Structure of PDB 6yo0 Chain C1 Binding Site BS01
Receptor Information
>6yo0 Chain C1 (length=513) Species:
5911
(Tetrahymena thermophila) [
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KKLSTGEASVVLAEKIKGITQQNDITEYGTVISIGDGIARVFGLTKVQAG
EMVEFKSGIRGMALNLETDNVGVVVLGNDRDIKEGDVVKRTGAIVDVPIG
EAMCGRVFDALGNPIDGLGPLKTTQRARVEIKAPGIIPRQSVRQPMQTGI
KCVDSLVPIGRGQRELIIGDRQTGKTAIAIDTILNQKEAFNTGDVKKQLY
CIYVAVGQKRSTIANLVSILKQHDCMKFTIVVCATASDAAPLQFLAPYSG
CAIGEFFRDNGKHALIIYDDLSKQAVAYRQMSLLLRRPPGREAYPGDVFY
LHSRLLERAAKMNDSLGGGSLTALPVIETQAGDVSAYIPTNVISITDGQI
FLETELFYKGIRPAINVGLSVSRVGSAAQIKAMKKIAGNLKLTLATYREL
AAFSQFGSDLDAKTQQQLNTGERLVEMLKQNQYTPMKVEEQVCIIFAGVK
GFLDALVTSEVLKFEKKFLEHVRTNHSALLKRIRDSGDLSEVDTNELNTI
IPLFIQEGGFKLK
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
6yo0 Chain C1 Residue 900 [
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Receptor-Ligand Complex Structure
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PDB
6yo0
Type III ATP synthase is a symmetry-deviated dimer that induces membrane curvature through tetramerization.
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
Q203 G205 K206 T207 A208 F388 R393 Q463
Binding residue
(residue number reindexed from 1)
Q172 G174 K175 T176 A177 F357 R362 Q432
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
K206 Q239 K240 R404
Catalytic site (residue number reindexed from 1)
K175 Q208 K209 R373
Enzyme Commision number
?
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
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:0016020
membrane
GO:0045261
proton-transporting ATP synthase complex, catalytic core F(1)
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6yo0
,
PDBe:6yo0
,
PDBj:6yo0
PDBsum
6yo0
PubMed
33093501
UniProt
Q24HY8
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