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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: E9ANJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0031119 | tRNA pseudouridine synthesis | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0009982 | pseudouridine synthase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016866 | intramolecular transferase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.654 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.230 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.674 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.694 |
CLV_PCSK_PC1ET2_1 | 602 | 604 | PF00082 | 0.346 |
CLV_PCSK_PC7_1 | 641 | 647 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.752 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.647 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.752 |
DEG_MDM2_SWIB_1 | 181 | 188 | PF02201 | 0.606 |
DEG_SCF_FBW7_1 | 658 | 665 | PF00400 | 0.468 |
DEG_SPOP_SBC_1 | 302 | 306 | PF00917 | 0.728 |
DEG_SPOP_SBC_1 | 512 | 516 | PF00917 | 0.418 |
DOC_ANK_TNKS_1 | 536 | 543 | PF00023 | 0.520 |
DOC_CKS1_1 | 636 | 641 | PF01111 | 0.425 |
DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.458 |
DOC_MAPK_DCC_7 | 251 | 260 | PF00069 | 0.685 |
DOC_MAPK_FxFP_2 | 32 | 35 | PF00069 | 0.628 |
DOC_MAPK_FxFP_2 | 462 | 465 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 583 | 591 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 650 | 660 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 700 | 708 | PF00069 | 0.368 |
DOC_MAPK_JIP1_4 | 543 | 549 | PF00069 | 0.369 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.686 |
DOC_MAPK_MEF2A_6 | 531 | 538 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 584 | 593 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 690 | 697 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 702 | 710 | PF00069 | 0.386 |
DOC_PP1_RVXF_1 | 603 | 610 | PF00149 | 0.376 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.744 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.593 |
DOC_PP4_FxxP_1 | 462 | 465 | PF00568 | 0.402 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.484 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 251 | 258 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 289 | 298 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 363 | 370 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 432 | 441 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 498 | 508 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 583 | 591 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 595 | 601 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 645 | 649 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 653 | 659 | PF00244 | 0.399 |
LIG_APCC_ABBA_1 | 258 | 263 | PF00400 | 0.672 |
LIG_APCC_ABBAyCdc20_2 | 681 | 687 | PF00400 | 0.393 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.727 |
LIG_BRCT_BRCA1_1 | 28 | 32 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_1 | 436 | 440 | PF00533 | 0.418 |
LIG_Clathr_ClatBox_1 | 669 | 673 | PF01394 | 0.405 |
LIG_eIF4E_1 | 145 | 151 | PF01652 | 0.625 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.671 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.715 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.727 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.612 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.560 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.468 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.407 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.435 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.346 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.682 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.664 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.595 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.447 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.673 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.470 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.448 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.593 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.696 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.578 |
LIG_LIR_Apic_2 | 375 | 379 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 502 | 513 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 665 | 670 | PF02991 | 0.490 |
LIG_MYND_1 | 468 | 472 | PF01753 | 0.590 |
LIG_NRBOX | 694 | 700 | PF00104 | 0.399 |
LIG_Pex14_2 | 181 | 185 | PF04695 | 0.605 |
LIG_Rb_pABgroove_1 | 26 | 34 | PF01858 | 0.619 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.487 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.481 |
LIG_SH2_CRK | 604 | 608 | PF00017 | 0.371 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 376 | 380 | PF00017 | 0.515 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.648 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.707 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.655 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.424 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.485 |
LIG_SUMO_SIM_par_1 | 492 | 497 | PF11976 | 0.701 |
LIG_SUMO_SIM_par_1 | 545 | 551 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 668 | 674 | PF11976 | 0.449 |
LIG_TRAF2_1 | 276 | 279 | PF00917 | 0.502 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.669 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.366 |
LIG_TYR_ITIM | 368 | 373 | PF00017 | 0.491 |
LIG_WRC_WIRS_1 | 446 | 451 | PF05994 | 0.496 |
LIG_WW_3 | 35 | 39 | PF00397 | 0.595 |
MOD_CDC14_SPxK_1 | 551 | 554 | PF00782 | 0.446 |
MOD_CDK_SPK_2 | 74 | 79 | PF00069 | 0.564 |
MOD_CDK_SPxK_1 | 548 | 554 | PF00069 | 0.429 |
MOD_CDK_SPxK_1 | 635 | 641 | PF00069 | 0.424 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.644 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.636 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.747 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.570 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.623 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.691 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.584 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.650 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.649 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.602 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.710 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.397 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.643 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.469 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.747 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.688 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.581 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.710 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.684 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.732 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.741 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.686 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.392 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.510 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.669 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.750 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.577 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.523 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.543 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.680 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.614 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.544 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.623 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.433 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.428 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.378 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.606 |
MOD_N-GLC_1 | 361 | 366 | PF02516 | 0.630 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.524 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.558 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.570 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.473 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.644 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.684 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.457 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.422 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.363 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.489 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.432 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.441 |
MOD_NEK2_2 | 587 | 592 | PF00069 | 0.486 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.643 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.404 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.392 |
MOD_PIKK_1 | 671 | 677 | PF00454 | 0.369 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.694 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.458 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.677 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.652 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.654 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.550 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.433 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.458 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.495 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.598 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.440 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.706 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.561 |
MOD_Plk_1 | 587 | 593 | PF00069 | 0.460 |
MOD_Plk_2-3 | 555 | 561 | PF00069 | 0.514 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.622 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.644 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.458 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.646 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.518 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.392 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.391 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.564 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.533 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.406 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.429 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.424 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.455 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.464 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.588 |
MOD_SUMO_for_1 | 209 | 212 | PF00179 | 0.683 |
MOD_SUMO_rev_2 | 597 | 601 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_2 | 540 | 546 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 455 | 460 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 650 | 655 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 562 | 564 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 582 | 584 | PF00400 | 0.230 |
TRG_ER_diArg_1 | 650 | 653 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.670 |
TRG_NES_CRM1_1 | 211 | 223 | PF08389 | 0.644 |
TRG_NES_CRM1_1 | 704 | 719 | PF08389 | 0.425 |
TRG_NLS_MonoExtC_3 | 287 | 293 | PF00514 | 0.654 |
TRG_NLS_MonoExtN_4 | 285 | 292 | PF00514 | 0.710 |
TRG_NLS_MonoExtN_4 | 600 | 606 | PF00514 | 0.342 |
TRG_Pf-PMV_PEXEL_1 | 537 | 541 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 612 | 616 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 630 | 635 | PF00026 | 0.533 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW55 | Leptomonas seymouri | 68% | 96% |
A0A0S4IV39 | Bodo saltans | 36% | 90% |
A0A1X0NVE2 | Trypanosomatidae | 45% | 100% |
A0A3S5H6I6 | Leishmania donovani | 92% | 100% |
A0A422MV99 | Trypanosoma rangeli | 44% | 100% |
A4H6H8 | Leishmania braziliensis | 83% | 100% |
A4HUW4 | Leishmania infantum | 92% | 100% |
D0A7I9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
Q4QH27 | Leishmania major | 93% | 100% |
V5BW97 | Trypanosoma cruzi | 45% | 100% |