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: E9ASU5
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 | 390 | 394 | PF00656 | 0.419 |
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.656 |
CLV_C14_Caspase3-7 | 673 | 677 | PF00656 | 0.556 |
CLV_C14_Caspase3-7 | 695 | 699 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.461 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 716 | 718 | PF00675 | 0.544 |
CLV_PCSK_FUR_1 | 714 | 718 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 716 | 718 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 824 | 828 | PF00082 | 0.675 |
CLV_Separin_Metazoa | 176 | 180 | PF03568 | 0.449 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.631 |
DEG_APCC_DBOX_1 | 453 | 461 | PF00400 | 0.638 |
DEG_APCC_DBOX_1 | 517 | 525 | PF00400 | 0.418 |
DOC_CKS1_1 | 835 | 840 | PF01111 | 0.657 |
DOC_CKS1_1 | 877 | 882 | PF01111 | 0.508 |
DOC_CYCLIN_RxL_1 | 713 | 724 | PF00134 | 0.686 |
DOC_CYCLIN_yCln2_LP_2 | 23 | 29 | PF00134 | 0.645 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.693 |
DOC_MAPK_FxFP_2 | 31 | 34 | PF00069 | 0.687 |
DOC_MAPK_gen_1 | 100 | 108 | PF00069 | 0.643 |
DOC_MAPK_gen_1 | 171 | 177 | PF00069 | 0.430 |
DOC_MAPK_gen_1 | 232 | 241 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 30 | 37 | PF00069 | 0.656 |
DOC_MAPK_gen_1 | 725 | 735 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 111 | 118 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 18 | 27 | PF00069 | 0.607 |
DOC_MAPK_MEF2A_6 | 235 | 243 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 399 | 406 | PF00069 | 0.487 |
DOC_PP1_RVXF_1 | 566 | 572 | PF00149 | 0.390 |
DOC_PP1_RVXF_1 | 627 | 634 | PF00149 | 0.526 |
DOC_PP1_RVXF_1 | 779 | 786 | PF00149 | 0.558 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.638 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.712 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.424 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.655 |
DOC_PP4_FxxP_1 | 619 | 622 | PF00568 | 0.533 |
DOC_PP4_FxxP_1 | 877 | 880 | PF00568 | 0.686 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 758 | 762 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 809 | 813 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 863 | 867 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 886 | 890 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 909 | 913 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 950 | 954 | PF00917 | 0.790 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 834 | 839 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 870 | 875 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 876 | 881 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 100 | 109 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 294 | 299 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 408 | 414 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 479 | 488 | PF00244 | 0.236 |
LIG_14-3-3_CanoR_1 | 539 | 543 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 572 | 576 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 578 | 586 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 922 | 926 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 951 | 960 | PF00244 | 0.752 |
LIG_Actin_WH2_2 | 345 | 361 | PF00022 | 0.581 |
LIG_Actin_WH2_2 | 661 | 677 | PF00022 | 0.535 |
LIG_AP2alpha_2 | 899 | 901 | PF02296 | 0.463 |
LIG_APCC_ABBA_1 | 643 | 648 | PF00400 | 0.390 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.745 |
LIG_BRCT_BRCA1_1 | 207 | 211 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_1 | 676 | 680 | PF00533 | 0.543 |
LIG_BRCT_BRCA1_1 | 911 | 915 | PF00533 | 0.487 |
LIG_Clathr_ClatBox_1 | 521 | 525 | PF01394 | 0.424 |
LIG_deltaCOP1_diTrp_1 | 632 | 640 | PF00928 | 0.548 |
LIG_EH_1 | 200 | 204 | PF12763 | 0.449 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.331 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.536 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.512 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.621 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.404 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.391 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.548 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.559 |
LIG_FHA_1 | 823 | 829 | PF00498 | 0.631 |
LIG_FHA_1 | 835 | 841 | PF00498 | 0.648 |
LIG_FHA_1 | 918 | 924 | PF00498 | 0.780 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.363 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.734 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.725 |
LIG_FHA_2 | 671 | 677 | PF00498 | 0.592 |
LIG_FHA_2 | 700 | 706 | PF00498 | 0.524 |
LIG_FHA_2 | 790 | 796 | PF00498 | 0.571 |
LIG_FHA_2 | 952 | 958 | PF00498 | 0.575 |
LIG_GBD_Chelix_1 | 469 | 477 | PF00786 | 0.418 |
LIG_GBD_Chelix_1 | 553 | 561 | PF00786 | 0.525 |
LIG_LIR_Apic_2 | 616 | 622 | PF02991 | 0.581 |
LIG_LIR_Apic_2 | 632 | 636 | PF02991 | 0.547 |
