| Analysis | Hit | start | end | length | Note | Hit coverage | Hit length | Hit pident | Hit pcons | eValue | Hit description |
| blastp_kegg | bfu:BC1G_00695 | 1 | 3605 | 3605 | n/a | 100.00 | 3605 | 99.06 | 0.00 | 0.0 | similar to polyketide synthase |
| pcs:Pc16g13930 | 3 | 3568 | 3566 | Gaps:218 | 88.67 | 3962 | 38.80 | 18.67 | 0.0 | Pc16g13930 |
| ani:AN8412.2 | 6 | 3583 | 3578 | Gaps:164 | 81.40 | 3930 | 38.29 | 18.88 | 0.0 | hypothetical protein |
| aor:AO090001000277 | 4 | 3571 | 3568 | Gaps:219 | 88.55 | 3946 | 36.52 | 18.49 | 0.0 | polyketide synthase modules and related proteins |
| afv:AFLA_066840 | 4 | 3571 | 3568 | Gaps:209 | 88.55 | 3946 | 36.43 | 18.55 | 0.0 | hybrid PKS/NRPS enzyme putative |
| ure:UREG_03815 | 5 | 3571 | 3567 | Gaps:295 | 88.43 | 3846 | 37.87 | 18.17 | 0.0 | similar to polyketide synthase |
| act:ACLA_078660 | 3 | 3587 | 3585 | Gaps:187 | 82.29 | 4043 | 38.50 | 17.49 | 0.0 | hybrid NRPS/PKS enzyme putative |
| act:ACLA_023380 | 4 | 3492 | 3489 | Gaps:231 | 82.93 | 3948 | 36.71 | 17.96 | 0.0 | equisetin synthetase putative |
| ang:An11g06460 | 3 | 3589 | 3587 | Gaps:332 | 89.40 | 3897 | 39.35 | 17.65 | 0.0 | hypothetical protein |
| pcs:Pc14g00080 | 4 | 3568 | 3565 | Gaps:168 | 84.12 | 3917 | 37.60 | 18.24 | 0.0 | Pc14g00080 |
| blastp_uniprot_sprot | sp|Q0C8M3|LNKS_ASPTN | 3 | 2602 | 2600 | Gaps:93 | 69.22 | 3038 | 36.28 | 16.88 | 0.0 | Lovastatin nonaketide synthase OS Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN lovB PE 3 SV 2 |
| sp|Q9Y8A5|LNKS_ASPTE | 3 | 2602 | 2600 | Gaps:91 | 69.22 | 3038 | 36.00 | 17.21 | 0.0 | Lovastatin nonaketide synthase OS Aspergillus terreus GN lovB PE 1 SV 1 |
| sp|Q10977|PPSA_MYCTU | 2 | 880 | 879 | Gaps:54 | 44.72 | 1876 | 35.88 | 19.07 | 1e-123 | Phenolpthiocerol synthesis polyketide synthase ppsA OS Mycobacterium tuberculosis GN ppsA PE 3 SV 2 |
| sp|O07798|PHAS_MYCTU | 5 | 1158 | 1154 | Gaps:119 | 51.51 | 2126 | 32.69 | 15.62 | 1e-121 | Phthioceranic/hydroxyphthioceranic acid synthase OS Mycobacterium tuberculosis GN pks2 PE 1 SV 1 |
| sp|A5U9F4|PHAS_MYCTA | 5 | 1158 | 1154 | Gaps:119 | 51.51 | 2126 | 32.69 | 15.62 | 1e-121 | Phthioceranic/hydroxyphthioceranic acid synthase OS Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN pks2 PE 3 SV 1 |
| sp|Q7TVK8|PHAS_MYCBO | 5 | 1158 | 1154 | Gaps:119 | 51.51 | 2126 | 32.69 | 15.62 | 1e-121 | Phthioceranic/hydroxyphthioceranic acid synthase OS Mycobacterium bovis GN pks2 PE 3 SV 1 |
| sp|A1KQG0|PHAS_MYCBP | 5 | 1158 | 1154 | Gaps:119 | 51.51 | 2126 | 32.69 | 15.62 | 1e-121 | Phthioceranic/hydroxyphthioceranic acid synthase OS Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN pks2 PE 3 SV 1 |
| sp|Q03131|ERYA1_SACER | 2 | 932 | 931 | Gaps:153 | 59.24 | 3491 | 34.19 | 18.38 | 1e-121 | Erythronolide synthase modules 1 and 2 OS Saccharopolyspora erythraea GN eryA PE 1 SV 1 |
| sp|Q07017|OL56_STRAT | 3 | 944 | 942 | Gaps:113 | 50.50 | 3519 | 35.12 | 17.73 | 1e-120 | Oleandomycin polyketide synthase modules 5 and 6 OS Streptomyces antibioticus GN orfB PE 3 SV 1 |
