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Pyridine nucleotide complexes with bacillus anthracis coenzyme a- disulfide reductase: a structural analysis of dual NAD(P)H specificity

Analyse Pyridine nucleotide complexes with bacillus anthracis coenzyme a- disulfide… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3CGE
Type
protein
Length
888 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pyridine nucleotide-disulfide oxidoreductase, class I
UniProt
Q81TK8
Ligands
FAD, COA, NDP
Pockets
3 · best druggability 0.84

Structure

x-ray diffraction · 1 distinct chain · 28% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPyridine nucleotide-disulfide oxidoreductase, class Iprotein44428% helix, 30% strandQ81TK8

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 2 copies · chains A, B
  • COA · Coenzyme A · ligand · 2 copies · chains A, B
  • NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · 2 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
110540.840.85105FAD, COA, NDP
211020.830.84107FAD, COA, NDP
33300.610.7938empty

Interfaces

1 interface between chains.

  • A–B · 2751 Ų buried · 32 hydrogen bonds · protein-protein

Compared structures

  • 3CGE · Pyridine Nucleotide Complexes with Bacillus anthracis Coenzyme A-Disulfide Reductase: A… · the same entry in another collection · chain A against A, TM-score 1.00

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