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:0005801 | cis-Golgi network | 5 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0017119 | Golgi transport complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0099023 | vesicle tethering complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7XAQ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0048193 | Golgi vesicle transport | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.262 |
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.621 |
CLV_C14_Caspase3-7 | 599 | 603 | PF00656 | 0.646 |
CLV_C14_Caspase3-7 | 663 | 667 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 685 | 689 | PF00656 | 0.581 |
CLV_C14_Caspase3-7 | 855 | 859 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 943 | 947 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.570 |
CLV_PCSK_FUR_1 | 704 | 708 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 830 | 834 | PF00082 | 0.687 |
CLV_Separin_Metazoa | 176 | 180 | PF03568 | 0.449 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.633 |
DEG_APCC_DBOX_1 | 443 | 451 | PF00400 | 0.622 |
DEG_APCC_DBOX_1 | 507 | 515 | PF00400 | 0.417 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.493 |
DEG_SPOP_SBC_1 | 820 | 824 | PF00917 | 0.725 |
DOC_CYCLIN_RxL_1 | 703 | 714 | PF00134 | 0.697 |
DOC_CYCLIN_yCln2_LP_2 | 23 | 29 | PF00134 | 0.655 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.719 |
DOC_MAPK_FxFP_2 | 31 | 34 | PF00069 | 0.703 |
DOC_MAPK_gen_1 | 100 | 108 | PF00069 | 0.643 |
DOC_MAPK_gen_1 | 171 | 177 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 232 | 241 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 30 | 37 | PF00069 | 0.676 |
DOC_MAPK_gen_1 | 715 | 725 | PF00069 | 0.615 |
DOC_MAPK_MEF2A_6 | 18 | 27 | PF00069 | 0.637 |
DOC_MAPK_MEF2A_6 | 235 | 243 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 391 | 398 | PF00069 | 0.483 |
DOC_PP1_RVXF_1 | 556 | 562 | PF00149 | 0.392 |
DOC_PP1_RVXF_1 | 617 | 624 | PF00149 | 0.526 |
DOC_PP1_RVXF_1 | 769 | 776 | PF00149 | 0.560 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.645 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.721 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.670 |
DOC_PP4_FxxP_1 | 609 | 612 | PF00568 | 0.533 |
DOC_PP4_FxxP_1 | 867 | 870 | PF00568 | 0.678 |
DOC_PP4_FxxP_1 | 905 | 908 | PF00568 | 0.702 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 799 | 803 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 820 | 824 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 853 | 857 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 876 | 880 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 881 | 885 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 940 | 944 | PF00917 | 0.760 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 904 | 909 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 925 | 930 | PF00397 | 0.743 |
LIG_14-3-3_CanoR_1 | 100 | 109 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 294 | 299 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 400 | 406 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 413 | 421 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 529 | 533 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 562 | 566 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 568 | 572 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 830 | 839 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 912 | 916 | PF00244 | 0.806 |
LIG_14-3-3_CanoR_1 | 941 | 950 | PF00244 | 0.757 |
LIG_Actin_WH2_2 | 337 | 353 | PF00022 | 0.577 |
LIG_Actin_WH2_2 | 651 | 667 | PF00022 | 0.557 |
LIG_APCC_ABBA_1 | 633 | 638 | PF00400 | 0.390 |
LIG_BRCT_BRCA1_1 | 207 | 211 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.553 |
LIG_BRCT_BRCA1_1 | 666 | 670 | PF00533 | 0.547 |
LIG_Clathr_ClatBox_1 | 511 | 515 | PF01394 | 0.421 |
LIG_deltaCOP1_diTrp_1 | 622 | 630 | PF00928 | 0.545 |
LIG_EH_1 | 200 | 204 | PF12763 | 0.449 |
LIG_EVH1_1 | 905 | 909 | PF00568 | 0.750 |
LIG_EVH1_2 | 863 | 867 | PF00568 | 0.566 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.341 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.546 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.554 |
LIG_FHA_1 | 739 | 745 | PF00498 | 0.578 |
LIG_FHA_1 | 908 | 914 | PF00498 | 0.800 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.400 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.390 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.759 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.730 |
LIG_FHA_2 | 661 | 667 | PF00498 | 0.596 |
LIG_FHA_2 | 690 | 696 | PF00498 | 0.508 |
LIG_FHA_2 | 780 | 786 | PF00498 | 0.579 |
LIG_GBD_Chelix_1 | 459 | 467 | PF00786 | 0.415 |
LIG_GBD_Chelix_1 | 543 | 551 | PF00786 | 0.528 |
LIG_LIR_Apic_2 | 606 | 612 | PF02991 | 0.580 |
LIG_LIR_Apic_2 | 622 | 626 | PF02991 | 0.539 |
LIG_LIR_Apic_2 | 72 | 77 | PF02991 | 0.645 |
LIG_LIR_Apic_2 | 858 | 863 | PF02991 | 0.644 |
LIG_LIR_Apic_2 | 866 | 870 | PF02991 | 0.584 |
