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1 otein trafficking even in the absence of the vacuolar ATPase.
2 -2 receptor beta and gamma chains and the H+ vacuolar ATPase.
3 ex containing RAG GTPases, RAGULATOR and the vacuolar ATPase.
4 olysis driven proton pumping activity of the vacuolar ATPase.
5 it C is not able to stably assemble with the vacuolar ATPase.
6 n a fashion analogous to that of the related vacuolar ATPase.
7 r effect of bafilomycin, an inhibitor of the vacuolar ATPase.
8 reversed by bafilomycin, an inhibitor of the vacuolar ATPase.
9  protein important for regulated assembly of vacuolar ATPase.
10  protein sorting, vesicle transport, and the vacuolar ATPase.
11 s acidification through its interaction with Vacuolar-ATPase.
12                            The a2-isoform of vacuolar ATPase (a2V) is uniquely and highly expressed o
13              Mechanistically, TMEM106B binds vacuolar-ATPase accessory protein 1 (AP1).
14 nomic screening, we hypothesize that loss of vacuolar ATPase activity reduces uptake of sertraline in
15 the endolysosomal compartments by inhibiting vacuolar ATPase activity.
16                        Here, by blocking the vacuolar ATPase, alkalinizing the extracellular pH, or e
17 nteracts with the 16-kDa component of the H+ vacuolar ATPase and cooperates with bovine papillomaviru
18 t of malic acid into the vacuole involving a vacuolar-ATPase and a tonoplast dicarboxylate transporte
19 ch, SWitch/sucrose nonfermentable (SWI/SNF), vacuolar ATPases) and identified novel recurrent mutatio
20 d phosphoinositide-3-class 3 (PIK3C3), Rab7, vacuolar ATPase, and lysosomal enzymes revealed that vac
21                  TMEM106B deficiency reduces vacuolar-ATPase AP1 and V0 subunits, impairing lysosomal
22                             Sestrin2 and the vacuolar ATPase are negative and positive regulators of
23                                              Vacuolar ATPases are ATP hydrolysis-driven proton pumps
24                        Giardia has a typical vacuolar ATPase as observed from the common motifs share
25 tive to other secretory tissues and identify vacuolar ATPases as the likely mechanisms driving acidif
26           A recent study identifies the host vacuolar-ATPase as essential to xenophagic clearance and
27          An exception is the assembly factor vacuolar ATPase assembly integral membrane protein (VMA2
28       These results suggest that assembly of vacuolar ATPase at the early endosome is required for tr
29 oncanamycin A (1), a well-known inhibitor of vacuolar ATPase, at concentrations below those that inte
30 screening and identified the V0 subunit C of vacuolar ATPase (ATP6V0C) as a Vpu-binding protein.
31  as overexpression of another subunit of the vacuolar ATPase, ATP6V0C", had no effect on tetherin exp
32                              An inhibitor of vacuolar ATPases, bafilomycin, selectively inhibits the
33 r the CHGB locus, with polymorphisms for the vacuolar-ATPase beta-subunit (ATP6V1B1, exon 1, Ile30Thr
34 e phenotypes suggest connections between the vacuolar ATPase, bud morphology, and cytokinesis that ha
35 the early steps in biosynthesis of the yeast vacuolar ATPase by biosynthetically labeling wild-type a
36 tes expression of glycolytic enzymes and the vacuolar ATPase complex, providing new insight into its
37 P-Ub, a modified subunit of the multiprotein vacuolar ATPase complex, which carries an in-frame fusio
38 ductase activity, as well as subunits of the vacuolar ATPase complex.
39 tone bafilomycin A(1), a potent inhibitor of vacuolar ATPases, could not be achieved.
40 presence of bafilomycin, an inhibitor of the vacuolar ATPase, did not block DC anti-Histoplasma activ
41          Together with the inhibition of the vacuolar ATPase (due to the interaction between E5 and 1
42 ized compartments and their acidification by vacuolar ATPase, enabling aggregate catabolism by lysoso
43 itionally, intercalated cells have increased vacuolar ATPase expression following in vivo experimenta
44 ls are involved in acid-base homeostasis via vacuolar ATPase expression.
45 ucturally more related to the proton-pumping vacuolar ATPase found in the endomembrane system of euka
46                         The structure of the vacuolar ATPase from bovine brain clathrin-coated vesicl
47 tructure of the proton channel domain of the vacuolar ATPase from bovine brain clathrin-coated vesicl
48 lution cryoEM structures of a proton-pumping vacuolar ATPase from human cells, illuminating the glyco
49 tation at three residues in subunit c of the vacuolar ATPase from Neurospora crassa conferred strong
50 ochondrial proteins, urea cycle enzymes, and vacuolar ATPase functions.
51                                          The vacuolar ATPase has been implicated in a variety of phys
52 highly potent and specific inhibitors of the vacuolar ATPase, have been widely used to investigate th
53  and replication, and also includes GTPases, vacuolar ATPase homologs, and most tRNA synthetases.
