Structure of PDB 1qbi Chain B Binding Site BS02
Receptor Information
>1qbi Chain B (length=436) Species:
471
(Acinetobacter calcoaceticus) [
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DVPLTPSQFAKAKSENFDKKVILSNLNKPHALLWGPDNQIWLTERATGKI
LRVNPESGSVKTVFQVPEIVNDADGQNGLLGFAFHPDFKNNPYIYISGTF
KNPKPNQTIIRRYTYNKSTDTLEKPVDLLAGLPSSKDHQSGRLVIGPDQK
IYYTIGDQGRNQLAYLFLPNQAQHTPTQQELNGKDYHTYMGKVLRLNLDG
SIPKDNPSFNGVVSHIYTLGHRNPQGLAFTPNGKLLQSEQGPNSDDEINL
IVKGGNYGWPNVAGYKDDSGYAYANYSAAANKSIKDLAQNGVKVAAGVPV
TKESEWTGKNFVPPLKTLYTVQDTYNYNCWPTVAPSSAYVYKGGKKAITG
WENTLLVPSLKRGVIFRIKLDPTYSTTYDDAVPMFKSNNRYRDVIASPDG
NVLYVLTDTAGNVQKDDGSVTNTLENPGSLIKFTYK
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
1qbi Chain B Residue 464 [
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Receptor-Ligand Complex Structure
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PDB
1qbi
The 1.7 A crystal structure of the apo form of the soluble quinoprotein glucose dehydrogenase from Acinetobacter calcoaceticus reveals a novel internal conserved sequence repeat.
Resolution
1.72 Å
Binding residue
(original residue number in PDB)
A269 Y271 D273 E309
Binding residue
(residue number reindexed from 1)
A263 Y265 D267 E303
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H144 D163 R228 A269 Y271 D273 E309
Catalytic site (residue number reindexed from 1)
H138 D157 R222 A263 Y265 D267 E303
Enzyme Commision number
1.1.5.2
: quinoprotein glucose dehydrogenase (PQQ, quinone).
Gene Ontology
Molecular Function
GO:0008876
quinoprotein glucose dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:1qbi
,
PDBe:1qbi
,
PDBj:1qbi
PDBsum
1qbi
PubMed
10366508
UniProt
P13650
|DHGB_ACICA Quinoprotein glucose dehydrogenase B (Gene Name=gdhB)
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