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Crystal structure of biotin carboxylase from E. COLI in complex with the triazine-2,4-diamine 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
2W6Q
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
OA5, CL
Pockets
6 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 37% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABiotin carboxylase (EC 6.3.4.14, 6.4.1.2)protein44637% helix, 28% strandP24182
BBiotin carboxylase (EC 6.3.4.14, 6.4.1.2)protein44537% helix, 27% strandP24182

Ligands and binding sites

  • OA5 · 6-(2-phenoxyethoxy)-1,3,5-triazine-2,4-diamine · ligand · 2 copies · chains A, B
  • 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, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17260.750.8075OA5, CL
23400.740.8650empty
37210.720.7863OA5, CL
4580.660.9525empty
5710.380.7815empty

Interfaces

1 interface between chains.

  • A–B · 1413 Ų buried · 24 hydrogen bonds · protein-protein

Compared structures

  • 2W6Q · 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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