ABCC7 p.Gln207Asp
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PMID: 24412276
[PubMed]
Loo TW et al: "The cystic fibrosis V232D mutation inhibits CFTR maturation by disrupting a hydrophobic pocket rather than formation of aberrant interhelical hydrogen bonds."
No.
Sentence
Comment
89
Further evidence for hydrogen bond formation was that the V232Q/Q207D mutant (reversal of the Gln and Asp positions) also migrated faster on SDS-PAGE gels [24].
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ABCC7 p.Gln207Asp 24412276:89:64
status: NEW