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Structure of quinolinate synthase in complex with 5-mercaptopyridine- 2,3-dicarboxylic acid

Analyse Structure of quinolinate synthase in complex with 5-mercaptopyridine… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6I0R
Type
protein
Length
303 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Quinolinate synthase a
EC
2.5.1.72
UniProt
Q9X1X7
Ligands
QAT, FE, H2S
Pockets
2 · best druggability 0.77

Structure

x-ray diffraction · 1 distinct chain · 46% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AQuinolinate synthase a (EC 2.5.1.72)protein30346% helix, 16% strandQ9X1X7

Ligands and binding sites

  • QAT · 5-mercaptopyridine-2,3-dicarboxylic acid · ligand · chains A
  • FE · Fe (III) ion · metal · 4 copies · chains A
  • H2S · Hydrosulfuric acid · ion · 4 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12020.770.9238FE, H2S, QAT
2510.270.7410empty

Compared structures

  • 6I0R · Structure of quinolinate synthase in complex with 5-mercaptopyridine-2,3-dicarboxylic acid · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9X1X7 · AlphaFold monomer V2.0 prediction for quinolinate synthase a (Q9X1X7) · a predicted model of the same protein · chain A against A, TM-score 0.98

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