Structure of PDB 7zcn Chain A Binding Site BS05
Receptor Information
>7zcn Chain A (length=341) Species:
566679
(Bradyrhizobium sp. ORS 375) [
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DDLKLPRQRVDLVAPPFVHVHEQATKQGPKIMEFKLVVQEKKMVIDEKGT
TFQAMTFNGSMPGPLMVVHEGDYVEVTLVNPATNTMPHNIDFHSATGALG
GGALTLINPGEQVVLRWKATRTGVFVYHCAPGGPMIPWHVVSGMNGAVMV
LPRDGLNDGHGHSLRYDRIYYIGEQDLYVPRDEKGNFKSYDSPGEAYSDT
EEVMRKLTPTHVVFNGKAGALTGKNALNANVGENVLIVHSQANRDSRPHL
IGGHGDYVWETGKFSNAPETGLETWFIRGGSAGAALYKFLQPGIYAYVTH
NLIEAANLGATAHFKVEGKWNDDLMTQVKAPADIPTGSTNE
Ligand information
Ligand ID
NO2
InChI
InChI=1S/HNO2/c2-1-3/h(H,2,3)/p-1
InChIKey
IOVCWXUNBOPUCH-UHFFFAOYSA-M
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
[O-]N=O
OpenEye OEToolkits 1.5.0
N(=O)[O-]
Formula
N O2
Name
NITRITE ION
ChEMBL
DrugBank
DB12529
ZINC
PDB chain
7zcn Chain A Residue 419 [
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Receptor-Ligand Complex Structure
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PDB
7zcn
Single crystal spectroscopy and multiple structures from one crystal (MSOX) define catalysis in copper nitrite reductases.
Resolution
1.19 Å
Binding residue
(original residue number in PDB)
P88 M136 H140
Binding residue
(residue number reindexed from 1)
P87 M135 H139
Annotation score
5
Enzymatic activity
Enzyme Commision number
1.7.2.1
: nitrite reductase (NO-forming).
Gene Ontology
Molecular Function
GO:0005507
copper ion binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0050421
nitrite reductase (NO-forming) activity
Biological Process
GO:0019333
denitrification pathway
GO:0042128
nitrate assimilation
Cellular Component
GO:0042597
periplasmic space
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Molecular Function
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Cellular Component
External links
PDB
RCSB:7zcn
,
PDBe:7zcn
,
PDBj:7zcn
PDBsum
7zcn
PubMed
35862453
UniProt
H0SLX7
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