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A chemiosmotic molecular mechanism for proton-translocating adenosine triphosphatases
FEBS Letters, 1974exaly
Adenosine triphosphatases of thermophilic archaeal double-stranded DNA viruses. [PDF]
Cell Biosci, 2014 Adenosine triphosphatases (ATPases) of double-stranded (ds) DNA archaeal viruses are structurally related to the AAA+ hexameric helicases and translocases.
Happonen LJ +3 more
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Purification and cryoelectron microscopy structure determination of human V-ATPase
STAR Protocols, 2021 Summary: Vesicular- or vacuolar-type adenosine triphosphatases (V-ATPases) are multi-component, ATP-driven proton pumps, which play important roles in many physiological processes by acidifying intracellular vesicles, organelles, and the extracellular ...
Longfei Wang +3 more
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Halobacterial adenosine triphosphatases and the adenosine triphosphatase fromHalobacterium saccharovorum [PDF]
FEMS Microbiology Letters, 1986 Membranes prepared from various members of the genus Halobacterium contained a Triton X-100 activated adenosine triphosphatase. The enzyme from Halobacterium saccharovorum was unstable in solutions of low ionic strength (< 3 M NaCl) and maximally active in the presence of 3.5 M NaCl. A variety of nucleotide triphosphates was hydrolyzed.
H, Kristjansson +2 more
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Cryo-EM structures and transport mechanism of human P5B type ATPase ATP13A2
Cell Discovery, 2021 Polyamines are important polycations that play critical roles in mammalian cells. ATP13A2 belongs to the orphan P5B adenosine triphosphatases (ATPase) family and has been established as a lysosomal polyamine exporter to maintain the normal function of ...
Xudong Chen +9 more
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Journal of Fungi, 2023 Colletotrichum gloeosporioides, a significant fungal pathogen of crops and trees, causes large economic losses worldwide. However, its pathogenic mechanism remains totally unclear.
Tian-Ci Deng +5 more
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ADENOSINE TRIPHOSPHATASE IN THE MITOTIC APPARATUS [PDF]
Proceedings of the National Academy of Sciences, 1961 Methods.-Isolation of the mitotic apparatus: The principle of the new method has been described in several publications, and a detailed account of the procedure will appear shortly.5 Sea urchin eggs (Stronglycentrotus purpuratus) are the source of material, providing large quantities of cells in synchronous division.
D, MAZIA, R R, CHAFFEE, R M, IVERSON
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DYT-TOR1A dystonia: an update on pathogenesis and treatment
Frontiers in Neuroscience, 2023 DYT-TOR1A dystonia is a neurological disorder characterized by involuntary muscle contractions and abnormal movements. It is a severe genetic form of dystonia caused by mutations in the TOR1A gene.
Yuhang Fan +3 more
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