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: E9AMQ4
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 | 0.632 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.526 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.486 |
CLV_C14_Caspase3-7 | 714 | 718 | PF00656 | 0.684 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.618 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 926 | 928 | PF00082 | 0.797 |
CLV_PCSK_PC1ET2_1 | 578 | 580 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 926 | 928 | PF00082 | 0.797 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.776 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 691 | 695 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.622 |
CLV_Separin_Metazoa | 512 | 516 | PF03568 | 0.531 |
DEG_APCC_DBOX_1 | 453 | 461 | PF00400 | 0.525 |
DEG_APCC_DBOX_1 | 487 | 495 | PF00400 | 0.602 |
DEG_SPOP_SBC_1 | 353 | 357 | PF00917 | 0.437 |
DOC_CDC14_PxL_1 | 282 | 290 | PF14671 | 0.570 |
DOC_CYCLIN_RxL_1 | 313 | 322 | PF00134 | 0.583 |
DOC_CYCLIN_RxL_1 | 439 | 447 | PF00134 | 0.448 |
DOC_CYCLIN_RxL_1 | 727 | 740 | PF00134 | 0.706 |
DOC_CYCLIN_yCln2_LP_2 | 393 | 396 | PF00134 | 0.573 |
DOC_CYCLIN_yCln2_LP_2 | 823 | 829 | PF00134 | 0.732 |
DOC_CYCLIN_yCln2_LP_2 | 862 | 865 | PF00134 | 0.725 |
DOC_CYCLIN_yCln2_LP_2 | 894 | 900 | PF00134 | 0.516 |
DOC_MAPK_DCC_7 | 316 | 325 | PF00069 | 0.580 |
DOC_MAPK_DCC_7 | 476 | 485 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 411 | 420 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 476 | 485 | PF00069 | 0.506 |
DOC_MAPK_HePTP_8 | 473 | 485 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.580 |
DOC_MAPK_MEF2A_6 | 476 | 485 | PF00069 | 0.550 |
DOC_PP2B_LxvP_1 | 318 | 321 | PF13499 | 0.432 |
DOC_PP2B_LxvP_1 | 392 | 395 | PF13499 | 0.497 |
DOC_PP2B_LxvP_1 | 481 | 484 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 494 | 497 | PF13499 | 0.495 |
DOC_PP2B_LxvP_1 | 818 | 821 | PF13499 | 0.712 |
DOC_PP2B_LxvP_1 | 823 | 826 | PF13499 | 0.673 |
DOC_PP2B_LxvP_1 | 862 | 865 | PF13499 | 0.725 |
DOC_PP4_FxxP_1 | 979 | 982 | PF00568 | 0.616 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 846 | 850 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 935 | 939 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 940 | 944 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 953 | 957 | PF00917 | 0.805 |
DOC_USP7_MATH_2 | 352 | 358 | PF00917 | 0.436 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 852 | 857 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 867 | 872 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 883 | 888 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 893 | 898 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 949 | 954 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 10 | 18 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 186 | 194 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 229 | 238 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 261 | 266 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 414 | 419 | PF00244 | 0.348 |
LIG_14-3-3_CanoR_1 | 425 | 433 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 498 | 504 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 532 | 537 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 554 | 562 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 596 | 603 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 90 | 99 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 957 | 967 | PF00244 | 0.674 |
LIG_APCC_Cbox_2 | 61 | 67 | PF00515 | 0.354 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.769 |
LIG_BRCT_BRCA1_1 | 263 | 267 | PF00533 | 0.541 |
LIG_BRCT_BRCA1_1 | 534 | 538 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_1 | 794 | 798 | PF00533 | 0.774 |
LIG_BRCT_BRCA1_1 | 937 | 941 | PF00533 | 0.704 |
LIG_FAT_LD_1 | 460 | 468 | PF03623 | 0.498 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.443 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.547 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.495 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.713 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.641 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.535 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.524 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.261 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.519 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.590 |
LIG_FHA_1 | 744 | 750 | PF00498 | 0.534 |
LIG_FHA_1 | 815 | 821 | PF00498 | 0.768 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.567 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.534 |
