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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7WYA1
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 13 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 741 | 745 | PF00656 | 0.324 |
CLV_C14_Caspase3-7 | 762 | 766 | PF00656 | 0.485 |
CLV_MEL_PAP_1 | 438 | 444 | PF00089 | 0.323 |
CLV_NRD_NRD_1 | 1082 | 1084 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.196 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.222 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.190 |
CLV_NRD_NRD_1 | 906 | 908 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 938 | 940 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 942 | 944 | PF00675 | 0.245 |
CLV_PCSK_KEX2_1 | 1081 | 1083 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.197 |
CLV_PCSK_KEX2_1 | 938 | 940 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 942 | 944 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 1081 | 1083 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.470 |
CLV_PCSK_PC7_1 | 366 | 372 | PF00082 | 0.538 |
CLV_PCSK_PC7_1 | 938 | 944 | PF00082 | 0.184 |
CLV_PCSK_SKI1_1 | 1072 | 1076 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 809 | 813 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 835 | 839 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 948 | 952 | PF00082 | 0.200 |
CLV_Separin_Metazoa | 384 | 388 | PF03568 | 0.300 |
DEG_APCC_DBOX_1 | 519 | 527 | PF00400 | 0.277 |
DEG_APCC_DBOX_1 | 608 | 616 | PF00400 | 0.406 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.664 |
DEG_SPOP_SBC_1 | 1013 | 1017 | PF00917 | 0.447 |
DEG_SPOP_SBC_1 | 1028 | 1032 | PF00917 | 0.590 |
DOC_ANK_TNKS_1 | 431 | 438 | PF00023 | 0.328 |
DOC_CYCLIN_RxL_1 | 287 | 298 | PF00134 | 0.571 |
DOC_CYCLIN_RxL_1 | 806 | 814 | PF00134 | 0.455 |
DOC_CYCLIN_yCln2_LP_2 | 581 | 587 | PF00134 | 0.313 |
DOC_CYCLIN_yCln2_LP_2 | 799 | 805 | PF00134 | 0.391 |
DOC_MAPK_gen_1 | 117 | 127 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 370 | 378 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 431 | 438 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 518 | 527 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 905 | 913 | PF00069 | 0.339 |
DOC_MAPK_HePTP_8 | 515 | 527 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 117 | 125 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 180 | 188 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 518 | 527 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 575 | 583 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 588 | 595 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 905 | 913 | PF00069 | 0.399 |
DOC_MAPK_NFAT4_5 | 520 | 528 | PF00069 | 0.281 |
DOC_PP1_RVXF_1 | 467 | 473 | PF00149 | 0.444 |
DOC_PP2B_LxvP_1 | 581 | 584 | PF13499 | 0.484 |
DOC_PP4_FxxP_1 | 838 | 841 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 1044 | 1048 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 1053 | 1057 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 912 | 916 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 937 | 941 | PF00917 | 0.417 |
DOC_USP7_UBL2_3 | 1067 | 1071 | PF12436 | 0.521 |
DOC_USP7_UBL2_3 | 842 | 846 | PF12436 | 0.496 |
DOC_WW_Pin1_4 | 1029 | 1034 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 1046 | 1051 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 643 | 648 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 801 | 806 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 886 | 891 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 1043 | 1053 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 41 | 48 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 708 | 718 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 719 | 726 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 740 | 744 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 773 | 777 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 938 | 944 | PF00244 | 0.424 |
LIG_Actin_WH2_2 | 466 | 482 | PF00022 | 0.286 |
LIG_Actin_WH2_2 | 501 | 516 | PF00022 | 0.346 |
LIG_Actin_WH2_2 | 636 | 653 | PF00022 | 0.366 |
LIG_BIR_III_2 | 2 | 6 | PF00653 | 0.539 |
LIG_BIR_III_2 | 644 | 648 | PF00653 | 0.476 |
LIG_BIR_III_2 | 765 | 769 | PF00653 | 0.454 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.314 |
LIG_BRCT_BRCA1_1 | 773 | 777 | PF00533 | 0.404 |
LIG_eIF4E_1 | 602 | 608 | PF01652 | 0.455 |
