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:0031931 | TORC1 complex | 4 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0038201 | TOR complex | 3 | 7 |
GO:0140535 | intracellular protein-containing complex | 2 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0007165 | signal transduction | 2 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0031929 | TOR signaling | 4 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
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 | 638 | 642 | PF00656 | 0.549 |
CLV_NRD_NRD_1 | 1028 | 1030 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 1035 | 1037 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 1071 | 1073 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 1323 | 1325 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.362 |
CLV_PCSK_FUR_1 | 621 | 625 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 1035 | 1037 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 1071 | 1073 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 1157 | 1159 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 819 | 821 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 1157 | 1159 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 623 | 625 | PF00082 | 0.530 |
CLV_PCSK_PC7_1 | 283 | 289 | PF00082 | 0.329 |
CLV_PCSK_PC7_1 | 517 | 523 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 1158 | 1162 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 1251 | 1255 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 1315 | 1319 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 759 | 763 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 765 | 769 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 825 | 829 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 858 | 862 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 882 | 886 | PF00082 | 0.415 |
DEG_APCC_DBOX_1 | 360 | 368 | PF00400 | 0.397 |
DEG_APCC_DBOX_1 | 521 | 529 | PF00400 | 0.341 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.607 |
DEG_ODPH_VHL_1 | 1380 | 1391 | PF01847 | 0.284 |
DEG_SPOP_SBC_1 | 1368 | 1372 | PF00917 | 0.525 |
DEG_SPOP_SBC_1 | 32 | 36 | PF00917 | 0.620 |
DEG_SPOP_SBC_1 | 635 | 639 | PF00917 | 0.495 |
DOC_CKS1_1 | 318 | 323 | PF01111 | 0.328 |
DOC_CYCLIN_RxL_1 | 1017 | 1028 | PF00134 | 0.439 |
DOC_CYCLIN_RxL_1 | 1072 | 1084 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 1187 | 1197 | PF00134 | 0.419 |
DOC_CYCLIN_RxL_1 | 1247 | 1258 | PF00134 | 0.401 |
DOC_CYCLIN_yCln2_LP_2 | 318 | 324 | PF00134 | 0.326 |
DOC_MAPK_gen_1 | 113 | 122 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 1383 | 1391 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 211 | 221 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 242 | 250 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 287 | 294 | PF00069 | 0.398 |
DOC_MAPK_JIP1_4 | 288 | 294 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 1324 | 1333 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 244 | 252 | PF00069 | 0.314 |
DOC_PP2B_LxvP_1 | 666 | 669 | PF13499 | 0.464 |
DOC_PP2B_PxIxI_1 | 261 | 267 | PF00149 | 0.314 |
DOC_USP7_MATH_1 | 1313 | 1317 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 1360 | 1364 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 1368 | 1372 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.239 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 901 | 905 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 769 | 773 | PF12436 | 0.413 |
DOC_WW_Pin1_4 | 1040 | 1045 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 933 | 938 | PF00397 | 0.567 |
LIG_14-3-3_CanoR_1 | 1009 | 1015 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 1035 | 1040 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 1071 | 1080 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 1111 | 1115 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 113 | 123 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 1158 | 1164 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 1199 | 1207 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 1232 | 1236 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 1324 | 1329 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 1386 | 1390 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 1440 | 1448 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 1458 | 1464 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 230 | 238 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 504 | 509 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 630 | 635 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 706 | 711 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 794 | 801 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 858 | 864 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 983 | 992 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 994 | 1003 | PF00244 | 0.446 |
