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Anthranilate phosphoribosyltransferase variant R193L from mycobacterium tuberculosis with PYROPHOSPHATE/PRPP and MG2+ bound

Analyse Anthranilate phosphoribosyltransferase variant R193L from mycobacterium… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4X5C
Type
protein
Length
692 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Anthranilate phosphoribosyltransferase
EC
2.4.2.18
UniProt
A5U4M0
Ligands
PRP, POP, MG
Pockets
6 · best druggability 0.76

Structure

x-ray diffraction · 2 distinct chains · 52% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAnthranilate phosphoribosyltransferase (EC 2.4.2.18)protein34752% helix, 12% strandA5U4M0
BAnthranilate phosphoribosyltransferase (EC 2.4.2.18)protein34552% helix, 11% strandA5U4M0

Ligands and binding sites

  • PRP · 1-O-pyrophosphono-5-O-phosphono-alpha-D-ribofuranose · ligand · chains A
  • POP · Pyrophosphate 2- · ligand · chains B
  • MG · Magnesium ion · metal · 4 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15090.760.8451PRP, MG
22810.610.8041POP, MG
3780.390.7821empty
4600.390.8016empty
5810.340.7516empty

Interfaces

1 interface between chains.

  • A–B · 867 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 4X5C · Anthranilate phosphoribosyltransferase variant R193L from Mycobacterium tuberculosis with… · the same entry in another collection · chain A against A, TM-score 1.00
  • A5U4M0 · AlphaFold monomer V2.0 prediction for anthranilate phosphoribosyltransferase (A5U4M0) · a predicted model of the same protein · chain A against A, TM-score 0.99

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