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MolNFT v1 · #46725 · protein

Crystal structure of YHST2 bound to the intermediate analogue ADP-hpd, and and aceylated H4 peptide

2OD7 · NAD-dependent deacetylase HST2: “Crystal structure of YHST2 bound to the intermediate analogue ADP-hpd, and and aceylated H4 peptide”. X-ray diffraction, 2 ligands (A1R, ZN), 2 pockets (best druggability 0.72). MolNFT v1 #46725 on…

PDB
2OD7
Type
protein
Length
297 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NAD-dependent deacetylase HST2; Acetylated histone H4 peptide
EC
3.5.1.-
UniProt
P53686
Ligands
A1R, ZN
Pockets
2 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANAD-dependent deacetylase HST2 (EC 3.5.1.-)protein28942% helix, 17% strandP53686
BAcetylated histone H4 peptideprotein80% helix, 38% strand—

Ligands and binding sites

  • A1R · 5'-O-[(S)-{[(S)-{[(2R,3R,4S)-3,4-dihydroxypyrrolidin-2-yl]methoxy}(hydroxy)phosphoryl]oxy}(hydroxy) phosphoryl]adenosine · ligand · chains A, B
  • ZN · Zinc ion · metal · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13690.720.8444A1R
2790.290.7220empty

Interfaces

1 interface between chains.

  • A–B · 640 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 modified (acetylation).

Compared structures

  • 2OD7 · Crystal Structure of yHst2 bound to the intermediate analogue ADP-HPD, and and aceylated… · the same entry in another collection · chain A against A, TM-score 1.00
  • P53686 · AlphaFold monomer V2.0 prediction for NAD-dependent protein deacetylase HST2 (P53686) · a predicted model of the same protein · chain A against A, TM-score 0.93

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