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Crystal structure of acetyl-coenzyme a synthetase from coccidioides immitis in complex with prx

Analyse Crystal structure of acetyl-coenzyme a synthetase from coccidioides immitis in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7KQ6
Type
protein
Length
1,808 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Acetyl-coenzyme a synthetase
EC
6.2.1.1
UniProt
J3KJC6
Ligands
PRX
Pockets
17 · best druggability 0.82

Structure

x-ray diffraction · 3 distinct chains · 33% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAcetyl-coenzyme a synthetase (EC 6.2.1.1)protein61032% helix, 25% strandJ3KJC6
BAcetyl-coenzyme a synthetase (EC 6.2.1.1)protein59034% helix, 24% strandJ3KJC6
CAcetyl-coenzyme a synthetase (EC 6.2.1.1)protein60833% helix, 25% strandJ3KJC6

Ligands and binding sites

  • PRX · Adenosine-5'-monophosphate-propyl ester · ligand · 3 copies · chains A, B, C
  • EDO · 1,2-ethanediol · additive · 32 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111360.820.83115EDO
27960.800.8382PRX
37300.800.8488PRX
46810.790.8476PRX
51050.670.9122EDO

Interfaces

3 interfaces between chains.

  • A–B · 759 Ų buried · 5 hydrogen bonds · protein-protein
  • B–C · 758 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 740 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 7KQ6 · Crystal Structure of Acetyl-coenzyme A synthetase from Coccidioides immitis in complex… · the same entry in another collection · chain A against A, TM-score 1.00

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