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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030686 | 90S preribosome | 4 | 1 |
GO:0030688 | preribosome, small subunit precursor | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 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 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AUY4
Term | Name | Level | Count |
---|---|---|---|
GO:0000054 | ribosomal subunit export from nucleus | 3 | 1 |
GO:0000056 | ribosomal small subunit export from nucleus | 4 | 1 |
GO:0000447 | endonucleolytic cleavage in ITS1 to separate SSU-rRNA from 5.8S rRNA and LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 1 |
GO:0000472 | endonucleolytic cleavage to generate mature 5'-end of SSU-rRNA from (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000478 | endonucleolytic cleavage involved in rRNA processing | 8 | 1 |
GO:0000479 | endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 1 |
GO:0000480 | endonucleolytic cleavage in 5'-ETS of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000966 | RNA 5'-end processing | 7 | 1 |
GO:0000967 | rRNA 5'-end processing | 9 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0033750 | ribosome localization | 3 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034471 | ncRNA 5'-end processing | 8 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0036260 | RNA capping | 7 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051656 | establishment of organelle localization | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 1 |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 467 | 471 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 738 | 740 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 758 | 760 | PF00675 | 0.331 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 720 | 722 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.666 |
CLV_PCSK_PC1ET2_1 | 445 | 447 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 623 | 625 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 720 | 722 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 758 | 762 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.495 |
DEG_APCC_DBOX_1 | 568 | 576 | PF00400 | 0.512 |
DEG_SCF_FBW7_1 | 453 | 459 | PF00400 | 0.403 |
DEG_SCF_FBW7_1 | 685 | 690 | PF00400 | 0.615 |
DOC_CDC14_PxL_1 | 430 | 438 | PF14671 | 0.462 |
DOC_CKS1_1 | 453 | 458 | PF01111 | 0.606 |
DOC_CYCLIN_RxL_1 | 755 | 764 | PF00134 | 0.677 |
DOC_MAPK_DCC_7 | 500 | 508 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 209 | 218 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 566 | 575 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 623 | 629 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 739 | 746 | PF00069 | 0.500 |
DOC_MAPK_HePTP_8 | 206 | 218 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 118 | 125 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 375 | 384 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 420 | 429 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 500 | 508 | PF00069 | 0.479 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.445 |
DOC_PP2B_LxvP_1 | 407 | 410 | PF13499 | 0.395 |
DOC_PP2B_LxvP_1 | 594 | 597 | PF13499 | 0.586 |
DOC_PP4_FxxP_1 | 431 | 434 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.307 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 681 | 686 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 713 | 718 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 631 | 641 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 677 | 685 | PF00244 | 0.685 |
LIG_14-3-3_CterR_2 | 759 | 764 | PF00244 | 0.680 |
LIG_Actin_RPEL_3 | 96 | 115 | PF02755 | 0.416 |
LIG_Actin_WH2_2 | 199 | 214 | PF00022 | 0.507 |
LIG_APCC_ABBA_1 | 670 | 675 | PF00400 | 0.495 |
LIG_eIF4E_1 | 139 | 145 | PF01652 | 0.476 |
LIG_eIF4E_1 | 306 | 312 | PF01652 | 0.526 |
LIG_eIF4E_1 | 400 | 406 | PF01652 | 0.398 |
LIG_FAT_LD_1 | 141 | 149 | PF03623 | 0.440 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.498 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.549 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.553 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.274 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.409 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.706 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.555 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.458 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.707 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.615 |
LIG_IRF3_LxIS_1 | 128 | 134 | PF10401 | 0.480 |
LIG_LIR_Gen_1 | 119 | 128 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 17 | 28 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 507 | 516 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 643 | 653 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 741 | 747 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.411 |
LIG_LIR_LC3C_4 | 276 | 280 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 507 | 511 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 639 | 645 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 741 | 746 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.400 |
LIG_MYND_1 | 434 | 438 | PF01753 | 0.526 |
LIG_NRBOX | 140 | 146 | PF00104 | 0.436 |
LIG_NRBOX | 311 | 317 | PF00104 | 0.378 |
LIG_NRBOX | 82 | 88 | PF00104 | 0.422 |
LIG_PCNA_yPIPBox_3 | 628 | 641 | PF02747 | 0.494 |
LIG_PCNA_yPIPBox_3 | 749 | 761 | PF02747 | 0.521 |
LIG_Rb_pABgroove_1 | 425 | 433 | PF01858 | 0.500 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.509 |
LIG_SH2_NCK_1 | 501 | 505 | PF00017 | 0.488 |
LIG_SH2_NCK_1 | 654 | 658 | PF00017 | 0.510 |
LIG_SH2_PTP2 | 122 | 125 | PF00017 | 0.404 |
LIG_SH2_PTP2 | 588 | 591 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 254 | 258 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 642 | 646 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 400 | 403 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 736 | 739 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.476 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.576 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.509 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.405 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.464 |
LIG_SH3_CIN85_PxpxPR_1 | 232 | 237 | PF14604 | 0.453 |
LIG_SUMO_SIM_anti_2 | 213 | 219 | PF11976 | 0.416 |
LIG_SUMO_SIM_anti_2 | 570 | 577 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.503 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.513 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.469 |
