Ancestral ML reconstructions were performed using FastML 2.02 (Pupko et al. 2000). The tool generates six outputs:
Name | Father | Distance to father | Sons |
4481821 | N1 | 0.605843 | - |
Bel | N2 | 0.982082 | - |
31230427 | N3 | 0.900315 | - |
Pao | N3 | 0.876113 | - |
31232862 | N5 | 0.67993 | - |
Tas | N6 | 0.849323 | - |
cer7 | N7 | 1.04376 | - |
cer10-1 | N8 | 0.89894 | - |
cer8 | N10 | 0.668781 | - |
Cer9 | N10 | 0.510442 | - |
cer12 | N11 | 0.195909 | - |
cer11 | N11 | 0.408461 | - |
31196163 | N13 | 0.340113 | - |
31232486 | N13 | 0.504037 | - |
31229813 | N14 | 0.839113 | - |
Tram | N14 | 0.562567 | - |
N1 | root! | - | 4481821 N2 N4 |
N2 | N1 | 0.104897 | Bel N3 |
N3 | N2 | 0.154047 | 31230427 Pao |
N4 | N1 | 0.0215427 | N5 N12 |
N5 | N4 | 0.0907278 | 31232862 N6 |
N6 | N5 | 0.105867 | Tas N7 |
N7 | N6 | 0.152459 | cer7 N8 |
N8 | N7 | 0.602639 | cer10-1 N9 |
N9 | N8 | 0.0147414 | N10 N11 |
N10 | N9 | 0.272264 | cer8 Cer9 |
N11 | N9 | 0.18207 | cer12 cer11 |
N12 | N4 | 0.0568487 | N13 N14 |
N13 | N12 | 0.08332 | 31196163 31232486 |
N14 | N12 | 0.0551009 | 31229813 Tram |
Position | Joint probability | Position | Joint probability | Position | Joint probability | Position | Joint probability |
0 | 7.24079e-013 | 34 | 6.67524e-018 | 68 | 9.25531e-015 | 102 | 1.05897e-014 |
1 | 2.68349e-009 | 35 | 2.56648e-011 | 69 | 2.12864e-012 | 103 | 1.31101e-015 |
2 | 6.78629e-018 | 36 | 3.65488e-019 | 70 | 5.26992e-013 | 104 | 1.69236e-018 |
3 | 3.30919e-011 | 37 | 1.48548e-020 | 71 | 6.56193e-012 | 105 | 5.43323e-019 |
4 | 6.80775e-013 | 38 | 4.53303e-020 | 72 | 8.6209e-010 | 106 | 1.98766e-016 |
5 | 1.63939e-016 | 39 | 1.62955e-021 | 73 | 2.65219e-014 | 107 | 1.00497e-012 |
6 | 3.25136e-021 | 40 | 5.89124e-016 | 74 | 2.15941e-013 | 108 | 5.54936e-017 |
7 | 1.03434e-015 | 41 | 9.21974e-015 | 75 | 6.10169e-018 | 109 | 3.45377e-012 |
8 | 2.35811e-019 | 42 | 7.73198e-018 | 76 | 3.87134e-017 | 110 | 1.63476e-016 |
9 | 6.7879e-014 | 43 | 5.66024e-018 | 77 | 3.29093e-021 | 111 | 1.75242e-017 |
10 | 2.09593e-010 | 44 | 4.84406e-018 | 78 | 9.93102e-015 | 112 | 7.81765e-015 |
11 | 6.17411e-018 | 45 | 3.7131e-022 | 79 | 4.81645e-019 | 113 | 1.61508e-010 |
12 | 1.94397e-019 | 46 | 2.58893e-022 | 80 | 6.89121e-021 | 114 | 6.30582e-015 |
13 | 1.04408e-016 | 47 | 2.012e-017 | 81 | 2.28779e-005 | 115 | 8.4195e-014 |
14 | 5.09335e-008 | 48 | 2.55826e-020 | 82 | 9.94124e-014 | 116 | 3.47742e-010 |
15 | 3.44399e-013 | 49 | 1.47673e-014 | 83 | 3.60274e-017 | 117 | 2.50277e-0005 |
16 | 3.13734e-019 | 50 | 2.46949e-020 | 84 | 3.54396e-022 | 118 | 1.91487e-018 |
17 | 1.51407e-018 | 51 | 3.68886e-018 | 85 | 7.47677e-025 | 119 | 1.26854e-012 |
18 | 1.31551e-013 | 52 | 2.05795e-018 | 86 | 1.28656e-014 | 120 | 1.866e-020 |
19 | 0.00638481 | 53 | 5.67067e-008 | 87 | 7.43157e-017 | 121 | 3.71025e-014 |
20 | 3.59042e-017 | 54 | 4.28831e-021 | 88 | 1.76192e-023 | 122 | 1.34089e-020 |
21 | 0.01754 | 55 | 1.60203e-021 | 89 | 5.23e-025 | 123 | 1.83162e-021 |
22 | 1.35151e-012 | 56 | 1.47567e-017 | 90 | 3.27538e-021 | 124 | 2.33163e-015 |
23 | 1.11149e-023 | 57 | 3.34195e-021 | 91 | 9.18958e-023 | 125 | 1.06646e-020 |
24 | 2.17225e-019 | 58 | 1.78885e-023 | 92 | 7.09424e-026 | 126 | 2.35218e-020 |
25 | 3.0828e-022 | 59 | 1.20206e-024 | 93 | 3.44895e-023 | 127 | 2.56223e-020 |
26 | 2.17729e-022 | 60 | 1.45963e-022 | 94 | 2.41005e-022 | 128 | 6.72408e-020 |
