RCAN1
Inhibits calcineurin-dependent transcriptional responses by binding to the catalytic domain of calcineurin A. Could play a role during central nervous system development. Belongs to the RCAN family. Highly expressed heart, brain and skeletal muscle. Also expressed in all other tissues. 4 alternatively spliced human isoforms have been reported. Note: This description may include information from UniProtKB.
|
Protein type: Inhibitor |
Chromosomal Location of human Ortholog: 21q22.12 |
Cellular Component:
cytoplasm; nucleus
|
Molecular Function:
calcium-dependent protein serine/threonine phosphatase regulator activity; nucleic acid binding; protein binding
|
Biological Process:
calcineurin-NFAT signaling cascade; calcium-mediated signaling; locomotion involved in locomotory behavior; negative regulation of calcineurin-NFAT signaling cascade; regulation of phosphoprotein phosphatase activity; response to ischemia; response to oxidative stress; short-term memory; skeletal muscle fiber development
|
Reference #:
P53805
(UniProtKB)
|
Alt. Names/Synonyms: ADAPT78; Calcipressin-1; calcium and oxidant-inducible mRNA; CSP1; Down syndrome candidate region 1; Down syndrome critical region gene 1; Down syndrome critical region protein 1; DSC1; DSCR1; MCIP1; modulatory calcineurin-interacting protein 1; Myocyte-enriched calcineurin-interacting protein 1; near DSCR proline-rich protein; RCAN1; RCN1; Regulator of calcineurin 1
|
Gene Symbols: RCAN1
|
Molecular weight:
28,079 Da
|
Basal Isoelectric point:
5.09
Predict pI for various phosphorylation states
|