Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 92 |
NetGPI | no | yes: 0, no: 93 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E8NHG8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 94 |
GO:0006807 | nitrogen compound metabolic process | 2 | 94 |
GO:0008152 | metabolic process | 1 | 94 |
GO:0019538 | protein metabolic process | 3 | 94 |
GO:0043170 | macromolecule metabolic process | 3 | 94 |
GO:0044238 | primary metabolic process | 2 | 94 |
GO:0071704 | organic substance metabolic process | 2 | 94 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 94 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 94 |
GO:0004175 | endopeptidase activity | 4 | 94 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 94 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 94 |
GO:0008233 | peptidase activity | 3 | 94 |
GO:0008234 | cysteine-type peptidase activity | 4 | 94 |
GO:0016787 | hydrolase activity | 2 | 94 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 94 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 566 | 570 | PF00656 | 0.505 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.449 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 759 | 761 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 759 | 761 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 696 | 700 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.466 |
DEG_APCC_DBOX_1 | 515 | 523 | PF00400 | 0.518 |
DEG_MDM2_SWIB_1 | 563 | 571 | PF02201 | 0.440 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.400 |
DEG_ODPH_VHL_1 | 713 | 725 | PF01847 | 0.249 |
DEG_SPOP_SBC_1 | 329 | 333 | PF00917 | 0.493 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.473 |
DOC_AGCK_PIF_1 | 429 | 434 | PF00069 | 0.503 |
DOC_ANK_TNKS_1 | 205 | 212 | PF00023 | 0.262 |
DOC_CKS1_1 | 467 | 472 | PF01111 | 0.450 |
DOC_CYCLIN_RxL_1 | 609 | 619 | PF00134 | 0.484 |
DOC_CYCLIN_RxL_1 | 633 | 643 | PF00134 | 0.477 |
DOC_MAPK_DCC_7 | 510 | 519 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 247 | 256 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 457 | 467 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 609 | 616 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 721 | 730 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 765 | 772 | PF00069 | 0.526 |
DOC_MAPK_HePTP_8 | 507 | 519 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 249 | 258 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 510 | 519 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 676 | 684 | PF00069 | 0.457 |
DOC_MAPK_RevD_3 | 596 | 610 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 611 | 617 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 722 | 728 | PF00149 | 0.367 |
DOC_PP4_FxxP_1 | 339 | 342 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 512 | 515 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 715 | 719 | PF00917 | 0.486 |
DOC_USP7_MATH_2 | 270 | 276 | PF00917 | 0.470 |
DOC_USP7_UBL2_3 | 402 | 406 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 163 | 167 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 303 | 311 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 54 | 64 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 550 | 558 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 696 | 705 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 724 | 728 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 738 | 744 | PF00244 | 0.459 |
LIG_Actin_WH2_2 | 38 | 56 | PF00022 | 0.382 |
LIG_Actin_WH2_2 | 723 | 740 | PF00022 | 0.232 |
LIG_APCC_ABBAyCdc20_2 | 132 | 138 | PF00400 | 0.346 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.256 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_2 | 146 | 152 | PF00533 | 0.259 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.399 |
LIG_deltaCOP1_diTrp_1 | 531 | 536 | PF00928 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 566 | 574 | PF00928 | 0.466 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.390 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.444 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.449 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.488 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.457 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.410 |
LIG_FHA_2 | 769 | 775 | PF00498 | 0.470 |
LIG_IRF3_LxIS_1 | 634 | 641 | PF10401 | 0.429 |
LIG_LIR_Apic_2 | 102 | 108 | PF02991 | 0.456 |
LIG_LIR_Apic_2 | 337 | 342 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 779 | 785 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 394 | 404 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 410 | 419 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 503 | 512 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 668 | 678 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 726 | 735 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 378 | 382 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 410 | 414 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 503 | 507 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 632 | 638 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 668 | 673 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 726 | 730 | PF02991 | 0.358 |
LIG_MLH1_MIPbox_1 | 448 | 452 | PF16413 | 0.512 |
LIG_Pex14_2 | 434 | 438 | PF04695 | 0.443 |
LIG_Pex14_2 | 563 | 567 | PF04695 | 0.448 |
LIG_Pex14_2 | 591 | 595 | PF04695 | 0.419 |
LIG_REV1ctd_RIR_1 | 449 | 457 | PF16727 | 0.465 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.330 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.422 |
