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:0005768 | endosome | 7 | 2 |
GO:0030897 | HOPS complex | 3 | 2 |
GO:0031410 | cytoplasmic vesicle | 6 | 2 |
GO:0031982 | vesicle | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0097708 | intracellular vesicle | 5 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0099023 | vesicle tethering complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0016020 | membrane | 2 | 9 |
Related structures:
AlphaFold database: E9AD68
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0006886 | intracellular protein transport | 4 | 10 |
GO:0006904 | vesicle docking involved in exocytosis | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007032 | endosome organization | 6 | 2 |
GO:0007033 | vacuole organization | 5 | 2 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016050 | vesicle organization | 5 | 2 |
GO:0022406 | membrane docking | 2 | 2 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0046907 | intracellular transport | 3 | 10 |
GO:0048278 | vesicle docking | 4 | 2 |
GO:0048284 | organelle fusion | 5 | 2 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051640 | organelle localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0051649 | establishment of localization in cell | 3 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0140029 | exocytic process | 2 | 2 |
GO:0140056 | organelle localization by membrane tethering | 3 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0060090 | molecular adaptor activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.605 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 757 | 761 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 1083 | 1085 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 853 | 855 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 936 | 938 | PF00675 | 0.429 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 853 | 855 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 963 | 965 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 507 | 509 | PF00082 | 0.341 |
CLV_PCSK_PC1ET2_1 | 963 | 965 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 1005 | 1009 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 874 | 878 | PF00082 | 0.563 |
DEG_APCC_DBOX_1 | 472 | 480 | PF00400 | 0.454 |
DEG_APCC_DBOX_1 | 65 | 73 | PF00400 | 0.565 |
DEG_APCC_KENBOX_2 | 639 | 643 | PF00400 | 0.330 |
DEG_COP1_1 | 337 | 348 | PF00400 | 0.610 |
DEG_SPOP_SBC_1 | 248 | 252 | PF00917 | 0.533 |
DOC_ANK_TNKS_1 | 416 | 423 | PF00023 | 0.220 |
DOC_CYCLIN_RxL_1 | 623 | 633 | PF00134 | 0.528 |
DOC_CYCLIN_RxL_1 | 729 | 742 | PF00134 | 0.555 |
DOC_CYCLIN_RxL_1 | 999 | 1012 | PF00134 | 0.347 |
DOC_CYCLIN_yCln2_LP_2 | 16 | 22 | PF00134 | 0.591 |
DOC_MAPK_DCC_7 | 732 | 741 | PF00069 | 0.562 |
DOC_MAPK_FxFP_2 | 1015 | 1018 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 201 | 209 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 269 | 277 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 378 | 388 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 52 | 59 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 729 | 739 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 937 | 944 | PF00069 | 0.454 |
DOC_MAPK_MEF2A_6 | 381 | 390 | PF00069 | 0.217 |
DOC_MAPK_MEF2A_6 | 732 | 741 | PF00069 | 0.562 |
DOC_PP1_RVXF_1 | 221 | 228 | PF00149 | 0.464 |
DOC_PP1_RVXF_1 | 330 | 336 | PF00149 | 0.577 |
DOC_PP1_RVXF_1 | 438 | 444 | PF00149 | 0.307 |
DOC_PP1_RVXF_1 | 513 | 519 | PF00149 | 0.480 |
DOC_PP2B_LxvP_1 | 847 | 850 | PF13499 | 0.602 |
DOC_PP4_FxxP_1 | 1015 | 1018 | PF00568 | 0.392 |
DOC_PP4_FxxP_1 | 429 | 432 | PF00568 | 0.454 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.378 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 868 | 872 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 910 | 914 | PF00917 | 0.586 |
DOC_WW_Pin1_4 | 1009 | 1014 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.401 |
LIG_14-3-3_CanoR_1 | 271 | 276 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 295 | 299 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 336 | 341 | PF00244 | 0.701 |
LIG_AP2alpha_2 | 444 | 446 | PF02296 | 0.322 |
LIG_APCC_ABBA_1 | 20 | 25 | PF00400 | 0.544 |
LIG_APCC_ABBA_1 | 836 | 841 | PF00400 | 0.307 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.688 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.697 |
LIG_BRCT_BRCA1_1 | 184 | 188 | PF00533 | 0.519 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.621 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.197 |
LIG_EH1_1 | 763 | 771 | PF00400 | 0.494 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.554 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.501 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.516 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.543 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.646 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.454 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.444 |
LIG_FHA_1 | 706 | 712 | PF00498 | 0.451 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.289 |
LIG_FHA_1 | 825 | 831 | PF00498 | 0.465 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.495 |
LIG_FHA_1 | 842 | 848 | PF00498 | 0.285 |
LIG_FHA_1 | 930 | 936 | PF00498 | 0.427 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.450 |
