Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0005737 | cytoplasm | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001101 | response to acid chemical | 3 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0007154 | cell communication | 2 | 2 |
GO:0009267 | cellular response to starvation | 4 | 2 |
GO:0009605 | response to external stimulus | 2 | 2 |
GO:0009719 | response to endogenous stimulus | 2 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009894 | regulation of catabolic process | 4 | 2 |
GO:0009896 | positive regulation of catabolic process | 5 | 2 |
GO:0009966 | regulation of signal transduction | 4 | 7 |
GO:0009968 | negative regulation of signal transduction | 5 | 7 |
GO:0009987 | cellular process | 1 | 2 |
GO:0009991 | response to extracellular stimulus | 3 | 2 |
GO:0010033 | response to organic substance | 3 | 2 |
GO:0010243 | response to organonitrogen compound | 4 | 2 |
GO:0010506 | regulation of autophagy | 6 | 2 |
GO:0010508 | positive regulation of autophagy | 7 | 2 |
GO:0010646 | regulation of cell communication | 4 | 7 |
GO:0010648 | negative regulation of cell communication | 5 | 7 |
GO:0016239 | positive regulation of macroautophagy | 8 | 2 |
GO:0016241 | regulation of macroautophagy | 7 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0023051 | regulation of signaling | 3 | 7 |
GO:0023057 | negative regulation of signaling | 4 | 7 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031329 | regulation of cellular catabolic process | 5 | 2 |
GO:0031331 | positive regulation of cellular catabolic process | 6 | 2 |
GO:0031667 | response to nutrient levels | 4 | 2 |
GO:0031668 | cellular response to extracellular stimulus | 3 | 2 |
GO:0031669 | cellular response to nutrient levels | 4 | 2 |
GO:0032006 | regulation of TOR signaling | 6 | 7 |
GO:0032007 | negative regulation of TOR signaling | 7 | 7 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034198 | cellular response to amino acid starvation | 5 | 2 |
GO:0042221 | response to chemical | 2 | 2 |
GO:0042594 | response to starvation | 3 | 2 |
GO:0043200 | response to amino acid | 4 | 2 |
GO:0043201 | response to leucine | 5 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 7 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 7 |
GO:0048583 | regulation of response to stimulus | 3 | 7 |
GO:0048585 | negative regulation of response to stimulus | 4 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0070887 | cellular response to chemical stimulus | 3 | 2 |
GO:0071229 | cellular response to acid chemical | 4 | 2 |
GO:0071230 | cellular response to amino acid stimulus | 5 | 2 |
GO:0071233 | cellular response to leucine | 6 | 2 |
GO:0071310 | cellular response to organic substance | 4 | 2 |
GO:0071417 | cellular response to organonitrogen compound | 4 | 2 |
GO:0071495 | cellular response to endogenous stimulus | 3 | 2 |
GO:0071496 | cellular response to external stimulus | 3 | 2 |
GO:0080134 | regulation of response to stress | 4 | 7 |
GO:1901031 | regulation of response to reactive oxygen species | 6 | 7 |
GO:1901698 | response to nitrogen compound | 3 | 2 |
GO:1901699 | cellular response to nitrogen compound | 4 | 2 |
GO:1901700 | response to oxygen-containing compound | 3 | 2 |
GO:1901701 | cellular response to oxygen-containing compound | 4 | 2 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 7 |
GO:1902532 | negative regulation of intracellular signal transduction | 6 | 7 |
GO:1902882 | regulation of response to oxidative stress | 5 | 7 |
GO:1903432 | regulation of TORC1 signaling | 7 | 2 |
GO:1904262 | negative regulation of TORC1 signaling | 8 | 2 |
GO:1990253 | cellular response to leucine starvation | 6 | 2 |
GO:1990928 | response to amino acid starvation | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 2 |
GO:0016597 | amino acid binding | 4 | 2 |
GO:0016684 | oxidoreductase activity, acting on peroxide as acceptor | 3 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043177 | organic acid binding | 3 | 2 |
GO:0070728 | leucine binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1222 | 1226 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.342 |
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.485 |
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 272 | 276 | PF00656 | 0.460 |
CLV_C14_Caspase3-7 | 654 | 658 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 857 | 861 | PF00656 | 0.458 |
