Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 3 |
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: 6 |
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 | 12 |
GO:0005737 | cytoplasm | 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 |
Related structures:
AlphaFold database: A4HKK5
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 12 |
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006913 | nucleocytoplasmic transport | 5 | 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:0033365 | protein localization to organelle | 5 | 12 |
GO:0034504 | protein localization to nucleus | 6 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051169 | nuclear transport | 4 | 12 |
GO:0051170 | import into nucleus | 6 | 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:0072594 | establishment of protein localization to organelle | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005048 | signal sequence binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008139 | nuclear localization sequence binding | 5 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0042277 | peptide binding | 3 | 1 |
GO:0061608 | nuclear import signal receptor activity | 3 | 1 |
GO:0140104 | molecular carrier activity | 1 | 1 |
GO:0140142 | nucleocytoplasmic carrier activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 466 | 470 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 549 | 553 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 659 | 663 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 832 | 836 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 1032 | 1034 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 817 | 819 | PF00675 | 0.351 |
CLV_PCSK_KEX2_1 | 1032 | 1034 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 816 | 818 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 824 | 826 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 816 | 818 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 824 | 826 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 824 | 828 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 863 | 867 | PF00082 | 0.392 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.523 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.337 |
DEG_SPOP_SBC_1 | 924 | 928 | PF00917 | 0.587 |
DOC_CYCLIN_RxL_1 | 61 | 70 | PF00134 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 101 | 107 | PF00134 | 0.572 |
DOC_MAPK_gen_1 | 1032 | 1039 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 560 | 569 | PF00069 | 0.501 |
DOC_MAPK_HePTP_8 | 803 | 815 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 272 | 280 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 488 | 497 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 806 | 815 | PF00069 | 0.592 |
DOC_PP2B_LxvP_1 | 548 | 551 | PF13499 | 0.339 |
DOC_PP4_FxxP_1 | 669 | 672 | PF00568 | 0.666 |
DOC_PP4_FxxP_1 | 866 | 869 | PF00568 | 0.592 |
DOC_SPAK_OSR1_1 | 668 | 672 | PF12202 | 0.660 |
DOC_USP7_MATH_1 | 1066 | 1070 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 924 | 928 | PF00917 | 0.582 |
DOC_USP7_UBL2_3 | 288 | 292 | PF12436 | 0.517 |
DOC_USP7_UBL2_3 | 408 | 412 | PF12436 | 0.557 |
DOC_USP7_UBL2_3 | 558 | 562 | PF12436 | 0.523 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 793 | 798 | PF00397 | 0.534 |
LIG_14-3-3_CanoR_1 | 21 | 28 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 415 | 420 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 455 | 464 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 610 | 619 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 786 | 791 | PF00244 | 0.602 |
LIG_APCC_ABBA_1 | 114 | 119 | PF00400 | 0.580 |
LIG_APCC_ABBA_1 | 491 | 496 | PF00400 | 0.534 |
LIG_APCC_ABBA_1 | 533 | 538 | PF00400 | 0.492 |
LIG_APCC_ABBA_1 | 541 | 546 | PF00400 | 0.398 |
LIG_BRCT_BRCA1_1 | 2 | 6 | PF00533 | 0.375 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.409 |
LIG_deltaCOP1_diTrp_1 | 121 | 127 | PF00928 | 0.433 |
LIG_EH1_1 | 937 | 945 | PF00400 | 0.397 |
LIG_eIF4E_1 | 973 | 979 | PF01652 | 0.555 |
LIG_FHA_1 | 1002 | 1008 | PF00498 | 0.435 |
LIG_FHA_1 | 1010 | 1016 | PF00498 | 0.447 |
LIG_FHA_1 | 1055 | 1061 | PF00498 | 0.334 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.458 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.547 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.490 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.324 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.313 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.558 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.462 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.365 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.521 |
LIG_FHA_1 | 798 | 804 | PF00498 | 0.549 |
LIG_FHA_1 | 916 | 922 | PF00498 | 0.469 |
LIG_FHA_1 | 951 | 957 | PF00498 | 0.660 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.517 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.541 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.506 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.537 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.696 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.569 |
