Structure of PDB 3h7v Chain A Binding Site BS01
Receptor Information
>3h7v Chain A (length=320) Species:
197221
(Thermosynechococcus vestitus BP-1) [
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LRWQWRIYEEPLQEPLTTAQGVWRSRSGIYLRLEDEQGQVGYGEIAPLPG
WGSETLNADIALCQQLPGHLTPEIMATIPEALPAAQFGFATAWQSVGRLP
YRVRPWPICALLGSGQAALEQWQQSWQRGQTTFKWKVGVMSPEEEQAILK
ALLAALPPGAKLRLDANGSWDRATANRWFAWLDRHGNGKIEYVEQPLPPD
QWQALLSLAQTVTTAIALDESVVSAAEVQRWVDRGWPGFFVIKTALFGDP
DSLSLLLRRGLEPQRLVFSSALEGAIARTAIFHLLETWQPCHALGFGVDR
WRSAPLLTTLTAYERLWERL
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
3h7v Chain A Residue 331 [
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Receptor-Ligand Complex Structure
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PDB
3h7v
Loss of quaternary structure is associated with rapid sequence divergence in the OSBS family.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
D165 E194 D219
Binding residue
(residue number reindexed from 1)
D165 E194 D219
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K134 K136 D165 E194 D219 K243
Catalytic site (residue number reindexed from 1)
K134 K136 D165 E194 D219 K243
Enzyme Commision number
4.2.1.113
: o-succinylbenzoate synthase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0016829
lyase activity
GO:0016836
hydro-lyase activity
GO:0043748
O-succinylbenzoate synthase activity
GO:0046872
metal ion binding
Biological Process
GO:0009234
menaquinone biosynthetic process
GO:0042372
phylloquinone biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3h7v
,
PDBe:3h7v
,
PDBj:3h7v
PDBsum
3h7v
PubMed
24872444
UniProt
Q8DJP8
|MENC_THEVB o-succinylbenzoate synthase (Gene Name=menC)
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