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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005829 | cytosol | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AWQ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 13 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009056 | catabolic process | 2 | 13 |
GO:0009057 | macromolecule catabolic process | 4 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016579 | protein deubiquitination | 6 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044248 | cellular catabolic process | 3 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 13 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 13 |
GO:0070646 | protein modification by small protein removal | 5 | 13 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:1901575 | organic substance catabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 13 |
GO:0008233 | peptidase activity | 3 | 13 |
GO:0008234 | cysteine-type peptidase activity | 4 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 13 |
GO:0101005 | deubiquitinase activity | 5 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:0004175 | endopeptidase activity | 4 | 2 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.385 |
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.385 |
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.384 |
CLV_C14_Caspase3-7 | 621 | 625 | PF00656 | 0.756 |
CLV_C14_Caspase3-7 | 63 | 67 | PF00656 | 0.720 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.818 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 805 | 807 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.582 |
CLV_PCSK_FUR_1 | 801 | 805 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 638 | 640 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.818 |
CLV_PCSK_KEX2_1 | 695 | 697 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 553 | 555 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 613 | 615 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 695 | 697 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 634 | 640 | PF00082 | 0.474 |
CLV_PCSK_PC7_1 | 801 | 807 | PF00082 | 0.710 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 680 | 684 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 772 | 776 | PF00082 | 0.750 |
CLV_PCSK_SKI1_1 | 795 | 799 | PF00082 | 0.634 |
DEG_APCC_DBOX_1 | 101 | 109 | PF00400 | 0.249 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.621 |
DOC_CKS1_1 | 738 | 743 | PF01111 | 0.615 |
DOC_CYCLIN_RxL_1 | 4 | 15 | PF00134 | 0.685 |
DOC_CYCLIN_RxL_1 | 634 | 642 | PF00134 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 156 | 162 | PF00134 | 0.385 |
DOC_MAPK_DCC_7 | 384 | 392 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 272 | 282 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 354 | 363 | PF00069 | 0.346 |
DOC_MAPK_HePTP_8 | 351 | 363 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 275 | 284 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 354 | 363 | PF00069 | 0.302 |
DOC_MAPK_MEF2A_6 | 717 | 724 | PF00069 | 0.494 |
DOC_MAPK_RevD_3 | 359 | 374 | PF00069 | 0.345 |
DOC_PP1_RVXF_1 | 17 | 24 | PF00149 | 0.493 |
DOC_PP1_RVXF_1 | 5 | 12 | PF00149 | 0.622 |
DOC_PP2B_LxvP_1 | 156 | 159 | PF13499 | 0.385 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.173 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.711 |
DOC_USP7_UBL2_3 | 283 | 287 | PF12436 | 0.431 |
DOC_USP7_UBL2_3 | 695 | 699 | PF12436 | 0.717 |
DOC_USP7_UBL2_3 | 773 | 777 | PF12436 | 0.701 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.263 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 208 | 215 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 240 | 250 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 308 | 313 | PF00244 | 0.173 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 473 | 479 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 608 | 613 | PF00244 | 0.782 |
LIG_14-3-3_CanoR_1 | 746 | 751 | PF00244 | 0.688 |
LIG_Actin_WH2_2 | 683 | 701 | PF00022 | 0.590 |
LIG_AP2alpha_2 | 313 | 315 | PF02296 | 0.292 |
LIG_AP2alpha_2 | 782 | 784 | PF02296 | 0.648 |
LIG_APCC_ABBA_1 | 787 | 792 | PF00400 | 0.648 |
LIG_BIR_III_4 | 584 | 588 | PF00653 | 0.529 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.327 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.659 |
LIG_EH_1 | 787 | 791 | PF12763 | 0.726 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.444 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.309 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.292 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.606 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.751 |
LIG_FHA_2 | 619 | 625 | PF00498 | 0.720 |
LIG_Integrin_isoDGR_2 | 565 | 567 | PF01839 | 0.501 |
LIG_Integrin_RGD_1 | 665 | 667 | PF01839 | 0.546 |
LIG_LIR_Apic_2 | 24 | 29 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 344 | 348 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 313 | 323 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 332 | 340 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 446 | 452 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 685 | 690 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 782 | 787 | PF02991 | 0.755 |
LIG_PCNA_yPIPBox_3 | 263 | 271 | PF02747 | 0.359 |
LIG_Pex14_2 | 145 | 149 | PF04695 | 0.327 |
LIG_Pex14_2 | 160 | 164 | PF04695 | 0.355 |
LIG_PTB_Apo_2 | 121 | 128 | PF02174 | 0.331 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.550 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.355 |
LIG_SH2_CRK | 687 | 691 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.605 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.232 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.607 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.431 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.588 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.375 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.326 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.555 |
LIG_SUMO_SIM_par_1 | 316 | 321 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 388 | 393 | PF11976 | 0.431 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.351 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.306 |
LIG_TRAF2_1 | 789 | 792 | PF00917 | 0.686 |
LIG_TYR_ITSM | 393 | 400 | PF00017 | 0.173 |
LIG_UBA3_1 | 193 | 202 | PF00899 | 0.351 |
LIG_UBA3_1 | 227 | 236 | PF00899 | 0.386 |
LIG_UBA3_1 | 690 | 699 | PF00899 | 0.668 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.431 |
MOD_CDK_SPK_2 | 344 | 349 | PF00069 | 0.292 |
MOD_CDK_SPK_2 | 499 | 504 | PF00069 | 0.555 |
