Structure of PDB 1gu6 Chain G Binding Site BS02
Receptor Information
>1gu6 Chain G (length=441) Species:
562
(Escherichia coli) [
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VEAKNETFAPQHPDQYLSWKATSEQSERVDALAEDPRLVILWAGYPFSRD
YNKPRGHAFAVTDVRETLRTGAPKNAEDGPLPMACWSCKSPDVARLIQKD
GEDGYFHGKWARGGPEIVNNLGCADCHNTASPEFAKGKPELTLSRPYAAR
AMEAIGKPFEKAGRFDQQSMVCGQCHVEYYFDGKNKAVKFPWDDGMKVEN
MEQYYDKIAFSDWTNSLSKTPMLKAQHPEYETWTAGIHGKNNVTCIDCHM
PKVQNAEGKLYTDHKIGNPFDNFAQTCANCHTQDKAALQKVVAERKQSIN
DLKIKVEDQLVHAHFEAKAALDAGATEAEMKPIQDDIRHAQWRWDLAIAS
HGIHMHAPEEGLRMLGTAMDKAADARTKLARLLATKGITHEIQIPDISTK
EKAQQAIGLNMEQIKAEKQDFIKTVIPQWEEQARKNGLLSQ
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1gu6 Chain G Residue 1479 [
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Receptor-Ligand Complex Structure
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PDB
1gu6
Structure and Spectroscopy of the Periplasmic Cytochrome C Nitrite Reductase from Escherichia Coli
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
E215 Y216 K261 Q263
Binding residue
(residue number reindexed from 1)
E178 Y179 K224 Q226
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.7.2.2
: nitrite reductase (cytochrome; ammonia-forming).
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0005509
calcium ion binding
GO:0016491
oxidoreductase activity
GO:0016966
nitric oxide reductase activity
GO:0020037
heme binding
GO:0042279
nitrite reductase (cytochrome, ammonia-forming) activity
GO:0046872
metal ion binding
Biological Process
GO:0009061
anaerobic respiration
GO:0019645
anaerobic electron transport chain
GO:0042128
nitrate assimilation
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
GO:0042597
periplasmic space
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Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1gu6
,
PDBe:1gu6
,
PDBj:1gu6
PDBsum
1gu6
PubMed
11863430
UniProt
P0ABK9
|NRFA_ECOLI Cytochrome c-552 (Gene Name=nrfA)
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