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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0031931 | TORC1 complex | 4 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0038201 | TOR complex | 3 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001101 | response to acid chemical | 3 | 2 |
GO:0001558 | regulation of cell growth | 4 | 2 |
GO:0001932 | regulation of protein phosphorylation | 7 | 2 |
GO:0001934 | positive regulation of protein phosphorylation | 8 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0007154 | cell communication | 2 | 2 |
GO:0007165 | signal transduction | 2 | 8 |
GO:0008361 | regulation of cell size | 5 | 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:0009966 | regulation of signal transduction | 4 | 2 |
GO:0009987 | cellular process | 1 | 8 |
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:0010562 | positive regulation of phosphorus metabolic process | 6 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0010646 | regulation of cell communication | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0023051 | regulation of signaling | 3 | 2 |
GO:0030307 | positive regulation of cell growth | 5 | 2 |
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:0031399 | regulation of protein modification process | 6 | 2 |
GO:0031401 | positive regulation of protein modification process | 7 | 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:0031929 | TOR signaling | 4 | 8 |
GO:0032006 | regulation of TOR signaling | 6 | 2 |
GO:0032535 | regulation of cellular component size | 4 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0033674 | positive regulation of kinase activity | 6 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 8 |
GO:0040008 | regulation of growth | 3 | 2 |
GO:0042221 | response to chemical | 2 | 2 |
GO:0042325 | regulation of phosphorylation | 7 | 2 |
GO:0042327 | positive regulation of phosphorylation | 8 | 2 |
GO:0042594 | response to starvation | 3 | 2 |
GO:0043085 | positive regulation of catalytic activity | 4 | 2 |
GO:0043200 | response to amino acid | 4 | 2 |
GO:0043549 | regulation of kinase activity | 5 | 2 |
GO:0044093 | positive regulation of molecular function | 3 | 2 |
GO:0045859 | regulation of protein kinase activity | 6 | 2 |
GO:0045860 | positive regulation of protein kinase activity | 7 | 2 |
GO:0045927 | positive regulation of growth | 4 | 2 |
GO:0045937 | positive regulation of phosphate metabolic process | 7 | 2 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0048583 | regulation of response to stimulus | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050790 | regulation of catalytic activity | 3 | 2 |
GO:0050794 | regulation of cellular process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051128 | regulation of cellular component organization | 4 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 2 |
GO:0051338 | regulation of transferase activity | 4 | 2 |
GO:0051347 | positive regulation of transferase activity | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0065009 | regulation of molecular function | 2 | 2 |
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: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:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0071900 | regulation of protein serine/threonine kinase activity | 7 | 2 |
GO:0071902 | positive regulation of protein serine/threonine kinase activity | 8 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090066 | regulation of anatomical structure size | 3 | 2 |
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 | 2 |
GO:1903432 | regulation of TORC1 signaling | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
GO:0060090 | molecular adaptor activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 638 | 642 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 1026 | 1028 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 1033 | 1035 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 1321 | 1323 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 817 | 819 | PF00675 | 0.424 |
CLV_PCSK_FUR_1 | 621 | 625 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 1033 | 1035 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 1155 | 1157 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 817 | 819 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 1155 | 1157 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 623 | 625 | PF00082 | 0.636 |
CLV_PCSK_PC7_1 | 283 | 289 | PF00082 | 0.443 |
CLV_PCSK_PC7_1 | 517 | 523 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 1249 | 1253 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 1313 | 1317 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 757 | 761 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 763 | 767 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 823 | 827 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 856 | 860 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 880 | 884 | PF00082 | 0.490 |
