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: A0A3Q8IBL1
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 | 0.563 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 675 | 677 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 712 | 714 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 754 | 756 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 785 | 787 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 807 | 809 | PF00675 | 0.335 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 711 | 713 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 754 | 756 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 807 | 809 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 307 | 309 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 518 | 520 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.760 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.395 |
DEG_APCC_DBOX_1 | 580 | 588 | PF00400 | 0.485 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.505 |
DEG_SPOP_SBC_1 | 639 | 643 | PF00917 | 0.380 |
DOC_ANK_TNKS_1 | 785 | 792 | PF00023 | 0.424 |
DOC_CKS1_1 | 798 | 803 | PF01111 | 0.424 |
DOC_CYCLIN_RxL_1 | 224 | 235 | PF00134 | 0.550 |
DOC_CYCLIN_RxL_1 | 495 | 507 | PF00134 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 490 | 496 | PF00134 | 0.639 |
DOC_MAPK_gen_1 | 479 | 488 | PF00069 | 0.667 |
DOC_MAPK_gen_1 | 568 | 576 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 578 | 584 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 772 | 779 | PF00069 | 0.424 |
DOC_MAPK_HePTP_8 | 252 | 264 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 241 | 250 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 481 | 490 | PF00069 | 0.723 |
DOC_MAPK_MEF2A_6 | 568 | 576 | PF00069 | 0.521 |
DOC_MAPK_MEF2A_6 | 772 | 779 | PF00069 | 0.332 |
DOC_MAPK_RevD_3 | 774 | 787 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 32 | 38 | PF00149 | 0.539 |
DOC_PP1_RVXF_1 | 497 | 504 | PF00149 | 0.603 |
DOC_PP2B_LxvP_1 | 488 | 491 | PF13499 | 0.593 |
DOC_PP2B_PxIxI_1 | 327 | 333 | PF00149 | 0.435 |
DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.473 |
DOC_PP4_FxxP_1 | 198 | 201 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.369 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 230 | 234 | PF12436 | 0.541 |
DOC_USP7_UBL2_3 | 597 | 601 | PF12436 | 0.497 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 797 | 802 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.530 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 543 | 550 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 581 | 591 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 711 | 719 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 807 | 811 | PF00244 | 0.355 |
LIG_Actin_WH2_2 | 225 | 243 | PF00022 | 0.414 |
LIG_Actin_WH2_2 | 659 | 677 | PF00022 | 0.457 |
LIG_Actin_WH2_2 | 744 | 759 | PF00022 | 0.342 |
LIG_Actin_WH2_2 | 791 | 809 | PF00022 | 0.332 |
LIG_APCC_ABBA_1 | 776 | 781 | PF00400 | 0.424 |
LIG_BIR_III_2 | 547 | 551 | PF00653 | 0.713 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.484 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.484 |
LIG_BRCT_BRCA1_1 | 636 | 640 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 742 | 746 | PF00533 | 0.424 |
LIG_Clathr_ClatBox_1 | 27 | 31 | PF01394 | 0.473 |
LIG_Clathr_ClatBox_1 | 776 | 780 | PF01394 | 0.387 |
LIG_CtBP_PxDLS_1 | 648 | 652 | PF00389 | 0.525 |
LIG_deltaCOP1_diTrp_1 | 38 | 45 | PF00928 | 0.473 |
LIG_eIF4E_1 | 176 | 182 | PF01652 | 0.473 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.470 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.563 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.365 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.406 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.539 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.621 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.561 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.610 |
LIG_FHA_1 | 683 | 689 | PF00498 | 0.406 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.424 |
LIG_FHA_1 | 798 | 804 | PF00498 | 0.424 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.495 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.566 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.572 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.412 |
LIG_FHA_2 | 732 | 738 | PF00498 | 0.368 |
LIG_GBD_Chelix_1 | 666 | 674 | PF00786 | 0.424 |
LIG_KLC1_Yacidic_2 | 402 | 407 | PF13176 | 0.576 |
LIG_LIR_Apic_2 | 106 | 112 | PF02991 | 0.563 |
LIG_LIR_Apic_2 | 179 | 185 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 521 | 527 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 300 | 309 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.693 |
LIG_LIR_Gen_1 | 764 | 775 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 8 | 15 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 764 | 770 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 809 | 814 | PF02991 | 0.333 |
LIG_Pex14_1 | 172 | 176 | PF04695 | 0.460 |
LIG_Pex14_1 | 41 | 45 | PF04695 | 0.473 |
LIG_Pex14_2 | 37 | 41 | PF04695 | 0.539 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.539 |
LIG_Rb_pABgroove_1 | 31 | 39 | PF01858 | 0.539 |
LIG_RPA_C_Fungi | 350 | 362 | PF08784 | 0.538 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.386 |
LIG_SH2_CRK | 24 | 28 | PF00017 | 0.432 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.372 |
LIG_SH2_CRK | 524 | 528 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 719 | 723 | PF00017 | 0.380 |
LIG_SH2_PTP2 | 405 | 408 | PF00017 | 0.538 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 656 | 660 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 814 | 818 | PF00017 | 0.588 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 658 | 661 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.529 |
LIG_SH3_1 | 52 | 58 | PF00018 | 0.380 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.450 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.350 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.438 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.717 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.380 |
LIG_SUMO_SIM_anti_2 | 359 | 366 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 26 | 31 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 359 | 366 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 647 | 653 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 774 | 781 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 790 | 797 | PF11976 | 0.386 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.409 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.562 |
LIG_TRAF2_1 | 529 | 532 | PF00917 | 0.628 |
LIG_TRAF2_1 | 760 | 763 | PF00917 | 0.468 |