LIG_EVH1_2 | 129 | 133 | PF00568 | 0.403 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.451 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.559 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.527 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.368 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.340 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.273 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.336 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.320 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.390 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.777 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.441 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.400 |
LIG_FHA_1 | 868 | 874 | PF00498 | 0.318 |
LIG_FHA_1 | 919 | 925 | PF00498 | 0.453 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.497 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.506 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.616 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.369 |
LIG_FHA_2 | 480 | 486 | PF00498 | 0.464 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.378 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.605 |
LIG_FHA_2 | 981 | 987 | PF00498 | 0.391 |
LIG_FHA_2 | 990 | 996 | PF00498 | 0.392 |
LIG_FXI_DFP_1 | 758 | 762 | PF00024 | 0.272 |
LIG_Integrin_RGD_1 | 520 | 522 | PF01839 | 0.451 |
LIG_Integrin_RGD_TGFB_3 | 520 | 526 | PF01839 | 0.420 |
LIG_LIR_Gen_1 | 489 | 499 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 760 | 769 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 897 | 906 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 986 | 994 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 716 | 721 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 897 | 902 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 941 | 947 | PF02991 | 0.415 |
LIG_MLH1_MIPbox_1 | 537 | 541 | PF16413 | 0.314 |
LIG_NRBOX | 231 | 237 | PF00104 | 0.515 |
LIG_NRBOX | 619 | 625 | PF00104 | 0.400 |
LIG_NRBOX | 806 | 812 | PF00104 | 0.496 |
LIG_PCNA_yPIPBox_3 | 41 | 52 | PF02747 | 0.530 |
LIG_Pex14_1 | 780 | 784 | PF04695 | 0.419 |
LIG_Pex14_2 | 537 | 541 | PF04695 | 0.314 |
LIG_PTAP_UEV_1 | 1049 | 1054 | PF05743 | 0.509 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.267 |
LIG_SH2_CRK | 947 | 951 | PF00017 | 0.422 |
LIG_SH2_GRB2like | 856 | 859 | PF00017 | 0.406 |
LIG_SH2_NCK_1 | 547 | 551 | PF00017 | 0.306 |
LIG_SH2_SRC | 547 | 550 | PF00017 | 0.293 |
LIG_SH2_SRC | 872 | 875 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.267 |
LIG_SH2_STAP1 | 726 | 730 | PF00017 | 0.472 |
LIG_SH2_STAT3 | 412 | 415 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 721 | 724 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 872 | 875 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 974 | 977 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 987 | 990 | PF00017 | 0.391 |
LIG_SH3_3 | 1047 | 1053 | PF00018 | 0.684 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.585 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.344 |
LIG_SH3_3 | 679 | 685 | PF00018 | 0.408 |
LIG_SH3_3 | 799 | 805 | PF00018 | 0.422 |
LIG_SH3_3 | 906 | 912 | PF00018 | 0.361 |
LIG_SH3_5 | 564 | 568 | PF00018 | 0.358 |
LIG_Sin3_3 | 808 | 815 | PF02671 | 0.395 |
LIG_SUMO_SIM_anti_2 | 181 | 188 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 391 | 398 | PF11976 | 0.414 |
LIG_SUMO_SIM_anti_2 | 621 | 627 | PF11976 | 0.391 |
LIG_SUMO_SIM_anti_2 | 744 | 752 | PF11976 | 0.268 |
LIG_SUMO_SIM_anti_2 | 859 | 867 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 121 | 126 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 394 | 401 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 492 | 498 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 621 | 627 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 744 | 752 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 986 | 992 | PF11976 | 0.400 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.564 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.707 |
LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.473 |
LIG_TYR_ITIM | 975 | 980 | PF00017 | 0.219 |
LIG_UBA3_1 | 509 | 514 | PF00899 | 0.312 |
LIG_UBA3_1 | 837 | 842 | PF00899 | 0.219 |
LIG_UBA3_1 | 902 | 908 | PF00899 | 0.322 |
LIG_WRC_WIRS_1 | 269 | 274 | PF05994 | 0.537 |
MOD_CK1_1 | 1015 | 1021 | PF00069 | 0.564 |
MOD_CK1_1 | 1039 | 1045 | PF00069 | 0.692 |
MOD_CK1_1 | 1048 | 1054 | PF00069 | 0.673 |
