Structure of PDB 1rku Chain B Binding Site BS01
Receptor Information
>1rku Chain B (length=206) Species:
208964
(Pseudomonas aeruginosa PAO1) [
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DMEIACLDLEGVLVPEIWIAFAEKTGIDALKATTRDIPDYDVLMKQRLRI
LDEHGLKLGDIQEVIATLKPLEGAVEFVDWLRERFQVVILSDTFYEFSQP
LMRQLGFPTLLCHKLEIDDSDRVVGYQLRQKDPKRQSVIAFKSLYYRVIA
AGDSYNDTTMLSEAHAGILFHAPENVIREFPQFPAVHTYEDLKREFLKAS
SRSLSL
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
1rku Chain B Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
1rku
The thrH Gene Product of Pseudomonas aeruginosa Is a Dual Activity Enzyme with a Novel Phosphoserine:Homoserine Phosphotransferase Activity.
Resolution
1.47 Å
Binding residue
(original residue number in PDB)
D7 E9 D152
Binding residue
(residue number reindexed from 1)
D8 E10 D153
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.1.3.3
: phosphoserine phosphatase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004413
homoserine kinase activity
GO:0016787
hydrolase activity
GO:0036424
L-phosphoserine phosphatase activity
GO:0043899
phosphoserine:homoserine phosphotransferase activity
GO:0046820
4-amino-4-deoxychorismate synthase activity
GO:0046872
metal ion binding
Biological Process
GO:0006564
L-serine biosynthetic process
GO:0009088
threonine biosynthetic process
GO:0016311
dephosphorylation
GO:0046654
tetrahydrofolate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1rku
,
PDBe:1rku
,
PDBj:1rku
PDBsum
1rku
PubMed
14699121
UniProt
Q9I2Y2
|THRH_PSEAE Phosphoserine phosphatase ThrH (Gene Name=thrH)
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