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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031931 | TORC1 complex | 4 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0038201 | TOR complex | 3 | 10 |
GO:0140535 | intracellular protein-containing complex | 2 | 10 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0007165 | signal transduction | 2 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0031929 | TOR signaling | 4 | 10 |
GO:0035556 | intracellular signal transduction | 3 | 10 |
GO:0050789 | regulation of biological process | 2 | 10 |
GO:0050794 | regulation of cellular process | 3 | 10 |
GO:0065007 | biological regulation | 1 | 10 |
GO:0001101 | response to acid chemical | 3 | 1 |
GO:0001558 | regulation of cell growth | 4 | 1 |
GO:0001932 | regulation of protein phosphorylation | 7 | 1 |
GO:0001934 | positive regulation of protein phosphorylation | 8 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0007154 | cell communication | 2 | 1 |
GO:0008361 | regulation of cell size | 5 | 1 |
GO:0009267 | cellular response to starvation | 4 | 1 |
GO:0009605 | response to external stimulus | 2 | 1 |
GO:0009719 | response to endogenous stimulus | 2 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0009991 | response to extracellular stimulus | 3 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0010243 | response to organonitrogen compound | 4 | 1 |
GO:0010506 | regulation of autophagy | 6 | 1 |
GO:0010562 | positive regulation of phosphorus metabolic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0030307 | positive regulation of cell growth | 5 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0031401 | positive regulation of protein modification process | 7 | 1 |
GO:0031667 | response to nutrient levels | 4 | 1 |
GO:0031668 | cellular response to extracellular stimulus | 3 | 1 |
GO:0031669 | cellular response to nutrient levels | 4 | 1 |
GO:0032006 | regulation of TOR signaling | 6 | 1 |
GO:0032535 | regulation of cellular component size | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0033674 | positive regulation of kinase activity | 6 | 1 |
GO:0040008 | regulation of growth | 3 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0042325 | regulation of phosphorylation | 7 | 1 |
GO:0042327 | positive regulation of phosphorylation | 8 | 1 |
GO:0042594 | response to starvation | 3 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0043200 | response to amino acid | 4 | 1 |
GO:0043549 | regulation of kinase activity | 5 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045859 | regulation of protein kinase activity | 6 | 1 |
GO:0045860 | positive regulation of protein kinase activity | 7 | 1 |
GO:0045927 | positive regulation of growth | 4 | 1 |
GO:0045937 | positive regulation of phosphate metabolic process | 7 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0070887 | cellular response to chemical stimulus | 3 | 1 |
GO:0071229 | cellular response to acid chemical | 4 | 1 |
GO:0071230 | cellular response to amino acid stimulus | 5 | 1 |
GO:0071310 | cellular response to organic substance | 4 | 1 |
GO:0071417 | cellular response to organonitrogen compound | 4 | 1 |
GO:0071495 | cellular response to endogenous stimulus | 3 | 1 |
GO:0071496 | cellular response to external stimulus | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0071900 | regulation of protein serine/threonine kinase activity | 7 | 1 |
GO:0071902 | positive regulation of protein serine/threonine kinase activity | 8 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090066 | regulation of anatomical structure size | 3 | 1 |
GO:1901698 | response to nitrogen compound | 3 | 1 |
GO:1901699 | cellular response to nitrogen compound | 4 | 1 |
GO:1901700 | response to oxygen-containing compound | 3 | 1 |
GO:1901701 | cellular response to oxygen-containing compound | 4 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
GO:1903432 | regulation of TORC1 signaling | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030674 | protein-macromolecule adaptor activity | 2 | 1 |
GO:0060090 | molecular adaptor activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 37 | 41 | PF00656 | 0.375 |
