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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 2 |
GO:0015629 | actin cytoskeleton | 6 | 2 |
GO:0016459 | myosin complex | 2 | 19 |
GO:0032991 | protein-containing complex | 1 | 19 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q4N5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0007015 | actin filament organization | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0030029 | actin filament-based process | 2 | 2 |
GO:0030048 | actin filament-based movement | 3 | 2 |
GO:0030050 | vesicle transport along actin filament | 4 | 2 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051640 | organelle localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051648 | vesicle localization | 3 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051650 | establishment of vesicle localization | 4 | 2 |
GO:0051656 | establishment of organelle localization | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0097435 | supramolecular fiber organization | 4 | 2 |
GO:0099515 | actin filament-based transport | 5 | 2 |
GO:0099518 | vesicle cytoskeletal trafficking | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000146 | microfilament motor activity | 2 | 2 |
GO:0000166 | nucleotide binding | 3 | 19 |
GO:0003774 | cytoskeletal motor activity | 1 | 19 |
GO:0003779 | actin binding | 4 | 19 |
GO:0005488 | binding | 1 | 19 |
GO:0005515 | protein binding | 2 | 19 |
GO:0005524 | ATP binding | 5 | 19 |
GO:0008092 | cytoskeletal protein binding | 3 | 19 |
GO:0017076 | purine nucleotide binding | 4 | 19 |
GO:0030554 | adenyl nucleotide binding | 5 | 19 |
GO:0032553 | ribonucleotide binding | 3 | 19 |
GO:0032555 | purine ribonucleotide binding | 4 | 19 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 19 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 19 |
GO:0036094 | small molecule binding | 2 | 19 |
GO:0043167 | ion binding | 2 | 19 |
GO:0043168 | anion binding | 3 | 19 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
GO:0051015 | actin filament binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 19 |
GO:0097367 | carbohydrate derivative binding | 2 | 19 |
GO:0140657 | ATP-dependent activity | 1 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 19 |
GO:1901363 | heterocyclic compound binding | 2 | 19 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1024 | 1028 | PF00656 | 0.671 |
CLV_C14_Caspase3-7 | 495 | 499 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 1002 | 1004 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 1033 | 1035 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 609 | 611 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 752 | 754 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 765 | 767 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 786 | 788 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 995 | 997 | PF00675 | 0.656 |
CLV_PCSK_FUR_1 | 772 | 776 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 1033 | 1035 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 751 | 753 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 765 | 767 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 781 | 783 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 672 | 674 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 781 | 783 | PF00082 | 0.594 |
CLV_PCSK_PC7_1 | 747 | 753 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 1029 | 1033 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 1044 | 1048 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 747 | 751 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 911 | 915 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 972 | 976 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 996 | 1000 | PF00082 | 0.599 |
DEG_APCC_DBOX_1 | 317 | 325 | PF00400 | 0.438 |
DEG_SCF_FBW7_2 | 489 | 495 | PF00400 | 0.421 |
DOC_ANK_TNKS_1 | 299 | 306 | PF00023 | 0.420 |
DOC_CKS1_1 | 489 | 494 | PF01111 | 0.421 |
DOC_CYCLIN_RxL_1 | 1041 | 1050 | PF00134 | 0.627 |
DOC_CYCLIN_RxL_1 | 115 | 124 | PF00134 | 0.449 |
DOC_CYCLIN_RxL_1 | 595 | 604 | PF00134 | 0.477 |
DOC_MAPK_gen_1 | 116 | 122 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 221 | 230 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 318 | 326 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 386 | 394 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 435 | 445 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 609 | 618 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 221 | 230 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 609 | 618 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 225 | 231 | PF00149 | 0.328 |
DOC_PP1_RVXF_1 | 417 | 424 | PF00149 | 0.453 |
DOC_PP1_RVXF_1 | 806 | 812 | PF00149 | 0.623 |
DOC_PP2B_LxvP_1 | 120 | 123 | PF13499 | 0.471 |
DOC_PP4_FxxP_1 | 546 | 549 | PF00568 | 0.408 |
DOC_PP4_MxPP_1 | 127 | 130 | PF00568 | 0.479 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.480 |
DOC_USP7_UBL2_3 | 1025 | 1029 | PF12436 | 0.583 |
DOC_USP7_UBL2_3 | 1044 | 1048 | PF12436 | 0.559 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 644 | 649 | PF00397 | 0.460 |
