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1  not effect maturation of a vacuolar enzyme (carboxypeptidase Y).
2 thetic intermediate of the vacuolar protein, carboxypeptidase Y.
3 se of the trimer cone, become susceptible to carboxypeptidase Y.
4  loop truncation mutants could be removed by carboxypeptidase Y.
5 ell wall assembly, and delayed maturation of carboxypeptidase Y.
6 cysteine) and by C-terminal truncation using carboxypeptidase Y.
7 s that secreted strong-to-moderate levels of carboxypeptidase Y.
8 f Saccharomyces cerevisiae for missorting of carboxypeptidase Y.
9 ducts were then degraded to dipeptides using carboxypeptidase Y.
10 c reticulum and a block in the maturation of carboxypeptidase Y.
11 onversion to the readily detectable SL8 with carboxypeptidase Y.
12 mately 50% of the soluble vacuolar hydrolase carboxypeptidase Y.
13 n the Golgi to vacuole transport pathway for carboxypeptidase Y.
14 ibody-specific epitopes from intact cells by carboxypeptidase Y.
15 ential for delivery of the vacuolar protease carboxypeptidase Y.
16 d processing of the soluble vacuolar protein carboxypeptidase Y.
17 ecause no effect on the rate of transport of carboxypeptidase Y, a non-GPI-anchored protein, was obse
18 ants grow poorly under reductive stress, and carboxypeptidase Y activity is less than 10% of that in
19 ail of Ste13p, and also caused missorting of carboxypeptidase Y and accelerated vacuolar degradation
20  Vps67p, appeared to be involved in both the carboxypeptidase Y and alkaline phosphatase pathways.
21 along two distinct routes referred to as the carboxypeptidase Y and alkaline phosphatase pathways.
22 ells depleted for Tlg2p missort a portion of carboxypeptidase Y and are defective in endocytosis.
23               Finally, using misfolded yeast carboxypeptidase Y and chicken ovalbumin as glycoprotein
24  degrees C and display normal trafficking of carboxypeptidase Y and KKXX-tagged proteins at a permiss
25 asmic reticulum form) of the vacuolar enzyme carboxypeptidase Y and morphological abnormalities consi
26 o redirect the vacuolar destination of plant carboxypeptidase Y and other proteins in Arabidopsis sus
27 e vacuolar proteins alkaline phosphatase and carboxypeptidase Y and the vacuolar membrane H(+)-ATPase
28  which secretes the serine carboxypeptidase, carboxypeptidase Y, and other proteins normally targeted
29 51p (Vps21p), the resident vacuolar protease carboxypeptidase Y, and the vacuolar H+-ATPase Vph1p.
30 turation and sorting of the vacuolar protein carboxypeptidase Y as measures of protein sorting at the
31  missorting of 70% of the vacuolar hydrolase carboxypeptidase Y as well as the mislocalization of lat
32 ve in the maturation of the vacuolar protein carboxypeptidase Y, as well as in the secretion of inver
33  enzyme reduces proper folding of endogenous carboxypeptidase Y by about 40%.
34 inaris, LcL) with the carbohydrate moiety of carboxypeptidase Y (CaY) was studied using both atomic f
35 characterized substrates of the Sec complex, carboxypeptidase Y (CPY) and Gas1p, when the protease cl
36  both GGA genes causes defects in sorting of carboxypeptidase Y (CPY) and proteinase A to the vacuole
37 omyces cerevisiae, vacuolar proteins such as carboxypeptidase Y (CPY) are actively sorted away from t
38  transport rate for an unglycosylated mutant carboxypeptidase Y (CPY) is markedly reduced.
39 sorting defect in which the vacuolar protein carboxypeptidase Y (CPY) is missorted and secreted from
40 he vacuole through a well defined route, the carboxypeptidase Y (CPY) pathway.
41  and secreted the soluble vacuolar hydrolase carboxypeptidase Y (CPY) rapidly and reversibly when vti
42 he sorting of the soluble vacuolar hydrolase carboxypeptidase Y (CPY) to the Saccharomyces cerevisiae
43                      In addition, sorting of carboxypeptidase Y (CPY) to the vacuole was delayed, and
44 VE domain-containing proteins, which mediate carboxypeptidase Y (CPY) transport to the vacuole by the
45                                              Carboxypeptidase Y (CPY) travels through a prevacuolar/e
46 mutant, which lacks the sorting receptor for carboxypeptidase Y (CPY), accumulates both invertase and
47 hagy, whereas complex II is required for the carboxypeptidase Y (CPY)-to-vacuole pathway.
48  ERAD, we studied a new misfolded variant of carboxypeptidase Y (CPY).
49 can protect its s10 part against cleavage by carboxypeptidase Y (CPY).
50 detected between PDI and the ER precursor of carboxypeptidase Y (CPY).
51 hat measures transport-coupled maturation of carboxypeptidase Y (CPY).
52 d protein mimics zeolin or a mutated form of carboxypeptidase Y (CPY*) also induced autophagy in an I
53                        In yeast, a mutant of carboxypeptidase Y (CPY*) was found to be a luminal ER s
54 d compare them with those for mutant form of carboxypeptidase Y (CPY*), a soluble luminal protein.
55  Zn2+ sensitivity and partially suppress the carboxypeptidase Y deficiency.
56 cational glycosylation was also observed for carboxypeptidase Y-derived reporter proteins that contai
57 sequence of peptides by their digestion with carboxypeptidase Y directly on ProteinChip surfaces coup
58  of linear peptides from the ERAD substrate, carboxypeptidase Y G255R (CPY*), and binds a model unfol
59 had extensive similarity to the yeast serine carboxypeptidase Y gene.
