Structure of PDB 5of6 Chain A Binding Site BS02
Receptor Information
>5of6 Chain A (length=334) Species:
223
(Achromobacter cycloclastes) [
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VDISTLPRVKVDLVKPPFVHAHDQVAKTGPRVVEFTMTIEEKKLVIDREG
TEIHAMTFNGSVPGPLMVVHENDYVELRLINPDTNTLLHNIDFHAATGAL
GGGALTQVNPGEETTLRFKATKPGVFVYHCAPEGMVPWHVTSGMNGAIMV
LPRDGLKDEKGQPLTYDKIYYVGEQDFYVPKDEAGNYKKYETPGEAYEDA
VKAMRTLTPTHIVFNGAVGALTGDHALTAAVGERVLVVHSQANRDTRPHL
IGGHGDYVWATGKFRNPPDLDQETWLIPGGTAGAAFYTFRQPGVYAYVNH
NLIEAFELGAAGHFKVTGEWNDDLMTSVVKPASM
Ligand information
Ligand ID
CU
InChI
InChI=1S/Cu/q+2
InChIKey
JPVYNHNXODAKFH-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Cu+2]
CACTVS 3.341
[Cu++]
Formula
Cu
Name
COPPER (II) ION
ChEMBL
DrugBank
DB14552
ZINC
PDB chain
5of6 Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5of6
Enzyme catalysis captured using multiple structures from one crystal at varying temperatures.
Resolution
1.08 Å
Binding residue
(original residue number in PDB)
H100 H135
Binding residue
(residue number reindexed from 1)
H94 H129
Annotation score
1
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:5of6
,
PDBe:5of6
,
PDBj:5of6
PDBsum
5of6
PubMed
29755744
UniProt
P25006
|NIR_ACHCY Copper-containing nitrite reductase (Gene Name=nirK)
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