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Crystal structure of biotin carboxylase from E. COLI in complex with the 3-(3-methyl-but-2-enyl)-3H-purin-6- ylamine fragment

Analyse Crystal structure of biotin carboxylase from E. COLI in complex with the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2W6Z
Type
protein
Length
891 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Biotin carboxylase
EC
6.3.4.14, 6.4.1.2
UniProt
P24182
Ligands
L21, CL
Pockets
6 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABiotin carboxylase (EC 6.3.4.14, 6.4.1.2)protein44637% helix, 27% strandP24182
BBiotin carboxylase (EC 6.3.4.14, 6.4.1.2)protein44536% helix, 27% strandP24182

Ligands and binding sites

  • L21 · 3-(3-methylbut-2-en-1-yl)-3H-purin-6-amine · ligand · chains A
  • CL · Chloride ion · ion · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17350.740.8072L21, CL
23140.740.8748empty
37170.730.7980CL
4620.370.7813empty
5700.370.7712empty

Interfaces

1 interface between chains.

  • A–B · 1440 Ų buried · 21 hydrogen bonds · protein-protein

Compared structures

  • 2W6Z · Crystal structure of Biotin carboxylase from E. coli in complex with the… · the same entry in another collection · chain A against A, TM-score 1.00
  • P24182 · AlphaFold monomer V2.0 prediction for biotin carboxylase (P24182) · a predicted model of the same protein · chain B against A, TM-score 1.00

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