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Squash Trypsin Inhibitors from Momordica cochinchinensis Exhibit an Atypical Macrocyclic Structure
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A biomimetic strategy in the synthesis and fragmentation of cyclic protein
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Comparative Protein Modelling by Satisfaction of Spatial Restraints
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High-resolution structure of a potent, cyclic proteinase inhibitor from sunflower seeds
inferredcites →https://doi.org/10.1006/jmbi.1999.3383openalex-snapshot
Plant cyclotides: A unique family of cyclic and knotted proteins that defines the cyclic cystine knot structural motif
inferredcites →https://doi.org/10.1007/bf01887398openalex-snapshot
Trypsin inhibitors from ridged gourd (Luffa acutangula Linn.) seeds: Purification, properties, and amino acid sequences
inferredcites →https://doi.org/10.1016/0006-291x(89)91964-5openalex-snapshot
Active site chemical mutagenesis of Ecballium elaterium Trypsin Inhibitor II: New microproteins inhibiting elastase and chymotrypsin
inferredcites →https://doi.org/10.1016/0014-5793(89)80486-7openalex-snapshot
The refined 2.0 Å X‐ray crystal structure of the complex formed between bovine β‐trypsin and CMTI‐I, a trypsin inhibitor from squash seeds (Cucurbita maxima) Topological similarity of the squash seed inhibitors with the carboxypeptidase A inhibitor from potatoes
inferredcites →https://doi.org/10.1016/s0014-5793(98)01119-3openalex-snapshot
Modifications outside the proteinase binding loop in Cucurbita maxima trypsin inhibitor III (CMTI‐III) analogues change the binding energy with bovine β‐trypsin
inferredcites →https://doi.org/10.1016/s1357-2725(99)00012-6openalex-snapshot
Isolation of a trypsin inhibitor with deletion of N-terminal pentapeptide from the seeds of Momordica cochinchinensis, the Chinese drug mubiezhi
inferredcites →https://doi.org/10.1021/ja00099a064openalex-snapshot
Circulins A and B. Novel human immunodeficiency virus (HIV)-inhibitory macrocyclic peptides from the tropical tree Chassalia parvifolia.
inferredcites →https://doi.org/10.1021/np50114a002openalex-snapshot
Cyclopsychotride A, a Biologically Active, 31-Residue Cyclic Peptide Isolated from Psychotria longipes
inferredcites →https://doi.org/10.1021/np970342ropenalex-snapshot
Fractionation Protocol for the Isolation of Polypeptides from Plant Biomass
inferredcites →https://doi.org/10.1021/np9803878openalex-snapshot
Seven Novel Macrocyclic Polypeptides fromViolaarvensis
inferredcites →https://doi.org/10.1034/j.1399-3011.1999.00137.xopenalex-snapshot
Grafting an RGD motif onto an epidermal growth factor‐like module: chemical synthesis and functional characterization of the chimeric molecule
inferredcites →https://doi.org/10.1073/pnas.96.16.8913openalex-snapshot
An unusual structural motif of antimicrobial peptides containing end-to-end macrocycle and cystine-knot disulfides
inferredcites →https://doi.org/10.1111/j.1399-3011.1986.tb01817.xopenalex-snapshot
Solid‐phase synthesis of trypsin inhibitor CMTI III from squash seeds (Cucurbita maxima)*
inferredcites →https://doi.org/10.1111/j.1399-3011.1989.tb00210.xopenalex-snapshot
Protease inhibitors from Ecballium elaterium seeds
inferredcites →https://doi.org/10.1111/j.1399-3011.1989.tb01399.xopenalex-snapshot
Solid phase synthesis of a trypsin inhibitor isolated from the Cucurbitaceae Ecballium elaterium
inferredcites →https://doi.org/10.1111/j.1432-1033.1995.837_3.xopenalex-snapshot
Folding of the Squash Trypsin Inhibitor EETI II
inferredcites →https://doi.org/10.18388/abp.1996_4475openalex-snapshot
Squash inhibitor family of serine proteinases.
inferredcites →https://doi.org/10.18388/abp.1996_4484openalex-snapshot
Isolation and amino-acid sequence of two inhibitors of serine proteinases, members of the squash inhibitor family, from Echinocystis lobata seeds.
inferredcites →https://doi.org/10.18388/abp.1996_4559openalex-snapshot
Expression of small synthetic genes coding for hEGF, human epidermal growth factor, and CPTI II, serine proteinase inhibitor from Cucurbitacea, cloned in a novel expression/secretion vector in Saccharomyces cerevisiae.
