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Crystal structure of oxidoreductase domain protein from kribbella flavida

Analyse Crystal structure of oxidoreductase domain protein from kribbella flavida in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4H3V
Type
protein
Length
760 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Oxidoreductase domain protein
UniProt
D2PU28
Pockets
7 · best druggability 0.64

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AOxidoreductase domain proteinprotein38538% helix, 25% strandD2PU28
BOxidoreductase domain proteinprotein37538% helix, 26% strandD2PU28

Ligands and binding sites

  • FMT · Formic acid · additive · 3 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11790.640.8531empty
22030.630.8330empty
32870.620.8023empty
4910.370.7516FMT
5930.340.7417empty

Interfaces

1 interface between chains.

  • A–B · 1837 Ų buried · 30 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 10 modified (engineered).

Compared structures

  • 4H3V · Crystal structure of oxidoreductase domain protein from Kribbella flavida · the same entry in another collection · chain A against A, TM-score 1.00

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