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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HPF6
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0032392 | DNA geometric change | 7 | 2 |
GO:0032508 | DNA duplex unwinding | 8 | 2 |
GO:0051276 | chromosome organization | 5 | 2 |
GO:0071103 | DNA conformation change | 6 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.392 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 847 | 849 | PF00675 | 0.524 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 784 | 786 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 847 | 849 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 784 | 786 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.509 |
DEG_APCC_DBOX_1 | 344 | 352 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 662 | 670 | PF00400 | 0.387 |
DEG_APCC_DBOX_1 | 784 | 792 | PF00400 | 0.517 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.499 |
DEG_SCF_FBW7_1 | 45 | 52 | PF00400 | 0.341 |
DEG_SCF_FBW7_1 | 496 | 501 | PF00400 | 0.354 |
DEG_SCF_FBW7_1 | 551 | 558 | PF00400 | 0.550 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.348 |
DOC_CDC14_PxL_1 | 172 | 180 | PF14671 | 0.477 |
DOC_CKS1_1 | 552 | 557 | PF01111 | 0.554 |
DOC_CYCLIN_RxL_1 | 131 | 142 | PF00134 | 0.551 |
DOC_MAPK_gen_1 | 404 | 410 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 783 | 791 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 124 | 132 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 321 | 328 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 345 | 352 | PF00069 | 0.415 |
DOC_MAPK_NFAT4_5 | 321 | 329 | PF00069 | 0.329 |
DOC_PP1_RVXF_1 | 117 | 123 | PF00149 | 0.464 |
DOC_PP1_RVXF_1 | 319 | 326 | PF00149 | 0.264 |
DOC_PP1_RVXF_1 | 785 | 791 | PF00149 | 0.512 |
DOC_PP2B_LxvP_1 | 620 | 623 | PF13499 | 0.733 |
DOC_PP4_FxxP_1 | 828 | 831 | PF00568 | 0.466 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.499 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.382 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 743 | 747 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 765 | 769 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.497 |
DOC_USP7_UBL2_3 | 779 | 783 | PF12436 | 0.473 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 741 | 746 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.523 |
LIG_14-3-3_CanoR_1 | 168 | 176 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 404 | 410 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 528 | 536 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 542 | 548 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.350 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.456 |
LIG_Clathr_ClatBox_1 | 788 | 792 | PF01394 | 0.514 |
LIG_deltaCOP1_diTrp_1 | 56 | 63 | PF00928 | 0.515 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.483 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.411 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.371 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.543 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.485 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.568 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.502 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.476 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.495 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.464 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.530 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.345 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.644 |
LIG_LIR_Apic_2 | 826 | 831 | PF02991 | 0.465 |
LIG_LIR_Apic_2 | 88 | 94 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 224 | 232 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 273 | 282 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 592 | 603 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 816 | 827 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 196 | 200 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 592 | 598 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 684 | 689 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 816 | 822 | PF02991 | 0.494 |
LIG_NRBOX | 817 | 823 | PF00104 | 0.429 |
LIG_PTAP_UEV_1 | 547 | 552 | PF05743 | 0.550 |
LIG_RPA_C_Fungi | 203 | 215 | PF08784 | 0.418 |
LIG_SH2_GRB2like | 21 | 24 | PF00017 | 0.281 |
LIG_SH2_GRB2like | 334 | 337 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 21 | 25 | PF00017 | 0.413 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.281 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 373 | 377 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.327 |
LIG_SH3_2 | 548 | 553 | PF14604 | 0.552 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.475 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.300 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.575 |
LIG_SUMO_SIM_anti_2 | 170 | 176 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 39 | 46 | PF11976 | 0.479 |
LIG_SUMO_SIM_anti_2 | 830 | 837 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 418 | 423 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 437 | 443 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 645 | 651 | PF11976 | 0.581 |
LIG_TRAF2_1 | 476 | 479 | PF00917 | 0.527 |
LIG_TRAF2_1 | 648 | 651 | PF00917 | 0.370 |
LIG_TYR_ITIM | 200 | 205 | PF00017 | 0.384 |
LIG_WRC_WIRS_1 | 595 | 600 | PF05994 | 0.429 |
LIG_WRC_WIRS_1 | 726 | 731 | PF05994 | 0.479 |
MOD_CDC14_SPxK_1 | 744 | 747 | PF00782 | 0.522 |
MOD_CDK_SPK_2 | 114 | 119 | PF00069 | 0.409 |
MOD_CDK_SPK_2 | 537 | 542 | PF00069 | 0.630 |
MOD_CDK_SPxK_1 | 551 | 557 | PF00069 | 0.732 |
MOD_CDK_SPxK_1 | 741 | 747 | PF00069 | 0.522 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.650 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.267 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.533 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.589 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.609 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.559 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.669 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.662 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.576 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.751 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.491 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.502 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.390 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.307 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.663 |
