[Cloning and determination of the primary structure of DNA complementary to the mRNA of human ribosomal protein L11].

Article Details

Citation

Mishin VP, Filipenko ML, Muravlev AI, Karpova GG, Mertvetsov NP

[Cloning and determination of the primary structure of DNA complementary to the mRNA of human ribosomal protein L11].

Bioorg Khim. 1995 Feb;21(2):158-60.

PubMed ID
7748210 [ View in PubMed
]
Abstract

A polymerase chain reaction strategy was employed to isolate cDNA encoding L11 human ribosomal protein. Based on the known nucleotide sequence of 5'-region of the ribosomal protein L11 mRNA, we have designed primers and used them in amplification of corresponding sequence of human cDNA from total placenta cDNA. The fragment of RPS26 cDNA was cloned in plasmid vector and sequenced. Sequence analysis showed that there is high homology (88%) between coding regions of RPS26 mRNAs in rat liver and human placenta. The amino acid exchanges were observed at positions: 91 (Asp-->Glu), 217 (Thr-->Ala), 352 (Lys-->Glu).

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
60S ribosomal protein L11P62913Details