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Ca. korarchaeum cryptofilum ACD1 in complex with coenzyme a

Analyse Ca. korarchaeum cryptofilum ACD1 in complex with coenzyme a in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4XYL
Type
protein
Length
1,377 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha subunit of acyl-CoA synthetase (ndp forming); Beta subunit of acyl-CoA synthetase…
UniProt
B1L3C9, B1L7P8
Ligands
COA, CL
Pockets
15 · best druggability 0.77

Structure

x-ray diffraction · 3 distinct chains · 40% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CAlpha subunit of acyl-CoA synthetase (ndp forming)protein46343% helix, 18% strandB1L3C9
BBeta subunit of acyl-CoA synthetase (ndp forming)protein22538% helix, 29% strandB1L7P8
DBeta subunit of acyl-CoA synthetase (ndp forming)protein22637% helix, 29% strandB1L7P8

Ligands and binding sites

  • COA · Coenzyme A · ligand · 2 copies · chains A, C
  • CL · Chloride ion · ion · 2 copies · chains A, C

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

Pockets

15 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19970.770.79104CL
28300.760.80100CL
39850.730.7679empty
44460.690.8143empty
51470.530.8018empty

Interfaces

4 interfaces between chains.

  • A–C · 1952 Ų buried · 24 hydrogen bonds · protein-protein
  • C–D · 823 Ų buried · 13 hydrogen bonds · protein-protein
  • A–B · 818 Ų buried · 13 hydrogen bonds · protein-protein
  • B–D · 534 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 4XYL · Ca. Korarchaeum cryptofilum ACD1 in complex with coenzyme A · the same entry in another collection · chain A against A, TM-score 1.00

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