LIG_FHA_2 | 825 | 831 | PF00498 | 0.592 |
LIG_LIR_Apic_2 | 864 | 869 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 225 | 233 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 3 | 13 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 993 | 1002 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 485 | 490 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 577 | 582 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 993 | 998 | PF02991 | 0.400 |
LIG_MLH1_MIPbox_1 | 297 | 301 | PF16413 | 0.611 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.517 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.517 |
LIG_Pex14_2 | 866 | 870 | PF04695 | 0.506 |
LIG_PTB_Apo_2 | 307 | 314 | PF02174 | 0.592 |
LIG_PTB_Phospho_1 | 307 | 313 | PF10480 | 0.592 |
LIG_Rb_LxCxE_1 | 739 | 758 | PF01857 | 0.560 |
LIG_RPA_C_Fungi | 369 | 381 | PF08784 | 0.288 |
LIG_SH2_GRB2like | 220 | 223 | PF00017 | 0.562 |
LIG_SH2_PTP2 | 494 | 497 | PF00017 | 0.530 |
LIG_SH2_PTP2 | 995 | 998 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 582 | 586 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 962 | 966 | PF00017 | 0.556 |
LIG_SH2_STAT3 | 220 | 223 | PF00017 | 0.562 |
LIG_SH2_STAT3 | 589 | 592 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 1078 | 1081 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 938 | 941 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 973 | 976 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 984 | 987 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 995 | 998 | PF00017 | 0.427 |
LIG_SH3_1 | 205 | 211 | PF00018 | 0.572 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.526 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.484 |
LIG_SH3_3 | 756 | 762 | PF00018 | 0.374 |
LIG_SH3_3 | 908 | 914 | PF00018 | 0.545 |
LIG_Sin3_3 | 377 | 384 | PF02671 | 0.501 |
LIG_SUMO_SIM_anti_2 | 565 | 571 | PF11976 | 0.496 |
LIG_SUMO_SIM_anti_2 | 57 | 62 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 546 | 552 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 676 | 684 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 88 | 97 | PF11976 | 0.332 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.595 |
LIG_TRFH_1 | 307 | 311 | PF08558 | 0.374 |
LIG_UBA3_1 | 133 | 138 | PF00899 | 0.347 |
LIG_UBA3_1 | 737 | 743 | PF00899 | 0.512 |
LIG_UBA3_1 | 854 | 863 | PF00899 | 0.477 |
LIG_Vh1_VBS_1 | 442 | 460 | PF01044 | 0.291 |
LIG_WRC_WIRS_1 | 464 | 469 | PF05994 | 0.424 |
MOD_CK1_1 | 1069 | 1075 | PF00069 | 0.533 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.522 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.518 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.581 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.403 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.448 |
MOD_CK1_1 | 772 | 778 | PF00069 | 0.475 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.504 |
MOD_CK1_1 | 919 | 925 | PF00069 | 0.567 |
MOD_CK1_1 | 949 | 955 | PF00069 | 0.676 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.620 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.547 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.374 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.374 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.288 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.589 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.531 |
MOD_CK2_1 | 772 | 778 | PF00069 | 0.522 |
MOD_CK2_1 | 882 | 888 | PF00069 | 0.538 |
MOD_Cter_Amidation | 350 | 353 | PF01082 | 0.374 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.330 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.519 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.518 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.374 |
MOD_GlcNHglycan | 45 | 49 | PF01048 | 0.533 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.468 |
MOD_GSK3_1 | 1009 | 1016 | PF00069 | 0.437 |
MOD_GSK3_1 | 1054 | 1061 | PF00069 | 0.556 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.564 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.499 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.505 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.512 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.559 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.339 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.399 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.547 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.396 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.539 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.462 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.445 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.434 |
MOD_GSK3_1 | 889 | 896 | PF00069 | 0.492 |
MOD_GSK3_1 | 905 | 912 | PF00069 | 0.427 |
MOD_GSK3_1 | 915 | 922 | PF00069 | 0.331 |
MOD_GSK3_1 | 946 | 953 | PF00069 | 0.558 |
MOD_GSK3_1 | 990 | 997 | PF00069 | 0.382 |
MOD_LATS_1 | 406 | 412 | PF00433 | 0.546 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.328 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.568 |