LIG_LIR_Apic_2 | 932 | 936 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 208 | 219 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 322 | 330 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 339 | 348 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 545 | 552 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 627 | 637 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 734 | 744 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 888 | 899 | PF02991 | 0.807 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 322 | 326 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 501 | 507 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 622 | 628 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 629 | 633 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 734 | 740 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 888 | 894 | PF02991 | 0.763 |
LIG_LYPXL_S_1 | 624 | 628 | PF13949 | 0.383 |
LIG_LYPXL_yS_3 | 625 | 628 | PF13949 | 0.390 |
LIG_MYND_1 | 493 | 497 | PF01753 | 0.542 |
LIG_NRBOX | 19 | 25 | PF00104 | 0.644 |
LIG_NRBOX | 785 | 791 | PF00104 | 0.627 |
LIG_PCNA_PIPBox_1 | 769 | 778 | PF02747 | 0.565 |
LIG_PCNA_yPIPBox_3 | 783 | 793 | PF02747 | 0.613 |
LIG_PDZ_Class_3 | 946 | 951 | PF00595 | 0.772 |
LIG_Rb_LxCxE_1 | 722 | 741 | PF01857 | 0.559 |
LIG_SH2_CRK | 860 | 864 | PF00017 | 0.565 |
LIG_SH2_CRK | 933 | 937 | PF00017 | 0.699 |
LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.645 |
LIG_SH2_NCK_1 | 915 | 919 | PF00017 | 0.717 |
LIG_SH2_NCK_1 | 933 | 937 | PF00017 | 0.488 |
LIG_SH2_SRC | 408 | 411 | PF00017 | 0.533 |
LIG_SH2_SRC | 610 | 613 | PF00017 | 0.412 |
LIG_SH2_SRC | 74 | 77 | PF00017 | 0.680 |
LIG_SH2_SRC | 776 | 779 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 566 | 569 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 776 | 779 | PF00017 | 0.580 |
LIG_SH3_1 | 900 | 906 | PF00018 | 0.682 |
LIG_SH3_2 | 809 | 814 | PF14604 | 0.634 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.686 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.421 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.766 |
LIG_SH3_3 | 737 | 743 | PF00018 | 0.495 |
LIG_SH3_3 | 806 | 812 | PF00018 | 0.606 |
LIG_SH3_3 | 834 | 840 | PF00018 | 0.801 |
LIG_SH3_3 | 896 | 902 | PF00018 | 0.770 |
LIG_SH3_3 | 903 | 909 | PF00018 | 0.749 |
LIG_SH3_5 | 929 | 933 | PF00018 | 0.665 |
LIG_SUMO_SIM_anti_2 | 21 | 26 | PF11976 | 0.645 |
LIG_SUMO_SIM_anti_2 | 644 | 649 | PF11976 | 0.501 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.646 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.474 |
LIG_UBA3_1 | 214 | 220 | PF00899 | 0.475 |
MOD_CDK_SPxK_1 | 572 | 578 | PF00069 | 0.523 |
MOD_CDK_SPxxK_3 | 267 | 274 | PF00069 | 0.403 |
MOD_CDK_SPxxK_3 | 287 | 294 | PF00069 | 0.547 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.441 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.355 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.705 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.638 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.352 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.554 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.430 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.583 |
MOD_CK1_1 | 714 | 720 | PF00069 | 0.509 |
MOD_CK1_1 | 856 | 862 | PF00069 | 0.778 |
MOD_CK1_1 | 907 | 913 | PF00069 | 0.759 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.473 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.533 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.501 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.672 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.496 |
MOD_CK2_1 | 689 | 695 | PF00069 | 0.499 |
MOD_CK2_1 | 710 | 716 | PF00069 | 0.535 |
MOD_CK2_1 | 748 | 754 | PF00069 | 0.596 |
MOD_CK2_1 | 815 | 821 | PF00069 | 0.605 |
MOD_CK2_1 | 828 | 834 | PF00069 | 0.801 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.552 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.427 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.348 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.358 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.413 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.312 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.695 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.566 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.602 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.710 |
MOD_GlcNHglycan | 744 | 747 | PF01048 | 0.523 |
MOD_GlcNHglycan | 830 | 833 | PF01048 | 0.783 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.739 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.758 |
MOD_GlcNHglycan | 878 | 881 | PF01048 | 0.723 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.769 |
MOD_GlcNHglycan | 883 | 886 | PF01048 | 0.734 |
MOD_GlcNHglycan | 916 | 919 | PF01048 | 0.753 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.355 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.344 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.362 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.377 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.400 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.654 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.663 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.731 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.726 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.524 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.501 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.438 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.575 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.536 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.446 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.413 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.687 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.714 |
