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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I0Q0
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 12 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009057 | macromolecule catabolic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016579 | protein deubiquitination | 6 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 12 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 12 |
GO:0070646 | protein modification by small protein removal | 5 | 12 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 12 |
GO:0008233 | peptidase activity | 3 | 12 |
GO:0008234 | cysteine-type peptidase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 12 |
GO:0101005 | deubiquitinase activity | 5 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 468 | 472 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 588 | 592 | PF00656 | 0.653 |
CLV_C14_Caspase3-7 | 624 | 628 | PF00656 | 0.773 |
CLV_C14_Caspase3-7 | 651 | 655 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 703 | 707 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.832 |
CLV_NRD_NRD_1 | 719 | 721 | PF00675 | 0.803 |
CLV_NRD_NRD_1 | 737 | 739 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.801 |
CLV_NRD_NRD_1 | 808 | 810 | PF00675 | 0.595 |
CLV_PCSK_FUR_1 | 804 | 808 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.832 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 748 | 750 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 806 | 808 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 616 | 618 | PF00082 | 0.771 |
CLV_PCSK_PC1ET2_1 | 698 | 700 | PF00082 | 0.672 |
CLV_PCSK_PC7_1 | 804 | 810 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 683 | 687 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 695 | 699 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 738 | 742 | PF00082 | 0.684 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.637 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.618 |
DOC_CKS1_1 | 741 | 746 | PF01111 | 0.679 |
DOC_CYCLIN_RxL_1 | 4 | 15 | PF00134 | 0.687 |
DOC_CYCLIN_yCln2_LP_2 | 160 | 166 | PF00134 | 0.396 |
DOC_CYCLIN_yCln2_LP_2 | 641 | 647 | PF00134 | 0.547 |
DOC_MAPK_DCC_7 | 388 | 396 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 276 | 286 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 358 | 367 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 634 | 643 | PF00069 | 0.561 |
DOC_MAPK_HePTP_8 | 355 | 367 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 279 | 288 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 358 | 367 | PF00069 | 0.316 |
DOC_MAPK_RevD_3 | 363 | 378 | PF00069 | 0.317 |
DOC_PP1_RVXF_1 | 17 | 24 | PF00149 | 0.393 |
DOC_PP1_RVXF_1 | 386 | 393 | PF00149 | 0.320 |
DOC_PP1_RVXF_1 | 5 | 12 | PF00149 | 0.655 |
DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.396 |
DOC_PP2B_LxvP_1 | 641 | 644 | PF13499 | 0.682 |
DOC_PP4_MxPP_1 | 503 | 506 | PF00568 | 0.653 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.737 |
DOC_USP7_UBL2_3 | 287 | 291 | PF12436 | 0.438 |
DOC_USP7_UBL2_3 | 698 | 702 | PF12436 | 0.734 |
DOC_USP7_UBL2_3 | 776 | 780 | PF12436 | 0.703 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 740 | 745 | PF00397 | 0.665 |
LIG_14-3-3_CanoR_1 | 212 | 219 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 244 | 254 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 400 | 405 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 476 | 482 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 611 | 616 | PF00244 | 0.800 |
LIG_14-3-3_CanoR_1 | 748 | 754 | PF00244 | 0.673 |
LIG_Actin_WH2_2 | 686 | 704 | PF00022 | 0.664 |
LIG_AP2alpha_2 | 317 | 319 | PF02296 | 0.306 |
LIG_AP2alpha_2 | 785 | 787 | PF02296 | 0.716 |
LIG_APCC_ABBA_1 | 790 | 795 | PF00400 | 0.704 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.341 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.668 |
LIG_BRCT_BRCA1_1 | 721 | 725 | PF00533 | 0.659 |
LIG_Clathr_ClatBox_1 | 391 | 395 | PF01394 | 0.250 |
LIG_EH_1 | 790 | 794 | PF12763 | 0.699 |
LIG_EVH1_2 | 368 | 372 | PF00568 | 0.250 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.332 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.311 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.595 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.735 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.771 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.658 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.742 |
LIG_FHA_2 | 649 | 655 | PF00498 | 0.554 |
LIG_LIR_Apic_2 | 24 | 29 | PF02991 | 0.551 |
LIG_LIR_Apic_2 | 348 | 352 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 317 | 327 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 336 | 344 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 399 | 405 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 688 | 693 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 785 | 790 | PF02991 | 0.734 |
LIG_PCNA_yPIPBox_3 | 267 | 275 | PF02747 | 0.372 |
LIG_Pex14_2 | 149 | 153 | PF04695 | 0.341 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.341 |
LIG_PTB_Apo_2 | 125 | 132 | PF02174 | 0.306 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.535 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.442 |
LIG_SH2_CRK | 690 | 694 | PF00017 | 0.605 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.685 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.577 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.442 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.488 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.371 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.425 |
LIG_SH3_3 | 744 | 750 | PF00018 | 0.556 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 392 | 397 | PF11976 | 0.400 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.365 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.372 |
LIG_TRAF2_1 | 534 | 537 | PF00917 | 0.664 |
LIG_TRAF2_1 | 792 | 795 | PF00917 | 0.666 |
LIG_UBA3_1 | 197 | 206 | PF00899 | 0.365 |
LIG_UBA3_1 | 231 | 240 | PF00899 | 0.398 |
LIG_UBA3_1 | 693 | 702 | PF00899 | 0.684 |
LIG_WRC_WIRS_1 | 150 | 155 | PF05994 | 0.438 |
MOD_CDK_SPK_2 | 348 | 353 | PF00069 | 0.306 |
