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1 tive acyl-CoA dehydrogenase with a consensus peroxisomal targeting signal.
2 (PTS-1) similar to the mammalian and fungal peroxisomal targeting signal.
3 298 Da that terminates in a consensus type-1 peroxisomal targeting signal.
4 ther a carboxy-terminal or an amino-terminal peroxisomal targeting signal.
5 an intraperoxisomal receptor for the type 2 peroxisomal targeting signal.
6 rix proteins that carry the type 1 or type 2 peroxisomal targeting signals.
7 resembles the consensus sequence for type-1 peroxisomal targeting signals.
8 f predicted HEAT repeats and has 2 predicted peroxisomal targeting signals.
10 eptor Pex5, which recognizes proteins with a peroxisomal targeting signal 1 (PTS1) in the cytosol and
13 nslocation across the glycosomal membrane of peroxisomal targeting signal 1 (PTS1)-harboring proteins
14 in Pex5 are important for processing of the peroxisomal targeting signal 1 receptor at the peroxisom
16 e Ser-Gln-Leu (SQL), which is similar to the peroxisomal targeting signal 1 utilized for protein impo
17 raperoxisomal localization, Pex8p contains a peroxisomal targeting signal 1, and it interacts with th
19 X5 and PEX7 that recognize proteins carrying peroxisomal targeting signals 1 or 2 (PTS1 or PTS2), res
20 l localization, the consensus sequence for a peroxisomal-targeting signal 1 (PTS1) is present at the
21 tain the COOH-terminal tripeptide glycosomal peroxisomal targeting signal-1 (PTS-1) similar to the ma
22 thin the lumen of the peroxisome contain the peroxisomal targeting signal-1 (PTS1), a C-terminal trip
23 ted to the peroxisomal matrix by virtue of a peroxisomal targeting signal-1 (PTS1), a short carboxy-t
24 roteins targeted to these organelles by the "peroxisomal targeting signal-1", a C-terminal tripeptide
26 ino terminus have sequence similarity to the peroxisomal targeting signal 2 of glyoxysomal proteins,
27 hese translated polypeptides have the type I peroxisomal targeting signal, AKL, at the carboxyl termi
29 o acids containing a highly conserved type 1 peroxisomal targeting signal and a serine lipase active
30 of encoding proteins with a type 1 or type 2 peroxisomal targeting signal and for genes containing th
31 have established that Pex5p binds the type 1 peroxisomal targeting signal and is the import receptor
32 human and mouse PECI proteins contain type-1 peroxisomal targeting signals, and human PECI was locali
34 quences of mpao and bpao have a -Pro-Arg-Leu peroxisomal targeting signal at the extreme C termini.
35 ins that contain either the type-1 or type-2 peroxisomal targeting signal but does not affect targeti
36 or for peroxisomal matrix cargo containing a peroxisomal targeting signal called PTS1, the protein Pe
38 terminal extension with characteristics of a peroxisomal targeting signal, designated PTS2, including
39 T. gondii catalase has a putative C-terminal peroxisomal targeting signal in the last 3 amino acids (
41 deduced product of YLR284C contains a type 1 peroxisomal targeting signal-like sequence at its C term
42 HcCNL contained a carboxyl-terminal type 1 peroxisomal targeting signal made up by the tripeptide S
44 g the nature and location of the glyoxysomal/peroxisomal targeting signal of isocitrate lyase (ICL).
46 ch encodes a protein with a canonical type-1 peroxisomal targeting signal of serine-lysine-leucine(CO
50 peroxisomes takes place via recognition of a peroxisomal targeting signal present at either the extre
51 The import of peroxisomal matrix proteins by peroxisomal targeting signal (PTS) receptors is an ATP-d
52 te, is targeted to peroxisomes by either the peroxisomal targeting signal (PTS) type 1 or PTS2 pathwa
54 roteins from other organisms and predicted a peroxisomal targeting signal (PTS-1) that steers protein
55 sequences, which have been characterized as peroxisomal targeting signals (PTS) residing either at t
58 reen fluorescent protein (GFP) to the matrix peroxisomal targeting signals PTS1 and PTS2, as well as
59 lly import proteins via one of two conserved peroxisomal targeting signal (PTS1 or 2) mediated pathwa
60 argeted to peroxisomes by virtue of a type-1 peroxisomal targeting signal (PTS1) at their extreme C t
61 ic pI and contains the previously identified peroxisomal targeting signal (PTS1) peptide, while the o
63 dy was to determine whether the plant type 1 peroxisomal targeting signal (PTS1) utilizes amino acid
64 to the peroxisomal matrix requires a type 1 peroxisomal targeting signal (PTS1) which essentially co
65 ansferase 2 (AGT2) contain a putative type 1 peroxisomal targeting signal (PTS1), but the metabolic s
66 roxisomal matrix proteins bear characterized Peroxisomal Targeting Signals (PTS1 or PTS2), which are
68 ysis of cellular fractions and prediction of peroxisomal targeting signals (PTS1/PTS2) identified 51
69 eroxisomes by virtue of an N-terminal type 2 peroxisomal targeting signal (PTS2) in a Pex7p-dependent
72 ldolases contain nonameric N-terminal type 2 peroxisomal targeting signals (PTS2s) to direct their im
75 ned for the peroxisomal matrix depend on the peroxisomal targeting signals (PTSs), which require the
78 rgeted to peroxisomes via the interaction of peroxisomal targeting signal sequences 1 and 2 (PTS1 or
79 he green fluorescent protein appended to the peroxisomal targeting signal, Ser-Lys-Leu (SKL), to labe
81 n agreement with the presence of a conserved peroxisomal targeting signal, the C-terminal tripeptide
83 terminal tripeptide targeting signal, termed peroxisomal targeting signal type 1 (PTS1), and follow a
85 n association between human myocilin and the peroxisomal targeting signal type 1 receptor (PTS1R).
89 ee mutations in the gene encoding Pex5p, the peroxisomal targeting signal type-1 (PTS1) receptor, hav