LIG_Actin_WH2_2 | 396 | 412 | PF00022 | 0.333 |
LIG_BRCT_BRCA1_1 | 1315 | 1319 | PF00533 | 0.346 |
LIG_BRCT_BRCA1_1 | 462 | 466 | PF00533 | 0.371 |
LIG_BRCT_BRCA1_1 | 607 | 611 | PF00533 | 0.674 |
LIG_BRCT_BRCA1_1 | 757 | 761 | PF00533 | 0.317 |
LIG_BRCT_BRCA1_1 | 903 | 907 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 980 | 984 | PF00533 | 0.489 |
LIG_Clathr_ClatBox_1 | 1152 | 1156 | PF01394 | 0.370 |
LIG_Clathr_ClatBox_1 | 577 | 581 | PF01394 | 0.355 |
LIG_deltaCOP1_diTrp_1 | 236 | 240 | PF00928 | 0.314 |
LIG_deltaCOP1_diTrp_1 | 327 | 334 | PF00928 | 0.320 |
LIG_EVH1_1 | 666 | 670 | PF00568 | 0.429 |
LIG_EVH1_2 | 381 | 385 | PF00568 | 0.329 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.303 |
LIG_FHA_1 | 1368 | 1374 | PF00498 | 0.485 |
LIG_FHA_1 | 1391 | 1397 | PF00498 | 0.478 |
LIG_FHA_1 | 1408 | 1414 | PF00498 | 0.368 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.314 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.314 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.362 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.349 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.361 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.293 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.345 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.606 |
LIG_FHA_1 | 774 | 780 | PF00498 | 0.390 |
LIG_FHA_1 | 781 | 787 | PF00498 | 0.363 |
LIG_FHA_1 | 913 | 919 | PF00498 | 0.408 |
LIG_FHA_1 | 925 | 931 | PF00498 | 0.527 |
LIG_FHA_2 | 1072 | 1078 | PF00498 | 0.446 |
LIG_FHA_2 | 1240 | 1246 | PF00498 | 0.451 |
LIG_FHA_2 | 1332 | 1338 | PF00498 | 0.503 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.492 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.366 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.485 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.520 |
LIG_FHA_2 | 743 | 749 | PF00498 | 0.406 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.566 |
LIG_FHA_2 | 917 | 923 | PF00498 | 0.511 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 144 | 149 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 1404 | 1413 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 1466 | 1472 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 333 | 342 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 374 | 385 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 541 | 551 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 571 | 580 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 751 | 760 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 780 | 786 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 1094 | 1099 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 1113 | 1117 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 1316 | 1321 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 1404 | 1408 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 1466 | 1472 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 418 | 422 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 571 | 577 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 751 | 755 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 758 | 764 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 780 | 785 | PF02991 | 0.342 |
LIG_LYPXL_yS_3 | 419 | 422 | PF13949 | 0.408 |
LIG_MLH1_MIPbox_1 | 1315 | 1319 | PF16413 | 0.431 |
LIG_MLH1_MIPbox_1 | 462 | 466 | PF16413 | 0.371 |
LIG_MYND_1 | 1378 | 1382 | PF01753 | 0.320 |
LIG_PCNA_TLS_4 | 323 | 330 | PF02747 | 0.320 |
LIG_PDZ_Class_2 | 1467 | 1472 | PF00595 | 0.333 |
LIG_Pex14_1 | 328 | 332 | PF04695 | 0.320 |
LIG_Pex14_2 | 385 | 389 | PF04695 | 0.334 |
LIG_Pex14_2 | 913 | 917 | PF04695 | 0.380 |
LIG_PTB_Apo_2 | 1399 | 1406 | PF02174 | 0.336 |
LIG_PTB_Apo_2 | 733 | 740 | PF02174 | 0.338 |
