Analysis | Hit | start | end | length | Note | Hit coverage | Hit length | Hit pident | Hit pcons | eValue | Hit description |
blastp_kegg | ssl:SS1G_03693 | 1 | 4741 | 4741 | n/a | 100.00 | 4741 | 97.38 | 0.00 | 0.0 | hypothetical protein |
bfu:BC1G_03511 | 61 | 4737 | 4677 | Gaps:1029 | 98.69 | 4513 | 77.68 | 11.65 | 0.0 | hypothetical protein |
act:ACLA_079690 | 7 | 4603 | 4597 | Gaps:834 | 95.15 | 5034 | 51.61 | 19.65 | 0.0 | nonribosomal siderophore peptide synthase putative |
cim:CIMG_00941 | 4 | 4725 | 4722 | Gaps:845 | 96.60 | 4995 | 49.28 | 19.98 | 0.0 | hypothetical protein |
fgr:FG05372.1 | 1 | 4634 | 4634 | Gaps:979 | 98.68 | 4841 | 51.25 | 20.79 | 0.0 | hypothetical protein |
pcs:Pc13g05250 | 9 | 4603 | 4595 | Gaps:965 | 94.45 | 5081 | 50.14 | 21.21 | 0.0 | Pc13g05250 |
pan:PODANSg3444 | 1 | 4616 | 4616 | Gaps:1159 | 97.78 | 5045 | 52.75 | 20.17 | 0.0 | hypothetical protein |
ncr:NCU07119 | 2 | 4644 | 4643 | Gaps:1304 | 98.42 | 5141 | 50.65 | 19.70 | 0.0 | hypothetical protein |
mgr:MGG_12175 | 78 | 4426 | 4349 | Gaps:1354 | 91.67 | 4778 | 56.37 | 20.09 | 0.0 | hypothetical protein |
pno:SNOG_02134 | 12 | 4627 | 4616 | Gaps:1444 | 97.33 | 4118 | 62.00 | 19.09 | 0.0 | hypothetical protein |
blastp_uniprot_sprot | sp|Q9P7T1|SIB1_SCHPO | 19 | 4584 | 4566 | Gaps:1830 | 91.77 | 4924 | 52.31 | 23.46 | 0.0 | Hydroxamate-type ferrichrome siderophore peptide synthetase OS Schizosaccharomyces pombe GN sib1 PE 1 SV 1 |
sp|O43103|SID2_USTMA | 43 | 4564 | 4522 | Gaps:1524 | 93.53 | 4114 | 51.09 | 21.31 | 1e-173 | Ferrichrome siderophore peptide synthetase OS Ustilago maydis GN SID2 PE 3 SV 2 |
sp|O30409|TYCC_BREPA | 28 | 3624 | 3597 | Gaps:2232 | 96.11 | 6486 | 46.68 | 24.29 | 1e-130 | Tyrocidine synthase 3 OS Brevibacillus parabrevis GN tycC PE 1 SV 1 |
sp|Q70LM4|LGRD_BREPA | 9 | 4010 | 4002 | Gaps:1415 | 82.77 | 5085 | 49.39 | 21.19 | 1e-128 | Linear gramicidin synthase subunit D OS Brevibacillus parabrevis GN lgrD PE 1 SV 1 |
sp|Q04747|SRFAB_BACSU | 19 | 4010 | 3992 | Gaps:1339 | 91.21 | 3583 | 48.84 | 23.01 | 1e-116 | Surfactin synthase subunit 2 OS Bacillus subtilis GN srfAB PE 1 SV 3 |
sp|P0C063|GRSB_ANEMI | 43 | 3478 | 3436 | Gaps:1456 | 93.44 | 4451 | 44.60 | 23.80 | 1e-115 | Gramicidin S synthase 2 OS Aneurinibacillus migulanus GN grsB PE 3 SV 2 |
sp|P0C064|GRSB_BREBE | 43 | 3478 | 3436 | Gaps:1334 | 93.44 | 4450 | 43.19 | 23.50 | 1e-115 | Gramicidin S synthase 2 OS Brevibacillus brevis GN grsB PE 1 SV 2 |