| sp|Q869W9|PKS16_DICDI | 3 | 988 | 986 | Gaps:73 | 37.30 | 2603 | 33.78 | 15.65 | 1e-120 | Probable polyketide synthase 16 OS Dictyostelium discoideum GN pks16 PE 2 SV 1 |
| blastp_pdb | 2qo3_B | 3 | 896 | 894 | Gaps:57 | 94.32 | 915 | 33.95 | 19.00 | 1e-118 | mol:protein length:915 EryAII Erythromycin polyketide synthase modul |
| 2qo3_A | 3 | 896 | 894 | Gaps:57 | 94.32 | 915 | 33.95 | 19.00 | 1e-118 | mol:protein length:915 EryAII Erythromycin polyketide synthase modul |
| 2hg4_F | 4 | 888 | 885 | Gaps:60 | 90.40 | 917 | 34.86 | 17.85 | 1e-113 | mol:protein length:917 6-Deoxyerythronolide B Synthase |
| 2hg4_E | 4 | 888 | 885 | Gaps:60 | 90.40 | 917 | 34.86 | 17.85 | 1e-113 | mol:protein length:917 6-Deoxyerythronolide B Synthase |
| 2hg4_D | 4 | 888 | 885 | Gaps:60 | 90.40 | 917 | 34.86 | 17.85 | 1e-113 | mol:protein length:917 6-Deoxyerythronolide B Synthase |
| 2hg4_C | 4 | 888 | 885 | Gaps:60 | 90.40 | 917 | 34.86 | 17.85 | 1e-113 | mol:protein length:917 6-Deoxyerythronolide B Synthase |
| 2hg4_B | 4 | 888 | 885 | Gaps:60 | 90.40 | 917 | 34.86 | 17.85 | 1e-113 | mol:protein length:917 6-Deoxyerythronolide B Synthase |
| 2hg4_A | 4 | 888 | 885 | Gaps:60 | 90.40 | 917 | 34.86 | 17.85 | 1e-113 | mol:protein length:917 6-Deoxyerythronolide B Synthase |
| 3hhd_D | 6 | 887 | 882 | Gaps:120 | 82.90 | 965 | 37.00 | 17.88 | 1e-105 | mol:protein length:965 Fatty acid synthase |
| 3hhd_C | 6 | 887 | 882 | Gaps:120 | 82.90 | 965 | 37.00 | 17.88 | 1e-105 | mol:protein length:965 Fatty acid synthase |
| rpsblast_cdd | gnl|CDD|129058 | 6 | 440 | 435 | Gaps:13 | 100.00 | 424 | 52.83 | 15.80 | 0.0 | smart00825 PKS_KS Beta-ketoacyl synthase. The structure of beta-ketoacyl synthase is similar to that of the thiolase family and also chalcone synthase. The active site of beta-ketoacyl synthase is located between the N and C-terminal domains. |
| gnl|CDD|33130 | 5 | 1024 | 1020 | Gaps:72 | 89.92 | 1061 | 37.00 | 16.98 | 0.0 | COG3321 COG3321 Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis transport and catabolism]. |
| gnl|CDD|29420 | 5 | 437 | 433 | Gaps:13 | 99.76 | 421 | 53.33 | 16.43 | 1e-159 | cd00833 PKS polyketide synthases (PKSs) polymerize simple fatty acids into a large variety of different products called polyketides by successive decarboxylating Claisen condensations. PKSs can be divided into 2 groups modular type I PKSs consisting of one or more large multifunctional proteins and iterative type II PKSs complexes of several monofunctional subunits.. |
| gnl|CDD|129060 | 559 | 872 | 314 | Gaps:17 | 99.66 | 298 | 39.06 | 14.81 | 4e-91 | smart00827 PKS_AT Acyl transferase domain in polyketide synthase (PKS) enzymes. |
| gnl|CDD|171521 | 2282 | 3215 | 934 | Gaps:255 | 68.33 | 3956 | 28.93 | 17.65 | 4e-85 | PRK12467 PRK12467 peptide synthase Provisional. |
