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:0000151 | ubiquitin ligase complex | 3 | 2 |
GO:0005930 | axoneme | 2 | 2 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 2 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
GO:0005929 | cilium | 4 | 6 |
GO:0042995 | cell projection | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 6 |
Related structures:
AlphaFold database: Q4QHX1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 722 | 726 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 781 | 785 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 875 | 877 | PF00675 | 0.686 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 875 | 877 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 934 | 936 | PF00082 | 0.746 |
CLV_PCSK_PC1ET2_1 | 586 | 588 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 934 | 936 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.581 |
CLV_Separin_Metazoa | 520 | 524 | PF03568 | 0.502 |
DEG_APCC_DBOX_1 | 461 | 469 | PF00400 | 0.524 |
DEG_APCC_DBOX_1 | 495 | 503 | PF00400 | 0.592 |
DEG_APCC_DBOX_1 | 698 | 706 | PF00400 | 0.577 |
DOC_CDC14_PxL_1 | 289 | 297 | PF14671 | 0.507 |
DOC_CKS1_1 | 35 | 40 | PF01111 | 0.560 |
DOC_CYCLIN_RxL_1 | 320 | 329 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 447 | 455 | PF00134 | 0.415 |
DOC_CYCLIN_RxL_1 | 735 | 748 | PF00134 | 0.655 |
DOC_CYCLIN_yCln2_LP_2 | 401 | 404 | PF00134 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 831 | 837 | PF00134 | 0.698 |
DOC_CYCLIN_yCln2_LP_2 | 870 | 873 | PF00134 | 0.699 |
DOC_MAPK_DCC_7 | 323 | 332 | PF00069 | 0.516 |
DOC_MAPK_DCC_7 | 484 | 493 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 419 | 428 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 484 | 493 | PF00069 | 0.500 |
DOC_MAPK_HePTP_8 | 481 | 493 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 323 | 332 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 484 | 493 | PF00069 | 0.544 |
DOC_PP2B_LxvP_1 | 325 | 328 | PF13499 | 0.402 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.443 |
DOC_PP2B_LxvP_1 | 489 | 492 | PF13499 | 0.466 |
DOC_PP2B_LxvP_1 | 502 | 505 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 826 | 829 | PF13499 | 0.686 |
DOC_PP2B_LxvP_1 | 831 | 834 | PF13499 | 0.658 |
DOC_PP2B_LxvP_1 | 870 | 873 | PF13499 | 0.699 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.824 |
DOC_USP7_MATH_1 | 854 | 858 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 929 | 933 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 943 | 947 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 975 | 979 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 988 | 992 | PF00917 | 0.631 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 860 | 865 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 875 | 880 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 891 | 896 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 901 | 906 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 12 | 22 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 234 | 243 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 422 | 427 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 433 | 441 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 496 | 505 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 506 | 512 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 540 | 545 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 604 | 611 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 875 | 879 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 95 | 104 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 958 | 966 | PF00244 | 0.749 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.725 |
LIG_BIR_III_4 | 849 | 853 | PF00653 | 0.667 |
LIG_BRCT_BRCA1_1 | 270 | 274 | PF00533 | 0.481 |
LIG_BRCT_BRCA1_1 | 542 | 546 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 802 | 806 | PF00533 | 0.726 |
LIG_BRCT_BRCA1_1 | 945 | 949 | PF00533 | 0.677 |
LIG_FAT_LD_1 | 468 | 476 | PF03623 | 0.458 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.493 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.633 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.476 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.457 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.294 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.372 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.502 |
LIG_FHA_1 | 660 | 666 | PF00498 | 0.533 |
LIG_FHA_1 | 823 | 829 | PF00498 | 0.678 |
LIG_FHA_1 | 967 | 973 | PF00498 | 0.571 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.562 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.549 |
LIG_FHA_2 | 779 | 785 | PF00498 | 0.714 |
LIG_FHA_2 | 876 | 882 | PF00498 | 0.689 |
LIG_GBD_Chelix_1 | 665 | 673 | PF00786 | 0.464 |
LIG_Integrin_isoDGR_2 | 526 | 528 | PF01839 | 0.619 |
LIG_LIR_LC3C_4 | 329 | 332 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 946 | 952 | PF02991 | 0.678 |
LIG_MAD2 | 450 | 458 | PF02301 | 0.408 |
LIG_NRBOX | 231 | 237 | PF00104 | 0.522 |
LIG_NRBOX | 339 | 345 | PF00104 | 0.501 |
LIG_PCNA_yPIPBox_3 | 183 | 191 | PF02747 | 0.500 |
LIG_Pex14_2 | 270 | 274 | PF04695 | 0.481 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.442 |
LIG_SH2_STAT3 | 130 | 133 | PF00017 | 0.522 |
LIG_SH2_STAT3 | 916 | 919 | PF00017 | 0.686 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 916 | 919 | PF00017 | 0.718 |
LIG_SH3_1 | 876 | 882 | PF00018 | 0.706 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.582 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.761 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.593 |
LIG_SH3_3 | 658 | 664 | PF00018 | 0.559 |
LIG_SH3_3 | 831 | 837 | PF00018 | 0.697 |
LIG_SH3_3 | 858 | 864 | PF00018 | 0.660 |
LIG_SH3_3 | 876 | 882 | PF00018 | 0.549 |
LIG_SUMO_SIM_anti_2 | 122 | 129 | PF11976 | 0.648 |
LIG_SUMO_SIM_anti_2 | 396 | 401 | PF11976 | 0.394 |
LIG_SUMO_SIM_anti_2 | 466 | 474 | PF11976 | 0.520 |
LIG_SUMO_SIM_anti_2 | 597 | 602 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 122 | 129 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 374 | 379 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 424 | 429 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 824 | 830 | PF11976 | 0.681 |
LIG_TRAF2_1 | 920 | 923 | PF00917 | 0.780 |
LIG_TRAF2_1 | 994 | 997 | PF00917 | 0.777 |
LIG_WRC_WIRS_1 | 205 | 210 | PF05994 | 0.416 |
LIG_WRC_WIRS_1 | 267 | 272 | PF05994 | 0.441 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.661 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.420 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.432 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.558 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.516 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.538 |