CLV_MEL_PAP_1 | 794 | 800 | PF00089 | 0.546 |
CLV_NRD_NRD_1 | 1051 | 1053 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 1164 | 1166 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 1287 | 1289 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 630 | 632 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.731 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.590 |
CLV_PCSK_FUR_1 | 628 | 632 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 1051 | 1053 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 1164 | 1166 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 1215 | 1217 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 1215 | 1217 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 704 | 706 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 1115 | 1119 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 1165 | 1169 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 1275 | 1279 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 729 | 733 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 902 | 906 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 935 | 939 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 990 | 994 | PF00082 | 0.451 |
CLV_Separin_Metazoa | 1185 | 1189 | PF03568 | 0.656 |
CLV_Separin_Metazoa | 754 | 758 | PF03568 | 0.330 |
DEG_APCC_DBOX_1 | 706 | 714 | PF00400 | 0.390 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.476 |
DEG_SPOP_SBC_1 | 294 | 298 | PF00917 | 0.438 |
DEG_SPOP_SBC_1 | 507 | 511 | PF00917 | 0.477 |
DOC_CDC14_PxL_1 | 465 | 473 | PF14671 | 0.488 |
DOC_CKS1_1 | 1192 | 1197 | PF01111 | 0.652 |
DOC_CKS1_1 | 142 | 147 | PF01111 | 0.561 |
DOC_CYCLIN_RxL_1 | 115 | 124 | PF00134 | 0.498 |
DOC_CYCLIN_RxL_1 | 744 | 754 | PF00134 | 0.418 |
DOC_CYCLIN_yCln2_LP_2 | 1296 | 1302 | PF00134 | 0.654 |
DOC_CYCLIN_yCln2_LP_2 | 718 | 721 | PF00134 | 0.393 |
DOC_CYCLIN_yCln2_LP_2 | 967 | 973 | PF00134 | 0.422 |
DOC_MAPK_gen_1 | 1215 | 1223 | PF00069 | 0.617 |
DOC_MAPK_gen_1 | 1288 | 1295 | PF00069 | 0.596 |
DOC_MAPK_gen_1 | 701 | 711 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 1275 | 1282 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 1288 | 1297 | PF00069 | 0.595 |
DOC_MAPK_MEF2A_6 | 166 | 173 | PF00069 | 0.449 |
DOC_MIT_MIM_1 | 792 | 801 | PF04212 | 0.346 |
DOC_PP1_RVXF_1 | 705 | 712 | PF00149 | 0.391 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 718 | 721 | PF13499 | 0.393 |
DOC_PP2B_LxvP_1 | 967 | 970 | PF13499 | 0.436 |
DOC_PP4_FxxP_1 | 872 | 875 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 1135 | 1139 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 1205 | 1209 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 873 | 877 | PF00917 | 0.532 |
DOC_WW_Pin1_4 | 1033 | 1038 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 1124 | 1129 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 1191 | 1196 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 1246 | 1251 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 922 | 927 | PF00397 | 0.391 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 1079 | 1085 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 314 | 320 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 644 | 648 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 797 | 805 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 902 | 909 | PF00244 | 0.427 |
LIG_APCC_ABBA_1 | 749 | 754 | PF00400 | 0.418 |
LIG_BIR_III_2 | 350 | 354 | PF00653 | 0.325 |
LIG_BIR_III_2 | 404 | 408 | PF00653 | 0.407 |
LIG_BIR_III_4 | 393 | 397 | PF00653 | 0.494 |
LIG_BRCT_BRCA1_1 | 1132 | 1136 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 246 | 250 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 80 | 84 | PF00533 | 0.461 |
LIG_Clathr_ClatBox_1 | 49 | 53 | PF01394 | 0.417 |
LIG_Clathr_ClatBox_1 | 978 | 982 | PF01394 | 0.609 |
LIG_eIF4E_1 | 244 | 250 | PF01652 | 0.362 |
LIG_eIF4E_1 | 768 | 774 | PF01652 | 0.374 |
LIG_FHA_1 | 1067 | 1073 | PF00498 | 0.738 |
LIG_FHA_1 | 1209 | 1215 | PF00498 | 0.693 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.572 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.495 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.394 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.437 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.431 |
LIG_FHA_2 | 1081 | 1087 | PF00498 | 0.546 |
LIG_FHA_2 | 1088 | 1094 | PF00498 | 0.546 |
LIG_FHA_2 | 1116 | 1122 | PF00498 | 0.546 |
