Structure of PDB 3h4h Chain B Binding Site BS02
Receptor Information
>3h4h Chain B (length=335) Species:
511
(Alcaligenes faecalis) [
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TAAEIAALPRQKVELVDPPFVHAHSQVAEGGPKVVEFTMVIEEKKIVIDD
AGTEVHAMAFNGTVPGPLMVVHQDDYLELTLINPETNTLTHNIDFHAATG
ALGGGGLTEINPGEKTILRFKATKPGVFVYHCAPPGMVPWHVVSGMNGAI
MVLPREGLHDGKGKALTYDKIYYVGEQDFYVPRDENGKYKKYEAPGDAYE
DTVKVMRTLTPTHVVFNGAVGALTGDKAMTAAVGEKVLIVHSQANRDTRP
HLIGGHGDYVWATGKFNTPPDVDQETWFIPGGAAGAAFYTFQQPGIYAYV
NHNLIEACELGAAAHFKVTGEWNDDLMTSVLAPSG
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
3h4h Chain B Residue 2502 [
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Receptor-Ligand Complex Structure
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PDB
3h4h
Directed evolution of copper nitrite reductase to a chromogenic reductant.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
H100 H135
Binding residue
(residue number reindexed from 1)
H96 H131
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)
H91 D94 H96 H131 C132 H141 M146 H251 E275 T276 H302
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:3h4h
,
PDBe:3h4h
,
PDBj:3h4h
PDBsum
3h4h
PubMed
20083495
UniProt
P38501
|NIR_ALCFA Copper-containing nitrite reductase (Gene Name=nirK)
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