Structure of PDB 7njs Chain B Binding Site BS01
Receptor Information
>7njs Chain B (length=503) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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TISAADIEGAIEDYVSSEEIGTVIDAGDGIAHVEGLPSVMTQELLEFPGG
VLGVALNLDEHSVGAVILGEFEKIEEGQQVKRTGEVLSVPVGDAFLGRVV
NPLGQPIDGQGDIAAETRRALELQAPSVVQRQSVSEPLQTGIKAIDAMTP
IGRGQRQLIIGDRKTGKTAVCVDTILNQREAWLTGDPKQQVRCVYVAIGQ
KGTTIASVKRALEEGGAMEYTTIVAAPASDAAGFKWLAPYTGSAIGQHWM
YNGKHVLIVFDDLSKQADAYRAISLLLRRPPGREAFPGDVFYLHSRLLER
CAKLSDELGGGSMTGLPIIETKANDISAFIPTNVISITDGQCFLESDLFN
QGVRPAINVGVSVSRVGGAAQIKAMKEVAGSLRLDLSQYRELEAFADAAS
KAQLDRGARLVELLKQPQYSPLAVEEQVVAIFLGTQGHLDSVPVEDVQRF
ESELLEHVKASHSDIFDGIRETKKLSEEAEEKLVSVINEFKKGFQASDGS
SVV
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
7njs Chain B Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
7njs
Structure of the ATP synthase from Mycobacterium smegmatis provides targets for treating tuberculosis.
Resolution
2.46 Å
Binding residue
(original residue number in PDB)
R174 K175 T176 G177 K178 T179 A180 F360 R365 Q435
Binding residue
(residue number reindexed from 1)
R163 K164 T165 G166 K167 T168 A169 F349 R354 Q418
Annotation score
5
Enzymatic activity
Enzyme Commision number
7.1.2.2
: H(+)-transporting two-sector ATPase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0032559
adenyl ribonucleotide binding
GO:0043531
ADP binding
GO:0046933
proton-transporting ATP synthase activity, rotational mechanism
GO:0046961
proton-transporting ATPase activity, rotational mechanism
Biological Process
GO:0006754
ATP biosynthetic process
GO:0015986
proton motive force-driven ATP synthesis
GO:0046034
ATP metabolic process
GO:1902600
proton transmembrane transport
Cellular Component
GO:0005886
plasma membrane
GO:0045259
proton-transporting ATP synthase complex
GO:0045261
proton-transporting ATP synthase complex, catalytic core F(1)
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:7njs
,
PDBe:7njs
,
PDBj:7njs
PDBsum
7njs
PubMed
34782468
UniProt
A0R202
|ATPA_MYCS2 ATP synthase subunit alpha (Gene Name=atpA)
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