LIG_14-3-3_CanoR_1 | 318 | 324 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 386 | 392 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 453 | 457 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 530 | 536 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 609 | 615 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 620 | 629 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 695 | 701 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 705 | 713 | PF00244 | 0.490 |
LIG_Actin_WH2_2 | 7 | 24 | PF00022 | 0.532 |
LIG_APCC_ABBA_1 | 226 | 231 | PF00400 | 0.436 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.344 |
LIG_BRCT_BRCA1_1 | 646 | 650 | PF00533 | 0.421 |
LIG_BRCT_BRCA1_1 | 709 | 713 | PF00533 | 0.421 |
LIG_BRCT_BRCA1_1 | 815 | 819 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_1 | 962 | 966 | PF00533 | 0.630 |
LIG_BRCT_BRCA1_2 | 218 | 224 | PF00533 | 0.344 |
LIG_Clathr_ClatBox_1 | 344 | 348 | PF01394 | 0.436 |
LIG_Clathr_ClatBox_1 | 371 | 375 | PF01394 | 0.408 |
LIG_deltaCOP1_diTrp_1 | 537 | 546 | PF00928 | 0.419 |
LIG_EH_1 | 102 | 106 | PF12763 | 0.339 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.358 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.383 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.421 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.399 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.399 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.436 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.409 |
LIG_FHA_1 | 666 | 672 | PF00498 | 0.351 |
LIG_FHA_1 | 695 | 701 | PF00498 | 0.451 |
LIG_FHA_1 | 822 | 828 | PF00498 | 0.624 |
LIG_FHA_1 | 908 | 914 | PF00498 | 0.622 |
LIG_FHA_2 | 1022 | 1028 | PF00498 | 0.613 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.499 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.442 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.435 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.424 |
LIG_FHA_2 | 824 | 830 | PF00498 | 0.585 |
LIG_FHA_2 | 834 | 840 | PF00498 | 0.548 |
LIG_FHA_2 | 930 | 936 | PF00498 | 0.648 |
LIG_FXI_DFP_1 | 819 | 823 | PF00024 | 0.604 |
LIG_GBD_Chelix_1 | 190 | 198 | PF00786 | 0.493 |
LIG_KLC1_Yacidic_2 | 10 | 15 | PF13176 | 0.329 |
LIG_LIR_Apic_2 | 199 | 203 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 259 | 270 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 313 | 321 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 455 | 464 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 583 | 591 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 740 | 750 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 83 | 92 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 858 | 867 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 288 | 292 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 436 | 442 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 455 | 459 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 583 | 589 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 740 | 745 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 816 | 822 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 858 | 863 | PF02991 | 0.567 |
LIG_NRBOX | 650 | 656 | PF00104 | 0.498 |
LIG_OCRL_FandH_1 | 84 | 96 | PF00620 | 0.486 |
LIG_Pex14_2 | 685 | 689 | PF04695 | 0.399 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.359 |
LIG_SH2_CRK | 475 | 479 | PF00017 | 0.410 |
LIG_SH2_CRK | 717 | 721 | PF00017 | 0.372 |
LIG_SH2_CRK | 923 | 927 | PF00017 | 0.644 |
LIG_SH2_GRB2like | 463 | 466 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 568 | 572 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 586 | 590 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 706 | 710 | PF00017 | 0.382 |
LIG_SH2_NCK_1 | 936 | 940 | PF00017 | 0.493 |
LIG_SH2_PTP2 | 225 | 228 | PF00017 | 0.436 |
LIG_SH2_PTP2 | 439 | 442 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 266 | 270 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 173 | 176 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.168 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 688 | 691 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 763 | 766 | PF00017 | 0.557 |
LIG_SH3_3 | 675 | 681 | PF00018 | 0.461 |
LIG_SUMO_SIM_anti_2 | 389 | 397 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 905 | 910 | PF11976 | 0.595 |
LIG_SxIP_EBH_1 | 548 | 559 | PF03271 | 0.493 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.469 |
LIG_TRFH_1 | 105 | 109 | PF08558 | 0.460 |
LIG_TYR_ITIM | 264 | 269 | PF00017 | 0.422 |
LIG_TYR_ITIM | 921 | 926 | PF00017 | 0.652 |
LIG_UBA3_1 | 1018 | 1025 | PF00899 | 0.649 |
LIG_UBA3_1 | 268 | 277 | PF00899 | 0.422 |
LIG_UBA3_1 | 371 | 378 | PF00899 | 0.503 |
LIG_WRC_WIRS_1 | 205 | 210 | PF05994 | 0.376 |
MOD_CDK_SPxxK_3 | 253 | 260 | PF00069 | 0.503 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.341 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.417 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.422 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.542 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.402 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.436 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.495 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.502 |
