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 | 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: A4HDC0
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 | 1 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 624 | 628 | PF00656 | 0.738 |
CLV_MEL_PAP_1 | 720 | 726 | PF00089 | 0.472 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 805 | 807 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 298 | 302 | PF00082 | 0.192 |
CLV_PCSK_FUR_1 | 801 | 805 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 378 | 380 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 557 | 559 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 616 | 618 | PF00082 | 0.737 |
CLV_PCSK_PC7_1 | 296 | 302 | PF00082 | 0.192 |
CLV_PCSK_PC7_1 | 801 | 807 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 683 | 687 | PF00082 | 0.703 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 772 | 776 | PF00082 | 0.724 |
DEG_APCC_DBOX_1 | 757 | 765 | PF00400 | 0.537 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.592 |
DEG_SPOP_SBC_1 | 411 | 415 | PF00917 | 0.367 |
DEG_SPOP_SBC_1 | 605 | 609 | PF00917 | 0.537 |
DOC_CDC14_PxL_1 | 138 | 146 | PF14671 | 0.192 |
DOC_CKS1_1 | 738 | 743 | PF01111 | 0.595 |
DOC_CYCLIN_yCln2_LP_2 | 159 | 165 | PF00134 | 0.362 |
DOC_MAPK_DCC_7 | 111 | 120 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 277 | 287 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 348 | 358 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 359 | 368 | PF00069 | 0.320 |
DOC_MAPK_MEF2A_6 | 280 | 289 | PF00069 | 0.414 |
DOC_MAPK_RevD_3 | 364 | 379 | PF00069 | 0.329 |
DOC_PP1_RVXF_1 | 17 | 24 | PF00149 | 0.418 |
DOC_PP1_RVXF_1 | 387 | 394 | PF00149 | 0.281 |
DOC_PP1_RVXF_1 | 5 | 12 | PF00149 | 0.596 |
DOC_PP1_RVXF_1 | 717 | 723 | PF00149 | 0.497 |
DOC_PP2B_LxvP_1 | 159 | 162 | PF13499 | 0.362 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 652 | 656 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.731 |
DOC_USP7_UBL2_3 | 288 | 292 | PF12436 | 0.414 |
DOC_USP7_UBL2_3 | 773 | 777 | PF12436 | 0.676 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 673 | 678 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 105 | 109 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 213 | 220 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 401 | 406 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 482 | 488 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 611 | 618 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 745 | 751 | PF00244 | 0.677 |
LIG_AP2alpha_2 | 318 | 320 | PF02296 | 0.268 |
LIG_AP2alpha_2 | 782 | 784 | PF02296 | 0.622 |
LIG_APCC_ABBA_1 | 787 | 792 | PF00400 | 0.629 |
LIG_BIR_III_4 | 587 | 591 | PF00653 | 0.552 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.302 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.628 |
LIG_EH_1 | 787 | 791 | PF12763 | 0.712 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.268 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.589 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.478 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.493 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.558 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.544 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.697 |
LIG_Integrin_RGD_1 | 668 | 670 | PF01839 | 0.537 |
LIG_LIR_Apic_2 | 24 | 29 | PF02991 | 0.539 |
LIG_LIR_Apic_2 | 349 | 353 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 318 | 328 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 337 | 345 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 400 | 410 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 22 | 26 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 688 | 693 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 782 | 787 | PF02991 | 0.746 |
LIG_PCNA_yPIPBox_3 | 268 | 276 | PF02747 | 0.335 |
LIG_Pex14_2 | 148 | 152 | PF04695 | 0.302 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.330 |
LIG_PTB_Apo_2 | 124 | 131 | PF02174 | 0.307 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.523 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.243 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.330 |
LIG_SH2_CRK | 690 | 694 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 639 | 643 | PF00017 | 0.729 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.398 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.550 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.414 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.544 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.367 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.367 |
LIG_SH3_3 | 674 | 680 | PF00018 | 0.606 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.545 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.548 |
LIG_SUMO_SIM_par_1 | 321 | 326 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 393 | 398 | PF11976 | 0.366 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.327 |
LIG_TRAF2_1 | 789 | 792 | PF00917 | 0.669 |
LIG_UBA3_1 | 198 | 207 | PF00899 | 0.327 |
LIG_UBA3_1 | 232 | 241 | PF00899 | 0.364 |
LIG_WRC_WIRS_1 | 149 | 154 | PF05994 | 0.414 |
MOD_CDK_SPK_2 | 349 | 354 | PF00069 | 0.268 |
MOD_CDK_SPK_2 | 673 | 678 | PF00069 | 0.517 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.342 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.414 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.414 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.432 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.370 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.699 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.604 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.605 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.584 |
MOD_CK1_1 | 586 | 592 | PF00069 | 0.768 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.622 |
MOD_CK1_1 | 708 | 714 | PF00069 | 0.630 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.312 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.211 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.383 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.675 |
