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A database built with INDRA combining content from numerous readers and databases. This page allows you to curate the loaded statements. For more information please see the manual.

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INDRA is developed by indralabs, a part of the Harvard Medical School Laboratory of Systems Pharmacology.

This project, indra_db, is also developed by the indralab team. For more information on how we procure our sources, you can go here. This work was funded by ARO grant W911NF‐15‐1‐0544 under the DARPA Communicating with Computers program.

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PKC phosphorylates KCNMA1. 3 / 3

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"The 20-HETE-GPR75 pairing initiates a signaling cascade that involves conventional G protein (Gα ) mediated changes alongside the promotion of a GIT1-mediated PKC-stimulated phosphorylation of MaxiKβ (BK channel β subunit) that facilitates vasoconstriction ."

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"The alpha-subunit of the reconstituted BK channel is phosphorylated by PKA and PKC."

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"PKC phosphorylation of MaxiK channel alpha-subunit occurs in the C-terminus at consensus PKC sites 642 S * PKKK 646 and 1097 KS * R 1099 with only one channel subunit requiring phosphorylation for channel inhibition [XREF_BIBR]."

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PKC phosphorylates KCNMA1. 3 / 3

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