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MolNFT v1 · #151116 · protein

Crystal structure of 2-hydroxyisobutyryl-CoA ligase (hcl) in complex with 2-hib-AMP and CoA in the thioesterfication state

6HE0 · 2-hydroxyisobutyryl-CoA synthetase: “Crystal structure of 2-hydroxyisobutyryl-CoA ligase (hcl) in complex with 2-hib-AMP and CoA in the…”. X-ray diffraction, 3 ligands (8LE, AMP, COA), 1 pocket (best druggability 0.82). MolNFT v1…

PDB
6HE0
Type
protein
Length
477 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
2-hydroxyisobutyryl-CoA synthetase
EC
6.2.1.-
UniProt
I3VE75
Ligands
8LE, AMP, COA
Pockets
1 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 38% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A2-hydroxyisobutyryl-CoA synthetase (EC 6.2.1.-)protein47738% helix, 21% strandI3VE75

Ligands and binding sites

  • 8LE · [[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] 2-methyl-2-oxidanyl-propanoate · ligand · chains A
  • AMP · Adenosine monophosphate · ligand · chains A
  • COA · Coenzyme A · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110160.820.831078LE, AMP, COA

Compared structures

  • 6HE0 · Crystal structure of 2-Hydroxyisobutyryl-CoA Ligase (HCL) in complex with 2-HIB-AMP and… · the same entry in another collection · chain A against A, TM-score 1.00

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