Structure of PDB 8dbu Chain D Binding Site BS01
Receptor Information
>8dbu Chain D (length=458) Species:
562
(Escherichia coli) [
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TGKIVQVIGAVVDVEFPQDAVPRVYDALEVQNGNERLVLEVQQQLGGGIV
RTIAMGSSDGLRRGLDVKDLEHPIEVPVGKATLGRIMNVLGEPVDMKGEI
GEEERWAIHRAAPSYEELSNSQELLETGIKVIDLMAPFAKGGKVGLFGGA
GVGKTVNMMELIRNIAIEHSGYSVFAGVGERTREGNDFYHEMTDSNVIDK
VSLVYGQMNEPPGNRLRVALTGLTMAEKFRDEGRDVLLFVDNIYRYTLAG
TEVSALLGRMPSAVGYQPTLAEEMGVLQERITSTKTGSITSVQAVYVPAD
DLTDPSPATTFAHLDATVVLSRQIASLGIYPAVDPLDSTSRQLDPLVVGQ
EHYDTARGVQSILQRYQELKDIIAILGMDELSEEDKLVVARARKIQRFLS
QPFFVAEVFTGSPGKYVSLKDTIRGFKGIMEGEYDHLPEQAFYMVGSIEE
AVEKAKKL
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
8dbu Chain D Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
8dbu
Changes within the central stalk of E. coli F 1 F o ATP synthase observed after addition of ATP.
Resolution
3.4 Å
Binding residue
(original residue number in PDB)
G152 V153 G154 K155 T156 V157 R182 Y331 F404 A407 F410
Binding residue
(residue number reindexed from 1)
G151 V152 G153 K154 T155 V156 R181 Y330 F403 A406 F409
Annotation score
5
Enzymatic activity
Enzyme Commision number
7.1.2.2
: H(+)-transporting two-sector ATPase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
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:0042777
proton motive force-driven plasma membrane ATP synthesis
GO:0046034
ATP metabolic process
GO:1902600
proton transmembrane transport
Cellular Component
GO:0005886
plasma membrane
GO:0016020
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:8dbu
,
PDBe:8dbu
,
PDBj:8dbu
PDBsum
8dbu
PubMed
36631659
UniProt
P0ABB4
|ATPB_ECOLI ATP synthase subunit beta (Gene Name=atpD)
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