MOD_GSK3_1 | 881 | 888 | PF00069 | 0.706 |
MOD_GSK3_1 | 907 | 914 | PF00069 | 0.741 |
MOD_GSK3_1 | 941 | 948 | PF00069 | 0.795 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.328 |
MOD_N-GLC_1 | 689 | 694 | PF02516 | 0.507 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.689 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.404 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.607 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.482 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.548 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.592 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.390 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.415 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.440 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.513 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.486 |
MOD_NEK2_1 | 710 | 715 | PF00069 | 0.649 |
MOD_NEK2_1 | 828 | 833 | PF00069 | 0.781 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.602 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.428 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.597 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.585 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.482 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.353 |
MOD_PIKK_1 | 738 | 744 | PF00454 | 0.558 |
MOD_PIKK_1 | 779 | 785 | PF00454 | 0.623 |
MOD_PIKK_1 | 821 | 827 | PF00454 | 0.666 |
MOD_PIKK_1 | 941 | 947 | PF00454 | 0.808 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.492 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.343 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.385 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.398 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.753 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.400 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.554 |
MOD_PKA_2 | 561 | 567 | PF00069 | 0.387 |
MOD_PKA_2 | 664 | 670 | PF00069 | 0.516 |
MOD_PKA_2 | 714 | 720 | PF00069 | 0.518 |
MOD_PKA_2 | 911 | 917 | PF00069 | 0.806 |
MOD_PKA_2 | 940 | 946 | PF00069 | 0.720 |
MOD_PKB_1 | 939 | 947 | PF00069 | 0.702 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.624 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.344 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.693 |
MOD_Plk_1 | 628 | 634 | PF00069 | 0.429 |
MOD_Plk_1 | 689 | 695 | PF00069 | 0.532 |
MOD_Plk_1 | 799 | 805 | PF00069 | 0.615 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.652 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.340 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.522 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.616 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.387 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.518 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.526 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.448 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.673 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.667 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.523 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.719 |
MOD_ProDKin_1 | 904 | 910 | PF00069 | 0.785 |
MOD_ProDKin_1 | 925 | 931 | PF00069 | 0.744 |
MOD_SUMO_for_1 | 173 | 176 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 415 | 422 | PF00179 | 0.647 |
MOD_SUMO_rev_2 | 660 | 670 | PF00179 | 0.554 |
TRG_DiLeu_BaEn_1 | 12 | 17 | PF01217 | 0.692 |
TRG_DiLeu_BaEn_1 | 754 | 759 | PF01217 | 0.608 |
TRG_DiLeu_BaLyEn_6 | 394 | 399 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 507 | 512 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 507 | 510 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 703 | 706 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 939 | 942 | PF00400 | 0.624 |
TRG_NES_CRM1_1 | 325 | 339 | PF08389 | 0.458 |
TRG_NLS_MonoExtC_3 | 170 | 176 | PF00514 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 469 | 474 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 510 | 515 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 550 | 554 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 706 | 711 | PF00026 | 0.707 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I905 | Leptomonas seymouri | 67% | 99% |
A0A0S4J053 | Bodo saltans | 30% | 100% |
A0A1X0P8U2 | Trypanosomatidae | 35% | 100% |
A0A3R7KGY7 | Trypanosoma rangeli | 34% | 100% |
A4HP37 | Leishmania braziliensis | 79% | 100% |
A4IDE4 | Leishmania infantum | 100% | 100% |
D0A320 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9ASU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q1Q1 | Leishmania major | 94% | 100% |
V5DKX4 | Trypanosoma cruzi | 35% | 100% |