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Mutations in the DLG motif disrupt the low-affinity binding of Keap1 with Nrf2, resulting in the stabilization of Nrf2, although the association between Keap1 and Nrf2 through the high-affinity binding site, ETGE, is retained
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PMID: 18703567
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The areas of scientific interest include: Nitric oxide signaling Angiogenesis-related pathways Growth-factor communication Gastrointestinal biology Tendon fibroblast models Peptide stability One reason BPC-157 continues to attract scientific interest is that published literature has linked it to multiple biological signaling pathways as opposed to a single molecular target