LIG_FHA_2 | 868 | 874 | PF00498 | 0.791 |
LIG_GBD_Chelix_1 | 657 | 665 | PF00786 | 0.507 |
LIG_Integrin_isoDGR_2 | 518 | 520 | PF01839 | 0.661 |
LIG_LIR_Apic_2 | 905 | 911 | PF02991 | 0.525 |
LIG_LIR_Apic_2 | 977 | 982 | PF02991 | 0.616 |
LIG_LIR_LC3C_4 | 322 | 325 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 938 | 944 | PF02991 | 0.711 |
LIG_MAD2 | 442 | 450 | PF02301 | 0.443 |
LIG_NRBOX | 226 | 232 | PF00104 | 0.577 |
LIG_NRBOX | 332 | 338 | PF00104 | 0.559 |
LIG_NRBOX | 404 | 410 | PF00104 | 0.269 |
LIG_PCNA_yPIPBox_3 | 178 | 186 | PF02747 | 0.516 |
LIG_Pex14_2 | 263 | 267 | PF04695 | 0.541 |
LIG_Pex14_2 | 979 | 983 | PF04695 | 0.620 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.488 |
LIG_SH2_CRK | 908 | 912 | PF00017 | 0.599 |
LIG_SH2_NCK_1 | 908 | 912 | PF00017 | 0.531 |
LIG_SH2_STAT3 | 125 | 128 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 908 | 911 | PF00017 | 0.744 |
LIG_SH3_1 | 868 | 874 | PF00018 | 0.745 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.674 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.588 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.761 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.633 |
LIG_SH3_3 | 650 | 656 | PF00018 | 0.616 |
LIG_SH3_3 | 822 | 828 | PF00018 | 0.721 |
LIG_SH3_3 | 868 | 874 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 117 | 124 | PF11976 | 0.710 |
LIG_SUMO_SIM_anti_2 | 388 | 393 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 458 | 466 | PF11976 | 0.526 |
LIG_SUMO_SIM_anti_2 | 589 | 594 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 117 | 124 | PF11976 | 0.682 |
LIG_SUMO_SIM_par_1 | 366 | 371 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 416 | 421 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 442 | 447 | PF11976 | 0.572 |
LIG_SUMO_SIM_par_1 | 816 | 822 | PF11976 | 0.705 |
LIG_TRAF2_1 | 870 | 873 | PF00917 | 0.790 |
LIG_TRAF2_1 | 912 | 915 | PF00917 | 0.834 |
LIG_TRAF2_1 | 982 | 985 | PF00917 | 0.799 |
LIG_WRC_WIRS_1 | 200 | 205 | PF05994 | 0.425 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.457 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.689 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.457 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.438 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.408 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.599 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.508 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.593 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.596 |
MOD_CK1_1 | 706 | 712 | PF00069 | 0.626 |
MOD_CK1_1 | 754 | 760 | PF00069 | 0.643 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.720 |
MOD_CK1_1 | 813 | 819 | PF00069 | 0.762 |
MOD_CK1_1 | 896 | 902 | PF00069 | 0.733 |
MOD_CK1_1 | 903 | 909 | PF00069 | 0.699 |
MOD_CK1_1 | 917 | 923 | PF00069 | 0.691 |
MOD_CK1_1 | 925 | 931 | PF00069 | 0.661 |
MOD_CK1_1 | 952 | 958 | PF00069 | 0.744 |
MOD_CK1_1 | 959 | 965 | PF00069 | 0.579 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.660 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.433 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.573 |
MOD_CK2_1 | 866 | 872 | PF00069 | 0.810 |
MOD_CK2_1 | 909 | 915 | PF00069 | 0.775 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.659 |
MOD_GlcNHglycan | 248 | 252 | PF01048 | 0.615 |
MOD_GlcNHglycan | 369 | 373 | PF01048 | 0.583 |
MOD_GlcNHglycan | 419 | 423 | PF01048 | 0.453 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.471 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.666 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.709 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.680 |
MOD_GlcNHglycan | 703 | 706 | PF01048 | 0.694 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.693 |
MOD_GlcNHglycan | 779 | 784 | PF01048 | 0.791 |
MOD_GlcNHglycan | 812 | 815 | PF01048 | 0.756 |
MOD_GlcNHglycan | 902 | 905 | PF01048 | 0.659 |
MOD_GlcNHglycan | 919 | 922 | PF01048 | 0.611 |
MOD_GlcNHglycan | 937 | 940 | PF01048 | 0.719 |
MOD_GlcNHglycan | 958 | 961 | PF01048 | 0.756 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.564 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.599 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.631 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.474 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.574 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.232 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.542 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.693 |
