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Which two structural components of CFTR protein regulate its a... | Filo

Which two structural components of CFTR protein regulate its a... | Filo

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The protein CFTR is made up of 1480 amino acids linked together in a chain. Some humans produce a version of the CFTR protein in which phenylalanine (an amino acid) has been deleted from the amino acid chain. Which of the following best predicts how the amino acid deletion will affect the structure of the CFTR protein?It will have no observable effect on the structure of the CFTR protein and tertiary structures of the CFTR protein, but it will affect the secondary structure of the CFTR protein;

The protein CFTR is made up of 1480 amino acids linked together in a chain. Some humans produce a version of the CFTR protein in which phenylalanine (an amino acid) has been deleted from the amino acid chain. Which of the following best predicts how the amino acid deletion will affect the structure of the CFTR protein?It will have no observable effect on the structure of the CFTR protein and tertiary structures of the CFTR protein, but it will affect the secondary structure of the CFTR protein;

2021年9月25日

one type of mutation in the cftr protein prevents the transport of chloride ions through the channel

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2021年12月15日

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DrRohit Kumar on Instagram: "Cystic fibrosis is a autosomal recessive genetic disorder with features that reflect mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene which encodes a protein expressed in the apical membrane of exocrine epithelial cells. Genetics ➤ The CFTR gene is found on the long (q) arm of human chromosome 7. ➤ Children need to inherit one copy of the gene from each parent in order to have the disease. ➤ If children inherit only one copy, they won'

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‎Cystic Fibrosis | التليف الكيسي‎ on Instagram‎: "السبب الرئيسي للتليف الكيسي .... The main cause of cystic fibrosis is CFTR located on chromosome 7. People with cystic fibrosis have two inactive copies (alleles) of the CFTR gene, so they are unable to make the CFTR protein, and sometimes they are able to make a little of it. People with CF inherit two inactive copies of the CFTR gene from both parents. The function of the CFTR protein is to help maintain salt and water balance. This is done thr

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Instagramwish.cf.iq

Visualize your CRISPR Experiment with MISSION™ Cas9-GFP Fusion Proteins

2021年4月21日

sigmaaldrich.com

🌹Trikafta doesn't modify genes in the traditional sense of altering DNA sequences. Instead, it works by correcting the function of the defective protein produced by the CFTR gene in people with cystic fibrosis (CF). The CFTR gene is responsible for the production of the CFTR protein, which is crucial for the regulation of salt and water movement across cell membranes. In people with CF, mutations in the CFTR gene lead to the production of a malfunctioning CFTR protein, resulting in thick and st

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