Structure of PDB 5c5h Chain A Binding Site BS03
Receptor Information
>5c5h Chain A (length=443) Species:
83333
(Escherichia coli K-12) [
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SHMIFSDWPWRHWRQVRGETIALRLNDEQLNWRELCARVDELASGFAVQG
VVEGSGVMLRAWNTPQTLLAWLALLQCGARVLPVNPQLPQPLLEELLPNL
TLQFALVPDGENTFPALTSLHIQLVEGAHAATWQPTRLCSMTLTSSTGLP
KAAVHTYQAHLASAQGVLSLIPFGDHDDWLLSLPLFHVSGQGIMWKWLYA
GARMTVRDKQPLEQMLAGCTHASLVPTQLWRLLVNRSSVSLKAVLLGGAA
IPVELTEQAREQGIRCFCGYGLTEFASTVCAKEADGLADVGSPLPGREVK
IVNNEVWLRAASMAEGYWRNGQLVSLVNDEGWYATRDRGEMHNGKLTIVG
RLDNLFFSGGEGIQPEEVERVIAAHPAVLQVFIVPVADKFGHRPVAVMEY
DHESVDLSEWVKDKLARFQQPVRWLTLPPKISRQALKEWVQRQ
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
5c5h Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5c5h
Mechanism of MenE Inhibition by Acyl-Adenylate Analogues and Discovery of Novel Antibacterial Agents.
Resolution
2.401 Å
Binding residue
(original residue number in PDB)
Q132 P133 T134
Binding residue
(residue number reindexed from 1)
Q134 P135 T136
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T142 S162 H186 G270 E273 F356 G361
Catalytic site (residue number reindexed from 1)
T144 S163 H187 G271 E274 F357 G362
Enzyme Commision number
6.2.1.26
: o-succinylbenzoate--CoA ligase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0008756
o-succinylbenzoate-CoA ligase activity
GO:0016874
ligase activity
GO:0016877
ligase activity, forming carbon-sulfur bonds
GO:0042802
identical protein binding
Biological Process
GO:0009234
menaquinone biosynthetic process
Cellular Component
GO:0032991
protein-containing complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5c5h
,
PDBe:5c5h
,
PDBj:5c5h
PDBsum
5c5h
PubMed
26394156
UniProt
P37353
|MENE_ECOLI 2-succinylbenzoate--CoA ligase (Gene Name=menE)
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