LIG_PTB_Phospho_1 | 1399 | 1405 | PF10480 | 0.336 |
LIG_Rb_pABgroove_1 | 901 | 909 | PF01858 | 0.375 |
LIG_SH2_CRK | 1207 | 1211 | PF00017 | 0.378 |
LIG_SH2_CRK | 182 | 186 | PF00017 | 0.314 |
LIG_SH2_CRK | 857 | 861 | PF00017 | 0.326 |
LIG_SH2_GRB2like | 1117 | 1120 | PF00017 | 0.422 |
LIG_SH2_GRB2like | 958 | 961 | PF00017 | 0.332 |
LIG_SH2_NCK_1 | 598 | 602 | PF00017 | 0.423 |
LIG_SH2_PTP2 | 247 | 250 | PF00017 | 0.314 |
LIG_SH2_SRC | 124 | 127 | PF00017 | 0.314 |
LIG_SH2_SRC | 460 | 463 | PF00017 | 0.407 |
LIG_SH2_SRC | 512 | 515 | PF00017 | 0.342 |
LIG_SH2_STAT3 | 1120 | 1123 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 1037 | 1040 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 1114 | 1117 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 696 | 699 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 834 | 837 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 872 | 875 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 972 | 975 | PF00017 | 0.393 |
LIG_SH3_2 | 653 | 658 | PF14604 | 0.577 |
LIG_SH3_2 | 923 | 928 | PF14604 | 0.467 |
LIG_SH3_3 | 1181 | 1187 | PF00018 | 0.431 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.283 |
LIG_SH3_3 | 1370 | 1376 | PF00018 | 0.476 |
LIG_SH3_3 | 1424 | 1430 | PF00018 | 0.450 |
LIG_SH3_3 | 1443 | 1449 | PF00018 | 0.457 |
LIG_SH3_3 | 1450 | 1456 | PF00018 | 0.455 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.563 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.365 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.452 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.678 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.546 |
LIG_SH3_3 | 920 | 926 | PF00018 | 0.464 |
LIG_SUMO_SIM_anti_2 | 102 | 107 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 1150 | 1156 | PF11976 | 0.372 |
LIG_SUMO_SIM_anti_2 | 795 | 803 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 1042 | 1049 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 1150 | 1156 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 1220 | 1227 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 492 | 497 | PF11976 | 0.322 |
LIG_TRAF2_1 | 1122 | 1125 | PF00917 | 0.596 |
LIG_TYR_ITIM | 122 | 127 | PF00017 | 0.314 |
LIG_TYR_ITIM | 596 | 601 | PF00017 | 0.415 |
LIG_UBA3_1 | 528 | 534 | PF00899 | 0.332 |
LIG_UBA3_1 | 760 | 769 | PF00899 | 0.322 |
LIG_WRC_WIRS_1 | 1460 | 1465 | PF05994 | 0.475 |
MOD_CDK_SPK_2 | 356 | 361 | PF00069 | 0.427 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.330 |
MOD_CDK_SPxxK_3 | 787 | 794 | PF00069 | 0.328 |
MOD_CK1_1 | 1113 | 1119 | PF00069 | 0.410 |
MOD_CK1_1 | 1147 | 1153 | PF00069 | 0.383 |
MOD_CK1_1 | 1172 | 1178 | PF00069 | 0.503 |
MOD_CK1_1 | 1243 | 1249 | PF00069 | 0.435 |
MOD_CK1_1 | 1363 | 1369 | PF00069 | 0.469 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.314 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.334 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.575 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.394 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.338 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.576 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.627 |
MOD_CK1_1 | 796 | 802 | PF00069 | 0.324 |
MOD_CK1_1 | 916 | 922 | PF00069 | 0.502 |
MOD_CK1_1 | 933 | 939 | PF00069 | 0.320 |
MOD_CK1_1 | 997 | 1003 | PF00069 | 0.448 |
MOD_CK2_1 | 1071 | 1077 | PF00069 | 0.446 |
MOD_CK2_1 | 1119 | 1125 | PF00069 | 0.485 |
MOD_CK2_1 | 1220 | 1226 | PF00069 | 0.415 |
MOD_CK2_1 | 1239 | 1245 | PF00069 | 0.455 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.314 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.332 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.340 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.532 |
MOD_CK2_1 | 742 | 748 | PF00069 | 0.432 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.619 |
MOD_CMANNOS | 432 | 435 | PF00535 | 0.342 |
MOD_Cter_Amidation | 519 | 522 | PF01082 | 0.339 |
MOD_DYRK1A_RPxSP_1 | 600 | 604 | PF00069 | 0.493 |
MOD_GlcNHglycan | 1062 | 1065 | PF01048 | 0.550 |
MOD_GlcNHglycan | 1083 | 1086 | PF01048 | 0.436 |
MOD_GlcNHglycan | 1133 | 1136 | PF01048 | 0.433 |
MOD_GlcNHglycan | 1148 | 1152 | PF01048 | 0.432 |
MOD_GlcNHglycan | 1180 | 1183 | PF01048 | 0.468 |
MOD_GlcNHglycan | 1200 | 1203 | PF01048 | 0.319 |
MOD_GlcNHglycan | 1235 | 1238 | PF01048 | 0.453 |
