Structure of PDB 1j9s Chain C Binding Site BS02
Receptor Information
>1j9s Chain C (length=336) Species:
511
(Alcaligenes faecalis) [
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ATAAEIAALPRQKVELVDPPFVHAHSQVAEGGPKVVEFTMVIEEKKIVID
DAGTEVHAMAFNGTVPGPLMVVHQDDYLELTLINPETNTLMHNIDFHAAT
GALGGGGLTEINPGEKTILRFKATKPGVFVYHCAPPGMVPWHVVSGMNGA
IMVLPREGLHDGKGKALTYDKIYYVGEQDFYVPRDENGKYKKYEAPGDAY
EDTVKVMRTLTPTHVVFNGAVGALTGDKAMTAAVGEKVLIVHSQANRDTR
PNLIGGHGDYVWATGKFNTPPDVDQETWFIPGGAAGAAFYTFQQPGIYAY
VNHNLIEAFELGAAAHFKVTGEWNDDLMTSVLAPSG
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
1j9s Chain C Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
1j9s
Alternate substrate binding modes to two mutant (D98N and H255N) forms of nitrite reductase from Alcaligenes faecalis S-6: structural model of a transient catalytic intermediate
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
H95 C136 H145 M150
Binding residue
(residue number reindexed from 1)
H92 C133 H142 M147
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H95 D98 H100 H135 C136 H145 M150 N255 E279 T280 H306
Catalytic site (residue number reindexed from 1)
H92 D95 H97 H132 C133 H142 M147 N252 E276 T277 H303
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:1j9s
,
PDBe:1j9s
,
PDBj:1j9s
PDBsum
1j9s
PubMed
11478880
UniProt
P38501
|NIR_ALCFA Copper-containing nitrite reductase (Gene Name=nirK)
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