MOD_N-GLC_2 | 819 | 821 | PF02516 | 0.505 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.622 |
MOD_NEK2_1 | 1001 | 1006 | PF00069 | 0.436 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.492 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.467 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.221 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.339 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.600 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.534 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.497 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.593 |
MOD_NEK2_1 | 854 | 859 | PF00069 | 0.441 |
MOD_NEK2_1 | 889 | 894 | PF00069 | 0.486 |
MOD_NEK2_1 | 946 | 951 | PF00069 | 0.531 |
MOD_NEK2_1 | 994 | 999 | PF00069 | 0.398 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.322 |
MOD_NEK2_2 | 172 | 177 | PF00069 | 0.519 |
MOD_NEK2_2 | 387 | 392 | PF00069 | 0.522 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.319 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.560 |
MOD_PIKK_1 | 423 | 429 | PF00454 | 0.422 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.603 |
MOD_PIKK_1 | 506 | 512 | PF00454 | 0.544 |
MOD_PIKK_1 | 94 | 100 | PF00454 | 0.607 |
MOD_PK_1 | 786 | 792 | PF00069 | 0.505 |
MOD_PK_1 | 893 | 899 | PF00069 | 0.282 |
MOD_PKA_1 | 824 | 830 | PF00069 | 0.479 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.483 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.573 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.443 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.587 |
MOD_PKA_2 | 730 | 736 | PF00069 | 0.395 |
MOD_PKA_2 | 824 | 830 | PF00069 | 0.253 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.625 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.318 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.495 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.571 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.324 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.300 |
MOD_Plk_1 | 772 | 778 | PF00069 | 0.549 |
MOD_Plk_2-3 | 225 | 231 | PF00069 | 0.566 |
MOD_Plk_2-3 | 546 | 552 | PF00069 | 0.584 |
MOD_Plk_4 | 1013 | 1019 | PF00069 | 0.312 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.485 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.483 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.380 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.526 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.491 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.419 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.339 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.425 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.506 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.481 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.541 |
MOD_Plk_4 | 733 | 739 | PF00069 | 0.397 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.505 |
MOD_Plk_4 | 854 | 860 | PF00069 | 0.439 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.330 |
MOD_Plk_4 | 893 | 899 | PF00069 | 0.386 |
MOD_Plk_4 | 905 | 911 | PF00069 | 0.495 |
MOD_Plk_4 | 994 | 1000 | PF00069 | 0.389 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.585 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.322 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.550 |
MOD_ProDKin_1 | 793 | 799 | PF00069 | 0.398 |
MOD_SUMO_for_1 | 407 | 410 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 15 | 24 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 182 | 189 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 409 | 414 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 684 | 691 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 746 | 751 | PF00179 | 0.619 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.479 |
TRG_DiLeu_BaEn_1 | 565 | 570 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_2 | 664 | 670 | PF01217 | 0.631 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 745 | 748 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 995 | 998 | PF00928 | 0.441 |
TRG_ER_diArg_1 | 1032 | 1034 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 603 | 606 | PF00400 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 1032 | 1036 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZF6 | Leptomonas seymouri | 77% | 100% |
A0A0S4JKP1 | Bodo saltans | 37% | 100% |
A0A1X0NU68 | Trypanosomatidae | 40% | 100% |
A0A3Q8ID72 | Leishmania donovani | 91% | 100% |
A0A3R7MFW4 | Trypanosoma rangeli | 42% | 100% |
A4I837 | Leishmania infantum | 91% | 100% |
D0AAA4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B2Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
O00410 | Homo sapiens | 21% | 99% |
O60518 | Homo sapiens | 21% | 98% |
O74476 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 99% |
P32337 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 99% |
Q4Q561 | Leishmania major | 90% | 100% |
Q8BIV3 | Mus musculus | 20% | 98% |
Q8BKC5 | Mus musculus | 21% | 99% |
V5BG77 | Trypanosoma cruzi | 42% | 100% |