LIG_TRFH_1 | 193 | 197 | PF08558 | 0.404 |
LIG_WRC_WIRS_1 | 104 | 109 | PF05994 | 0.438 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.386 |
LIG_WW_2 | 367 | 370 | PF00397 | 0.560 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.457 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.483 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.578 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.243 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.346 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.566 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.529 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.476 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.579 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.376 |
MOD_CK1_1 | 720 | 726 | PF00069 | 0.333 |
MOD_CK1_1 | 797 | 803 | PF00069 | 0.342 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.403 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.493 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.344 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.589 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.418 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.386 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.554 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.582 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.406 |
MOD_CK2_1 | 731 | 737 | PF00069 | 0.368 |
MOD_CK2_1 | 757 | 763 | PF00069 | 0.468 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.505 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.380 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.585 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.370 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.611 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.514 |
MOD_GlcNHglycan | 586 | 590 | PF01048 | 0.409 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.500 |
MOD_GlcNHglycan | 694 | 698 | PF01048 | 0.456 |
MOD_GlcNHglycan | 742 | 745 | PF01048 | 0.424 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.382 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.259 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.335 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.313 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.552 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.339 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.684 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.355 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.665 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.417 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.570 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.376 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.439 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.332 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.288 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.412 |
MOD_GSK3_1 | 757 | 764 | PF00069 | 0.424 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.324 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.443 |
MOD_LATS_1 | 497 | 503 | PF00433 | 0.729 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.656 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.418 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.418 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.477 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.419 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.444 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.386 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.605 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.573 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.351 |
MOD_NEK2_1 | 756 | 761 | PF00069 | 0.355 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.443 |
MOD_NEK2_1 | 806 | 811 | PF00069 | 0.374 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.334 |
MOD_NEK2_2 | 185 | 190 | PF00069 | 0.269 |
MOD_PIKK_1 | 726 | 732 | PF00454 | 0.420 |
MOD_PIKK_1 | 812 | 818 | PF00454 | 0.481 |
MOD_PKA_1 | 711 | 717 | PF00069 | 0.424 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.404 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.589 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.477 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.430 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.386 |
MOD_PKA_2 | 711 | 717 | PF00069 | 0.424 |
MOD_PKA_2 | 756 | 762 | PF00069 | 0.366 |
MOD_PKA_2 | 806 | 812 | PF00069 | 0.355 |
MOD_PKB_1 | 755 | 763 | PF00069 | 0.424 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.300 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.361 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.512 |
MOD_Plk_1 | 662 | 668 | PF00069 | 0.424 |
MOD_Plk_2-3 | 334 | 340 | PF00069 | 0.387 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.390 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.424 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.445 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.355 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.463 |
MOD_Plk_4 | 742 | 748 | PF00069 | 0.386 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.416 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.424 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.475 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.322 |
MOD_ProDKin_1 | 797 | 803 | PF00069 | 0.324 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 437 | 440 | PF00179 | 0.714 |
MOD_SUMO_rev_2 | 300 | 309 | PF00179 | 0.573 |
TRG_DiLeu_BaEn_1 | 531 | 536 | PF01217 | 0.487 |
TRG_DiLeu_BaEn_4 | 531 | 537 | PF01217 | 0.649 |
TRG_DiLeu_BaLyEn_6 | 772 | 777 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 767 | 770 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 578 | 581 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 674 | 676 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 711 | 713 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 753 | 755 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 806 | 808 | PF00400 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 754 | 758 | PF00026 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEP3 | Leptomonas seymouri | 75% | 99% |
A0A0S4JJR9 | Bodo saltans | 30% | 86% |
A0A1X0P5N3 | Trypanosomatidae | 51% | 100% |
A0A422NF58 | Trypanosoma rangeli | 51% | 100% |
A4HDW4 | Leishmania braziliensis | 89% | 100% |
A4I159 | Leishmania infantum | 100% | 100% |
A8XUS3 | Caenorhabditis briggsae | 23% | 97% |
D0A5E4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AX93 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4QA79 | Leishmania major | 95% | 100% |
Q652P4 | Oryza sativa subsp. japonica | 23% | 100% |
Q9V3D6 | Drosophila melanogaster | 25% | 100% |