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Cellular uptake of cyclotide MCoTI-I follows multiple endocytic pathways
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Violae Herba: A comprehensive review of the traditional uses, phytochemistry, pharmacology, quality control and clinical applications
inferred← citeshttps://doi.org/10.1016/j.jff.2018.05.034openalex-snapshot
Biochemical requirements of bioactive peptides for nutraceutical efficacy
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2020.104025openalex-snapshot
Behavioral and physiological effects of Viola spp. cyclotides on Myzus persicae (Sulz.)
inferred← citeshttps://doi.org/10.1016/j.jmb.2005.11.005openalex-snapshot
Barnase Fusion as a Tool to Determine the Crystal Structure of the Small Disulfide-rich Protein McoEeTI
inferred← citeshttps://doi.org/10.1016/j.jmb.2009.10.028openalex-snapshot
Engineered Cystine Knot Miniproteins as Potent Inhibitors of Human Mast Cell Tryptase β
inferred← citeshttps://doi.org/10.1016/j.mocell.2025.100252openalex-snapshot
Cyclotides as novel plant-derived scaffolds for orally active cyclic peptide therapeutics
inferred← citeshttps://doi.org/10.1016/j.mrgentox.2012.05.006openalex-snapshot
Genotoxicity and cellular uptake of cyclotides: Evidence for multiple modes of action
inferred← citeshttps://doi.org/10.1016/j.pep.2004.09.016openalex-snapshot
A fusion protein system for the recombinant production of short disulfide bond rich cystine knot peptides using barnase as a purification handle
inferred← citeshttps://doi.org/10.1016/j.peptides.2004.01.002openalex-snapshot
Multiple trypsin inhibitors from Momordica cochinchinensis seeds, the Chinese drug mubiezhi
inferred← citeshttps://doi.org/10.1016/j.peptides.2007.04.025openalex-snapshot
Plant cyclotides: An unusual class of defense compounds
inferred← citeshttps://doi.org/10.1016/j.peptides.2011.06.016openalex-snapshot
Isolation and characterization of cytotoxic cyclotides from Viola philippica
inferred← citeshttps://doi.org/10.1016/j.peptides.2012.09.018openalex-snapshot
A new family of cystine knot peptides from the seeds of Momordica cochinchinensis
inferred← citeshttps://doi.org/10.1016/j.peptides.2020.170430openalex-snapshot
An insight into biological activities of native cyclotides for potential applications in agriculture and pharmaceutics
inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.09.023openalex-snapshot
Cyclotide proteins and precursors from the genus Gloeospermum: Filling a blank spot in the cyclotide map of Violaceae
inferred← citeshttps://doi.org/10.1016/j.phytol.2012.09.001openalex-snapshot
Optimization of cyclotide extraction parameters
inferred← citeshttps://doi.org/10.1016/j.str.2008.02.023openalex-snapshot
The Structure of a Two-Disulfide Intermediate Assists in Elucidating the Oxidative Folding Pathway of a Cyclic Cystine Knot Protein
inferred← citeshttps://doi.org/10.1016/j.toxicon.2006.11.018openalex-snapshot
Insecticidal plant cyclotides and related cystine knot toxins
inferred← citeshttps://doi.org/10.1016/j.toxicon.2010.02.021openalex-snapshot
Discovery and applications of the plant cyclotides
inferred← citeshttps://doi.org/10.1016/j.toxicon.2019.10.244openalex-snapshot
Cyclotides: Disulfide-rich peptide toxins in plants
inferred← citeshttps://doi.org/10.1016/j.toxicon.2023.107173openalex-snapshot
Cysteine-rich peptides: From bioactivity to bioinsecticide applications
inferred← citeshttps://doi.org/10.1016/j.tplants.2009.03.003openalex-snapshot
Circling the enemy: cyclic proteins in plant defence
inferred← citeshttps://doi.org/10.1016/s0003-2697(03)00114-3openalex-snapshot
Expression of Viola cyclotides by liquid chromatography–mass spectrometry and tandem mass spectrometry sequencing of intercysteine loops after introduction of charges and cleavage sites by aminoethylation