LIG_FHA_2 | 1249 | 1255 | PF00498 | 0.765 |
LIG_FHA_2 | 1268 | 1274 | PF00498 | 0.604 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.376 |
LIG_FHA_2 | 926 | 932 | PF00498 | 0.400 |
LIG_FHA_2 | 941 | 947 | PF00498 | 0.364 |
LIG_LIR_Apic_2 | 194 | 199 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 241 | 246 | PF02991 | 0.359 |
LIG_LIR_Apic_2 | 583 | 589 | PF02991 | 0.459 |
LIG_LIR_Apic_2 | 866 | 870 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 1083 | 1092 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 1108 | 1117 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 1153 | 1163 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 796 | 806 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 81 | 92 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 946 | 955 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 1048 | 1053 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 1083 | 1087 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 1108 | 1113 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 1133 | 1139 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 1153 | 1159 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 340 | 344 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 730 | 736 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 744 | 749 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 750 | 755 | PF02991 | 0.183 |
LIG_LIR_Nem_3 | 796 | 801 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 946 | 951 | PF02991 | 0.411 |
LIG_LYPXL_S_1 | 751 | 755 | PF13949 | 0.546 |
LIG_LYPXL_yS_3 | 752 | 755 | PF13949 | 0.346 |
LIG_MYND_1 | 145 | 149 | PF01753 | 0.618 |
LIG_MYND_1 | 469 | 473 | PF01753 | 0.491 |
LIG_NRBOX | 1292 | 1298 | PF00104 | 0.597 |
LIG_NRBOX | 418 | 424 | PF00104 | 0.429 |
LIG_PCNA_yPIPBox_3 | 1104 | 1115 | PF02747 | 0.574 |
LIG_Pex14_1 | 1078 | 1082 | PF04695 | 0.546 |
LIG_PTB_Apo_2 | 866 | 873 | PF02174 | 0.369 |
LIG_SH2_CRK | 1050 | 1054 | PF00017 | 0.598 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.396 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.440 |
LIG_SH2_CRK | 586 | 590 | PF00017 | 0.450 |
LIG_SH2_CRK | 746 | 750 | PF00017 | 0.346 |
LIG_SH2_CRK | 867 | 871 | PF00017 | 0.457 |
LIG_SH2_GRB2like | 867 | 870 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 1156 | 1160 | PF00017 | 0.546 |
LIG_SH2_SRC | 1110 | 1113 | PF00017 | 0.545 |
LIG_SH2_SRC | 1130 | 1133 | PF00017 | 0.475 |
LIG_SH2_SRC | 867 | 870 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 436 | 440 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 805 | 809 | PF00017 | 0.360 |
LIG_SH2_STAT3 | 436 | 439 | PF00017 | 0.351 |
LIG_SH2_STAT3 | 878 | 881 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 1110 | 1113 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 1142 | 1145 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 1190 | 1193 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 765 | 768 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 793 | 796 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.506 |
LIG_SH3_3 | 1069 | 1075 | PF00018 | 0.595 |
LIG_SH3_3 | 1189 | 1195 | PF00018 | 0.662 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.613 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.339 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.409 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.532 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.383 |
LIG_SH3_3 | 967 | 973 | PF00018 | 0.439 |
LIG_SUMO_SIM_anti_2 | 1217 | 1222 | PF11976 | 0.619 |
LIG_SUMO_SIM_anti_2 | 1273 | 1280 | PF11976 | 0.595 |
LIG_SUMO_SIM_anti_2 | 326 | 331 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 1219 | 1226 | PF11976 | 0.631 |
LIG_SUMO_SIM_par_1 | 1278 | 1284 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 234 | 241 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 770 | 776 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 979 | 985 | PF11976 | 0.612 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.529 |
LIG_TYR_ITIM | 339 | 344 | PF00017 | 0.474 |
LIG_WW_2 | 145 | 148 | PF00397 | 0.770 |
MOD_CK1_1 | 1004 | 1010 | PF00069 | 0.616 |
MOD_CK1_1 | 1080 | 1086 | PF00069 | 0.507 |
MOD_CK1_1 | 1201 | 1207 | PF00069 | 0.582 |
