Structure of PDB 6tmh Chain C Binding Site BS01
Receptor Information
>6tmh Chain C (length=487) Species:
507601
(Toxoplasma gondii GT1) [
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EVGRVVSVGDGIARLFGLEGVQAGELVEFQNGMTGMALNLETDNVGVVIF
GDDRSVLEGDSVKRTGRIVDVPIGPGLLGRVVDALGNPIDGKGPIPAKER
RRVELKAPGIIPRKSVHEPMMTGLKCVDALVPVGRGQRELIIGDRQTGKT
AVAVDAIINQKEINDSTDDESKKLYCIYVAVGQKRSTVAQIVKALEQRDA
MKYTTVVAATASEAAPLQFLAPYSGCAMGEWFRDSGRHCVIIYDDLSKQA
TAYRQMSLLLRRPPGREAYPGDVFYLHSRLLERAAKMGDKSGGGSLTALP
VIETQAGDVSAYIPTNVISITDGQIFLETELFYKGIRPAINVGLSVSRVG
SAAQVKAMKQVAGTMKLELAQYREVAAFAQFGSDLDASTRQLLTRGTALT
ELLKQRQYSPMKNSVQVCVLYCGVKGYLDPLDPKEISRFESLFIDYINAN
HQDILKTIETEKELSEKTEAKLRAAVDEFVAMNEFKK
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
6tmh Chain C Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
6tmh
ATP synthase hexamer assemblies shape cristae of Toxoplasma mitochondria.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
Q223 T224 G225 K226 T227 A228 F409 R414 Q482 Q484
Binding residue
(residue number reindexed from 1)
Q146 T147 G148 K149 T150 A151 F332 R337 Q405 Q407
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
K226 Q260 K261 R425
Catalytic site (residue number reindexed from 1)
K149 Q183 K184 R348
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016787
hydrolase 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:0016020
membrane
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:6tmh
,
PDBe:6tmh
,
PDBj:6tmh
PDBsum
6tmh
PubMed
33402698
UniProt
S7UU80
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