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Mycobacterium tuberculosis biotin ligase complexed with bisubstrate inhibitor 46 with azide in place of 2'OH

Analyse Mycobacterium tuberculosis biotin ligase complexed with bisubstrate inhibitor… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4XTW
Type
protein
Length
525 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional LIGASE/REPRESSOR bira
EC
6.3.4.15
UniProt
A0A045H8W3
Ligands
44M
Pockets
6 · best druggability 0.64

Structure

x-ray diffraction · 2 distinct chains · 30% helix, 32% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABifunctional LIGASE/REPRESSOR bira (EC 6.3.4.15)protein26631% helix, 31% strandA0A045H8W3
BBifunctional LIGASE/REPRESSOR bira (EC 6.3.4.15)protein25929% helix, 32% strandA0A045H8W3

Ligands and binding sites

  • 44M · 2'-azido-2',5'-dideoxy-5'-[({5-[(3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoyl}sulfamoyl)amino]adenosine · ligand · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · chains A

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
12250.640.834144M
22970.610.7930EDO
32270.610.824344M
41690.480.7724empty
5510.360.7910empty

Interfaces

1 interface between chains.

  • A–B · 790 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 4XTW · Mycobacterium tuberculosis biotin ligase complexed with bisubstrate inhibitor 46 with… · the same entry in another collection · chain A against A, TM-score 1.00

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