6H3C
Cryo-EM structure of the BRISC complex bound to SHMT2
6H3C の概要
エントリーDOI | 10.2210/pdb6h3c/pdb |
関連するPDBエントリー | 6GVW |
EMDBエントリー | 0132 |
分子名称 | BRISC complex subunit Abraxas 2, Lys-63-specific deubiquitinase BRCC36, BRISC and BRCA1-A complex member 2, ... (7 entities in total) |
機能のキーワード | deubiquitinase complex, dub, lysine-63 linkage specific, brcc36-containing, brca1a binding, signaling protein |
由来する生物種 | Homo sapiens (Human) 詳細 |
タンパク質・核酸の鎖数 | 10 |
化学式量合計 | 458077.08 |
構造登録者 | |
主引用文献 | Rabl, J.,Bunker, R.D.,Schenk, A.D.,Cavadini, S.,Gill, M.E.,Abdulrahman, W.,Andres-Pons, A.,Luijsterburg, M.S.,Ibrahim, A.F.M.,Branigan, E.,Aguirre, J.D.,Marceau, A.H.,Guerillon, C.,Bouwmeester, T.,Hassiepen, U.,Peters, A.H.F.M.,Renatus, M.,Gelman, L.,Rubin, S.M.,Mailand, N.,van Attikum, H.,Hay, R.T.,Thoma, N.H. Structural Basis of BRCC36 Function in DNA Repair and Immune Regulation. Mol.Cell, 75:483-497.e9, 2019 Cited by PubMed Abstract: In mammals, ∼100 deubiquitinases act on ∼20,000 intracellular ubiquitination sites. Deubiquitinases are commonly regarded as constitutively active, with limited regulatory and targeting capacity. The BRCA1-A and BRISC complexes serve in DNA double-strand break repair and immune signaling and contain the lysine-63 linkage-specific BRCC36 subunit that is functionalized by scaffold subunits ABRAXAS and ABRO1, respectively. The molecular basis underlying BRCA1-A and BRISC function is currently unknown. Here we show that in the BRCA1-A complex structure, ABRAXAS integrates the DNA repair protein RAP80 and provides a high-affinity binding site that sequesters the tumor suppressor BRCA1 away from the break site. In the BRISC structure, ABRO1 binds SHMT2α, a metabolic enzyme enabling cancer growth in hypoxic environments, which we find prevents BRCC36 from binding and cleaving ubiquitin chains. Our work explains modularity in the BRCC36 DUB family, with different adaptor subunits conferring diversified targeting and regulatory functions. PubMed: 31253574DOI: 10.1016/j.molcel.2019.06.002 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.9 Å) |
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