LIG_SH2_CRK | 35 | 39 | PF00017 | 0.384 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.565 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.450 |
LIG_SH2_CRK | 411 | 415 | PF00017 | 0.451 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.470 |
LIG_SH2_CRK | 589 | 593 | PF00017 | 0.332 |
LIG_SH2_CRK | 635 | 639 | PF00017 | 0.399 |
LIG_SH2_PTP2 | 692 | 695 | PF00017 | 0.419 |
LIG_SH2_SRC | 290 | 293 | PF00017 | 0.474 |
LIG_SH2_SRC | 463 | 466 | PF00017 | 0.437 |
LIG_SH2_SRC | 670 | 673 | PF00017 | 0.489 |
LIG_SH2_SRC | 692 | 695 | PF00017 | 0.397 |
LIG_SH2_SRC | 782 | 785 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 393 | 397 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 504 | 508 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 670 | 674 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 692 | 695 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.556 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.295 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.668 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.558 |
LIG_SH3_3 | 661 | 667 | PF00018 | 0.456 |
LIG_SH3_3 | 725 | 731 | PF00018 | 0.413 |
LIG_SH3_3 | 738 | 744 | PF00018 | 0.446 |
LIG_SUMO_SIM_anti_2 | 324 | 333 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 463 | 469 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 638 | 643 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 653 | 660 | PF11976 | 0.522 |
LIG_TRAF2_1 | 295 | 298 | PF00917 | 0.349 |
LIG_TRAF2_1 | 442 | 445 | PF00917 | 0.485 |
LIG_TYR_ITIM | 33 | 38 | PF00017 | 0.377 |
LIG_UBA3_1 | 614 | 621 | PF00899 | 0.389 |
LIG_WRC_WIRS_1 | 431 | 436 | PF05994 | 0.498 |
MOD_CDC14_SPxK_1 | 74 | 77 | PF00782 | 0.601 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.587 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.433 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.438 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.678 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.510 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.421 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.420 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.444 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.454 |
MOD_CMANNOS | 564 | 567 | PF00535 | 0.253 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.450 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.283 |
MOD_GlcNHglycan | 473 | 477 | PF01048 | 0.258 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.268 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.308 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.628 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.315 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.293 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.491 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.461 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.473 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.506 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.673 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.511 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.692 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.627 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.297 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.282 |
MOD_N-GLC_1 | 715 | 720 | PF02516 | 0.536 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.285 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.279 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.460 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.461 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.464 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.456 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.578 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.467 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.517 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.323 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.318 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.358 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.435 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.405 |
MOD_NEK2_2 | 162 | 167 | PF00069 | 0.346 |
MOD_NEK2_2 | 768 | 773 | PF00069 | 0.256 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.390 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.560 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.451 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.581 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.526 |
MOD_PIKK_1 | 616 | 622 | PF00454 | 0.364 |
MOD_PIKK_1 | 648 | 654 | PF00454 | 0.527 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.653 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.311 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.508 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.514 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.501 |
MOD_PKA_2 | 723 | 729 | PF00069 | 0.397 |
MOD_Plk_1 | 136 | 142 | PF00069 | 0.303 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.486 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.432 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.523 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.452 |
MOD_Plk_1 | 773 | 779 | PF00069 | 0.428 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.313 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.480 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.495 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.425 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.446 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.470 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.493 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.456 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.349 |
