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Crystal structure of an oxidoreductase from Burkholderia vietnamiensis in complex with NADP

Analyse Crystal structure of an oxidoreductase from Burkholderia vietnamiensis in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5IDY
Type
protein
Length
526 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.85
Source
Burkholderia vietnamiensis (strain G4 / LMG 22486)
Molecule
Short-chain dehydrogenase/reductase SDR
UniProt
A4JGH3
Ligands
NAP, SO4, CL
Pockets
3 · best druggability 0.71

Structure

x-ray diffraction · resolution 1.85 · 2 distinct chains · 50% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AShort-chain dehydrogenase/reductase SDRprotein26250% helix, 16% strandA4JGH3
BShort-chain dehydrogenase/reductase SDRprotein26449% helix, 16% strandA4JGH3

Ligands and binding sites

  • NAP · Nadp nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 3 copies · chains A, B
  • CL · Chloride ion · ion · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 3 copies · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17100.710.7865NAP
26510.680.7760SO4, NAP
34640.630.7729empty

Interfaces

1 interface between chains.

  • A–B · 1434 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 5IDY · Crystal structure of an oxidoreductase from burkholderia vietnamiensis in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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