MOD_GlcNHglycan | 1315 | 1318 | PF01048 | 0.343 |
MOD_GlcNHglycan | 1442 | 1445 | PF01048 | 0.505 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.314 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.314 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.314 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.337 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.314 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.448 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.464 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.361 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.469 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.378 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.342 |
MOD_GlcNHglycan | 91 | 96 | PF01048 | 0.587 |
MOD_GlcNHglycan | 996 | 999 | PF01048 | 0.461 |
MOD_GSK3_1 | 1035 | 1042 | PF00069 | 0.557 |
MOD_GSK3_1 | 1067 | 1074 | PF00069 | 0.441 |
MOD_GSK3_1 | 1087 | 1094 | PF00069 | 0.371 |
MOD_GSK3_1 | 1193 | 1200 | PF00069 | 0.402 |
MOD_GSK3_1 | 1210 | 1217 | PF00069 | 0.350 |
MOD_GSK3_1 | 1239 | 1246 | PF00069 | 0.506 |
MOD_GSK3_1 | 1363 | 1370 | PF00069 | 0.451 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.291 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.289 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.314 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.362 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.388 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.459 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.327 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.659 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.609 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.412 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.354 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.326 |
MOD_GSK3_1 | 912 | 919 | PF00069 | 0.402 |
MOD_GSK3_1 | 990 | 997 | PF00069 | 0.448 |
MOD_N-GLC_1 | 1368 | 1373 | PF02516 | 0.498 |
MOD_N-GLC_1 | 1401 | 1406 | PF02516 | 0.343 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.314 |
MOD_N-GLC_1 | 702 | 707 | PF02516 | 0.409 |
MOD_N-GLC_1 | 867 | 872 | PF02516 | 0.315 |
MOD_NEK2_1 | 1067 | 1072 | PF00069 | 0.553 |
MOD_NEK2_1 | 1099 | 1104 | PF00069 | 0.400 |
MOD_NEK2_1 | 1194 | 1199 | PF00069 | 0.417 |
MOD_NEK2_1 | 1233 | 1238 | PF00069 | 0.437 |
MOD_NEK2_1 | 1331 | 1336 | PF00069 | 0.409 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.314 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.314 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.352 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.328 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.336 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.345 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.379 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.423 |
MOD_NEK2_1 | 755 | 760 | PF00069 | 0.281 |
MOD_NEK2_1 | 800 | 805 | PF00069 | 0.321 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.339 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.321 |
MOD_NEK2_1 | 907 | 912 | PF00069 | 0.357 |
MOD_NEK2_1 | 913 | 918 | PF00069 | 0.386 |
MOD_NEK2_2 | 1278 | 1283 | PF00069 | 0.417 |
MOD_NEK2_2 | 691 | 696 | PF00069 | 0.384 |
MOD_PIKK_1 | 1119 | 1125 | PF00454 | 0.406 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.290 |
MOD_PIKK_1 | 1246 | 1252 | PF00454 | 0.418 |
MOD_PIKK_1 | 1430 | 1436 | PF00454 | 0.573 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.342 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.318 |
MOD_PIKK_1 | 534 | 540 | PF00454 | 0.346 |
MOD_PIKK_1 | 628 | 634 | PF00454 | 0.596 |
MOD_PIKK_1 | 891 | 897 | PF00454 | 0.386 |
MOD_PIKK_1 | 930 | 936 | PF00454 | 0.404 |
MOD_PIKK_1 | 978 | 984 | PF00454 | 0.483 |
MOD_PK_1 | 680 | 686 | PF00069 | 0.442 |
MOD_PKA_1 | 1035 | 1041 | PF00069 | 0.533 |
MOD_PKA_1 | 1071 | 1077 | PF00069 | 0.418 |
MOD_PKA_1 | 1324 | 1330 | PF00069 | 0.467 |
MOD_PKA_2 | 1010 | 1016 | PF00069 | 0.409 |
MOD_PKA_2 | 1035 | 1041 | PF00069 | 0.483 |
MOD_PKA_2 | 1071 | 1077 | PF00069 | 0.390 |
MOD_PKA_2 | 1110 | 1116 | PF00069 | 0.454 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.305 |
MOD_PKA_2 | 1198 | 1204 | PF00069 | 0.349 |
MOD_PKA_2 | 1231 | 1237 | PF00069 | 0.500 |
MOD_PKA_2 | 1385 | 1391 | PF00069 | 0.359 |
