Science · 1996 · 268 citations · 26 references
Life SciencesBiochemistryMolecular BiologyCell SignalingElectrophysiologySignal TransductionCardiac Ion ChannelsIon Channel PhysiologyIon Channel RegulationIon Channel SignalingIon ChannelsPotassium Channel BiophysicsCardiac Ion Channel RegulationPotassium Channel GatingPotassium Channel RegulationProline-rich MotifSh3 Domain InteractionsSh3 DomainsSrc Homology 3 DomainsVoltage-gated Potassium Channels
The human Kv1.5 potassium channel (hKv1.5) contains proline-rich sequences identical to those that bind to Src homology 3 (SH3) domains. Direct association of the Src tyrosine kinase with cloned hKv1.5 and native hKv1.5 in human myocardium was observed. This interaction was mediated by the proline-rich motif of hKv1.5 and the SH3 domain of Src. Furthermore, hKv1.5 was tyrosine phosphorylated, and the channel current was suppressed, in cells coexpressing v-Src. These results provide direct biochemical evidence for a signaling complex composed of a potassium channel and a protein tyrosine kinase.
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Identification of a Ten-Amino Acid Proline-Rich SH3 Binding Site
Ruibao Ren, Bruce J. Mayer, Piera Cicchetti et al. · Science · 1993 · 1.2K citations
Structural basis for the binding of proline-rich peptides to SH3 domains
Hongtao Yu, James Chen, Sibo Feng et al. · Cell · 1994 · 1K citations