This article provides a comprehensive comparative analysis of the Src Homology 2 (SH2) domains found in STAT and Src-family proteins, two classes of proteins central to cellular signaling.
The development of selective inhibitors for STAT (Signal Transducer and Activator of Transcription) SH2 domains represents a promising therapeutic strategy for cancers and inflammatory diseases.
The development of specific STAT SH2 domain inhibitors represents a promising therapeutic strategy for cancers and inflammatory diseases.
This article provides a comprehensive comparison for researchers and drug development professionals on two primary strategies for inhibiting SH2 domain-mediated protein-protein interactions: small molecules and peptidomimetics.
This review provides a comprehensive comparative analysis of the Src Homology 2 (SH2) domains of STAT1 and STAT3, transcription factors critical in immunity, inflammation, and cancer.
Constitutive activation of the JAK-STAT pathway is a hallmark of numerous cancers and autoimmune diseases, driving the development of targeted inhibitors.
Targeting Src Homology 2 (SH2) domains represents a promising therapeutic strategy for modulating dysregulated cell signaling in cancer and other diseases.
This article provides a comprehensive analysis of rapid off-rates in SH2 domain-phosphopeptide interactions, a critical feature for ensuring dynamic and specific cellular signaling.
Targeting the shallow binding surfaces of Src Homology 2 (SH2) domains represents a significant challenge and opportunity in therapeutic development, particularly for cancer and neurodegenerative diseases.
The Signal Transducer and Activator of Transcription (STAT) proteins are critical transcription factors whose dysregulation drives numerous diseases, particularly cancer.