Analysis | Hit | start | end | length | Note | Hit coverage | Hit length | Hit pident | Hit pcons | eValue | Hit description |
blastp_kegg | ssl:SS1G_04250 | 1 | 1974 | 1974 | n/a | 100.00 | 1974 | 95.04 | 0.00 | 0.0 | hypothetical protein |
bfu:BC1G_10567 | 284 | 1974 | 1691 | Gaps:4 | 95.05 | 1777 | 82.24 | 7.05 | 0.0 | similar to nonribosomal peptide synthetase 6 |
afv:AFLA_010620 | 3 | 1974 | 1972 | Gaps:77 | 95.38 | 2100 | 63.40 | 12.33 | 0.0 | nonribosomal siderophore peptide synthase Sid2 |
aor:AO090103000167 | 185 | 1974 | 1790 | Gaps:12 | 92.46 | 1923 | 68.50 | 12.32 | 0.0 | non-ribosomal peptide synthetase modules and related proteins |
afm:AFUA_3G03420 | 1 | 1974 | 1974 | Gaps:84 | 94.34 | 2083 | 61.02 | 13.28 | 0.0 | nonribosomal peptide synthase SidD |
nfi:NFIA_005590 | 1 | 1974 | 1974 | Gaps:21 | 89.97 | 2083 | 64.73 | 13.50 | 0.0 | nonribosomal peptide synthase SidD |
pcs:Pc22g20400 | 1 | 1971 | 1971 | Gaps:22 | 90.37 | 2076 | 64.98 | 12.95 | 0.0 | Pc22g20400 |
act:ACLA_061000 | 30 | 1970 | 1941 | Gaps:29 | 90.37 | 2066 | 64.70 | 12.75 | 0.0 | nonribosomal peptide synthase SidD |
ani:AN6236.2 | 183 | 1971 | 1789 | Gaps:97 | 89.17 | 2086 | 58.87 | 13.66 | 0.0 | hypothetical protein |
ang:An03g03520 | 185 | 1960 | 1776 | Gaps:33 | 84.29 | 2113 | 63.05 | 13.59 | 0.0 | hypothetical protein |
blastp_uniprot_sprot | sp|Q01886|HTS1_COCCA | 161 | 1869 | 1709 | Gaps:598 | 69.87 | 5218 | 34.31 | 20.05 | 1e-120 | HC-toxin synthetase OS Cochliobolus carbonum GN HTS1 PE 1 SV 2 |
sp|Q00869|ESYN_FUSEQ | 171 | 1875 | 1705 | Gaps:403 | 66.59 | 3131 | 29.78 | 19.95 | 3e-62 | Enniatin synthase OS Fusarium equiseti GN ESYN1 PE 1 SV 2 |
sp|O68008|BACC_BACLI | 185 | 1742 | 1558 | Gaps:1155 | 84.93 | 6359 | 27.70 | 21.26 | 9e-55 | Bacitracin synthase 3 OS Bacillus licheniformis GN bacC PE 3 SV 1 |
sp|O43103|SID2_USTMA | 194 | 1883 | 1690 | Gaps:666 | 76.86 | 4114 | 29.89 | 20.34 | 6e-53 | Ferrichrome siderophore peptide synthetase OS Ustilago maydis GN SID2 PE 3 SV 2 |
sp|P25464|ACVS_CEPAC | 275 | 1714 | 1440 | Gaps:524 | 56.73 | 3712 | 33.81 | 19.18 | 2e-51 | N-(5-amino-5-carboxypentanoyl)-L-cysteinyl-D-valine synthase OS Cephalosporium acremonium GN PCBAB PE 1 SV 1 |
sp|Q70LM5|LGRC_BREPA | 185 | 1742 | 1558 | Gaps:1347 | 79.93 | 7756 | 28.78 | 20.25 | 2e-50 | Linear gramicidin synthase subunit C OS Brevibacillus parabrevis GN lgrC PE 3 SV 1 |
sp|O30409|TYCC_BREPA | 193 | 1723 | 1531 | Gaps:1052 | 74.64 | 6486 | 29.08 | 21.42 | 6e-49 | Tyrocidine synthase 3 OS Brevibacillus parabrevis GN tycC PE 1 SV 1 |