MOD_CK1_1 | 1056 | 1062 | PF00069 | 0.688 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.514 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.447 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.468 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.494 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.608 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.684 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.529 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.389 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.339 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.339 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.373 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.349 |
MOD_CK1_1 | 742 | 748 | PF00069 | 0.299 |
MOD_CK1_1 | 857 | 863 | PF00069 | 0.362 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.643 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.659 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.613 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.611 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.388 |
MOD_CK2_1 | 731 | 737 | PF00069 | 0.386 |
MOD_CK2_1 | 980 | 986 | PF00069 | 0.219 |
MOD_CK2_1 | 989 | 995 | PF00069 | 0.221 |
MOD_Cter_Amidation | 347 | 350 | PF01082 | 0.408 |
MOD_GlcNHglycan | 1053 | 1056 | PF01048 | 0.694 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.676 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.600 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.569 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.453 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.745 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.643 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.639 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.384 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.342 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.336 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.317 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.258 |
MOD_GlcNHglycan | 67 | 71 | PF01048 | 0.663 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.286 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.256 |
MOD_GlcNHglycan | 962 | 965 | PF01048 | 0.243 |
MOD_GSK3_1 | 1011 | 1018 | PF00069 | 0.564 |
MOD_GSK3_1 | 1027 | 1034 | PF00069 | 0.591 |
MOD_GSK3_1 | 1042 | 1049 | PF00069 | 0.639 |
MOD_GSK3_1 | 1051 | 1058 | PF00069 | 0.689 |
MOD_GSK3_1 | 1063 | 1070 | PF00069 | 0.633 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.592 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.533 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.629 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.545 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.579 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.607 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.709 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.688 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.389 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.347 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.374 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.278 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.549 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.322 |
MOD_GSK3_1 | 850 | 857 | PF00069 | 0.265 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.585 |
MOD_LATS_1 | 54 | 60 | PF00433 | 0.550 |
MOD_LATS_1 | 852 | 858 | PF00433 | 0.339 |
MOD_N-GLC_1 | 857 | 862 | PF02516 | 0.232 |
MOD_NEK2_1 | 1036 | 1041 | PF00069 | 0.755 |
MOD_NEK2_1 | 1077 | 1082 | PF00069 | 0.641 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.430 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.426 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.452 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.463 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.548 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.407 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.450 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.451 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.265 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.209 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.247 |
MOD_NEK2_1 | 749 | 754 | PF00069 | 0.371 |
MOD_NEK2_1 | 811 | 816 | PF00069 | 0.233 |
MOD_NEK2_1 | 980 | 985 | PF00069 | 0.260 |
MOD_NEK2_1 | 999 | 1004 | PF00069 | 0.120 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.466 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.531 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.522 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.332 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.732 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.324 |
