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Proteolysis in plants: mechanisms and functions

https://doi.org/10.1007/bf00039386
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Outgoing claims: the papers this work cites, builds on, or argues with.

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The genomic organization and transcription of the ubiquitin genes of Trypanosoma cruzi.
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Perturbation of the ubiquitin system causes leaf curling, vascular tissue alterations and necrotic lesions in a higher plant.
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb07940.xopenalex-snapshot
UBA 1: an essential yeast gene encoding ubiquitin‐activating enzyme.
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05379.xopenalex-snapshot
In vivo function of the proteasome in the ubiquitin pathway.
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05540.xopenalex-snapshot
Identification of two structurally related proteins involved in proteolytic processing of precursors targeted to the chloroplast.
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb06080.xopenalex-snapshot
Degradation of Mos by the N‐terminal proline (Pro2)‐dependent ubiquitin pathway on fertilization of Xenopus eggs: possible significance of natural selection for Pro2 in Mos.
inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06878.xopenalex-snapshot
A proteasome inhibitor prevents activation of NF‐kappa B and stabilizes a newly phosphorylated form of I kappa B‐alpha that is still bound to NF‐kappa B.
inferredcites →https://doi.org/10.1002/j.1460-2075.1994.tb06948.xopenalex-snapshot
Regulated degradation of the transcription factor Gcn4.
inferredcites →https://doi.org/10.1006/bbrc.1993.2381openalex-snapshot
Characterization of cDNA for a Dehydration-Inducible Gene That Encodes a CLP A, B-like Protein in Arabidopsis thaliana L.
inferredcites →https://doi.org/10.1006/bbrc.1994.1342openalex-snapshot
Calcium-Dependent Proteinase Activity in Root Cultures of Arabidopsis
inferredcites →https://doi.org/10.1006/dbio.1994.1271openalex-snapshot
Genetic and Molecular Analysis of hyperplastic discs, a Gene Whose Product Is Required for Regulation of Cell Proliferation in Drosophila melanogaster Imaginal Discs and Germ Cells
inferredcites →https://doi.org/10.1006/jmbi.1995.0400openalex-snapshot
Homology in Structural Organization BetweenE. coliClpAP Protease and the Eukaryotic 26 S Proteasome
inferredcites →https://doi.org/10.1007/978-94-011-1884-2_7openalex-snapshot
Phytochrome degradation
inferredcites →https://doi.org/10.1007/bf00014491openalex-snapshot
Expression of stress-responsive ubiquitin genes in potato tubers
inferredcites →https://doi.org/10.1007/bf00020010openalex-snapshot
Maize polyubiquitin genes: structure, thermal perturbation of expression and transcript splicing, and promoter activity following transfer to protoplasts by electroporation
inferredcites →https://doi.org/10.1007/bf00023561openalex-snapshot
Homologues of wheat ubiquitin-conjugating enzymes - TaUBC1 and TaUBC4 are encoded by small multigene families in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00027161openalex-snapshot
Ubiquitin genes are differentially regulated in protoplast-derived cultures of Nicotiana sylvestris and in response to various stresses
inferredcites →https://doi.org/10.1007/bf00028809openalex-snapshot
Characterization of a cDNA clone encoding a chloroplast-targeted Clp homologue
inferredcites →https://doi.org/10.1007/bf00029013openalex-snapshot
Functional expression and molecular characterization of AtUBC2-1, a novel ubiquitin-conjugating enzyme (E2) from Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00039435openalex-snapshot
Nucleotide sequence of a wheat chloroplast gene encoding the proteolytic subunit of an ATP-dependent protease
inferredcites →https://doi.org/10.1007/bf00040634openalex-snapshot
Structure and expression of sunflower ubiquitin genes
inferredcites →https://doi.org/10.1007/bf00042223openalex-snapshot
Members of two gene families encoding ubiquitin-conjugating enzymes, AtUBC1-3 and AtUBC4-6, fromArabidopsis thaliana are differentially expressed
inferredcites →https://doi.org/10.1007/bf00279901openalex-snapshot
An Arabidopsis gene homologous to mammalian and insect genes encoding the largest proteasome subunit
inferredcites →https://doi.org/10.1007/bf00282648openalex-snapshot
A plastome mutation affects processing of both chloroplast and nuclear DNA-encoded plastid proteins
inferredcites →https://doi.org/10.1007/bf00339613openalex-snapshot
Characterization of a polyubiquitin gene from Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf00583906openalex-snapshot
Differential expression of several E2-type ubiquitin carrier protein genes at different developmental stages inArabidopsis thaliana andNicotiana sylvestris
inferredcites →https://doi.org/10.1007/bf01923511openalex-snapshot
Proteases and protein degradation inEscherichia coli
inferredcites →https://doi.org/10.1016/0014-5793(84)80089-7openalex-snapshot
ATP‐dependent proteolysis in pea chloroplasts
inferredcites →https://doi.org/10.1016/0014-5793(84)80090-3openalex-snapshot
Newly synthesized proteins are degraded by an ATP‐stimulated proteolytic process in isolated pea chloroplasts
inferredcites →https://doi.org/10.1016/0014-5793(92)80179-kopenalex-snapshot
Characterization of a prolyl endopeptidase from spinach thylakoids
inferredcites →https://doi.org/10.1016/0014-5793(92)80796-jopenalex-snapshot
Cloning and sequence analysis of a cDNA clone from Arabidopsis thaliana homologous to a proteasome α subunit from Drosophila
inferredcites →https://doi.org/10.1016/0014-5793(93)81757-qopenalex-snapshot
Ubiquitin found in the archaebacterium Thermoplasma acidophilum
inferredcites →https://doi.org/10.1016/0014-5793(94)00665-2openalex-snapshot
Existence of a molecular ruler in proteasomes suggested by analysis of degradation products
inferredcites →https://doi.org/10.1016/0092-8674(90)90104-mopenalex-snapshot
Protein degradation in the endoplasmic reticulum
inferredcites →https://doi.org/10.1016/0092-8674(91)90129-mopenalex-snapshot
Mammalian subtilisins: The long-sought dibasic processing endoproteases
inferredcites →https://doi.org/10.1016/0092-8674(92)90285-kopenalex-snapshot
The N-end rule
inferredcites →https://doi.org/10.1016/0092-8674(93)90364-vopenalex-snapshot
Anaphase is initiated by proteolysis rather than by the inactivation of maturation-promoting factor
inferredcites →https://doi.org/10.1016/0092-8674(93)90384-3openalex-snapshot
The HPV-16 E6 and E6-AP complex functions as a ubiquitin-protein ligase in the ubiquitination of p53
inferredcites →https://doi.org/10.1016/0092-8674(93)90426-qopenalex-snapshot
Multiple ubiquitin-conjugating enzymes participate in the in vivo degradation of the yeast MATα2 repressor
inferredcites →https://doi.org/10.1016/0092-8674(94)90193-7openalex-snapshot
The B-type cyclin kinase inhibitor p40SIC1 controls the G1 to S transition in S. cerevisiae
inferredcites →https://doi.org/10.1016/0092-8674(94)90396-4openalex-snapshot
The ubiquitin-proteasome proteolytic pathway
inferredcites →https://doi.org/10.1016/0092-8674(94)90509-6openalex-snapshot
Arabidopsis homeotic gene APETALA3 ectopic expression: Transcriptional and posttranscriptional regulation determine floral organ identity
inferredcites →https://doi.org/10.1016/0092-8674(95)90322-4openalex-snapshot
Cyclin Ubiquitination: The destructive end of mitosis
inferredcites →https://doi.org/10.1016/0092-8674(95)90338-0openalex-snapshot
A 20s complex containing CDC27 and CDC16 catalyzes the mitosis-specific conjugation of ubiquitin to cyclin B
inferredcites →https://doi.org/10.1016/0092-8674(95)90413-1openalex-snapshot
Ubiquitin is attached to membranes of baculovirus particles by a novel type of phospholipid anchor
inferredcites →https://doi.org/10.1016/0378-1119(91)90035-aopenalex-snapshot
The ubiquitin-encoding multigene family of flax, Linum usitatissimum
inferredcites →https://doi.org/10.1016/0896-6273(93)90182-qopenalex-snapshot
The Drosophila bendless gene encodes a neural protein related to ubiquitin-conjugating enzymes
inferredcites →https://doi.org/10.1016/0955-0674(95)80031-xopenalex-snapshot
Ubiquitin, proteasomes, and the regulation of intracellular protein degradation
inferredcites →https://doi.org/10.1016/0958-1669(92)90144-8openalex-snapshot
Novel applications of the ubiquitin-dependent proteolytic pathway in plant genetic engineering
inferredcites →https://doi.org/10.1016/s0021-9258(17)31879-3openalex-snapshot
The Pichia pastoris PAS4 gene encodes a ubiquitin-conjugating enzyme required for peroxisome assembly.
inferredcites →https://doi.org/10.1016/s0021-9258(17)31904-xopenalex-snapshot
PA700, an ATP-dependent activator of the 20 S proteasome, is an ATPase containing multiple members of a nucleotide-binding protein family.
