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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 8 |
GO:0042995 | cell projection | 2 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 8 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4H5N0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 17 | 21 | PF00656 | 0.638 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.454 |
CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.491 |
CLV_C14_Caspase3-7 | 605 | 609 | PF00656 | 0.371 |
CLV_C14_Caspase3-7 | 722 | 726 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 940 | 942 | PF00675 | 0.565 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 920 | 922 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 940 | 942 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 920 | 922 | PF00082 | 0.790 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.762 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 917 | 921 | PF00082 | 0.799 |
DEG_APCC_DBOX_1 | 459 | 467 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 493 | 501 | PF00400 | 0.586 |
DEG_SPOP_SBC_1 | 777 | 781 | PF00917 | 0.536 |
DOC_CDC14_PxL_1 | 288 | 296 | PF14671 | 0.579 |
DOC_CYCLIN_RxL_1 | 319 | 328 | PF00134 | 0.580 |
DOC_CYCLIN_RxL_1 | 445 | 453 | PF00134 | 0.445 |
DOC_CYCLIN_RxL_1 | 735 | 748 | PF00134 | 0.706 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 402 | PF00134 | 0.572 |
DOC_MAPK_DCC_7 | 322 | 331 | PF00069 | 0.574 |
DOC_MAPK_DCC_7 | 482 | 491 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 417 | 426 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 482 | 491 | PF00069 | 0.497 |
DOC_MAPK_HePTP_8 | 479 | 491 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 10 | 18 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 322 | 331 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 405 | 414 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 462 | 470 | PF00069 | 0.317 |
DOC_MAPK_MEF2A_6 | 482 | 491 | PF00069 | 0.541 |
DOC_PP2B_LxvP_1 | 324 | 327 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 38 | 41 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.497 |
DOC_PP2B_LxvP_1 | 487 | 490 | PF13499 | 0.526 |
DOC_PP2B_LxvP_1 | 500 | 503 | PF13499 | 0.480 |
DOC_PP4_MxPP_1 | 44 | 47 | PF00568 | 0.519 |
DOC_SPAK_OSR1_1 | 557 | 561 | PF12202 | 0.321 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 787 | 791 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 800 | 804 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 915 | 919 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 929 | 933 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 947 | 951 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 979 | 983 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 758 | 763 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 878 | 883 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 887 | 892 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 943 | 948 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 259 | 265 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 405 | 412 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 420 | 425 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 431 | 439 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 504 | 510 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 538 | 543 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 557 | 565 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 604 | 611 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 766 | 770 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 94 | 103 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 940 | 944 | PF00244 | 0.764 |
LIG_APCC_ABBA_1 | 968 | 973 | PF00400 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.776 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.549 |
LIG_BRCT_BRCA1_1 | 540 | 544 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 802 | 806 | PF00533 | 0.791 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.558 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.492 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.572 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.595 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.528 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.529 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.543 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.254 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.597 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.308 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.518 |
LIG_FHA_1 | 660 | 666 | PF00498 | 0.584 |
LIG_FHA_1 | 762 | 768 | PF00498 | 0.559 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.469 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.413 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.574 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.563 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.514 |
LIG_Integrin_isoDGR_2 | 524 | 526 | PF01839 | 0.655 |
