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MolNFT v1 · #12444 · protein

Crystal structure analysis of the anthranilate phosphoribosyltransferase from erwinia carotovora (current name, pectobacterium carotovorum)

1KGZ: “Crystal structure analysis of the anthranilate phosphoribosyltransferase from erwinia carotovora (current…”. X-ray diffraction, 3 ligands (PRP, MN, HG), 4 pockets (best druggability 0.71). MolNFT v1 #12444 on GenesisL1: 3D…

PDB
1KGZ
Type
protein
Length
658 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Anthranilate phosphoribosyltransferase
EC
2.4.2.18
UniProt
Q8VP84
Ligands
PRP, MN, HG
Pockets
4 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 51% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAnthranilate phosphoribosyltransferase (EC 2.4.2.18)protein32850% helix, 12% strandQ8VP84
BAnthranilate phosphoribosyltransferase (EC 2.4.2.18)protein33052% helix, 13% strandQ8VP84

Ligands and binding sites

  • PRP · 1-O-pyrophosphono-5-O-phosphono-alpha-D-ribofuranose · ligand · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 4 copies · chains A, B
  • HG · Mercury (II) ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15180.710.8156MN, PRP
24320.680.8051MN, PRP
3970.390.7613empty
4780.360.7614empty

Interfaces

1 interface between chains.

  • A–B · 890 Ų buried · 9 hydrogen bonds · protein-protein

Compared structures

  • 1KGZ · Crystal Structure Analysis of the Anthranilate Phosphoribosyltransferase from Erwinia… · the same entry in another collection · chain A against A, TM-score 1.00

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