| First Author | Darnis S | Year | 1999 |
| Journal | Biochim Biophys Acta | Volume | 1430 |
| Issue | 2 | Pages | 281-9 |
| PubMed ID | 10082956 | Mgi Jnum | J:53899 |
| Mgi Id | MGI:1333615 | Doi | 10.1016/s0167-4838(99)00011-4 |
| Citation | Darnis S, et al. (1999) Molecular cloning and primary structure analysis of porcine pancreatic alpha-amylase. Biochim Biophys Acta 1430(2):281-9 |
| abstractText | A cDNA library was constructed in a Uni-ZAP XR vector using mRNA isolated from porcine pancreas. A full-length alpha-amylase cDNA was obtained using a combination of library screening and nested polymerase chain reaction. Sequencing of the clone revealed a 1536-nucleotide (nt) open reading frame encoding a protein of 496 amino acid (aa) residues with a signal peptide of 15 aa. The calculated molecular mass of the enzyme was 55354 Da, in accordance with those of the purified porcine pancreatic alpha-amylase forms (PPAI and PPAII) as determined by mass spectrometry. A comparison of the deduced aa sequence with published peptidic sequences of PPAI identified a number of mismatches. The sequence of the cDNA reported here provides a sequence reference for PPA in excellent agreement with the refined three-dimensional structures of both PPAI and PPAII. No evidence for a second variant was found in the cDNA library and it is most likely that PPAI and PPAII are two forms of the same protein. The primary structure of PPA shows high homology with human, mouse and rat pancreatic alpha-amylases. The 304-310 region, corresponding to a mobile loop involved in substrate binding and processing near the active site, is fully conserved. |