LIG_TRFH_1 | 452 | 456 | PF08558 | 0.584 |
LIG_TYR_ITIM | 120 | 125 | PF00017 | 0.393 |
LIG_TYR_ITIM | 499 | 504 | PF00017 | 0.429 |
LIG_UBA3_1 | 572 | 580 | PF00899 | 0.477 |
LIG_UBA3_1 | 83 | 88 | PF00899 | 0.447 |
LIG_WRC_WIRS_1 | 449 | 454 | PF05994 | 0.586 |
MOD_CDK_SPxxK_3 | 24 | 31 | PF00069 | 0.593 |
MOD_CDK_SPxxK_3 | 713 | 720 | PF00069 | 0.559 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.417 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.591 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.660 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.435 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.443 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.665 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.670 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.502 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.758 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.462 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.544 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.513 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.487 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.530 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.594 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.550 |
MOD_Cter_Amidation | 7 | 10 | PF01082 | 0.736 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.450 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.515 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.416 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.733 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.579 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.558 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.545 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.483 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.587 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.736 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.757 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.673 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.375 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.426 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.504 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.475 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.618 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.682 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.474 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.428 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.645 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.326 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.593 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.594 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.493 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.695 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.419 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.421 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.456 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.488 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.500 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.474 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.477 |
MOD_NEK2_2 | 219 | 224 | PF00069 | 0.435 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.477 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.495 |
MOD_PIKK_1 | 675 | 681 | PF00454 | 0.657 |
MOD_PIKK_1 | 715 | 721 | PF00454 | 0.532 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.561 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.452 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.569 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.455 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.456 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.384 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.382 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.413 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.378 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.418 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.454 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.537 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.429 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.537 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.298 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.444 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.398 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.440 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.485 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.451 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.355 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.366 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.596 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.453 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.428 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.627 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.513 |
MOD_ProDKin_1 | 681 | 687 | PF00069 | 0.773 |
MOD_ProDKin_1 | 713 | 719 | PF00069 | 0.585 |
MOD_SUMO_rev_2 | 617 | 625 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 703 | 713 | PF00179 | 0.482 |
TRG_DiLeu_BaEn_1 | 383 | 388 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 82 | 87 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_2 | 543 | 549 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 307 | 312 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 752 | 757 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 645 | 648 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 673 | 676 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 725 | 728 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 630 | 632 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 757 | 759 | PF00400 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 489 | 494 | PF00026 | 0.274 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 759 | 764 | PF00026 | 0.680 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4K4 | Leptomonas seymouri | 68% | 97% |
A0A0S4J166 | Bodo saltans | 34% | 100% |
A0A1X0NXL8 | Trypanosomatidae | 42% | 96% |
A0A3S5IR95 | Trypanosoma rangeli | 39% | 100% |
A0A3S7WW94 | Leishmania donovani | 92% | 100% |
A4HBL6 | Leishmania braziliensis | 84% | 100% |
A4HZA4 | Leishmania infantum | 92% | 100% |
D0A1L0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
Q4QCJ8 | Leishmania major | 91% | 100% |
V5B0J8 | Trypanosoma cruzi | 43% | 100% |