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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9B4V0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006259 | DNA metabolic process | 4 | 9 |
GO:0006260 | DNA replication | 5 | 9 |
GO:0006261 | DNA-templated DNA replication | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003677 | DNA binding | 4 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016779 | nucleotidyltransferase activity | 4 | 9 |
GO:0034061 | DNA polymerase activity | 4 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 44 | 48 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 792 | 794 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 824 | 826 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 879 | 881 | PF00675 | 0.360 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.822 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.209 |
CLV_PCSK_KEX2_1 | 681 | 683 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 792 | 794 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 824 | 826 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.832 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.822 |
CLV_PCSK_PC1ET2_1 | 747 | 749 | PF00082 | 0.325 |
CLV_PCSK_PC7_1 | 743 | 749 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 748 | 752 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 830 | 834 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 854 | 858 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 881 | 885 | PF00082 | 0.337 |
DEG_APCC_DBOX_1 | 400 | 408 | PF00400 | 0.471 |
DEG_APCC_DBOX_1 | 444 | 452 | PF00400 | 0.525 |
DEG_APCC_DBOX_1 | 879 | 887 | PF00400 | 0.538 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.603 |
DEG_SPOP_SBC_1 | 717 | 721 | PF00917 | 0.597 |
DOC_CYCLIN_RxL_1 | 453 | 461 | PF00134 | 0.538 |
DOC_CYCLIN_RxL_1 | 62 | 72 | PF00134 | 0.730 |
DOC_CYCLIN_yCln2_LP_2 | 901 | 907 | PF00134 | 0.501 |
DOC_MAPK_DCC_7 | 208 | 218 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 383 | 392 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 859 | 867 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 880 | 888 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 120 | 128 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 177 | 186 | PF00069 | 0.551 |
DOC_MAPK_MEF2A_6 | 305 | 312 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 383 | 392 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 396 | 404 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 881 | 890 | PF00069 | 0.538 |
DOC_MAPK_NFAT4_5 | 387 | 395 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 745 | 752 | PF00149 | 0.525 |
DOC_PP2B_LxvP_1 | 901 | 904 | PF13499 | 0.501 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 832 | 836 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 889 | 893 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.555 |
DOC_USP7_UBL2_3 | 35 | 39 | PF12436 | 0.788 |
DOC_USP7_UBL2_3 | 456 | 460 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.822 |
LIG_14-3-3_CanoR_1 | 164 | 173 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 208 | 216 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 479 | 487 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 584 | 593 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 626 | 632 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 644 | 652 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 65 | 71 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 818 | 822 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 824 | 828 | PF00244 | 0.548 |
LIG_Actin_WH2_2 | 444 | 462 | PF00022 | 0.538 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.619 |
LIG_Clathr_ClatBox_1 | 692 | 696 | PF01394 | 0.501 |
LIG_EH1_1 | 896 | 904 | PF00400 | 0.501 |
LIG_eIF4E_1 | 292 | 298 | PF01652 | 0.508 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.436 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.583 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.569 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.485 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.467 |
LIG_FHA_1 | 775 | 781 | PF00498 | 0.599 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.510 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.501 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.560 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.596 |
LIG_FHA_2 | 718 | 724 | PF00498 | 0.608 |
LIG_LIR_Apic_2 | 191 | 197 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 105 | 115 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 167 | 176 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 293 | 301 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 694 | 705 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 94 | 104 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 694 | 700 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 781 | 787 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.485 |
LIG_NRBOX | 226 | 232 | PF00104 | 0.375 |
LIG_NRBOX | 367 | 373 | PF00104 | 0.492 |
LIG_NRBOX | 390 | 396 | PF00104 | 0.430 |
LIG_PCNA_APIM_2 | 454 | 460 | PF02747 | 0.538 |
LIG_PCNA_yPIPBox_3 | 224 | 235 | PF02747 | 0.470 |
LIG_Pex14_2 | 581 | 585 | PF04695 | 0.504 |
LIG_Pex14_2 | 680 | 684 | PF04695 | 0.525 |
LIG_Rb_LxCxE_1 | 640 | 661 | PF01857 | 0.542 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.459 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.405 |
LIG_SH2_CRK | 365 | 369 | PF00017 | 0.420 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.554 |
LIG_SH2_CRK | 520 | 524 | PF00017 | 0.530 |
LIG_SH2_CRK | 628 | 632 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 194 | 198 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 697 | 701 | PF00017 | 0.520 |
LIG_SH2_PTP2 | 97 | 100 | PF00017 | 0.570 |
LIG_SH2_SRC | 292 | 295 | PF00017 | 0.468 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 294 | 298 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 457 | 460 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 813 | 816 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.495 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.640 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.733 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.571 |
LIG_SUMO_SIM_anti_2 | 183 | 188 | PF11976 | 0.501 |
LIG_SUMO_SIM_anti_2 | 863 | 869 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 565 | 571 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 691 | 696 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 848 | 853 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 903 | 908 | PF11976 | 0.525 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.604 |
LIG_TRAF2_1 | 739 | 742 | PF00917 | 0.525 |
LIG_TYR_ITIM | 501 | 506 | PF00017 | 0.560 |
LIG_TYR_ITIM | 695 | 700 | PF00017 | 0.501 |
LIG_TYR_ITIM | 95 | 100 | PF00017 | 0.579 |
