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Crystal structure of T. maritima GDP-mannose pyrophosphorylase in complex with GDP-mannose.

Analyse Crystal structure of T. maritima GDP-mannose pyrophosphorylase in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2X5Z
Type
protein
Length
666 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Mannose-1-phosphate guanylyltransferase
EC
2.7.7.13
UniProt
Q9X0C3
Ligands
GDD, MG
Pockets
6 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 38% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BMannose-1-phosphate guanylyltransferase (EC 2.7.7.13)protein33338% helix, 28% strandQ9X0C3

Ligands and binding sites

  • GDD · Guanosine-5'-diphosphate-alpha-D-mannose · ligand · 2 copies · chains A, B
  • MG · Magnesium ion · metal · 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16500.730.8068GDD, MG
26030.720.8055GDD
3570.420.8217empty
41010.390.7619empty
5560.360.7912empty

Interfaces

1 interface between chains.

  • A–B · 1402 Ų buried · 22 hydrogen bonds · protein-protein

Compared structures

  • 2X5Z · Crystal structure of T. maritima GDP-mannose pyrophosphorylase in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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