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A recent study introduces a peptide PROTAC specifically designed to target and degrade the cysteine-histidine-rich 1 (CH1) domain of p300, a vital co-activator involved in oncogenic signaling pathways, particularly in PCa (Zhang et al., 2024)

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The phenyl ring of F23 Cagri forms extensive van der Waals contact with L16 Cagri , Y149 1.40 , Y146 1.37 (superscript numbers for receptor residues refer to the class B1 GPCR numbering scheme 17 ), anchoring the peptide segment with the CTR transmembrane (TM) bundle level with the micelle interface