DEG_APCC_DBOX_1 | 360 | 368 | PF00400 | 0.514 |
DEG_APCC_DBOX_1 | 521 | 529 | PF00400 | 0.456 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.664 |
DEG_SPOP_SBC_1 | 1367 | 1371 | PF00917 | 0.664 |
DEG_SPOP_SBC_1 | 33 | 37 | PF00917 | 0.669 |
DEG_SPOP_SBC_1 | 635 | 639 | PF00917 | 0.569 |
DOC_CKS1_1 | 259 | 264 | PF01111 | 0.369 |
DOC_CKS1_1 | 318 | 323 | PF01111 | 0.385 |
DOC_CYCLIN_RxL_1 | 1015 | 1026 | PF00134 | 0.556 |
DOC_CYCLIN_RxL_1 | 1070 | 1082 | PF00134 | 0.543 |
DOC_CYCLIN_RxL_1 | 1185 | 1195 | PF00134 | 0.533 |
DOC_CYCLIN_RxL_1 | 1245 | 1256 | PF00134 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 318 | 324 | PF00134 | 0.388 |
DOC_MAPK_gen_1 | 113 | 122 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 1382 | 1390 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 211 | 221 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 242 | 250 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 287 | 294 | PF00069 | 0.483 |
DOC_MAPK_JIP1_4 | 288 | 294 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 1322 | 1331 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 244 | 252 | PF00069 | 0.375 |
DOC_PP2B_PxIxI_1 | 261 | 267 | PF00149 | 0.429 |
DOC_USP7_MATH_1 | 1311 | 1315 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 1358 | 1362 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 1367 | 1371 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 1384 | 1388 | PF00917 | 0.294 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 899 | 903 | PF00917 | 0.481 |
DOC_USP7_UBL2_3 | 767 | 771 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 1038 | 1043 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 663 | 668 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 785 | 790 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 931 | 936 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 1007 | 1013 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 1109 | 1113 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 113 | 123 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 1156 | 1162 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 1197 | 1205 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 1230 | 1234 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 1322 | 1327 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 1385 | 1389 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 1439 | 1447 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 1457 | 1463 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 212 | 221 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 230 | 238 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 448 | 457 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 504 | 509 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 630 | 635 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 704 | 709 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 792 | 799 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 856 | 862 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 969 | 977 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 981 | 990 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 992 | 1001 | PF00244 | 0.464 |
LIG_Actin_WH2_2 | 396 | 412 | PF00022 | 0.395 |
LIG_BRCT_BRCA1_1 | 1313 | 1317 | PF00533 | 0.424 |
LIG_BRCT_BRCA1_1 | 462 | 466 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 607 | 611 | PF00533 | 0.664 |
LIG_BRCT_BRCA1_1 | 755 | 759 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 901 | 905 | PF00533 | 0.472 |
LIG_BRCT_BRCA1_1 | 978 | 982 | PF00533 | 0.544 |
LIG_Clathr_ClatBox_1 | 1150 | 1154 | PF01394 | 0.503 |
LIG_Clathr_ClatBox_1 | 577 | 581 | PF01394 | 0.480 |
LIG_deltaCOP1_diTrp_1 | 236 | 240 | PF00928 | 0.375 |
LIG_deltaCOP1_diTrp_1 | 327 | 334 | PF00928 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 474 | 479 | PF00928 | 0.376 |
LIG_EVH1_2 | 381 | 385 | PF00568 | 0.390 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.375 |
LIG_FHA_1 | 1286 | 1292 | PF00498 | 0.359 |
LIG_FHA_1 | 1367 | 1373 | PF00498 | 0.623 |
LIG_FHA_1 | 1390 | 1396 | PF00498 | 0.405 |
LIG_FHA_1 | 1407 | 1413 | PF00498 | 0.367 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.375 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.375 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.453 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.354 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.393 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.377 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.447 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.704 |
LIG_FHA_1 | 779 | 785 | PF00498 | 0.404 |
LIG_FHA_1 | 911 | 917 | PF00498 | 0.451 |
LIG_FHA_1 | 923 | 929 | PF00498 | 0.491 |
LIG_FHA_2 | 1238 | 1244 | PF00498 | 0.568 |
LIG_FHA_2 | 1330 | 1336 | PF00498 | 0.594 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.460 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.434 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.538 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.578 |
