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Structure of a deazaflavin-dependent nitroreductase from nocardia farcinica, with co-factor F420

Analyse Structure of a deazaflavin-dependent nitroreductase from nocardia farcinica… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3R5Y
Type
protein
Length
565 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative uncharacterized protein
UniProt
Q5YUF0
Ligands
F42
Pockets
6 · best druggability 0.59

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 33% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CPutative uncharacterized proteinprotein14132% helix, 33% strandQ5YUF0
DPutative uncharacterized proteinprotein14232% helix, 33% strandQ5YUF0

Ligands and binding sites

  • F42 · Coenzyme F420 · ligand · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12870.590.7835F42
23200.590.7737F42
33140.580.7734F42
42670.580.7835F42
51930.490.7622empty

Interfaces

3 interfaces between chains.

  • C–D · 503 Ų buried · 10 hydrogen bonds · protein-protein
  • B–C · 99 Ų buried · 0 hydrogen bonds · protein-protein
  • A–B · 11 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 3R5Y · Structure of a Deazaflavin-dependent nitroreductase from Nocardia farcinica, with… · the same entry in another collection · chain A against A, TM-score 1.00

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