Structure of PDB 6tmh Chain D Binding Site BS01

Receptor Information
>6tmh Chain D (length=475) Species: 507601 (Toxoplasma gondii GT1) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
NHGRITQVIGAVVDVHFDEQLPPILNSLEVQGHTNRLVLEVAQHLGENTV
RTIAMDATEGLVRGQKVVDTGAPIQVPVGVETLGRIMNVIGEPVDECGPV
PAKKTYSIHRAAPLFADQSTEPGLLQTGIKVVDLLAPYAKGGKIGLFGGA
GVGKTVLIMELINNVANKHGGFSVFAGVGERTREGNDLYHEMMTTGVIKR
KKLEDGKFDFTGSKAALVYGQMNEPPGARARVALTALSVAEYFRDEQGQD
VLLFIDNIYRFTQAGSEVSALLGRIPSAVGYQPTLATDLGQLQERITTTK
KGSITSVQAVYVPADDLTDPAPATTFAHLDATTVLSRQIAELGIYPAVDP
LDSTSRMLAPEIVGQEHYDTARATQKLLQDYKSLQDIIAILGMDELSEED
KLVVSRARKIQRFLSQPFTVAEVFTGKPGRFVELPETIKSAQTILRGECD
DLPEMAFYMCGGLEEVRSKAVKMAQ
Ligand information
Ligand IDADP
InChIInChI=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
InChIKeyXTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0c1nc(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 3.341Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
FormulaC10 H15 N5 O10 P2
NameADENOSINE-5'-DIPHOSPHATE
ChEMBLCHEMBL14830
DrugBankDB16833
ZINCZINC000012360703
PDB chain6tmh Chain D Residue 601 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB6tmh ATP synthase hexamer assemblies shape cristae of Toxoplasma mitochondria.
Resolution3.1 Å
Binding residue
(original residue number in PDB)		G232 K233 Y424 F503
Binding residue
(residue number reindexed from 1)		G153 K154 Y345 F424
Annotation score5
Enzymatic activity
Catalytic site (original residue number in PDB) K233 E259 R260 R435
Catalytic site (residue number reindexed from 1) K154 E180 R181 R356
Enzyme Commision number 7.1.2.2: H(+)-transporting two-sector ATPase.
Gene Ontology
Molecular Function
GO:0005524 ATP binding
GO:0016787 hydrolase activity
GO:0016887 ATP hydrolysis activity
GO:0046933 proton-transporting ATP synthase activity, rotational mechanism
GO:0046961 proton-transporting ATPase activity, rotational mechanism
Biological Process
GO:0006754 ATP biosynthetic process
GO:0015986 proton motive force-driven ATP synthesis
GO:0042776 proton motive force-driven mitochondrial ATP synthesis
GO:0046034 ATP metabolic process
GO:1902600 proton transmembrane transport
Cellular Component
GO:0005739 mitochondrion
GO:0009507 chloroplast
GO:0016020 membrane
GO:0045261 proton-transporting ATP synthase complex, catalytic core F(1)

View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB RCSB:6tmh, PDBe:6tmh, PDBj:6tmh
PDBsum6tmh
PubMed33402698
UniProtA0A125YYY4

[Back to BioLiP]