Abstract:Using as a primary standard a representative set of 208 proteins whose amino-acid-residue mole frequencies have been accurately established, a set of standard distributions of mole frequencies is defined for each amino acids, in terms of which percentile values for the observed mole frequencies of the amino-acid residues in any other protein can be determined. Data so transformed have a distribution much closer to Gaussian than untransformed values, and allow meaningful determinations of correlations between t… Show more
“…FASTA analysis also indicated similarity between ORF1904 and an unidentified ORF (ORF35) from the lactococcal bacteriophage bIL67 (19) and less similarity to the lactococcal lytic bacteriophage US3 lytic enzyme (16) and the Bacillus subtilis xylose isomerase (22). Analysis by COMPARE (18) indicated similarity between ORF1904 and numerous proteins involved in binding and/or degradation of cell wall glycoproteins. These sequence similarities and the observation that a number of cell wall-lytic en-zymes contain repeated sequence motifs (5,8,10,12) suggest that ORF1904 may be involved in cell lysis during the lytic cycle of BK5-T or in cell wall hydrolysis to enable phage DNA injection.…”
Spontaneous deletion mutants of the temperate lactococcal bacteriophage BK5-T were obtained when the phage was grown vegetatively on the indicator strain Lactococcus lactis subsp. cremoris H2. One deletion mutant was unable to form stable lysogens, and analysis of this mutant led to the identification of the BK5-T attP site and the integrase gene (int). The core sequences of the BK5-T attP and host attB regions are conserved in a number of lactococcal phages and L. lactis strains.
“…FASTA analysis also indicated similarity between ORF1904 and an unidentified ORF (ORF35) from the lactococcal bacteriophage bIL67 (19) and less similarity to the lactococcal lytic bacteriophage US3 lytic enzyme (16) and the Bacillus subtilis xylose isomerase (22). Analysis by COMPARE (18) indicated similarity between ORF1904 and numerous proteins involved in binding and/or degradation of cell wall glycoproteins. These sequence similarities and the observation that a number of cell wall-lytic en-zymes contain repeated sequence motifs (5,8,10,12) suggest that ORF1904 may be involved in cell lysis during the lytic cycle of BK5-T or in cell wall hydrolysis to enable phage DNA injection.…”
Spontaneous deletion mutants of the temperate lactococcal bacteriophage BK5-T were obtained when the phage was grown vegetatively on the indicator strain Lactococcus lactis subsp. cremoris H2. One deletion mutant was unable to form stable lysogens, and analysis of this mutant led to the identification of the BK5-T attP site and the integrase gene (int). The core sequences of the BK5-T attP and host attB regions are conserved in a number of lactococcal phages and L. lactis strains.
“…5). ORF63, however, showed no significant homology to Cro or any other characterized proteins, as determined by COMPARE (24) or FASTA (18) comparison with proteins in the GenBank database. The amino acid sequence of ORF63 was analyzed for the presence of possible helix-turn-helix structures, but no sequence fulfilling all the requirements of a helix-turn-helix motif was identified.…”
Bacteriophage BK5-T is a small isometric-headed temperate phage that infects Lactococcus lactis subsp. cremoris. Northern (RNA) analysis of mRNA produced by lysogenic strains containing BK5-T prophage revealed four major BK5-T transcripts that are 0.8, 1.3, 1.8, and 1.8 kb in size and enabled a transcription map of the prophage genome to be prepared. The position and size of each transcript corresponded closely to the position and size of open reading frames predicted from the nucleotide sequence of BK5-T. Analysis of the transcripts suggested that one of them was derived from the gene encoding the BK5-T integrase and another was from the gene encoding the BK5-T homolog of the cI repressor. Computer analysis of the nucleotide sequence upstream of the BK5-T cI homolog predicted the presence of a pair of divergent promoters and three inverted repeat sequences, features characteristic of temperate-phage immunity regions. By analogy with , the three inverted repeat sequences could be binding sites for cI or Cro homologs and the two divergent promoters could initiate transcription through the BK5-T equivalents of cI and cro.
“…The method for deriving the correlation statistic (r) for amino acid residues is based on a concept developed previously [5] which utilizes the amino acid residue composition of a standard set of proteins [6] and which uses a table look-up to perform a percentile transformation. As a result, the analysis is based on a near normal distribution and a meaningful estimate of the probability for a given "r" can be given.…”
A suite of some dozen programmes written in FORTRAN77 to run on VAX computers using the VMS operating system, and which utilizes a Digital Command Language (DCL) shell to allow it to be menu driven has been in use at the Division of Molecular Biology for about nine months.
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