Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | yes | yes: 2 |
Pissara et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 8 |
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 | 2 |
GO:0008540 | proteasome regulatory particle, base subcomplex | 2 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0034515 | proteasome storage granule | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q893
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009894 | regulation of catabolic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 12 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0042176 | regulation of protein catabolic process | 5 | 12 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 12 |
GO:0051246 | regulation of protein metabolic process | 5 | 12 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030234 | enzyme regulator activity | 2 | 12 |
GO:0098772 | molecular function regulator activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 295 | 299 | PF00656 | 0.775 |
CLV_C14_Caspase3-7 | 377 | 381 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 505 | 509 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 839 | 841 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 848 | 850 | PF00675 | 0.499 |
CLV_PCSK_FUR_1 | 455 | 459 | PF00082 | 0.558 |
CLV_PCSK_FUR_1 | 846 | 850 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 824 | 826 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 848 | 850 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 880 | 882 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 824 | 826 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 880 | 882 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 818 | 822 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 824 | 828 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.379 |
DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.427 |
DEG_APCC_KENBOX_2 | 704 | 708 | PF00400 | 0.588 |
DEG_COP1_1 | 958 | 968 | PF00400 | 0.722 |
DEG_SPOP_SBC_1 | 293 | 297 | PF00917 | 0.796 |
DEG_SPOP_SBC_1 | 835 | 839 | PF00917 | 0.453 |
DOC_AGCK_PIF_2 | 259 | 264 | PF00069 | 0.434 |
DOC_ANK_TNKS_1 | 848 | 855 | PF00023 | 0.464 |
DOC_CKS1_1 | 117 | 122 | PF01111 | 0.659 |
DOC_CYCLIN_RxL_1 | 201 | 211 | PF00134 | 0.450 |
DOC_CYCLIN_RxL_1 | 95 | 104 | PF00134 | 0.495 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 631 | 640 | PF00134 | 0.499 |
DOC_CYCLIN_yCln2_LP_2 | 904 | 910 | PF00134 | 0.421 |
DOC_CYCLIN_yCln2_LP_2 | 951 | 957 | PF00134 | 0.692 |
DOC_MAPK_FxFP_2 | 969 | 972 | PF00069 | 0.757 |
DOC_MAPK_gen_1 | 202 | 208 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 709 | 717 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 758 | 766 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 930 | 938 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 130 | 138 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 632 | 640 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 653 | 662 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 688 | 697 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 761 | 768 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 930 | 938 | PF00069 | 0.499 |
DOC_MAPK_RevD_3 | 189 | 203 | PF00069 | 0.472 |
DOC_PP1_RVXF_1 | 162 | 168 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 249 | 256 | PF00149 | 0.553 |
DOC_PP2B_LxvP_1 | 798 | 801 | PF13499 | 0.376 |
DOC_PP2B_LxvP_1 | 951 | 954 | PF13499 | 0.658 |
DOC_PP4_FxxP_1 | 631 | 634 | PF00568 | 0.453 |
DOC_PP4_FxxP_1 | 969 | 972 | PF00568 | 0.664 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 853 | 857 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 860 | 864 | PF00917 | 0.452 |
DOC_USP7_UBL2_3 | 601 | 605 | PF12436 | 0.464 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 646 | 651 | PF00397 | 0.464 |
LIG_14-3-3_CanoR_1 | 178 | 187 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 358 | 362 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 410 | 419 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 619 | 626 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 62 | 68 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 746 | 751 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 825 | 835 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 909 | 917 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.437 |
LIG_AP2alpha_2 | 579 | 581 | PF02296 | 0.415 |
LIG_BIR_III_4 | 298 | 302 | PF00653 | 0.735 |
LIG_BIR_III_4 | 742 | 746 | PF00653 | 0.390 |
LIG_deltaCOP1_diTrp_1 | 579 | 588 | PF00928 | 0.387 |
LIG_DLG_GKlike_1 | 63 | 71 | PF00625 | 0.544 |
LIG_eIF4E_1 | 190 | 196 | PF01652 | 0.536 |
LIG_eIF4E_1 | 774 | 780 | PF01652 | 0.422 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.419 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.557 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.428 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.503 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.427 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.452 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.456 |
LIG_FHA_1 | 787 | 793 | PF00498 | 0.375 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.499 |
LIG_FHA_1 | 826 | 832 | PF00498 | 0.532 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.494 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.603 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.447 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.568 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.384 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.216 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.443 |
LIG_FHA_2 | 837 | 843 | PF00498 | 0.361 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.602 |
LIG_FHA_2 | 940 | 946 | PF00498 | 0.519 |
LIG_GBD_Chelix_1 | 253 | 261 | PF00786 | 0.480 |
LIG_GBD_Chelix_1 | 273 | 281 | PF00786 | 0.579 |
LIG_LIR_Apic_2 | 630 | 634 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 812 | 817 | PF02991 | 0.373 |
LIG_LIR_Apic_2 | 967 | 972 | PF02991 | 0.664 |
LIG_LIR_Gen_1 | 132 | 143 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 35 | 46 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 494 | 504 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 579 | 589 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 674 | 684 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 898 | 908 | PF02991 | 0.373 |
LIG_LIR_LC3C_4 | 19 | 23 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 494 | 500 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 674 | 680 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 712 | 716 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 730 | 735 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 898 | 904 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 923 | 929 | PF02991 | 0.369 |
LIG_LYPXL_yS_3 | 776 | 779 | PF13949 | 0.524 |
LIG_MAD2 | 642 | 650 | PF02301 | 0.376 |
LIG_PCNA_PIPBox_1 | 417 | 426 | PF02747 | 0.562 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.467 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.488 |
LIG_Pex14_2 | 769 | 773 | PF04695 | 0.383 |
LIG_PTB_Apo_2 | 183 | 190 | PF02174 | 0.430 |
LIG_PTB_Apo_2 | 263 | 270 | PF02174 | 0.424 |
LIG_PTB_Apo_2 | 534 | 541 | PF02174 | 0.569 |
LIG_PTB_Phospho_1 | 263 | 269 | PF10480 | 0.567 |
LIG_PTB_Phospho_1 | 534 | 540 | PF10480 | 0.564 |
LIG_SH2_CRK | 448 | 452 | PF00017 | 0.545 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.504 |
LIG_SH2_CRK | 814 | 818 | PF00017 | 0.477 |
LIG_SH2_GRB2like | 79 | 82 | PF00017 | 0.568 |
LIG_SH2_PTP2 | 926 | 929 | PF00017 | 0.499 |
LIG_SH2_SRC | 336 | 339 | PF00017 | 0.460 |
LIG_SH2_SRC | 435 | 438 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 497 | 501 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 79 | 83 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.441 |
LIG_SH2_STAT3 | 686 | 689 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 734 | 737 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 803 | 806 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 926 | 929 | PF00017 | 0.499 |
LIG_SH3_1 | 925 | 931 | PF00018 | 0.376 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.578 |
LIG_SH3_3 | 925 | 931 | PF00018 | 0.376 |
LIG_SH3_3 | 962 | 968 | PF00018 | 0.669 |
LIG_SUMO_SIM_anti_2 | 19 | 25 | PF11976 | 0.577 |
LIG_SUMO_SIM_par_1 | 10 | 17 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 319 | 325 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 520 | 526 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 604 | 610 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 778 | 783 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 953 | 959 | PF11976 | 0.709 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.600 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.435 |
LIG_TRAF2_1 | 539 | 542 | PF00917 | 0.562 |
LIG_TRAF2_1 | 895 | 898 | PF00917 | 0.435 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.516 |
LIG_TYR_ITIM | 446 | 451 | PF00017 | 0.522 |
LIG_TYR_ITIM | 924 | 929 | PF00017 | 0.405 |
LIG_UBA3_1 | 134 | 140 | PF00899 | 0.441 |
LIG_UBA3_1 | 195 | 204 | PF00899 | 0.481 |
LIG_UBA3_1 | 24 | 28 | PF00899 | 0.566 |
LIG_UBA3_1 | 47 | 56 | PF00899 | 0.575 |
LIG_WRC_WIRS_1 | 34 | 39 | PF05994 | 0.537 |
LIG_WRC_WIRS_1 | 628 | 633 | PF05994 | 0.453 |
MOD_CDK_SPxxK_3 | 646 | 653 | PF00069 | 0.464 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.537 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.487 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.645 |
MOD_CK1_1 | 856 | 862 | PF00069 | 0.378 |
MOD_CK1_1 | 916 | 922 | PF00069 | 0.457 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.431 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.566 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.442 |
MOD_CK2_1 | 836 | 842 | PF00069 | 0.361 |
MOD_CK2_1 | 939 | 945 | PF00069 | 0.510 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.465 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.478 |
MOD_GlcNHglycan | 302 | 306 | PF01048 | 0.723 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.459 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.470 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.463 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.574 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.417 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.584 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.529 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.421 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.569 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.419 |
MOD_GlcNHglycan | 862 | 865 | PF01048 | 0.467 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.527 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.596 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.548 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.632 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.480 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.569 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.514 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.487 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.408 |
MOD_GSK3_1 | 852 | 859 | PF00069 | 0.453 |
MOD_LATS_1 | 350 | 356 | PF00433 | 0.585 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.629 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.434 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.418 |
MOD_N-GLC_1 | 746 | 751 | PF02516 | 0.416 |
MOD_N-GLC_1 | 794 | 799 | PF02516 | 0.499 |
MOD_N-GLC_2 | 635 | 637 | PF02516 | 0.499 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.398 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.533 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.526 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.413 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.449 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.459 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.410 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.414 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.378 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.361 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.429 |
MOD_NEK2_1 | 780 | 785 | PF00069 | 0.391 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.361 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.523 |
MOD_NEK2_1 | 939 | 944 | PF00069 | 0.401 |
MOD_NEK2_2 | 627 | 632 | PF00069 | 0.361 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.469 |
MOD_NEK2_2 | 801 | 806 | PF00069 | 0.396 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.506 |
MOD_PK_1 | 319 | 325 | PF00069 | 0.543 |
MOD_PK_1 | 426 | 432 | PF00069 | 0.646 |
MOD_PK_1 | 605 | 611 | PF00069 | 0.373 |
MOD_PKA_1 | 28 | 34 | PF00069 | 0.530 |
MOD_PKA_1 | 352 | 358 | PF00069 | 0.617 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.562 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.606 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.546 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.511 |
MOD_PKA_2 | 727 | 733 | PF00069 | 0.529 |
MOD_PKA_2 | 908 | 914 | PF00069 | 0.383 |
MOD_PKA_2 | 939 | 945 | PF00069 | 0.319 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.557 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.431 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.460 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.417 |
MOD_Plk_1 | 746 | 752 | PF00069 | 0.410 |
MOD_Plk_1 | 794 | 800 | PF00069 | 0.422 |
MOD_Plk_1 | 801 | 807 | PF00069 | 0.366 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.607 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.420 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.438 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.528 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.450 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.500 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.529 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.376 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.547 |
MOD_Plk_4 | 816 | 822 | PF00069 | 0.377 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.650 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.575 |
MOD_ProDKin_1 | 646 | 652 | PF00069 | 0.464 |
MOD_SUMO_for_1 | 129 | 132 | PF00179 | 0.619 |
MOD_SUMO_rev_2 | 145 | 155 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 314 | 321 | PF00179 | 0.574 |
MOD_SUMO_rev_2 | 712 | 721 | PF00179 | 0.572 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 711 | 716 | PF01217 | 0.543 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 776 | 779 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 926 | 929 | PF00928 | 0.396 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 756 | 759 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 845 | 848 | PF00400 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 418 | 422 | PF00026 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 642 | 646 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 714 | 718 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 98 | 103 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8Y0 | Leptomonas seymouri | 82% | 98% |
A0A0S4JC57 | Bodo saltans | 51% | 94% |
A0A1X0NQV9 | Trypanosomatidae | 56% | 96% |
A0A3Q8IEW8 | Leishmania donovani | 96% | 98% |
A0A3R7KVS9 | Trypanosoma rangeli | 59% | 100% |
A4HGM6 | Leishmania braziliensis | 91% | 98% |
A4I3Q0 | Leishmania infantum | 96% | 98% |
D0A8B2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 99% |
E9AZZ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 98% |
O48844 | Arabidopsis thaliana | 38% | 97% |
O74762 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
P32565 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
Q18115 | Caenorhabditis elegans | 29% | 100% |
Q54JM5 | Dictyostelium discoideum | 34% | 100% |
Q5F418 | Gallus gallus | 38% | 100% |
Q6FIP2 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 31% | 100% |
Q75CF3 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 31% | 100% |
Q9MAT0 | Arabidopsis thaliana | 38% | 97% |
Q9V3P6 | Drosophila melanogaster | 38% | 95% |
V5AV92 | Trypanosoma cruzi | 59% | 100% |