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Inosine 5'-monophosphate dehydrogenase from vibrio cholerae, deletion mutant, in complex with xmp and NAD

Analyse Inosine 5'-monophosphate dehydrogenase from vibrio cholerae, deletion mutant… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4X3Z
Type
protein
Length
690 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Inosine-5'-monophosphate dehydrogenase
EC
1.1.1.205
UniProt
Q9KTW3
Ligands
XMP, NAD, K, PO4
Pockets
8 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AInosine-5'-monophosphate dehydrogenase (EC 1.1.1.205)protein34237% helix, 18% strandQ9KTW3
BInosine-5'-monophosphate dehydrogenase (EC 1.1.1.205)protein34835% helix, 19% strandQ9KTW3

Ligands and binding sites

  • XMP · Xanthosine-5'-monophosphate · ligand · 2 copies · chains A, B
  • NAD · Nicotinamide-adenine-dinucleotide · ligand · 2 copies · chains A, B
  • K · Potassium ion · metal · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · chains B
  • GOL · Glycerol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14670.770.8558XMP, NAD
23520.740.8539XMP, NAD
33700.570.7543empty
42610.520.7524empty
52150.500.7522empty

Interfaces

1 interface between chains.

  • A–B · 400 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 4X3Z · Inosine 5'-monophosphate dehydrogenase from Vibrio cholerae, deletion mutant, in complex… · the same entry in another collection · chain A against A, TM-score 1.00

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