Literature DB >> 15463935

Cystic fibrosis: recent structural insights.

Michael Dorwart1, Patrick Thibodeau, Philip Thomas.   

Abstract

Cystic fibrosis (CF) is a debilitating human disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The recently solved crystal structures of the murine CFTR nucleotide binding domain (NBD) provide insight into the molecular basis of several CF-causing mutations. In addition, the NBD structures reveal several unexpected findings that may have implications concerning CFTR function. In this mini-review, we discuss the key structural features of ATP Binding Cassette (ABC) transporter NBDs, as well as highlight how structural information has aided our understanding of the ATP-regulated solute transport cycle.

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Year:  2004        PMID: 15463935     DOI: 10.1016/j.jcf.2004.05.020

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  3 in total

1.  Processing and function of CFTR-DeltaF508 are species-dependent.

Authors:  Lynda S Ostedgaard; Christopher S Rogers; Qian Dong; Christoph O Randak; Daniel W Vermeer; Tatiana Rokhlina; Philip H Karp; Michael J Welsh
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-14       Impact factor: 11.205

2.  First report of c. 1499G>C mutation in a 6-month-child with cystic fibrosis.

Authors:  Abbas Sahami; Nourkhoda Sadeghifard; Alireza Monsef; Hadi Peyman
Journal:  Indian J Hum Genet       Date:  2014-04

3.  Mutation Analysis of Exons 10 and 17a of CFTR Gene in Patients with Cystic Fibrosis in Kermanshah Province, Western Iran.

Authors:  Abbas Sahami; Reza Alibakhshi; Keyghobad Ghadiri; Hamid Sadeghi
Journal:  J Reprod Infertil       Date:  2014-01
  3 in total

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