Systematic and quantitative analysis of protein phosphorylation is revealing dynamic regulatory networks underlying cellular responses to environmental cues. However, matching these sites to the kinases that phosphorylate them and the phosphorylation-dependent binding domains that may subsequently bind to them remains a challenge. NetPhorest is an atlas of consensus sequence motifs that covers 179 kinases and 104 phosphorylation-dependent binding domains [Src homology 2 (SH2), phosphotyrosine binding (PTB), BRCA1 C-terminal (BRCT), WW, and 14-3-3]. The atlas reveals new aspects of signaling systems, including the observation that tyrosine kinases mutated in cancer have lower specificity than their non-oncogenic relatives. The resource is ma...
Phosphorylation is an important mechanism for regulation of protein function and aktivity. Tyrosine ...
The functional diversity of kinases enables specificity in cellular signal transduction. Yet how mor...
Protein phosphorylation is the most abundant reversible covalent modification. Human protein kinases...
Systematic and quantitative analysis of protein phosphorylation is revealing dynamic regulatory netw...
The coordinated regulation of protein kinases is a rapid mechanism that integrates diverse cues and ...
SummaryProtein kinases control cellular decision processes by phosphorylating specific substrates. T...
The coordinated regulation of protein kinases is a rapid mechanism that integrates diverse cues and ...
To investigate signal regulation models of gastric cancer, databases and literature were used to con...
Network motifs of kinases phosphorylating other kinases represent a unique control system for cellul...
<p>(A) Sequence motif analysis was performed using IceLogo and motif-x. Amino acid sequences of diff...
Abstract Background Phosphorylation events direct the flow of signals and metabolites along cellular...
Thesis (Ph.D.)--University of Washington, 2016-05Signal transduction is the process by which cells c...
Signal transduction systems coordinate complex cellular information to regulate biological events su...
<p>For each domain family (SH2, WW, PDZ and SH3), the bars denote the percent of motifs found to be ...
Motivation: Modification of proteins via phosphorylation is a primary mechanism for signal transduct...
Phosphorylation is an important mechanism for regulation of protein function and aktivity. Tyrosine ...
The functional diversity of kinases enables specificity in cellular signal transduction. Yet how mor...
Protein phosphorylation is the most abundant reversible covalent modification. Human protein kinases...
Systematic and quantitative analysis of protein phosphorylation is revealing dynamic regulatory netw...
The coordinated regulation of protein kinases is a rapid mechanism that integrates diverse cues and ...
SummaryProtein kinases control cellular decision processes by phosphorylating specific substrates. T...
The coordinated regulation of protein kinases is a rapid mechanism that integrates diverse cues and ...
To investigate signal regulation models of gastric cancer, databases and literature were used to con...
Network motifs of kinases phosphorylating other kinases represent a unique control system for cellul...
<p>(A) Sequence motif analysis was performed using IceLogo and motif-x. Amino acid sequences of diff...
Abstract Background Phosphorylation events direct the flow of signals and metabolites along cellular...
Thesis (Ph.D.)--University of Washington, 2016-05Signal transduction is the process by which cells c...
Signal transduction systems coordinate complex cellular information to regulate biological events su...
<p>For each domain family (SH2, WW, PDZ and SH3), the bars denote the percent of motifs found to be ...
Motivation: Modification of proteins via phosphorylation is a primary mechanism for signal transduct...
Phosphorylation is an important mechanism for regulation of protein function and aktivity. Tyrosine ...
The functional diversity of kinases enables specificity in cellular signal transduction. Yet how mor...
Protein phosphorylation is the most abundant reversible covalent modification. Human protein kinases...