LIG_FHA_2 | 741 | 747 | PF00498 | 0.490 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.612 |
LIG_FHA_2 | 915 | 921 | PF00498 | 0.617 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.429 |
LIG_LIR_Apic_2 | 144 | 149 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 1403 | 1412 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 1465 | 1471 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 189 | 200 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 333 | 342 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 374 | 385 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 541 | 551 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 571 | 580 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 749 | 758 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 778 | 784 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 1092 | 1097 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 1111 | 1115 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 1314 | 1319 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 1335 | 1340 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 1403 | 1407 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 1465 | 1471 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 418 | 422 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 571 | 577 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 749 | 753 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 756 | 762 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 778 | 783 | PF02991 | 0.397 |
LIG_LYPXL_yS_3 | 419 | 422 | PF13949 | 0.521 |
LIG_MLH1_MIPbox_1 | 1313 | 1317 | PF16413 | 0.538 |
LIG_MLH1_MIPbox_1 | 462 | 466 | PF16413 | 0.433 |
LIG_PCNA_TLS_4 | 323 | 330 | PF02747 | 0.435 |
LIG_PDZ_Class_2 | 1466 | 1471 | PF00595 | 0.458 |
LIG_Pex14_1 | 328 | 332 | PF04695 | 0.382 |
LIG_Pex14_2 | 385 | 389 | PF04695 | 0.395 |
LIG_Pex14_2 | 911 | 915 | PF04695 | 0.441 |
LIG_PTAP_UEV_1 | 1377 | 1382 | PF05743 | 0.406 |
LIG_PTB_Apo_2 | 1398 | 1405 | PF02174 | 0.455 |
LIG_PTB_Apo_2 | 731 | 738 | PF02174 | 0.399 |
LIG_PTB_Phospho_1 | 1398 | 1404 | PF10480 | 0.455 |
LIG_Rb_pABgroove_1 | 899 | 907 | PF01858 | 0.490 |
LIG_SH2_CRK | 1169 | 1173 | PF00017 | 0.316 |
LIG_SH2_CRK | 1205 | 1209 | PF00017 | 0.439 |
LIG_SH2_CRK | 182 | 186 | PF00017 | 0.429 |
LIG_SH2_CRK | 855 | 859 | PF00017 | 0.386 |
LIG_SH2_GRB2like | 1115 | 1118 | PF00017 | 0.531 |
LIG_SH2_GRB2like | 956 | 959 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 1169 | 1173 | PF00017 | 0.316 |
LIG_SH2_NCK_1 | 598 | 602 | PF00017 | 0.542 |
LIG_SH2_PTP2 | 247 | 250 | PF00017 | 0.375 |
LIG_SH2_SRC | 124 | 127 | PF00017 | 0.429 |
LIG_SH2_SRC | 460 | 463 | PF00017 | 0.504 |
LIG_SH2_SRC | 512 | 515 | PF00017 | 0.403 |
LIG_SH2_STAT3 | 1118 | 1121 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 1037 | 1040 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 1112 | 1115 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 694 | 697 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.435 |
LIG_SH3_2 | 653 | 658 | PF14604 | 0.672 |
LIG_SH3_2 | 921 | 926 | PF14604 | 0.579 |
LIG_SH3_3 | 1179 | 1185 | PF00018 | 0.537 |
LIG_SH3_3 | 1369 | 1375 | PF00018 | 0.563 |
LIG_SH3_3 | 1423 | 1429 | PF00018 | 0.566 |
LIG_SH3_3 | 1449 | 1455 | PF00018 | 0.478 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.673 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.406 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.425 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.467 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.570 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.690 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.609 |
LIG_SH3_3 | 918 | 924 | PF00018 | 0.561 |
LIG_SUMO_SIM_anti_2 | 102 | 110 | PF11976 | 0.554 |
LIG_SUMO_SIM_anti_2 | 1148 | 1154 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 793 | 801 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 1148 | 1154 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 1218 | 1225 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 492 | 497 | PF11976 | 0.386 |
LIG_TRAF2_1 | 1120 | 1123 | PF00917 | 0.583 |
LIG_TRAF2_1 | 882 | 885 | PF00917 | 0.497 |
LIG_TYR_ITIM | 122 | 127 | PF00017 | 0.429 |
LIG_TYR_ITIM | 596 | 601 | PF00017 | 0.538 |
LIG_UBA3_1 | 528 | 534 | PF00899 | 0.447 |
LIG_UBA3_1 | 758 | 767 | PF00899 | 0.382 |
LIG_WRC_WIRS_1 | 1459 | 1464 | PF05994 | 0.551 |
MOD_CDK_SPK_2 | 356 | 361 | PF00069 | 0.543 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.392 |
MOD_CDK_SPxxK_3 | 785 | 792 | PF00069 | 0.389 |
MOD_CK1_1 | 1045 | 1051 | PF00069 | 0.536 |
MOD_CK1_1 | 1111 | 1117 | PF00069 | 0.461 |
MOD_CK1_1 | 1145 | 1151 | PF00069 | 0.506 |
MOD_CK1_1 | 1170 | 1176 | PF00069 | 0.524 |
MOD_CK1_1 | 1241 | 1247 | PF00069 | 0.551 |
MOD_CK1_1 | 1361 | 1367 | PF00069 | 0.599 |
