ライフサイエンスコーパス: glyoxysome

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します

1 ltransferase (CAT) from the cytosol into the glyoxysomes.

2 the mechanism(s) of import of proteins into glyoxysomes.

3 e of the AtSACX and other genes expressed in glyoxysomes.

4 prevent oligomerization did not import into glyoxysomes.

5 protein import into pumpkin (Cucurbita pepo) glyoxysomes, a class of peroxisome found in the cotyledo

6 ix enzymes are imported into peroxisomes and glyoxysomes, a subclass of peroxisomes involved in lipid

7 as able to be imported by isolated sunflower glyoxysomes and by tobacco leaf peroxisomes when express

8 e fusion protein binds to the surface of the glyoxysomes and competes the binding of authentic matrix

9 acterial chaperones dnaK and groEL, binds to glyoxysomes and is partially translocated in an ATP-depe

10 argeting and actual import of these ILs into glyoxysomes, and ARM-COOH was sufficient for redirecting

11 h binding and translocation of proteins into glyoxysomes, and inhibition is determined by the ratio o

12 Glyoxysomes are a class of peroxisomes found primarily i

13 in import to inhibition by NADPH declines as glyoxysomes are converted to leaf-type peroxisomes.

14 of action of NADPH is most likely within the glyoxysome because (1) pretreatment of glyoxysomes with

15 oteins involved in peroxisome, glycosome and glyoxysome biogenesis.

16 out these tripeptides were still acquired by glyoxysomes, but only when wild-type IL or CAT-SKL subun

17 CAT was redirected from the cytosol into glyoxysomes by a wide range of residues, i.e. A/C/G/S/T-

18 bunits are being piggybacked as multimers to glyoxysomes by association with subunits possessing a PT

19 ing a PTS2 (CAT-HA), were 'piggybacked' into glyoxysomes by PTS2-bearing CAT subunits (rthio-CAT), wh

20 ent residues, however, did not target CAT to glyoxysomes, i.e. F or P at the -3 position (-FKL, -PKL)

21 eir ability to target CAT fusion proteins to glyoxysomes in tobacco (Nicotiana tabacum L.) cv Bright

22 We have studied the import of proteins into glyoxysomes in vitro and show that this process is speci

23 rsus sunflower, leaf peroxisomes versus seed glyoxysomes) is not responsible for observed differences

24 Glyoxysome-like bodies were observed by electron microsc

25 ADPH inhibited binding of proteins to broken glyoxysome membranes.

26 we discovered a local defect of peroxisomes (glyoxysomes) mostly confined to the cotyledons of the ma

27 t functions in the regeneration of NAD(+) in glyoxysomes of germinated oilseeds and protection of per

28 The glyoxysomes of growing oilseed seedlings produce H2O2, a

29 ld therefore appear to possess an additional glyoxysome/peroxisome targeting signal that is lacking i

30 anslocation are dependent upon the amount of glyoxysomes present.

31 HA-Ccat resulted in the import of Ccat into glyoxysomes, the specialized type of peroxisome in BY-2

32 remodeling of peroxisome matrix contents as glyoxysomes transition to leaf peroxisomes.

33 acetyltransferase (CAT) from the cytosol to glyoxysomes, whereas the Ccat tetrapeptide RPSI-COOH was

34 n the glyoxysome because (1) pretreatment of glyoxysomes with NADPH, followed by re-isolation of the

35 re transported into pumpkin (Cucurbita pepo) glyoxysomes with no apparent differences in efficiency o

36 Finally, pretreatment of the isolated glyoxysomes with protease virtually abolished subsequent

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。