Mutational analysis of the ras converting enzyme reveals a requirement for glutamate and histidine residues
about
USP17 regulates Ras activation and cell proliferation by blocking RCE1 activityMechanism of farnesylated CAAX protein processing by the intramembrane protease Rce1Small-molecule inhibitors of the Rce1p CaaX proteaseSte24p Mediates Proteolysis of Both Isoprenylated and Non-prenylated Oligopeptides.Chemical inhibition of CaaX protease activity disrupts yeast Ras localization.The Abi-domain protein Abx1 interacts with the CovS histidine kinase to control virulence gene expression in group B Streptococcus.Modulation of the inhibitor properties of dipeptidyl (acyloxy)methyl ketones toward the CaaX proteases.Therapeutic intervention based on protein prenylation and associated modificationsPhotoaffinity labeling of Ras converting enzyme 1 (Rce1p) using a benzophenone-containing peptide substrate.HIV protease inhibitors block streptolysin S productionExpansion of type II CAAX proteases reveals evolutionary origin of γ-secretase subunit APH-1Photoaffinity labeling of Ras converting enzyme using peptide substrates that incorporate benzoylphenylalanine (Bpa) residues: improved labeling and structural implications8-Hydroxyquinoline-based inhibitors of the Rce1 protease disrupt Ras membrane localization in human cells.Inhibition of the CaaX proteases Rce1p and Ste24p by peptidyl (acyloxy)methyl ketones.Biogenesis of the Saccharomyces cerevisiae pheromone a-factor, from yeast mating to human disease.Topology of the yeast Ras converting enzyme as inferred from cysteine accessibility studies.Heterologous expression studies of Saccharomyces cerevisiae reveal two distinct trypanosomatid CaaX protease activities and identify their potential targets.YcaO-Dependent Posttranslational Amide Activation: Biosynthesis, Structure, and Function.A shunt pathway limits the CaaX processing of Hsp40 Ydj1p and regulates Ydj1p-dependent phenotypes.A common genetic system for functional studies of pitrilysin and related M16A proteases.Saccharomyces cerevisiae a-factor mutants reveal residues critical for processing, activity, and export.Proteolytic processing of certain CaaX motifs can occur in the absence of the Rce1p and Ste24p CaaX proteases.A novel RCE1 isoform is required for H-Ras plasma membrane localization and is regulated by USP17.Rce1: mechanism and inhibition.
P2860
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P2860
Mutational analysis of the ras converting enzyme reveals a requirement for glutamate and histidine residues
description
2006 nî lūn-bûn
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2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Mutational analysis of the ras ...... utamate and histidine residues
@ast
Mutational analysis of the ras ...... utamate and histidine residues
@en
Mutational analysis of the ras ...... utamate and histidine residues
@nl
type
label
Mutational analysis of the ras ...... utamate and histidine residues
@ast
Mutational analysis of the ras ...... utamate and histidine residues
@en
Mutational analysis of the ras ...... utamate and histidine residues
@nl
prefLabel
Mutational analysis of the ras ...... utamate and histidine residues
@ast
Mutational analysis of the ras ...... utamate and histidine residues
@en
Mutational analysis of the ras ...... utamate and histidine residues
@nl
P2093
P2860
P3181
P356
P1476
Mutational analysis of the ras ...... utamate and histidine residues
@en
P2093
Emily R Hildebrandt
Lisa J Plummer
Stephen B Porter
Victoria A Rogers
Walter K Schmidt
P2860
P304
P3181
P356
10.1074/JBC.M506284200
P407
P577
2005-12-17T00:00:00Z