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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 2 |
GO:0030684 | preribosome | 3 | 2 |
GO:0030686 | 90S preribosome | 4 | 2 |
GO:0030688 | preribosome, small subunit precursor | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QCJ8
Term | Name | Level | Count |
---|---|---|---|
GO:0000054 | ribosomal subunit export from nucleus | 3 | 2 |
GO:0000056 | ribosomal small subunit export from nucleus | 4 | 2 |
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 | 2 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 2 |
GO:0000472 | endonucleolytic cleavage to generate mature 5'-end of SSU-rRNA from (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 2 |
GO:0000478 | endonucleolytic cleavage involved in rRNA processing | 8 | 2 |
GO:0000479 | endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 2 |
GO:0000480 | endonucleolytic cleavage in 5'-ETS of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 2 |
GO:0000966 | RNA 5'-end processing | 7 | 2 |
GO:0000967 | rRNA 5'-end processing | 9 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0031503 | protein-containing complex localization | 2 | 2 |
GO:0033750 | ribosome localization | 3 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034471 | ncRNA 5'-end processing | 8 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0036260 | RNA capping | 7 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051168 | nuclear export | 6 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051640 | organelle localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051656 | establishment of organelle localization | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 2 |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | 7 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.763 |
CLV_C14_Caspase3-7 | 467 | 471 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.401 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 640 | 642 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 729 | 731 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 747 | 749 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 767 | 769 | PF00675 | 0.315 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 640 | 642 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 729 | 731 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 767 | 769 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 445 | 447 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 632 | 634 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.185 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 767 | 771 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.421 |
DEG_APCC_DBOX_1 | 568 | 576 | PF00400 | 0.453 |
DOC_CDC14_PxL_1 | 223 | 231 | PF14671 | 0.340 |
DOC_CDC14_PxL_1 | 430 | 438 | PF14671 | 0.382 |
DOC_CYCLIN_RxL_1 | 764 | 773 | PF00134 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 229 | 235 | PF00134 | 0.368 |
DOC_MAPK_DCC_7 | 500 | 508 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 209 | 218 | PF00069 | 0.286 |
DOC_MAPK_gen_1 | 566 | 575 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 632 | 638 | PF00069 | 0.438 |
DOC_MAPK_HePTP_8 | 206 | 218 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 118 | 125 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.297 |
DOC_MAPK_MEF2A_6 | 375 | 384 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 420 | 429 | PF00069 | 0.333 |
DOC_MAPK_MEF2A_6 | 500 | 508 | PF00069 | 0.402 |
DOC_PP2B_LxvP_1 | 329 | 332 | PF13499 | 0.358 |
DOC_PP2B_LxvP_1 | 407 | 410 | PF13499 | 0.330 |
DOC_PP2B_LxvP_1 | 594 | 597 | PF13499 | 0.516 |
DOC_PP4_FxxP_1 | 431 | 434 | PF00568 | 0.446 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.288 |
DOC_USP7_MATH_2 | 11 | 17 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 489 | 493 | PF12436 | 0.352 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 722 | 727 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 640 | 650 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 686 | 694 | PF00244 | 0.502 |
LIG_14-3-3_CterR_2 | 768 | 773 | PF00244 | 0.492 |
LIG_Actin_RPEL_3 | 96 | 115 | PF02755 | 0.326 |
LIG_Actin_WH2_2 | 199 | 214 | PF00022 | 0.447 |
LIG_Actin_WH2_2 | 655 | 673 | PF00022 | 0.326 |
LIG_APCC_ABBA_1 | 679 | 684 | PF00400 | 0.405 |
LIG_eIF4E_1 | 139 | 145 | PF01652 | 0.415 |
LIG_eIF4E_1 | 306 | 312 | PF01652 | 0.468 |
LIG_eIF4E_1 | 400 | 406 | PF01652 | 0.333 |
LIG_FAT_LD_1 | 141 | 149 | PF03623 | 0.355 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.485 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.496 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.550 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.452 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.321 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.568 |
LIG_FHA_1 | 691 | 697 | PF00498 | 0.489 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.513 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.428 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.630 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.712 |
LIG_FHA_2 | 708 | 714 | PF00498 | 0.597 |
LIG_FHA_2 | 718 | 724 | PF00498 | 0.583 |
LIG_IRF3_LxIS_1 | 128 | 134 | PF10401 | 0.427 |
LIG_LIR_Gen_1 | 119 | 128 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 17 | 28 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 652 | 662 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.322 |
LIG_LIR_LC3C_4 | 276 | 280 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 648 | 654 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 750 | 755 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.348 |
LIG_MYND_1 | 434 | 438 | PF01753 | 0.353 |
LIG_NRBOX | 140 | 146 | PF00104 | 0.410 |
LIG_NRBOX | 311 | 317 | PF00104 | 0.308 |
LIG_NRBOX | 82 | 88 | PF00104 | 0.331 |
LIG_PCNA_yPIPBox_3 | 637 | 650 | PF02747 | 0.419 |
LIG_PCNA_yPIPBox_3 | 758 | 770 | PF02747 | 0.442 |
LIG_Rb_pABgroove_1 | 425 | 433 | PF01858 | 0.442 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.452 |
LIG_SH2_CRK | 734 | 738 | PF00017 | 0.254 |
LIG_SH2_NCK_1 | 501 | 505 | PF00017 | 0.434 |
LIG_SH2_NCK_1 | 663 | 667 | PF00017 | 0.436 |
LIG_SH2_PTP2 | 122 | 125 | PF00017 | 0.312 |
LIG_SH2_PTP2 | 588 | 591 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 651 | 655 | PF00017 | 0.355 |
LIG_SH2_STAT3 | 400 | 403 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 745 | 748 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.443 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.468 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.432 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.321 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.411 |
LIG_SH3_CIN85_PxpxPR_1 | 232 | 237 | PF14604 | 0.333 |