CLV_NRD_NRD_1 | 1023 | 1025 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 1030 | 1032 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 1065 | 1067 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 1318 | 1320 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 814 | 816 | PF00675 | 0.316 |
CLV_PCSK_FUR_1 | 622 | 626 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 1030 | 1032 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 1152 | 1154 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 814 | 816 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 1152 | 1154 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 522 | 524 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 624 | 626 | PF00082 | 0.635 |
CLV_PCSK_PC7_1 | 518 | 524 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 1246 | 1250 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 1342 | 1346 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 760 | 764 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 820 | 824 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 853 | 857 | PF00082 | 0.415 |
DEG_APCC_DBOX_1 | 361 | 369 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 522 | 530 | PF00400 | 0.417 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.638 |
DEG_SPOP_SBC_1 | 1364 | 1368 | PF00917 | 0.512 |
DEG_SPOP_SBC_1 | 51 | 55 | PF00917 | 0.448 |
DEG_SPOP_SBC_1 | 614 | 618 | PF00917 | 0.567 |
DOC_ANK_TNKS_1 | 664 | 671 | PF00023 | 0.376 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.285 |
DOC_CYCLIN_RxL_1 | 1012 | 1023 | PF00134 | 0.457 |
DOC_CYCLIN_RxL_1 | 1067 | 1079 | PF00134 | 0.526 |
DOC_CYCLIN_RxL_1 | 1182 | 1192 | PF00134 | 0.492 |
DOC_CYCLIN_RxL_1 | 1242 | 1253 | PF00134 | 0.478 |
DOC_CYCLIN_RxL_1 | 1337 | 1349 | PF00134 | 0.308 |
DOC_CYCLIN_yCln2_LP_2 | 1284 | 1290 | PF00134 | 0.378 |
DOC_CYCLIN_yCln2_LP_2 | 319 | 325 | PF00134 | 0.283 |
DOC_MAPK_gen_1 | 114 | 123 | PF00069 | 0.317 |
DOC_MAPK_gen_1 | 1379 | 1387 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 212 | 222 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 288 | 295 | PF00069 | 0.451 |
DOC_MAPK_JIP1_4 | 289 | 295 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 1319 | 1328 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 245 | 253 | PF00069 | 0.296 |
DOC_MAPK_RevD_3 | 199 | 213 | PF00069 | 0.277 |
DOC_PP1_RVXF_1 | 801 | 807 | PF00149 | 0.216 |
DOC_PP2B_LxvP_1 | 1284 | 1287 | PF13499 | 0.292 |
DOC_PP2B_LxvP_1 | 1361 | 1364 | PF13499 | 0.346 |
DOC_PP2B_PxIxI_1 | 262 | 268 | PF00149 | 0.388 |
DOC_USP7_MATH_1 | 1308 | 1312 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 1355 | 1359 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 1364 | 1368 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 1423 | 1427 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 1457 | 1461 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 531 | 535 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.244 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 851 | 855 | PF00917 | 0.323 |
DOC_USP7_UBL2_3 | 764 | 768 | PF12436 | 0.346 |
DOC_WW_Pin1_4 | 1035 | 1040 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.225 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 782 | 787 | PF00397 | 0.286 |
DOC_WW_Pin1_4 | 854 | 859 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 928 | 933 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 1004 | 1010 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 1030 | 1040 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 1066 | 1075 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 108 | 115 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 1153 | 1159 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 116 | 124 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 1194 | 1202 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 1227 | 1231 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 1319 | 1324 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 1382 | 1386 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 1456 | 1462 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 181 | 187 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 231 | 239 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 391 | 400 | PF00244 | 0.213 |
LIG_14-3-3_CanoR_1 | 4 | 14 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 505 | 510 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 701 | 706 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 789 | 796 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 978 | 987 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 989 | 998 | PF00244 | 0.372 |