inferred← citeshttps://doi.org/10.1016/s0031-9422(01)00173-xopenalex-snapshot
First cyclotide from Hybanthus (Violaceae)
inferred← citeshttps://doi.org/10.1016/s0031-9422(03)00239-5openalex-snapshot
Bitter gourd proteinase inhibitors: potential growth inhibitors of Helicoverpa armigera and Spodoptera litura
inferred← citeshttps://doi.org/10.1016/s0968-0004(02)02057-1openalex-snapshot
Circular proteins — no end in sight
inferred← citeshttps://doi.org/10.1016/s1572-5995(03)80015-7openalex-snapshot
Protein and Non-Protein Protease Inhibitors from Plants
inferred← citeshttps://doi.org/10.1021/acs.analchem.9b03671openalex-snapshot
Gas-Phase Sequencing of Cyclotides: Introduction of Selective Ring Opening at Dehydroalanine via Ion/Ion Reaction
inferred← citeshttps://doi.org/10.1021/acs.biochem.5b00529openalex-snapshot
Using the MCoTI-II Cyclotide Scaffold To Design a Stable Cyclic Peptide Antagonist of SET, a Protein Overexpressed in Human Cancer
inferred← citeshttps://doi.org/10.1021/acs.biochem.6b01212openalex-snapshot
Cyclotide Structure and Function: The Role of Membrane Binding and Permeation
inferred← citeshttps://doi.org/10.1021/acs.chemrev.9b00402openalex-snapshot
Cyclotides: From Structure to Function
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c01080openalex-snapshot
Engineering the Cyclization Loop of MCoTI-II Generates Targeted Cyclotides that Potently Inhibit Factor XIIa
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b00557openalex-snapshot
Substrate-Guided Design of Selective FXIIa Inhibitors Based on the Plant-Derived Momordica cochinchinensis Trypsin Inhibitor-II (MCoTI-II) Scaffold
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01045openalex-snapshot
Evaluation of the in Vivo Aphrodisiac Activity of a Cyclotide Extract from Hybanthus enneaspermus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01065openalex-snapshot
In Planta Discovery and Chemical Synthesis of Bracelet Cystine Knot Peptides from Rinorea bengalensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01069openalex-snapshot
Cyclotides from Brazilian Palicourea sessilis and Their Effects on Human Lymphocytes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c01129openalex-snapshot
Cytotoxic Cyclotides from Anchietea pyrifolia, a South American Plant Species
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00762openalex-snapshot
Cysteine-Rich Peptide Family with Unusual Disulfide Connectivity from Jasminum sambac
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c01216openalex-snapshot
Discovery, Isolation, and Bactericidal Activity of a Cyclotide from Spigelia anthelmia L. (Loganiaceae)
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00061openalex-snapshot
Understanding the Diversity and Distribution of Cyclotides from Plants of Varied Genetic Origin
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00969openalex-snapshot
Inhibition of Breast Cancer Cell Migration by Cyclotides Isolated from Pombalia calceolaria
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00572openalex-snapshot
Discovery and Characterization of Cyclotides from Rinorea Species
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00716openalex-snapshot
Discovery and Characterization of Cyclic and Acyclic Trypsin Inhibitors from Momordica dioica
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00111openalex-snapshot
An Orbitide from Ratibida columnifera Seed Containing 16 Amino Acid Residues
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01209openalex-snapshot
Cyclic Peptides in Seed of Annona muricata Are Ribosomally Synthesized
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01218openalex-snapshot
Exploring the Sequence Diversity of Cyclotides from VietnameseViolaSpecies
inferred← citeshttps://doi.org/10.1021/acs.jpcb.9b07547openalex-snapshot