MOD_CK1_1 | 886 | 892 | PF00069 | 0.556 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.461 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.554 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.407 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.316 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.417 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.439 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.498 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.505 |
MOD_CK2_1 | 655 | 661 | PF00069 | 0.371 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.520 |
MOD_CK2_1 | 833 | 839 | PF00069 | 0.576 |
MOD_CK2_1 | 899 | 905 | PF00069 | 0.552 |
MOD_CK2_1 | 929 | 935 | PF00069 | 0.605 |
MOD_CMANNOS | 536 | 539 | PF00535 | 0.422 |
MOD_GlcNHglycan | 1035 | 1038 | PF01048 | 0.557 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.342 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.343 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.592 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.401 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.591 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.359 |
MOD_GlcNHglycan | 742 | 745 | PF01048 | 0.559 |
MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.602 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.555 |
MOD_GlcNHglycan | 878 | 881 | PF01048 | 0.603 |
MOD_GlcNHglycan | 885 | 888 | PF01048 | 0.540 |
MOD_GSK3_1 | 1017 | 1024 | PF00069 | 0.671 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.373 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.376 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.460 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.389 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.401 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.447 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.490 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.436 |
MOD_GSK3_1 | 895 | 902 | PF00069 | 0.575 |
MOD_GSK3_1 | 907 | 914 | PF00069 | 0.585 |
MOD_GSK3_1 | 953 | 960 | PF00069 | 0.507 |
MOD_LATS_1 | 181 | 187 | PF00433 | 0.493 |
MOD_N-GLC_1 | 1008 | 1013 | PF02516 | 0.660 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.371 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.437 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.351 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.421 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.561 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.439 |
MOD_N-GLC_1 | 464 | 469 | PF02516 | 0.264 |
MOD_NEK2_1 | 1021 | 1026 | PF00069 | 0.683 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.449 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.432 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.548 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.357 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.357 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.390 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.435 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.419 |
MOD_NEK2_1 | 966 | 971 | PF00069 | 0.626 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.410 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.478 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.482 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.494 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.602 |
MOD_PIKK_1 | 655 | 661 | PF00454 | 0.436 |
MOD_PIKK_1 | 707 | 713 | PF00454 | 0.421 |
MOD_PKA_1 | 1033 | 1039 | PF00069 | 0.589 |
MOD_PKA_1 | 610 | 616 | PF00069 | 0.408 |
MOD_PKA_1 | 911 | 917 | PF00069 | 0.465 |
MOD_PKA_2 | 1033 | 1039 | PF00069 | 0.584 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.406 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.610 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.446 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.441 |
MOD_PKA_2 | 694 | 700 | PF00069 | 0.451 |
MOD_PKA_2 | 704 | 710 | PF00069 | 0.490 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.371 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.482 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.344 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.344 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.401 |
MOD_Plk_1 | 966 | 972 | PF00069 | 0.584 |
MOD_Plk_2-3 | 624 | 630 | PF00069 | 0.498 |
MOD_Plk_2-3 | 823 | 829 | PF00069 | 0.614 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.371 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.498 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.422 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.458 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.426 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.422 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.398 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.532 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.478 |
MOD_Plk_4 | 696 | 702 | PF00069 | 0.481 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.355 |
MOD_Plk_4 | 823 | 829 | PF00069 | 0.600 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.325 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.503 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.486 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.500 |
MOD_ProDKin_1 | 644 | 650 | PF00069 | 0.460 |
MOD_SUMO_rev_2 | 10 | 18 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 375 | 379 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 433 | 440 | PF00179 | 0.453 |
MOD_SUMO_rev_2 | 501 | 511 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 773 | 783 | PF00179 | 0.636 |