MOD_PIKK_1 | 695 | 701 | PF00454 | 0.279 |
MOD_PIKK_1 | 867 | 873 | PF00454 | 0.416 |
MOD_PKA_1 | 440 | 446 | PF00069 | 0.331 |
MOD_PKA_1 | 535 | 541 | PF00069 | 0.457 |
MOD_PKA_1 | 942 | 948 | PF00069 | 0.319 |
MOD_PKA_2 | 1039 | 1045 | PF00069 | 0.614 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.556 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.489 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.519 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.331 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.447 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.700 |
MOD_PKA_2 | 683 | 689 | PF00069 | 0.392 |
MOD_PKA_2 | 710 | 716 | PF00069 | 0.378 |
MOD_PKA_2 | 739 | 745 | PF00069 | 0.348 |
MOD_PKA_2 | 772 | 778 | PF00069 | 0.317 |
MOD_PKA_2 | 937 | 943 | PF00069 | 0.231 |
MOD_PKB_1 | 305 | 313 | PF00069 | 0.474 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.618 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.329 |
MOD_Plk_1 | 660 | 666 | PF00069 | 0.264 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.542 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.485 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.323 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.311 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.243 |
MOD_Plk_4 | 742 | 748 | PF00069 | 0.278 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.367 |
MOD_Plk_4 | 861 | 867 | PF00069 | 0.232 |
MOD_ProDKin_1 | 1029 | 1035 | PF00069 | 0.743 |
MOD_ProDKin_1 | 1046 | 1052 | PF00069 | 0.645 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.689 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.438 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.393 |
MOD_ProDKin_1 | 643 | 649 | PF00069 | 0.302 |
MOD_ProDKin_1 | 801 | 807 | PF00069 | 0.436 |
MOD_ProDKin_1 | 886 | 892 | PF00069 | 0.443 |
MOD_SUMO_rev_2 | 1059 | 1069 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 205 | 214 | PF00179 | 0.565 |
MOD_SUMO_rev_2 | 279 | 289 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 831 | 837 | PF00179 | 0.226 |
TRG_DiLeu_BaEn_1 | 210 | 215 | PF01217 | 0.582 |
TRG_DiLeu_BaEn_1 | 285 | 290 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_1 | 995 | 1000 | PF01217 | 0.250 |
TRG_DiLeu_LyEn_5 | 946 | 951 | PF01217 | 0.310 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 947 | 950 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 977 | 980 | PF00928 | 0.219 |
TRG_ENDOCYTIC_2 | 987 | 990 | PF00928 | 0.219 |
TRG_ER_diArg_1 | 1082 | 1084 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 369 | 371 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 517 | 520 | PF00400 | 0.334 |
TRG_ER_diArg_1 | 608 | 611 | PF00400 | 0.232 |
TRG_ER_diArg_1 | 942 | 944 | PF00400 | 0.352 |
TRG_NLS_Bipartite_1 | 1071 | 1085 | PF00514 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 1004 | 1008 | PF00026 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 291 | 296 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 387 | 391 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 610 | 614 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 809 | 813 | PF00026 | 0.274 |
TRG_Pf-PMV_PEXEL_1 | 835 | 839 | PF00026 | 0.219 |
TRG_PTS1 | 1083 | 1086 | PF00515 | 0.640 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKA7 | Leptomonas seymouri | 76% | 100% |
A0A0N1PEU4 | Leptomonas seymouri | 35% | 100% |
A0A0S4ITR4 | Bodo saltans | 48% | 100% |
A0A1X0NVG5 | Trypanosomatidae | 55% | 100% |
A0A1X0P872 | Trypanosomatidae | 35% | 100% |
A0A3Q8II71 | Leishmania donovani | 35% | 100% |
A0A3Q8IJ24 | Leishmania donovani | 35% | 100% |
A0A422N8L3 | Trypanosoma rangeli | 56% | 100% |
A4HAT8 | Leishmania braziliensis | 36% | 100% |
A4HDG6 | Leishmania braziliensis | 82% | 100% |
A4HNU7 | Leishmania braziliensis | 34% | 100% |
A4I0U7 | Leishmania infantum | 100% | 100% |
A4IA06 | Leishmania infantum | 35% | 100% |
A4ICP7 | Leishmania infantum | 34% | 100% |
D0A778 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AWV1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
P20095 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 100% |
P45018 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 33% | 83% |
Q4Q1Y9 | Leishmania major | 34% | 100% |
Q4Q2X4 | Leishmania major | 35% | 100% |
Q4QAM3 | Leishmania major | 95% | 100% |
Q54MH3 | Dictyostelium discoideum | 39% | 98% |
Q9HDY4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 92% |
V5BV22 | Trypanosoma cruzi | 36% | 100% |
V5C0I9 | Trypanosoma cruzi | 64% | 100% |