In Silico Investigation of the Binding of MCoTI-II Plant Defense Knottin to the γ-NGF Serine Protease of the 7S Nerve Growth Factor Complex and Biological Activity of Its NGF Mimetic Properties
inferred← citeshttps://doi.org/10.1021/acschembio.0c00907openalex-snapshot
Tuning the Anti-Angiogenic Effect of the P15 Peptide Using Cyclic Trypsin Inhibitor Scaffolds
inferred← citeshttps://doi.org/10.1021/acschembio.5b00454openalex-snapshot
Lysine-rich Cyclotides: A New Subclass of Circular Knotted Proteins from Violaceae
inferred← citeshttps://doi.org/10.1021/acschembio.6c00509openalex-snapshot
Direct Heterologous Expression of Cyclic Conotoxin [G22N]Vc1.1 in Yeast
inferred← citeshttps://doi.org/10.1021/acschembio.8b00653openalex-snapshot
Targeted Delivery of Cyclotides via Conjugation to a Nanobody
inferred← citeshttps://doi.org/10.1021/acsinfecdis.4c00957openalex-snapshot
Small and Versatile Cyclotides as Anti-infective Agents
inferred← citeshttps://doi.org/10.1021/bi027323nopenalex-snapshot
Linearization of a Naturally Occurring Circular Protein Maintains Structure but Eliminates Hemolytic Activity,
inferred← citeshttps://doi.org/10.1021/cb100388jopenalex-snapshot
Discovery of Cyclotides in the Fabaceae Plant Family Provides New Insights into the Cyclization, Evolution, and Distribution of Circular Proteins
inferred← citeshttps://doi.org/10.1021/cb200395fopenalex-snapshot
Importance of the Cell Membrane on the Mechanism of Action of Cyclotides
inferred← citeshttps://doi.org/10.1021/ja0367703openalex-snapshot
Microcin J25 Has a Threaded Sidechain-to-Backbone Ring Structure and Not a Head-to-Tail Cyclized Backbone
inferred← citeshttps://doi.org/10.1021/jacs.4c11589openalex-snapshot
Enhancing Sensitivity of Nuclear Magnetic Resonance in Biomolecules: Parahydrogen-Induced Hyperpolarization in Synthetic Disulfide-Rich Miniproteins
inferred← citeshttps://doi.org/10.1021/jacs.4c11964openalex-snapshot
Highly Efficient Transpeptidase-Catalyzed Isopeptide Ligation
inferred← citeshttps://doi.org/10.1021/jacs.5b03504openalex-snapshot
Chemical Protein Synthesis Using a Second-Generation N-Acylurea Linker for the Preparation of Peptide-Thioester Precursors
inferred← citeshttps://doi.org/10.1021/jm301468kopenalex-snapshot
Design of a Novel Cyclotide-Based CXCR4 Antagonist with Anti-Human Immunodeficiency Virus (HIV)-1 Activity
inferred← citeshttps://doi.org/10.1021/jm800704eopenalex-snapshot
Engineering Stabilized Vascular Endothelial Growth Factor-A Antagonists: Synthesis, Structural Characterization, and Bioactivity of Grafted Analogues of Cyclotides
inferred← citeshttps://doi.org/10.1021/jo500699mopenalex-snapshot
Fmoc-Based Synthesis of Disulfide-Rich Cyclic Peptides
inferred← citeshttps://doi.org/10.1021/np0499719openalex-snapshot
Reversible Antifouling Effect of the Cyclotide Cycloviolacin O2 against Barnacles
inferred← citeshttps://doi.org/10.1021/np050317iopenalex-snapshot
Cycloviolacin H4, a Hydrophobic Cyclotide fromViola hederaceae
inferred← citeshttps://doi.org/10.1021/np1000413openalex-snapshot
Isolation, Sequencing, and Structure−Activity Relationships of Cyclotides
inferred← citeshttps://doi.org/10.1021/np100790fopenalex-snapshot
Cyclotides from an Extreme Habitat: Characterization of Cyclic Peptides from Viola abyssinica of the Ethiopian Highlands
inferred← citeshttps://doi.org/10.1021/np401055jopenalex-snapshot
Chemistry and Biology of Cyclotides: Circular Plant Peptides Outside the Box
inferred← citeshttps://doi.org/10.1021/np501061topenalex-snapshot
Inhibition of Human Prolyl Oligopeptidase Activity by the Cyclotide Psysol 2 Isolated from Psychotria solitudinum
inferred← citeshttps://doi.org/10.1021/np900174nopenalex-snapshot
Isolation and Characterization of Peptides from Momordica cochinchinensis Seeds
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