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:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AZY2
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
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:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0004730 | pseudouridylate synthase activity | 5 | 2 |
GO:0016829 | lyase activity | 2 | 2 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 2 |
GO:0016836 | hydro-lyase activity | 4 | 2 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.325 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.219 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 734 | 736 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 751 | 753 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 802 | 804 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 805 | 807 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 818 | 820 | PF00675 | 0.617 |
CLV_PCSK_FUR_1 | 309 | 313 | PF00082 | 0.421 |
CLV_PCSK_FUR_1 | 802 | 806 | PF00082 | 0.591 |
CLV_PCSK_FUR_1 | 816 | 820 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 751 | 753 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 760 | 762 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 794 | 796 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 802 | 804 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 818 | 820 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 760 | 762 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 794 | 796 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 804 | 806 | PF00082 | 0.542 |
CLV_PCSK_PC7_1 | 429 | 435 | PF00082 | 0.303 |
CLV_PCSK_PC7_1 | 747 | 753 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 760 | 764 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.493 |
CLV_Separin_Metazoa | 610 | 614 | PF03568 | 0.303 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.319 |
DEG_APCC_DBOX_1 | 339 | 347 | PF00400 | 0.340 |
DOC_ANK_TNKS_1 | 326 | 333 | PF00023 | 0.171 |
DOC_CDC14_PxL_1 | 445 | 453 | PF14671 | 0.315 |
DOC_CDC14_PxL_1 | 76 | 84 | PF14671 | 0.458 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 613 | 625 | PF00134 | 0.388 |
DOC_CYCLIN_RxL_1 | 758 | 767 | PF00134 | 0.580 |
DOC_MAPK_gen_1 | 308 | 319 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 428 | 440 | PF00069 | 0.381 |
DOC_PP1_RVXF_1 | 758 | 765 | PF00149 | 0.634 |
DOC_PP2B_LxvP_1 | 667 | 670 | PF13499 | 0.508 |
DOC_PP2B_LxvP_1 | 725 | 728 | PF13499 | 0.567 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.431 |
DOC_PP4_FxxP_1 | 608 | 611 | PF00568 | 0.303 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.628 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 789 | 793 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.719 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 807 | 812 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 819 | 824 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 165 | 174 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 275 | 280 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 373 | 377 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 497 | 502 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 532 | 538 | PF00244 | 0.193 |
LIG_14-3-3_CanoR_1 | 818 | 823 | PF00244 | 0.692 |
LIG_Actin_WH2_2 | 464 | 482 | PF00022 | 0.405 |
LIG_AP2alpha_2 | 732 | 734 | PF02296 | 0.635 |
LIG_APCC_ABBA_1 | 544 | 549 | PF00400 | 0.171 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.696 |
LIG_BRCT_BRCA1_1 | 846 | 850 | PF00533 | 0.642 |
LIG_CaM_IQ_9 | 124 | 139 | PF13499 | 0.588 |
LIG_CtBP_PxDLS_1 | 619 | 623 | PF00389 | 0.319 |
LIG_deltaCOP1_diTrp_1 | 542 | 547 | PF00928 | 0.424 |
LIG_EH1_1 | 22 | 30 | PF00400 | 0.394 |
LIG_eIF4E_1 | 324 | 330 | PF01652 | 0.337 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.692 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.419 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.315 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.319 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.319 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.659 |
LIG_FHA_1 | 832 | 838 | PF00498 | 0.720 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.743 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.321 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.754 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.324 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.454 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.259 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.180 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.360 |
LIG_FHA_2 | 558 | 564 | PF00498 | 0.358 |
LIG_FHA_2 | 685 | 691 | PF00498 | 0.579 |
LIG_LIR_Apic_2 | 607 | 611 | PF02991 | 0.304 |
LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 382 | 393 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 542 | 551 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 481 | 486 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 542 | 547 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 570 | 574 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 671 | 677 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 690 | 695 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 839 | 843 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.481 |
LIG_NRBOX | 408 | 414 | PF00104 | 0.303 |
LIG_PCNA_PIPBox_1 | 578 | 587 | PF02747 | 0.337 |
LIG_PCNA_yPIPBox_3 | 578 | 591 | PF02747 | 0.430 |
LIG_PCNA_yPIPBox_3 | 641 | 653 | PF02747 | 0.303 |
LIG_Pex14_1 | 543 | 547 | PF04695 | 0.424 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.448 |
LIG_Pex14_2 | 335 | 339 | PF04695 | 0.303 |
LIG_Pex14_2 | 395 | 399 | PF04695 | 0.319 |
LIG_RPA_C_Fungi | 143 | 155 | PF08784 | 0.382 |
LIG_SH2_CRK | 585 | 589 | PF00017 | 0.384 |
LIG_SH2_CRK | 644 | 648 | PF00017 | 0.303 |
LIG_SH2_CRK | 797 | 801 | PF00017 | 0.651 |
LIG_SH2_GRB2like | 644 | 647 | PF00017 | 0.303 |
LIG_SH2_NCK_1 | 626 | 630 | PF00017 | 0.369 |
LIG_SH2_NCK_1 | 644 | 648 | PF00017 | 0.235 |
LIG_SH2_SRC | 626 | 629 | PF00017 | 0.431 |
LIG_SH2_SRC | 644 | 647 | PF00017 | 0.222 |
LIG_SH2_SRC | 695 | 698 | PF00017 | 0.663 |
LIG_SH2_STAP1 | 626 | 630 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 644 | 648 | PF00017 | 0.236 |
LIG_SH2_STAP1 | 797 | 801 | PF00017 | 0.651 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 584 | 587 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.482 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.680 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.300 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.303 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.303 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.303 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.546 |
LIG_SH3_3 | 782 | 788 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 661 | 668 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 26 | 36 | PF11976 | 0.608 |
