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MolNFT v1 · #43556 · protein

NMR structure of UHRF1 phd domains in a complex with histone H3 peptide

2LGK · E3 ubiquitin-protein ligase UHRF1: “NMR structure of UHRF1 phd domains in a complex with histone H3 peptide”. Solution nmr, 1 ligand (ZN), 1 pocket (best druggability 0.58). MolNFT v1 #43556 on GenesisL1: 3D structure, binding sites…

PDB
2LGK
Type
protein
Length
81 residues
Chains
2
Method
solution nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
E3 ubiquitin-protein ligase UHRF1; Histone H3 peptide
EC
6.3.2.-
UniProt
Q96T88
Ligands
ZN
Pockets
1 · best druggability 0.58

Structure

solution nmr · 2 distinct chains · 9% helix, 5% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AE3 ubiquitin-protein ligase UHRF1 (EC 6.3.2.-)protein6910% helix, 6% strandQ96T88
BHistone H3 peptideprotein120% helix, 0% strand—

Ligands and binding sites

  • ZN · Zinc ion · metal · 3 copies · chains A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1990.580.8622empty

Interfaces

1 interface between chains.

  • A–B · 606 Ų buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (methylation).

Compared structures

  • 2LGK · NMR Structure of UHRF1 PHD domains in a complex with histone H3 peptide · the same entry in another collection · chain A against A, TM-score 1.00
  • Q96T88 · AlphaFold monomer V2.0 prediction for E3 ubiquitin-protein ligase UHRF1 (Q96T88) · a predicted model of the same protein · chain A against A, TM-score 0.59

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