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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0043229 | intracellular organelle | 3 | 6 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005643 | nuclear pore | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4ICX8
Term | Name | Level | Count |
---|---|---|---|
GO:0006611 | protein export from nucleus | 5 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005049 | nuclear export signal receptor activity | 3 | 7 |
GO:0140104 | molecular carrier activity | 1 | 7 |
GO:0140142 | nucleocytoplasmic carrier activity | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 701 | 705 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 822 | 826 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 910 | 914 | PF00656 | 0.458 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 747 | 751 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 782 | 786 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 963 | 967 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 973 | 977 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 984 | 988 | PF00082 | 0.418 |
DEG_APCC_DBOX_1 | 797 | 805 | PF00400 | 0.416 |
DEG_APCC_DBOX_1 | 983 | 991 | PF00400 | 0.522 |
DEG_MDM2_SWIB_1 | 521 | 528 | PF02201 | 0.466 |
DEG_SCF_FBW7_1 | 101 | 107 | PF00400 | 0.502 |
DEG_SCF_FBW7_2 | 517 | 522 | PF00400 | 0.481 |
DEG_SCF_FBW7_2 | 632 | 639 | PF00400 | 0.480 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 186 | 198 | PF00134 | 0.469 |
DOC_CYCLIN_RxL_1 | 207 | 215 | PF00134 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 575 | 581 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 300 | 309 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 977 | 987 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 179 | 187 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 798 | 805 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 980 | 989 | PF00069 | 0.490 |
DOC_MAPK_NFAT4_5 | 798 | 806 | PF00069 | 0.489 |
DOC_PP1_RVXF_1 | 527 | 534 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 59 | 66 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 689 | 696 | PF00149 | 0.462 |
DOC_PP1_RVXF_1 | 971 | 977 | PF00149 | 0.426 |
DOC_PP2B_LxvP_1 | 882 | 885 | PF13499 | 0.472 |
DOC_PP4_FxxP_1 | 174 | 177 | PF00568 | 0.469 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.504 |
DOC_SPAK_OSR1_1 | 325 | 329 | PF12202 | 0.523 |
DOC_USP7_MATH_1 | 1022 | 1026 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 1030 | 1034 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 1044 | 1048 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 820 | 824 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 909 | 913 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 922 | 926 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 994 | 998 | PF00917 | 0.516 |
DOC_USP7_MATH_2 | 636 | 642 | PF00917 | 0.479 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 713 | 718 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 946 | 951 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 325 | 335 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 382 | 390 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 39 | 49 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 437 | 447 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 497 | 503 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 658 | 663 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 79 | 89 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 839 | 845 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 880 | 885 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 932 | 938 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 967 | 976 | PF00244 | 0.487 |
LIG_Actin_WH2_2 | 106 | 124 | PF00022 | 0.421 |
LIG_Actin_WH2_2 | 618 | 635 | PF00022 | 0.518 |
LIG_Actin_WH2_2 | 793 | 811 | PF00022 | 0.495 |
LIG_AP2alpha_1 | 468 | 472 | PF02296 | 0.514 |
LIG_APCC_ABBA_1 | 634 | 639 | PF00400 | 0.482 |
LIG_BH_BH3_1 | 115 | 131 | PF00452 | 0.526 |
LIG_BRCT_BRCA1_1 | 237 | 241 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 411 | 415 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 911 | 915 | PF00533 | 0.383 |
LIG_CSL_BTD_1 | 105 | 108 | PF09270 | 0.550 |
LIG_FHA_1 | 1049 | 1055 | PF00498 | 0.469 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.538 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.475 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.470 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.504 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.478 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.503 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.496 |
LIG_FHA_1 | 835 | 841 | PF00498 | 0.431 |
LIG_FHA_1 | 857 | 863 | PF00498 | 0.447 |
LIG_FHA_1 | 936 | 942 | PF00498 | 0.448 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.551 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.547 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.524 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.527 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.458 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.520 |
LIG_FHA_2 | 820 | 826 | PF00498 | 0.577 |
LIG_FHA_2 | 891 | 897 | PF00498 | 0.509 |
LIG_GBD_Chelix_1 | 327 | 335 | PF00786 | 0.468 |
LIG_GBD_Chelix_1 | 725 | 733 | PF00786 | 0.478 |
LIG_LIR_Apic_2 | 369 | 374 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 1034 | 1045 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 260 | 270 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 336 | 345 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 347 | 357 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 365 | 374 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 518 | 528 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 56 | 67 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 667 | 676 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 889 | 899 | PF02991 | 0.403 |
