General Information of Drug Therapeutic Target (DTT) (ID: TT2Q719)

DTT Name HUMAN vacuolar-type proton ATPase catalytic A (v-ATPase-A)
Synonyms Vacuolar proton pump subunit alpha; Vacuolar ATPase isoform VA68; VPP2; V-ATPase subunit A; V-ATPase 69 kDa subunit; ATP6V1A1; ATP6V1A; ATP6A1
Gene Name ATP6V1A
BioChemical Class
Acid anhydrides hydrolase
UniProt ID
VATA_HUMAN
TTD ID
T01965
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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EC Number
EC 7.1.2.2
Sequence
MDFSKLPKILDEDKESTFGYVHGVSGPVVTACDMAGAAMYELVRVGHSELVGEIIRLEGD
MATIQVYEETSGVSVGDPVLRTGKPLSVELGPGIMGAIFDGIQRPLSDISSQTQSIYIPR
GVNVSALSRDIKWDFTPCKNLRVGSHITGGDIYGIVSENSLIKHKIMLPPRNRGTVTYIA
PPGNYDTSDVVLELEFEGVKEKFTMVQVWPVRQVRPVTEKLPANHPLLTGQRVLDALFPC
VQGGTTAIPGAFGCGKTVISQSLSKYSNSDVIIYVGCGERGNEMSEVLRDFPELTMEVDG
KVESIMKRTALVANTSNMPVAAREASIYTGITLSEYFRDMGYHVSMMADSTSRWAEALRE
ISGRLAEMPADSGYPAYLGARLASFYERAGRVKCLGNPEREGSVSIVGAVSPPGGDFSDP
VTSATLGIVQVFWGLDKKLAQRKHFPSVNWLISYSKYMRALDEYYDKHFTEFVPLRTKAK
EILQEEEDLAEIVQLVGKASLAETDKITLEVAKLIKDDFLQQNGYTPYDRFCPFYKTVGM
LSNMIAFYDMARRAVETTAQSDNKITWSIIREHMGDILYKLSSMKFKDPLKDGEAKIKSD
YAQLLEDMQNAFRSLED
Function Human protein ATPase H+ transporting V1 subunit A interacts with SARS-CoV-2 M protein with high significance, which indicates ATP6V1A as a potential therapeutic target.
KEGG Pathway
Oxidative phosphorylation (hsa00190 )
Metabolic pathways (hsa01100 )
Phagosome (hsa04145 )
mTOR signaling pathway (hsa04150 )
Synaptic vesicle cycle (hsa04721 )
Collecting duct acid secretion (hsa04966 )
Vibrio cholerae infection (hsa05110 )
Epithelial cell signaling in Helicobacter pylori infection (hsa05120 )
Human papillomavirus infection (hsa05165 )
Rheumatoid arthritis (hsa05323 )
Reactome Pathway
Insulin receptor recycling (R-HSA-77387 )
Transferrin endocytosis and recycling (R-HSA-917977 )
Amino acids regulate mTORC1 (R-HSA-9639288 )
Ion channel transport (R-HSA-983712 )
ROS and RNS production in phagocytes (R-HSA-1222556 )
BioCyc Pathway
MetaCyc:HS03781-MON

References

1 A SARS-CoV-2 Protein Interaction Map Reveals Targets for Drug Repurposing. Nature. 2020 Apr 30. doi: 10.1038/s41586-020-2286-9.