sp|O30408|TYCB_BREPA | 5 | 3287 | 3283 | Gaps:1040 | 92.61 | 3587 | 44.25 | 23.39 | 1e-114 | Tyrocidine synthase 2 OS Brevibacillus parabrevis GN tycB PE 3 SV 1 |
sp|O68006|BACA_BACLI | 2 | 3631 | 3630 | Gaps:1832 | 93.64 | 5255 | 46.21 | 24.28 | 1e-113 | Bacitracin synthase 1 OS Bacillus licheniformis GN bacA PE 3 SV 1 |
sp|Q70LM5|LGRC_BREPA | 27 | 4010 | 3984 | Gaps:2193 | 83.75 | 7756 | 46.63 | 21.66 | 1e-112 | Linear gramicidin synthase subunit C OS Brevibacillus parabrevis GN lgrC PE 3 SV 1 |
blastp_pdb | 3ite_B | 94 | 3192 | 3099 | Gaps:158 | 95.91 | 562 | 52.88 | 21.34 | 1e-76 | mol:protein length:562 SidN siderophore synthetase |
3ite_A | 94 | 3192 | 3099 | Gaps:158 | 95.91 | 562 | 52.88 | 21.34 | 1e-76 | mol:protein length:562 SidN siderophore synthetase |
2vsq_A | 24 | 3173 | 3150 | Gaps:269 | 77.61 | 1304 | 44.96 | 23.02 | 2e-65 | mol:protein length:1304 SURFACTIN SYNTHETASE SUBUNIT 3 |
1amu_B | 78 | 3173 | 3096 | Gaps:105 | 85.79 | 563 | 54.24 | 21.95 | 2e-60 | mol:protein length:563 GRAMICIDIN SYNTHETASE 1 |
1amu_A | 78 | 3173 | 3096 | Gaps:105 | 85.79 | 563 | 54.24 | 21.95 | 2e-60 | mol:protein length:563 GRAMICIDIN SYNTHETASE 1 |
3dhv_A | 87 | 3180 | 3094 | Gaps:124 | 98.44 | 512 | 46.03 | 25.00 | 8e-36 | mol:protein length:512 D-alanine-poly(phosphoribitol) ligase |
3fce_A | 87 | 3180 | 3094 | Gaps:124 | 98.44 | 512 | 46.03 | 25.00 | 9e-36 | mol:protein length:512 D-alanine--poly(phosphoribitol) ligase subuni |
3fcc_A | 87 | 3180 | 3094 | Gaps:124 | 98.44 | 512 | 46.03 | 25.00 | 9e-36 | mol:protein length:512 D-alanine--poly(phosphoribitol) ligase subuni |
3lgx_D | 80 | 3179 | 3100 | Gaps:150 | 93.09 | 521 | 48.25 | 22.47 | 1e-32 | mol:protein length:521 D-alanine--poly(phosphoribitol) ligase subuni |
3lgx_C | 80 | 3179 | 3100 | Gaps:150 | 93.09 | 521 | 48.25 | 22.47 | 1e-32 | mol:protein length:521 D-alanine--poly(phosphoribitol) ligase subuni |
rpsblast_cdd | gnl|CDD|171521 | 9 | 4495 | 4487 | Gaps:1337 | 85.47 | 3956 | 47.97 | 19.14 | 1e-154 | PRK12467 PRK12467 peptide synthase Provisional. |
gnl|CDD|168184 | 19 | 4132 | 4114 | Gaps:1322 | 88.30 | 4334 | 41.94 | 20.04 | 1e-120 | PRK05691 PRK05691 peptide synthase Validated. |
gnl|CDD|162508 | 49 | 3093 | 3045 | Gaps:74 | 100.00 | 408 | 58.58 | 13.73 | 1e-112 | 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|171397 | 79 | 4427 | 4349 | Gaps:1358 | 88.65 | 4131 | 47.76 | 18.79 | 1e-104 | PRK12316 PRK12316 peptide synthase Provisional. |