MOD_CDK_SPxxK_3 | 719 | 726 | PF00069 | 0.698 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.380 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.370 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.438 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.439 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.438 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.402 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.682 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.788 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.730 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.624 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.775 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.320 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.648 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.503 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.697 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.547 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.673 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.718 |
MOD_Cter_Amidation | 294 | 297 | PF01082 | 0.372 |
MOD_Cter_Amidation | 804 | 807 | PF01082 | 0.568 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.410 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.607 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.285 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.726 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.528 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.774 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.686 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.466 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.744 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.356 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.442 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.370 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.364 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.424 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.502 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.733 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.750 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.627 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.705 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.719 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.615 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.745 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.545 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.386 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.652 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.673 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.638 |
MOD_N-GLC_2 | 128 | 130 | PF02516 | 0.312 |
MOD_N-GLC_2 | 568 | 570 | PF02516 | 0.558 |
MOD_N-GLC_2 | 648 | 650 | PF02516 | 0.736 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.521 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.316 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.344 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.295 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.438 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.435 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.400 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.344 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.424 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.364 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.684 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.708 |
MOD_NEK2_2 | 685 | 690 | PF00069 | 0.729 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.462 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.396 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.719 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.540 |
MOD_PK_1 | 206 | 212 | PF00069 | 0.423 |
MOD_PK_1 | 361 | 367 | PF00069 | 0.442 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.442 |
MOD_PKA_1 | 494 | 500 | PF00069 | 0.605 |
MOD_PKA_1 | 77 | 83 | PF00069 | 0.567 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.509 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.440 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.389 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.374 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.673 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.631 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.567 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.421 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.377 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.713 |
MOD_Plk_2-3 | 446 | 452 | PF00069 | 0.475 |
MOD_Plk_2-3 | 627 | 633 | PF00069 | 0.704 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.321 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.396 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.372 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.728 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.531 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.294 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.306 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.423 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.468 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.372 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.665 |
MOD_ProDKin_1 | 740 | 746 | PF00069 | 0.669 |
MOD_SUMO_for_1 | 286 | 289 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 282 | 288 | PF00179 | 0.365 |
MOD_SUMO_rev_2 | 289 | 298 | PF00179 | 0.365 |
TRG_DiLeu_BaEn_1 | 270 | 275 | PF01217 | 0.365 |
TRG_DiLeu_BaEn_1 | 549 | 554 | PF01217 | 0.588 |
TRG_DiLeu_BaEn_1 | 580 | 585 | PF01217 | 0.709 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 690 | 693 | PF00928 | 0.605 |
TRG_ER_diArg_1 | 747 | 749 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.795 |
TRG_ER_diArg_1 | 803 | 806 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 807 | 809 | PF00400 | 0.574 |
TRG_NES_CRM1_1 | 159 | 172 | PF08389 | 0.442 |
TRG_NES_CRM1_1 | 758 | 770 | PF08389 | 0.672 |
TRG_NLS_MonoExtN_4 | 358 | 364 | PF00514 | 0.438 |
TRG_NLS_MonoExtN_4 | 773 | 779 | PF00514 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.672 |
TRG_Pf-PMV_PEXEL_1 | 699 | 703 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Z2 | Leptomonas seymouri | 62% | 100% |
A0A0S4JHR5 | Bodo saltans | 35% | 100% |
A0A1X0NIL8 | Trypanosomatidae | 38% | 100% |
A0A3S7WY54 | Leishmania donovani | 100% | 100% |
A0A422P3Z4 | Trypanosoma rangeli | 39% | 100% |
A4HDC0 | Leishmania braziliensis | 76% | 99% |
D0A726 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AWQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QAS1 | Leishmania major | 92% | 100% |
V5BR83 | Trypanosoma cruzi | 37% | 100% |