protein phosphatase 1 catalytic subunit beta
The information on this page was automatically extracted from online scientific databases.
From NCBI Gene:
The protein encoded by this gene is one of the three catalytic subunits of protein phosphatase 1 (PP1). PP1 is a serine/threonine specific protein phosphatase known to be involved in the regulation of a variety of cellular processes, such as cell division, glycogen metabolism, muscle contractility, protein synthesis, and HIV-1 viral transcription. Mouse studies suggest that PP1 functions as a suppressor of learning and memory. Two alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]
Protein phosphatase that associates with over 200 regulatory proteins to form highly specific holoenzymes which dephosphorylate hundreds of biological targets. Protein phosphatase (PP1) is essential for cell division, it participates in the regulation of glycogen metabolism, muscle contractility and protein synthesis. Involved in regulation of ionic conductances and long-term synaptic plasticity. Component of the PTW/PP1 phosphatase complex, which plays a role in the control of chromatin structure and cell cycle progression during the transition from mitosis into interphase. In balance with CSNK1D and CSNK1E, determines the circadian period length, through the regulation of the speed and rhythmicity of PER1 and PER2 phosphorylation. May dephosphorylate CSNK1D and CSNK1E. Dephosphorylates the 'Ser-418' residue of FOXP3 in regulatory T-cells (Treg) from patients with rheumatoid arthritis, thereby inactivating FOXP3 and rendering Treg cells functionally defective (PubMed:23396208).
From NCBI Gene:
- NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2
Variants in PPP1CB may be a cause of susceptibility to rasopathy reminiscent of Noonan syndrome-like disorder with loose anagen hair (NSLH). Affected individuals show Noonan dysmorphic features such as macrocephaly, high forehead and low-set and posteriorly rotated ears, in association with some hair abnormality (slow-growing, very fine hair or unruly hair texture), developmental delay and mild ventriculomegaly.