ライフサイエンスコーパス: dilysine

1 By coassembling dilysine (+2) and carboxylate (-1) amphiphiles of variou

2 ulsion resulting from the protonation of the dilysines at lower pH may be the trigger to open the cle

3 connexin constructs containing a C-terminal dilysine-based ER retention/retrieval signal (HKKSL) tra

4 tro binding and results in mistrafficking of dilysine-containing cargo in yeast without compromising

5 often interacts with proteins via C-terminal dilysine domains.

6 Recently, we identified a dilysine endoplasmic reticulum (ER) retrieval signal and

7 th a net loss of 44 amino acids, including a dilysine endoplasmic reticulum retention motif.

8 bronchitis virus (IBV) contains a canonical dilysine endoplasmic reticulum retrieval signal (-KKXX-C

9 Domains that contained dilysine endoplasmic reticulum retrieval signals bound t

10 or a GFP chimera that contained a C-terminal dilysine ER retention signal and entered the recycling p

11 ent with the presence of a carboxyl-terminal dilysine ER retrieval motif, although we find that mutat

12 r by expression of exogenous APP bearing the dilysine ER retrieval motif.

13 lly linked to the COP I-dependent C-terminal dilysine ER retrieval pathway.

14 (S) protein that was similar to a canonical dilysine ER retrieval signal.

15 e N-terminal lobe of ovotransferrin create a dilysine interaction and suggest that this is the trigge

16 eaction specificity for the second lysine in dilysine (KK) motifs, and this may be a common character

17 The unique structural feature of the dilysine (Lys206-Lys296) pair in the transferrin N-lobe

18 Retrograde dilysine-mediated transport also appeared to be ineffici

19 plasmic reticulum (ER) retrieval signal, the dilysine motif (KKXX), that functions to localize the hu

20 gradation was confirmed, but surprisingly, a dilysine motif adjacent to thr-61 proved not to be the u

21 mic domain (CD) of the alpha-chain carries a dilysine motif at positions -3/-7 from the C terminus th

22 n proliferating mammalian cells, a canonical dilysine motif at the C-terminus of Sac1 is required for

23 Targeted deletion of the dilysine motif at the C-terminus of the protein resulted

24 eporter protein in the ERGIC, similar to the dilysine motif in IBV S.

25 We also show that the dilysine motif in OST48 functions as an ER localization

26 Mutation of a dilysine motif in the beta sandwich core of the domain e

27 bound to Golgi COPI coat proteins through a dilysine motif in the carboxyl terminal domain consisten

28 This study analyzed the function of the dilysine motif in the context of infectious molecular cl

29 action with MHC-I and MICA/B molecules and a dilysine motif in the cytoplasmic tail that confers retr

30 We conclude that the dilysine motif is responsible for ER sorting of the FV g

31 HFV glycoproteins encoding seven different dilysine motif mutations were then expressed.

32 t as COPI and that GAP binds directly to the dilysine motif of cargo proteins.

33 We conclude that the dilysine motif of HFV imposes a partial restriction on t

34 that via interaction between the C-terminal dilysine motif of Nucleolin and the WD40 domain of alpha

35 nner and is proposed to involve masking of a dilysine motif present at the cytoplasmic C terminus of

36 ic reticulum by introduction of a C-terminal dilysine motif prevented complex carbohydrate processing

37 Dilysine motif recognition involves lysine side-chain in

38 he results indicated that disruptions of the dilysine motif resulted in higher levels of forward tran

39 , the Erv25p tail sequence, which contains a dilysine motif, bound COPI more efficiently.

40 for type I transmembrane proteins carrying a dilysine motif, specific retrieval mechanisms have been

41 ility of COPI to bind ubiquitin, but not the dilysine motif, through its N-terminal WD repeat domain

42 oplasmic reticulum (ER) retrieval signal-the dilysine motif-in the glycoproteins of all five foamy vi

43 clones of HFV that encoded mutations in the dilysine motif.

44 ng of beta'-COP to RGS4 occurred through two dilysine motifs in RGS4, similar to those contained in s

45 Cytoplasmic dilysine motifs on transmembrane proteins are captured b

46 ndidate RNA binding proteins with C-terminal dilysine motifs yielded Nucleolin, which terminates in a

47 -type virions but not in ones containing the dilysine-mutated variant of MA.

48 gistic anion for metal binding) and then the dilysine pair form the driving force to loosen the cleft

49 nter has also led to the suggestion that the dilysine pair is an anion-binding site for chelators.

50 dependent iron release studies show that the dilysine pair is part of an active anion-binding site wh

51 The fact that the dilysine pair is positively charged and resides in a loc

52 s comprehensive evidence to confirm that the dilysine pair plays this dual role in modulating release

53 recycling of membrane proteins containing a dilysine retrieval motif.

54 By contrast, the dilysine retrieval signal, which competes for the same b

55 alanine-scanning mutagenesis we identified a dilysine sequence (Lys(212)-Lys(216)) proximal to the tr

56 d their infectivity, but viruses lacking the dilysine signal budded at the plasma membrane to a great

57 have further explored the role of the -3/-7 dilysine signal in controlling steady-state alpha-chain

58 ytosis signal (in combination with a mutated dilysine signal or alone) could not be recovered, even t

59 he Lys(212)-Lys(216) residues with the -3/-7 dilysine signal produced a dramatic increase in alpha-ch

60 the motif was less potent than the canonical dilysine signal.

61 n, the most susceptible being Lys351 and the dilysine site Lys413-414.

62 rning a GTPase discard pathway that excludes dilysine-tagged proteins from one class of COPI-coated v

63 glutamate residue and the disruption of the "dilysine trigger".

64 ing motif, in concert with the action of the dilysine trigger, elicits iron release from the N lobe.