On the public citation graph

Biochemical, Biophysical, and Functional Analyses of Two Isoforms of the SnRK2 inhibitor AtSCS

https://doi.org/10.1101/813717
0 signed · 63 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/prot.10104openalex-snapshot
Increasing the precision of comparative models with YASARA NOVA—a self‐parameterizing force field
inferredcites →https://doi.org/10.1002/prot.22570openalex-snapshot
Improving physical realism, stereochemistry, and side‐chain accuracy in homology modeling: Four approaches that performed well in CASP8
inferredcites →https://doi.org/10.1006/meth.1997.0522openalex-snapshot
Identification of Autonomously Replicating Sequence (ARS) Elements in Eukaryotic Cells
inferredcites →https://doi.org/10.1007/978-1-4939-3115-6_15openalex-snapshot
Assessing Kinase Activity in Plants with In-Gel Kinase Assays
inferredcites →https://doi.org/10.1007/s00299-013-1418-1openalex-snapshot
ABA signaling in stress-response and seed development
inferredcites →https://doi.org/10.1007/s10265-011-0412-3openalex-snapshot
ABA-mediated transcriptional regulation in response to osmotic stress in plants
inferredcites →https://doi.org/10.1007/s11103-005-0340-5openalex-snapshot
pSAT vectors: a modular series of plasmids for autofluorescent protein tagging and expression of multiple genes in plants
inferredcites →https://doi.org/10.1016/0003-2697(92)90279-gopenalex-snapshot
Statistical determination of the average values of the extinction coefficients of tryptophan and tyrosine in native proteins
inferredcites →https://doi.org/10.1016/j.bbagen.2011.10.012openalex-snapshot
Analysis of calcium signaling pathways in plants
inferredcites →https://doi.org/10.1016/j.bbamcr.2008.10.006openalex-snapshot
Plant calcineurin B-like proteins and their interacting protein kinases
inferredcites →https://doi.org/10.1016/j.cell.2006.06.054openalex-snapshot
Plant Stomata Function in Innate Immunity against Bacterial Invasion
inferredcites →https://doi.org/10.1016/j.febslet.2009.08.033openalex-snapshot
Phosphorylation of the Arabidopsis AtrbohF NADPH oxidase by OST1 protein kinase
inferredcites →https://doi.org/10.1016/j.phytochem.2004.04.033openalex-snapshot
Proteomics of calcium-signaling components in plants
inferredcites →https://doi.org/10.1016/j.tig.2015.01.001openalex-snapshot
Alternative mRNA transcription, processing, and translation: insights from RNA sequencing
inferredcites →https://doi.org/10.1016/j.tplants.2008.10.005openalex-snapshot
The CBL–CIPK network in plant calcium signaling
inferredcites →https://doi.org/10.1016/s0076-6879(97)78013-3openalex-snapshot
[11] Fluorescence methods for studying equilibrium macromolecule-ligand interactions
inferredcites →https://doi.org/10.1023/a:1009253808876openalex-snapshot
Structures of EF-hand Ca 2+-binding proteins: Diversity in the organization, packing and response to Ca 2+ Binding
inferredcites →https://doi.org/10.1038/aps.2014.5openalex-snapshot
Abscisic acid perception and signaling: structural mechanisms and applications
inferredcites →https://doi.org/10.1038/ncomms3219openalex-snapshot
Group A PP2Cs evolved in land plants as key regulators of intrinsic desiccation tolerance
inferredcites →https://doi.org/10.1038/nplants.2016.204openalex-snapshot
ABA-unresponsive SnRK2 protein kinases regulate mRNA decay under osmotic stress in plants
inferredcites →https://doi.org/10.1038/nprot.2006.97openalex-snapshot
Agrobacterium-mediated transformation of Arabidopsis thaliana using the floral dip method
inferredcites →https://doi.org/10.1038/s42003-019-0281-1openalex-snapshot
SnRK2 protein kinases represent an ancient system in plants for adaptation to a terrestrial environment
inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot
Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0407758101openalex-snapshot
SRK2C, a SNF1-related protein kinase 2, improves drought tolerance by controlling stress-responsive gene expression in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.0903144106openalex-snapshot
Arabidopsis mutant deficient in 3 abscisic acid-activated protein kinases reveals critical roles in growth, reproduction, and stress
inferredcites →https://doi.org/10.1073/pnas.0907095106openalex-snapshot
Type 2C protein phosphatases directly regulate abscisic acid-activated protein kinases in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0912030107openalex-snapshot
Guard cell anion channel SLAC1 is regulated by CDPK protein kinases with distinct Ca 2+ affinities
inferredcites →https://doi.org/10.1073/pnas.1018367108openalex-snapshot
Arabidopsis decuple mutant reveals the importance of SnRK2 kinases in osmotic stress responses in vivo
inferredcites →https://doi.org/10.1073/pnas.1116590109openalex-snapshot
Reconstitution of abscisic acid activation of SLAC1 anion channel by CPK6 and OST1 kinases and branched ABI1 PP2C phosphatase action
inferredcites →https://doi.org/10.1073/pnas.1600385113openalex-snapshot
Conserved properties of individual Ca 2+ -binding sites in calmodulin
inferredcites →https://doi.org/10.1074/jbc.m110.115535openalex-snapshot
SNF1-related Protein Kinases 2 Are Negatively Regulated by a Plant-specific Calcium Sensor
inferredcites →https://doi.org/10.1089/omi.2011.0091openalex-snapshot
SnRK2 Protein Kinases—Key Regulators of Plant Response to Abiotic Stresses
inferredcites →https://doi.org/10.1093/pcp/pcf188openalex-snapshot
ABA-Activated SnRK2 Protein Kinase is Required for Dehydration Stress Signaling in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcp083openalex-snapshot
Three Arabidopsis SnRK2 Protein Kinases, SRK2D/SnRK2.2, SRK2E/SnRK2.6/OST1 and SRK2I/SnRK2.3, Involved in ABA Signaling are Essential for the Control of Seed Development and Dormancy
inferredcites →https://doi.org/10.1093/pcp/pcp147openalex-snapshot
Three SnRK2 Protein Kinases are the Main Positive Regulators of Abscisic Acid Signaling in Response to Water Stress in Arabidopsis
inferredcites →https://doi.org/10.1093/pcp/pcq041openalex-snapshot
Two Closely Related Subclass II SnRK2 Protein Kinases Cooperatively Regulate Drought-Inducible Gene Expression
inferredcites →https://doi.org/10.1093/pcp/pcq156openalex-snapshot
Molecular Basis of the Core Regulatory Network in ABA Responses: Sensing, Signaling and Transport
inferredcites →https://doi.org/10.1093/pcp/pcv060openalex-snapshot
Omics Approaches Toward Defining the Comprehensive Abscisic Acid Signaling Network in Plants
inferredcites →https://doi.org/10.1093/protein/5.3.191openalex-snapshot
Quantitative analysis of protein far UV circular dichroism spectra by neural networks
inferredcites →https://doi.org/10.1101/gad.1953910openalex-snapshot
Early abscisic acid signal transduction mechanisms: newly discovered components and newly emerging questions
inferredcites →https://doi.org/10.1104/pp.108.131656openalex-snapshot
Highly Diversified Molecular Evolution of Downstream Transcription Start Sites in Rice and Arabidopsis
inferredcites →https://doi.org/10.1104/pp.109.137174openalex-snapshot
Triple Loss of Function of Protein Phosphatases Type 2C Leads to Partial Constitutive Response to Endogenous Abscisic Acid
inferredcites →https://doi.org/10.1104/pp.112.194472openalex-snapshot
SNF1-Related Protein Kinases Type 2 Are Involved in Plant Responses to Cadmium Stress
inferredcites →https://doi.org/10.1104/pp.113.220608openalex-snapshot
PYR/RCAR Receptors Contribute to Ozone-, Reduced Air Humidity-, Darkness-, and CO2-Induced Stomatal Regulation
inferredcites →https://doi.org/10.1104/pp.113.222539openalex-snapshot
Calcium-Dependent Protein Kinases: Hubs in Plant Stress Signaling and Development
inferredcites →https://doi.org/10.1105/tpc.007906openalex-snapshot
Arabidopsis OST1 Protein Kinase Mediates the Regulation of Stomatal Aperture by Abscisic Acid and Acts Upstream of Reactive Oxygen Species Production
inferredcites →https://doi.org/10.1105/tpc.106.048538openalex-snapshot
Identification of Two Protein Kinases Required for Abscisic Acid Regulation of Seed Germination, Root Growth, and Gene Expression in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.069179openalex-snapshot
Protein Phosphatases 2C Regulate the Activation of the Snf1-Related Kinase OST1 by Abscisic Acid in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2012.05089.xopenalex-snapshot
The Snf1‐related protein kinases SnRK2.4 and SnRK2.10 are involved in maintenance of root system architecture during salt stress
inferredcites →https://doi.org/10.1111/nph.15543openalex-snapshot
Fine‐tuning of RBOHF activity is achieved by differential phosphorylation and Ca 2+ binding
inferredcites →https://doi.org/10.1111/pce.13465openalex-snapshot
Phosphoproteomic analysis reveals that dehydrins ERD10 and ERD14 are phosphorylated by SNF1‐related protein kinase 2.10 in response to osmotic stress
inferredcites →https://doi.org/10.1126/science.1215106openalex-snapshot
Molecular Mimicry Regulates ABA Signaling by SnRK2 Kinases and PP2C Phosphatases
inferredcites →https://doi.org/10.1186/gb-2002-3-10-research0056openalex-snapshot
Analysis of EF-hand-containing proteins in Arabidopsis
inferredcites →https://doi.org/10.1186/s12870-016-0817-1openalex-snapshot
Phosphatase ABI1 and okadaic acid-sensitive phosphoprotein phosphatases inhibit salt stress-activated SnRK2.4 kinase
inferredcites →https://doi.org/10.1271/bbb.100184openalex-snapshot
Gateway Binary Vectors with the Bialaphos Resistance Gene, bar , as a Selection Marker for Plant Transformation
inferredcites →https://doi.org/10.1271/bbb.68.1966openalex-snapshot
Rapid Response ofArabidopsisT87 Cultured Cells to Cytokinin through His-to-Asp Phosphorelay Signal Transduction
inferredcites →https://doi.org/10.1371/journal.pgen.1005835openalex-snapshot
Type One Protein Phosphatase 1 and Its Regulatory Protein Inhibitor 2 Negatively Regulate ABA Signaling
inferredcites →https://doi.org/10.1371/journal.pone.0001705openalex-snapshot
Natural Variation in Arabidopsis thaliana as a Tool for Highlighting Differential Drought Responses
inferredcites →https://doi.org/10.1371/journal.pone.0076353openalex-snapshot
Oligomerization Interface of RAGE Receptor Revealed by MS-Monitored Hydrogen Deuterium Exchange
inferredcites →https://doi.org/10.3389/fpls.2017.00395openalex-snapshot
Evolutionary Analysis of Snf1-Related Protein Kinase2 (SnRK2) and Calcium Sensor (SCS) Gene Lineages, and Dimerization of Rice Homologs, Suggest Deep Biochemical Conservation across Angiosperms
inferredcites →https://doi.org/10.3390/ijms14035734openalex-snapshot
Structural Biology of a Major Signaling Network that Regulates Plant Abiotic Stress: The CBL-CIPK Mediated Pathway
inferredcites →https://doi.org/10.4161/psb.19694openalex-snapshot
Catalytic mechanism and kinase interactions of ABA-signaling PP2C phosphatases
inferredcites →https://doi.org/10.7554/elife.03599openalex-snapshot
Calcium specificity signaling mechanisms in abscisic acid signal transduction in Arabidopsis guard cells
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.