sp|Q70LM4|LGRD_BREPA | 193 | 1178 | 986 | Gaps:605 | 75.00 | 5085 | 27.32 | 19.72 | 1e-48 | Linear gramicidin synthase subunit D OS Brevibacillus parabrevis GN lgrD PE 1 SV 1 |
sp|P39845|PPSA_BACSU | 158 | 1124 | 967 | Gaps:381 | 67.01 | 2561 | 26.22 | 18.07 | 1e-48 | Plipastatin synthase subunit A OS Bacillus subtilis GN ppsA PE 1 SV 2 |
sp|P27742|ACVS_EMENI | 193 | 1062 | 870 | Gaps:381 | 54.77 | 3770 | 27.80 | 17.72 | 7e-47 | N-(5-amino-5-carboxypentanoyl)-L-cysteinyl-D-valine synthase OS Emericella nidulans GN acvA PE 1 SV 2 |
blastp_pdb | 2vsq_A | 384 | 1060 | 677 | Gaps:87 | 47.62 | 1304 | 29.47 | 21.90 | 8e-29 | mol:protein length:1304 SURFACTIN SYNTHETASE SUBUNIT 3 |
1amu_B | 286 | 663 | 378 | Gaps:64 | 60.04 | 563 | 32.25 | 18.93 | 9e-28 | mol:protein length:563 GRAMICIDIN SYNTHETASE 1 |
1amu_A | 286 | 663 | 378 | Gaps:64 | 60.04 | 563 | 32.25 | 18.93 | 9e-28 | mol:protein length:563 GRAMICIDIN SYNTHETASE 1 |
3ite_B | 281 | 639 | 359 | Gaps:48 | 60.68 | 562 | 32.84 | 17.01 | 3e-27 | mol:protein length:562 SidN siderophore synthetase |
3ite_A | 281 | 639 | 359 | Gaps:48 | 60.68 | 562 | 32.84 | 17.01 | 3e-27 | mol:protein length:562 SidN siderophore synthetase |
3e7x_A | 295 | 622 | 328 | Gaps:48 | 60.67 | 511 | 30.00 | 18.39 | 2e-16 | mol:protein length:511 D-alanine--poly(phosphoribitol) ligase subuni |
3e7w_A | 295 | 622 | 328 | Gaps:48 | 60.67 | 511 | 30.00 | 18.39 | 2e-16 | mol:protein length:511 D-alanine--poly(phosphoribitol) ligase subuni |
3dhv_A | 295 | 622 | 328 | Gaps:60 | 60.55 | 512 | 29.68 | 17.10 | 5e-15 | mol:protein length:512 D-alanine-poly(phosphoribitol) ligase |
3fce_A | 295 | 622 | 328 | Gaps:60 | 60.55 | 512 | 29.68 | 17.10 | 5e-15 | mol:protein length:512 D-alanine--poly(phosphoribitol) ligase subuni |
3fcc_A | 295 | 622 | 328 | Gaps:60 | 60.55 | 512 | 29.68 | 17.10 | 5e-15 | mol:protein length:512 D-alanine--poly(phosphoribitol) ligase subuni |
rpsblast_cdd | gnl|CDD|162508 | 194 | 1313 | 1120 | Gaps:115 | 100.00 | 408 | 33.58 | 14.22 | 2e-70 | 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|171521 | 183 | 1891 | 1709 | Gaps:895 | 76.72 | 3956 | 32.52 | 18.62 | 5e-62 | PRK12467 PRK12467 peptide synthase Provisional. |
gnl|CDD|171397 | 190 | 1893 | 1704 | Gaps:1046 | 85.60 | 4131 | 34.22 | 19.91 | 2e-57 | PRK12316 PRK12316 peptide synthase Provisional. |
gnl|CDD|144190 | 194 | 543 | 350 | Gaps:112 | 100.00 | 412 | 25.73 | 14.32 | 2e-51 | pfam00501 AMP-binding AMP-binding enzyme. |
gnl|CDD|168184 | 330 | 1894 | 1565 | Gaps:788 | 54.71 | 4334 | 36.31 | 20.46 | 3e-39 | PRK05691 PRK05691 peptide synthase Validated. |