LIG_SUMO_SIM_par_1 | 618 | 623 | PF11976 | 0.446 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.529 |
LIG_WRC_WIRS_1 | 498 | 503 | PF05994 | 0.424 |
LIG_WRC_WIRS_1 | 837 | 842 | PF05994 | 0.710 |
LIG_WW_2 | 77 | 80 | PF00397 | 0.681 |
LIG_WW_3 | 610 | 614 | PF00397 | 0.303 |
MOD_CDK_SPK_2 | 807 | 812 | PF00069 | 0.665 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.755 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.317 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.728 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.530 |
MOD_CK1_1 | 810 | 816 | PF00069 | 0.489 |
MOD_CK1_1 | 825 | 831 | PF00069 | 0.713 |
MOD_CK1_1 | 833 | 839 | PF00069 | 0.624 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.585 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.630 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.419 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.730 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.327 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.343 |
MOD_CK2_1 | 709 | 715 | PF00069 | 0.657 |
MOD_DYRK1A_RPxSP_1 | 819 | 823 | PF00069 | 0.704 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.553 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.754 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.581 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.613 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.673 |
MOD_GlcNHglycan | 32 | 38 | PF01048 | 0.451 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.372 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.626 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.388 |
MOD_GlcNHglycan | 711 | 714 | PF01048 | 0.652 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.637 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.739 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.761 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.639 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.705 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.621 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.363 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.337 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.515 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.712 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.765 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.729 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.496 |
MOD_LATS_1 | 273 | 279 | PF00433 | 0.424 |
MOD_N-GLC_1 | 296 | 301 | PF02516 | 0.296 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.378 |
MOD_N-GLC_1 | 789 | 794 | PF02516 | 0.651 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.448 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.265 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.530 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.646 |
MOD_NEK2_1 | 764 | 769 | PF00069 | 0.523 |
MOD_NEK2_1 | 817 | 822 | PF00069 | 0.718 |
MOD_NEK2_2 | 631 | 636 | PF00069 | 0.446 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.544 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.446 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.474 |
MOD_PIKK_1 | 739 | 745 | PF00454 | 0.622 |
MOD_PIKK_1 | 767 | 773 | PF00454 | 0.593 |
MOD_PK_1 | 275 | 281 | PF00069 | 0.395 |
MOD_PK_1 | 344 | 350 | PF00069 | 0.446 |
MOD_PKA_1 | 491 | 497 | PF00069 | 0.303 |
MOD_PKA_1 | 531 | 537 | PF00069 | 0.171 |
MOD_PKA_1 | 818 | 824 | PF00069 | 0.720 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.643 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.303 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.292 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.258 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.443 |
MOD_PKA_2 | 557 | 563 | PF00069 | 0.121 |
MOD_PKA_2 | 746 | 752 | PF00069 | 0.614 |
MOD_PKA_2 | 817 | 823 | PF00069 | 0.683 |
MOD_PKB_1 | 220 | 228 | PF00069 | 0.531 |
MOD_PKB_1 | 816 | 824 | PF00069 | 0.735 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.642 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.631 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.317 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.416 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.337 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.414 |
MOD_Plk_1 | 764 | 770 | PF00069 | 0.633 |
MOD_Plk_2-3 | 237 | 243 | PF00069 | 0.321 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.575 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.313 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.584 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.303 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.429 |
MOD_ProDKin_1 | 807 | 813 | PF00069 | 0.670 |
MOD_ProDKin_1 | 819 | 825 | PF00069 | 0.576 |
MOD_SUMO_for_1 | 229 | 232 | PF00179 | 0.659 |
MOD_SUMO_rev_2 | 69 | 75 | PF00179 | 0.742 |
MOD_SUMO_rev_2 | 709 | 718 | PF00179 | 0.650 |
MOD_SUMO_rev_2 | 753 | 762 | PF00179 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 758 | 763 | PF01217 | 0.642 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 585 | 588 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 797 | 800 | PF00928 | 0.649 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 292 | 295 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 427 | 430 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 530 | 532 | PF00400 | 0.237 |
TRG_ER_diArg_1 | 556 | 559 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 801 | 803 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 805 | 807 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 815 | 818 | PF00400 | 0.654 |
TRG_NES_CRM1_1 | 284 | 296 | PF08389 | 0.360 |
TRG_NLS_Bipartite_1 | 794 | 808 | PF00514 | 0.613 |
TRG_NLS_MonoCore_2 | 802 | 807 | PF00514 | 0.666 |
TRG_NLS_MonoExtN_4 | 802 | 808 | PF00514 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 407 | 411 | PF00026 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 433 | 437 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 491 | 496 | PF00026 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 518 | 523 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 657 | 662 | PF00026 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 66 | 71 | PF00026 | 0.654 |
TRG_Pf-PMV_PEXEL_1 | 761 | 765 | PF00026 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 766 | 771 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P820 | Leptomonas seymouri | 66% | 86% |
A0A0S4K0L8 | Bodo saltans | 45% | 84% |
A0A1X0NQX7 | Trypanosomatidae | 56% | 93% |
A0A3Q8II50 | Leishmania donovani | 91% | 100% |
A0A3S5ISD4 | Trypanosoma rangeli | 58% | 97% |
A4HGL5 | Leishmania braziliensis | 85% | 99% |
A4I3P1 | Leishmania infantum | 94% | 100% |
D0A8C3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 92% |
Q08647 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
Q4Q8A3 | Leishmania major | 90% | 100% |
V5BFB8 | Trypanosoma cruzi | 56% | 92% |