60 dividuals induced defective glycosylation of carboxypeptidase Y in a wild-type yeast strain and expre
61 spholipid-anchored surface protein) and CPY (carboxypeptidase Y), in the cytosol.
62 e newly synthesized soluble vacuolar protein carboxypeptidase Y is missorted in nhx1 delta cells, and
63 essing and sorting of the vacuolar hydrolase carboxypeptidase Y is normal.
64 e-sensitive ero1-1 mutant, newly synthesized carboxypeptidase Y is retained in the ER and lacks disul
65                             More than 95% of carboxypeptidase Y is secreted from these cells in its G
66 l in luv1 mutants, but some portion (28%) of carboxypeptidase Y is secreted.
67 aturation of isomerase-requiring substrates (carboxypeptidase Y) is impaired.
68 four carboxypeptidases, Arabidopsis thaliana carboxypeptidase Y-like protein, rice serine carboxypept
69 mperature were also found to have defects in carboxypeptidase Y maturation, giving emphasis to our pr
70 2p, Eug1p, Eps1p) are required for efficient carboxypeptidase Y maturation.
71 ps28 null mutant cells (approximately 40-50% carboxypeptidase Y missorted).
72  Gga function was studied using an assay for carboxypeptidase Y missorting and synthetic temperature-
73                The Kex2p mislocalization and carboxypeptidase Y missorting phenotypes were exhibited
74 idative protein folding of the model protein carboxypeptidase Y occurs with similar kinetics to the w
75          Although maturation of glycosylated carboxypeptidase Y occurs with wild-type kinetics in Del
76  Most surprisingly, Och1p can use either the carboxypeptidase Y or AP-3 pathways to reach the vacuole
77 hibited a significant defect in transport of carboxypeptidase Y or carboxypeptidase S to the vacuole
78  be released by trypsin treatment but not by carboxypeptidase Y or chymotrypsin treatment, we suggest
79 degrees C and accumulate the ER precursor of carboxypeptidase Y (p1 CPY).
80 vacuole was observed: transport via both the carboxypeptidase Y pathway and the alkaline phosphatase
81 ovel gene products were involved only in the carboxypeptidase Y pathway, whereas a few, including Mon
82 s and for proper protein sorting through the carboxypeptidase Y pathway.
83 on of CER1 slowed the folding of reduced pro-carboxypeptidase Y (pro-CPY) approximately twofold in ye
84 e Golgi-precursors of the soluble hydrolases carboxypeptidase Y, proteinase A, and proteinase B to th
85                        Proper cycling of the carboxypeptidase Y receptor Vps10p between the TGN and p
86 ntial for endosome-to-Golgi retrieval of the carboxypeptidase Y receptor Vps10p.
87  mediates endosome-to-Golgi transport of the carboxypeptidase Y receptor Vps10p.
88 ase experiments monitoring the maturation of carboxypeptidase Y reveal that oxidative folding is grea
89 HX20 affected protein sorting as measured by carboxypeptidase Y secretion in yeast mutants grown at a
90 whole Arabidopsis seedlings also resulted in carboxypeptidase Y secretion, indicating that the drug h
91                         The recycling of the carboxypeptidase Y sorting receptor, Vps10p, between the
92                          Defects are seen in carboxypeptidase Y sorting, alkaline phosphatase transpo
93  the portion of the receptor responsible for carboxypeptidase Y sorting, is also coimmunoprecipitated
94 s the route that several proteins, including carboxypeptidase Y, take from the late Golgi to the vacu
95                             No difference in carboxypeptidase Y targeting or processing is observed b
96 for the ERAD of CPY* (a misfolded version of carboxypeptidase Y that has five disulfide bonds).
97 ogy and defects related to the maturation of carboxypeptidase Y that is not dependent on the catalyti
98 ect in the transport of the vacuolar protein carboxypeptidase Y through the Golgi.
99 d results in a slight missorting of vacuolar carboxypeptidase Y to the cell surface.
100 n BET5 (bet5-1) that blocks the transport of carboxypeptidase Y to the vacuole and prevents secretion
101                                 Transport of carboxypeptidase Y to the vacuole is also perturbed, but
102 ane Golgi receptor responsible for targeting carboxypeptidase Y to the vacuole, causes the mutant hyb
103 ent alpha-factor maturation and transport of carboxypeptidase Y to the vacuole.
104 t for the delivery of the biosynthetic cargo carboxypeptidase Y to the vacuole.
105 in yeast resulted in impaired trafficking of carboxypeptidase Y to the vacuole.
106 ave colocalized antibodies against Ste2p and carboxypeptidase Y to this compartment, thereby identify
107 re-sensitive mutants of Vti1p show a similar carboxypeptidase Y trafficking defect, but the secretion
108 anisms; overexpressing VipA has an effect on carboxypeptidase Y trafficking, whereas VipD interferes
109 e in yeast causes defects in both growth and carboxypeptidase Y trafficking/processing.
110 omyces cerevisiae, vacuolar proteins such as carboxypeptidase Y transit from the Golgi to the lysosom
111              At semipermissive temperatures, carboxypeptidase Y transit time to the vacuole was slowe
112 e adaptor protein-1 complex, and Vps10p, the carboxypeptidase Y vacuolar protein receptor, are associ
113 nonpermissive temperature, newly synthesized carboxypeptidase Y was secreted, indicating that Vps9p f
114 osphatase, and a soluable vacuolar protease, carboxypeptidase Y. were also detected outside spores af
115       PA28 was inactivated by treatment with carboxypeptidase Y, which cleaved Tyr and Ile residues f
116 s for compounds that induce the secretion of carboxypeptidase Y, which is normally targeted to the va

 
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