gnl|CDD|144190 | 74 | 3102 | 3029 | Gaps:95 | 100.00 | 412 | 58.25 | 12.86 | 1e-93 | pfam00501 AMP-binding AMP-binding enzyme. |
gnl|CDD|31223 | 8 | 4143 | 4136 | Gaps:140 | 99.84 | 642 | 49.61 | 18.88 | 6e-88 | COG1020 EntF Non-ribosomal peptide synthetase modules and related proteins [Secondary metabolites biosynthesis transport and catabolism]. |
gnl|CDD|170335 | 47 | 3276 | 3230 | Gaps:307 | 70.82 | 1299 | 42.28 | 19.13 | 5e-77 | PRK10252 entF enterobactin synthase subunit F Provisional. |
gnl|CDD|30666 | 26 | 3179 | 3154 | Gaps:153 | 97.57 | 534 | 47.98 | 18.04 | 3e-65 | COG0318 CaiC Acyl-CoA synthetases (AMP-forming)/AMP-acid ligases II [Lipid metabolism / Secondary metabolites biosynthesis transport and catabolism]. |
gnl|CDD|162509 | 20 | 3178 | 3159 | Gaps:163 | 99.60 | 502 | 46.20 | 24.20 | 6e-54 | 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. |
gnl|CDD|167846 | 45 | 3178 | 3134 | Gaps:229 | 99.21 | 504 | 50.80 | 21.00 | 4e-50 | PRK04813 PRK04813 D-alanine--poly(phosphoribitol) ligase subunit 1 Provisional. |
rpsblast_kog | gnl|CDD|36393 | 72 | 3341 | 3270 | Gaps:286 | 88.57 | 1032 | 34.79 | 18.05 | 5e-55 | KOG1178 KOG1178 KOG1178 Non-ribosomal peptide synthetase/alpha-aminoadipate reductase and related enzymes [Secondary metabolites biosynthesis transport and catabolism]. |
gnl|CDD|36391 | 32 | 3184 | 3153 | Gaps:176 | 97.39 | 537 | 43.40 | 19.89 | 1e-42 | KOG1176 KOG1176 KOG1176 Acyl-CoA synthetase [Lipid transport and metabolism]. |
gnl|CDD|36390 | 58 | 3167 | 3110 | Gaps:235 | 87.38 | 626 | 41.13 | 17.73 | 1e-27 | KOG1175 KOG1175 KOG1175 Acyl-CoA synthetase [Lipid transport and metabolism]. |
gnl|CDD|36392 | 38 | 3177 | 3140 | Gaps:251 | 96.48 | 596 | 37.74 | 21.57 | 5e-23 | KOG1177 KOG1177 KOG1177 Long chain fatty acid acyl-CoA ligase [Lipid transport and metabolism]. |
gnl|CDD|36394 | 1067 | 3102 | 2036 | Gaps:107 | 70.42 | 649 | 27.79 | 14.88 | 6e-16 | KOG1179 KOG1179 KOG1179 Very long-chain acyl-CoA synthetase/fatty acid transporter [Lipid transport and metabolism]. |
gnl|CDD|36470 | 1044 | 3095 | 2052 | Gaps:89 | 61.65 | 691 | 31.46 | 17.61 | 8e-13 | KOG1256 KOG1256 KOG1256 Long-chain acyl-CoA synthetases (AMP-forming) [Lipid transport and metabolism]. |
gnl|CDD|36395 | 370 | 2854 | 2485 | Gaps:34 | 42.63 | 678 | 27.34 | 14.53 | 2e-11 | KOG1180 KOG1180 KOG1180 Acyl-CoA synthetase [Lipid transport and metabolism]. |