gnl|CDD|31223 | 139 | 1183 | 1045 | Gaps:91 | 96.88 | 642 | 23.47 | 18.01 | 4e-38 | COG1020 EntF Non-ribosomal peptide synthetase modules and related proteins [Secondary metabolites biosynthesis transport and catabolism]. |
gnl|CDD|170335 | 184 | 715 | 532 | Gaps:53 | 27.17 | 1299 | 32.01 | 19.55 | 2e-35 | PRK10252 entF enterobactin synthase subunit F Provisional. |
gnl|CDD|144314 | 757 | 1826 | 1070 | Gaps:63 | 100.00 | 300 | 33.67 | 22.00 | 1e-32 | pfam00668 Condensation Condensation domain. This domain is found in many multi-domain enzymes which synthesize peptide antibiotics. This domain catalyses a condensation reaction to form peptide bonds in non- ribosomal peptide biosynthesis. It is usually found to the carboxy side of a phosphopantetheine binding domain (pfam00550). It has been shown that mutations in the HHXXXDG motif abolish activity suggesting this is part of the active site. |
gnl|CDD|163268 | 423 | 715 | 293 | Gaps:44 | 22.25 | 1389 | 33.01 | 17.15 | 3e-31 | TIGR03443 alpha_am_amid L-aminoadipate-semialdehyde dehydrogenase. Members of this protein family are L-aminoadipate-semialdehyde dehydrogenase (EC 1.2.1.31) product of the LYS2 gene. It is also called alpha-aminoadipate reductase. In fungi lysine is synthesized via aminoadipate. Currently all members of this family are fungal. |
gnl|CDD|30666 | 306 | 634 | 329 | Gaps:55 | 56.93 | 534 | 31.91 | 12.50 | 7e-27 | COG0318 CaiC Acyl-CoA synthetases (AMP-forming)/AMP-acid ligases II [Lipid metabolism / Secondary metabolites biosynthesis transport and catabolism]. |
rpsblast_kog | gnl|CDD|36393 | 483 | 1498 | 1016 | Gaps:94 | 25.29 | 1032 | 32.57 | 25.67 | 1e-22 | KOG1178 KOG1178 KOG1178 Non-ribosomal peptide synthetase/alpha-aminoadipate reductase and related enzymes [Secondary metabolites biosynthesis transport and catabolism]. |
gnl|CDD|36391 | 306 | 625 | 320 | Gaps:54 | 54.00 | 537 | 28.28 | 17.93 | 7e-18 | KOG1176 KOG1176 KOG1176 Acyl-CoA synthetase [Lipid transport and metabolism]. |
gnl|CDD|36390 | 315 | 634 | 320 | Gaps:63 | 48.40 | 626 | 28.05 | 14.52 | 1e-13 | KOG1175 KOG1175 KOG1175 Acyl-CoA synthetase [Lipid transport and metabolism]. |
gnl|CDD|36470 | 382 | 525 | 144 | Gaps:27 | 18.09 | 691 | 35.20 | 19.20 | 3e-11 | KOG1256 KOG1256 KOG1256 Long-chain acyl-CoA synthetases (AMP-forming) [Lipid transport and metabolism]. |
gnl|CDD|36392 | 286 | 624 | 339 | Gaps:59 | 52.68 | 596 | 22.29 | 17.83 | 3e-09 | KOG1177 KOG1177 KOG1177 Long chain fatty acid acyl-CoA ligase [Lipid transport and metabolism]. |
gnl|CDD|36395 | 385 | 527 | 143 | Gaps:40 | 19.03 | 678 | 31.78 | 19.38 | 1e-08 | KOG1180 KOG1180 KOG1180 Acyl-CoA synthetase [Lipid transport and metabolism]. |