LIG_LIR_Gen_1 | 226 | 233 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 467 | 478 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 552 | 560 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 591 | 600 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 863 | 872 | PF02991 | 0.715 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 552 | 558 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 591 | 595 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 863 | 867 | PF02991 | 0.720 |
LIG_MAD2 | 448 | 456 | PF02301 | 0.439 |
LIG_NRBOX | 232 | 238 | PF00104 | 0.623 |
LIG_NRBOX | 338 | 344 | PF00104 | 0.543 |
LIG_PCNA_yPIPBox_3 | 504 | 514 | PF02747 | 0.328 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.549 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.529 |
LIG_SH2_CRK | 227 | 231 | PF00017 | 0.448 |
LIG_SH2_NCK_1 | 227 | 231 | PF00017 | 0.361 |
LIG_SH2_SRC | 353 | 356 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.447 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.666 |
LIG_SH3_3 | 658 | 664 | PF00018 | 0.610 |
LIG_SH3_3 | 756 | 762 | PF00018 | 0.631 |
LIG_SUMO_SIM_anti_2 | 121 | 129 | PF11976 | 0.676 |
LIG_SUMO_SIM_anti_2 | 396 | 401 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 464 | 472 | PF11976 | 0.520 |
LIG_SUMO_SIM_anti_2 | 597 | 602 | PF11976 | 0.556 |
LIG_SUMO_SIM_par_1 | 12 | 20 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 121 | 129 | PF11976 | 0.647 |
LIG_SUMO_SIM_par_1 | 372 | 377 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 383 | 388 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 422 | 427 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 448 | 453 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 857 | 863 | PF11976 | 0.602 |
LIG_TRAF2_1 | 863 | 866 | PF00917 | 0.784 |
LIG_TRAF2_1 | 906 | 909 | PF00917 | 0.810 |
LIG_TRAF2_1 | 911 | 914 | PF00917 | 0.733 |
LIG_TRAF2_1 | 985 | 988 | PF00917 | 0.808 |
LIG_TYR_ITIM | 225 | 230 | PF00017 | 0.440 |
LIG_UBA3_1 | 123 | 130 | PF00899 | 0.435 |
LIG_WRC_WIRS_1 | 266 | 271 | PF05994 | 0.470 |
LIG_WRC_WIRS_1 | 589 | 594 | PF05994 | 0.357 |
LIG_WRC_WIRS_1 | 861 | 866 | PF05994 | 0.724 |
LIG_WW_3 | 40 | 44 | PF00397 | 0.640 |
MOD_CDK_SPK_2 | 758 | 763 | PF00069 | 0.513 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.501 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.621 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.459 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.445 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.595 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.500 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.391 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.609 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.291 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.585 |
MOD_CK1_1 | 761 | 767 | PF00069 | 0.623 |
MOD_CK1_1 | 821 | 827 | PF00069 | 0.785 |
MOD_CK1_1 | 844 | 850 | PF00069 | 0.593 |
MOD_CK1_1 | 860 | 866 | PF00069 | 0.550 |
MOD_CK1_1 | 878 | 884 | PF00069 | 0.811 |
MOD_CK1_1 | 890 | 896 | PF00069 | 0.726 |
MOD_CK1_1 | 897 | 903 | PF00069 | 0.687 |
MOD_CK1_1 | 942 | 948 | PF00069 | 0.765 |
MOD_CK1_1 | 950 | 956 | PF00069 | 0.635 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.676 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.429 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.569 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.541 |
MOD_CK2_1 | 765 | 771 | PF00069 | 0.539 |
MOD_CK2_1 | 787 | 793 | PF00069 | 0.651 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.779 |
MOD_CK2_1 | 903 | 909 | PF00069 | 0.760 |
MOD_DYRK1A_RPxSP_1 | 758 | 762 | PF00069 | 0.506 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.514 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.541 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.666 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.516 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.619 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.551 |
MOD_GlcNHglycan | 360 | 364 | PF01048 | 0.575 |
MOD_GlcNHglycan | 375 | 379 | PF01048 | 0.574 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.258 |
MOD_GlcNHglycan | 425 | 429 | PF01048 | 0.444 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.444 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.495 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.460 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.708 |
MOD_GlcNHglycan | 711 | 714 | PF01048 | 0.681 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.688 |
MOD_GlcNHglycan | 788 | 792 | PF01048 | 0.796 |
MOD_GlcNHglycan | 820 | 823 | PF01048 | 0.783 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.668 |
MOD_GlcNHglycan | 896 | 899 | PF01048 | 0.646 |
MOD_GlcNHglycan | 931 | 934 | PF01048 | 0.724 |
MOD_GlcNHglycan | 949 | 952 | PF01048 | 0.810 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.713 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.563 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.637 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.467 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.362 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.571 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.225 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.539 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.412 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.396 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.660 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.518 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.790 |
