Structure of PDB 7njk Chain F Binding Site BS01
Receptor Information
>7njk Chain F (length=469) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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KTAGRVVRITGPVVDVEFPRGSVPELFNALHAEITFGALAKTLTLEVAQH
LGDSLVRCISMQPTDGLVRGVEVTDTGASISVPVGDGVKGHVFNALGDCL
DDPGYGKDFEHWSIHRKPPAFSDLEPRTEMLETGLKVVDLLTPYVRGGKI
ALFGGAGVGKTVLIQEMINRIARNFGGTSVFAGVGERTREGNDLWVELAD
ANVLKDTALVFGQMDEPPGTRMRVALSALTMAEFFRDEQGQDVLLFIDNI
FRFTQAGSEVSTLLGRMPSAVGYQPTLADEMGELQERITSTRGRSITSMQ
AVYVPADDYTDPAPATTFAHLDATTELSRAVFSKGIFPAVDPLASSSTIL
DPAIVGDEHYRVAQEVIRILQRYKDLQDIIAILGIDELSEEDKQLVNRAR
RIERFLSQNMMAAEQFTGQPGSTVPLKETIEAFDKLTKGEFDHLPEQAFF
LIGGLDDLAKKAESLGAKL
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
7njk Chain F Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
7njk
Structure of the ATP synthase from Mycobacterium smegmatis provides targets for treating tuberculosis.
Resolution
2.52 Å
Binding residue
(original residue number in PDB)
G163 G165 K166 T167 V168 R193 F343 A419 F422
Binding residue
(residue number reindexed from 1)
G157 G159 K160 T161 V162 R187 F337 A413 F416
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:0016887
ATP hydrolysis activity
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:7njk
,
PDBe:7njk
,
PDBj:7njk
PDBsum
7njk
PubMed
34782468
UniProt
A0R200
|ATPB_MYCS2 ATP synthase subunit beta (Gene Name=atpD)
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