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. 2015 Aug 11;10(8):e0135239. doi: 10.1371/journal.pone.0135239

Table 3. P. insidiosum’s transcriptome-derived Exo1 homologous proteins that share the Peptide-A, -B, or -C sequences.

Predicted structures of these proteins are shown in Fig 2. NCBI accession number, protein length, calculated protein molecular weight (MW), number of 454-derived transcript reads (when P. insidiosum grew at 37°C), and sequence alignment analysis against Exo1 (including: query sequence coverage, E-value, and sequence identity), corresponding to each transcriptome-derived protein, are summarized in the table.

Subject sequence Accession number Protein length (amino acids) MW (kDa) Number of transcript reads Exo1 peptide Alignment against Exo1 (Query sequence)
A B C Query coverage a E-value Sequence identity b
UN05080 FX532070 751 82.8 109 Yes Yes Yes 98% 0.0 93%
UN00475 FX527465 682 76.1 17 Yes Yes - 86% 0.0 92%
UN03240 FX530230 290 32.7 1 - Yes - 38% 0.0 97%
UN01457 FX528447 257 28.3 1 - - Yes 37% 5.00E-174 93%
UN24957 FX551947 242 26.9 4 - Yes - 32% 2.00E-157 100%
UN22794 FX549784 177 19.6 1 - Yes - 20% 3.00E-87 88%

a Percent length value of a query sequence (i.e., Exo1) that covers or can align with a subject sequence

b Percent identity value of query (Exo1) and subject sequences within the Query coverage region