54 cys4 mutants arises from inactivation of the vacuolar ATPase in the less reducing cytosol resulting f
55 ransfer process is impaired by inhibition of vacuolar ATPases in T cells as well as by fixation of de
56 oncanamycin A (CCA), a specific inhibitor of vacuolar ATPases, inhibited growth of Neurospora crassa
57 ysosomotropic agent chloroquine (CQ) and the vacuolar ATPase inhibitor bafilomycin A1 (Baf A1).
58 hibition of endosomal acidification with the vacuolar ATPase inhibitor bafilomycin A1 or concanamycin
59                       As bafilomycin A1 is a vacuolar ATPase inhibitor that inhibits autophagic prote
60 aturally occurring enantiomer of this potent vacuolar ATPase inhibitor, is described.
61 minant negative form of dynamin (K44A) and a vacuolar-ATPase inhibitor, concanamycin.
62 f the gene cosegregated, indicating that the vacuolar ATPase is essential in Neurospora crassa.
63 investigated whether Atp6v0a2 (a2 isoform of vacuolar ATPase) is associated with abnormal semen quali
64 nd subsequent recruitment and maintenance of vacuolar ATPase/lgp-containing membranes that enclose re
65 ing vesicles within both cell lines acquired vacuolar-ATPase, lysosomal markers LAMP 1 and 2, and the
66 llomavirus E5 proteins with a subunit of the vacuolar ATPase may also contribute to transformation.
67 levant to osmosis control (e.g., aquaporins, vacuolar-ATPases, Na+/K+-ATPases, and carbonic anhydrase
68       Raised pH triggers the assembly of the vacuolar ATPase on the vacuole membrane where it binds A
69 lomycin A1 and concanamycin A, inhibitors of vacuolar ATPases, prevented HCV entry when they were pre
70 luster into distinct pathways, including the vacuolar ATPase proton pump, Retromer, and Commander com
71 etical models of proton translocation by the vacuolar ATPase require that Glu140 should be protonated
72 2 is an essential accessory component of the vacuolar ATPase required for lysosomal degradative funct
73 2 is an essential accessory component of the vacuolar ATPase required for lysosomal degradative funct
74      The resulting atomic model of the yeast vacuolar ATPase serves as a framework to help understand
75       Within these proteins, subunits of the vacuolar ATPase, small GTPases, actinin 4, and, of speci
76 riants of the yeast Saccharomyces cerevisiae vacuolar ATPase subunit (VMA) intein inserted within Gal
77 The protein splicing element (intein) of the vacuolar ATPase subunit (VMA) of Saccharomyces cerevisia
78 himeric protein containing the intein of the vacuolar ATPase subunit (VMA) of Saccharomyces cerevisia
79 (GAPDH), ribosomal protein subunit (RPS) 18, vacuolar ATPase subunit A (VhaA), and elongation factor
80 ts, E5 interacts with both the 16-kilodalton vacuolar ATPase subunit and the platelet-derived growth
81 ctivity and decreased N-glycoyslation of the vacuolar ATPase subunit V0a1, a modification required fo
82              Mechanistically, iAs suppressed Vacuolar ATPase subunit VMA5 expression, impairing lysos
83                                          The vacuolar ATPase subunit Vph1p transits to the vacuole in
84 phorylated tau (e.g. synaptic protein VAMP2, vacuolar-ATPase subunit ATP6V0D1); therefore, we provide