MOD_CK1_1 | 693 | 699 | PF00069 | 0.596 |
MOD_CK1_1 | 714 | 720 | PF00069 | 0.643 |
MOD_CK1_1 | 776 | 782 | PF00069 | 0.691 |
MOD_CK1_1 | 821 | 827 | PF00069 | 0.737 |
MOD_CK1_1 | 904 | 910 | PF00069 | 0.717 |
MOD_CK1_1 | 911 | 917 | PF00069 | 0.660 |
MOD_CK1_1 | 960 | 966 | PF00069 | 0.797 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.563 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.667 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.419 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.567 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.558 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.663 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.551 |
MOD_GlcNHglycan | 377 | 381 | PF01048 | 0.513 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.534 |
MOD_GlcNHglycan | 427 | 431 | PF01048 | 0.452 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.453 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.665 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.801 |
MOD_GlcNHglycan | 711 | 714 | PF01048 | 0.551 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.653 |
MOD_GlcNHglycan | 788 | 792 | PF01048 | 0.746 |
MOD_GlcNHglycan | 820 | 823 | PF01048 | 0.696 |
MOD_GlcNHglycan | 856 | 859 | PF01048 | 0.639 |
MOD_GlcNHglycan | 945 | 948 | PF01048 | 0.762 |
MOD_GlcNHglycan | 977 | 980 | PF01048 | 0.588 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.495 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.483 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.643 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.532 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.274 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.517 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.707 |
MOD_GSK3_1 | 818 | 825 | PF00069 | 0.623 |
MOD_GSK3_1 | 903 | 910 | PF00069 | 0.733 |
MOD_GSK3_1 | 914 | 921 | PF00069 | 0.660 |
MOD_GSK3_1 | 929 | 936 | PF00069 | 0.569 |
MOD_GSK3_1 | 957 | 964 | PF00069 | 0.812 |
MOD_GSK3_1 | 966 | 973 | PF00069 | 0.594 |
MOD_LATS_1 | 266 | 272 | PF00433 | 0.499 |
MOD_LATS_1 | 574 | 580 | PF00433 | 0.532 |
MOD_N-GLC_2 | 580 | 582 | PF02516 | 0.366 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.697 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.563 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.426 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.447 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.406 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.359 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.510 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.410 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.458 |
MOD_NEK2_1 | 778 | 783 | PF00069 | 0.811 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.645 |
MOD_NEK2_1 | 874 | 879 | PF00069 | 0.617 |
MOD_NEK2_1 | 933 | 938 | PF00069 | 0.806 |
MOD_NEK2_2 | 142 | 147 | PF00069 | 0.496 |
MOD_NEK2_2 | 929 | 934 | PF00069 | 0.726 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.571 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.520 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.541 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.567 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.470 |
MOD_PIKK_1 | 918 | 924 | PF00454 | 0.706 |
MOD_PK_1 | 268 | 274 | PF00069 | 0.494 |
MOD_PK_1 | 540 | 546 | PF00069 | 0.517 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.522 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.675 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.556 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.524 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.550 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.536 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.560 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.458 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.738 |
MOD_PKA_2 | 874 | 880 | PF00069 | 0.680 |
MOD_PKA_2 | 957 | 963 | PF00069 | 0.730 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.480 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.503 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.416 |
MOD_Plk_1 | 635 | 641 | PF00069 | 0.523 |
MOD_Plk_1 | 988 | 994 | PF00069 | 0.639 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.440 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.526 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.368 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.618 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.529 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.563 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.470 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.544 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.562 |
MOD_Plk_4 | 773 | 779 | PF00069 | 0.692 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.524 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.791 |
MOD_ProDKin_1 | 860 | 866 | PF00069 | 0.766 |
MOD_ProDKin_1 | 875 | 881 | PF00069 | 0.598 |
MOD_ProDKin_1 | 891 | 897 | PF00069 | 0.765 |
MOD_ProDKin_1 | 901 | 907 | PF00069 | 0.716 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.545 |
TRG_DiLeu_BaEn_1 | 122 | 127 | PF01217 | 0.643 |
TRG_DiLeu_BaEn_4 | 122 | 128 | PF01217 | 0.648 |
TRG_DiLeu_BaEn_4 | 73 | 79 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 231 | 236 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 339 | 344 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 130 | 132 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 522 | 524 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 874 | 876 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.529 |
TRG_NES_CRM1_1 | 647 | 659 | PF08389 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 450 | 455 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 604 | 608 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 612 | 616 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 640 | 644 | PF00026 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 740 | 745 | PF00026 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 935 | 939 | PF00026 | 0.737 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQP1 | Leishmania donovani | 92% | 100% |
A0A422NV64 | Trypanosoma rangeli | 28% | 92% |
A4H5N0 | Leishmania braziliensis | 70% | 100% |
A4HTW7 | Leishmania infantum | 92% | 100% |
D0A9D1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 95% |
E9AMQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |