Analysis | Hit | start | end | length | Note | Hit coverage | Hit length | Hit pident | Hit pcons | eValue | Hit description |
blastp_kegg | ssl:SS1G_01265 | 1 | 2223 | 2223 | n/a | 100.00 | 2223 | 97.12 | 0.00 | 0.0 | hypothetical protein |
bfu:BC1G_02495 | 1 | 2034 | 2034 | Gaps:380 | 93.42 | 2385 | 73.52 | 11.58 | 0.0 | hypothetical protein |
pno:SNOG_09081 | 5 | 1898 | 1894 | Gaps:784 | 74.77 | 5149 | 43.27 | 21.92 | 0.0 | hypothetical protein |
afv:AFLA_038600 | 9 | 1883 | 1875 | Gaps:444 | 90.66 | 2975 | 42.71 | 20.43 | 0.0 | nonribosomal peptide synthase putative |
ani:AN7884.2 | 9 | 2222 | 2214 | Gaps:1193 | 92.78 | 7214 | 40.52 | 21.80 | 0.0 | hypothetical protein |
aor:AO090011000043 | 3 | 1897 | 1895 | Gaps:964 | 87.22 | 6885 | 40.63 | 20.77 | 0.0 | non-ribosomal peptide synthetase modules and related proteins |
cim:CIMG_09750 | 3 | 1898 | 1896 | Gaps:1049 | 70.26 | 7862 | 40.70 | 21.36 | 0.0 | hypothetical protein |
act:ACLA_098420 | 2 | 1898 | 1897 | Gaps:1258 | 83.30 | 8202 | 38.85 | 21.52 | 0.0 | nonribosomal peptide synthase putative |
pno:SNOG_14834 | 1 | 1897 | 1897 | Gaps:1007 | 75.23 | 7038 | 39.43 | 21.00 | 0.0 | hypothetical protein |
aor:AO090001000009 | 7 | 1893 | 1887 | Gaps:480 | 92.17 | 3143 | 43.39 | 19.68 | 0.0 | non-ribosomal peptide synthetase modules and related proteins |
blastp_uniprot_sprot | sp|Q01886|HTS1_COCCA | 9 | 1898 | 1890 | Gaps:1082 | 88.33 | 5218 | 36.82 | 20.05 | 1e-139 | HC-toxin synthetase OS Cochliobolus carbonum GN HTS1 PE 1 SV 2 |
sp|Q00869|ESYN_FUSEQ | 11 | 1842 | 1832 | Gaps:407 | 71.89 | 3131 | 29.81 | 20.75 | 4e-95 | Enniatin synthase OS Fusarium equiseti GN ESYN1 PE 1 SV 2 |
sp|Q70LM5|LGRC_BREPA | 1 | 1835 | 1835 | Gaps:1394 | 75.90 | 7756 | 34.86 | 22.47 | 2e-72 | Linear gramicidin synthase subunit C OS Brevibacillus parabrevis GN lgrC PE 3 SV 1 |
sp|Q70LM4|LGRD_BREPA | 4 | 2088 | 2085 | Gaps:1074 | 86.45 | 5085 | 34.92 | 22.57 | 3e-68 | Linear gramicidin synthase subunit D OS Brevibacillus parabrevis GN lgrD PE 1 SV 1 |
sp|O30409|TYCC_BREPA | 1 | 1893 | 1893 | Gaps:1345 | 83.98 | 6486 | 31.12 | 21.08 | 3e-62 | Tyrocidine synthase 3 OS Brevibacillus parabrevis GN tycC PE 1 SV 1 |
sp|O68006|BACA_BACLI | 11 | 1898 | 1888 | Gaps:1243 | 86.28 | 5255 | 30.92 | 22.12 | 5e-62 | Bacitracin synthase 1 OS Bacillus licheniformis GN bacA PE 3 SV 1 |
sp|O68008|BACC_BACLI | 11 | 1895 | 1885 | Gaps:1283 | 75.64 | 6359 | 34.39 | 22.81 | 3e-61 | Bacitracin synthase 3 OS Bacillus licheniformis GN bacC PE 3 SV 1 |
sp|P27206|SRFAA_BACSU | 3 | 1893 | 1891 | Gaps:769 | 68.97 | 3587 | 35.29 | 22.51 | 1e-59 | Surfactin synthase subunit 1 OS Bacillus subtilis GN srfAA PE 1 SV 4 |
sp|P0C064|GRSB_BREBE | 9 | 1898 | 1890 | Gaps:960 | 81.17 | 4450 | 31.31 | 23.75 | 2e-58 | Gramicidin S synthase 2 OS Brevibacillus brevis GN grsB PE 1 SV 2 |
sp|O68007|BACB_BACLI | 11 | 1898 | 1888 | Gaps:451 | 69.47 | 2607 | 32.97 | 21.31 | 2e-57 | Bacitracin synthase 2 OS Bacillus licheniformis GN bacB PE 3 SV 1 |
blastp_pdb | 2vsq_A | 9 | 1898 | 1890 | Gaps:315 | 78.91 | 1304 | 35.08 | 23.71 | 8e-49 | mol:protein length:1304 SURFACTIN SYNTHETASE SUBUNIT 3 |
1amu_B | 596 | 1808 | 1213 | Gaps:90 | 66.25 | 563 | 40.48 | 19.03 | 5e-34 | mol:protein length:563 GRAMICIDIN SYNTHETASE 1 |
1amu_A | 596 | 1808 | 1213 | Gaps:90 | 66.25 | 563 | 40.48 | 19.03 | 5e-34 | mol:protein length:563 GRAMICIDIN SYNTHETASE 1 |
3fce_A | 594 | 1815 | 1222 | Gaps:68 | 71.29 | 512 | 36.71 | 21.10 | 2e-31 | mol:protein length:512 D-alanine--poly(phosphoribitol) ligase subuni |
3fcc_A | 594 | 1815 | 1222 | Gaps:68 | 71.29 | 512 | 36.71 | 21.10 | 2e-31 | mol:protein length:512 D-alanine--poly(phosphoribitol) ligase subuni |
3dhv_A | 594 | 1815 | 1222 | Gaps:68 | 71.29 | 512 | 36.71 | 21.10 | 2e-31 | mol:protein length:512 D-alanine-poly(phosphoribitol) ligase |
3lgx_D | 596 | 1804 | 1209 | Gaps:97 | 81.00 | 521 | 35.31 | 19.67 | 2e-24 | mol:protein length:521 D-alanine--poly(phosphoribitol) ligase subuni |
3lgx_C | 596 | 1804 | 1209 | Gaps:97 | 81.00 | 521 | 35.31 | 19.67 | 2e-24 | mol:protein length:521 D-alanine--poly(phosphoribitol) ligase subuni |
3lgx_B | 596 | 1804 | 1209 | Gaps:97 | 81.00 | 521 | 35.31 | 19.67 | 2e-24 | mol:protein length:521 D-alanine--poly(phosphoribitol) ligase subuni |
3lgx_A | 596 | 1804 | 1209 | Gaps:97 | 81.00 | 521 | 35.31 | 19.67 | 2e-24 | mol:protein length:521 D-alanine--poly(phosphoribitol) ligase subuni |
rpsblast_cdd | gnl|CDD|171521 | 9 | 1899 | 1891 | Gaps:740 | 67.11 | 3956 | 37.18 | 20.26 | 1e-82 | PRK12467 PRK12467 peptide synthase Provisional. |
gnl|CDD|171397 | 9 | 1828 | 1820 | Gaps:867 | 84.27 | 4131 | 34.96 | 19.76 | 3e-75 | PRK12316 PRK12316 peptide synthase Provisional. |
gnl|CDD|162508 | 464 | 1724 | 1261 | Gaps:56 | 100.00 | 408 | 41.67 | 16.42 | 1e-73 | TIGR01733 AA-adenyl-dom amino acid adenylation domain. This domain is a subset of the AMP-binding domain found in Pfam (pfam00501) which also hits substrate--CoA ligases and luciferases. Sequences scoring in between trusted and noise for this model may be ambiguous as to whether they activate amino acids or other molecules lacking an alpha amino group. |
gnl|CDD|144190 | 463 | 1724 | 1262 | Gaps:107 | 100.00 | 412 | 38.11 | 19.90 | 2e-60 | pfam00501 AMP-binding AMP-binding enzyme. |
gnl|CDD|31223 | 223 | 1717 | 1495 | Gaps:114 | 97.66 | 642 | 30.78 | 22.33 | 2e-51 | COG1020 EntF Non-ribosomal peptide synthetase modules and related proteins [Secondary metabolites biosynthesis transport and catabolism]. |
