Unique D box and KEN box sequences limit ubiquitination of Acm1 and promote pseudosubstrate inhibition of the anaphase-promoting complex
about
Modulation of cell cycle control during oocyte-to-embryo transitionsCasein kinase 1δ is an APC/C(Cdh1) substrate that regulates cerebellar granule cell neurogenesis.The polyglutamine-expanded androgen receptor responsible for spinal and bulbar muscular atrophy inhibits the APC/C(Cdh1) ubiquitin ligase complex.Structural analysis of human Cdc20 supports multisite degron recognition by APC/CStructure of the mitotic checkpoint complexInsights into Degron Recognition by APC/C Coactivators from the Structure of an Acm1-Cdh1 ComplexMechanisms of pseudosubstrate inhibition of the anaphase promoting complex by Acm1.Ama1p-activated anaphase-promoting complex regulates the destruction of Cdc20p during meiosis II.The eukaryotic linear motif resource ELM: 10 years and countingMes1 controls the meiosis I to meiosis II transition by distinctly regulating the anaphase-promoting complex/cyclosome coactivators Fzr1/Mfr1 and Slp1 in fission yeastTimely activation of budding yeast APCCdh1 involves degradation of its inhibitor, Acm1, by an unconventional proteolytic mechanism.Proteome-wide discovery of evolutionary conserved sequences in disordered regions.Mutually dependent degradation of Ama1p and Cdc20p terminates APC/C ubiquitin ligase activity at the completion of meiotic development in yeast.Substrate Recognition by the Cdh1 Destruction Box Receptor Is a General Requirement for APC/CCdh1-mediated ProteolysisEmi1 preferentially inhibits ubiquitin chain elongation by the anaphase-promoting complex.Structure, function and mechanism of the anaphase promoting complex (APC/C).Structural insights into anaphase-promoting complex function and mechanism.Fulfilling the metabolic requirements for cell proliferation.Panta rhei: the APC/C at steady state.Understanding the structural basis for controlling chromosome division.Ubiquitination site preferences in anaphase promoting complex/cyclosome (APC/C) substrates.Acm1 contributes to nuclear positioning by inhibiting Cdh1-substrate interactions.Emi2-mediated inhibition of E2-substrate ubiquitin transfer by the anaphase-promoting complex/cyclosome through a D-box-independent mechanism.Degradation of mouse NTE-related esterase by macroautophagy and the proteasome.The destruction box is involved in the degradation of the NTE family proteins by the proteasome.
P2860
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P2860
Unique D box and KEN box sequences limit ubiquitination of Acm1 and promote pseudosubstrate inhibition of the anaphase-promoting complex
description
2008 nî lūn-bûn
@nan
2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Unique D box and KEN box seque ...... the anaphase-promoting complex
@ast
Unique D box and KEN box seque ...... the anaphase-promoting complex
@en
Unique D box and KEN box seque ...... he anaphase-promoting complex.
@nl
type
label
Unique D box and KEN box seque ...... the anaphase-promoting complex
@ast
Unique D box and KEN box seque ...... the anaphase-promoting complex
@en
Unique D box and KEN box seque ...... he anaphase-promoting complex.
@nl
prefLabel
Unique D box and KEN box seque ...... the anaphase-promoting complex
@ast
Unique D box and KEN box seque ...... the anaphase-promoting complex
@en
Unique D box and KEN box seque ...... he anaphase-promoting complex.
@nl
P2093
P2860
P3181
P356
P1476
Unique D box and KEN box seque ...... the anaphase-promoting complex
@en
P2093
Dah-Eun Jeong
Eunyoung Choi
J Michael Dial
P2860
P304
23701-23710
P3181
P356
10.1074/JBC.M803695200
P407
P50
P577
2008-07-02T00:00:00Z