Literature DB >> 14731969

Intracellular protein trafficking defects in human disease.

J F Amara1, S H Cheng, A E Smith.   

Abstract

Secretory proteins and integral membrane proteins travel through the secretory pathway to a variety of destinations. Their targets are often specified by signals in the amino acid sequence or signals added post-translationally. The KDEL sequence that retains soluble proteins in the endoplasmic reticulum and the mannose 6-phosphate group of lysosomal enzymes are well-characterized examples of targeting signals; other signals are less well understood. Given the complexity and importance of the intracellular trafficking pathways, it is perhaps not surprising that mutations that affect the trafficking of proteins are associated with some human genetic diseases.

Entities:  

Year:  1992        PMID: 14731969     DOI: 10.1016/0962-8924(92)90101-r

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  24 in total

1.  Possible interference between tissue-non-specific alkaline phosphatase with an Arg54-->Cys substitution and acounterpart with an Asp277-->Ala substitution found in a compound heterozygote associated with severe hypophosphatasia.

Authors:  M Fukushi-Irié; M Ito; Y Amaya; N Amizuka; H Ozawa; S Omura; Y Ikehara; K Oda
Journal:  Biochem J       Date:  2000-06-15       Impact factor: 3.857

2.  Minor folding defects trigger local modification of glycoproteins by the ER folding sensor GT.

Authors:  Christiane Ritter; Katharina Quirin; Michael Kowarik; Ari Helenius
Journal:  EMBO J       Date:  2005-04-14       Impact factor: 11.598

Review 3.  Strategies for correcting the delta F508 CFTR protein-folding defect.

Authors:  C R Brown; L Q Hong-Brown; W J Welch
Journal:  J Bioenerg Biomembr       Date:  1997-10       Impact factor: 2.945

Review 4.  In vitro systems in the study of peroxisomal protein import.

Authors:  A Baker
Journal:  Experientia       Date:  1996-12-15

5.  Interdomain conformational flexibility underpins the activity of UGGT, the eukaryotic glycoprotein secretion checkpoint.

Authors:  Pietro Roversi; Lucia Marti; Alessandro T Caputo; Dominic S Alonzi; Johan C Hill; Kyle C Dent; Abhinav Kumar; Mikail D Levasseur; Andrea Lia; Thomas Waksman; Souradeep Basu; Yentli Soto Albrecht; Kristin Qian; James Patrick McIvor; Colette B Lipp; Dritan Siliqi; Snežana Vasiljević; Shabaz Mohammed; Petra Lukacik; Martin A Walsh; Angelo Santino; Nicole Zitzmann
Journal:  Proc Natl Acad Sci U S A       Date:  2017-07-24       Impact factor: 11.205

6.  Aberrant retention of tyrosinase in the endoplasmic reticulum mediates accelerated degradation of the enzyme and contributes to the dedifferentiated phenotype of amelanotic melanoma cells.

Authors:  R Halaban; E Cheng; Y Zhang; G Moellmann; D Hanlon; M Michalak; V Setaluri; D N Hebert
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-10       Impact factor: 11.205

7.  The chondrodystrophy, nanomelia: biosynthesis and processing of the defective aggrecan precursor.

Authors:  B M Vertel; B L Grier; H Li; N B Schwartz
Journal:  Biochem J       Date:  1994-07-01       Impact factor: 3.857

Review 8.  Rous-Whipple Award Lecture. Contributions to the physiology and pathology of the Golgi apparatus.

Authors:  N K Gonatas
Journal:  Am J Pathol       Date:  1994-10       Impact factor: 4.307

9.  Comparative analysis of the apo(a) gene, apo(a) glycoprotein, and plasma concentrations of Lp(a) in three ethnic groups. Evidence for no common "null" allele at the apo(a) locus.

Authors:  A Gaw; E Boerwinkle; J C Cohen; H H Hobbs
Journal:  J Clin Invest       Date:  1994-06       Impact factor: 14.808

10.  In Alzheimer's disease the Golgi apparatus of a population of neurons without neurofibrillary tangles is fragmented and atrophic.

Authors:  A Stieber; Z Mourelatos; N K Gonatas
Journal:  Am J Pathol       Date:  1996-02       Impact factor: 4.307

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