LIG_Actin_WH2_2 | 397 | 413 | PF00022 | 0.290 |
LIG_BRCT_BRCA1_1 | 1037 | 1041 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 1310 | 1314 | PF00533 | 0.361 |
LIG_BRCT_BRCA1_1 | 463 | 467 | PF00533 | 0.349 |
LIG_BRCT_BRCA1_1 | 608 | 612 | PF00533 | 0.634 |
LIG_BRCT_BRCA1_1 | 752 | 756 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 975 | 979 | PF00533 | 0.441 |
LIG_Clathr_ClatBox_1 | 1147 | 1151 | PF01394 | 0.459 |
LIG_Clathr_ClatBox_1 | 578 | 582 | PF01394 | 0.420 |
LIG_deltaCOP1_diTrp_1 | 237 | 241 | PF00928 | 0.295 |
LIG_deltaCOP1_diTrp_1 | 328 | 335 | PF00928 | 0.300 |
LIG_EVH1_2 | 382 | 386 | PF00568 | 0.396 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.322 |
LIG_FHA_1 | 1364 | 1370 | PF00498 | 0.609 |
LIG_FHA_1 | 1387 | 1393 | PF00498 | 0.338 |
LIG_FHA_1 | 1404 | 1410 | PF00498 | 0.332 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.202 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.295 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.373 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.247 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.287 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.291 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.479 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.331 |
LIG_FHA_1 | 908 | 914 | PF00498 | 0.390 |
LIG_FHA_1 | 920 | 926 | PF00498 | 0.480 |
LIG_FHA_2 | 1067 | 1073 | PF00498 | 0.399 |
LIG_FHA_2 | 1235 | 1241 | PF00498 | 0.529 |
LIG_FHA_2 | 1327 | 1333 | PF00498 | 0.421 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.346 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.330 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.391 |
LIG_FHA_2 | 738 | 744 | PF00498 | 0.342 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.527 |
LIG_FHA_2 | 912 | 918 | PF00498 | 0.442 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.443 |
LIG_FHA_2 | 989 | 995 | PF00498 | 0.333 |
LIG_LIR_Apic_2 | 145 | 150 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 1400 | 1409 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 1464 | 1470 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 375 | 386 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 542 | 552 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 746 | 755 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 775 | 781 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 1089 | 1094 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 1111 | 1115 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 1311 | 1316 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 1400 | 1404 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 1464 | 1470 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 246 | 251 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 419 | 423 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 587 | 593 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 746 | 750 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 753 | 759 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 775 | 780 | PF02991 | 0.352 |
LIG_LYPXL_yS_3 | 420 | 423 | PF13949 | 0.419 |
LIG_MLH1_MIPbox_1 | 1310 | 1314 | PF16413 | 0.352 |
LIG_MLH1_MIPbox_1 | 463 | 467 | PF16413 | 0.349 |
LIG_NRBOX | 574 | 580 | PF00104 | 0.241 |
LIG_PCNA_TLS_4 | 324 | 331 | PF02747 | 0.393 |
LIG_PDZ_Class_2 | 1465 | 1470 | PF00595 | 0.409 |
LIG_Pex14_1 | 1108 | 1112 | PF04695 | 0.282 |
LIG_Pex14_1 | 329 | 333 | PF04695 | 0.277 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.312 |
LIG_Pex14_2 | 908 | 912 | PF04695 | 0.393 |
LIG_PTB_Apo_2 | 1395 | 1402 | PF02174 | 0.410 |
LIG_PTB_Apo_2 | 728 | 735 | PF02174 | 0.351 |
LIG_PTB_Phospho_1 | 1395 | 1401 | PF10480 | 0.410 |
LIG_Rb_pABgroove_1 | 896 | 904 | PF01858 | 0.435 |
LIG_SH2_CRK | 1202 | 1206 | PF00017 | 0.359 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.388 |
LIG_SH2_CRK | 852 | 856 | PF00017 | 0.316 |
LIG_SH2_GRB2like | 1112 | 1115 | PF00017 | 0.457 |
LIG_SH2_GRB2like | 953 | 956 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 1032 | 1036 | PF00017 | 0.372 |
LIG_SH2_PTP2 | 248 | 251 | PF00017 | 0.295 |
LIG_SH2_SRC | 125 | 128 | PF00017 | 0.388 |
