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Structural and functional studies of the yeast class II HDA1 hdac complex

Analyse Structural and functional studies of the yeast class II HDA1 hdac complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3HGQ
Type
protein
Length
1,169 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
HDA1 complex subunit 3
UniProt
Q06623
Pockets
15 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHDA1 complex subunit 3protein29941% helix, 12% strandQ06623
B, C, DHDA1 complex subunit 3protein29043% helix, 12% strandQ06623

Pockets

15 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18690.720.7772empty
211630.720.7677empty
34670.640.7744empty
42720.530.7643empty
52700.530.7542empty

Interfaces

4 interfaces between chains.

  • C–D · 875 Ų buried · 8 hydrogen bonds · protein-protein
  • A–B · 872 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 496 Ų buried · 5 hydrogen bonds · protein-protein
  • B–D · 31 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 32 modified (engineered).

Compared structures

  • 3HGQ · Structural and functional studies of the yeast class II Hda1 HDAC complex · the same entry in another collection · chain A against A, TM-score 1.00
  • Q06623 · AlphaFold monomer V2.0 prediction for HDA1 complex subunit 3 (Q06623) · a predicted model of the same protein · chain B against A, TM-score 1.00

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