z-logo
open-access-imgOpen Access
Nucleotide and deduced amino acid sequence of an actin cDNA clone fromPlasmodium falciparum
Author(s) -
Helmut Blum,
M. Hannappel,
Georg J. Arnold
Publication year - 1990
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/18.23.7140
Subject(s) - biology , nucleic acid sequence , plasmodium falciparum , complementary dna , peptide sequence , clone (java method) , genetics , nucleotide , sequence alignment , sequence (biology) , microbiology and biotechnology , gene , malaria , immunology
A full length cDNA clone (XZPfac) coding for actin of Plasmodium falciparum (strain FCB1) was isolated from a X-ZAP cDNA library by hybridization with synthetic oligonucleotides. The cDNA was synthesized from poly(A) mRNA of the asexual blood-stage (merozoite) of the parasite. A comparison of our sequence data with the actin sequence of isolate NF54, Amsterdam Airport strain (1) reveals several differences on the nucleotide level, most of which are located within the 5' nontranscribed region. Isolate NF54 contains an AT insertion at position 132 and an additional A at position 170 compared to XZPfac. Further, the nucleotides at positions 71 and 104 are deleted and the bases at positions 188/189 differ. Within the coding region, base alterations at position 349/350 and 1264 result in amino acid changes from a V to a D and a T to an I, respectively. The base alteration at position 1385 does not affect the amino acid sequence. A remarkable feature of the actin sequence in XZPfac is a stretch of 45 T nucleotides at the 5' end.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom