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Yang M, et al
Journal of Investigative Dermatology 117(6):1350-1356. [doi.org]
These probes, termed roGFP-iX were developed by insertion of a single amino acid (denoted by the X) adjacent to cysteine 147 resulting in a decreased stability of the disulfide bond and midpoint potentials of 229 to 246 mV compared to 280 mV of roGFP2
PGC-1 expression and activity are controlled by p38 MAPK, and a CAMK inhibitor prevented p38 activation in response to increased cytosolic Ca 2+ , demonstrating that p38 MAPK is a downstream target of CAMK [77,78,79,80]
In plant proteins, there is no cysteine in the signature (often SLDS) (Lallement et al., 2014)
