Structure of PDB 8h9e Chain E Binding Site BS01
Receptor Information
>8h9e Chain E (length=456) Species:
9606
(Homo sapiens) [
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ATGRIVAVIGAVVDVQFDEGLPPILNALEVQGRETRLVLEVAQHLGESTV
RTIAMDGTEGLVRGQKVLDSGAPIKIPVGPETLGRIMNVIGEPIDERGPI
KTKQFAPIHAEAPEFMEMSVEQEILVTGIKVVDLLAPYAKGGKIGLFGGA
GVGKTVLIMELINNVAKAHGGYSVFAGVGERTREGNDLYHEMIESGVINL
KDATSKVALVYGQMNEPPGARARVALTGLTVAEYFRDQEGQDVLLFIDNI
FRFTQAGSEVSALLGRIPSAVGYQPTLATDMGTMQERITTTKKGSITSVQ
AIYVPADDLTDPAPATTFAHLDATTVLSRAIAELGIYPAVDPLDSTSRIM
DPNIVGSEHYDVARGVQKILQDYKSLQDIISEEDKLTVSRARKIQRFLSQ
PFQVAEVFTGHMGKLVPLKETIKGFQQILAGEYDHLPEQAFYMVGPIEEA
VAKADK
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
8h9e Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
8h9e
Structure of the human ATP synthase.
Resolution
2.53 Å
Binding residue
(original residue number in PDB)
R359 D362
Binding residue
(residue number reindexed from 1)
R348 D351
Annotation score
5
Enzymatic activity
Enzyme Commision number
7.1.2.2
: H(+)-transporting two-sector ATPase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
GO:0042288
MHC class I protein binding
GO:0043532
angiostatin binding
GO:0046933
proton-transporting ATP synthase activity, rotational mechanism
GO:0046961
proton-transporting ATPase activity, rotational mechanism
Biological Process
GO:0001525
angiogenesis
GO:0001649
osteoblast differentiation
GO:0006091
generation of precursor metabolites and energy
GO:0006629
lipid metabolic process
GO:0006754
ATP biosynthetic process
GO:0006933
negative regulation of cell adhesion involved in substrate-bound cell migration
GO:0015986
proton motive force-driven ATP synthesis
GO:0042776
proton motive force-driven mitochondrial ATP synthesis
GO:0043536
positive regulation of blood vessel endothelial cell migration
GO:0046034
ATP metabolic process
GO:0051453
regulation of intracellular pH
GO:0098761
cellular response to interleukin-7
GO:1902600
proton transmembrane transport
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
GO:0005759
mitochondrial matrix
GO:0005886
plasma membrane
GO:0009986
cell surface
GO:0016020
membrane
GO:0016469
proton-transporting two-sector ATPase complex
GO:0031090
organelle membrane
GO:0031966
mitochondrial membrane
GO:0042645
mitochondrial nucleoid
GO:0045259
proton-transporting ATP synthase complex
GO:0045261
proton-transporting ATP synthase complex, catalytic core F(1)
GO:0045267
proton-transporting ATP synthase, catalytic core
GO:0070062
extracellular exosome
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8h9e
,
PDBe:8h9e
,
PDBj:8h9e
PDBsum
8h9e
PubMed
37244256
UniProt
P06576
|ATPB_HUMAN ATP synthase subunit beta, mitochondrial (Gene Name=ATP5F1B)
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