LIG_SH2_SRC | 461 | 464 | PF00017 | 0.454 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.323 |
LIG_SH2_SRC | 574 | 577 | PF00017 | 0.248 |
LIG_SH2_STAT3 | 1115 | 1118 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 1032 | 1035 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 1109 | 1112 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 590 | 593 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 691 | 694 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 829 | 832 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.378 |
LIG_SH3_2 | 918 | 923 | PF14604 | 0.529 |
LIG_SH3_3 | 1176 | 1182 | PF00018 | 0.501 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.319 |
LIG_SH3_3 | 1369 | 1375 | PF00018 | 0.521 |
LIG_SH3_3 | 1441 | 1447 | PF00018 | 0.416 |
LIG_SH3_3 | 1448 | 1454 | PF00018 | 0.344 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.363 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.321 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.395 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.496 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.631 |
LIG_SH3_3 | 852 | 858 | PF00018 | 0.307 |
LIG_SH3_3 | 890 | 896 | PF00018 | 0.429 |
LIG_SH3_3 | 915 | 921 | PF00018 | 0.465 |
LIG_SH3_CIN85_PxpxPR_1 | 1374 | 1379 | PF14604 | 0.387 |
LIG_SUMO_SIM_anti_2 | 103 | 108 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 1145 | 1151 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 204 | 211 | PF11976 | 0.202 |
LIG_SUMO_SIM_anti_2 | 790 | 798 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 1145 | 1151 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 493 | 498 | PF11976 | 0.300 |
LIG_TRAF2_1 | 1117 | 1120 | PF00917 | 0.451 |
LIG_TRAF2_1 | 879 | 882 | PF00917 | 0.446 |
LIG_TYR_ITIM | 123 | 128 | PF00017 | 0.388 |
LIG_UBA3_1 | 529 | 535 | PF00899 | 0.351 |
LIG_UBA3_1 | 575 | 580 | PF00899 | 0.464 |
LIG_UBA3_1 | 755 | 764 | PF00899 | 0.302 |
LIG_WRC_WIRS_1 | 1121 | 1126 | PF05994 | 0.392 |
LIG_WRC_WIRS_1 | 1458 | 1463 | PF05994 | 0.372 |
LIG_WW_3 | 662 | 666 | PF00397 | 0.388 |
MOD_CDK_SPK_2 | 357 | 362 | PF00069 | 0.490 |
MOD_CDK_SPxK_1 | 318 | 324 | PF00069 | 0.310 |
MOD_CDK_SPxxK_3 | 782 | 789 | PF00069 | 0.286 |
MOD_CDK_SPxxK_3 | 854 | 861 | PF00069 | 0.235 |
MOD_CK1_1 | 1034 | 1040 | PF00069 | 0.484 |
MOD_CK1_1 | 1058 | 1064 | PF00069 | 0.399 |
MOD_CK1_1 | 1142 | 1148 | PF00069 | 0.460 |
MOD_CK1_1 | 1167 | 1173 | PF00069 | 0.534 |
MOD_CK1_1 | 1238 | 1244 | PF00069 | 0.459 |
MOD_CK1_1 | 1349 | 1355 | PF00069 | 0.392 |
MOD_CK1_1 | 1362 | 1368 | PF00069 | 0.567 |
MOD_CK1_1 | 1426 | 1432 | PF00069 | 0.630 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.225 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.584 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.312 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.344 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.594 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.456 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.355 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.578 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.629 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.325 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.282 |
MOD_CK1_1 | 854 | 860 | PF00069 | 0.411 |
MOD_CK1_1 | 911 | 917 | PF00069 | 0.563 |
MOD_CK1_1 | 928 | 934 | PF00069 | 0.316 |
MOD_CK1_1 | 988 | 994 | PF00069 | 0.406 |
MOD_CK2_1 | 1066 | 1072 | PF00069 | 0.397 |
MOD_CK2_1 | 1114 | 1120 | PF00069 | 0.406 |
MOD_CK2_1 | 1215 | 1221 | PF00069 | 0.407 |
MOD_CK2_1 | 1234 | 1240 | PF00069 | 0.439 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.330 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.371 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.313 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.404 |
MOD_CK2_1 | 737 | 743 | PF00069 | 0.425 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.631 |
MOD_CK2_1 | 988 | 994 | PF00069 | 0.578 |
MOD_CMANNOS | 433 | 436 | PF00535 | 0.288 |
MOD_Cter_Amidation | 520 | 523 | PF01082 | 0.356 |
MOD_GlcNHglycan | 1033 | 1036 | PF01048 | 0.371 |
MOD_GlcNHglycan | 1051 | 1054 | PF01048 | 0.465 |
MOD_GlcNHglycan | 1057 | 1060 | PF01048 | 0.497 |
MOD_GlcNHglycan | 1078 | 1081 | PF01048 | 0.469 |
MOD_GlcNHglycan | 1128 | 1131 | PF01048 | 0.459 |
MOD_GlcNHglycan | 1143 | 1147 | PF01048 | 0.460 |
