Table 1.
Fold recognition from 3D-PSSM and FUGUE servers for the C-terminal region of BMV 1a
PBD code | Name | SF | Description | 3D-PSSM | FUGUE | ||
---|---|---|---|---|---|---|---|
e-Value | Percentage of identity | Z-score | Percentage of identity | ||||
1pjr and 3pjr | PcrA | 1 | DNA helicase from Bacillus stearothermophilus | – | – | 2.33 | 6% (of 632 residues) |
1uaa | RepA | 1 | DNA helicase from E.Coli | 1.01 | 12% (of 306 residues) | 2.33 | 5% (of 623 residues) |
1hv8 | MjDEAD | 2 | RNA helicase from Methanococcus jannaschii | 1.53 | 12% (of 353 residues) | – | – |
1a1v | NS3 | 2 | RNA helicase from Hepatitis C virus | 0.176 | 11% (of 135 residues) | – | – |
First ranked e-values (and Z-scores) for the alignment of BMV 1a C-terminal region (residues 448–961) with the sequences of helicases with known structure hinted by means of the fold recognition server 3D-PSSM. Scores and alignments obtained by FUGUE are also given for the UvrD-helicases (sequences of PcrA and RepA). The percentage of identity and the total number of residues aligned with the query are shown. PDB codes are used to identify the helicase proteins: HCV helicase NS3 (1a1v), MjDEAD (1hv8), UvrD helicase RepA (1uaa), and PcrA (1pjr). The largest number of residues aligned is obtained with MjDEAD