inferredcites →https://doi.org/10.1016/s0021-9258(17)36780-7openalex-snapshot
Activation-dependent ubiquitination of a T cell antigen receptor subunit on multiple intracellular lysines.
inferredcites →https://doi.org/10.1016/s0021-9258(17)37244-7openalex-snapshot
A 26 S protease subunit that binds ubiquitin conjugates.
inferredcites →https://doi.org/10.1016/s0021-9258(17)38978-0openalex-snapshot
Purification and initial characterization of ubiquitin from the higher plant, Avena sativa.
inferredcites →https://doi.org/10.1016/s0021-9258(18)41573-6openalex-snapshot
ClpX, an alternative subunit for the ATP-dependent Clp protease of Escherichia coli. Sequence and in vivo activities.
inferredcites →https://doi.org/10.1016/s0021-9258(18)42026-1openalex-snapshot
Structure of a diubiquitin conjugate and a model for interaction with ubiquitin conjugating enzyme (E2).
inferredcites →https://doi.org/10.1016/s0021-9258(18)42110-2openalex-snapshot
Multiple forms of ubiquitin-activating enzyme E1 from wheat. Identification of an essential cysteine by in vitro mutagenesis.
inferredcites →https://doi.org/10.1016/s0021-9258(18)42154-0openalex-snapshot
THREE-DIMENSIONAL STRUCTURE OF A UBIQUITIN-CONJUGATING ENZYME (E2)
inferredcites →https://doi.org/10.1016/s0021-9258(18)42585-9openalex-snapshot
The interferon-inducible 15-kDa ubiquitin homolog conjugates to intracellular proteins.
inferredcites →https://doi.org/10.1016/s0021-9258(18)45583-4openalex-snapshot
Comparison of the three-dimensional structures of human, yeast, and oat ubiquitin.
inferredcites →https://doi.org/10.1016/s0021-9258(18)48343-3openalex-snapshot
A ubiquitin C-terminal isopeptidase that acts on polyubiquitin chains. Role in protein degradation.
inferredcites →https://doi.org/10.1016/s0021-9258(18)53218-xopenalex-snapshot
The multicatalytic and 26 S proteases.
inferredcites →https://doi.org/10.1016/s0021-9258(18)53509-2openalex-snapshot
PRE2, highly homologous to the human major histocompatibility complex-linked RING10 gene, codes for a yeast proteasome subunit necessary for chrymotryptic activity and degradation of ubiquitinated proteins.
inferredcites →https://doi.org/10.1016/s0021-9258(18)54026-6openalex-snapshot
A major ubiquitin conjugation system in wheat germ extracts involves a 15-kDa ubiquitin-conjugating enzyme (E2) homologous to the yeast UBC4/UBC5 gene products.
inferredcites →https://doi.org/10.1016/s0021-9258(18)54365-9openalex-snapshot
Cloning of a 16-kDa ubiquitin carrier protein from wheat and Arabidopsis thaliana. Identification of functional domains by in vitro mutagenesis.
inferredcites →https://doi.org/10.1016/s0021-9258(18)55470-3openalex-snapshot
Cloning of ubiquitin activating enzyme from wheat and expression of a functional protein in Escherichia coli.
inferredcites →https://doi.org/10.1016/s0021-9258(18)66641-4openalex-snapshot
Rapid degradation of apoplastocyanin in Cu(II)-deficient cells of Chlamydomonas reinhardtii.
inferredcites →https://doi.org/10.1016/s0021-9258(18)71584-6openalex-snapshot
Lysosomal (Vacuolar) Proteinases of Yeast Are Essential Catalysts for Protein Degradation, Differentiation, and Cell Survival
inferredcites →https://doi.org/10.1016/s0021-9258(18)83293-8openalex-snapshot
Increasing gene expression in yeast by fusion to ubiquitin
inferredcites →https://doi.org/10.1016/s0021-9258(18)83690-0openalex-snapshot
Ubiquitin-Phytochrome Conjugates
inferredcites →https://doi.org/10.1016/s0021-9258(18)92922-4openalex-snapshot
Three proteolytic systems in the yeast saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/s0021-9258(18)98465-6openalex-snapshot
Isolation of a cDNA encoding a mammalian multiubiquitinating enzyme (E225K) and overexpression of the functional enzyme in Escherichia coli
inferredcites →https://doi.org/10.1016/s0021-9258(19)36665-7openalex-snapshot
Purification and initial characterization of the proteasome from the higher plant Spinacia oleracea.
inferredcites →https://doi.org/10.1016/s0021-9258(19)38372-3openalex-snapshot
Ubiquitin extension proteins of Arabidopsis thaliana. Structure, localization, and expression of their promoters in transgenic tobacco.
inferredcites →https://doi.org/10.1016/s0021-9258(19)38379-6openalex-snapshot
Clp P represents a unique family of serine proteases.
inferredcites →https://doi.org/10.1016/s0021-9258(19)49552-5openalex-snapshot
Subcellular localization of ubiquitin and ubiquitinated proteins in Arabidopsis thaliana.
inferredcites →https://doi.org/10.1016/s0021-9258(19)74530-xopenalex-snapshot
Multiubiquitin chains linked through lysine 48 are abundant in vivo and are competent intermediates in the ubiquitin proteolytic pathway.
inferredcites →https://doi.org/10.1016/s0021-9258(20)30051-xopenalex-snapshot
Cucumisin, a serine protease from melon fruits, shares structural homology with subtilisin and is generated from a large precursor
inferredcites →https://doi.org/10.1016/s0031-9422(00)94191-8openalex-snapshot
Encyclopedia of plant physiology, New series
inferredcites →https://doi.org/10.1016/s0092-8674(00)80982-4openalex-snapshot
Ubiquitination of a Yeast Plasma Membrane Receptor Signals Its Ligand-Stimulated Endocytosis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81256-8openalex-snapshot
Plant Cells Contain Two Functionally Distinct Vacuolar Compartments
inferredcites →https://doi.org/10.1016/s0092-8674(85)80031-3openalex-snapshot
Production of abnormal proteins in E. coli stimulates transcription of ion and other heat shock genes
inferredcites →https://doi.org/10.1016/s0092-8674(94)90462-6openalex-snapshot
Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules
inferredcites →https://doi.org/10.1016/s0092-8674(94)90482-0openalex-snapshot
The ubiquitinproteasome pathway is required for processing the NF-κB1 precursor protein and the activation of NF-κB
inferredcites →https://doi.org/10.1016/s0092-8674(94)90502-9openalex-snapshot
Ubiquitin-dependent c-Jun degradation in vivo is mediated by the δ domain
inferredcites →https://doi.org/10.1016/s0960-9822(95)00153-9openalex-snapshot
The first characterization of a eubacterial proteasome: the 20S complex of Rhodococcus
inferredcites →https://doi.org/10.1021/bi00034a025openalex-snapshot
Scanning Transmission Electron Microscopy and Small-Angle Scattering Provide Evidence that Native Escherichia coli ClpP is a Tetradecamer with an Axial Pore
inferredcites →https://doi.org/10.1021/bi00213a009openalex-snapshot
Tertiary structures of class I ubiquitin-conjugating enzymes are highly conserved: Crystal structure of yeast Ubc4
inferredcites →https://doi.org/10.1021/bi00421a001openalex-snapshot
Cotranslational processing and protein turnover in eukaryotic cells
inferredcites →https://doi.org/10.1021/bi00428a048openalex-snapshot
Ubiquitin-dependent proteolytic pathway in wheat germ: isolation of multiple forms of ubiquitin-activating enzyme, E1
inferredcites →https://doi.org/10.1021/bi00440a046openalex-snapshot
Partial purification and peptide mapping of ubiquitin-phytochrome conjugates from oat
inferredcites →https://doi.org/10.1034/j.1399-3054.1994.910210.xopenalex-snapshot
Changes in protein ubiquitination and the expression of ubiquitin-encoding transcripts in daylily petals during floral development and senescence
inferredcites →https://doi.org/10.1038/333090a0openalex-snapshot
Heavy-chain binding protein recognizes aberrant polypeptides translocated in vitro
inferredcites →https://doi.org/10.1038/338394a0openalex-snapshot
The tails of ubiquitin precursors are ribosomal proteins whose fusion to ubiquitin facilitates ribosome biogenesis
inferredcites →https://doi.org/10.1038/346287a0openalex-snapshot
Cis-trans recognition and subunit-specific degradation of short-lived proteins
inferredcites →https://doi.org/10.1038/349132a0openalex-snapshot
Cyclin is degraded by the ubiquitin pathway
inferredcites →https://doi.org/10.1038/357375a0openalex-snapshot
