Structure of chymotrypsin-trifluoromethyl ketone inhibitor complexes: comparison of slowly and rapidly equilibrating inhibitors
about
Kinetic and crystallographic analysis of complexes formed between elastase and peptides from beta-caseinStructure of a serine protease poised to resynthesize a peptide bondInhibition of Chymotrypsin by a Complex of Ortho-Vanadate and Benzohydroxamic Acid: Structure of the Inert Complex and Its Mechanistic Interpretation †Inhibition of dd -Peptidases by a Specific Trifluoroketone: Crystal Structure of a Complex with the Actinomadura R39 dd -PeptidaseAttempts to convert chymotrypsin to trypsinA study of the stabilization of tetrahedral adducts by trypsin and delta-chymotrypsin.Fractionation factors and activation energies for exchange of the low barrier hydrogen bonding proton in peptidyl trifluoromethyl ketone complexes of chymotrypsinStructural and energetic determinants of the S1-site specificity in serine proteases.High-precision measurement of hydrogen bond lengths in proteins by nuclear magnetic resonance methods.Transient intermediates in enzymology, 1964-2008.Identification of selective covalent inhibitors of platelet activating factor acetylhydrolase 1B2 from the screening of an oxadiazolone-capped peptoid-azapeptoid hybrid library.Influence of sulfur oxidation state and steric bulk upon trifluoromethyl ketone (TFK) binding kinetics to carboxylesterases and fatty acid amide hydrolase (FAAH).An Update on the Status of Potent Inhibitors of Metallo-β-Lactamases.Similarity search for local protein structures at atomic resolution by exploiting a database management system.Use of Fluorinated Functionality in Enzyme Inhibitor Development: Mechanistic and Analytical AdvantagesPhosphinic peptides, the first potent inhibitors of astacin, behave as extremely slow-binding inhibitors.Studies on the specificity of acetylaminoacyl-peptide hydrolase.Steric complementarity in the decoding center is important for tRNA selection by the ribosomeStereoselective synthesis of peptidyl trifluoromethyl alcohols and ketones: inhibitory potency against human leucocyte elastase, cathepsin G, porcine pancreatic elastase and HIV-1 protease.Effects of water content on the tetrahedral intermediate of chymotrypsin - trifluoromethylketone in polar and non-polar media: observations from molecular dynamics simulation.The low barrier hydrogen bond in enzymatic catalysis.Structural Analyses on Intermediates in Serine Protease Catalysis13C and1H NMR Studies of Ionizations and Hydrogen Bonding in Chymotrypsin-Glyoxal Inhibitor Complexes
P2860
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P2860
Structure of chymotrypsin-trifluoromethyl ketone inhibitor complexes: comparison of slowly and rapidly equilibrating inhibitors
description
1990 nî lūn-bûn
@nan
1990 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@ast
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@en
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@nl
type
label
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@ast
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@en
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@nl
prefLabel
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@ast
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@en
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@nl
P2093
P356
P1433
P1476
Structure of chymotrypsin-trif ...... pidly equilibrating inhibitors
@en
P2093
P304
P356
10.1021/BI00485A009
P407
P577
1990-08-21T00:00:00Z