27 | 6.85255e-024 | 61 | 5.68431e-024 | 95 | 1.36756e-021 | 129 | 3.35338e-019 |
28 | 2.60033e-019 | 62 | 1.8189e-024 | 96 | 2.62404e-019 | 130 | 2.15279e-013 |
29 | 5.44278e-023 | 63 | 2.48176e-015 | 97 | 4.67537e-020 | 131 | 1.95258e-015 |
30 | 1.49934e-024 | 64 | 2.04719e-021 | 98 | 8.85395e-025 | 132 | 4.16501e-020 |
31 | 1.22314e-016 | 65 | 7.22613e-019 | 99 | 4.18348e-022 | ||
32 | 4.58009e-014 | 66 | 7.09438e-015 | 100 | 5.28986e-021 | ||
33 | 5.90595e-015 | 67 | 2.31307e-018 | 101 | 1.4181e-016 | ||
Total log likelihood of joint reconstruction: | -5119.68 |
There are two methods of ancestral reconstruction - Joint and Marginal. In this section, we provide a multiple alignment including both input peptidases and ancestral ML sequences reconstructed using the Joint method.The alignment is available in several formats clicking below the option "Set 1". To build HMM profiles and MRC sequences we removed non-informative amino acid stretches and gaps from several ancestral ML reconstruction analyses You can also retrieve the processed Jrof output, clicking below the option "Set 2". Note however that should you cannot select option 2 is because the output was not processed. <align id="bel" folder="jrof"></align>
Position | Joint probability | Position | Joint probability | Position | Joint probability | Position | Joint probability |
0 | 1.20933e-012 | 34 | 1.49619e-016 | 68 | 3.67905e-013 | 102 | 3.48661e-014 |
1 | 3.18353e-009 | 35 | 2.80475e-011 | 69 | 6.89171e-011 | 103 | 5.10143e-015 |
2 | 4.68936e-017 | 36 | 3.3949e-018 | 70 | 5.73377e-012 | 104 | 4.47252e-017 |
3 | 4.91468e-011 | 37 | 2.49775e-019 | 71 | 2.5537e-010 | 105 | 2.57809e-018 |
4 | 2.28352e-012 | 38 | 2.36324e-018 | 72 | 7.70509e-009 | 106 | 3.37011e-016 |
5 | 1.29576e-015 | 39 | 5.86935e-020 | 73 | 1.51407e-013 | 107 | 2.2831e-011 |
6 | 3.49334e-020 | 40 | 3.2562e-015 | 74 | 1.00456e-012 | 108 | 9.87034e-017 |
7 | 1.05727e-014 | 41 | 9.95213e-014 | 75 | 1.45354e-016 | 109 | 7.66121e-012 |
8 | 1.03308e-018 | 42 | 1.03583e-016 | 76 | 3.27055e-016 | 110 | 8.41827e-016 |
9 | 3.05514e-013 | 43 | 1.72577e-016 | 77 | 1.14996e-019 | 111 | 6.68686e-017 |
10 | 5.10297e-009 | 44 | 7.03409e-018 | 78 | 5.60563e-014 | 112 | 1.63216e-014 |
11 | 6.69407e-017 | 45 | 3.99522e-021 | 79 | 8.54649e-018 | 113 | 2.53941e-010 |
12 | 4.17905e-019 | 46 | 2.92391e-021 | 80 | 9.49646e-020 | 114 | 1.20777e-014 |
13 | 7.02481e-016 | 47 | 9.25281e-017 | 81 | 0.000366755 | 115 | 8.89004e-013 |
14 | 1.19722e-006 | 48 | 1.92281e-019 | 82 | 4.32825e-013 | 116 | 4.63823e-010 |
15 | 7.34026e-013 | 49 | 3.25962e-014 | 83 | 1.17017e-016 | 117 | 2.51097e-005 |
16 | 9.58329e-018 | 50 | 2.91814e-019 | 84 | 8.63672e-021 | 118 | 1.3137e-017 |
17 | 8.93173e-018 | 51 | 1.70463e-017 | 85 | 4.14766e-023 | 119 | 1.82813e-012 |
18 | 8.22776e-013 | 52 | 4.84789e-017 | 86 | 2.18976e-013 | 120 | 4.02189e-019 |
19 | 0.058676 | 53 | 1.6389e-006 | 87 | 2.7775e-015 | 121 | 1.15408e-013 |
20 | 7.93522e-017 | 54 | 7.27982e-019 | 88 | 2.46608e-021 | 122 | 5.08949e-020 |
21 | 0.091904 | 55 | 2.80801e-020 | 89 | 1.35577e-023 | 123 | 3.62168e-020 |
22 | 4.21524e-012 | 56 | 5.87536e-017 | 90 | 4.32135e-020 | 124 | 3.67156e-015 |
23 | 1.18037e-022 | 57 | 1.0556e-020 | 91 | 4.22484e-022 | 125 | 4.67236e-020 |
24 | 1.42526e-017 | 58 | 3.97277e-022 | 92 | 8.67628e-025 | 126 | 1.68928e-019 |
