Structure of PDB 1so3 Chain A Binding Site BS01
Receptor Information
>1so3 Chain A (length=214) Species:
562
(Escherichia coli) [
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SLPMLQVALDNQTMDSAYETTRLIAEEVDIIEVGTILCVGEGVRAVRDLK
ALYPHKIVLADAKIADAGKILSRMCFEANADWVTVICCADINTAKGALDV
AKEFNGDVQIELTGYWTWEQAQQWRDAGIGQVVYARSRDAQAAGVAWGEA
DITAIKRLSDMGFKVTVTGGLALEDLPLFKGIPIHVFIAGRSIRDAASPV
EAARQFKRSIAELW
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
1so3 Chain A Residue 2300 [
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Receptor-Ligand Complex Structure
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PDB
1so3
Evolution of Enzymatic Activities in the Orotidine 5'-Monophosphate Decarboxylase Suprafamily: Crystallographic Evidence for a Proton Relay System in the Active Site of 3-Keto-l-gulonate 6-Phosphate Decarboxylase(,)
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
E33 D62
Binding residue
(residue number reindexed from 1)
E32 D61
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T36 I37 K64 D67 A68 L72 E112 A136 R139
Catalytic site (residue number reindexed from 1)
T35 I36 K63 D66 A67 L71 E111 A135 R138
Enzyme Commision number
4.1.1.85
: 3-dehydro-L-gulonate-6-phosphate decarboxylase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004590
orotidine-5'-phosphate decarboxylase activity
GO:0016831
carboxy-lyase activity
GO:0033982
3-dehydro-L-gulonate-6-phosphate decarboxylase activity
GO:0046872
metal ion binding
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0019854
L-ascorbic acid catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1so3
,
PDBe:1so3
,
PDBj:1so3
PDBsum
1so3
PubMed
15157078
UniProt
P39304
|ULAD_ECOLI 3-keto-L-gulonate-6-phosphate decarboxylase UlaD (Gene Name=ulaD)
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