Structure of PDB 1aq8 Chain C Binding Site BS02
Receptor Information
>1aq8 Chain C (length=331) Species:
511
(Alcaligenes faecalis) [
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IAALPRQKVELVDPPFVHAHSQVAEGGPKVVEFTMVIEEKKIVIDDAGTE
VHAMAFNGTVPGPLMVVHQDDYLELTLINPETNTLMHNIDFHAATGALGG
GGLTEINPGEKTILRFKATKPGVFVYHCAPPGMVPWHVVSGMNGAIMVLP
REGLHDGKGKALTYDKIYYVGEQDFYVPRDENGKYKKYEAPGDAYEDTVK
VMRTLTPTHVVFNGAVGALTGDKAMTAAVGEKVLIVHSQANRDTRPHLIG
GHGDYVWATGKFNTPPDVDQETWFIPGGAAGAAFYTFQQPGIYAYVNHNL
IEAFELGAAAHFKVTGEWNDDLMTSVLAPSG
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
1aq8 Chain C Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
1aq8
Structure of nitrite bound to copper-containing nitrite reductase from Alcaligenes faecalis. Mechanistic implications.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
H100 H135
Binding residue
(residue number reindexed from 1)
H92 H127
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)
H87 D90 H92 H127 C128 H137 M142 H247 E271 T272 H298
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:1aq8
,
PDBe:1aq8
,
PDBj:1aq8
PDBsum
1aq8
PubMed
9353305
UniProt
P38501
|NIR_ALCFA Copper-containing nitrite reductase (Gene Name=nirK)
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