Structure of PDB 1up6 Chain A Binding Site BS02
Receptor Information
>1up6 Chain A (length=413) Species:
243274
(Thermotoga maritima MSB8) [
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HMRIAVIGGGSSYTPELVKGLLDISEDVRIDEVIFYDIDEEKQKIVVDFV
KRLVKDRFKVLISDTFEGAVVDAKYVIFQFRPGGLKGRENDEGIPLKYGL
IGQETTGVGGFSAALRAFPIVEEYVDTVRKTSNATIVNFTNPSGHITEFV
RNYLEYEKFIGLCNVPINFIREIAEMFSARLEDVFLKYYGLNHLSFIEKV
FVKGEDVTEKVFENLKLKLPDEDFPTWFYDSVRLIVNPYLRYYLMEKKMF
KKISTHELRAREVMKIEKELFEKYRTAVEIPEELTKRGGSMYSTAAAHLI
RDLETDEGKIHIVNTRNNGSIENLPDDYVLEIPCYVRSGRVHTLSQGKGD
HFALSFIHAVKMYERLTIEAYLKRSKKLALKALLSHPLGPDVEDAKDLLE
EILEANREYVKLG
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
1up6 Chain A Residue 1417 [
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Receptor-Ligand Complex Structure
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PDB
1up6
An Unusual Mechanism of Glycoside Hydrolysis Involving Redox and Elimination Steps by a Family 4 Beta-Glycosidase from Thermotoga Maritima.
Resolution
2.55 Å
Binding residue
(original residue number in PDB)
C162 N163 H192
Binding residue
(residue number reindexed from 1)
C163 N164 H193
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.2.1.86
: 6-phospho-beta-glucosidase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004553
hydrolase activity, hydrolyzing O-glycosyl compounds
GO:0008706
6-phospho-beta-glucosidase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0016798
hydrolase activity, acting on glycosyl bonds
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1up6
,
PDBe:1up6
,
PDBj:1up6
PDBsum
1up6
PubMed
15237973
UniProt
Q9X108
|BGLT_THEMA 6-phospho-beta-glucosidase BglT (Gene Name=bglT)
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