5JG6
APC11-Ubv shows role of noncovalent RING-Ubiquitin interactions in processive multiubiquitination and Ubiquitin chain elongation by APC/C
Summary for 5JG6
Entry DOI | 10.2210/pdb5jg6/pdb |
Descriptor | Anaphase-promoting complex subunit 11, Polyubiquitin-B, ZINC ION, ... (4 entities in total) |
Functional Keywords | ring ubiquitin cell cycle anaphase-promoting complex-cyclosome, cell cycle |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 4 |
Total formula weight | 35004.73 |
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 citation | Brown, 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: 27259151DOI: 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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