| Name | calmodulin |
|---|---|
| Synonyms | CALM; CAM; CALM 1; CALM 2; CALM 3; CALM1; CALM2; CALM3… |
| Name | mercuric chloride |
|---|---|
| CAS |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 2153338 | Clifton GG, Oelsner D, Anderson CR, Pearce CJ, Wallin JD: The effects of mercuric chloride on calmodulin-mediated Ca2+ transport in rat brain. Am J Med Sci. 1990 Jan;299(1):26-31. |
32(0,1,1,2) | Details |
| 19546257 | Peltz A, Sherwani SI, Kotha SR, Mazerik JN, O'Connor Butler ES, Kuppusamy ML, Hagele T, Magalang UJ, Kuppusamy P, Marsh CB, Parinandi NL: and calmodulin regulate mercury-induced phospholipase D activation in vascular endothelial cells. Int J Toxicol. 2009 May-Jun;28(3):190-206. |
4(0,0,0,4) | Details |
| 11346962 | Chen TH, Hsu CS, Tsai PJ, Ho YF, Lin NS: Heterotrimeric G-protein and signal transduction in the nematode-trapping fungus Arthrobotrys dactyloides. Planta. 2001 Apr;212(5-6):858-63. The activation leads to an increase in cytoplasmic Ca2+, activation of calmodulin, and finally the opening of water channels. |
1(0,0,0,1) | Details |
| 7707359 | Shoshan-Barmatz V, Weil S, Meyer H, Varsanyi M, Heilmeyer LM: Endogenous, Ca (2+)-dependent -protease cleaves specifically the ryanodine receptor/Ca2+ release channel in skeletal muscle. J Membr Biol. 1994 Dec;142(3):281-8. The activity of this protease is strongly stimulated by (DTT), and beta-mercaptoethanol, and is inhibited by iodoacetamide, mercuric chloride and leupeptin, but not by PMSF. The calpain binding site is identified as a PEST glutamic acid, serine, -rich) region in the amino acid sequence GTPGGTPQPGVE, at positions 1356-1367 of the RyR and the cleavage site, the calmodulin binding site, at residues 1383-1400. |
1(0,0,0,1) | Details |
| 7825186 | Yamamoto H: A hypothesis for -induced tonic seizures with supporting evidence. Toxicology. 1995 Jan 6;95(1-3):19-26. The ED50 value of as measured by induction of tonic seizures was significantly increased in a dose-dependent manner when mercuric chloride (0.5 or 5.0 nmol/body), gangliosides (GGS) (90 nmol/body), a protein kinase C inhibitor or trifluoperazine (TFP) (45 or 90 nmol/body), a calmodulin inhibitor were preinjected intracerebroventricularly (i.v.t.) and NG-nitro- (NNA) (300 mg/kg), a (NO) synthase inhibitor was preinjected intraperitoneally (i.p.) in mice. |
32(0,1,1,2) | Details |