Difference between revisions of "Phosphatase Subfamily PPP3C"
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Revision as of 20:15, 5 July 2015
Phosphatase Classification: Fold MTDP: Superfamily MTDP: Family PPP: Subfamily PPP3C (PP2B, calcineurin)
PPP3C, the catalytic subunit of PP2B (calcineurin) holoeynzme, is a calcium-dependent serine/threonine phosphatase conserved in eukaryotes. It is involved in various biological processes and has significantly clinic relevance.
Evolution
PPP3C is found throughout eukaryotes, including opisthokonta, amoebazoa, plants and etc.
Domain
PPP3C has a single domain - phosphatase domain.
Functions
PPP3C is the catalytic subunit of Protein Phosphatase 2B (PP2B) holoenzyme (aka calcineurin). The holoenzyme is heterodimer complex consisting of one catalytic subunit and one regulatory subunit participates in very various cellular processes, from cell cycle progression to cardiac hypertrophy [1]. Below are some examples of its function:
- PP2B (calcineurin) activates the T cells of the immune system in mammals. When an antigen-preseting cell interacts with a T cell receptor on T cells, the cytoplasmic level of calcium increases, which activates calcineurin. PP2B (calcineurin) is used as a target for several immunosuppressive drugs, e.g. tacrolimus which is an immunosuppressive drug used mainly after allogeneic organ transplant to reduce the activity of the patient's immune system and so lower the risk of organ rejection [2].
- PP2B (calcineurin) is included as a key player in mediating calcium-triggered and -accelerated vesicle endocytosis [3].
- PP2B (calcineurin) activates a vertebrate-specific transcription factor called NFATc.
- PPP3C (PP2B, calcineurin) modulates potassium channel, perhaps by directly controlling the phosphorylation state of potassium channel in collaboration with PKA [4, 5].
- PPP3C interacts with Nuclear factor (NF)-κB-inducing kinase (NIK) and attenuates NIK-dependent gene expression [6].
This phosphatase has clinical significance for schizophrenia and diabetes (see wikipedia).
Besides, PPP3C (PP2B, calcineurin) is an attractive antifungal drug target [7], and its inhibitor (FK506 or cyclosporin A) can be combined with azoles or echinocandins for use against multidrug-resistant Candida species [8].
References
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- Error fetching PMID 11015619:
- Error fetching PMID 25452304:
- Error fetching PMID 24835995:
- Error fetching PMID 19422382:
- Error fetching PMID 25793374:
- Error fetching PMID 26029823:
- Error fetching PMID 26106221:
- Error fetching PMID 25878052: