Structure of PDB 5lqy Chain C Binding Site BS01
Receptor Information
>5lqy Chain C (length=505) Species:
870730
(Ogataea angusta) [
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KAAPTEVSSILESKIRVSDEANLDETGRVLSVGDGIARVFGLNNCQAEEL
VEFASGVKGMALNLEPGQVGIVLFGSDREVKEGEIVKRTGKIVDVPIGPG
MLGRVVDALGNPIDGKGPIEATGYAIAQLKAPGILPRRSVFEPMQTGLKA
VDALVPIGRGQRELIIGDRQTGKTAVALDTILNQKRWNDGNDESKKLYCV
YVAVGQKRSTVAQLVQTLEQNDAMKYSIVVAATASEAAPLQYLAPFTACA
IAEWFRDNGKHALIVYDDLSKQAVAYRQLSLLLRRPPGREAYPGDVFYLH
SRLLERAAKMSDANGGGSLTALPVIETQGGDVSAYIPTNVISITDGQIFL
EAELFYKGIRPAINVGLSVSRVGSAAQVKAMKQVAGSLKLFLAQYREVAA
FAQFGSDLDASTKQTLSRGERLTQLLKQKQYSPQASEEQVPVIYAGVNGF
LDNIPIERIPEFEEQFIAYLKANEGDILEAIRTKGELSSELLDKLKSATE
TFVAT
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=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)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
5lqy Chain C Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
5lqy
Structure of the mitochondrial ATP synthase fromPichia angustadetermined by electron cryo-microscopy.
Resolution
7.8 Å
Binding residue
(original residue number in PDB)
R173 Q174 G176 K177 T178 A179 R364 K433 Q434
Binding residue
(residue number reindexed from 1)
R169 Q170 G172 K173 T174 A175 R360 K429 Q430
Annotation score
5
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0032559
adenyl ribonucleotide binding
GO:0046933
proton-transporting ATP synthase activity, rotational mechanism
Biological Process
GO:0015986
proton motive force-driven ATP synthesis
GO:0046034
ATP metabolic process
GO:1902600
proton transmembrane transport
Cellular Component
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:5lqy
,
PDBe:5lqy
,
PDBj:5lqy
PDBsum
5lqy
PubMed
27791192
UniProt
C0HK51
|ATPA_PICAN ATP synthase subunit alpha, mitochondrial (Gene Name=ATP1)
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