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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005622 | intracellular anatomical structure | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005773 | vacuole | 5 | 2 |
GO:0005776 | autophagosome | 6 | 2 |
GO:0016234 | inclusion body | 3 | 2 |
GO:0016235 | aggresome | 4 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0044753 | amphisome | 7 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QD14
Term | Name | Level | Count |
---|---|---|---|
GO:0000422 | autophagy of mitochondrion | 4 | 2 |
GO:0000423 | mitophagy | 5 | 2 |
GO:0006914 | autophagy | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007005 | mitochondrion organization | 5 | 2 |
GO:0007032 | endosome organization | 6 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016050 | vesicle organization | 5 | 2 |
GO:0016236 | macroautophagy | 4 | 2 |
GO:0022411 | cellular component disassembly | 4 | 2 |
GO:0035973 | aggrephagy | 6 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0061726 | mitochondrion disassembly | 6 | 2 |
GO:0061912 | selective autophagy | 5 | 2 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1903008 | organelle disassembly | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005080 | protein kinase C binding | 6 | 2 |
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0019899 | enzyme binding | 3 | 2 |
GO:0019900 | kinase binding | 4 | 2 |
GO:0019901 | protein kinase binding | 5 | 2 |
GO:0031593 | polyubiquitin modification-dependent protein binding | 4 | 2 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0070530 | K63-linked polyubiquitin modification-dependent protein binding | 5 | 2 |
GO:0140030 | modification-dependent protein binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.569 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.627 |
CLV_MEL_PAP_1 | 75 | 81 | PF00089 | 0.306 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.784 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.517 |
CLV_PCSK_FUR_1 | 458 | 462 | PF00082 | 0.789 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.782 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 721 | 723 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 341 | 343 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 721 | 723 | PF00082 | 0.597 |
CLV_PCSK_PC7_1 | 717 | 723 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.336 |
DEG_APCC_DBOX_1 | 250 | 258 | PF00400 | 0.514 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.527 |
DEG_SPOP_SBC_1 | 170 | 174 | PF00917 | 0.588 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.479 |
DOC_CKS1_1 | 123 | 128 | PF01111 | 0.580 |
DOC_CKS1_1 | 583 | 588 | PF01111 | 0.496 |
DOC_CKS1_1 | 752 | 757 | PF01111 | 0.672 |
DOC_CYCLIN_RxL_1 | 278 | 287 | PF00134 | 0.526 |
DOC_CYCLIN_RxL_1 | 495 | 507 | PF00134 | 0.520 |
DOC_CYCLIN_yClb1_LxF_4 | 204 | 210 | PF00134 | 0.568 |
DOC_CYCLIN_yCln2_LP_2 | 120 | 126 | PF00134 | 0.489 |
DOC_CYCLIN_yCln2_LP_2 | 637 | 643 | PF00134 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 646 | 652 | PF00134 | 0.423 |
DOC_MAPK_gen_1 | 341 | 348 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 436 | 444 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 459 | 471 | PF00069 | 0.708 |
DOC_MAPK_gen_1 | 500 | 506 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 341 | 350 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 464 | 471 | PF00069 | 0.708 |
DOC_PP2B_LxvP_1 | 646 | 649 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 770 | 773 | PF13499 | 0.506 |
DOC_PP2B_LxvP_1 | 784 | 787 | PF13499 | 0.518 |
DOC_PP4_FxxP_1 | 783 | 786 | PF00568 | 0.580 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 759 | 763 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 337 | 341 | PF12436 | 0.592 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 744 | 749 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 751 | 756 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 251 | 255 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 517 | 525 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 691 | 696 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 78 | 82 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 29 | 47 | PF00022 | 0.567 |
LIG_AP2alpha_2 | 309 | 311 | PF02296 | 0.424 |
LIG_AP2alpha_2 | 523 | 525 | PF02296 | 0.520 |
LIG_Clathr_ClatBox_1 | 347 | 351 | PF01394 | 0.388 |
LIG_Clathr_ClatBox_1 | 395 | 399 | PF01394 | 0.590 |
LIG_deltaCOP1_diTrp_1 | 277 | 284 | PF00928 | 0.515 |
LIG_deltaCOP1_diTrp_1 | 309 | 314 | PF00928 | 0.408 |
LIG_DLG_GKlike_1 | 691 | 699 | PF00625 | 0.447 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.530 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.364 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.694 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.642 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.775 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.428 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.402 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.489 |
LIG_FHA_1 | 752 | 758 | PF00498 | 0.727 |
LIG_FHA_1 | 787 | 793 | PF00498 | 0.534 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.758 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.538 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.545 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.544 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.498 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.570 |
LIG_IBAR_NPY_1 | 518 | 520 | PF08397 | 0.630 |
LIG_Integrin_RGD_1 | 735 | 737 | PF01839 | 0.656 |
LIG_LIR_Apic_2 | 782 | 786 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 19 | 26 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 299 | 310 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 30 | 39 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 359 | 368 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 475 | 483 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 533 | 543 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 19 | 23 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 522 | 528 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 533 | 538 | PF02991 | 0.403 |
LIG_PCNA_PIPBox_1 | 389 | 398 | PF02747 | 0.562 |
LIG_PCNA_yPIPBox_3 | 389 | 397 | PF02747 | 0.488 |
LIG_Pex14_1 | 136 | 140 | PF04695 | 0.443 |
LIG_Pex14_1 | 268 | 272 | PF04695 | 0.499 |
LIG_PTAP_UEV_1 | 572 | 577 | PF05743 | 0.491 |
LIG_SH2_CRK | 302 | 306 | PF00017 | 0.626 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.444 |
LIG_SH2_PTP2 | 535 | 538 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.644 |