| gnl|CDD|163029 | 5 | 776 | 772 | Gaps:97 | 31.02 | 2582 | 30.21 | 15.98 | 8e-84 | TIGR02813 omega_3_PfaA polyketide-type polyunsaturated fatty acid synthase PfaA. Members of the seed for this alignment are involved in omega-3 polyunsaturated fatty acid biosynthesis such as the protein PfaA from the eicosapentaenoic acid biosynthesis operon in Photobacterium profundum strain SS9. PfaA is encoded together with PfaB PfaC and PfaD and the functions of the individual polypeptides have not yet been described. More distant homologs of PfaA also included with the reach of this model appear to be involved in polyketide-like biosynthetic mechanisms of polyunsaturated fatty acid biosynthesis an alternative to the more familiar iterated mechanism of chain extension and desaturation and in most cases are encoded near genes for homologs of PfaB PfaC and/or PfaD. |
| gnl|CDD|162508 | 2657 | 3058 | 402 | Gaps:42 | 100.00 | 408 | 33.58 | 15.44 | 2e-83 | 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 | 2657 | 3058 | 402 | Gaps:46 | 100.00 | 412 | 33.25 | 14.32 | 7e-79 | pfam00501 AMP-binding AMP-binding enzyme. |
| gnl|CDD|171397 | 2373 | 3256 | 884 | Gaps:278 | 57.06 | 4131 | 28.43 | 16.67 | 2e-76 | PRK12316 PRK12316 peptide synthase Provisional. |
| gnl|CDD|31223 | 2428 | 3048 | 621 | Gaps:51 | 95.33 | 642 | 30.07 | 16.99 | 3e-76 | COG1020 EntF Non-ribosomal peptide synthetase modules and related proteins [Secondary metabolites biosynthesis transport and catabolism]. |
| rpsblast_kog | gnl|CDD|36416 | 3 | 1188 | 1186 | Gaps:195 | 44.32 | 2376 | 32.76 | 17.47 | 1e-132 | KOG1202 KOG1202 KOG1202 Animal-type fatty acid synthase and related proteins [Lipid transport and metabolism]. |
| gnl|CDD|36393 | 2654 | 3376 | 723 | Gaps:102 | 76.84 | 1032 | 23.71 | 16.02 | 7e-48 | KOG1178 KOG1178 KOG1178 Non-ribosomal peptide synthetase/alpha-aminoadipate reductase and related enzymes [Secondary metabolites biosynthesis transport and catabolism]. |
| gnl|CDD|36608 | 155 | 440 | 286 | Gaps:23 | 62.05 | 440 | 30.04 | 16.48 | 1e-33 | KOG1394 KOG1394 KOG1394 3-oxoacyl-(acyl-carrier-protein) synthase (I and II) [Lipid transport and metabolism Secondary metabolites biosynthesis transport and catabolism]. |
| gnl|CDD|36391 | 2653 | 3119 | 467 | Gaps:70 | 89.20 | 537 | 26.10 | 15.24 | 2e-33 | KOG1176 KOG1176 KOG1176 Acyl-CoA synthetase [Lipid transport and metabolism]. |
| gnl|CDD|36392 | 2653 | 3059 | 407 | Gaps:92 | 73.99 | 596 | 24.04 | 15.87 | 6e-24 | KOG1177 KOG1177 KOG1177 Long chain fatty acid acyl-CoA ligase [Lipid transport and metabolism]. |
| gnl|CDD|36390 | 2657 | 3119 | 463 | Gaps:103 | 78.91 | 626 | 22.87 | 14.37 | 1e-17 | KOG1175 KOG1175 KOG1175 Acyl-CoA synthetase [Lipid transport and metabolism]. |
| gnl|CDD|36435 | 3255 | 3505 | 251 | Gaps:72 | 62.74 | 467 | 23.55 | 19.80 | 2e-13 | KOG1221 KOG1221 KOG1221 Acyl-CoA reductase [Lipid transport and metabolism]. |
| gnl|CDD|36470 | 2897 | 3080 | 184 | Gaps:25 | 23.59 | 691 | 30.06 | 15.34 | 2e-12 | KOG1256 KOG1256 KOG1256 Long-chain acyl-CoA synthetases (AMP-forming) [Lipid transport and metabolism]. |
| gnl|CDD|38137 | 558 | 779 | 222 | Gaps:23 | 57.77 | 386 | 26.91 | 16.59 | 2e-10 | KOG2926 KOG2926 KOG2926 Malonyl-CoA:ACP transacylase [Lipid transport and metabolism]. |
| gnl|CDD|36395 | 2656 | 3081 | 426 | Gaps:71 | 50.44 | 678 | 27.78 | 17.25 | 2e-09 | KOG1180 KOG1180 KOG1180 Acyl-CoA synthetase [Lipid transport and metabolism]. |
Gene Identifier
Genome Report System - copyright INRA 2011