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1 ced pex4 defects, confirming that PEX22 is a peroxin.
2 p, and the intraperoxisomal presence of this peroxin.
3 d that the encoded protein, Pex22p, is a new peroxin.
4 ng and subsequent budding of the RING-domain peroxins.
5 suggesting distinct roles of individual RING peroxins.
6 PEX13 and possibly PEX14 and all three RING peroxins.
7 ikely to require interaction with additional peroxins.
8 , showing distinct differences between these peroxins.
9 hich is required for recognition by the AAA+ peroxins.
10 on requires the peroxisomal membrane protein Peroxin 11 (Pex11p), which remodels the membrane, result
11 stimuli such as arsenic and is regulated by peroxin 11a (PEX11a), as Arabidopsis pex11a RNAi lines a
13 ort that the peroxisomal E3 ubiquitin ligase peroxin 2 (PEX2) is the causative agent for mammalian pe
14 The predicted Gim1 protein is related the peroxin 2 family of integral membrane proteins, which ar
17 uman MCD onto the peroxisomal import protein peroxin 5, which revealed interactions that extend beyon
18 have revealed numerous Arabidopsis thaliana peroxins acting in peroxisomal matrix protein import; th
19 4p, Pex17p) and RING (Pex2p, Pex10p, Pex12p) peroxins and is also implicated in cargo release of PTS1
20 the peroxisome membrane via interaction with peroxins, and during pexophagy it colocalizes transientl
25 (Pp) Pex8p, the only known intraperoxisomal peroxin at steady state, is targeted to peroxisomes by e
26 Mutations in peroxisome biogenesis proteins (peroxins) can lead to developmental deficiencies in vari
27 etermine whether destabilization of the RING peroxin complex observed in pex12-1 stems from PEX4-depe
31 as of progress are the identification of new peroxins, definition of protein-protein interactions amo
32 Peroxisomal defects were exacerbated in RING peroxin double mutants, suggesting distinct roles of ind
33 and that AMC functions in gametophytes as a peroxin essential for protein import into peroxisomes.
34 indicating that they constitute a two-member peroxin family specifically required for Pex7p and PTS2
35 he adrenoleukodystrophy-related gene and the peroxin gene, PEX11alpha, was found in PBD fibroblasts.
36 uing possibility that other "yeast-specific" peroxins have eluded discovery in plants and mammals bec
38 ummary, AtPex16p is the only authentic plant peroxin homolog known to coexist at steady state within
40 es, aspects of import/biogenesis the role of peroxins in human disease, and involvement of the endopl
44 ort of peroxisomal enzymes is facilitated by peroxins including PEX5, a receptor that delivers cargo
47 ling was used to identify PEX genes encoding peroxins involved in peroxisome assembly and genes invol
53 nition of protein-protein interactions among peroxins leading to the recognition of complexes involve
54 rved that disruption of any Arabidopsis RING peroxin led to decreased PEX10 levels, as seen in yeast
55 ation and characterization of an Arabidopsis peroxin mutant, pex7-1, which displays peroxisome-defect
56 tination-related mutants and found that RING peroxin mutants displayed elevated PEX5 and PEX7 levels,
58 matrix protein import, suggesting that this peroxin pair may have novel plant targets in addition to
62 y enzymes enter peroxisomes with the help of peroxin (PEX) proteins is increasing, mechanisms by whic
63 amoeba balamuthi We found a conserved set of peroxin (Pex) proteins that are required for protein imp
64 eroxisome biogenesis require the function of peroxin (PEX) proteins, among which PEX12 is a RING fing
65 rganelle matrix depends on more than a dozen peroxin (PEX) proteins, with PEX5 and PEX7 serving as re
67 import proteins to the peroxisome matrix by peroxins (PEX proteins), but how the function of the PEX
68 teins from the cytosol through the action of peroxins (PEX proteins), many of which are conserved amo
70 We also show that another integral PMP, the peroxin PEX13, also contains two independent sets of per
73 5 ubiquitination, we found that all the RING peroxins (Pex2, Pex10, and Pex12) are required as E3 ubi
77 ructure of the first three TPR-motifs of the peroxin PEX5 from Trypanosoma brucei, the causative agen
80 which the functional roles of many of the 23 peroxins (proteins involved in peroxisomal protein impor
81 study, we report that two integral membrane peroxins (proteins required for peroxisome biogenesis) i
82 8p and Pex21p are structurally related yeast peroxins (proteins required for peroxisome biogenesis) t
86 Pex18p and ScPex21p, two novel S. cerevisiae peroxins required for protein targeting via the PTS2 bra
88 usly uncharacterized protein, is a cytosolic peroxin that facilitates the import of PTS2-containing p
90 GPT1 contacted two oxidoreductases and also peroxins that mediate import of peroxisomal membrane pro
91 EX genes and the altering of their proteins, peroxins, which are necessary for the importation of tar
92 e biogenesis is mediated by proteins called "peroxins," which are considered to be promising drug tar