MOD_CK1_1 | 1442 | 1448 | PF00069 | 0.476 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.375 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.443 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.584 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.499 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.399 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.709 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.385 |
MOD_CK1_1 | 914 | 920 | PF00069 | 0.552 |
MOD_CK1_1 | 931 | 937 | PF00069 | 0.468 |
MOD_CK1_1 | 995 | 1001 | PF00069 | 0.509 |
MOD_CK2_1 | 1117 | 1123 | PF00069 | 0.541 |
MOD_CK2_1 | 1218 | 1224 | PF00069 | 0.461 |
MOD_CK2_1 | 1237 | 1243 | PF00069 | 0.518 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.369 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.444 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.427 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.472 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.494 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.662 |
MOD_CMANNOS | 432 | 435 | PF00535 | 0.403 |
MOD_CMANNOS | 476 | 479 | PF00535 | 0.315 |
MOD_Cter_Amidation | 519 | 522 | PF01082 | 0.401 |
MOD_DYRK1A_RPxSP_1 | 600 | 604 | PF00069 | 0.569 |
MOD_GlcNHglycan | 1060 | 1063 | PF01048 | 0.527 |
MOD_GlcNHglycan | 1081 | 1084 | PF01048 | 0.503 |
MOD_GlcNHglycan | 1131 | 1134 | PF01048 | 0.527 |
MOD_GlcNHglycan | 1146 | 1150 | PF01048 | 0.474 |
MOD_GlcNHglycan | 1178 | 1181 | PF01048 | 0.494 |
MOD_GlcNHglycan | 1198 | 1201 | PF01048 | 0.203 |
MOD_GlcNHglycan | 1233 | 1236 | PF01048 | 0.501 |
MOD_GlcNHglycan | 1313 | 1316 | PF01048 | 0.385 |
MOD_GlcNHglycan | 1378 | 1381 | PF01048 | 0.404 |
MOD_GlcNHglycan | 1441 | 1444 | PF01048 | 0.604 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.404 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.362 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.411 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.354 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.534 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.564 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.476 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.359 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.401 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.641 |
MOD_GlcNHglycan | 91 | 96 | PF01048 | 0.676 |
MOD_GlcNHglycan | 994 | 997 | PF01048 | 0.558 |
MOD_GSK3_1 | 1038 | 1045 | PF00069 | 0.537 |
MOD_GSK3_1 | 1085 | 1092 | PF00069 | 0.404 |
MOD_GSK3_1 | 1191 | 1198 | PF00069 | 0.448 |
MOD_GSK3_1 | 1208 | 1215 | PF00069 | 0.421 |
MOD_GSK3_1 | 1237 | 1244 | PF00069 | 0.509 |
MOD_GSK3_1 | 1358 | 1365 | PF00069 | 0.635 |
MOD_GSK3_1 | 1438 | 1445 | PF00069 | 0.555 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.357 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.429 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.557 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.465 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.334 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.537 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.442 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.616 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.703 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.452 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.387 |
MOD_GSK3_1 | 910 | 917 | PF00069 | 0.459 |
MOD_GSK3_1 | 988 | 995 | PF00069 | 0.501 |
MOD_N-GLC_1 | 1367 | 1372 | PF02516 | 0.537 |
MOD_N-GLC_1 | 1400 | 1405 | PF02516 | 0.455 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.394 |
MOD_N-GLC_1 | 609 | 614 | PF02516 | 0.660 |
MOD_N-GLC_1 | 700 | 705 | PF02516 | 0.493 |
MOD_NEK2_1 | 1065 | 1070 | PF00069 | 0.585 |
MOD_NEK2_1 | 1097 | 1102 | PF00069 | 0.481 |
MOD_NEK2_1 | 1192 | 1197 | PF00069 | 0.498 |
MOD_NEK2_1 | 1231 | 1236 | PF00069 | 0.548 |
MOD_NEK2_1 | 1329 | 1334 | PF00069 | 0.501 |
MOD_NEK2_1 | 1362 | 1367 | PF00069 | 0.550 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.389 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.357 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.467 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.445 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.381 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.361 |
MOD_NEK2_1 | 740 | 745 | PF00069 | 0.518 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.433 |
MOD_NEK2_1 | 798 | 803 | PF00069 | 0.432 |
MOD_NEK2_1 | 821 | 826 | PF00069 | 0.383 |
MOD_NEK2_1 | 834 | 839 | PF00069 | 0.311 |
MOD_NEK2_1 | 905 | 910 | PF00069 | 0.459 |
MOD_NEK2_1 | 911 | 916 | PF00069 | 0.441 |
MOD_NEK2_2 | 1276 | 1281 | PF00069 | 0.543 |
MOD_NEK2_2 | 689 | 694 | PF00069 | 0.496 |
MOD_PIKK_1 | 1042 | 1048 | PF00454 | 0.580 |
MOD_PIKK_1 | 1117 | 1123 | PF00454 | 0.461 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.348 |
MOD_PIKK_1 | 1244 | 1250 | PF00454 | 0.532 |
MOD_PIKK_1 | 1429 | 1435 | PF00454 | 0.662 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.407 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.380 |
MOD_PIKK_1 | 534 | 540 | PF00454 | 0.385 |
