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Crystal structure of biotin protein ligase from pyrococcus horikoshii OT3 in complex with biotinyl-5'-AMP, mutation ARG51ALA

Analyse Crystal structure of biotin protein ligase from pyrococcus horikoshii OT3 in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2DVE
Type
protein
Length
470 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Biotin protein ligase
EC
6.3.4.15
UniProt
O57883
Ligands
BT5
Pockets
5 · best druggability 0.61

Structure

x-ray diffraction · 1 distinct chain · 28% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BBiotin protein ligase (EC 6.3.4.15)protein23528% helix, 31% strandO57883

Ligands and binding sites

  • BT5 · Biotinyl-5-amp · ligand · 2 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12620.610.8144BT5
21820.590.8239BT5
31460.450.7627empty
41230.450.7822empty
51040.420.7718empty

Interfaces

1 interface between chains.

  • A–B · 1032 Ų buried · 26 hydrogen bonds · protein-protein

Compared structures

  • 2DVE · Crystal Structure Of Biotin Protein Ligase From Pyrococcus Horikoshii OT3 in Complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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