Title : Activation of inwardly rectifying K+ channels by distinct PtdIns(4,5)P2 interactions.

Pub. Date : 1999 Jul

PMID : 10559906






11 Functional Relationships(s)
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1 Between these two arginines, a conservative change of isoleucine residue 229 in GIRK4 to the corresponding leucine found in IRK1 strengthens GIRK4-PtdIns(4,5)P2 interactions, eliminating the need for extra gating molecules. Arginine potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
2 Between these two arginines, a conservative change of isoleucine residue 229 in GIRK4 to the corresponding leucine found in IRK1 strengthens GIRK4-PtdIns(4,5)P2 interactions, eliminating the need for extra gating molecules. Arginine potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
3 Between these two arginines, a conservative change of isoleucine residue 229 in GIRK4 to the corresponding leucine found in IRK1 strengthens GIRK4-PtdIns(4,5)P2 interactions, eliminating the need for extra gating molecules. Isoleucine potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
4 Between these two arginines, a conservative change of isoleucine residue 229 in GIRK4 to the corresponding leucine found in IRK1 strengthens GIRK4-PtdIns(4,5)P2 interactions, eliminating the need for extra gating molecules. Isoleucine potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
5 Between these two arginines, a conservative change of isoleucine residue 229 in GIRK4 to the corresponding leucine found in IRK1 strengthens GIRK4-PtdIns(4,5)P2 interactions, eliminating the need for extra gating molecules. Leucine potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
6 Between these two arginines, a conservative change of isoleucine residue 229 in GIRK4 to the corresponding leucine found in IRK1 strengthens GIRK4-PtdIns(4,5)P2 interactions, eliminating the need for extra gating molecules. Leucine potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
7 Between these two arginines, a conservative change of isoleucine residue 229 in GIRK4 to the corresponding leucine found in IRK1 strengthens GIRK4-PtdIns(4,5)P2 interactions, eliminating the need for extra gating molecules. Phosphatidylinositol 4,5-Diphosphate potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
8 Between these two arginines, a conservative change of isoleucine residue 229 in GIRK4 to the corresponding leucine found in IRK1 strengthens GIRK4-PtdIns(4,5)P2 interactions, eliminating the need for extra gating molecules. Phosphatidylinositol 4,5-Diphosphate potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
9 A negatively charged GIRK4 residue, two positions away from the most strongly interacting arginine, mediates stimulation of channel activity by sodium by strengthening channel-PtdIns(4,5)P2 interactions. Arginine potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
10 A negatively charged GIRK4 residue, two positions away from the most strongly interacting arginine, mediates stimulation of channel activity by sodium by strengthening channel-PtdIns(4,5)P2 interactions. Sodium potassium inwardly rectifying channel subfamily J member 5 Homo sapiens
11 A negatively charged GIRK4 residue, two positions away from the most strongly interacting arginine, mediates stimulation of channel activity by sodium by strengthening channel-PtdIns(4,5)P2 interactions. Phosphatidylinositol 4,5-Diphosphate potassium inwardly rectifying channel subfamily J member 5 Homo sapiens