Structure of PDB 6qpu Chain D Binding Site BS02
Receptor Information
>6qpu Chain D (length=319) Species:
658080
(Ralstonia sp. 5_2_56FAA) [
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PGDFGPPRGEPIHAVLTSPPLVPPPVNRTYPAKVIVELEVVEKEMQISEG
VSYTFWTFGGTVPGSFIRVRQGDTVEFHLKNHPSSKMPHNIDLHGVTGPG
GGAASSFTAPGHESQFTFKALNEGIYVYHCATAPVGMHIANGMYGLILVE
PPEGLPKVDHEYYVMQGDFYTAGKYREKGLQPFDMEKAIDERPSYVLFNG
AEGALTGDKALHAKVGETVRIFVGNGGPNLVSSFHVIGAIFDQVRYEGGT
NVQKNVQTTLIPAGGAAVVKFTARVPGSYVLVDHSIFRAFNKGAMAILKI
DGAENKLVYSGKELDSVYL
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
6qpu Chain D Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
6qpu
Unexpected Roles of a Tether Harboring a Tyrosine Gatekeeper Residue in Modular Nitrite Reductase Catalysis.
Resolution
2.25 Å
Binding residue
(original residue number in PDB)
H99 H134
Binding residue
(residue number reindexed from 1)
H94 H129
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H94 D97 H99 H134 C135 H143 M148 H240 Q262 T263 H289
Catalytic site (residue number reindexed from 1)
H89 D92 H94 H129 C130 H138 M143 H235 Q257 T258 H284
Enzyme Commision number
1.7.2.1
: nitrite reductase (NO-forming).
Gene Ontology
Molecular Function
GO:0005507
copper ion binding
GO:0050421
nitrite reductase (NO-forming) activity
View graph for
Molecular Function
External links
PDB
RCSB:6qpu
,
PDBe:6qpu
,
PDBj:6qpu
PDBsum
6qpu
PubMed
32051772
UniProt
U3G913
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