LIG_SH2_STAP1 | 302 | 306 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 719 | 723 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 688 | 691 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.533 |
LIG_SH3_2 | 323 | 328 | PF14604 | 0.677 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.504 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.531 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.469 |
LIG_SH3_3 | 649 | 655 | PF00018 | 0.513 |
LIG_SH3_3 | 738 | 744 | PF00018 | 0.735 |
LIG_SH3_3 | 747 | 753 | PF00018 | 0.692 |
LIG_SUMO_SIM_anti_2 | 375 | 380 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 236 | 242 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 431 | 438 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 467 | 473 | PF11976 | 0.770 |
LIG_TYR_ITIM | 74 | 79 | PF00017 | 0.456 |
LIG_UBA3_1 | 335 | 341 | PF00899 | 0.594 |
MOD_CDC14_SPxK_1 | 8 | 11 | PF00782 | 0.515 |
MOD_CDK_SPK_2 | 451 | 456 | PF00069 | 0.684 |
MOD_CDK_SPxK_1 | 5 | 11 | PF00069 | 0.663 |
MOD_CDK_SPxxK_3 | 451 | 458 | PF00069 | 0.742 |
MOD_CDK_SPxxK_3 | 582 | 589 | PF00069 | 0.557 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.542 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.705 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.670 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.754 |
MOD_CK1_1 | 622 | 628 | PF00069 | 0.513 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.646 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.700 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.556 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.725 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.534 |
MOD_CK2_1 | 356 | 362 | PF00069 | 0.560 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.503 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.562 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.652 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.761 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.588 |
MOD_GlcNHglycan | 227 | 231 | PF01048 | 0.575 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.574 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.580 |
MOD_GlcNHglycan | 572 | 576 | PF01048 | 0.490 |
MOD_GlcNHglycan | 623 | 627 | PF01048 | 0.441 |
MOD_GlcNHglycan | 778 | 781 | PF01048 | 0.607 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.701 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.628 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.777 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.516 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.526 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.707 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.595 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.775 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.511 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.544 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.546 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.684 |
MOD_GSK3_1 | 759 | 766 | PF00069 | 0.421 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.450 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.703 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.503 |
MOD_N-GLC_1 | 566 | 571 | PF02516 | 0.556 |
MOD_N-GLC_2 | 690 | 692 | PF02516 | 0.369 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.682 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.498 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.473 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.528 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.474 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.598 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.488 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.534 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.460 |
MOD_NEK2_1 | 711 | 716 | PF00069 | 0.429 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.613 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.582 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.601 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.533 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.582 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.687 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.623 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.498 |
MOD_PKA_2 | 696 | 702 | PF00069 | 0.487 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.491 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.679 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.519 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.515 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.562 |
MOD_Plk_1 | 622 | 628 | PF00069 | 0.516 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.406 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.488 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.531 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.410 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.513 |
MOD_Plk_4 | 779 | 785 | PF00069 | 0.589 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.529 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.445 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.678 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.625 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.475 |
MOD_ProDKin_1 | 744 | 750 | PF00069 | 0.673 |
MOD_ProDKin_1 | 751 | 757 | PF00069 | 0.651 |
TRG_DiLeu_BaEn_1 | 213 | 218 | PF01217 | 0.606 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.473 |
TRG_DiLeu_BaEn_2 | 398 | 404 | PF01217 | 0.580 |
TRG_DiLeu_BaLyEn_6 | 655 | 660 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 69 | 74 | PF01217 | 0.570 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.623 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.432 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 457 | 460 | PF00400 | 0.789 |
TRG_ER_diArg_1 | 500 | 502 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.555 |
TRG_NES_CRM1_1 | 386 | 399 | PF08389 | 0.568 |
TRG_NES_CRM1_1 | 560 | 572 | PF08389 | 0.572 |
TRG_NLS_MonoExtN_4 | 154 | 160 | PF00514 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 163 | 168 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 281 | 286 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJU9 | Leptomonas seymouri | 47% | 100% |
A0A1X0NY20 | Trypanosomatidae | 31% | 100% |
A0A3S7WVR9 | Leishmania donovani | 93% | 100% |
A0A422NEI4 | Trypanosoma rangeli | 30% | 100% |
A4HYM1 | Leishmania infantum | 93% | 100% |
C9ZHT5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AI85 | Leishmania braziliensis | 73% | 100% |
E9AUH0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |