Structure of PDB 3d1r Chain A Binding Site BS04

Receptor Information
>3d1r Chain A (length=321) Species: 83333 (Escherichia coli K-12) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MRRELAIEFSRVTESAALAGYKWLGRGDKNTADGAAVNAMRIMLNQVNID
GTIVIGEGEIAEAPMLYIGEKVGTGRGDAVDIAVDPIEGTRMTAMGQANA
LAVLAVGDKGCFLNAPDMYMEKLIVGPGAKGTIDLNLPLADNLRNVAAAL
GKPLSELTVTILAKPRHDAVIAEMQQLGVRVFAIPDGDVAASILTCMPDS
EVDVLYGIGGAPEGVVSAAVIRALDGDMNGRLLARHDVKGDNENRRIGEQ
ELARCKAMGIEAGKVLRLGDMARSDNVIFSATGITKGDLLEGISRKGNIA
TTETLLIRGKSTIRRIQSIHY
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain3d1r Chain A Residue 3504 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB3d1r Structural and Biochemical Characterization of the Type II Fructose-1,6-bisphosphatase GlpX from Escherichia coli.
Resolution1.85 Å
Binding residue
(original residue number in PDB)
L194 M197 S200 V202
Binding residue
(residue number reindexed from 1)
L194 M197 S200 V202
Annotation score1
Enzymatic activity
Enzyme Commision number 3.1.3.11: fructose-bisphosphatase.
Gene Ontology
Molecular Function
GO:0016787 hydrolase activity
GO:0030145 manganese ion binding
GO:0042132 fructose 1,6-bisphosphate 1-phosphatase activity
GO:0042803 protein homodimerization activity
GO:0046872 metal ion binding
Biological Process
GO:0006071 glycerol metabolic process
GO:0006094 gluconeogenesis
GO:0030388 fructose 1,6-bisphosphate metabolic process
Cellular Component
GO:0005737 cytoplasm

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Biological Process

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Cellular Component
External links
PDB RCSB:3d1r, PDBe:3d1r, PDBj:3d1r
PDBsum3d1r
PubMed19073594
UniProtP0A9C9|GLPX_ECOLI Fructose-1,6-bisphosphatase 1 class 2 (Gene Name=glpX)

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