LIG_FHA_2 | 967 | 973 | PF00498 | 0.410 |
LIG_FHA_2 | 974 | 980 | PF00498 | 0.383 |
LIG_Integrin_isoDGR_2 | 288 | 290 | PF01839 | 0.541 |
LIG_LIR_Apic_2 | 1012 | 1018 | PF02991 | 0.415 |
LIG_LIR_Apic_2 | 415 | 419 | PF02991 | 0.429 |
LIG_LIR_Apic_2 | 427 | 432 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 393 | 402 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 474 | 485 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 552 | 561 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 575 | 586 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 596 | 607 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 621 | 632 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 706 | 712 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 86 | 92 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 1011 | 1017 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 552 | 557 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 596 | 602 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 621 | 627 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 706 | 710 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 747 | 751 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 946 | 951 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 954 | 959 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 989 | 994 | PF02991 | 0.394 |
LIG_PCNA_yPIPBox_3 | 44 | 56 | PF02747 | 0.438 |
LIG_PCNA_yPIPBox_3 | 893 | 903 | PF02747 | 0.529 |
LIG_Rb_pABgroove_1 | 312 | 320 | PF01858 | 0.409 |
LIG_SH2_CRK | 558 | 562 | PF00017 | 0.370 |
LIG_SH2_CRK | 788 | 792 | PF00017 | 0.220 |
LIG_SH2_NCK_1 | 298 | 302 | PF00017 | 0.471 |
LIG_SH2_PTP2 | 87 | 90 | PF00017 | 0.433 |
LIG_SH2_SRC | 751 | 754 | PF00017 | 0.469 |
LIG_SH2_SRC | 848 | 851 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 645 | 649 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 751 | 755 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 788 | 792 | PF00017 | 0.220 |
LIG_SH2_STAP1 | 815 | 819 | PF00017 | 0.337 |
LIG_SH2_STAT3 | 959 | 962 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 1014 | 1017 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 673 | 676 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 848 | 851 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 955 | 958 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 993 | 996 | PF00017 | 0.307 |
LIG_SH3_1 | 428 | 434 | PF00018 | 0.454 |
LIG_SH3_3 | 1075 | 1081 | PF00018 | 0.546 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.591 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.531 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.442 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.454 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.477 |
LIG_SUMO_SIM_par_1 | 1074 | 1079 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 235 | 241 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 715 | 721 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 765 | 771 | PF11976 | 0.462 |
LIG_TRAF2_1 | 976 | 979 | PF00917 | 0.418 |
LIG_UBA3_1 | 598 | 606 | PF00899 | 0.481 |
LIG_UBA3_1 | 723 | 729 | PF00899 | 0.536 |
LIG_WRC_WIRS_1 | 1039 | 1044 | PF05994 | 0.500 |
LIG_WRC_WIRS_1 | 745 | 750 | PF05994 | 0.523 |
LIG_WW_2 | 431 | 434 | PF00397 | 0.454 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.618 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.509 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.629 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.389 |
MOD_CK2_1 | 1028 | 1034 | PF00069 | 0.437 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.590 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.686 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.705 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.411 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.491 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.672 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.431 |
MOD_CK2_1 | 966 | 972 | PF00069 | 0.409 |
MOD_CK2_1 | 973 | 979 | PF00069 | 0.389 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.685 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.491 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.528 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.435 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.464 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.368 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.503 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.550 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.516 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.510 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.536 |
MOD_GlcNHglycan | 780 | 783 | PF01048 | 0.429 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.633 |
MOD_GlcNHglycan | 925 | 928 | PF01048 | 0.353 |
MOD_GSK3_1 | 1003 | 1010 | PF00069 | 0.426 |
MOD_GSK3_1 | 1028 | 1035 | PF00069 | 0.535 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.631 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.530 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.599 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.376 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.447 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.522 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.495 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.461 |