85                   Eleven of the twelve known vacuolar-ATPase subunits were identified.
86 e to bafilomycin A1, a specific inhibitor of vacuolar ATPase, suggesting that activation was dependen
87 its proteolipid subunit and other eukaryotic vacuolar ATPases, suggesting that the former enzyme work
88 active oxygen intermediates inactivate human vacuolar ATPase, supporting the validity of the yeast sc
89 t is an essential assembly chaperone for the vacuolar ATPase, the major proton pump of cellular membr
90 oles that progressively acquire lgps and the vacuolar ATPase, the majority of sifA(-) bacteria lost t
91 reted virulence factors that target the host vacuolar ATPase to withstand phagosomal acidity, the Mgt
92 uming large amounts of energy, including the vacuolar-ATPase, translation, and phosphoinositide metab
93 ve RANKL-mediated induction of d2 isoform of vacuolar ATPase V(o) domain that is involved in cell fus
94                     The proton-translocating vacuolar ATPase (V-ATPase) acidifies the endocytic netwo
95 y bafilomycin A1 that binds and inhibits the vacuolar ATPase (V-ATPase) and by SopF, a bacterial effe
96 similarity with the catalytic subunit of the vacuolar ATPase (V-ATPase) and complements the loss of t
97     Using this technique, we have found that Vacuolar ATPase (V-ATPase) and the V-ATPase regulator Ra
98                             Here we identify vacuolar ATPase (V-ATPase) as an essential regulator of
99                                    The yeast vacuolar ATPase (V-ATPase) contains three proteolipid su
100          The structure of the proton-pumping vacuolar ATPase (V-ATPase) from bovine brain clathrin co
101 regulation, we evaluated the function of the vacuolar ATPase (V-ATPase) in RAW264.7 Mo infected with
102 ession of the gene encoding the C subunit of vacuolar ATPase (V-ATPase) in the medial cells of the ri
103 Retardation of endosomal trafficking through vacuolar ATPase (V-ATPase) inhibition enhanced caspase-8
104                      Pre-incubation with the vacuolar ATPase (V-ATPase) inhibitors bafilomycin A(1) a
105 s, as indicated by brief treatments with the vacuolar ATPase (V-ATPase) inhibitors Bafilomycin A1 or
106                                          The vacuolar ATPase (V-ATPase) is a 1MDa transmembrane proto
107           The yeast Saccharomyces cerevisiae vacuolar ATPase (V-ATPase) is a multisubunit complex div
108                                          The vacuolar ATPase (V-ATPase) is a multisubunit complex tha
109                                          The vacuolar ATPase (V-ATPase) is a multisubunit enzyme that
110                                          The vacuolar ATPase (V-ATPase) is a multisubunit enzyme that
111                                          The vacuolar ATPase (V-ATPase) is a rotary motor proton pump
112                 The Saccharomyces cerevisiae vacuolar ATPase (V-ATPase) is composed of at least 13 po
113                                   Eukaryotic vacuolar ATPase (V-ATPase) is regulated by a reversible
114 he proton pumping activity of the eukaryotic vacuolar ATPase (V-ATPase) is regulated by a unique mech
115 ere, we reveal that the V(1)H subunit of the vacuolar ATPase (V-ATPase) proton pump binds directly to
116 Drosophila genes that encode subunits of the vacuolar ATPase (V-ATPase) proton pump.
117 ssion of ATP6v1g1, a critical subunit of the vacuolar ATPase (V-ATPase) pump.
118 the transport of mature V0a1 subunits of the vacuolar ATPase (V-ATPase) to lysosomes.
119        The subunit architecture of the yeast vacuolar ATPase (V-ATPase) was analyzed by single partic
120                             In cancer cells, vacuolar ATPase (V-ATPase), a multi-subunit enzyme, is e
121                             In cancer cells, vacuolar ATPase (V-ATPase), a multi-subunit enzyme, is e
122 encoding ATP6V1A, a catalytic subunit of the vacuolar ATPase (v-ATPase), and serves as a substrate fo
123  required for the biogenesis of a functional vacuolar ATPase (V-ATPase), but are not part of the fina
124         TFEB targets include subunits of the vacuolar ATPase (v-ATPase), which are essential for lyso
125 y and function of the lysosomal proton pump, vacuolar ATPase (v-ATPase).
126 ng its interaction with V(1) subunits of the vacuolar ATPase (V-ATPase).
127 hich includes the Rag GTPases, Ragulator and vacuolar ATPase (V-ATPase).
128 entified mutants in vacuolar sorting and the vacuolar ATPase (V-ATPase).
129  within VMA1, the catalytic subunit A of the vacuolar ATPase (V-ATPase).
130 e membrane sector (Vo) of the proton pumping vacuolar ATPase (V-ATPase, V1Vo-ATPase) from Saccharomyc
131 s achieved by means of rotary motors, namely vacuolar ATPases (V-ATPase), which are present at many o
132                                              Vacuolar ATPases (V-ATPases) are essential proton pumps
133                                              Vacuolar ATPases (V-ATPases) are important for many cell
134                                          The vacuolar ATPases (V-ATPases) are multisubunit complexes
135                                              Vacuolar ATPases (V-ATPases) are multisubunit enzymes th
136   There has been no previous indication that vacuolar ATPases (V-ATPases) require sphingolipids for f
137 ilomycin A(1) is a specific inhibitor of the vacuolar-ATPase (V-ATPase), which is responsible for pH
138 g and cnj encode the E and G subunits of the vacuolar ATPase (vATPase) and showed that both the V0 an
139 filomycin A1 (BafA), a specific inhibitor of vacuolar ATPase (vATPase) required for lysosomal functio
140 ysoTracker red and acquisition of the proton vacuolar ATPase (vATPase) using immunofluorescence withi
141 using AD impedes acidification via defective vacuolar ATPase (vATPase) V0a1 subunit delivery to lysos
142 d that zymogen activation is mediated by the vacuolar ATPase (vATPase), a proton transporter.
143 duced expression of the lysosome proton pump vacuolar-ATPase (vATPase) subunits (V1B2 and V0a1), resu
144 address questions about the structure of the vacuolar ATPase, we have generated mutant strains of Neu
145 o analyze the phenotype of cells lacking the vacuolar ATPase, we inactivated the vma-1 gene, which en

 
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