Linked Life Data

12821141

Source:http://linkedlifedata.com/resource/pubmed/id/12821141

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pubmed-article:12821141pubmed:abstractTextReceptors for activated C kinases (RACKs) are scaffold proteins that anchor diverse signaling proteins and are involved in modulating cell cycle. We report the cloning and cellular localization of a RACK ortholog (PfRACK) in the human malaria parasite Plasmodium falciparum. The full-length transcript obtained by 3(') and 5(') RACE has 1.4 kbp with a predicted ORF of 972 bp, coding for a protein with 323 residues of 35.8 kDa molecular weight and pI 6.38. PfRACK has 59% and 60% identity at the amino acid level to Chlamydomonas reinhardtii and Danio rerio RACKs, respectively, presenting seven WD40 motifs and retaining the conserved domains in repeats III (DVFSVSF) and VI (STINSLCF) that are important for PKC binding. Semi-quantitative RT-PCR revealed that PfRACK is constitutively expressed in the intraerythrocytic stages of P. falciparum. Using confocal microscopy, PfRACK was immunolocalized in all parasite stages, being conspicuously spread throughout the schizont. The high similarity of PfRACK to those previously described in other organisms, as well as its constitutive expression in Plasmodium asexual stages, suggests that it might play a key role in the regulatory processes of malaria parasite life cycle.lld:pubmed
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pubmed-article:12821141pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:12821141pubmed:year2003lld:pubmed
pubmed-article:12821141pubmed:articleTitleHuman malaria parasites display a receptor for activated C kinase ortholog.lld:pubmed
pubmed-article:12821141pubmed:affiliationDepartamento de Parasitologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, 05508-900, São Paulo, SP, Brazil.lld:pubmed
pubmed-article:12821141pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12821141pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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