8UQA: PDB entry 8UQA

Crystal structure of RNF168 (RING)-UbcH5c fused to H2A-H2B via a 12-residue linker. Determined by X-ray diffraction at 2.05 Å resolution. Released 17 Jan 2024.

Method
X-ray diffraction
Resolution
2.05 Å
Organism
Homo sapiens
Chains
1
Atoms
3,645
Mol. weight
49.87 kDa
Ligands
ZN
Released
17 Jan 2024

Explore 8UQA in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

8UQA contains 22 α-helices and 20 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain K: 22 helices, 20 β-strands

ElementResiduesLengthSheet
β-strand15-1621
β-strand21-2221
β-strand26-2832
β-strand34-3632
α-helix37-404
α-helix41-488
β-strand5013
β-strand5713
α-helix59-668
β-strand7212
α-helix74-8310
α-helix85-939
α-helix101-101515
α-helix1017-10182
β-strand1021-102664
β-strand1029-1038104
α-helix1039-10402
β-strand1049-105574
α-helix1064-10652
β-strand1066-106944
β-strand107515
β-strand107815
β-strand108415
α-helix1087-10893
α-helix1099-111113
α-helix1121-11299
α-helix1131-114515
β-strand115416
β-strand115616
α-helix2038-204811
β-strand2053-205427
α-helix2056-208328
β-strand2088-208928
α-helix2091-210111
α-helix2104-212219
α-helix3017-30215
α-helix3027-303610
β-strand3042-304328
α-helix3046-307227
β-strand3077-307827
α-helix3080-30889
α-helix3091-30977

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
E3 ubiquitin-protein ligase RNF168,Ubiquitin-conjugating enzyme E2 D3,Histone H2B type 2-E,Histone…Kprotein447Homo sapiensP04908 (AlphaFold model), P61077 (AlphaFold model), Q16778 (AlphaFold model), Q8IYW5 (AlphaFold model)
Sequence of entity 1 (K), FASTA
>8UQA_1 E3 ubiquitin-protein ligase RNF168,Ubiquitin-conjugating enzyme E2 D3,Histone H2B type 2-E,Histone H2A type 1-B/E (chains K)
GHMALPKDAIPSLSECQCGICMEILVEPVTLPCNHTLCKPCFQSTVEKASLCCPFCRRRV
SSWTRYHTRRNSLVNVELWTIIQKHYPRECKLRASGSGSGSGSALKRINKELSDLARDPP
AQCSAGPVGDDMFHWQATIMGPNDSPYQGGVFFLTIHFPTDYPFKPPKVAFTTRIYHPNI
NSNGSIKLDILRSQWSPALTISKVLLSICSLLCDPNPDDPLVPEIARIYKTDRDKYNRIS
REWTQKYAMGSGGSGGSGSGSRKESYSIYVYKVLKQVHPDTGISSKAMGIMNSFVNDIFE
RIAGEASRLAHYNKRSTITSREIQTAVRLLLPGELAKHAVSEGTKAVTKYTSSAKAKTRS
SRAGLQFPVGRVHRLLRKGNYSERVGAGAPVYLAAVLEYLTAEILELAGNAARDNKKTRI
IPRHLQLAIRNDEELNKLLGRVTIAQG

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn2

Water and common crystallization additives (NA, CL) are not listed.

Primary citation

Mechanisms of RNF168 nucleosome recognition and ubiquitylation. Hu, Q., Zhao, D., Cui, G. et al. Mol Cell (2024) 84:839-853.e12. DOI 10.1016/j.molcel.2023.12.036 · PubMed

Other PDB entries of the same protein (UniProt P04908 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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