LIG_UBA3_1 | 226 | 235 | PF00899 | 0.470 |
LIG_UBA3_1 | 390 | 396 | PF00899 | 0.508 |
LIG_UBA3_1 | 901 | 910 | PF00899 | 0.501 |
LIG_WRC_WIRS_1 | 218 | 223 | PF05994 | 0.373 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.764 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.569 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.724 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.730 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.829 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.737 |
MOD_CK1_1 | 778 | 784 | PF00069 | 0.542 |
MOD_CK1_1 | 823 | 829 | PF00069 | 0.560 |
MOD_CK1_1 | 863 | 869 | PF00069 | 0.597 |
MOD_CK1_1 | 893 | 899 | PF00069 | 0.560 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.529 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.501 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.548 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.797 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.626 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.501 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.681 |
MOD_CK2_1 | 736 | 742 | PF00069 | 0.505 |
MOD_CK2_1 | 823 | 829 | PF00069 | 0.525 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.510 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.553 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.617 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.733 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.597 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.500 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.720 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.386 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.774 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.825 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.368 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.298 |
MOD_GlcNHglycan | 839 | 842 | PF01048 | 0.299 |
MOD_GlcNHglycan | 892 | 895 | PF01048 | 0.360 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.638 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.539 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.492 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.380 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.738 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.598 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.470 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.622 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.506 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.787 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.791 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.487 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.647 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.542 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.505 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.560 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.640 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.560 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.539 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.541 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.463 |
MOD_N-GLC_1 | 613 | 618 | PF02516 | 0.526 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.738 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.590 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.470 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.538 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.504 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.499 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.806 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.631 |
MOD_NEK2_1 | 774 | 779 | PF00069 | 0.520 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.548 |
MOD_NEK2_1 | 890 | 895 | PF00069 | 0.554 |
MOD_NEK2_1 | 905 | 910 | PF00069 | 0.436 |
MOD_NEK2_1 | 911 | 916 | PF00069 | 0.501 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.471 |
MOD_NEK2_2 | 483 | 488 | PF00069 | 0.560 |
MOD_NEK2_2 | 627 | 632 | PF00069 | 0.529 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.375 |
MOD_PIKK_1 | 866 | 872 | PF00454 | 0.560 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.552 |
MOD_PKA_1 | 41 | 47 | PF00069 | 0.655 |
MOD_PKA_1 | 504 | 510 | PF00069 | 0.560 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.582 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.560 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.756 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.501 |
MOD_PKA_2 | 817 | 823 | PF00069 | 0.570 |
MOD_PKB_1 | 502 | 510 | PF00069 | 0.597 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.529 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.665 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.636 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.501 |
MOD_Plk_1 | 741 | 747 | PF00069 | 0.503 |
MOD_Plk_1 | 863 | 869 | PF00069 | 0.597 |
MOD_Plk_1 | 919 | 925 | PF00069 | 0.463 |
MOD_Plk_2-3 | 281 | 287 | PF00069 | 0.701 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.454 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.665 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.482 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.525 |
MOD_Plk_4 | 775 | 781 | PF00069 | 0.525 |
MOD_Plk_4 | 817 | 823 | PF00069 | 0.541 |
MOD_Plk_4 | 832 | 838 | PF00069 | 0.436 |
MOD_Plk_4 | 863 | 869 | PF00069 | 0.597 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.788 |
MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.789 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.707 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.819 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 628 | 631 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.570 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.815 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 680 | 682 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 792 | 794 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 810 | 813 | PF00400 | 0.501 |
TRG_NLS_Bipartite_1 | 18 | 40 | PF00514 | 0.807 |
TRG_NLS_MonoCore_2 | 35 | 40 | PF00514 | 0.815 |
TRG_NLS_MonoExtC_3 | 34 | 39 | PF00514 | 0.824 |
TRG_NLS_MonoExtN_4 | 160 | 167 | PF00514 | 0.601 |
TRG_NLS_MonoExtN_4 | 35 | 40 | PF00514 | 0.765 |
TRG_Pf-PMV_PEXEL_1 | 113 | 117 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 726 | 730 | PF00026 | 0.283 |
TRG_Pf-PMV_PEXEL_1 | 812 | 816 | PF00026 | 0.378 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I668 | Leptomonas seymouri | 63% | 73% |
A0A1X0P9E5 | Trypanosomatidae | 42% | 94% |
A0A3Q8IH45 | Leishmania donovani | 92% | 100% |
A4HAP3 | Leishmania braziliensis | 79% | 100% |
A4I9T9 | Leishmania infantum | 92% | 74% |
C9ZMU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 97% |
Q8IS90 | Leishmania major | 91% | 100% |