MOD_Plk_4 | 723 | 729 | PF00069 | 0.456 |
MOD_Plk_4 | 778 | 784 | PF00069 | 0.518 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.418 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.465 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.613 |
MOD_SUMO_for_1 | 604 | 607 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 214 | 222 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 297 | 302 | PF00179 | 0.349 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 670 | 673 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 549 | 551 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 623 | 625 | PF00400 | 0.489 |
TRG_NLS_MonoExtC_3 | 608 | 613 | PF00514 | 0.419 |
TRG_NLS_MonoExtN_4 | 247 | 253 | PF00514 | 0.508 |
TRG_NLS_MonoExtN_4 | 609 | 614 | PF00514 | 0.418 |
TRG_PTS2 | 1 | 27 | PF00400 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 66% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 27% | 80% |
A0A0N1IGQ2 | Leptomonas seymouri | 35% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 33% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 34% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 33% | 92% |
A0A0N1PCA9 | Leptomonas seymouri | 30% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 24% | 88% |
A0A0N1PFI4 | Leptomonas seymouri | 33% | 100% |
A0A0S4JLK6 | Bodo saltans | 30% | 97% |
A0A0S4JS70 | Bodo saltans | 25% | 100% |
A0A0S4KGT2 | Bodo saltans | 40% | 100% |
A0A0S4KKP7 | Bodo saltans | 20% | 100% |
A0A1X0NJ61 | Trypanosomatidae | 40% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 42% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 34% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 29% | 99% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 96% |
A0A1X0NMT3 | Trypanosomatidae | 34% | 92% |
A0A1X0NW84 | Trypanosomatidae | 33% | 100% |
A0A1X0NW85 | Trypanosomatidae | 32% | 100% |
A0A1X0NW89 | Trypanosomatidae | 34% | 91% |
A0A1X0NWA6 | Trypanosomatidae | 26% | 90% |
A0A1X0NWW1 | Trypanosomatidae | 33% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 34% | 86% |
A0A3Q8IDD4 | Leishmania donovani | 36% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 24% | 100% |
A0A3S5H5A5 | Leishmania donovani | 31% | 92% |
A0A3S5ISG2 | Trypanosoma rangeli | 35% | 100% |
A0A3S7WW13 | Leishmania donovani | 25% | 71% |
A0A3S7WW18 | Leishmania donovani | 34% | 96% |
A0A3S7WW41 | Leishmania donovani | 29% | 100% |
A0A3S7WW71 | Leishmania donovani | 34% | 100% |
A0A3S7X430 | Leishmania donovani | 34% | 100% |
A0A3S7X438 | Leishmania donovani | 31% | 84% |
A0A3S7X460 | Leishmania donovani | 88% | 100% |
A0A3S7X463 | Leishmania donovani | 28% | 84% |
A0A3S7X470 | Leishmania donovani | 31% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 33% | 85% |
A0A422MYX0 | Trypanosoma rangeli | 32% | 100% |
A4H3W4 | Leishmania braziliensis | 31% | 100% |
A4HE81 | Leishmania braziliensis | 36% | 100% |
A4HJ14 | Leishmania braziliensis | 33% | 100% |
A4HJ21 | Leishmania braziliensis | 25% | 100% |
A4HJ22 | Leishmania braziliensis | 30% | 100% |
A4HJ24 | Leishmania braziliensis | 80% | 100% |
A4HS39 | Leishmania infantum | 31% | 92% |
A4HYN0 | Leishmania infantum | 34% | 96% |
A4HYW1 | Leishmania infantum | 34% | 78% |
A4HYW2 | Leishmania infantum | 34% | 100% |
A4HYW3 | Leishmania infantum | 29% | 100% |
A4HYW4 | Leishmania infantum | 26% | 79% |
A4I1J4 | Leishmania infantum | 36% | 100% |
A4I6E4 | Leishmania infantum | 32% | 100% |
A4I6E6 | Leishmania infantum | 88% | 100% |
A4I6F0 | Leishmania infantum | 31% | 84% |
A4I6K4 | Leishmania infantum | 34% | 100% |
A4I6K5 | Leishmania infantum | 28% | 84% |
A4I6K6 | Leishmania infantum | 24% | 100% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 73% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 99% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 98% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 92% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E9AIH1 | Leishmania braziliensis | 35% | 100% |
E9AIH3 | Leishmania braziliensis | 34% | 100% |
E9AIH4 | Leishmania braziliensis | 30% | 100% |
E9AIH6 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 99% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 84% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 84% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
O08688 | Mus musculus | 27% | 100% |
O15484 | Homo sapiens | 27% | 100% |
Q4Q6L7 | Leishmania major | 87% | 100% |
Q4Q6L9 | Leishmania major | 32% | 100% |
Q4Q6M0 | Leishmania major | 31% | 100% |
Q4Q6M2 | Leishmania major | 24% | 100% |
Q4Q6M3 | Leishmania major | 29% | 100% |
Q4Q6M4 | Leishmania major | 34% | 100% |
Q4Q9U3 | Leishmania major | 36% | 100% |
Q4QCS6 | Leishmania major | 30% | 100% |
Q4QCS7 | Leishmania major | 34% | 100% |
Q4QCS8 | Leishmania major | 33% | 100% |
Q4QCS9 | Leishmania major | 34% | 100% |
Q8R4C0 | Rattus norvegicus | 27% | 100% |
Q9D805 | Mus musculus | 27% | 100% |
Q9U0T9 | Leishmania major | 31% | 100% |
V5AYJ1 | Trypanosoma cruzi | 40% | 100% |
V5B5I4 | Trypanosoma cruzi | 33% | 94% |
V5BA05 | Trypanosoma cruzi | 35% | 100% |
V5BEL3 | Trypanosoma cruzi | 33% | 100% |
V5BN20 | Trypanosoma cruzi | 34% | 100% |
V5D5V8 | Trypanosoma cruzi | 29% | 100% |
V5D9Y2 | Trypanosoma cruzi | 31% | 92% |
V5DES7 | Trypanosoma cruzi | 35% | 99% |