Proteolysis, proteasomes and antigen presentation
inferredcites →https://doi.org/10.1038/359073a0openalex-snapshot
The Pas2 protein essential for peroxisome biogenesis is related to ubiquitin-conjugating enzymes
inferredcites →https://doi.org/10.1038/360597a0openalex-snapshot
Ornithine decarboxylase is degraded by the 26S proteasome without ubiquitination
inferredcites →https://doi.org/10.1038/364161a0openalex-snapshot
Arabidopsis auxin-resistance gene AXR1 encodes a protein related to ubiquitin-activating enzyme E1
inferredcites →https://doi.org/10.1038/365264a0openalex-snapshot
γ-Interferon and expression of MHC genes regulate peptide hydrolysis by proteasomes
inferredcites →https://doi.org/10.1038/366313a0openalex-snapshot
The yeast DOA4 gene encodes a deubiquitinating enzyme related to a product of the human tre-2 oncogene
inferredcites →https://doi.org/10.1038/366355a0openalex-snapshot
Defective mitosis due to a mutation in the gene for a fission yeast 26S protease subunit
inferredcites →https://doi.org/10.1038/366358a0openalex-snapshot
S. cerevisiae 26S protease mutants arrest cell division in G2/metaphase
inferredcites →https://doi.org/10.1038/373078a0openalex-snapshot
Role of a ubiquitin-conjugating enzyme in degradation of S- and M-phase cyclins
inferredcites →https://doi.org/10.1038/373081a0openalex-snapshot
Protein ubiquitination involving an E1–E2–E3 enzyme ubiquitin thioester cascade
inferredcites →https://doi.org/10.1038/379066a0openalex-snapshot
A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis
inferredcites →https://doi.org/10.1042/bj2910001openalex-snapshot
Proteasomes: multicatalytic proteinase complexes
inferredcites →https://doi.org/10.1046/j.1365-313x.1992.t01-5-00999.xopenalex-snapshot
Temporal and spatial expression of a thiolprotease gene during pea ovary senescence, and its regulation by gibberellin
inferredcites →https://doi.org/10.1046/j.1365-313x.1993.03040545.xopenalex-snapshot
Homologs of the essential ubiquitin conjugating enzymes UBC1, 4, and 5 in yeast are encoded by a multigene family in Arabidopsis thaliana
inferredcites →https://doi.org/10.1046/j.1365-313x.1993.04020327.xopenalex-snapshot
Arabidopsis mutants compromised for the control of cellular damage during pathogenesis and aging
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6040537.xopenalex-snapshot
Molecular characterization of a β‐type proteasome subunit from Arabidopsis thaliana co‐expressed at a high level with an α‐type proteasome subunit early in the cell cycle
inferredcites →https://doi.org/10.1046/j.1365-313x.1997.11020213.xopenalex-snapshot
The ubiquitin‐activating enzyme (E1) gene family in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.79.6.1869openalex-snapshot
Liver mitochondria contain an ATP-dependent, vanadate-sensitive pathway for the degradation of proteins.
inferredcites →https://doi.org/10.1073/pnas.80.9.2632openalex-snapshot
Rapid degradation of unassembled ribulose 1,5-bisphosphate carboxylase small subunits in chloroplasts
inferredcites →https://doi.org/10.1073/pnas.81.5.1380openalex-snapshot
Regulation of protein metabolism: Coupling of photosynthetic electron transport to in vivo degradation of the rapidly metabolized 32-kilodalton protein of the chloroplast membranes
inferredcites →https://doi.org/10.1073/pnas.84.2.359openalex-snapshot
Red light-induced formation of ubiquitin-phytochrome conjugates: Identification of possible intermediates of phytochrome degradation
inferredcites →https://doi.org/10.1073/pnas.86.24.9861openalex-snapshot
A ubiquitin carrier protein from wheat germ is structurally and functionally similar to the yeast DNA repair enzyme encoded by RAD6.
inferredcites →https://doi.org/10.1073/pnas.86.8.2540openalex-snapshot
Ubiquitin fusion augments the yield of cloned gene products in Escherichia coli.
inferredcites →https://doi.org/10.1073/pnas.87.11.4038openalex-snapshot
Chlorophyll regulates accumulation of the plastid-encoded chlorophyll apoproteins CP43 and D1 by increasing apoprotein stability.
inferredcites →https://doi.org/10.1073/pnas.87.9.3513openalex-snapshot
Conservation of the regulatory subunit for the Clp ATP-dependent protease in prokaryotes and eukaryotes.
inferredcites →https://doi.org/10.1073/pnas.88.22.10297openalex-snapshot
Cloning and characterization of a 20-kDa ubiquitin carrier protein from wheat that catalyzes multiubiquitin chain formation in vitro.
inferredcites →https://doi.org/10.1073/pnas.89.1.295openalex-snapshot
Tsp: a tail-specific protease that selectively degrades proteins with nonpolar C termini.
inferredcites →https://doi.org/10.1073/pnas.89.6.2017openalex-snapshot
Early hydrogen-bonding events in the folding reaction of ubiquitin.
inferredcites →https://doi.org/10.1073/pnas.90.2.418openalex-snapshot
Use of a reporter transgene to generate arabidopsis mutants in ubiquitin-dependent protein degradation.
inferredcites →https://doi.org/10.1073/pnas.91.1.326openalex-snapshot
Early auxin-induced genes encode short-lived nuclear proteins.
inferredcites →https://doi.org/10.1073/pnas.91.17.8082openalex-snapshot
The ctpA gene encodes the C-terminal processing protease for the D1 protein of the photosystem II reaction center complex.
inferredcites →https://doi.org/10.1073/pnas.91.25.11802openalex-snapshot
Identification of a 50-kDa systemin-binding protein in tomato plasma membranes having Kex2p-like properties.
inferredcites →https://doi.org/10.1073/pnas.91.25.12218openalex-snapshot
A molecular chaperone, ClpA, functions like DnaK and DnaJ.
inferredcites →https://doi.org/10.1073/pnas.92.20.9117openalex-snapshot
Redirecting the specificity of ubiquitination by modifying ubiquitin-conjugating enzymes.
inferredcites →https://doi.org/10.1073/pnas.92.7.2563openalex-snapshot
A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase.
inferredcites →https://doi.org/10.1073/pnas.93.2.856openalex-snapshot
Arabidopsis MBP1 gene encodes a conserved ubiquitin recognition component of the 26S proteasome.
inferredcites →https://doi.org/10.1073/pnas.93.2.861openalex-snapshot
Surface hydrophobic residues of multiubiquitin chains essential for proteolytic targeting.
inferredcites →https://doi.org/10.1074/jbc.270.29.17442openalex-snapshot
A Proteolytic Pathway That Recognizes Ubiquitin as a Degradation Signal
inferredcites →https://doi.org/10.1074/jbc.270.30.18099openalex-snapshot
An Essential Yeast Gene Encoding a Homolog of Ubiquitin-activating Enzyme
inferredcites →https://doi.org/10.1074/jbc.270.40.23726openalex-snapshot
Molecular Cloning and Expression of a 26 S Protease Subunit Enriched in Dileucine Repeats
inferredcites →https://doi.org/10.1074/jbc.270.50.29660openalex-snapshot
Inhibition of Ubiquitin-mediated Proteolysis by the Arabidopsis 26 S Protease Subunit S5a
inferredcites →https://doi.org/10.1074/jbc.270.8.3720openalex-snapshot
Ubiquitin in the Prokaryote Anabaena variabilis
inferredcites →https://doi.org/10.1074/jbc.271.1.302openalex-snapshot
Isolation, Characterization, and Partial Purification of a Novel Ubiquitin-Protein Ligase, E3
inferredcites →https://doi.org/10.1074/jbc.271.21.12150openalex-snapshot
The Arabidopsis thaliana UBC7/13/14 Genes Encode a Family of Multiubiquitin Chain-forming E2 Enzymes
inferredcites →https://doi.org/10.1093/genetics/139.2.921openalex-snapshot
Structure and evolution of genes encoding polyubiquitin and ubiquitin-like proteins in Arabidopsis thaliana ecotype Columbia.
inferredcites →https://doi.org/10.1093/oso/9780198577355.003.0001openalex-snapshot
Ubiquitin and Ubiquitin Genes in Higher Plants
inferredcites →https://doi.org/10.1096/fasebj.1.5.2824267openalex-snapshot
Molecular determinants of protein half‐lives in eukaryotic cells
inferredcites →https://doi.org/10.1101/gad.8.7.811openalex-snapshot
Specific complex formation between yeast RAD6 and RAD18 proteins: a potential mechanism for targeting RAD6 ubiquitin-conjugating activity to DNA damage sites.
inferredcites →https://doi.org/10.1104/pp.100.3.1126openalex-snapshot
Turnover of 1-Aminocyclopropane-1-Carboxylic Acid Synthase Protein in Wounded Tomato Fruit Tissue
inferredcites →https://doi.org/10.1104/pp.102.1.125openalex-snapshot
Group 3 Late Embryogenesis Abundant Proteins in Desiccation-Tolerant Seedlings of Wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1104/pp.103.2.585openalex-snapshot
A Purified Zinc Protease of Pea Chloroplasts, EP1, Degrades the Large Subunit of Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase
inferredcites →https://doi.org/10.1104/pp.103.3.805openalex-snapshot
Gene Expression Patterns Associated with in Vitro Tracheary Element Formation in Isolated Single Mesophyll Cells of Zinnia elegans
inferredcites →https://doi.org/10.1104/pp.106.2.529openalex-snapshot
The Apparent Turnover of 1-Aminocyclopropane-1-Carboxylate Synthase in Tomato Cells Is Regulated by Protein Phosphorylation and Dephosphorylation
inferredcites →https://doi.org/10.1104/pp.106.3.817openalex-snapshot
Posttranslational Regulation of Nitrate Reductase in Higher Plants
inferredcites →https://doi.org/10.1104/pp.108.2.489openalex-snapshot
In Situ Detection of nDNA Fragmentation during the Differentiation of Tracheary Elements in Higher Plants
inferredcites →https://doi.org/10.1104/pp.109.4.1309openalex-snapshot
Examination of the Contribution of Vacuolar Proteases to Intracellular Protein Degradation in Chara corallina
inferredcites →https://doi.org/10.1104/pp.109.4.1371openalex-snapshot
Isolation of a Polyubiquitin Promoter and Its Expression in Transgenic Potato Plants
inferredcites →https://doi.org/10.1104/pp.110.1.241openalex-snapshot
Induction and Regulation of Heat-Shock Gene Expression by an Amino Acid Analog in Soybean Seedlings
inferredcites →https://doi.org/10.1104/pp.110.2.521openalex-snapshot
Isolation of Intact Protein Storage Vacuoles from Barley Aleurone (Identification of Aspartic and Cysteine Proteases)
inferredcites →https://doi.org/10.1104/pp.81.2.603openalex-snapshot
Neutral Peptidases in the Stroma of Pea Chloroplasts
inferredcites →https://doi.org/10.1104/pp.84.2.225openalex-snapshot
Catalase Degradation in Sunflower Cotyledons during Peroxisome Transition from Glyoxysomal to Leaf Peroxisomal Function
inferredcites →https://doi.org/10.1104/pp.84.2.332openalex-snapshot
Demonstration of ATP-Dependent, Ubiquitin-Conjugating Activities in Higher Plants
inferredcites →https://doi.org/10.1104/pp.90.2.380openalex-snapshot
Red Light-Induced Accumulation of Ubiquitin-Phytochrome Conjugates in Both Monocots and Dicots
inferredcites →https://doi.org/10.1104/pp.94.2.710openalex-snapshot
High Performance Liquid Chromatography Resolution of Ubiquitin Pathway Enzymes from Wheat Germ
inferredcites →https://doi.org/10.1105/tpc.1.4.447openalex-snapshot
Functional Implications of the Subcellular Localization of Ethylene-Induced Chitinase and [beta]-1,3-Glucanase in Bean Leaves.
inferredcites →https://doi.org/10.1105/tpc.2.8.769openalex-snapshot
Hormonal Regulation, Processing, and Secretion of Cysteine Proteinases in Barley Aleurone Layers
inferredcites →https://doi.org/10.1105/tpc.3.5.497openalex-snapshot
Increased expression of the maize immunoglobulin binding protein homolog b-70 in three zein regulatory mutants.
inferredcites →https://doi.org/10.1105/tpc.4.3.307openalex-snapshot
Proaleurain Vacuolar Targeting Is Mediated by Short Contiguous Peptide Interactions
inferredcites →https://doi.org/10.1105/tpc.5.5.553openalex-snapshot
Developmental and age-related processes that influence the longevity and senescence of photosynthetic tissues in arabidopsis.
inferredcites →https://doi.org/10.1105/tpc.6.7.967openalex-snapshot
Novel vascular cell-specific genes whose expression is regulated temporally and spatially during vascular system development.
inferredcites →https://doi.org/10.1105/tpc.6.9.1289openalex-snapshot
An Arabidopsis peptide transporter is a member of a new class of membrane transport proteins.
inferredcites →https://doi.org/10.1105/tpc.7.10.1713openalex-snapshot
The stroma of higher plant plastids contain ClpP and ClpC, functional homologs of Escherichia coli ClpP and ClpA: an archetypal two-component ATP-dependent protease.
inferredcites →https://doi.org/10.1105/tpc.7.11.1893openalex-snapshot
Induction of wound response genes in tomato leaves by bestatin, an inhibitor of aminopeptidases.
inferredcites →https://doi.org/10.1105/tpc.7.5.611openalex-snapshot
Post-transcriptional regulation of nitrate reductase by light is abolished by an N-terminal deletion.
inferredcites →https://doi.org/10.1105/tpc.7.6.785openalex-snapshot
A nodule-specific gene encoding a subtilisin-like protease is expressed in early stages of actinorhizal nodule development.
inferredcites →https://doi.org/10.1105/tpc.7.7.845openalex-snapshot
Regulation of Protein Degradation
inferredcites →https://doi.org/10.1105/tpc.7.7.859openalex-snapshot
Nitrate: Nutrient and Signal for Plant Growth
inferredcites →https://doi.org/10.1111/j.1399-3054.1994.tb05343.xopenalex-snapshot
Molecular analysis of natural leaf senescence in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-6576.1974.tb00708.xopenalex-snapshot
Regulation of Protein Metabolism
inferredcites →https://doi.org/10.1111/j.1432-1033.1992.tb19822.xopenalex-snapshot
The mechanism and functions of ATP‐dependent proteases in bacterial and animal cells
inferredcites →https://doi.org/10.1111/j.1751-1097.1990.tb01746.xopenalex-snapshot
PHOTOMORPHOGENESIS IN PLANTS
inferredcites →https://doi.org/10.1126/science.1962196openalex-snapshot
The N-End Rule in Bacteria
inferredcites →https://doi.org/10.1126/science.253.5022.895openalex-snapshot
A Polypeptide from Tomato Leaves Induces Wound-Inducible Proteinase Inhibitor Proteins
inferredcites →https://doi.org/10.1126/science.2530630openalex-snapshot
The Neuron-Specific Protein PGP 9.5 Is a Ubiquitin Carboxyl-Terminal Hydrolase
inferredcites →https://doi.org/10.1126/science.2538923openalex-snapshot
A Multiubiquitin Chain Is Confined to Specific Lysine in a Targeted Short-Lived Protein
inferredcites →https://doi.org/10.1126/science.270.5243.1828openalex-snapshot
Control of Cell Fate by a Deubiquitinating Enzyme Encoded by the fat facets Gene
inferredcites →https://doi.org/10.1126/science.271.5251.990openalex-snapshot
Role of a Peptide Tagging System in Degradation of Proteins Synthesized from Damaged Messenger RNA
inferredcites →https://doi.org/10.1126/science.2799391openalex-snapshot
A Role for a 70-Kilodalton Heat Shock Protein in Lysosomal Degradation of Intracellular Proteins
inferredcites →https://doi.org/10.1126/science.3018930openalex-snapshot
In Vivo Half-Life of a Protein Is a Function of Its Amino-Terminal Residue
inferredcites →https://doi.org/10.1126/science.3083508openalex-snapshot
Abnormal Proteins Serve as Eukaryotic Stress Signals and Trigger the Activation of Heat Shock Genes
inferredcites →https://doi.org/10.1126/science.7624798openalex-snapshot
Role of the Ubiquitin-Proteasome Pathway in Regulating Abundance of the Cyclin-Dependent Kinase Inhibitor p27
inferredcites →https://doi.org/10.1126/science.7725095openalex-snapshot
Functions of the Proteasome: the Lysis at the End of the Tunnel
inferredcites →https://doi.org/10.1126/science.7725096openalex-snapshot
From the Cradle to the Grave: Ring Complexes in the Life of a Protein
inferredcites →https://doi.org/10.1126/science.7725097openalex-snapshot
Crystal Structure of the 20 S Proteasome from the Archaeon T. acidophilum at 3.4 Å Resolution
inferredcites →https://doi.org/10.1126/science.7725107openalex-snapshot
Proteasome from Thermoplasma acidophilum : a Threonine Protease
inferredcites →https://doi.org/10.1126/science.7732382openalex-snapshot
Inhibition of Proteasome Activities and Subunit-Specific Amino-Terminal Threonine Modification by Lactacystin
inferredcites →https://doi.org/10.1126/science.7878466openalex-snapshot
Control of IκB-α Proteolysis by Site-Specific, Signal-Induced Phosphorylation
inferredcites →https://doi.org/10.1126/science.8073290openalex-snapshot
Degradation of G alpha by the N-end rule pathway
inferredcites →https://doi.org/10.1126/science.8122109openalex-snapshot
Heat-Inducible Degron: a Method for Constructing Temperature-Sensitive Mutants
inferredcites →https://doi.org/10.1126/science.8493533openalex-snapshot
Regulation of V(D)J Recombination Activator Protein RAG-2 by Phosphorylation
inferredcites →https://doi.org/10.1128/mcb.14.12.7876openalex-snapshot
Stress resistance in Saccharomyces cerevisiae is strongly correlated with assembly of a novel type of multiubiquitin chain.
inferredcites →https://doi.org/10.1128/mcb.14.12.7876-7883.1994openalex-snapshot
Stress Resistance in Saccharomyces cerevisiae Is Strongly Correlated with Assembly of a Novel Type of Multiubiquitin Chain
inferredcites →https://doi.org/10.1128/mcb.15.2.731openalex-snapshot
p34 Cdc28 -Mediated Control of Cln3 Cyclin Degradation
inferredcites →https://doi.org/10.1128/mcb.15.3.1265openalex-snapshot
A Ubiquitin Mutant with Specific Defects in DNA Repair and Multiubiquitination
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Oligopeptidase B of Dioscorea Opposita “Nagaimo”: Isolation, Biochemical Characterization, and Primary Structure
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Programmed Cell Death in Plants in Response to Pathogen Attack
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Proteinase Inhibitors
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The PCI Complexes and the Ubiquitin Proteasome System ( UPS ) in Plant Development
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The PCI Complexes and the Ubiquitin Proteasome System (UPS) in Plant Development
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Advances in Protein Production Technologies
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Characterization of Helicoverpa armigera gut proteinases and their interaction with proteinase inhibitors using gel X‐ray film contact print technique
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Ripening tomato fruit after chilling storage alters protein turnover
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Effect of early cold stress on the maturation of rice anthers
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Degradation mechanisms of the Tomato yellow leaf curl virus coat protein following inoculation of tomato plants by the whitefly Bemisia tabaci
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Partial Purification and Characterization of a Ca2+-Dependent Proteinase fromArabidopsisRoots
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Catalytic Activities of the 20 S Proteasome, a Multicatalytic Proteinase Complex
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The impact of potato cysteine proteinases in plant growth and development
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Purification of a Multicatalytic Protease Complex from Developing Winged Bean Seeds by Indirect Immunoaffinity Chromatography
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PHYTOCHROME DEGRADATION AND DARK REVERSION
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Programmed Cell Death in Dinoflagellates
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Fate and Activities of Plastids During Leaf Senescence
inferred← citeshttps://doi.org/10.1007/978-1-4615-4707-5_7openalex-snapshot
Transformation of Cereals
inferred← citeshttps://doi.org/10.1007/978-1-4615-5925-2_7openalex-snapshot
Regulation of Protein Degradation in Plants
inferred← citeshttps://doi.org/10.1007/978-1-4939-2202-4_5openalex-snapshot
Towards Using Biotechnology to Modify Soybean Seeds as Protein Bioreactors
inferred← citeshttps://doi.org/10.1007/978-1-4939-2639-8_8openalex-snapshot
A Flowchart to Analyze Protease Activity in Plant Mitochondria
inferred← citeshttps://doi.org/10.1007/978-1-59259-346-0_11openalex-snapshot
Expression of Recombinant Proteins via the Plastid Genome
inferred← citeshttps://doi.org/10.1007/978-3-662-04064-5_11openalex-snapshot
Protein Hydrolysis and Nitrogen Remobilisation in Plant Life and Senescence
inferred← citeshttps://doi.org/10.1007/978-81-322-1620-9openalex-snapshot
Approaches to Plant Stress and their Management
inferred← citeshttps://doi.org/10.1007/978-81-322-1620-9_10openalex-snapshot
Photosynthesis and Associated Aspects Under Abiotic Stresses Environment
inferred← citeshttps://doi.org/10.1007/978-94-010-0934-8_12openalex-snapshot
Plant proteolytic enzymes: possible roles during programmed cell death
inferred← citeshttps://doi.org/10.1007/978-94-010-0934-8_13openalex-snapshot
Caspase-like protease involvement in the control of plant cell death
inferred← citeshttps://doi.org/10.1007/978-94-010-0934-8_3openalex-snapshot
Programmed cell death in plant reproduction
inferred← citeshttps://doi.org/10.1007/978-94-017-2687-0_10openalex-snapshot
Pathogenesis-Related Proteins and Disease Resistance
inferred← citeshttps://doi.org/10.1007/bf03355953openalex-snapshot
Characterization of Insect Proteinases and Their Inhibition by Finger and Little Millet Inhibitors
inferred← citeshttps://doi.org/10.1007/s002940050282openalex-snapshot
Arabidopsis thaliana RAD6 homolog AtUBC2 complements UV sensitivity, but not N-end rule degradation deficiency, of Saccharomyces cerevisiae rad6 mutants
inferred← citeshttps://doi.org/10.1007/s00299-002-0493-5openalex-snapshot
A test of fusion protein stability in the plant Arabidopsis thaliana reveals degradation signals from ACC synthase and from the plant N-end rule pathway
inferred← citeshttps://doi.org/10.1007/s00299-016-2067-yopenalex-snapshot
Differential proteome analysis during early somatic embryogenesis in Musa spp. AAA cv. Grand Naine
inferred← citeshttps://doi.org/10.1007/s002990050501openalex-snapshot
Tobacco plants perturbed in the ubiquitin-dependent protein degradation system accumulate callose, salicylic acid, and pathogenesis-related protein 1
inferred← citeshttps://doi.org/10.1007/s00425-006-0292-2openalex-snapshot
A nuclear-encoded ClpP subunit of the chloroplast ATP-dependent Clp protease is essential for early development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00425-006-0469-8openalex-snapshot
Characterization of a stress responsive proteinase inhibitor gene with positive effect in improving drought resistance in rice
inferred← citeshttps://doi.org/10.1007/s00425-011-1554-1openalex-snapshot
From callus to embryo: a proteomic view on the development and maturation of somatic embryos in Cyclamen persicum
inferred← citeshttps://doi.org/10.1007/s00425-015-2346-9openalex-snapshot
Zebra chip disease decreases tuber (Solanum tuberosum L.) protein content by attenuating protease inhibitor levels and increasing protease activities
inferred← citeshttps://doi.org/10.1007/s00425-015-2374-5openalex-snapshot
Quantitative proteomics analysis reveals that S-nitrosoglutathione reductase (GSNOR) and nitric oxide signaling enhance poplar defense against chilling stress
inferred← citeshttps://doi.org/10.1007/s004250050045openalex-snapshot
Leucine aminopeptidases: the ubiquity of LAP-N and the specificity of LAP-A
inferred← citeshttps://doi.org/10.1007/s004250050344openalex-snapshot
Degradation of active-oxygen-modified ribulose-1,5-bisphosphate carboxylase/oxygenase by chloroplastic proteases requires ATP-hydrolysis
inferred← citeshttps://doi.org/10.1007/s004250050637openalex-snapshot
Proteolytic cleavage of plant proteins by peroxisomal endoproteases from senescent pea leaves
inferred← citeshttps://doi.org/10.1007/s004250050698openalex-snapshot
A survey of proteinases active during meiotic development
inferred← citeshttps://doi.org/10.1007/s00497-003-0182-8openalex-snapshot
Involvement of the ubiquitin/proteasome pathway in the organisation and polarised growth of kiwifruit pollen tubes
inferred← citeshttps://doi.org/10.1007/s004970050196openalex-snapshot
Ubiquitin and ubiquitin-conjugated proteins in the olive ( olea europaea l.) pollen
inferred← citeshttps://doi.org/10.1007/s00726-010-0820-zopenalex-snapshot
Prey-induced changes in the accumulation of amino acids and phenolic metabolites in the leaves of Drosera capensis L
inferred← citeshttps://doi.org/10.1007/s10142-008-0081-zopenalex-snapshot
Dehydrin gene expression provides an indicator of low temperature and drought stress: transcriptome-based analysis of Barley (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1007/s10535-008-0133-1openalex-snapshot
Involvement of exopeptidases in dehydration tolerance of spring wheat seedlings
inferred← citeshttps://doi.org/10.1007/s10709-019-00080-4openalex-snapshot
Genome-wide identification, phylogenetic and expression analysis of the maize HECT E3 ubiquitin ligase genes
inferred← citeshttps://doi.org/10.1007/s10725-006-9163-xopenalex-snapshot
Nickel toxicity inhibits ribonuclease and protease activities in rice seedlings: protective effects of proline
