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MolNFT v1 · #137134 · protein

Solution NMR structure of histone H2A-H2B mono-ubiquitylated at H2A LYS15 in complex with RNF169 (653-708)

5VEY · Histone H2B type 1-J,HISTONE H2A type 1-B/E: “Solution NMR structure of histone H2A-H2B mono-ubiquitylated at H2A LYS15 in complex with RNF169 (653-708)”. Solution nmr, 2 pockets (best druggability 0.51). MolNFT v1 #137134 on…

PDB
5VEY
Type
protein
Length
321 residues
Chains
3
Method
solution nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histone H2B type 1-J,HISTONE H2A type 1-B/E; Polyubiquitin-B; E3 ubiquitin-protein ligase…
EC
2.3.2.27
UniProt
P06899, P04908, P0CG47, Q8NCN4
Pockets
2 · best druggability 0.51

Structure

solution nmr · 3 distinct chains · 55% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistone H2B type 1-J,HISTONE H2A type 1-B/Eprotein18669% helix, 4% strandP06899, P04908
BPolyubiquitin-Bprotein7625% helix, 34% strandP0CG47
CE3 ubiquitin-protein ligase RNF169 (EC 2.3.2.27)protein5951% helix, 0% strandQ8NCN4

Pockets

2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11970.510.7719empty
21790.420.7333empty

Interfaces

3 interfaces between chains.

  • B–C · 629 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 526 Ų buried · 7 hydrogen bonds · protein-protein
  • A–B · 217 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 isopeptide (isopeptide).

Compared structures

  • 5VEY · Solution NMR structure of histone H2A-H2B mono-ubiquitylated at H2A Lys15 in complex with… · the same entry in another collection · chain A against A, TM-score 1.00
  • Q8NCN4 · AlphaFold monomer V2.0 prediction for E3 ubiquitin-protein ligase RNF169 (Q8NCN4) · a predicted model of the same protein · chain C against A, TM-score 0.55

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