MOD_Cter_Amidation | 801 | 804 | PF01082 | 0.549 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.432 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.306 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.602 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.266 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.298 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.467 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.669 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.489 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.591 |
MOD_GlcNHglycan | 587 | 591 | PF01048 | 0.730 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.549 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.538 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.779 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.390 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.325 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.317 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.404 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.479 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.588 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.568 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.735 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.683 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.671 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.591 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.769 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.292 |
MOD_N-GLC_1 | 475 | 480 | PF02516 | 0.350 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.618 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.610 |
MOD_N-GLC_1 | 568 | 573 | PF02516 | 0.510 |
MOD_N-GLC_2 | 127 | 129 | PF02516 | 0.316 |
MOD_N-GLC_2 | 648 | 650 | PF02516 | 0.633 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.531 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.285 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.306 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.390 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.283 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.376 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.197 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.415 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.528 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.336 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.518 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.510 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.726 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.620 |
MOD_NEK2_1 | 693 | 698 | PF00069 | 0.517 |
MOD_NEK2_1 | 707 | 712 | PF00069 | 0.773 |
MOD_NEK2_2 | 685 | 690 | PF00069 | 0.617 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.362 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.192 |
MOD_PIKK_1 | 423 | 429 | PF00454 | 0.440 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.737 |
MOD_PIKK_1 | 642 | 648 | PF00454 | 0.683 |
MOD_PIKK_1 | 663 | 669 | PF00454 | 0.581 |
MOD_PK_1 | 362 | 368 | PF00069 | 0.330 |
MOD_PKA_1 | 300 | 306 | PF00069 | 0.192 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.330 |
MOD_PKA_1 | 500 | 506 | PF00069 | 0.565 |
MOD_PKA_1 | 634 | 640 | PF00069 | 0.491 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.412 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.414 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.358 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.336 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.530 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.460 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.643 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.407 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.377 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.600 |
MOD_Plk_1 | 708 | 714 | PF00069 | 0.577 |
MOD_Plk_2-3 | 452 | 458 | PF00069 | 0.330 |
MOD_Plk_2-3 | 621 | 627 | PF00069 | 0.650 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.468 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.327 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.362 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.443 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.651 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.441 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.268 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.446 |
MOD_ProDKin_1 | 673 | 679 | PF00069 | 0.542 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.675 |
MOD_SUMO_for_1 | 287 | 290 | PF00179 | 0.414 |
MOD_SUMO_rev_2 | 283 | 289 | PF00179 | 0.327 |
MOD_SUMO_rev_2 | 290 | 299 | PF00179 | 0.327 |
MOD_SUMO_rev_2 | 54 | 62 | PF00179 | 0.626 |
MOD_SUMO_rev_2 | 627 | 637 | PF00179 | 0.497 |
TRG_DiLeu_BaEn_1 | 271 | 276 | PF01217 | 0.327 |
TRG_DiLeu_BaEn_1 | 550 | 555 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 200 | 205 | PF01217 | 0.414 |
TRG_DiLeu_BaLyEn_6 | 677 | 682 | PF01217 | 0.634 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 690 | 693 | PF00928 | 0.578 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 641 | 643 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 697 | 699 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 717 | 720 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 744 | 746 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 800 | 803 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 804 | 806 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.538 |
TRG_NES_CRM1_1 | 158 | 171 | PF08389 | 0.330 |
TRG_NES_CRM1_1 | 755 | 767 | PF08389 | 0.691 |
TRG_NLS_MonoExtC_3 | 296 | 301 | PF00514 | 0.192 |
TRG_NLS_MonoExtN_4 | 296 | 301 | PF00514 | 0.192 |
TRG_NLS_MonoExtN_4 | 359 | 365 | PF00514 | 0.414 |
TRG_NLS_MonoExtN_4 | 770 | 776 | PF00514 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 47 | 51 | PF00026 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 544 | 548 | PF00026 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 641 | 646 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Z2 | Leptomonas seymouri | 60% | 100% |
A0A0S4JHR5 | Bodo saltans | 34% | 99% |
A0A1X0NIL8 | Trypanosomatidae | 38% | 100% |
A0A3S7WY54 | Leishmania donovani | 76% | 100% |
A0A422P3Z4 | Trypanosoma rangeli | 38% | 100% |
A4HZ39 | Leishmania infantum | 22% | 100% |
A4I0Q0 | Leishmania infantum | 76% | 100% |
D0A726 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AWQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QAS1 | Leishmania major | 75% | 99% |
V5BR83 | Trypanosoma cruzi | 42% | 100% |