LIG_LIR_Apic_2 | 932 | 938 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 208 | 219 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 330 | 338 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 347 | 356 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 555 | 562 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 637 | 647 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 744 | 754 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 898 | 909 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 511 | 517 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 632 | 638 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 639 | 643 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 744 | 750 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 898 | 904 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 912 | 918 | PF02991 | 0.521 |
LIG_LYPXL_S_1 | 634 | 638 | PF13949 | 0.386 |
LIG_LYPXL_yS_3 | 635 | 638 | PF13949 | 0.393 |
LIG_MYND_1 | 503 | 507 | PF01753 | 0.542 |
LIG_NRBOX | 19 | 25 | PF00104 | 0.609 |
LIG_NRBOX | 795 | 801 | PF00104 | 0.550 |
LIG_PCNA_PIPBox_1 | 779 | 788 | PF02747 | 0.563 |
LIG_PCNA_yPIPBox_3 | 793 | 803 | PF02747 | 0.606 |
LIG_PDZ_Class_3 | 956 | 961 | PF00595 | 0.765 |
LIG_Rb_LxCxE_1 | 732 | 751 | PF01857 | 0.557 |
LIG_SH2_CRK | 935 | 939 | PF00017 | 0.607 |
LIG_SH2_NCK_1 | 925 | 929 | PF00017 | 0.710 |
LIG_SH2_SRC | 416 | 419 | PF00017 | 0.549 |
LIG_SH2_SRC | 620 | 623 | PF00017 | 0.413 |
LIG_SH2_SRC | 74 | 77 | PF00017 | 0.678 |
LIG_SH2_SRC | 786 | 789 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.466 |
LIG_SH2_STAT3 | 576 | 579 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 786 | 789 | PF00017 | 0.543 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.415 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.767 |
LIG_SH3_3 | 747 | 753 | PF00018 | 0.492 |
LIG_SH3_3 | 846 | 852 | PF00018 | 0.799 |
LIG_SH3_3 | 913 | 919 | PF00018 | 0.702 |
LIG_SUMO_SIM_anti_2 | 21 | 26 | PF11976 | 0.604 |
LIG_SUMO_SIM_anti_2 | 484 | 489 | PF11976 | 0.314 |
LIG_SUMO_SIM_anti_2 | 654 | 659 | PF11976 | 0.500 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.614 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.470 |
LIG_UBA3_1 | 214 | 220 | PF00899 | 0.475 |
MOD_CDK_SPxK_1 | 582 | 588 | PF00069 | 0.518 |
MOD_CDK_SPxxK_3 | 267 | 274 | PF00069 | 0.402 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.441 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.337 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.645 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.598 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.661 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.703 |
MOD_CK1_1 | 582 | 588 | PF00069 | 0.533 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.428 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.579 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.502 |
MOD_CK1_1 | 866 | 872 | PF00069 | 0.776 |
MOD_CK1_1 | 910 | 916 | PF00069 | 0.784 |
MOD_CK1_1 | 917 | 923 | PF00069 | 0.762 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.512 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.537 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.665 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.501 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.454 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.517 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.511 |
MOD_CK2_1 | 758 | 764 | PF00069 | 0.595 |
MOD_CK2_1 | 838 | 844 | PF00069 | 0.786 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.550 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.400 |
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 | 0.266 |
MOD_GlcNHglycan | 281 | 286 | PF01048 | 0.666 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.517 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.652 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.557 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.608 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.728 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.516 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.734 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.807 |
MOD_GlcNHglycan | 865 | 868 | PF01048 | 0.801 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.763 |
MOD_GlcNHglycan | 888 | 891 | PF01048 | 0.720 |
MOD_GlcNHglycan | 909 | 912 | PF01048 | 0.752 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.696 |
MOD_GlcNHglycan | 926 | 929 | PF01048 | 0.763 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.328 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.344 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.361 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.636 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.592 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.657 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.576 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.734 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.486 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.525 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.494 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.435 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.571 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.609 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.525 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.435 |