MOD_CK2_1 | 810 | 816 | PF00069 | 0.536 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.549 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.645 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.363 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.550 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.579 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.638 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.602 |
MOD_GlcNHglycan | 478 | 482 | PF01048 | 0.554 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.683 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.656 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.658 |
MOD_GlcNHglycan | 706 | 709 | PF01048 | 0.677 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.515 |
MOD_GlcNHglycan | 802 | 805 | PF01048 | 0.634 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.526 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.448 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.477 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.454 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.434 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.273 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.455 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.576 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.564 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.447 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.523 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.572 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.616 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.585 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.655 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.663 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.470 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.608 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.513 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.586 |
MOD_GSK3_1 | 806 | 813 | PF00069 | 0.470 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.542 |
MOD_LATS_1 | 522 | 528 | PF00433 | 0.638 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.444 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.711 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.450 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.467 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.491 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.614 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.438 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.437 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.560 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.683 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.653 |
MOD_NEK2_1 | 774 | 779 | PF00069 | 0.546 |
MOD_NEK2_2 | 32 | 37 | PF00069 | 0.356 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.523 |
MOD_PIKK_1 | 167 | 173 | PF00454 | 0.499 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.406 |
MOD_PIKK_1 | 506 | 512 | PF00454 | 0.488 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.723 |
MOD_PIKK_1 | 541 | 547 | PF00454 | 0.706 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.410 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.349 |
MOD_PIKK_1 | 774 | 780 | PF00454 | 0.480 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.554 |
MOD_PIKK_1 | 834 | 840 | PF00454 | 0.594 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.531 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.522 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.364 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.603 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.644 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.691 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.636 |
MOD_PKA_2 | 746 | 752 | PF00069 | 0.646 |
MOD_PKA_2 | 800 | 806 | PF00069 | 0.573 |
MOD_PKB_1 | 155 | 163 | PF00069 | 0.462 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.463 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.326 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.582 |
MOD_Plk_1 | 806 | 812 | PF00069 | 0.374 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.474 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.301 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.445 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.333 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.481 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.555 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.302 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.788 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.476 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.599 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.486 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.337 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.678 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.613 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.475 |
MOD_ProDKin_1 | 741 | 747 | PF00069 | 0.497 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 755 | 758 | PF00179 | 0.495 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.499 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_1 | 841 | 846 | PF01217 | 0.491 |
TRG_DiLeu_BaEn_4 | 841 | 847 | PF01217 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 243 | 248 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 434 | 439 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 785 | 788 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 794 | 797 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 799 | 802 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 846 | 848 | PF00400 | 0.498 |
TRG_NLS_MonoExtC_3 | 782 | 787 | PF00514 | 0.530 |
TRG_NLS_MonoExtN_4 | 781 | 788 | PF00514 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 76 | 81 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P797 | Leptomonas seymouri | 45% | 100% |
A0A1X0NKL2 | Trypanosomatidae | 26% | 100% |
A0A3R7LZS8 | Trypanosoma rangeli | 26% | 100% |
A0A3S5H829 | Leishmania donovani | 75% | 95% |
A4ID78 | Leishmania infantum | 75% | 95% |
E9AT68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q1C9 | Leishmania major | 75% | 100% |
V5B0C2 | Trypanosoma cruzi | 26% | 100% |