Structure of PDB 3f1y Chain C Binding Site BS01
Receptor Information
>3f1y Chain C (length=318) Species:
32630
(synthetic construct) [
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LGPASAAEWFRQRSYDYGQFPPEDLARRKRELGLTVSAVLPSRNVADTVG
GIIDEIHALNERAPLIDQILVVDADSEDGTAGVAASHGAEVYSENELMSG
YGDAHGKGDAMWRALSVTRGDLVLYIDADTRDFRPQLAYGVLGPVLEVPG
VRFVKAAYRRPEEDGGGRVTELTAKPLFNLFYPELAGFVQPLAGEFVADR
ELFCSIPFLTGYAVETGIMIDVLKKVGLGAMAQVDLGERQNRHQHLRDLS
RMSYAVVRAVARRLRQEGRLQQLREPGLPESFFQLSDYLHAVATPEGLKL
QEYVEELVERPPINEVLR
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
3f1y Chain C Residue 336 [
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Receptor-Ligand Complex Structure
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PDB
3f1y
Functional and structural characterization of a novel mannosyl-3-phosphoglycerate synthase from Rubrobacter xylanophilus reveals its dual substrate specificity
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
Q299 D302
Binding residue
(residue number reindexed from 1)
Q284 D287
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
P72 T231 Q248 E253 R254
Catalytic site (residue number reindexed from 1)
P64 T216 Q233 E238 R239
Enzyme Commision number
2.4.1.266
: glucosyl-3-phosphoglycerate synthase.
Gene Ontology
Molecular Function
GO:0016757
glycosyltransferase activity
GO:0046872
metal ion binding
GO:0050504
mannosyl-3-phosphoglycerate synthase activity
View graph for
Molecular Function
External links
PDB
RCSB:3f1y
,
PDBe:3f1y
,
PDBj:3f1y
PDBsum
3f1y
PubMed
21166895
UniProt
B7SY86
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