inferred← citeshttps://doi.org/10.1007/s10725-011-9609-7openalex-snapshot
Two calcium dependent protein kinases are differently regulated by light and have different activity patterns during seedling growth in Pharbitis nil
inferred← citeshttps://doi.org/10.1007/s11032-018-0868-0openalex-snapshot
Association mapping of days to flowering in common bean (Phaseolus vulgaris L.) revealed by DArT markers
inferred← citeshttps://doi.org/10.1007/s11033-007-9124-0openalex-snapshot
A novel Otubain-like cysteine protease gene is preferentially expressed during somatic embryogenesis in Pinus radiata
inferred← citeshttps://doi.org/10.1007/s11103-007-9241-0openalex-snapshot
Genome-wide analysis of Arabidopsis responsive transcriptome to nitrogen limitation and its regulation by the ubiquitin ligase gene NLA
inferred← citeshttps://doi.org/10.1007/s11103-008-9300-1openalex-snapshot
Identification of early senescence-associated genes in rice flag leaves
inferred← citeshttps://doi.org/10.1007/s11103-017-0633-5openalex-snapshot
UBIQUITIN-SPECIFIC PROTEASES function in plant development and stress responses
inferred← citeshttps://doi.org/10.1007/s11103-021-01177-1openalex-snapshot
Calmodulin7: recent insights into emerging roles in plant development and stress
inferred← citeshttps://doi.org/10.1007/s11306-017-1267-yopenalex-snapshot
A combination of stomata deregulation and a distinctive modulation of amino acid metabolism are associated with enhanced tolerance of wheat varieties to transient drought
inferred← citeshttps://doi.org/10.1007/s11738-003-0012-5openalex-snapshot
Proteolysis and expression of the cysteine protease gene in senescing cut leaves of Hosta ‘Undulata Erromena’ and Zantedeschia aethiopica Spr. treated with BA or GA3
inferred← citeshttps://doi.org/10.1007/s11738-008-0219-6openalex-snapshot
Purification and characterization of a salinity induced alkaline protease from isolated spinach chloroplasts
inferred← citeshttps://doi.org/10.1007/s11738-013-1288-8openalex-snapshot
Micropropagation of Hohenbergia penduliflora (A. Rich.) Mez. for sustainable production of plant proteases
inferred← citeshttps://doi.org/10.1007/s11738-018-2683-yopenalex-snapshot
Drought stress during soybean seed filling affects storage compounds through regulation of lipid and protein metabolism
inferred← citeshttps://doi.org/10.1007/s11816-012-0265-9openalex-snapshot
Proteome analysis of chlorotic leaves of the Arabidopsis mex1 mutant defective in the mobilization of starch degradation products
inferred← citeshttps://doi.org/10.1007/s11816-021-00736-8openalex-snapshot
Comparative transcriptome analysis of spinach in response to insect herbivory
inferred← citeshttps://doi.org/10.1007/s12010-012-9882-6openalex-snapshot
Use of Transgenic Oryzacystatin-I-Expressing Plants Enhances Recombinant Protein Production
inferred← citeshttps://doi.org/10.1007/s12010-013-0342-8openalex-snapshot
Molecular Dynamic and Docking Interaction Study of Heterodera glycines Serine Proteinase with Vigna mungo Proteinase Inhibitor
inferred← citeshttps://doi.org/10.1007/s12010-014-1376-2openalex-snapshot
A Cysteine Protease Isolated from the Latex of Ficus microcarpa: Purification and Biochemical Characterization
inferred← citeshttps://doi.org/10.1007/s12298-012-0128-4openalex-snapshot
Proteolytic activities in Phaseolus vulgaris cotyledons under copper stress
inferred← citeshttps://doi.org/10.1007/s12374-016-0455-zopenalex-snapshot
Sugar starvation induces the central vacuolation with coordinated increase in expression of tonoplast intrinsic protein genes in suspension-cultured rice cells
inferred← citeshttps://doi.org/10.1007/s13237-018-0255-6openalex-snapshot
Ubiquitination: a tool for plant adaptation to changing environments
inferred← citeshttps://doi.org/10.1007/s13562-016-0385-3openalex-snapshot
Transcriptomic and proteomic analysis of yellow mosaic diseased soybean
inferred← citeshttps://doi.org/10.1016/b978-0-12-801536-0.00004-9openalex-snapshot
Use of proteomics to evaluate soybean response under abiotic stresses
inferred← citeshttps://doi.org/10.1016/b978-0-12-813066-7.00009-7openalex-snapshot
Genome-Wide Association Studies (GWAS) for Abiotic Stress Tolerance in Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-817562-0.00003-3openalex-snapshot
Effect of High Temperature on Protein Metabolism in Plants
inferred← citeshttps://doi.org/10.1016/b978-012372484-7/50014-xopenalex-snapshot
Cyanophytochromes, Bacteriophytochromes, and Plant Phytochromes
inferred← citeshttps://doi.org/10.1016/j.algal.2026.104825openalex-snapshot
Comparative genomics reveals the ecological adaptation of Paralia guyana to both planktonic and benthic habitats
inferred← citeshttps://doi.org/10.1016/j.anifeedsci.2019.03.003openalex-snapshot
Influence of storage length and inoculation with Lactobacillus buchneri on the fermentation, aerobic stability, and ruminal degradability of high-moisture corn and rehydrated corn grain silage
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2004.10.005openalex-snapshot
Ubiquitin family proteins and their relationship to the proteasome: a structural perspective
inferred← citeshttps://doi.org/10.1016/j.bbrep.2025.102071openalex-snapshot
Isolation, biochemical characterization, and primary structure and active site determination of Dioscorea opposita (‘Nagaimo’) oligopeptidase B
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2014.01.047openalex-snapshot
Identification and characterization of MOR-CP, a cysteine protease induced by ozone and developmental senescence in maize (Zea mays L.) leaves
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2014.07.005openalex-snapshot
Roles of ubiquitination-mediated protein degradation in plant responses to abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.fitote.2004.04.006openalex-snapshot
Proteolytic properties of Funastrum clausum latex
inferred← citeshttps://doi.org/10.1016/j.hal.2012.03.007openalex-snapshot
Occurrence of toxic Prymnesium parvum blooms with high protease activity is related to fish mortality in Hungarian ponds
inferred← citeshttps://doi.org/10.1016/j.indcrop.2018.11.036openalex-snapshot
Latex from Tabernaemontana catharinensis (A. DC)—Apocynaceae: An alternative for the sustainable production of biologically active compounds
inferred← citeshttps://doi.org/10.1016/j.jafr.2023.100496openalex-snapshot
Potentials of baobab: A complement to cocoa production
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.122063openalex-snapshot
Transcriptome sequencing analysis reveals silver nanoparticles antifungal molecular mechanism of the soil fungi Fusarium solani species complex
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2022.112443openalex-snapshot
SWATH-based quantitative proteomic analysis of Morus alba L. leaves after exposure to ultraviolet-B radiation and incubation in the dark
inferred← citeshttps://doi.org/10.1016/j.jplph.2006.03.009openalex-snapshot
Physiology and biochemistry of source-regulated protein accumulation in the wheat grain
inferred← citeshttps://doi.org/10.1016/j.jplph.2009.05.007openalex-snapshot
Cytokinin-induced changes of nitrogen remobilization and chloroplast ultrastructure in wheat (Triticum aestivum)
inferred← citeshttps://doi.org/10.1016/j.jplph.2013.06.007openalex-snapshot
A novel aspartic acid protease gene from pineapple fruit (Ananas comosus): Cloning, characterization and relation to postharvest chilling stress resistance
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.05.005openalex-snapshot
Transcriptome analysis reveals potential roles of a barley ASR gene that confers stress tolerance in transgenic rice
inferred← citeshttps://doi.org/10.1016/j.jplph.2019.153055openalex-snapshot
Beneficial implications of sugar beet proteinase inhibitor BvSTI on plant architecture and salt stress tolerance in Lotus corniculatus L.
inferred← citeshttps://doi.org/10.1016/j.jprot.2016.04.048openalex-snapshot
Proteomic analysis of two divergently responding potato genotypes ( Solanum tuberosum L.) following osmotic stress treatment in vitro
inferred← citeshttps://doi.org/10.1016/j.jprot.2021.104475openalex-snapshot
TMT-based comparative proteomic analysis of the male-sterile mutant ms01 sheds light on sporopollenin production and pollen development in wucai (Brassica campestris L.)
