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PMID: 11478590
Linsdell P
Thiocyanate as a probe of the cystic fibrosis transmembrane conductance regulator chloride channel pore.
Can J Physiol Pharmacol. 2001 Jul;79(7):573-9.,
[PubMed]
Sentences
No.
Mutations
Sentence
Comment
131
ABCC7 p.Thr338Ala
X
ABCC7 p.Thr338Ala 11478590:131:190
status:
NEW
view ABCC7 p.Thr338Ala details
ABCC7 p.Phe337Ser
X
ABCC7 p.Phe337Ser 11478590:131:183
status:
NEW
view ABCC7 p.Phe337Ser details
In spite of this caveat, it is interesting to note that the effects of mutations within the pore that drastically alter SCN- permeability but have only small effects on SCN- binding (
F337S
,
T338A
; Linsdell 2001) may result in such a model from alterations in barrier height, implying that the effects of these mutations may result primarily from changes in anion access to the pore.
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