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PMID: 10381582
Reimann F, Tucker SJ, Proks P, Ashcroft FM
Involvement of the n-terminus of Kir6.2 in coupling to the sulphonylurea receptor.
J Physiol. 1999 Jul 15;518 ( Pt 2):325-36.,
[PubMed]
Sentences
No.
Mutations
Sentence
Comment
25
ABCC8 p.Lys719Ala
X
ABCC8 p.Lys719Ala 10381582:25:108
status:
NEW
view ABCC8 p.Lys719Ala details
ABCC8 p.Lys719Ala
X
ABCC8 p.Lys719Ala 10381582:25:195
status:
NEW
view ABCC8 p.Lys719Ala details
However, when the Pï was decreased (by ATP), tolbutamide was unable to block Kir6.2ÄN14ÏSUR1-
K719A
,K1385M currents, despite the fact that the drug inhibited Kir6.2-C166SÏSUR1-
K719A
,K1385M currents (which in the absence of ATP have a Pï of > 0·8 and are not blocked by tolbutamide).
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46
ABCC8 p.Lys719Ala
X
ABCC8 p.Lys719Ala 10381582:46:93
status:
NEW
view ABCC8 p.Lys719Ala details
We use the abbreviation SUR1-KAKM to refer to mutation of the Walker A lysines in both NBD1 (
K719A
) and NBD2 (K1385M) of SUR1.
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169
ABCC8 p.Lys719Ala
X
ABCC8 p.Lys719Ala 10381582:169:160
status:
NEW
view ABCC8 p.Lys719Ala details
Figure 9Ab shows that the ability of tolbutamide to block the channel in the presence of MgATP was also abolished when both Walker A lysines were mutated (SUR1-
K719A
,K1385M, abbreviated SUR1-KAKM).
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