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Cytochrome CD1 nitrite reductase, reduced form

Analyse Cytochrome CD1 nitrite reductase, reduced form in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1AOF
Type
protein
Length
1,074 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Nitrite reductase
UniProt
P72181
Ligands
HEM, DHE, SO2
Pockets
8 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 16% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ANitrite reductaseprotein53215% helix, 38% strandP72181
BNitrite reductaseprotein54216% helix, 37% strandP72181

Ligands and binding sites

  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
  • DHE · Heme D · ligand · 2 copies · chains A, B
  • SO2 · Sulfur dioxide · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12160.840.9732empty
25490.770.8457DHE, SO2
36350.740.8172DHE, SO2
49160.740.7861empty
51670.640.8526HEM

Interfaces

1 interface between chains.

  • A–B · 1548 Ų buried · 31 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 cofactor (heme attachment).

Compared structures

  • 1AOF · Cytochrome CD1 nitrite reductase, reduced form · the same entry in another collection · chain B against B, TM-score 1.00
  • P72181 · AlphaFold monomer V2.0 prediction for nitrite reductase (P72181) · a predicted model of the same protein · chain B against A, TM-score 0.98

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