Structure of PDB 6cp3 Chain C Binding Site BS01
Receptor Information
>6cp3 Chain C (length=508) Species:
559292
(Saccharomyces cerevisiae S288C) [
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TKAQPTEVSSILEERIKGVSDEANLNETGRVLAVGDGIARVFGLNNIQAE
ELVEFSSGVKGMALNLEPGQVGIVLFGSDRLVKEGELVKRTGNIVDVPVG
PGLLGRVVDALGNPIDGKGPIDAAGRSRAQVKAPGILPRRSVHEPVQTGL
KAVDALVPIGRGQRELIIGDRQTGKTAVALDTILNQKRWNNGSDESKKLY
CVYVAVGQKRSTVAQLVQTLEQHDAMKYSIIVAATASEAAPLQYLAPFTA
ASIGEWFRDNGKHALIVYDDLSKQAVAYRQLSLLLRRPPGREAYPGDVFY
LHSRLLERAAKLSEKEGSGSLTALPVIETQGGDVSAYIPTNVISITDGQI
FLEAELFYKGIRPAINVGLSVSRVGSAAQVKALKQVAGSLKLFLAQYREV
AAFAQFGSDLDASTKQTLVRGERLTQLLKQNQYSPLATEEQVPLIYAGVN
GHLDGIELSRIGEFESSFLSYLKSNHNELLTEIREKGELSKELLASLKSA
TESFVATF
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
6cp3 Chain C Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
6cp3
High-resolution cryo-EM analysis of the yeast ATP synthase in a lipid membrane.
Resolution
3.8 Å
Binding residue
(original residue number in PDB)
R173 Q174 G176 K177 T178 A179 R364 Q434
Binding residue
(residue number reindexed from 1)
R171 Q172 G174 K175 T176 A177 R362 Q432
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
K177 Q210 K211 R375
Catalytic site (residue number reindexed from 1)
K175 Q208 K209 R373
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
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:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
GO:0005758
mitochondrial intermembrane space
GO:0005829
cytosol
GO:0016020
membrane
GO:0042645
mitochondrial nucleoid
GO:0045261
proton-transporting ATP synthase complex, catalytic core F(1)
GO:0045267
proton-transporting ATP synthase, catalytic core
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:6cp3
,
PDBe:6cp3
,
PDBj:6cp3
PDBsum
6cp3
PubMed
29650704
UniProt
P07251
|ATPA_YEAST ATP synthase subunit alpha, mitochondrial (Gene Name=ATP1)
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