Structure of PDB 1h6d Chain K Binding Site BS03
Receptor Information
>1h6d Chain K (length=382) Species:
542
(Zymomonas mobilis) [
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AATLPAGASQVPTTPAGRPMPYAIRPMPEDRRFGYAIVGLGKYALNQILP
GFAGCQHSRIEALVSGNAEKAKIVAAEYGVDPRKIYDYSNFDKIAKDPKI
DAVYIILPNSLHAEFAIRAFKAGKHVMCEKPMATSVADCQRMIDAAKAAN
KKLMIGYRCHYDPMNRAAVKLIRENQLGKLGMVTTDNSDVMDQNDPAQQW
RLRRELAGGGSLMDIGIYGLNGTRYLLGEEPIEVRAYTYSDPNDERFVEV
EDRIIWQMRFRSGALSHGASSYSTTTTSRFSVQGDKAVLLMDPATGYYQN
LISVQTPGHANQSMMPQFIMPANNQFSAQLDHLAEAVINNKPVRSPGEEG
MQDVRLIQAIYEAARTGRPVNTDWGYVRQGGY
Ligand information
Ligand ID
GOL
InChI
InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2
InChIKey
PEDCQBHIVMGVHV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(C(CO)O)O
ACDLabs 12.01
CACTVS 3.370
OCC(O)CO
Formula
C3 H8 O3
Name
GLYCEROL;
GLYCERIN;
PROPANE-1,2,3-TRIOL
ChEMBL
CHEMBL692
DrugBank
DB09462
ZINC
ZINC000000895048
PDB chain
1h6d Chain K Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1h6d
Crystal Structures of the Precursor Form of Glucose-Fructose Oxidoreductase from Zymomonas Mobilis and its Complexes with Bound Ligands
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
K181 R252 D265 Y269
Binding residue
(residue number reindexed from 1)
K130 R201 D214 Y218
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K181 Y269
Catalytic site (residue number reindexed from 1)
K130 Y218
Enzyme Commision number
1.1.99.28
: glucose-fructose oxidoreductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
View graph for
Molecular Function
External links
PDB
RCSB:1h6d
,
PDBe:1h6d
,
PDBj:1h6d
PDBsum
1h6d
PubMed
11705375
UniProt
Q07982
|GFO_ZYMMO Glucose--fructose oxidoreductase (Gene Name=gfo)
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