A human peptidyl-prolyl isomerase essential for regulation of mitosis.

Article Details

Citation

Lu KP, Hanes SD, Hunter T

A human peptidyl-prolyl isomerase essential for regulation of mitosis.

Nature. 1996 Apr 11;380(6574):544-7.

PubMed ID
8606777 [ View in PubMed
]
Abstract

The NIMA kinase is essential for progression through mitosis in Aspergillus nidulans, and there is evidence for a similar pathway in other eukaryotic cells. Here we describe the human protein Pin1, a peptidyl-prolyl cis/trans isomerase (PPIase) that interacts with NIMA. PPIases are important in protein folding, assembly and/or transport, but none has so far been shown to be required for cell viability. Pin1 is nuclear PPIase containing a WW protein interaction domain, and is structurally and functionally related to Ess1/Ptf1, an essential protein in budding yeast. PPIase activity is necessary for Ess1/Pin1 function in yeast. Depletion of Pin1/Ess1 from yeast or HeLa cells induces mitotic arrest, whereas HeLa cells overexpressing Pin1 arrest in the G2 phase of the cell cycle. Pin1 is thus an essential PPIase that regulates mitosis presumably by interacting with NIMA and attenuating its mitosis-promoting activity.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1Q13526Details