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:0005847 | mRNA cleavage and polyadenylation specificity factor complex | 4 | 11 |
GO:0005849 | mRNA cleavage factor complex | 3 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0140513 | nuclear protein-containing complex | 2 | 11 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AX93
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006378 | mRNA polyadenylation | 7 | 11 |
GO:0006379 | mRNA cleavage | 7 | 11 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006397 | mRNA processing | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016071 | mRNA metabolic process | 6 | 11 |
GO:0031123 | RNA 3'-end processing | 7 | 11 |
GO:0031124 | mRNA 3'-end processing | 8 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043631 | RNA polyadenylation | 6 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 11 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0006398 | mRNA 3'-end processing by stem-loop binding and cleavage | 8 | 1 |
GO:0008334 | histone mRNA metabolic process | 7 | 1 |
GO:0098787 | mRNA cleavage involved in mRNA processing | 8 | 1 |
GO:0098789 | pre-mRNA cleavage required for polyadenylation | 9 | 1 |
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 | 118 | 122 | PF00656 | 0.460 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 716 | 718 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 758 | 760 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 811 | 813 | PF00675 | 0.270 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 811 | 813 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 307 | 309 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 522 | 524 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 542 | 544 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.770 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.338 |
DEG_APCC_DBOX_1 | 584 | 592 | PF00400 | 0.443 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.439 |
DEG_SPOP_SBC_1 | 643 | 647 | PF00917 | 0.329 |
DOC_ANK_TNKS_1 | 789 | 796 | PF00023 | 0.381 |
DOC_CKS1_1 | 802 | 807 | PF01111 | 0.381 |
DOC_CYCLIN_RxL_1 | 224 | 235 | PF00134 | 0.402 |
DOC_CYCLIN_RxL_1 | 499 | 511 | PF00134 | 0.582 |
DOC_CYCLIN_yCln2_LP_2 | 494 | 500 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 483 | 492 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 572 | 580 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 582 | 588 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 776 | 783 | PF00069 | 0.381 |
DOC_MAPK_HePTP_8 | 252 | 264 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 241 | 250 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.262 |
DOC_MAPK_MEF2A_6 | 485 | 494 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 572 | 580 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 776 | 783 | PF00069 | 0.267 |
DOC_MAPK_RevD_3 | 778 | 791 | PF00069 | 0.381 |
DOC_PP1_RVXF_1 | 32 | 38 | PF00149 | 0.509 |
DOC_PP1_RVXF_1 | 501 | 508 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 492 | 495 | PF13499 | 0.546 |
DOC_PP2B_PxIxI_1 | 327 | 333 | PF00149 | 0.425 |
DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.427 |
DOC_PP4_FxxP_1 | 198 | 201 | PF00568 | 0.329 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.308 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.509 |
DOC_USP7_UBL2_3 | 230 | 234 | PF12436 | 0.395 |
DOC_USP7_UBL2_3 | 601 | 605 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 801 | 806 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 547 | 554 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 585 | 595 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 715 | 723 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 811 | 815 | PF00244 | 0.291 |
LIG_Actin_WH2_2 | 225 | 243 | PF00022 | 0.346 |
LIG_Actin_WH2_2 | 663 | 681 | PF00022 | 0.313 |
LIG_Actin_WH2_2 | 748 | 763 | PF00022 | 0.277 |
LIG_Actin_WH2_2 | 795 | 813 | PF00022 | 0.267 |
LIG_APCC_ABBA_1 | 780 | 785 | PF00400 | 0.381 |
LIG_BIR_III_2 | 551 | 555 | PF00653 | 0.675 |
LIG_BIR_III_4 | 473 | 477 | PF00653 | 0.496 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 640 | 644 | PF00533 | 0.428 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.346 |
LIG_BRCT_BRCA1_1 | 746 | 750 | PF00533 | 0.381 |
LIG_Clathr_ClatBox_1 | 27 | 31 | PF01394 | 0.427 |
LIG_Clathr_ClatBox_1 | 780 | 784 | PF01394 | 0.329 |
LIG_CtBP_PxDLS_1 | 652 | 656 | PF00389 | 0.400 |
LIG_deltaCOP1_diTrp_1 | 38 | 45 | PF00928 | 0.427 |
LIG_eIF4E_1 | 176 | 182 | PF01652 | 0.427 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.424 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.427 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.351 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.339 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.509 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.569 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.562 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.575 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.353 |
LIG_FHA_1 | 794 | 800 | PF00498 | 0.381 |
LIG_FHA_1 | 802 | 808 | PF00498 | 0.381 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.450 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.548 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.362 |
LIG_FHA_2 | 736 | 742 | PF00498 | 0.306 |
LIG_GBD_Chelix_1 | 670 | 678 | PF00786 | 0.381 |
LIG_KLC1_Yacidic_2 | 402 | 407 | PF13176 | 0.541 |
LIG_LIR_Apic_2 | 106 | 112 | PF02991 | 0.460 |
LIG_LIR_Apic_2 | 179 | 185 | PF02991 | 0.427 |
LIG_LIR_Apic_2 | 525 | 531 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 300 | 309 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 768 | 779 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 8 | 15 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 506 | 510 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 768 | 774 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 813 | 818 | PF02991 | 0.268 |
LIG_Pex14_1 | 172 | 176 | PF04695 | 0.414 |
LIG_Pex14_1 | 41 | 45 | PF04695 | 0.427 |
LIG_Pex14_2 | 37 | 41 | PF04695 | 0.509 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.509 |
LIG_Rb_pABgroove_1 | 31 | 39 | PF01858 | 0.509 |
LIG_RPA_C_Fungi | 350 | 362 | PF08784 | 0.492 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.381 |
LIG_SH2_CRK | 24 | 28 | PF00017 | 0.385 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.307 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.462 |
LIG_SH2_NCK_1 | 723 | 727 | PF00017 | 0.269 |
LIG_SH2_PTP2 | 405 | 408 | PF00017 | 0.488 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 660 | 664 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 818 | 822 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.369 |
LIG_SH2_STAT3 | 662 | 665 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.205 |
LIG_SH3_1 | 52 | 58 | PF00018 | 0.269 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.386 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.286 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.373 |
LIG_SH3_3 | 490 | 496 | PF00018 | 0.697 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.269 |
LIG_SUMO_SIM_anti_2 | 359 | 366 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 26 | 31 | PF11976 | 0.248 |
LIG_SUMO_SIM_par_1 | 359 | 366 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 651 | 657 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 778 | 785 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 794 | 801 | PF11976 | 0.327 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.344 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.528 |
LIG_TRAF2_1 | 533 | 536 | PF00917 | 0.602 |
LIG_TRAF2_1 | 764 | 767 | PF00917 | 0.458 |
LIG_TRFH_1 | 193 | 197 | PF08558 | 0.338 |
LIG_WRC_WIRS_1 | 104 | 109 | PF05994 | 0.313 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.327 |
LIG_WW_2 | 367 | 370 | PF00397 | 0.514 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.313 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.559 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.292 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.562 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.487 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.433 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.448 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.289 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.268 |
MOD_CK1_1 | 801 | 807 | PF00069 | 0.277 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.426 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.461 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.381 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.350 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.322 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.519 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.538 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.359 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.306 |
MOD_CK2_1 | 761 | 767 | PF00069 | 0.458 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.466 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.320 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.450 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.308 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.546 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.466 |
MOD_GlcNHglycan | 590 | 594 | PF01048 | 0.344 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.452 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.382 |
MOD_GlcNHglycan | 698 | 702 | PF01048 | 0.436 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.381 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.323 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.201 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.289 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.248 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.442 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.557 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.648 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.290 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.668 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.354 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.580 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.327 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.417 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.352 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.169 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.363 |
MOD_GSK3_1 | 761 | 768 | PF00069 | 0.381 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.259 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.313 |
MOD_LATS_1 | 501 | 507 | PF00433 | 0.595 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.506 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.354 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.353 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.401 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.393 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.384 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.327 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.562 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.447 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.286 |
MOD_NEK2_1 | 760 | 765 | PF00069 | 0.291 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.458 |
MOD_NEK2_1 | 810 | 815 | PF00069 | 0.313 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.269 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.300 |
MOD_NEK2_2 | 185 | 190 | PF00069 | 0.212 |
MOD_PIKK_1 | 730 | 736 | PF00454 | 0.375 |
MOD_PIKK_1 | 816 | 822 | PF00454 | 0.409 |
MOD_PKA_1 | 715 | 721 | PF00069 | 0.381 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.340 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.455 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.367 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.335 |
MOD_PKA_2 | 715 | 721 | PF00069 | 0.381 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.303 |
MOD_PKA_2 | 810 | 816 | PF00069 | 0.291 |
MOD_PKB_1 | 759 | 767 | PF00069 | 0.381 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.252 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.297 |
MOD_Plk_1 | 524 | 530 | PF00069 | 0.462 |
MOD_Plk_1 | 666 | 672 | PF00069 | 0.381 |
MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.323 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.323 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.464 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.424 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.291 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.409 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.327 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.381 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.381 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.462 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.267 |
MOD_ProDKin_1 | 801 | 807 | PF00069 | 0.259 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.267 |
MOD_SUMO_for_1 | 223 | 226 | PF00179 | 0.278 |
MOD_SUMO_for_1 | 437 | 440 | PF00179 | 0.603 |
MOD_SUMO_rev_2 | 300 | 309 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_4 | 535 | 541 | PF01217 | 0.620 |
TRG_DiLeu_BaLyEn_6 | 776 | 781 | PF01217 | 0.381 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 771 | 774 | PF00928 | 0.381 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 582 | 585 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 678 | 680 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 715 | 717 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 757 | 759 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 810 | 812 | PF00400 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.248 |
TRG_Pf-PMV_PEXEL_1 | 417 | 422 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 758 | 762 | PF00026 | 0.313 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEP3 | Leptomonas seymouri | 75% | 99% |
A0A0S4JJR9 | Bodo saltans | 30% | 87% |
A0A1X0P5N3 | Trypanosomatidae | 50% | 100% |
A0A3Q8IBL1 | Leishmania donovani | 95% | 100% |
A0A422NF58 | Trypanosoma rangeli | 51% | 100% |
A4HDW4 | Leishmania braziliensis | 89% | 100% |
A4I159 | Leishmania infantum | 95% | 100% |
A8XUS3 | Caenorhabditis briggsae | 22% | 98% |
D0A5E4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
O17403 | Caenorhabditis elegans | 22% | 98% |
Q4QA79 | Leishmania major | 96% | 100% |
Q652P4 | Oryza sativa subsp. japonica | 22% | 100% |
Q9LKF9 | Arabidopsis thaliana | 23% | 100% |