MOD_CK1_1 | 1208 | 1214 | PF00069 | 0.457 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.759 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.635 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.503 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.659 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.653 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.542 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.603 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.543 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.649 |
MOD_CK1_1 | 796 | 802 | PF00069 | 0.411 |
MOD_CK1_1 | 824 | 830 | PF00069 | 0.551 |
MOD_CK1_1 | 841 | 847 | PF00069 | 0.604 |
MOD_CK1_1 | 887 | 893 | PF00069 | 0.675 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.471 |
MOD_CK2_1 | 1080 | 1086 | PF00069 | 0.406 |
MOD_CK2_1 | 1087 | 1093 | PF00069 | 0.419 |
MOD_CK2_1 | 1179 | 1185 | PF00069 | 0.411 |
MOD_CK2_1 | 1248 | 1254 | PF00069 | 0.721 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.508 |
MOD_CK2_1 | 925 | 931 | PF00069 | 0.487 |
MOD_CK2_1 | 940 | 946 | PF00069 | 0.442 |
MOD_Cter_Amidation | 642 | 645 | PF01082 | 0.682 |
MOD_GlcNHglycan | 1003 | 1006 | PF01048 | 0.576 |
MOD_GlcNHglycan | 1007 | 1010 | PF01048 | 0.608 |
MOD_GlcNHglycan | 1202 | 1206 | PF01048 | 0.630 |
MOD_GlcNHglycan | 1225 | 1228 | PF01048 | 0.536 |
MOD_GlcNHglycan | 1236 | 1239 | PF01048 | 0.688 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.752 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.656 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.679 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.567 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.572 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.653 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.776 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.679 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.441 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.380 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.377 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.544 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.392 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.470 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.636 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.627 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.411 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.579 |
MOD_GlcNHglycan | 823 | 826 | PF01048 | 0.597 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.471 |
MOD_GlcNHglycan | 844 | 847 | PF01048 | 0.550 |
MOD_GlcNHglycan | 888 | 892 | PF01048 | 0.570 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.406 |
MOD_GSK3_1 | 1018 | 1025 | PF00069 | 0.502 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.717 |
MOD_GSK3_1 | 1073 | 1080 | PF00069 | 0.408 |
MOD_GSK3_1 | 1177 | 1184 | PF00069 | 0.404 |
MOD_GSK3_1 | 1197 | 1204 | PF00069 | 0.419 |
MOD_GSK3_1 | 1219 | 1226 | PF00069 | 0.446 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.646 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.582 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.483 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.605 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.544 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.675 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.537 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.609 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.655 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.526 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.512 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.620 |
MOD_GSK3_1 | 997 | 1004 | PF00069 | 0.556 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.629 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.486 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.546 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.558 |
MOD_NEK2_1 | 1077 | 1082 | PF00069 | 0.411 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.467 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.418 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.687 |
MOD_NEK2_1 | 713 | 718 | PF00069 | 0.468 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.411 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.645 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.369 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.619 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.471 |
MOD_NEK2_1 | 997 | 1002 | PF00069 | 0.632 |