25 | 3.6845e-021 | 59 | 2.37544e-023 | 93 | 6.64886e-022 | 127 | 2.04828e-019 |
26 | 8.47903e-021 | 60 | 2.67693e-021 | 94 | 3.25259e-021 | 128 | 8.28625e-019 |
27 | 1.99243e-022 | 61 | 2.01123e-022 | 95 | 3.19519e-021 | 129 | 5.79831e-018 |
28 | 2.40691e-018 | 62 | 2.84222e-022 | 96 | 2.78944e-018 | 130 | 8.53888e-013 |
29 | 1.16817e-021 | 63 | 2.88751e-015 | 97 | 2.65096e-019 | 131 | 9.78542e-015 |
30 | 8.05691e-024 | 64 | 1.32177e-020 | 98 | 4.9208e-023 | 132 | 5.50002e-019 |
31 | 8.95322e-016 | 65 | 7.81395e-018 | 99 | 1.39842e-020 | ||
32 | 8.27644e-014 | 66 | 2.31555e-013 | 100 | 5.14462e-020 | ||
33 | 1.15308e-014 | 67 | 9.51129e-018 | 101 | 6.84153e-016 | ||
Total log likelihood of joint reconstruction: | -4832.94 |
There are two methods of ancestral reconstruction - Joint and Marginal. In this section, we provide a multiple alignment including both input peptidases and ancestral ML sequences reconstructed using the Joint method.The alignment is available in several formats clicking below the option "Set 1". To build HMM profiles and MRC sequences we removed non-informative amino acid stretches and gaps from several ancestral ML reconstruction analyses You can also retrieve the processed Jrof output, clicking below the option "Set 2". Note however that should you cannot select option 2 is because the output was not processed. <align id="bel" folder="mrof"></align>
Sequence logo constructed from the input of the processed Jrof alignment. In every position, each residue is a letter whose height is proportional to its frequency multiplied by the information content of each position measured in bits. Letters are placed such that the most common is at the top.
The logo was constructed using ChekAlign server with the Shannon's algorithm (Shannon 1997) and options "include gaps" and "Correction factor". Gaps are not represented by any symbol but occupy a blank also proportional to its frequency and, for aesthetic reasons, always at the top. Maximum entropy is log221. The alignment gap is considered to be another state or amino acid species.
>AP_Bel profile HMM generated consensus sequence DsGSqvslIterlAqqLgLkrtraslhIsgiGgnkattsksrivklsirsrnSliagle slvltqvtaplpsnqdltdvdnwkiphneiladptfnkpgrIDiiiGnDvladllaasr
Domain 1 of 1, from 1 to 119: score 62.6, E = 1.4e-19 DTG_ILG template *->vDTGAsvlsviskecklaqklgltrkkafdpSSYvCivtllsysqPs D+G++v s+i+++ laq+lgl+r +++s AP_Bel 1 -DSGSQV-SLITER--LAQQLGLKR------------------TRAS 25 sktsttaqdtirgagGqskiyvSklktsgqirknllslvtikitkGnv.. + i g+gG++++ +Sk++++ +++ +s+ +++ G ++ AP_Bel 26 LH--------ISGIGGNKAT-TSKSRIVKLSI---RSRNSLIA--GLEsl 61 ...............Tevenrslpsdgvflvvtdpedqks.rydvILGrl ++ + + +++++ T+v+n+++p+++ + ++ dp ++k++r+d+I+G+ AP_Bel 62 vltqvtaplpsnqdlTDVDNWKIPHNE-I-LA-DPTFNKPgRIDIIIGN- 107 dfLrqlnsvhidl<-* d+L +l + ++ AP_Bel 108 DVLADLLAA-SRI 119
Llorens, C. Futami, R. Renaud, G. and A. Moya (2009). Bioinformatic Flowchart and Database to Investigate the Diversity of Clan AA Peptidases.Biology Direct, 4:3.
Llorens, C., Futami, R., Covelli, L., Dominguez-Escriba, L., Viu, J.M., Tamarit, D., Aguilar-Rodriguez, J. Vicente-Ripolles, M., Fuster, G., Bernet, G.P., Maumus, F., Munoz-Pomer, A., Sempere, J.M., LaTorre, A., Moya, A. (2011) The Gypsy Database (GyDB) of Mobile Genetic Elements: Release 2.0 Nucleic Acids Research (NARESE) 39 (suppl 1): D70-D74 doi: 10.1093/nar/gkq1061