MOD_GSK3_1 | 915 | 922 | PF00069 | 0.795 |
MOD_GSK3_1 | 939 | 946 | PF00069 | 0.762 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.713 |
MOD_LATS_1 | 265 | 271 | PF00433 | 0.571 |
MOD_LATS_1 | 572 | 578 | PF00433 | 0.586 |
MOD_N-GLC_1 | 440 | 445 | PF02516 | 0.471 |
MOD_N-GLC_1 | 841 | 846 | PF02516 | 0.621 |
MOD_N-GLC_2 | 275 | 277 | PF02516 | 0.352 |
MOD_N-GLC_2 | 370 | 372 | PF02516 | 0.326 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.707 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.563 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.444 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.472 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.345 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.707 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.425 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.402 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.430 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.344 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.464 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.450 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.478 |
MOD_NEK2_1 | 778 | 783 | PF00069 | 0.787 |
MOD_NEK2_1 | 831 | 836 | PF00069 | 0.781 |
MOD_NEK2_2 | 260 | 265 | PF00069 | 0.478 |
MOD_NEK2_2 | 533 | 538 | PF00069 | 0.409 |
MOD_NEK2_2 | 684 | 689 | PF00069 | 0.461 |
MOD_NEK2_2 | 915 | 920 | PF00069 | 0.761 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.535 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.311 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.583 |
MOD_PIKK_1 | 558 | 564 | PF00454 | 0.584 |
MOD_PIKK_1 | 875 | 881 | PF00454 | 0.565 |
MOD_PIKK_1 | 900 | 906 | PF00454 | 0.789 |
MOD_PK_1 | 111 | 117 | PF00069 | 0.388 |
MOD_PK_1 | 267 | 273 | PF00069 | 0.564 |
MOD_PK_1 | 538 | 544 | PF00069 | 0.565 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.642 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.534 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.559 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.548 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.647 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.749 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.755 |
MOD_PKA_2 | 939 | 945 | PF00069 | 0.749 |
MOD_PKA_2 | 953 | 959 | PF00069 | 0.649 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.581 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.499 |
MOD_Plk_1 | 545 | 551 | PF00069 | 0.471 |
MOD_Plk_1 | 635 | 641 | PF00069 | 0.576 |
MOD_Plk_1 | 979 | 985 | PF00069 | 0.657 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.535 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.720 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.565 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.557 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.549 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.371 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.612 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.641 |
MOD_ProDKin_1 | 758 | 764 | PF00069 | 0.515 |
MOD_ProDKin_1 | 878 | 884 | PF00069 | 0.715 |
MOD_ProDKin_1 | 887 | 893 | PF00069 | 0.687 |
MOD_ProDKin_1 | 943 | 949 | PF00069 | 0.680 |
MOD_SUMO_for_1 | 69 | 72 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 375 | 384 | PF00179 | 0.326 |
TRG_DiLeu_BaEn_1 | 121 | 126 | PF01217 | 0.621 |
TRG_DiLeu_BaEn_4 | 121 | 127 | PF01217 | 0.674 |
TRG_DiLeu_BaEn_4 | 534 | 540 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_4 | 72 | 78 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.597 |
TRG_DiLeu_BaLyEn_6 | 232 | 237 | PF01217 | 0.617 |
TRG_DiLeu_BaLyEn_6 | 737 | 742 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 343 | 346 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 520 | 522 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 671 | 673 | PF00400 | 0.449 |
TRG_NES_CRM1_1 | 365 | 380 | PF08389 | 0.333 |
TRG_NES_CRM1_1 | 647 | 659 | PF08389 | 0.551 |
TRG_NES_CRM1_1 | 973 | 987 | PF08389 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 235 | 240 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 448 | 453 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 557 | 562 | PF00026 | 0.316 |
TRG_Pf-PMV_PEXEL_1 | 604 | 608 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 640 | 644 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 671 | 675 | PF00026 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 740 | 745 | PF00026 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 921 | 925 | PF00026 | 0.782 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NN23 | Trypanosomatidae | 27% | 76% |
A0A3S7WQP1 | Leishmania donovani | 71% | 99% |
A0A422NV64 | Trypanosoma rangeli | 27% | 91% |
A4HTW7 | Leishmania infantum | 71% | 99% |
D0A9D1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 94% |
E9AMQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
Q4QHX1 | Leishmania major | 70% | 99% |