Structure of PDB 6zud Chain A Binding Site BS03
Receptor Information
>6zud Chain A (length=333) Species:
223
(Achromobacter cycloclastes) [
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VDISTLPRVKVDLVKPPFVHAHDQVAKTGPRVVEFTMTIEEKKLVIDREG
TEIHAMTFNGSVPGPLMVVHENDYVELRLINPDTNTLLHNIDFHAATGAL
GGGALTQVNPGEETTLRFKATKPGVFVYHCAPEGMVPWHVTSGMNGAIMV
LPRDGLKDEKGQPLTYDKIYYVGEQDFYVPKDEAGNYKKYETPGEAYEDA
VKAMRTLTPTHIVFNGAVGALTGDHALTAAVGERVLVVHSQANRDTRPHL
IGGHGDYVWATGKFRNPPDLDQETWLIPGGTAGAAFYTFRQPGVYAYVNH
NLIEAFELGAAGHFKVTGEWNDDLMTSVVKPAS
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
6zud Chain A Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
6zud
Nature of the copper-nitrosyl intermediates of copper nitrite reductases during catalysis.
Resolution
1.1 Å
Binding residue
(original residue number in PDB)
D98 H100 H135
Binding residue
(residue number reindexed from 1)
D92 H94 H129
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H95 D98 H100 H135 C136 H145 M150 H255 E279 T280 H306
Catalytic site (residue number reindexed from 1)
H89 D92 H94 H129 C130 H139 M144 H249 E273 T274 H300
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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Biological Process
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Cellular Component
External links
PDB
RCSB:6zud
,
PDBe:6zud
,
PDBj:6zud
PDBsum
6zud
PubMed
34094452
UniProt
P25006
|NIR_ACHCY Copper-containing nitrite reductase (Gene Name=nirK)
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