MOD_NEK2_2 | 623 | 628 | PF00069 | 0.625 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.753 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.592 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.557 |
MOD_PIKK_1 | 549 | 555 | PF00454 | 0.419 |
MOD_PKA_1 | 108 | 114 | PF00069 | 0.543 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.525 |
MOD_PKA_2 | 1080 | 1086 | PF00069 | 0.512 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.555 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.693 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.369 |
MOD_PKA_2 | 697 | 703 | PF00069 | 0.521 |
MOD_PKA_2 | 796 | 802 | PF00069 | 0.411 |
MOD_PKA_2 | 842 | 848 | PF00069 | 0.570 |
MOD_PKB_1 | 900 | 908 | PF00069 | 0.558 |
MOD_Plk_1 | 1152 | 1158 | PF00069 | 0.512 |
MOD_Plk_1 | 1205 | 1211 | PF00069 | 0.579 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.570 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.483 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.451 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.561 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.562 |
MOD_Plk_2-3 | 1152 | 1158 | PF00069 | 0.512 |
MOD_Plk_2-3 | 1219 | 1225 | PF00069 | 0.530 |
MOD_Plk_2-3 | 269 | 275 | PF00069 | 0.524 |
MOD_Plk_4 | 1073 | 1079 | PF00069 | 0.515 |
MOD_Plk_4 | 1098 | 1104 | PF00069 | 0.411 |
MOD_Plk_4 | 1205 | 1211 | PF00069 | 0.523 |
MOD_Plk_4 | 1219 | 1225 | PF00069 | 0.478 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.563 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.565 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.559 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.401 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.508 |
MOD_Plk_4 | 727 | 733 | PF00069 | 0.411 |
MOD_Plk_4 | 741 | 747 | PF00069 | 0.411 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.562 |
MOD_Plk_4 | 873 | 879 | PF00069 | 0.679 |
MOD_Plk_4 | 974 | 980 | PF00069 | 0.580 |
MOD_ProDKin_1 | 1033 | 1039 | PF00069 | 0.689 |
MOD_ProDKin_1 | 1124 | 1130 | PF00069 | 0.411 |
MOD_ProDKin_1 | 1191 | 1197 | PF00069 | 0.559 |
MOD_ProDKin_1 | 1246 | 1252 | PF00069 | 0.724 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.713 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.635 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.735 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.638 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.670 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.599 |
MOD_ProDKin_1 | 922 | 928 | PF00069 | 0.474 |
MOD_SUMO_for_1 | 1214 | 1217 | PF00179 | 0.490 |
MOD_SUMO_rev_2 | 400 | 407 | PF00179 | 0.674 |
TRG_DiLeu_BaEn_1 | 1274 | 1279 | PF01217 | 0.479 |
TRG_DiLeu_BaEn_1 | 946 | 951 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 575 | 580 | PF01217 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 769 | 774 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 1050 | 1053 | PF00928 | 0.672 |
TRG_ENDOCYTIC_2 | 1110 | 1113 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 1156 | 1159 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 733 | 736 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 745 | 748 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 752 | 755 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 1050 | 1052 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 1078 | 1081 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 1163 | 1165 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 627 | 630 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 705 | 707 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 900 | 903 | PF00400 | 0.553 |
TRG_NES_CRM1_1 | 1213 | 1225 | PF08389 | 0.514 |
TRG_NES_CRM1_1 | 318 | 332 | PF08389 | 0.580 |
TRG_NES_CRM1_1 | 792 | 807 | PF08389 | 0.411 |
TRG_NLS_MonoCore_2 | 703 | 708 | PF00514 | 0.474 |
TRG_NLS_MonoExtN_4 | 701 | 708 | PF00514 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 1051 | 1056 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 108 | 112 | PF00026 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 578 | 582 | PF00026 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 645 | 650 | PF00026 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA38 | Leptomonas seymouri | 52% | 100% |
A0A3S7WUZ0 | Leishmania donovani | 91% | 100% |
A4H9H5 | Leishmania braziliensis | 73% | 100% |
A4HXU1 | Leishmania infantum | 91% | 100% |
E9ARK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |