Structure of PDB 8h9t Chain B Binding Site BS01
Receptor Information
>8h9t Chain B (length=487) Species:
9606
(Homo sapiens) [
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EMSSILEERILGADTSVDLEETGRVLSIGDGIARVHGLRNVQAEEMVEFS
SGLKGMSLNLEPDNVGVVVFGNDKLIKEGDIVKRTGAIVDVPVGEELLGR
VVDALGNAIDGKGPIGSKTRRRVGLKAPGIIPRISVREPMQTGIKAVDSL
VPIGRGQRELIIGDRQTGKTSIAIDTIINQKRFNDGSDEKKKLYCIYVAI
GQKRSTVAQLVKRLTDADAMKYTIVVSATASDAAPLQYLAPYSGCSMGEY
FRDNGKHALIIYDDLSKQAVAYRQMSLLLRRPPGREAYPGDVFYLHSRLL
ERAAKMNDAFGGGSLTALPVIETQAGDVSAYIPTNVISITDGQIFLETEL
FYKGIRPAINVGLSVSRVGSAAQTRAMKQVAGTMKLELAQYREVALLSRG
VRLTELLKQGQYSPMAIEEQVAVIYAGVRGYLDKLEPSKITKFENAFLSH
VVSQHQALLGTIRADGKISEQSDAKLKEIVTNFLAGF
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
8h9t Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
8h9t
Structure of the human ATP synthase.
Resolution
2.77 Å
Binding residue
(original residue number in PDB)
Q172 G174 K175 T176 S177 F357 R362 Q432
Binding residue
(residue number reindexed from 1)
Q166 G168 K169 T170 S171 F351 R356 Q411
Annotation score
5
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0002020
protease binding
GO:0003723
RNA binding
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
GO:0032559
adenyl ribonucleotide binding
GO:0042288
MHC class I protein binding
GO:0043531
ADP binding
GO:0043532
angiostatin binding
GO:0046933
proton-transporting ATP synthase activity, rotational mechanism
Biological Process
GO:0001937
negative regulation of endothelial cell proliferation
GO:0006629
lipid metabolic process
GO:0006754
ATP biosynthetic process
GO:0014850
response to muscle activity
GO:0015986
proton motive force-driven ATP synthesis
GO:0042776
proton motive force-driven mitochondrial ATP synthesis
GO:0043536
positive regulation of blood vessel endothelial cell migration
GO:0045471
response to ethanol
GO:0046034
ATP metabolic process
GO:0071549
cellular response to dexamethasone stimulus
GO:0071732
cellular response to nitric oxide
GO:1902600
proton transmembrane transport
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
GO:0005759
mitochondrial matrix
GO:0005886
plasma membrane
GO:0008180
COP9 signalosome
GO:0009986
cell surface
GO:0016020
membrane
GO:0016469
proton-transporting two-sector ATPase complex
GO:0031090
organelle membrane
GO:0045121
membrane raft
GO:0045259
proton-transporting ATP synthase complex
GO:0045261
proton-transporting ATP synthase complex, catalytic core F(1)
GO:0045267
proton-transporting ATP synthase, catalytic core
GO:0070062
extracellular exosome
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8h9t
,
PDBe:8h9t
,
PDBj:8h9t
PDBsum
8h9t
PubMed
37244256
UniProt
P25705
|ATPA_HUMAN ATP synthase subunit alpha, mitochondrial (Gene Name=ATP5F1A)
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