메뉴 건너뛰기




Volumn 153, Issue 5, 2001, Pages 957-970

COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments

Author keywords

Cystic fibrosis; Functional complementation; Lysosomal proteolysis; Structural destabilization; Ubiquitination

Indexed keywords

CHLORIDE CHANNEL; CYCLIC AMP; PROTEASOME; TRANSMEMBRANE CONDUCTANCE REGULATOR; UBIQUITIN;

EID: 0035947777     PISSN: 00219525     EISSN: None     Source Type: Journal    
DOI: 10.1083/jcb.153.5.957     Document Type: Article
Times cited : (78)

References (93)
  • 18
    • 0000073862 scopus 로고
    • Mutational analysis of protein folding and stability
    • T.E. Creighton, editor. W.H. Freeman and Co., New York
    • (1992) Protein Folding , pp. 353-403
    • Goldenberg, D.P.1
  • 24
    • 0033106369 scopus 로고    scopus 로고
    • Gettin' down with ubiquitin: Turning off cell-surface receptors, transporters and channels
    • (1999) Trends Cell Biol. , vol.9 , pp. 107-112
    • Hicke, L.1
  • 39
    • 0031950846 scopus 로고    scopus 로고
    • Role for the ubiquitin-proteasome system in the vacuolar degradation of Ste6p, the a-factor transporter in Saccharomyces cerevisiae
    • (1998) Mol. Cell. Biol. , vol.18 , pp. 779-789
    • Loayza, D.1    Michaelis, S.2
  • 41
    • 0034162692 scopus 로고    scopus 로고
    • CFTR: The purified NBF1+R protein interacts with the purified NBF2 domain to form a stable NBF1+R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region
    • (2000) Arch. Biochem. Biophys. , vol.375 , pp. 7-20
    • Lu, N.T.1    Pedersen, P.L.2
  • 51
    • 0034716887 scopus 로고    scopus 로고
    • Tripartite management of unfolded proteins in the endoplasmic reticulum
    • (2000) Cell , vol.101 , pp. 451-454
    • Mori, K.1
  • 53
    • 0026714435 scopus 로고
    • Ornithine decarboxylase is degraded by the 26S proteasome without ubiquitination
    • (1992) Nature , vol.360 , pp. 348-351
    • Murakami, Y.1
  • 61
  • 65
    • 0033361889 scopus 로고    scopus 로고
    • Cystic fibrosis as a disease of misprocessing of the cystic fibrosis transmembrane conductance regulator glycoprotein
    • (1999) Am. J. Hum. Genet. , vol.64 , pp. 1499-1504
    • Riordan, J.R.1
  • 85
    • 0027162649 scopus 로고
    • Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
    • (1993) Cell , vol.73 , pp. 1251-1254
    • Welsh, M.J.1    Smith, A.E.2
  • 90
    • 0033614038 scopus 로고    scopus 로고
    • Evidence that endoplasmic reticulum (ER)-associated degradation of CFTR is linked to retrograde translocation from the ER membrane
    • (1999) J. Biol. Chem. , vol.274 , pp. 2616-2624
    • Xiong, X.1    Chong, E.2    Skach, W.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.