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2003.07.001openalex-snapshot
The development of cysteine proteases in freesia corms during responses to chilling
inferred← citeshttps://doi.org/10.1016/j.molp.2016.03.008openalex-snapshot
Tobacco RING E3 Ligase NtRFP1 Mediates Ubiquitination and Proteasomal Degradation of a Geminivirus-Encoded βC1
inferred← citeshttps://doi.org/10.1016/j.pbi.2005.01.013openalex-snapshot
Autophagic recycling: lessons from yeast help define the process in plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2004.08.007openalex-snapshot
Leucine aminopeptidase from etiolated barley seedlings: characterization and partial purification of isoforms
inferred← citeshttps://doi.org/10.1016/j.plantsci.2008.05.012openalex-snapshot
Identification of stress-induced genes from the drought tolerant semi-arid legume crop horsegram (Macrotyloma uniflorum (Lam.) Verdc.) through analysis of subtracted expressed sequence tags
inferred← citeshttps://doi.org/10.1016/j.plantsci.2010.07.011openalex-snapshot
Molecular mechanisms underlying frost tolerance in perennial grasses adapted to cold climates
inferred← citeshttps://doi.org/10.1016/j.plantsci.2011.11.014openalex-snapshot
Ubiquitin/proteasome-mediated proteolysis is involved in the response to flooding stress in soybean roots, independent of oxygen limitation
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.01.003openalex-snapshot
The banana E2 gene family: Genomic identification, characterization, expression profiling analysis
inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.01.013openalex-snapshot
Qualitative and quantitative modifications of root mitochondria during senescence of above-ground parts of Arabidopis thaliana
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111818openalex-snapshot
Systems biology of root development in Populus: Review and perspectives
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112600openalex-snapshot
Rapid Alkalinization Factor – A cryptide regulating developmental and stress responses
inferred← citeshttps://doi.org/10.1016/j.plaphy.2007.02.002openalex-snapshot
Water deficit induces variation in expression of stress-responsive genes in two peanut (Arachis hypogaea L.) cultivars with different tolerance to drought
inferred← citeshttps://doi.org/10.1016/j.plaphy.2007.11.003openalex-snapshot
Isolation and characterization of a dual function protein from Allium sativum bulbs which exhibits proteolytic and hemagglutinating activities
inferred← citeshttps://doi.org/10.1016/j.plaphy.2012.10.022openalex-snapshot
Characterization of two novel subtilases from common bean (Phaseolus vulgaris L.) and their responses to drought
inferred← citeshttps://doi.org/10.1016/j.plaphy.2015.09.017openalex-snapshot
Investigation of plant latices of Asteraceae and Campanulaceae regarding proteolytic activity
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2014.06.006openalex-snapshot
Overexpression of the protease inhibitor BoCPI-1 in broccoli delays chlorophyll loss after harvest and causes down-regulation of cysteine protease gene expression
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2020.111165openalex-snapshot
Nanosilver and sucrose delay the senescence of cut snapdragon flowers
inferred← citeshttps://doi.org/10.1016/j.sajb.2018.01.022openalex-snapshot
Co-evolution of enzyme activities and latex in fig (Ficus carica L.) during fruit maturity process
inferred← citeshttps://doi.org/10.1016/j.snb.2016.12.120openalex-snapshot
A nanostructured cell-free photosynthetic biocomposite via molecularly controlled layer-by-layer assembly
inferred← citeshttps://doi.org/10.1016/j.soilbio.2012.04.004openalex-snapshot
Biochar but not earthworms enhances rice growth through increased protein turnover
inferred← citeshttps://doi.org/10.1016/j.tplants.2011.05.008openalex-snapshot
Protein degradation – an alternative respiratory substrate for stressed plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2012.05.006openalex-snapshot
Autophagy: a multifaceted intracellular system for bulk and selective recycling
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.04.025openalex-snapshot
Molecular evolution and diversification of plant cysteine proteinase inhibitors: New insights after the poplar genome
inferred← citeshttps://doi.org/10.1016/s0014-5793(00)01107-8openalex-snapshot
The N‐terminal domain of the light‐harvesting chlorophyll a/b‐binding protein complex (LHCII) is essential for its acclimative proteolysis
inferred← citeshttps://doi.org/10.1016/s0014-5793(01)02259-1openalex-snapshot
Aspartic protease in leaves of common bean ( Phaseolus vulgaris L.) and cowpea ( Vigna unguiculata L. Walp): enzymatic activity, gene expression and relation to drought susceptibility
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00075-3openalex-snapshot
Isolation and characterization of a serine protease from the sprouts of Pleioblastus hindsii Nakai
inferred← citeshttps://doi.org/10.1016/s0031-9422(98)00740-7openalex-snapshot
Purification and partial characterization of an ATP-hydrolyzing serine protease from lettuce leaves
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00605-6openalex-snapshot
Cucumisin-like protease from the latex of Euphorbia supina
inferred← citeshttps://doi.org/10.1016/s0065-2164(01)50008-8openalex-snapshot
Archaeal proteasomes: Proteolytic nanocompartments of the cell
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)62181-6openalex-snapshot
Intracellular Proteinases of Invertebrates: Calcium-Dependent and Proteasome/Ubiquitin-Dependent Systems
inferred← citeshttps://doi.org/10.1016/s0168-9452(00)00255-7openalex-snapshot
Structure, expression and promoter activity of two polyubiquitin genes from rice (Oryza sativa L.)
inferred← citeshttps://doi.org/10.1016/s0168-9452(02)00085-7openalex-snapshot
Isolation and characterization of proteolytic enzymes from the latex of Synadenium grantii Hook, ‘f’
inferred← citeshttps://doi.org/10.1016/s0168-9452(02)00277-7openalex-snapshot
Characterization and tissue-regulated expression of genes involved in pineapple (Ananas comosus L.) root development
inferred← citeshttps://doi.org/10.1016/s0168-9452(98)00215-5openalex-snapshot
Tobacco cultures transformed with cyclin-promoter-gus constructs reveal a discrepancy between gus mRNA levels and GUS protein activity upon leaving the stationary state
inferred← citeshttps://doi.org/10.1016/s0168-9452(99)00140-5openalex-snapshot
Purification and characterization of the 26S proteasome from cultured rice (Oryza sativa) cells
inferred← citeshttps://doi.org/10.1016/s0981-9428(01)01349-3openalex-snapshot
The activity of the 20S proteasome is maintained in detached wheat leaves during senescence in darkness
inferred← citeshttps://doi.org/10.1016/s0981-9428(02)01404-3openalex-snapshot
Plant proteases, protein degradation, and oxidative stress: role of peroxisomes
inferred← citeshttps://doi.org/10.1016/s1016-8478(23)13538-2openalex-snapshot
Analysis of cDNAs Expressed during First Cell Division of Petunia Petal Protoplast Cultures Using Expressed Sequence Tags
inferred← citeshttps://doi.org/10.1016/s1360-1385(00)01769-6openalex-snapshot
F-box proteins in Arabidopsis
inferred← citeshttps://doi.org/10.1016/s1360-1385(03)00014-1openalex-snapshot
The ubiquitin/26S proteasome pathway, the complex last chapter in the life of many plant proteins
inferred← citeshttps://doi.org/10.1016/s1360-1385(99)01382-5openalex-snapshot
Function of the ubiquitin–proteosome pathway in auxin response
inferred← citeshttps://doi.org/10.1016/s1673-8527(08)60081-8openalex-snapshot
Floret-specific differences in gene expression and support for the hypothesis that tapetal degeneration of Zea mays L. occurs via programmed cell death
inferred← citeshttps://doi.org/10.1021/acs.jproteome.7b00621openalex-snapshot
Proteome Comparisons between Hemolymph of Two Honeybee Strains (Apis mellifera ligustica) Reveal Divergent Molecular Basis in Driving Hemolymph Function and High Royal Jelly Secretion
inferred← citeshttps://doi.org/10.1021/jf034989vopenalex-snapshot
Cloning, Functional Expression, and Characterization of Cystatin in Sesame Seed
inferred← citeshttps://doi.org/10.1023/a:1002123627361openalex-snapshot
Mobilization of Reserve Proteins During Early Stages of Seed Germination in Fagopyrum Esculentum
inferred← citeshttps://doi.org/10.1023/a:1005848828368openalex-snapshot
A model for the evolution of polyubiquitin genes from the study of Arabidopsis thaliana ecotypes
inferred← citeshttps://doi.org/10.1023/a:1006089924093openalex-snapshot
Engineering in vivo instability of firefly luciferase and Escherichia coli β-glucuronidase in higher plants using recognition elements from the ubiquitin pathway
inferred← citeshttps://doi.org/10.1023/a:1006102110889openalex-snapshot
Expression of a proteasome α-type subunit gene during tobacco development and senescence
inferred← citeshttps://doi.org/10.1023/a:1006223908044openalex-snapshot
The restorer Rfo gene acts post-translationally on the stability of the ORF138 Ogura CMS-associated protein in reproductive tissues of rapeseed cybrids
inferred← citeshttps://doi.org/10.1023/a:1006316422400openalex-snapshot
Rice calcium-dependent protein kinase isoforms OsCDPK2 and OsCDPK11 show different responses to light and different expression patterns during seed development
inferred← citeshttps://doi.org/10.1023/a:1006323317890openalex-snapshot
Polypeptide tags, ubiquitous modifiers for plant protein regulation
inferred← citeshttps://doi.org/10.1023/a:1006926322501openalex-snapshot
