Structure of PDB 5x8f Chain C Binding Site BS02
Receptor Information
>5x8f Chain C (length=484) Species:
224308
(Bacillus subtilis subsp. subtilis str. 168) [
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TEQPNWLMQRAQLTPERIALIYEDQTVTFAELFAASKRMAEQLAAHSVRK
GDTAAILLQNRAEMVYAVHACFLLGVKAVLLNTKLSTHERLFQLEDSGSG
FLLTDSSFEKKEYEHIVQTIDVDELMKEAAEEIEIEAYMQMDATATLMYT
SGTTGKPKGVQQTFGNHYFSAVSSALNLGITEQDRWLIALPLFHISGLSA
LFKSVIYGMTVVLHQRFSVSDVLHSINRHEVTMISAVQTMLASLLEETNR
CPESIRCILLGGGPAPLPLLEECREKGFPVFQSYGMTETCSQIVTLSPEF
SMEKLGSAGKPLFSCEIKIERDGQVCEPYEHGEIMVKGPNVMKSYFNRES
ANEASFQNGWLKTGDLGYLDNEGFLYVLDRRSDLIISGGENIYPAEVESV
LLSHPAVAEAGVSGAEDKKWGKVPHAYLVLHKPVSAGELTDYCKERLAKY
KRPKKFFVLDRLPRNASNKLLRNQLKDARKGELL
Ligand information
Ligand ID
AMP
InChI
InChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(22-10)1-21-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
UDMBCSSLTHHNCD-KQYNXXCUSA-N
SMILES
Software
SMILES
CACTVS 3.370
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(O)=O)[CH](O)[CH]3O
CACTVS 3.370
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N
ACDLabs 12.01
O=P(O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)O)O)O)N
Formula
C10 H14 N5 O7 P
Name
ADENOSINE MONOPHOSPHATE
ChEMBL
CHEMBL752
DrugBank
DB00131
ZINC
ZINC000003860156
PDB chain
5x8f Chain C Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
5x8f
Crystal structure of the thioesterification conformation of Bacillus subtilis o-succinylbenzoyl-CoA synthetase reveals a distinct substrate-binding mode
Resolution
1.763 Å
Binding residue
(original residue number in PDB)
T152 G265 P266 S285 Y286 G287 M288 T289 D367 I388 N393
Binding residue
(residue number reindexed from 1)
T150 G263 P264 S283 Y284 G285 M286 T287 D365 I386 N391
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
T152 S172 H196 T289 E290 I388 N393 K471
Catalytic site (residue number reindexed from 1)
T150 S170 H194 T287 E288 I386 N391 K469
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:0016405
CoA-ligase activity
GO:0016874
ligase activity
Biological Process
GO:0009234
menaquinone biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5x8f
,
PDBe:5x8f
,
PDBj:5x8f
PDBsum
5x8f
PubMed
28559280
UniProt
P23971
|MENE_BACSU 2-succinylbenzoate--CoA ligase (Gene Name=menE)
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