Structure of PDB 5bur Chain A Binding Site BS01
Receptor Information
>5bur Chain A (length=475) Species:
224308
(Bacillus subtilis subsp. subtilis str. 168) [
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TEQPNWLMQRAQLTPERIALIYEDQTVTFAELFAASKRMAEQLAAHSVRK
GDTAAILLQNRAEMVYAVHACFLLGVKAVLLNTKLSTHERLFQLEDSGSG
FLLTDSSFEKKEYEHIVQTIDVDELMKEAAEEIEIEAYMQMDATATLMYT
SGTTGKPKGVQQTFGNHYFSAVSSALNLGITEQDRWLIALPLFHISGLSA
LFKSVIYGMTVVLHQRFSVSDVLHSINRHEVTMISAVQTMLASLLEETNR
CPESIRCILLGGGPAPLPLLEECREKGFPVFQSYGMTETCSQIVTLSPEF
SMEKLGSAGKPLFSCEIKIERDGQVCEPYEHGEIMVKGPNVMKSYFNRES
ANEASFQNGWLKTGDLGYLDNEGFLYVLDRRSDLIISGGENIYPAEVESV
LLSHPAVAEAGVSGAEDKGKVPHAYLVLHKPVSAGELTDYCKERLAKYKI
PAKFFVLDRLPRNASNKLLRNQLKD
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
5bur Chain A Residue 506 [
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Receptor-Ligand Complex Structure
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PDB
5bur
Structural Basis for the ATP-dependent Configuration of Adenylation Active Site in Bacillus subtilis o-Succinylbenzoyl-CoA Synthetase
Resolution
2.82 Å
Binding residue
(original residue number in PDB)
T152 S153 T155 T156 K160 G265 S285 T289 D367 V379 R382
Binding residue
(residue number reindexed from 1)
T150 S151 T153 T154 K158 G263 S283 T287 D365 V377 R380
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
T152 S172 H196 T289 E290
Catalytic site (residue number reindexed from 1)
T150 S170 H194 T287 E288
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:5bur
,
PDBe:5bur
,
PDBj:5bur
PDBsum
5bur
PubMed
26276389
UniProt
P23971
|MENE_BACSU 2-succinylbenzoate--CoA ligase (Gene Name=menE)
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