MOD_PKA_2 | 1439 | 1445 | PF00069 | 0.471 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.338 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.256 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.333 |
MOD_PKA_2 | 793 | 799 | PF00069 | 0.326 |
MOD_PKA_2 | 899 | 905 | PF00069 | 0.389 |
MOD_PKB_1 | 502 | 510 | PF00069 | 0.322 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.370 |
MOD_Plk_1 | 1099 | 1105 | PF00069 | 0.394 |
MOD_Plk_1 | 1368 | 1374 | PF00069 | 0.499 |
MOD_Plk_1 | 1401 | 1407 | PF00069 | 0.338 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.314 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.314 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.307 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.354 |
MOD_Plk_1 | 823 | 829 | PF00069 | 0.337 |
MOD_Plk_1 | 836 | 842 | PF00069 | 0.320 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.619 |
MOD_Plk_1 | 907 | 913 | PF00069 | 0.357 |
MOD_Plk_1 | 930 | 936 | PF00069 | 0.421 |
MOD_Plk_2-3 | 1002 | 1008 | PF00069 | 0.456 |
MOD_Plk_2-3 | 1346 | 1352 | PF00069 | 0.455 |
MOD_Plk_2-3 | 461 | 467 | PF00069 | 0.369 |
MOD_Plk_2-3 | 582 | 588 | PF00069 | 0.386 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.425 |
MOD_Plk_4 | 1087 | 1093 | PF00069 | 0.367 |
MOD_Plk_4 | 1099 | 1105 | PF00069 | 0.394 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.314 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.371 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.303 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.345 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.339 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.384 |
MOD_Plk_4 | 796 | 802 | PF00069 | 0.326 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.464 |
MOD_Plk_4 | 823 | 829 | PF00069 | 0.337 |
MOD_Plk_4 | 902 | 908 | PF00069 | 0.369 |
MOD_Plk_4 | 913 | 919 | PF00069 | 0.403 |
MOD_ProDKin_1 | 1040 | 1046 | PF00069 | 0.526 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.290 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.357 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.393 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.330 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.425 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.408 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.556 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.643 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.602 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.328 |
MOD_ProDKin_1 | 933 | 939 | PF00069 | 0.562 |
MOD_SUMO_for_1 | 141 | 144 | PF00179 | 0.314 |
MOD_SUMO_for_1 | 578 | 581 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 1025 | 1031 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 353 | 360 | PF00179 | 0.445 |
TRG_AP2beta_CARGO_1 | 780 | 789 | PF09066 | 0.338 |
TRG_DiLeu_BaEn_1 | 1148 | 1153 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_1 | 582 | 587 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_1 | 824 | 829 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 1041 | 1046 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 404 | 409 | PF01217 | 0.332 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 730 | 735 | PF01217 | 0.321 |
TRG_DiLeu_BaLyEn_6 | 781 | 786 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 1405 | 1408 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 696 | 699 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 857 | 860 | PF00928 | 0.325 |
TRG_ER_diArg_1 | 1035 | 1037 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.317 |
TRG_ER_diArg_1 | 818 | 820 | PF00400 | 0.364 |
TRG_NES_CRM1_1 | 1132 | 1145 | PF08389 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 1020 | 1025 | PF00026 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 1324 | 1328 | PF00026 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 407 | 411 | PF00026 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 784 | 788 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 819 | 824 | PF00026 | 0.356 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P678 | Leptomonas seymouri | 74% | 97% |
A4HEF7 | Leishmania braziliensis | 86% | 100% |
A4I1A2 | Leishmania infantum | 100% | 100% |
E9AXD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QA34 | Leishmania major | 95% | 100% |