Structure of PDB 2b08 Chain B Binding Site BS03
Receptor Information
>2b08 Chain B (length=336) Species:
511
(Alcaligenes faecalis) [
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ATAAEIAALPRQKVELVDPPFVHAHSQVAEGGPKVVEFTMVIEEKKIVID
DAGTEVHAMAFNGTVPGPLMVVHQDDYLELTLINPETNTLMHNIDFHAAT
GALGGGGLTEINPGEKTILRFKATKPGVFVYHCAPPGMVPWHVVSGGNGA
IMVLPREGLHDGKGKALTYDKIYYVGEQDFYVPRDENGKYKKYEAPGDAY
EDTVKVMRTLTPTHVVFNGAVGALTGDKAMTAAVGEKVLIVHSQANRDTR
PHLIGGHGDYVWATGKFNTPPDVDQETWFIPGGAAGAAFYTFQQPGIYAY
VNHNLIEAFELGAAAHFKVTGEWNDDLMTSVLAPSG
Ligand information
Ligand ID
CU1
InChI
InChI=1S/Cu/q+1
InChIKey
VMQMZMRVKUZKQL-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Cu+]
Formula
Cu
Name
COPPER (I) ION
ChEMBL
DrugBank
ZINC
PDB chain
2b08 Chain B Residue 2505 [
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Receptor-Ligand Complex Structure
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PDB
2b08
Effect of the methionine ligand on the reorganization energy of the type-1 copper site of nitrite reductase.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
C136 P138 H145
Binding residue
(residue number reindexed from 1)
C133 P135 H142
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H95 D98 H100 H135 C136 H145 G150 H255 E279 T280 H306
Catalytic site (residue number reindexed from 1)
H92 D95 H97 H132 C133 H142 G147 H252 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:2b08
,
PDBe:2b08
,
PDBj:2b08
PDBsum
2b08
PubMed
17227014
UniProt
P38501
|NIR_ALCFA Copper-containing nitrite reductase (Gene Name=nirK)
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