MOD_PIKK_1 | 628 | 634 | PF00454 | 0.682 |
MOD_PIKK_1 | 889 | 895 | PF00454 | 0.471 |
MOD_PIKK_1 | 976 | 982 | PF00454 | 0.589 |
MOD_PK_1 | 678 | 684 | PF00069 | 0.548 |
MOD_PKA_1 | 1322 | 1328 | PF00069 | 0.511 |
MOD_PKA_2 | 1008 | 1014 | PF00069 | 0.493 |
MOD_PKA_2 | 1108 | 1114 | PF00069 | 0.503 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.382 |
MOD_PKA_2 | 1196 | 1202 | PF00069 | 0.464 |
MOD_PKA_2 | 1229 | 1235 | PF00069 | 0.546 |
MOD_PKA_2 | 1384 | 1390 | PF00069 | 0.502 |
MOD_PKA_2 | 1438 | 1444 | PF00069 | 0.620 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.511 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.351 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.450 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.387 |
MOD_PKA_2 | 897 | 903 | PF00069 | 0.450 |
MOD_PKB_1 | 502 | 510 | PF00069 | 0.437 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.440 |
MOD_Plk_1 | 1097 | 1103 | PF00069 | 0.493 |
MOD_Plk_1 | 1367 | 1373 | PF00069 | 0.683 |
MOD_Plk_1 | 1400 | 1406 | PF00069 | 0.447 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.429 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.342 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.365 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.406 |
MOD_Plk_1 | 821 | 827 | PF00069 | 0.398 |
MOD_Plk_1 | 834 | 840 | PF00069 | 0.382 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.679 |
MOD_Plk_1 | 905 | 911 | PF00069 | 0.419 |
MOD_Plk_2-3 | 1000 | 1006 | PF00069 | 0.571 |
MOD_Plk_2-3 | 1344 | 1350 | PF00069 | 0.512 |
MOD_Plk_2-3 | 461 | 467 | PF00069 | 0.484 |
MOD_Plk_2-3 | 582 | 588 | PF00069 | 0.451 |
MOD_Plk_4 | 1085 | 1091 | PF00069 | 0.432 |
MOD_Plk_4 | 1097 | 1103 | PF00069 | 0.408 |
MOD_Plk_4 | 1442 | 1448 | PF00069 | 0.454 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.402 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.597 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.431 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.361 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.481 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.406 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.495 |
MOD_Plk_4 | 794 | 800 | PF00069 | 0.423 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.571 |
MOD_Plk_4 | 821 | 827 | PF00069 | 0.398 |
MOD_Plk_4 | 900 | 906 | PF00069 | 0.432 |
MOD_Plk_4 | 911 | 917 | PF00069 | 0.556 |
MOD_ProDKin_1 | 1038 | 1044 | PF00069 | 0.664 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.688 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.348 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.423 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.424 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.319 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.459 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.499 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.662 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.593 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.642 |
MOD_ProDKin_1 | 663 | 669 | PF00069 | 0.529 |
MOD_ProDKin_1 | 785 | 791 | PF00069 | 0.389 |
MOD_ProDKin_1 | 931 | 937 | PF00069 | 0.601 |
MOD_SUMO_for_1 | 141 | 144 | PF00179 | 0.429 |
MOD_SUMO_for_1 | 578 | 581 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 1023 | 1029 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 353 | 360 | PF00179 | 0.511 |
TRG_AP2beta_CARGO_1 | 778 | 787 | PF09066 | 0.448 |
TRG_DiLeu_BaEn_1 | 1146 | 1151 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.348 |
TRG_DiLeu_BaEn_1 | 582 | 587 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_1 | 822 | 827 | PF01217 | 0.396 |
TRG_DiLeu_BaLyEn_6 | 1039 | 1044 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 404 | 409 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 728 | 733 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 779 | 784 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 1340 | 1343 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 1404 | 1407 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 694 | 697 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 855 | 858 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 1033 | 1035 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 816 | 818 | PF00400 | 0.426 |
TRG_NES_CRM1_1 | 1130 | 1143 | PF08389 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 1018 | 1023 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 1322 | 1326 | PF00026 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 407 | 411 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 782 | 786 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 817 | 822 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P678 | Leptomonas seymouri | 74% | 97% |
A0A3S7WYY1 | Leishmania donovani | 95% | 100% |
A4HEF7 | Leishmania braziliensis | 86% | 100% |
A4I1A2 | Leishmania infantum | 95% | 100% |
E9AXD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5DP89 | Trypanosoma cruzi | 50% | 100% |