LIG_SUMO_SIM_anti_2 | 213 | 218 | PF11976 | 0.318 |
LIG_SUMO_SIM_anti_2 | 570 | 577 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.436 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.459 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.380 |
LIG_TRFH_1 | 452 | 456 | PF08558 | 0.459 |
LIG_TYR_ITIM | 120 | 125 | PF00017 | 0.301 |
LIG_TYR_ITIM | 499 | 504 | PF00017 | 0.367 |
LIG_TYR_ITIM | 732 | 737 | PF00017 | 0.243 |
LIG_UBA3_1 | 572 | 580 | PF00899 | 0.417 |
LIG_UBA3_1 | 83 | 88 | PF00899 | 0.358 |
LIG_WRC_WIRS_1 | 449 | 454 | PF05994 | 0.395 |
MOD_CDK_SPxxK_3 | 24 | 31 | PF00069 | 0.528 |
MOD_CDK_SPxxK_3 | 722 | 729 | PF00069 | 0.424 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.612 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.324 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.521 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.632 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.596 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.358 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.579 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.567 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.442 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.575 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.457 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.532 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.452 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.425 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.534 |
MOD_Cter_Amidation | 7 | 10 | PF01082 | 0.661 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.394 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.424 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.323 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.638 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.495 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.531 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.591 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.464 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.658 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.496 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.698 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.655 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.573 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.299 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.298 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.450 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.462 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.609 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.422 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.600 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.360 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.457 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.523 |
MOD_N-GLC_1 | 717 | 722 | PF02516 | 0.591 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.336 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.336 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.388 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.445 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.353 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.418 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.425 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.392 |
MOD_NEK2_2 | 219 | 224 | PF00069 | 0.340 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.391 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.478 |
MOD_PIKK_1 | 684 | 690 | PF00454 | 0.474 |
MOD_PIKK_1 | 724 | 730 | PF00454 | 0.396 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.468 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.386 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.500 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.404 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.497 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.370 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.385 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.524 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.293 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.288 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.404 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.381 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.316 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.344 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.396 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.531 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.464 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.355 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.327 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.381 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.401 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.364 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.420 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.299 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.531 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.385 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.496 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.588 |
MOD_ProDKin_1 | 722 | 728 | PF00069 | 0.551 |
TRG_DiLeu_BaEn_1 | 383 | 388 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_1 | 82 | 87 | PF01217 | 0.322 |
TRG_DiLeu_BaEn_2 | 543 | 549 | PF01217 | 0.336 |
TRG_DiLeu_BaLyEn_6 | 224 | 229 | PF01217 | 0.311 |
TRG_DiLeu_BaLyEn_6 | 307 | 312 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 761 | 766 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 588 | 591 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 682 | 685 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 734 | 737 | PF00928 | 0.441 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 34 | 36 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 639 | 641 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 729 | 731 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 766 | 768 | PF00400 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 57 | 61 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 768 | 773 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4K4 | Leptomonas seymouri | 67% | 98% |
A0A0S4J166 | Bodo saltans | 34% | 100% |
A0A1X0NXL8 | Trypanosomatidae | 41% | 97% |
A0A3S7WW94 | Leishmania donovani | 93% | 100% |
A4HBL6 | Leishmania braziliensis | 82% | 100% |
A4HZA4 | Leishmania infantum | 93% | 100% |
D0A1L0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AUY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B0J8 | Trypanosoma cruzi | 44% | 100% |