Structure of PDB 8h9p Chain F Binding Site BS01
Receptor Information
>8h9p Chain F (length=466) Species:
9606
(Homo sapiens) [
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ATGRIVAVIGAVVDVQFDEGLPPILNALEVQGRETRLVLEVAQHLGESTV
RTIAMDGTEGLVRGQKVLDSGAPIKIPVGPETLGRIMNVIGEPIDERGPI
KTKQFAPIHAEAPEFMEMSVEQEILVTGIKVVDLLAPYAKGGKIGLFGGA
GVGKTVLIMELINNVAKAHGGYSVFAGVGERTREGNDLYHEMIESGVINL
KDATSKVALVYGQMNEPPGARARVALTGLTVAEYFRDQEGQDVLLFIDNI
FRFTQAGSEVSALLGRIPSAVGYQPTLATDMGTMQERITTTKKGSITSVQ
AIYVPADDLTDPAPATTFAHLDATTVLSRAIAELGIYPAVDPLDSTSRIM
DPNIVGSEHYDVARGVQKILQDYKSLQDIIAILGMDELSEEDKLTVSRAR
KIQRFLSQPFQVAEVFTGHMGKLVPLKETIKGFQQILAGEYDHLPEQAFY
MVGPIEEAVAKADKLA
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
8h9p Chain F Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
8h9p
Structure of the human ATP synthase.
Resolution
3.02 Å
Binding residue
(original residue number in PDB)
G162 G164 K165 T166 V167 Y348 F421 A424 F427
Binding residue
(residue number reindexed from 1)
G151 G153 K154 T155 V156 Y337 F410 A413 F416
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8h9p
,
PDBe:8h9p
,
PDBj:8h9p
PDBsum
8h9p
PubMed
37244256
UniProt
P06576
|ATPB_HUMAN ATP synthase subunit beta, mitochondrial (Gene Name=ATP5F1B)
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