gnl|CDD|162515 | 1889 | 2176 | 288 | Gaps:21 | 79.29 | 367 | 29.90 | 19.24 | 4e-43 | TIGR01746 Thioester-redct thioester reductase domain. It has been suggested that a NADP-binding motif can be found in the N-terminal portion of this domain that may form a Rossman-type fold. |
gnl|CDD|167846 | 595 | 1810 | 1216 | Gaps:123 | 82.94 | 504 | 35.41 | 17.70 | 2e-42 | PRK04813 PRK04813 D-alanine--poly(phosphoribitol) ligase subunit 1 Provisional. |
gnl|CDD|33129 | 1888 | 2171 | 284 | Gaps:31 | 78.27 | 382 | 28.76 | 13.04 | 2e-37 | COG3320 COG3320 Putative dehydrogenase domain of multifunctional non-ribosomal peptide synthetases and related enzymes [Secondary metabolites biosynthesis transport and catabolism]. |
gnl|CDD|170335 | 126 | 1892 | 1767 | Gaps:204 | 66.82 | 1299 | 28.46 | 17.63 | 5e-37 | PRK10252 entF enterobactin synthase subunit F Provisional. |
gnl|CDD|162509 | 596 | 1808 | 1213 | Gaps:93 | 82.87 | 502 | 31.97 | 17.79 | 2e-36 | TIGR01734 D-ala-DACP-lig D-alanine--poly(phosphoribitol) ligase subunit 1. This model represents the enzyme (also called D-alanine-D-alanyl carrier protein ligase) which activates D-alanine as an adenylate via the reaction D-ala + ATP -> D-ala-AMP + PPi and further catalyzes the condensation of the amino acid adenylate with the D-alanyl carrier protein (D-ala-ACP). The D-alanine is then further transferred to teichoic acid in the biosynthesis of lipoteichoic acid (LTA) and wall teichoic acid (WTA) in gram positive bacteria both polysacchatides. |
rpsblast_kog | gnl|CDD|36391 | 440 | 1816 | 1377 | Gaps:115 | 76.72 | 537 | 34.22 | 22.57 | 5e-25 | KOG1176 KOG1176 KOG1176 Acyl-CoA synthetase [Lipid transport and metabolism]. |
gnl|CDD|36393 | 649 | 2119 | 1471 | Gaps:185 | 84.30 | 1032 | 25.52 | 15.52 | 3e-22 | KOG1178 KOG1178 KOG1178 Non-ribosomal peptide synthetase/alpha-aminoadipate reductase and related enzymes [Secondary metabolites biosynthesis transport and catabolism]. |
gnl|CDD|36392 | 596 | 1810 | 1215 | Gaps:97 | 60.23 | 596 | 29.81 | 20.61 | 1e-20 | KOG1177 KOG1177 KOG1177 Long chain fatty acid acyl-CoA ligase [Lipid transport and metabolism]. |
gnl|CDD|36390 | 569 | 1817 | 1249 | Gaps:144 | 68.53 | 626 | 29.37 | 15.15 | 6e-15 | KOG1175 KOG1175 KOG1175 Acyl-CoA synthetase [Lipid transport and metabolism]. |
gnl|CDD|36395 | 610 | 789 | 180 | Gaps:36 | 26.84 | 678 | 31.87 | 14.29 | 7e-11 | KOG1180 KOG1180 KOG1180 Acyl-CoA synthetase [Lipid transport and metabolism]. |
gnl|CDD|36435 | 1879 | 2072 | 194 | Gaps:47 | 46.90 | 467 | 20.55 | 18.72 | 7e-07 | KOG1221 KOG1221 KOG1221 Acyl-CoA reductase [Lipid transport and metabolism]. |