MOD_LATS_1 | 851 | 857 | PF00433 | 0.507 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.463 |
MOD_N-GLC_2 | 525 | 527 | PF02516 | 0.434 |
MOD_NEK2_1 | 1007 | 1012 | PF00069 | 0.344 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.559 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.513 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.504 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.359 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.553 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.408 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.448 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.400 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.535 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.404 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.501 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.525 |
MOD_NEK2_1 | 804 | 809 | PF00069 | 0.316 |
MOD_NEK2_1 | 810 | 815 | PF00069 | 0.308 |
MOD_NEK2_2 | 883 | 888 | PF00069 | 0.534 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.464 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.641 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.640 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.571 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.599 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.530 |
MOD_PIKK_1 | 966 | 972 | PF00454 | 0.372 |
MOD_PIKK_1 | 994 | 1000 | PF00454 | 0.412 |
MOD_PK_1 | 1032 | 1038 | PF00069 | 0.443 |
MOD_PK_1 | 336 | 342 | PF00069 | 0.618 |
MOD_PKA_1 | 853 | 859 | PF00069 | 0.704 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.521 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.634 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.460 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.491 |
MOD_PKA_2 | 853 | 859 | PF00069 | 0.701 |
MOD_Plk_1 | 1085 | 1091 | PF00069 | 0.515 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.542 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.662 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.547 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.447 |
MOD_Plk_1 | 751 | 757 | PF00069 | 0.548 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.673 |
MOD_Plk_1 | 863 | 869 | PF00069 | 0.674 |
MOD_Plk_1 | 883 | 889 | PF00069 | 0.535 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.500 |
MOD_Plk_4 | 1038 | 1044 | PF00069 | 0.493 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.455 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.479 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.461 |
MOD_Plk_4 | 744 | 750 | PF00069 | 0.486 |
MOD_Plk_4 | 805 | 811 | PF00069 | 0.387 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.475 |
MOD_ProDKin_1 | 1009 | 1015 | PF00069 | 0.354 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.476 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.416 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.401 |
MOD_SUMO_rev_2 | 866 | 876 | PF00179 | 0.642 |
TRG_DiLeu_BaEn_1 | 174 | 179 | PF01217 | 0.442 |
TRG_DiLeu_BaEn_1 | 329 | 334 | PF01217 | 0.570 |
TRG_DiLeu_BaEn_1 | 64 | 69 | PF01217 | 0.590 |
TRG_DiLeu_BaEn_1 | 940 | 945 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 647 | 652 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 787 | 792 | PF01217 | 0.376 |
TRG_DiLeu_LyEn_5 | 329 | 334 | PF01217 | 0.570 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 645 | 648 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 788 | 791 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 833 | 836 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.320 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 440 | 443 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 505 | 508 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 529 | 531 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 670 | 673 | PF00400 | 0.443 |
TRG_ER_FFAT_1 | 950 | 961 | PF00635 | 0.437 |
TRG_NES_CRM1_1 | 594 | 608 | PF08389 | 0.427 |
TRG_NES_CRM1_1 | 934 | 947 | PF08389 | 0.368 |
TRG_NLS_MonoExtC_3 | 505 | 511 | PF00514 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 1005 | 1009 | PF00026 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 650 | 654 | PF00026 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 725 | 730 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 735 | 740 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 790 | 794 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 937 | 941 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAX5 | Leptomonas seymouri | 63% | 99% |
A0A0S4JVP2 | Bodo saltans | 30% | 100% |
A0A1X0P439 | Trypanosomatidae | 35% | 98% |
A0A3R7NS00 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X0J6 | Leishmania donovani | 95% | 100% |
A4HFL4 | Leishmania braziliensis | 81% | 100% |
A4I2P5 | Leishmania infantum | 96% | 100% |
D0A5Q6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 99% |
E9AYZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
F4IDS7 | Arabidopsis thaliana | 24% | 100% |
P59015 | Danio rerio | 22% | 100% |
V5BE49 | Trypanosoma cruzi | 39% | 100% |