Nucleotide and amino acid sequence analysis of the porcine adenovirus 23K protein

The genomic location of the viral encoded protease (23K) of porcine adenovirus serotype 3 (PAV3) was determined and the appropriate fragment cloned and sequenced. An open reading frame (ORF) coding for a polypeptide of 203 amino acids and a calculated molecular weight of 23.3 kDa was found. The ORF...

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Veröffentlicht in:DNA sequence 1996, Vol.6 (4), p.251-254
Hauptverfasser: McCoy, Richard J., Johnson, Michael A., Sheppard, Michael
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container_title DNA sequence
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creator McCoy, Richard J.
Johnson, Michael A.
Sheppard, Michael
description The genomic location of the viral encoded protease (23K) of porcine adenovirus serotype 3 (PAV3) was determined and the appropriate fragment cloned and sequenced. An open reading frame (ORF) coding for a polypeptide of 203 amino acids and a calculated molecular weight of 23.3 kDa was found. The ORF was situated in a position similar to that of the human adenovirus 23K, that is, between a putative stop codon for the hexon gene and the polyadenylation signal, AATAAA, for the late region 3. Amino acid sequence alignment of the predicted polypeptide with the sequences of the 23K proteins from other mammalian adenoviruses revealed homology of between 50% and 60% for all except the bovine adenovirus type 7, which displayed appreciable variance from the PAV3 putative 23K with an overall sequence homology of approximately 35%. Conserved cysteine, histidine and proline residues believed to be important in the activity of the 23K protein of human adenoviruses were also present in the PAV3 protein. The genomic location and amino acid sequence of the characterised reading frame suggests that this gene is that of the 23K protein of PAV3.
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An open reading frame (ORF) coding for a polypeptide of 203 amino acids and a calculated molecular weight of 23.3 kDa was found. The ORF was situated in a position similar to that of the human adenovirus 23K, that is, between a putative stop codon for the hexon gene and the polyadenylation signal, AATAAA, for the late region 3. Amino acid sequence alignment of the predicted polypeptide with the sequences of the 23K proteins from other mammalian adenoviruses revealed homology of between 50% and 60% for all except the bovine adenovirus type 7, which displayed appreciable variance from the PAV3 putative 23K with an overall sequence homology of approximately 35%. Conserved cysteine, histidine and proline residues believed to be important in the activity of the 23K protein of human adenoviruses were also present in the PAV3 protein. The genomic location and amino acid sequence of the characterised reading frame suggests that this gene is that of the 23K protein of PAV3.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>8912929</pmid><doi>10.3109/10425179609008451</doi><tpages>4</tpages></addata></record>
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ispartof DNA sequence, 1996, Vol.6 (4), p.251-254
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language eng
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source MEDLINE; Taylor & Francis:Master (3349 titles)
subjects Adenovirus
Adenoviruses, Human - enzymology
Adenoviruses, Human - genetics
Amino Acid Sequence
Animals
Base Sequence
Capsid - biosynthesis
Capsid - chemistry
Capsid - genetics
Capsid Proteins
Cattle
Conserved Sequence
Cysteine
Cysteine Endopeptidases - chemistry
Cysteine Endopeptidases - genetics
Hexon
Histidine
Humans
Mastadenovirus - enzymology
Mastadenovirus - genetics
Molecular Sequence Data
Molecular Weight
Open Reading Frames
Proline
Proteinase
Sequence Homology, Amino Acid
Swine
Viral Proteins
title Nucleotide and amino acid sequence analysis of the porcine adenovirus 23K protein
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