MOD_CDK_SPxxK_3 | 716 | 723 | PF00069 | 0.633 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.363 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.346 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.423 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.446 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.431 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.391 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.655 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.782 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.693 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.813 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.307 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.448 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.649 |
MOD_Cter_Amidation | 290 | 293 | PF01082 | 0.306 |
MOD_Cter_Amidation | 565 | 568 | PF01082 | 0.679 |
MOD_Cter_Amidation | 801 | 804 | PF01082 | 0.560 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.397 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.324 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.665 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.722 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.648 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.513 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.521 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.767 |
MOD_GlcNHglycan | 584 | 588 | PF01048 | 0.624 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.554 |
MOD_GlcNHglycan | 706 | 709 | PF01048 | 0.554 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.768 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.331 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.425 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.369 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.354 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.415 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.498 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.731 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.749 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.629 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.663 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.699 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.563 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.374 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.665 |
MOD_N-GLC_1 | 603 | 608 | PF02516 | 0.620 |
MOD_N-GLC_2 | 124 | 126 | PF02516 | 0.340 |
MOD_N-GLC_2 | 645 | 647 | PF02516 | 0.641 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.552 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.511 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.293 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.298 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.303 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.408 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.231 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.401 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.431 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.354 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.735 |
MOD_NEK2_2 | 682 | 687 | PF00069 | 0.625 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.469 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.385 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.638 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.748 |
MOD_PIKK_1 | 639 | 645 | PF00454 | 0.689 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.518 |
MOD_PK_1 | 202 | 208 | PF00069 | 0.415 |
MOD_PK_1 | 357 | 363 | PF00069 | 0.355 |
MOD_PKA_1 | 357 | 363 | PF00069 | 0.355 |
MOD_PKA_1 | 491 | 497 | PF00069 | 0.598 |
MOD_PKA_1 | 567 | 573 | PF00069 | 0.490 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.429 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.173 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.431 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.375 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.361 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.666 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.588 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.420 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.398 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.631 |
MOD_Plk_2-3 | 443 | 449 | PF00069 | 0.475 |
MOD_Plk_2-3 | 622 | 628 | PF00069 | 0.683 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.347 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.351 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.571 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.306 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.707 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.564 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.263 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.292 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.374 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.458 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.464 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.525 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.820 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.656 |
MOD_SUMO_for_1 | 282 | 285 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 278 | 284 | PF00179 | 0.363 |
MOD_SUMO_rev_2 | 285 | 294 | PF00179 | 0.359 |
TRG_DiLeu_BaEn_1 | 266 | 271 | PF01217 | 0.351 |
TRG_DiLeu_BaEn_1 | 546 | 551 | PF01217 | 0.570 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.605 |
TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 636 | 641 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 687 | 690 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 637 | 639 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 800 | 803 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 804 | 806 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.569 |
TRG_NES_CRM1_1 | 155 | 168 | PF08389 | 0.355 |
TRG_NES_CRM1_1 | 755 | 767 | PF08389 | 0.709 |
TRG_NLS_MonoExtN_4 | 354 | 360 | PF00514 | 0.431 |
TRG_NLS_MonoExtN_4 | 770 | 776 | PF00514 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 540 | 544 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 638 | 643 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 696 | 700 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Z2 | Leptomonas seymouri | 61% | 100% |
A0A0S4JHR5 | Bodo saltans | 36% | 99% |
A0A1X0NIL8 | Trypanosomatidae | 38% | 100% |
A0A3S7WY54 | Leishmania donovani | 90% | 100% |
A0A422P3Z4 | Trypanosoma rangeli | 39% | 100% |
A4HDC0 | Leishmania braziliensis | 77% | 99% |
A4I0Q0 | Leishmania infantum | 90% | 100% |
D0A726 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
Q4QAS1 | Leishmania major | 88% | 100% |
Q4QCH5 | Leishmania major | 23% | 100% |
V5BR83 | Trypanosoma cruzi | 42% | 100% |