LIG_LIR_LC3C_4 | 802 | 805 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 1017 | 1023 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 1034 | 1040 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 667 | 672 | PF02991 | 0.537 |
LIG_MYND_3 | 884 | 888 | PF01753 | 0.520 |
LIG_NRBOX | 208 | 214 | PF00104 | 0.433 |
LIG_NRBOX | 523 | 529 | PF00104 | 0.458 |
LIG_PCNA_yPIPBox_3 | 200 | 213 | PF02747 | 0.510 |
LIG_PCNA_yPIPBox_3 | 39 | 49 | PF02747 | 0.566 |
LIG_PDZ_Class_2 | 1051 | 1056 | PF00595 | 0.430 |
LIG_Pex14_2 | 468 | 472 | PF04695 | 0.490 |
LIG_Pex14_2 | 521 | 525 | PF04695 | 0.476 |
LIG_Pex14_2 | 902 | 906 | PF04695 | 0.378 |
LIG_REV1ctd_RIR_1 | 973 | 981 | PF16727 | 0.374 |
LIG_RPA_C_Fungi | 834 | 846 | PF08784 | 0.431 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.457 |
LIG_SH2_CRK | 995 | 999 | PF00017 | 0.555 |
LIG_SH2_NCK_1 | 610 | 614 | PF00017 | 0.387 |
LIG_SH2_SRC | 600 | 603 | PF00017 | 0.529 |
LIG_SH2_SRC | 610 | 613 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 610 | 614 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 769 | 773 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 810 | 814 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 995 | 999 | PF00017 | 0.555 |
LIG_SH2_STAT3 | 93 | 96 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.414 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.415 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.568 |
LIG_Sin3_3 | 870 | 877 | PF02671 | 0.456 |
LIG_SUMO_SIM_anti_2 | 624 | 630 | PF11976 | 0.504 |
LIG_SUMO_SIM_anti_2 | 983 | 989 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 725 | 732 | PF11976 | 0.519 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.426 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.656 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.528 |
LIG_TRAF2_1 | 636 | 639 | PF00917 | 0.540 |
LIG_TRAF2_1 | 675 | 678 | PF00917 | 0.451 |
LIG_TRFH_1 | 350 | 354 | PF08558 | 0.525 |
LIG_TYR_ITIM | 993 | 998 | PF00017 | 0.478 |
LIG_UBA3_1 | 306 | 314 | PF00899 | 0.451 |
LIG_UBA3_1 | 520 | 529 | PF00899 | 0.480 |
LIG_UBA3_1 | 560 | 566 | PF00899 | 0.378 |
LIG_UBA3_1 | 840 | 848 | PF00899 | 0.472 |
LIG_WRC_WIRS_1 | 310 | 315 | PF05994 | 0.509 |
LIG_WRC_WIRS_1 | 659 | 664 | PF05994 | 0.541 |
MOD_CDK_SPK_2 | 151 | 156 | PF00069 | 0.571 |
MOD_CDK_SPxxK_3 | 149 | 156 | PF00069 | 0.575 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.543 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.455 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.398 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.575 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.392 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.446 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.544 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.474 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.530 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.484 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.457 |
MOD_CK1_1 | 716 | 722 | PF00069 | 0.461 |
MOD_CK1_1 | 739 | 745 | PF00069 | 0.479 |
MOD_CK1_1 | 819 | 825 | PF00069 | 0.549 |
MOD_CK1_1 | 863 | 869 | PF00069 | 0.410 |
MOD_CK1_1 | 883 | 889 | PF00069 | 0.404 |
MOD_CK1_1 | 953 | 959 | PF00069 | 0.536 |
MOD_CK1_1 | 968 | 974 | PF00069 | 0.413 |
MOD_CK2_1 | 1032 | 1038 | PF00069 | 0.470 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.431 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.577 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.602 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.555 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.434 |
MOD_CK2_1 | 632 | 638 | PF00069 | 0.406 |
MOD_CK2_1 | 890 | 896 | PF00069 | 0.440 |
MOD_Cter_Amidation | 77 | 80 | PF01082 | 0.506 |
MOD_GlcNHglycan | 1024 | 1027 | PF01048 | 0.536 |
MOD_GlcNHglycan | 1028 | 1031 | PF01048 | 0.627 |
MOD_GlcNHglycan | 1034 | 1037 | PF01048 | 0.595 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.456 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.473 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.523 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.530 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.223 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.655 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.449 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.482 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.452 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.467 |
MOD_GlcNHglycan | 818 | 821 | PF01048 | 0.572 |
MOD_GlcNHglycan | 822 | 825 | PF01048 | 0.602 |
MOD_GlcNHglycan | 916 | 919 | PF01048 | 0.489 |
MOD_GlcNHglycan | 955 | 958 | PF01048 | 0.437 |
MOD_GlcNHglycan | 970 | 973 | PF01048 | 0.522 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.579 |
MOD_GSK3_1 | 1022 | 1029 | PF00069 | 0.529 |
MOD_GSK3_1 | 1044 | 1051 | PF00069 | 0.514 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.418 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.461 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.573 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.414 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.582 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.455 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.480 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.578 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.542 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.332 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.394 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.439 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.442 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.479 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.520 |
MOD_GSK3_1 | 780 | 787 | PF00069 | 0.436 |
MOD_GSK3_1 | 810 | 817 | PF00069 | 0.449 |
MOD_GSK3_1 | 852 | 859 | PF00069 | 0.452 |
MOD_GSK3_1 | 933 | 940 | PF00069 | 0.431 |
MOD_GSK3_1 | 946 | 953 | PF00069 | 0.535 |
MOD_GSK3_1 | 994 | 1001 | PF00069 | 0.505 |
MOD_N-GLC_1 | 1030 | 1035 | PF02516 | 0.649 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.695 |
MOD_N-GLC_2 | 490 | 492 | PF02516 | 0.375 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.571 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.476 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.485 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.173 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.461 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.483 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.268 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.388 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.342 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.423 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.398 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.340 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.379 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.396 |
MOD_NEK2_1 | 815 | 820 | PF00069 | 0.568 |
MOD_NEK2_1 | 840 | 845 | PF00069 | 0.387 |
MOD_NEK2_1 | 945 | 950 | PF00069 | 0.407 |
MOD_NEK2_2 | 1044 | 1049 | PF00069 | 0.538 |
MOD_NEK2_2 | 276 | 281 | PF00069 | 0.540 |
MOD_NEK2_2 | 443 | 448 | PF00069 | 0.489 |
MOD_NEK2_2 | 498 | 503 | PF00069 | 0.480 |
MOD_NEK2_2 | 780 | 785 | PF00069 | 0.420 |
MOD_OFUCOSY | 487 | 492 | PF10250 | 0.484 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.454 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.551 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.472 |
MOD_PIKK_1 | 591 | 597 | PF00454 | 0.517 |
MOD_PIKK_1 | 739 | 745 | PF00454 | 0.496 |
MOD_PK_1 | 860 | 866 | PF00069 | 0.455 |
MOD_PKA_1 | 392 | 398 | PF00069 | 0.584 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.495 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.542 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.580 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.498 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.447 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.526 |
MOD_Plk_1 | 878 | 884 | PF00069 | 0.460 |
MOD_Plk_2-3 | 245 | 251 | PF00069 | 0.585 |
MOD_Plk_4 | 1001 | 1007 | PF00069 | 0.493 |
MOD_Plk_4 | 1049 | 1055 | PF00069 | 0.591 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.460 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.429 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.442 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.402 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.415 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.452 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.326 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.475 |
MOD_Plk_4 | 994 | 1000 | PF00069 | 0.517 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.501 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.578 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.531 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.391 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.505 |
MOD_ProDKin_1 | 713 | 719 | PF00069 | 0.526 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.498 |
MOD_ProDKin_1 | 946 | 952 | PF00069 | 0.586 |
MOD_SUMO_rev_2 | 449 | 456 | PF00179 | 0.536 |
TRG_DiLeu_BaEn_1 | 261 | 266 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_1 | 305 | 310 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_1 | 567 | 572 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_4 | 604 | 610 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 570 | 575 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 644 | 649 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 688 | 693 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 756 | 761 | PF01217 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 787 | 792 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 836 | 841 | PF01217 | 0.490 |
TRG_DiLeu_LyEn_5 | 261 | 266 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 995 | 998 | PF00928 | 0.559 |
TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 689 | 692 | PF00400 | 0.399 |
TRG_NES_CRM1_1 | 322 | 336 | PF08389 | 0.464 |
TRG_NES_CRM1_1 | 623 | 638 | PF08389 | 0.448 |
TRG_NES_CRM1_1 | 796 | 807 | PF08389 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 161 | 165 | PF00026 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 192 | 197 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 264 | 269 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 437 | 442 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 798 | 802 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 977 | 981 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 991 | 996 | PF00026 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0T0 | Leptomonas seymouri | 66% | 100% |
A0A1X0P8G9 | Trypanosomatidae | 29% | 100% |
A0A3R7MB24 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H812 | Leishmania donovani | 99% | 100% |
A4HNL6 | Leishmania braziliensis | 82% | 100% |
D0A2H1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 94% |
E9ASC7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q269 | Leishmania major | 94% | 100% |
V5C008 | Trypanosoma cruzi | 29% | 100% |