Molecular recognition. Conformational analysis of limited proteolytic sites and serine proteinase protein inhibitors.
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A systematic comparative and structural analysis of protein phosphorylation sites based on the mtcPTM databaseStructure of human brain fructose 1,6-(bis)phosphate aldolase: linking isozyme structure with functionThe structure of Saccharomyces cerevisiae Met8p, a bifunctional dehydrogenase and ferrochelatase.Crystal structures and enzymatic properties of three formyltransferases from archaea: environmental adaptation and evolutionary relationshipGlobal sequencing of proteolytic cleavage sites in apoptosis by specific labeling of protein N terminiFunctional annotation by identification of local surface similarities: a novel tool for structural genomicsCrystal structure of the peptidyl-cysteine decarboxylase EpiD complexed with a pentapeptide substrateCrystal structure and substrate binding modeling of the uroporphyrinogen-III decarboxylase from Nicotiana tabacum. Implications for the catalytic mechanismStructures of F420H2:NADP+ oxidoreductase with and without its substrates bound.Crystal structure of the yeast cytochrome bc1 complex with its bound substrate cytochrome cA clogged gutter mechanism for protease inhibitors.Unbound form of tomato inhibitor-II reveals interdomain flexibility and conformational variability in the reactive site loopsSolution structure and thermal stability of ribosomal protein L30e from hyperthermophilic archaeonThermococcus celerThe solution structure of bovine pancreatic trypsin inhibitor at high pressureStructural determinants of nitroxide motion in spin-labeled proteins: Tertiary contact and solvent-inaccessible sites in helix G of T4 lysozymeLigand-specific regulation of the extracellular surface of a G-protein-coupled receptorDual GPCR and GAG mimicry by the M3 chemokine decoy receptorStructural basis for accelerated cleavage of bovine pancreatic trypsin inhibitor (BPTI) by human mesotrypsinStructural Basis for a Distinct Catalytic Mechanism in Trypanosoma brucei Tryparedoxin PeroxidaseCrystal Structure of a Trypanocidal 4,4′-Bis(imidazolinylamino)diphenylamine Bound to DNA ,Long-range Electrostatic Complementarity Governs Substrate Recognition by Human Chymotrypsin C, a Key Regulator of Digestive Enzyme ActivationStructure of theAeropyrum pernixL7Ae multifunctional protein and insight into its extreme thermostabilityStructure of the prolyl-acyl carrier protein oxidase involved in the biosynthesis of the cyanotoxin anatoxin-aHydrophilic side chains in the third and seventh transmembrane helical domains of human A2A adenosine receptors are required for ligand recognitionSpatial clustering of isozyme-specific residues reveals unlikely determinants of isozyme specificity in fructose-1,6-bisphosphate aldolaseStructure of a serpin-enzyme complex probed by cysteine substitutions and fluorescence spectroscopy.Structural and functional similarities between osmotin from Nicotiana tabacum seeds and human adiponectinβ-lactoglobulin's conformational requirements for ligand binding at the calyx and the dimer interphase: a flexible docking studyStructural determinants of the half-life and cleavage site preference in the autolytic inactivation of chymotrypsinMastering the canonical loop of serine protease inhibitors: enhancing potency by optimising the internal hydrogen bond networkIn vitro recombination of non-homologous genes can result in gene fusions that confer a switching phenotype to cellsPredicted structure of the extracellular region of ligand-gated ion-channel receptors shows SH2-like and SH3-like domains forming the ligand-binding siteA localized specific interaction alters the unfolding pathways of structural homologues.Energetics of aliphatic deletions in protein coresHow well can the accuracy of comparative protein structure models be predicted?Structural determinants of limited proteolysis.Probing the 3-D structure, dynamics, and stability of bacterial collagenase collagen binding domain (apo- versus holo-) by limited proteolysis MALDI-TOF MS.High-throughput characterization of intrinsic disorder in proteins from the Protein Structure Initiative.Design of synthetic hexapeptide substrates for prostate-specific antigen using single-position minilibraries.A multi-factor model for caspase degradome prediction
P2860
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P2860
Molecular recognition. Conformational analysis of limited proteolytic sites and serine proteinase protein inhibitors.
description
1991 nî lūn-bûn
@nan
1991 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
name
Molecular recognition. Conform ...... proteinase protein inhibitors.
@ast
Molecular recognition. Conform ...... proteinase protein inhibitors.
@en
Molecular recognition. Conform ...... proteinase protein inhibitors.
@nl
type
label
Molecular recognition. Conform ...... proteinase protein inhibitors.
@ast
Molecular recognition. Conform ...... proteinase protein inhibitors.
@en
Molecular recognition. Conform ...... proteinase protein inhibitors.
@nl
prefLabel
Molecular recognition. Conform ...... proteinase protein inhibitors.
@ast
Molecular recognition. Conform ...... proteinase protein inhibitors.
@en
Molecular recognition. Conform ...... proteinase protein inhibitors.
@nl
P1476
Molecular recognition. Conform ...... proteinase protein inhibitors.
@en
P2093
Campbell SF
Hubbard SJ
P304
P356
10.1016/0022-2836(91)90027-4
P407
P577
1991-07-01T00:00:00Z