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Structure of acetyl-coenzyme a synthase alpha subunit C-terminal domain F598H mutant

Analyse Structure of acetyl-coenzyme a synthase alpha subunit C-terminal domain F598H… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5H6W
Type
protein
Length
504 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Carbon monoxide DEHYDROGENASE/ACETYL-CoA synthase subunit alpha
EC
2.3.1.169
UniProt
P27988
Pockets
4 · best druggability 0.66

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CCarbon monoxide DEHYDROGENASE/ACETYL-CoA synthase subunit alpha (EC 2.3.1.169)protein12546% helix, 16% strandP27988
B, DCarbon monoxide DEHYDROGENASE/ACETYL-CoA synthase subunit alpha (EC 2.3.1.169)protein12746% helix, 16% strandP27988

Pockets

4 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11530.660.8631empty
21640.630.8427empty
33460.530.7436empty
41180.500.8027empty

Interfaces

4 interfaces between chains.

  • C–D · 588 Ų buried · 9 hydrogen bonds · protein-protein
  • A–B · 572 Ų buried · 8 hydrogen bonds · protein-protein
  • B–D · 409 Ų buried · 1 hydrogen bond · protein-protein
  • A–C · 375 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 5H6W · Structure of acetyl-Coenzyme A synthase Alpha subunit C-terminal domain F598H mutant · the same entry in another collection · chain D against D, TM-score 1.00
  • P27988 · AlphaFold monomer V2.0 prediction for carbon monoxide DEHYDROGENASE/ACETYL-CoA synthase… · a predicted model of the same protein · chain C against A, TM-score 0.99

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