MOD_GSK3_1 | 810 | 817 | PF00069 | 0.616 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.797 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.716 |
MOD_GSK3_1 | 906 | 913 | PF00069 | 0.720 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.775 |
MOD_LATS_1 | 259 | 265 | PF00433 | 0.559 |
MOD_LATS_1 | 566 | 572 | PF00433 | 0.596 |
MOD_N-GLC_2 | 572 | 574 | PF02516 | 0.394 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.597 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.452 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.459 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.434 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.428 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.353 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.464 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.454 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.490 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.480 |
MOD_NEK2_1 | 770 | 775 | PF00069 | 0.805 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.625 |
MOD_NEK2_1 | 866 | 871 | PF00069 | 0.793 |
MOD_NEK2_1 | 898 | 903 | PF00069 | 0.643 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.612 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.531 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.590 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.588 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.596 |
MOD_PIKK_1 | 906 | 912 | PF00454 | 0.799 |
MOD_PK_1 | 261 | 267 | PF00069 | 0.554 |
MOD_PK_1 | 532 | 538 | PF00069 | 0.568 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.521 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.609 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.557 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.564 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.554 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.498 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.757 |
MOD_PKA_2 | 956 | 962 | PF00069 | 0.665 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.561 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.596 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.533 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.429 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.479 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.580 |
MOD_Plk_1 | 858 | 864 | PF00069 | 0.692 |
MOD_Plk_2-3 | 354 | 360 | PF00069 | 0.419 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.258 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.430 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.537 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.384 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.554 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.564 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.503 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.492 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.647 |
MOD_Plk_4 | 765 | 771 | PF00069 | 0.753 |
MOD_Plk_4 | 858 | 864 | PF00069 | 0.678 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.603 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.646 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.783 |
MOD_ProDKin_1 | 852 | 858 | PF00069 | 0.756 |
MOD_ProDKin_1 | 867 | 873 | PF00069 | 0.829 |
MOD_ProDKin_1 | 883 | 889 | PF00069 | 0.727 |
MOD_ProDKin_1 | 893 | 899 | PF00069 | 0.688 |
MOD_ProDKin_1 | 949 | 955 | PF00069 | 0.687 |
MOD_SUMO_for_1 | 65 | 68 | PF00179 | 0.505 |
TRG_DiLeu_BaEn_1 | 117 | 122 | PF01217 | 0.658 |
TRG_DiLeu_BaEn_4 | 117 | 123 | PF01217 | 0.709 |
TRG_DiLeu_BaEn_4 | 68 | 74 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.473 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.573 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.618 |
TRG_NES_CRM1_1 | 639 | 651 | PF08389 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 442 | 447 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 596 | 600 | PF00026 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 604 | 608 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 632 | 636 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 732 | 737 | PF00026 | 0.701 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 927 | 931 | PF00026 | 0.788 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NN23 | Trypanosomatidae | 28% | 76% |
A0A3S7WQP1 | Leishmania donovani | 88% | 99% |
A0A422NV64 | Trypanosoma rangeli | 26% | 91% |
A4H5N0 | Leishmania braziliensis | 68% | 98% |
A4HTW7 | Leishmania infantum | 88% | 99% |
D0A9D1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 94% |
Q4QHX1 | Leishmania major | 88% | 100% |