MOD_GSK3_1 | 748 | 755 | PF00069 | 0.389 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.658 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.707 |
MOD_GSK3_1 | 866 | 873 | PF00069 | 0.600 |
MOD_GSK3_1 | 886 | 893 | PF00069 | 0.670 |
MOD_GSK3_1 | 910 | 917 | PF00069 | 0.689 |
MOD_GSK3_1 | 951 | 958 | PF00069 | 0.783 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.328 |
MOD_N-GLC_1 | 699 | 704 | PF02516 | 0.511 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.687 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.404 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.579 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.485 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.519 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.585 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.375 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.400 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.441 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.511 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.484 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.637 |
MOD_NEK2_2 | 348 | 353 | PF00069 | 0.583 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.602 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.602 |
MOD_PIKK_1 | 548 | 554 | PF00454 | 0.484 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.352 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.510 |
MOD_PIKK_1 | 748 | 754 | PF00454 | 0.556 |
MOD_PIKK_1 | 789 | 795 | PF00454 | 0.616 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.457 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.436 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.378 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.437 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.715 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.523 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.376 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.490 |
MOD_PKA_2 | 724 | 730 | PF00069 | 0.501 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.415 |
MOD_PKA_2 | 921 | 927 | PF00069 | 0.790 |
MOD_PKA_2 | 950 | 956 | PF00069 | 0.715 |
MOD_PKB_1 | 949 | 957 | PF00069 | 0.699 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.344 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.680 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.751 |
MOD_Plk_1 | 638 | 644 | PF00069 | 0.428 |
MOD_Plk_1 | 699 | 705 | PF00069 | 0.533 |
MOD_Plk_1 | 809 | 815 | PF00069 | 0.607 |
MOD_Plk_1 | 843 | 849 | PF00069 | 0.576 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.340 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.680 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.503 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.611 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.379 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.493 |
MOD_Plk_4 | 930 | 936 | PF00069 | 0.662 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.524 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.673 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.725 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.504 |
MOD_ProDKin_1 | 834 | 840 | PF00069 | 0.652 |
MOD_ProDKin_1 | 870 | 876 | PF00069 | 0.652 |
MOD_SUMO_for_1 | 173 | 176 | PF00179 | 0.413 |
MOD_SUMO_for_1 | 826 | 829 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 422 | 430 | PF00179 | 0.658 |
MOD_SUMO_rev_2 | 670 | 680 | PF00179 | 0.550 |
TRG_DiLeu_BaEn_1 | 12 | 17 | PF01217 | 0.666 |
TRG_DiLeu_BaLyEn_6 | 402 | 407 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 517 | 522 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 517 | 520 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 713 | 716 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 949 | 952 | PF00400 | 0.739 |
TRG_NES_CRM1_1 | 333 | 347 | PF08389 | 0.458 |
TRG_NES_CRM1_1 | 484 | 496 | PF08389 | 0.328 |
TRG_NLS_MonoExtC_3 | 170 | 176 | PF00514 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 479 | 484 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 520 | 525 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 560 | 564 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 716 | 721 | PF00026 | 0.688 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I905 | Leptomonas seymouri | 61% | 100% |
A0A0S4J053 | Bodo saltans | 29% | 100% |
A0A1X0P8U2 | Trypanosomatidae | 35% | 100% |
A0A3R7KGY7 | Trypanosoma rangeli | 35% | 100% |
A0A3S7XAQ6 | Leishmania donovani | 90% | 100% |
A4HP37 | Leishmania braziliensis | 79% | 100% |
A4IDE4 | Leishmania infantum | 90% | 100% |
D0A320 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4Q1Q1 | Leishmania major | 88% | 99% |
V5DKX4 | Trypanosoma cruzi | 35% | 100% |