ライフサイエンスコーパス: ribophorin

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1 membrane-bound endoplasmic reticulum marker ribophorin.

2 Moreover, expression of ASB11 can increase Ribophorin 1 protein turnover in vivo.

3 o interact and promote the ubiquitination of Ribophorin 1, an integral protein of the oligosaccharylt

4 One protein was identified as ribophorin and another as immunoglobulin-binding protein

5 ear membrane site that overlaps with PDI and ribophorin and has the characteristics of the endoplasmi

6 asmic site that does not overlap with PDI or ribophorin and may be another cytoplasmic structure or p

7 nts precisely with OST activity and with the ribophorins and OST48.

8 only affects the stability of OST48 and the ribophorins but also results in the functional inactivat

9 age ACAT pattern did not overlap with PDI or ribophorin, but was found in as yet unidentified cytopla

10 RNA) inhibits the degradation of a misfolded ribophorin fragment (RI332) independently of the presenc

11 hin the three type I transmembrane proteins, ribophorin I (RI), ribophorin II (RII), and OST48.

12 be composed of three transmembrane proteins, ribophorin I (RI), ribophorin II (RII), and OST48.

13 brane proteins of the endoplasmic reticulum: ribophorin I (RI), ribophorin II (RII), and OST48.

14 = 0.30) and a region of replication found in ribophorin I (RPN1) (P-value = 2.63x10(-16), beta = -0.2

15 ectrometry analysis, we have identified that Ribophorin I (RPNI), a component of the oligosaccharide

16 n-RNA adducts identified Sec61alpha,beta and ribophorin I as ER-poly(A) mRNA-binding proteins, sugges

17 ts are located between the previously mapped Ribophorin I gene and the most centromeric breakpoint; t

18 1) gene in 3q26 and GR6 and between EVI1 and Ribophorin I that maps 30 kb telomeric to GR6 in 3q21.

19 eins that are considered markers of the RER (ribophorin I) and GA (p58, alpha-mannosidase II, galacto

20 One predicts a plant homologue of ribophorin I, a subunit of the oligosaccharyltransferase

21 ntaining the translocon proteins Sec61alpha, ribophorin I, and TRAPalpha, and endoplasmic reticulum p

22 tionally, both preparations contained FSP27, ribophorin I, EHD2, diaphorase I, and ancient ubiquitous

23 teractions between ribosomes and Sec61alpha, ribophorin I, or TRAPalpha were observed following solub

24 is associated with an oligomeric complex of ribophorin I, ribophorin II, and OST48.

25 All known mammalian OST subunits (STT3-A, ribophorin I, ribophorin II, OST48, and DAD1) were prese

26 ereas translocon accessory proteins, such as ribophorin I, were present in all subpopulations of ER-a

27 The Ribophorin I-EVI1 fusion in particular may be a common o

28 1-ribophorin II-OST48 heterotrimers and DAD1-ribophorin I-ribophorin II-OST48 heterotetramers also we

29 previously described mammalian OST subunits (ribophorins I and II, OST48, and DAD1) into complexes th

30 I transmembrane proteins, ribophorin I (RI), ribophorin II (RII), and OST48.

31 e transmembrane proteins, ribophorin I (RI), ribophorin II (RII), and OST48.

32 he endoplasmic reticulum: ribophorin I (RI), ribophorin II (RII), and OST48.

33 hich correlates with acquisition of the SWP1/ribophorin II subunit of the OST complex.

34 with an oligomeric complex of ribophorin I, ribophorin II, and OST48.

35 ammalian OST subunits (STT3-A, ribophorin I, ribophorin II, OST48, and DAD1) were present in all comp

36 Crosslinked ribophorin II-OST48 heterodimers, DAD1-ribophorin II-OST

37 II-OST48 heterotrimers and DAD1-ribophorin I-ribophorin II-OST48 heterotetramers also were detected.

38 inked ribophorin II-OST48 heterodimers, DAD1-ribophorin II-OST48 heterotrimers and DAD1-ribophorin I-

39 ts of the oligosaccharyltransferase complex (ribophorins, OST48, and STT3A) and an ER chaperone, caln

40 Furthermore, N-glycosylation of the ribophorins was seriously affected 6 h after shifting th

41 sive temperature, steady-state levels of the ribophorins were reduced by about 50%, and OST48 was bar

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