MOD_GlcNHglycan | 1175 | 1178 | PF01048 | 0.424 |
MOD_GlcNHglycan | 1195 | 1198 | PF01048 | 0.359 |
MOD_GlcNHglycan | 1230 | 1233 | PF01048 | 0.423 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.521 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.388 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.719 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.295 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.568 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.434 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.561 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.352 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.320 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.515 |
MOD_GlcNHglycan | 92 | 97 | PF01048 | 0.521 |
MOD_GlcNHglycan | 991 | 994 | PF01048 | 0.469 |
MOD_GSK3_1 | 1030 | 1037 | PF00069 | 0.550 |
MOD_GSK3_1 | 1058 | 1065 | PF00069 | 0.434 |
MOD_GSK3_1 | 1188 | 1195 | PF00069 | 0.364 |
MOD_GSK3_1 | 1205 | 1212 | PF00069 | 0.350 |
MOD_GSK3_1 | 1234 | 1241 | PF00069 | 0.467 |
MOD_GSK3_1 | 1315 | 1322 | PF00069 | 0.378 |
MOD_GSK3_1 | 1355 | 1362 | PF00069 | 0.525 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.388 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.612 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.371 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.234 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.566 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.350 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.552 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.465 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.356 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.288 |
MOD_GSK3_1 | 907 | 914 | PF00069 | 0.376 |
MOD_GSK3_1 | 985 | 992 | PF00069 | 0.424 |
MOD_LATS_1 | 1029 | 1035 | PF00433 | 0.448 |
MOD_N-GLC_1 | 1346 | 1351 | PF02516 | 0.422 |
MOD_N-GLC_1 | 1397 | 1402 | PF02516 | 0.410 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.349 |
MOD_N-GLC_1 | 697 | 702 | PF02516 | 0.498 |
MOD_NEK2_1 | 1062 | 1067 | PF00069 | 0.552 |
MOD_NEK2_1 | 1094 | 1099 | PF00069 | 0.445 |
MOD_NEK2_1 | 1189 | 1194 | PF00069 | 0.439 |
MOD_NEK2_1 | 1228 | 1233 | PF00069 | 0.511 |
MOD_NEK2_1 | 1282 | 1287 | PF00069 | 0.288 |
MOD_NEK2_1 | 1326 | 1331 | PF00069 | 0.425 |
MOD_NEK2_1 | 1359 | 1364 | PF00069 | 0.524 |
MOD_NEK2_1 | 1381 | 1386 | PF00069 | 0.556 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.344 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.312 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.367 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.315 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.401 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.295 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.567 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.441 |
MOD_NEK2_1 | 750 | 755 | PF00069 | 0.228 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.312 |
MOD_NEK2_1 | 818 | 823 | PF00069 | 0.343 |
MOD_NEK2_1 | 831 | 836 | PF00069 | 0.252 |
MOD_NEK2_1 | 902 | 907 | PF00069 | 0.354 |
MOD_NEK2_1 | 908 | 913 | PF00069 | 0.419 |
MOD_NEK2_1 | 925 | 930 | PF00069 | 0.318 |
MOD_NEK2_2 | 1273 | 1278 | PF00069 | 0.442 |
MOD_NEK2_2 | 1308 | 1313 | PF00069 | 0.218 |
MOD_NEK2_2 | 686 | 691 | PF00069 | 0.389 |
MOD_OFUCOSY | 702 | 707 | PF10250 | 0.274 |
MOD_PIKK_1 | 1039 | 1045 | PF00454 | 0.438 |
MOD_PIKK_1 | 1114 | 1120 | PF00454 | 0.361 |
MOD_PIKK_1 | 1241 | 1247 | PF00454 | 0.495 |
MOD_PIKK_1 | 1426 | 1432 | PF00454 | 0.609 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.270 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.362 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.302 |
MOD_PIKK_1 | 535 | 541 | PF00454 | 0.397 |
MOD_PIKK_1 | 625 | 631 | PF00454 | 0.711 |
MOD_PIKK_1 | 873 | 879 | PF00454 | 0.368 |
MOD_PIKK_1 | 886 | 892 | PF00454 | 0.394 |
MOD_PIKK_1 | 973 | 979 | PF00454 | 0.468 |
MOD_PK_1 | 675 | 681 | PF00069 | 0.518 |
MOD_PKA_1 | 1030 | 1036 | PF00069 | 0.442 |
MOD_PKA_1 | 1066 | 1072 | PF00069 | 0.374 |
MOD_PKA_1 | 1319 | 1325 | PF00069 | 0.427 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.578 |
MOD_PKA_2 | 1005 | 1011 | PF00069 | 0.408 |
MOD_PKA_2 | 1030 | 1036 | PF00069 | 0.442 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.402 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.342 |
MOD_PKA_2 | 1193 | 1199 | PF00069 | 0.422 |
MOD_PKA_2 | 1226 | 1232 | PF00069 | 0.512 |
MOD_PKA_2 | 1381 | 1387 | PF00069 | 0.481 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.284 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.235 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.215 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.405 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.578 |
MOD_PKA_2 | 788 | 794 | PF00069 | 0.285 |
MOD_PKA_2 | 894 | 900 | PF00069 | 0.328 |
MOD_PKA_2 | 988 | 994 | PF00069 | 0.388 |
MOD_PKB_1 | 503 | 511 | PF00069 | 0.401 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.356 |
MOD_Plk_1 | 1094 | 1100 | PF00069 | 0.449 |
MOD_Plk_1 | 1397 | 1403 | PF00069 | 0.410 |
MOD_Plk_1 | 1424 | 1430 | PF00069 | 0.428 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.388 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.330 |
MOD_Plk_1 | 818 | 824 | PF00069 | 0.308 |
MOD_Plk_1 | 831 | 837 | PF00069 | 0.279 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.631 |
MOD_Plk_1 | 902 | 908 | PF00069 | 0.367 |
MOD_Plk_2-3 | 1346 | 1352 | PF00069 | 0.414 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.440 |
MOD_Plk_2-3 | 997 | 1003 | PF00069 | 0.535 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.483 |
MOD_Plk_4 | 1058 | 1064 | PF00069 | 0.373 |
MOD_Plk_4 | 1094 | 1100 | PF00069 | 0.443 |
MOD_Plk_4 | 1414 | 1420 | PF00069 | 0.383 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.334 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.355 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.408 |
MOD_Plk_4 | 686 | 692 | PF00069 | 0.389 |
MOD_Plk_4 | 791 | 797 | PF00069 | 0.299 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.569 |
MOD_Plk_4 | 818 | 824 | PF00069 | 0.297 |
MOD_Plk_4 | 902 | 908 | PF00069 | 0.366 |
MOD_Plk_4 | 955 | 961 | PF00069 | 0.327 |
MOD_ProDKin_1 | 1035 | 1041 | PF00069 | 0.555 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.681 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.388 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.224 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.373 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.398 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.538 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.639 |
MOD_ProDKin_1 | 782 | 788 | PF00069 | 0.286 |
MOD_ProDKin_1 | 854 | 860 | PF00069 | 0.234 |
MOD_ProDKin_1 | 928 | 934 | PF00069 | 0.527 |
MOD_SUMO_for_1 | 142 | 145 | PF00179 | 0.388 |
MOD_SUMO_for_1 | 579 | 582 | PF00179 | 0.360 |
MOD_SUMO_rev_2 | 1020 | 1026 | PF00179 | 0.465 |
MOD_SUMO_rev_2 | 354 | 361 | PF00179 | 0.413 |
TRG_AP2beta_CARGO_1 | 775 | 784 | PF09066 | 0.408 |
TRG_DiLeu_BaEn_1 | 1143 | 1148 | PF01217 | 0.367 |
TRG_DiLeu_BaEn_1 | 255 | 260 | PF01217 | 0.303 |
TRG_DiLeu_BaEn_1 | 819 | 824 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 405 | 410 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 725 | 730 | PF01217 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 776 | 781 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 1401 | 1404 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 593 | 596 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 691 | 694 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 852 | 855 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 1030 | 1032 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 502 | 505 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 813 | 815 | PF00400 | 0.317 |
TRG_NES_CRM1_1 | 1127 | 1140 | PF08389 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 1015 | 1020 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 1319 | 1323 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 1342 | 1346 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 779 | 783 | PF00026 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 814 | 819 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P678 | Leptomonas seymouri | 72% | 97% |
A0A0S4JFH5 | Bodo saltans | 35% | 100% |
A0A3S7WYY1 | Leishmania donovani | 86% | 100% |
A4I1A2 | Leishmania infantum | 86% | 100% |
D0A5J4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AXD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QA34 | Leishmania major | 86% | 100% |
V5DP89 | Trypanosoma cruzi | 43% | 100% |