Structure of PDB 1mzz Chain C Binding Site BS01
Receptor Information
>1mzz Chain C (length=334) Species:
1063
(Cereibacter sphaeroides) [
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VDLSNLPRVKHTLVPPPFAHAHEQVAASGPVINEFEMRIIEKEVQLDEDA
YLQAMTFDGSIPGPLMIVHEGDYVELTLINPPENTMPHNIDFHAATGALG
GGGLTLINPGEKVVLRFKATRAGAFVYHCAPGGPMIPWHVVSGTAGCIMV
LPRDGLKDHEGKPVRYDTVYYIGESDHYIPKDEDGTYMRFSDPSEGYEDM
VAVMDTLIPSHIVFNGAVGALTGEGALKAKVGDNVLFVHSQPNRDSRPHL
IGGHGDLVWETGKFHNAPERDLETWFIRGGTAGAALYKFLQPGVYAYVNH
NLIEAVHKGATAHVLVEGEWDNDLMEQVVAPVGL
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
1mzz Chain C Residue 2401 [
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Receptor-Ligand Complex Structure
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PDB
1mzz
The High resolution Crystal Structures of Nitrite Reductase and its mutant Met182Thr from Rhodobacter Sphaeroides Reveal a Gating Mechanism for the Electron Transfer to the Type 1 Copper Center
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
H2126 C2167 H2177
Binding residue
(residue number reindexed from 1)
H88 C129 H139
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H2126 D2129 H2131 H2166 C2167 H2177 T2182 H2287 E2311 T2312 H2338
Catalytic site (residue number reindexed from 1)
H88 D91 H93 H128 C129 H139 T144 H249 E273 T274 H300
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:1mzz
,
PDBe:1mzz
,
PDBj:1mzz
PDBsum
1mzz
PubMed
UniProt
Q53239
|NIR_CERS5 Copper-containing nitrite reductase (Gene Name=nirK)
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