Structure and functional analyses of the 26S proteasome subunits from plants – Plant 26S proteasome
inferred← citeshttps://doi.org/10.1023/a:1009656002068openalex-snapshot
Expression of a sulfur-rich maize seed storage protein, δ-zein, in white clover (shape Trifolium repens) to improve forage quality
inferred← citeshttps://doi.org/10.1023/a:1010671405594openalex-snapshot
Effects of the polyubiquitin gene Ubi.U4 leader intron and first ubiquitin monomer on reporter gene expression in Nicotiana tabacum
inferred← citeshttps://doi.org/10.1023/a:1012400104001openalex-snapshot
Vacuole Cysteine Proteases and Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase Degradation during Monocarpic Senescence in Cowpea Leaves
inferred← citeshttps://doi.org/10.1023/a:1019906031305openalex-snapshot
Characterization of the expression of a wheat cystatin gene during caryopsis development
inferred← citeshttps://doi.org/10.1023/a:1021291522243openalex-snapshot
Protein complexes mediate signalling in plant responses to hormones, light, sucrose and pathogens
inferred← citeshttps://doi.org/10.1023/a:1022319821591openalex-snapshot
Nuclease activities and DNA fragmentation during programmed cell death of megagametophyte cells of white spruce (Picea glauca) seeds
inferred← citeshttps://doi.org/10.1023/a:1026509012695openalex-snapshot
Caspase-like protease involvement in the control of plant cell death
inferred← citeshttps://doi.org/10.1023/a:1026536324081openalex-snapshot
Programmed cell death in plant reproduction
inferred← citeshttps://doi.org/10.1023/a:1026546004942openalex-snapshot
Circadian and senescence-enhanced expression of a tobacco cysteine protease gene
inferred← citeshttps://doi.org/10.1023/a:1026556928624openalex-snapshot
Plant proteolytic enzymes: possible roles during programmed cell death
inferred← citeshttps://doi.org/10.1023/b:phot.0000046158.60446.07openalex-snapshot
Ribulose-1,5-bisphosphate Carboxylase/Oxygenase Content and Degradation in Diploid, Tetraploid, and Hexaploid Wheat Species during Monocarpic Senescence
inferred← citeshttps://doi.org/10.1034/j.1399-3054.2003.00142.xopenalex-snapshot
Purification and characterization of a subtilisin‐like serine protease induced during the senescence of wheat leaves
inferred← citeshttps://doi.org/10.1038/73796openalex-snapshot
High-yield production of a human therapeutic protein in tobacco chloroplasts
inferred← citeshttps://doi.org/10.1038/nrg1228openalex-snapshot
The diverse roles of ubiquitin and the 26S proteasome in the life of plants
inferred← citeshttps://doi.org/10.1038/s41598-017-16909-xopenalex-snapshot
Reducing biomass recalcitrance by heterologous expression of a bacterial peroxidase in tobacco (Nicotiana benthamiana)
inferred← citeshttps://doi.org/10.1038/s41598-018-27003-1openalex-snapshot
Identifying differentially expressed proteins in sorghum cell cultures exposed to osmotic stress
inferred← citeshttps://doi.org/10.1038/s41598-020-65734-2openalex-snapshot
Duplication and divergence: New insights into AXR1 and AXL functions in DNA repair and meiosis
inferred← citeshttps://doi.org/10.1038/s41598-020-68735-3openalex-snapshot
Comparative physiological and root proteome analyses of two sorghum varieties responding to water limitation
inferred← citeshttps://doi.org/10.1038/s44383-026-00021-zopenalex-snapshot
Biotechnological approaches for producing therapeutic peptides in plants
inferred← citeshttps://doi.org/10.1038/srep24901openalex-snapshot
The transcriptomics of an experimentally evolved plant-virus interaction
inferred← citeshttps://doi.org/10.1042/0264-6021:3490417openalex-snapshot
Evidence for phosphorylation and ubiquitinylation of the turnip yellow mosaic virus RNA-dependent RNA polymerase domain expressed in a baculovirus‒insect cell system
inferred← citeshttps://doi.org/10.1042/bc20040516openalex-snapshot
Starvation‐induced expression of autophagy‐related genes in Arabidopsis
inferred← citeshttps://doi.org/10.1042/bj20081146openalex-snapshot
Identification of new protein substrates for the chloroplast ATP-dependent Clp protease supports its constitutive role in Arabidopsis
inferred← citeshttps://doi.org/10.1042/bj3270399openalex-snapshot
Characterization of endoproteases from plant peroxisomes
inferred← citeshttps://doi.org/10.1046/j.1364-3703.2003.00169.xopenalex-snapshot
The role of proteolysis in R gene mediated defence in plants
inferred← citeshttps://doi.org/10.1046/j.1365-3040.1997.d01-107.xopenalex-snapshot
Phytochrome degradation
inferred← citeshttps://doi.org/10.1046/j.1365-3040.1997.d01-108.xopenalex-snapshot
An emerging molecular map of the phytochromes
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00360.xopenalex-snapshot
Sequences within both the N‐ and C‐terminal domains of phytochrome A are required for PFR ubiquitination and degradation
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00370.xopenalex-snapshot
Expression of cysteine proteinase during developmental events associated with programmed cell death in brinjal
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00479.xopenalex-snapshot
Structural and functional analysis of the six regulatory particle triple‐A ATPase subunits from the Arabidopsis 26S proteasome
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00590.xopenalex-snapshot
UPL1 and 2, two 405 kDa ubiquitin–protein ligases from Arabidopsis thaliana related to the HECT‐domain protein family
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2000.00677.xopenalex-snapshot
Induction of competence for elicitation of defense responses in cucumber hypocotyls requires proteasome activity
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2001.01093.xopenalex-snapshot
Degradation signals within both terminal domains of the cauliflower mosaic virus capsid protein precursor
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2001.01106.xopenalex-snapshot
The ubiquitin‐specific protease UBP14 is essential for early embryo development in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1046/j.1432-1327.1999.00463.xopenalex-snapshot
The inhibitory properties and primary structure of a novel serine proteinase inhibitor from the fruiting body of the basidiomycete, Lentinus edodes
inferred← citeshttps://doi.org/10.1046/j.1432-1327.1999.00548.xopenalex-snapshot
Overexpression, purification and biochemical characterization of the wound‐induced leucine aminopeptidase of tomato
inferred← citeshttps://doi.org/10.1046/j.1432-1327.2000.01116.xopenalex-snapshot
Specificity of the wound‐induced leucine aminopeptidase (LAP‐A) of tomato
inferred← citeshttps://doi.org/10.1046/j.1432-1327.2001.02383.xopenalex-snapshot
Rapid, ATP‐dependent degradation of a truncated D1 protein in the chloroplast
inferred← citeshttps://doi.org/10.1046/j.1439-0434.2002.00724.xopenalex-snapshot
Changes in Wheat Leaf Extracellular Proteolytic Activity after Infection with Septoria tritici
inferred← citeshttps://doi.org/10.1046/j.1469-8137.1997.00737.xopenalex-snapshot
Chlorophyll: a symptom and a regulator of plastid development
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2000.00733.xopenalex-snapshot
Tansley Review No. 118
inferred← citeshttps://doi.org/10.1071/fp03010openalex-snapshot
Growth, carbon allocation and proteolytic activity in the seagrass Zostera noltii shaded by Ulva canopies
inferred← citeshttps://doi.org/10.1071/fp07121openalex-snapshot
Identification and characterisation of acidic and novel basic forms of actinidin, the highly abundant cysteine protease from kiwifruit
inferred← citeshttps://doi.org/10.1071/fp10140openalex-snapshot
Characterisation of HvALMT1 function in transgenic barley plants
inferred← citeshttps://doi.org/10.1073/pnas.0703758104openalex-snapshot
Proteolysis of the barley receptor-like protein kinase RPG1 by a proteasome pathway is correlated with Rpg1 -mediated stem rust resistance
inferred← citeshttps://doi.org/10.1073/pnas.1307637110openalex-snapshot
Organellar oligopeptidase (OOP) provides a complementary pathway for targeting peptide degradation in mitochondria and chloroplasts
inferred← citeshttps://doi.org/10.1073/pnas.251386098openalex-snapshot
Ricin A chain without its partner B chain is degraded after retrotranslocation from the endoplasmic reticulum to the cytosol in plant cells
inferred← citeshttps://doi.org/10.1073/pnas.95.14.7904openalex-snapshot
PRT1 of Arabidopsis thaliana encodes a component of the plant N-end rule pathway
inferred← citeshttps://doi.org/10.1073/pnas.96.11.6547openalex-snapshot
GTP bound to chloroplast thylakoid membranes is required for light-induced, multienzyme degradation of the photosystem II D1 protein
inferred← citeshttps://doi.org/10.1073/pnas.98.4.1507openalex-snapshot
The quorum-sensing transcriptional regulator TraR requires its cognate signaling ligand for protein folding, protease resistance, and dimerization
inferred← citeshttps://doi.org/10.1074/jbc.273.4.1970openalex-snapshot
Multiubiquitin Chain Binding and Protein Degradation Are Mediated by Distinct Domains within the 26 S Proteasome Subunit Mcb1
inferred← citeshttps://doi.org/10.1074/jbc.274.8.5222openalex-snapshot
Fragmentation of the Large Subunit of Ribulose-1,5-bisphosphate Carboxylase by Reactive Oxygen Species Occurs near Gly-329
inferred← citeshttps://doi.org/10.1074/jbc.m006721200openalex-snapshot
Arabidopsis eIF3e (INT-6) Associates with Both eIF3c and the COP9 Signalosome Subunit CSN7
inferred← citeshttps://doi.org/10.1074/jbc.m109.035394openalex-snapshot
Evidence for the Existence in Arabidopsis thaliana of the Proteasome Proteolytic Pathway
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