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5JG6

APC11-Ubv shows role of noncovalent RING-Ubiquitin interactions in processive multiubiquitination and Ubiquitin chain elongation by APC/C

Summary for 5JG6
Entry DOI10.2210/pdb5jg6/pdb
DescriptorAnaphase-promoting complex subunit 11, Polyubiquitin-B, ZINC ION, ... (4 entities in total)
Functional Keywordsring ubiquitin cell cycle anaphase-promoting complex-cyclosome, cell cycle
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains4
Total formula weight35004.73
Authors
Brown, N.G.,Zhang, W.,Yu, S.,Miller, D.J.,Sidhu, S.S.,Schulman, B.A. (deposition date: 2016-04-19, release date: 2016-06-15, Last modification date: 2023-09-27)
Primary citationBrown, N.G.,VanderLinden, R.,Watson, E.R.,Weissmann, F.,Ordureau, A.,Wu, K.P.,Zhang, W.,Yu, S.,Mercredi, P.Y.,Harrison, J.S.,Davidson, I.F.,Qiao, R.,Lu, Y.,Dube, P.,Brunner, M.R.,Grace, C.R.,Miller, D.J.,Haselbach, D.,Jarvis, M.A.,Yamaguchi, M.,Yanishevski, D.,Petzold, G.,Sidhu, S.S.,Kuhlman, B.,Kirschner, M.W.,Harper, J.W.,Peters, J.M.,Stark, H.,Schulman, B.A.
Dual RING E3 Architectures Regulate Multiubiquitination and Ubiquitin Chain Elongation by APC/C.
Cell, 165:1440-1453, 2016
Cited by
PubMed Abstract: Protein ubiquitination involves E1, E2, and E3 trienzyme cascades. E2 and RING E3 enzymes often collaborate to first prime a substrate with a single ubiquitin (UB) and then achieve different forms of polyubiquitination: multiubiquitination of several sites and elongation of linkage-specific UB chains. Here, cryo-EM and biochemistry show that the human E3 anaphase-promoting complex/cyclosome (APC/C) and its two partner E2s, UBE2C (aka UBCH10) and UBE2S, adopt specialized catalytic architectures for these two distinct forms of polyubiquitination. The APC/C RING constrains UBE2C proximal to a substrate and simultaneously binds a substrate-linked UB to drive processive multiubiquitination. Alternatively, during UB chain elongation, the RING does not bind UBE2S but rather lures an evolving substrate-linked UB to UBE2S positioned through a cullin interaction to generate a Lys11-linked chain. Our findings define mechanisms of APC/C regulation, and establish principles by which specialized E3-E2-substrate-UB architectures control different forms of polyubiquitination.
PubMed: 27259151
DOI: 10.1016/j.cell.2016.05.037
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.0013 Å)
Structure validation

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數據於2024-11-06公開中

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