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1 sion of BAP2, the gene encoding the branched-amino acid permease.
2 ns generated vesicles containing the general amino acid permease.
3 whereas many of the underexpressed genes are amino acid permeases.
4 T8 impair the activities of a broader set of amino acid permeases.
5 Arabidopsis mutant that is deficient in the amino acid permease 1 (AAP1, At1g58360) and resistant to
8 ransporters of amino acids, i.e. the general amino acid permease (Aap) and the branched-chain amino a
9 theanine transport ability of nine tea plant amino acid permease (AAP) family members, with six exhib
13 D40-repeat protein required for targeting of amino acid permeases (AAPs) to the plasma membrane, bypa
14 amino acid analogues, have very low general amino acid permease activity and do not accumulate treha
16 ginine uptake, decreased expression of three amino acid permeases, and low intracellular levels of fo
17 e ammonium transporter AMT1;1 as well as the amino acid permease APP1 and dipeptide transporter NPF7.
19 tion factor that regulates the expression of amino acid permeases, are impaired in multiple aspects o
20 e and utilization were altered: the aromatic amino acid permease (aroP) and tryptophanyl-tRNA synthet
21 dentified, including many SNARE proteins and amino acid permeases as well as many other participants
22 y homologous to each other and homologous to amino acid permease BAT1 proteins from other plant speci
23 o acid permease (Aap) and the branched-chain amino acid permease (Bra) of Rhizobium leguminosarum and
26 ng of ubiquitinated proteins such as general amino acid permease (Gap1) from the trans-Golgi network
28 n either ammonia or urea medium, the general amino acid permease (Gap1p) is transported from the Golg
29 that a plasma membrane protein, the general amino acid permease (Gap1p), is enriched approximately t
30 ew is the nitrogen regulation of the general amino acid permease, Gap1p, and the proline permease, Pu
31 y blocks transport of the nitrogen-regulated amino acid permease, Gap1p, from the Golgi to the plasma
34 livery to the plasma membrane of the general amino acid permease, Gap1p, of Saccharomyces cerevisiae
37 eracts genetically with Stp1, a regulator of amino acid permease genes and, with Sfp1, a key regulato
38 nylalanine codon, highly conserved among the amino acid permease genes, to a serine codon in a region
40 of GAP1, the structural gene for the general amino acid permease, in glutamine-grown cells in respons
45 rt systems: PA1971 (braZ) for branched-chain amino acids permease; PA2042 for a putative sodium:serin
47 pression of Can1p, the plasma membrane basic amino acid permease, results in increased cell volume an
48 rate-transport elicited endocytosis of other amino acid permeases similarly involves unmasking of a c
52 lular amino acids and activate expression of amino acid permeases through the SPS-sensing pathway, wh
53 cilitates not only the polarized delivery of amino acid permeases to the PM but also participates in
54 biosynthesis (HOM3, HOM2, HOM6, THR1, THR4), amino acid permease trafficking (LST4, LST7), and threon
55 , were identified that are also required for amino acid permease transport from the Golgi to the cell
56 of GAP1, the structural gene for the general amino acid permease, which contains the sites required f