MOD_SUMO_rev_2 | 791 | 798 | PF00179 | 0.667 |
MOD_SUMO_rev_2 | 879 | 885 | PF00179 | 0.573 |
MOD_SUMO_rev_2 | 889 | 899 | PF00179 | 0.303 |
MOD_SUMO_rev_2 | 951 | 958 | PF00179 | 0.637 |
TRG_DiLeu_BaEn_4 | 778 | 784 | PF01217 | 0.657 |
TRG_DiLeu_BaLyEn_6 | 985 | 990 | PF01217 | 0.570 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 688 | 691 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 717 | 720 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 923 | 926 | PF00928 | 0.628 |
TRG_ER_diArg_1 | 1032 | 1034 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 678 | 680 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 750 | 753 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 764 | 766 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 774 | 776 | PF00400 | 0.535 |
TRG_NES_CRM1_1 | 332 | 348 | PF08389 | 0.505 |
TRG_NES_CRM1_1 | 402 | 418 | PF08389 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 620 | 624 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 680 | 684 | PF00026 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 766 | 770 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 775 | 779 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 787 | 791 | PF00026 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 911 | 915 | PF00026 | 0.609 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3V8 | Leptomonas seymouri | 78% | 100% |
A0A0N1HTE8 | Leptomonas seymouri | 27% | 76% |
A0A0S4INK0 | Bodo saltans | 36% | 79% |
A0A0S4IVZ8 | Bodo saltans | 50% | 89% |
A0A0S4J0R8 | Bodo saltans | 34% | 88% |
A0A0S4J9E1 | Bodo saltans | 25% | 83% |
A0A0S4JAC9 | Bodo saltans | 33% | 73% |
A0A0S4JJT9 | Bodo saltans | 36% | 95% |
A0A0S4JP47 | Bodo saltans | 32% | 92% |
A0A0S4JPX4 | Bodo saltans | 33% | 80% |
A0A0S4JUM6 | Bodo saltans | 35% | 91% |
A0A0S4KL03 | Bodo saltans | 31% | 91% |
A0A1X0NNV7 | Trypanosomatidae | 35% | 87% |
A0A1X0NQ39 | Trypanosomatidae | 31% | 86% |
A0A1X0NTN9 | Trypanosomatidae | 60% | 100% |
A0A1X0NVL2 | Trypanosomatidae | 34% | 86% |
A0A1X0NZ71 | Trypanosomatidae | 33% | 71% |
A0A1X0P0P8 | Trypanosomatidae | 35% | 88% |
A0A1X0P4G3 | Trypanosomatidae | 27% | 77% |
A0A1X0P8M1 | Trypanosomatidae | 34% | 96% |
A0A3R7KLV0 | Trypanosoma rangeli | 27% | 81% |
A0A3R7LHC0 | Trypanosoma rangeli | 35% | 90% |
A0A3S7X666 | Leishmania donovani | 96% | 100% |
A0A422MU89 | Trypanosoma rangeli | 31% | 85% |
A0A422NAD7 | Trypanosoma rangeli | 32% | 71% |
A1C4A5 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 32% | 84% |
A1DBH2 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 33% | 84% |
A2R5J1 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 32% | 83% |
A3LYL7 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 29% | 84% |
A4HL24 | Leishmania braziliensis | 85% | 100% |
A4I8K5 | Leishmania infantum | 96% | 100% |
A4RE77 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 31% | 87% |
A5DKH0 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 29% | 82% |
A5E4A8 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 30% | 82% |
A6SED8 | Botryotinia fuckeliana (strain B05.10) | 31% | 86% |
A6ZMG6 | Saccharomyces cerevisiae (strain YJM789) | 30% | 86% |
A6ZZJ1 | Saccharomyces cerevisiae (strain YJM789) | 30% | 83% |
A7EK16 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 31% | 85% |
A7TDZ8 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 30% | 86% |
A8N2Y6 | Coprinopsis cinerea (strain Okayama-7 / 130 / ATCC MYA-4618 / FGSC 9003) | 30% | 82% |
A8PWF6 | Malassezia globosa (strain ATCC MYA-4612 / CBS 7966) | 31% | 79% |
B0CRJ3 | Laccaria bicolor (strain S238N-H82 / ATCC MYA-4686) | 31% | 84% |
B0I1T2 | Homo sapiens | 31% | 100% |
B0Y9Q4 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 33% | 84% |
C9ZMY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 90% |
D0AAL0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 99% |
E1BPK6 | Bos taurus | 31% | 81% |
E7F9L8 | Danio rerio | 30% | 100% |
E9B3G5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9Q634 | Mus musculus | 30% | 95% |
F1PRN2 | Canis lupus familiaris | 30% | 100% |
F4HWY6 | Arabidopsis thaliana | 34% | 69% |
F4HXP9 | Arabidopsis thaliana | 33% | 68% |
F4I460 | Arabidopsis thaliana | 33% | 70% |
F4I507 | Arabidopsis thaliana | 34% | 91% |
F4IRU3 | Arabidopsis thaliana | 33% | 67% |
F4IUG9 | Arabidopsis thaliana | 34% | 70% |
F4JIU4 | Arabidopsis thaliana | 34% | 93% |
F4JM19 | Arabidopsis thaliana | 32% | 69% |
F4K5J1 | Arabidopsis thaliana | 34% | 69% |
K7U9N8 | Zea mays | 33% | 69% |
O00936 | Toxoplasma gondii | 29% | 90% |
O74805 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 71% |
O94477 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 69% |
O94832 | Homo sapiens | 31% | 100% |
P05659 | Acanthamoeba castellanii | 32% | 70% |
P10568 | Bos taurus | 31% | 100% |
P10676 | Drosophila melanogaster | 26% | 70% |
P19524 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 67% |
P19706 | Acanthamoeba castellanii | 32% | 92% |
P32492 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 71% |
P36006 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 83% |
P42522 | Dictyostelium discoideum | 32% | 89% |
P47807 | Gallus gallus | 31% | 100% |
P47808 | Acanthamoeba castellanii | 31% | 67% |
Q00647 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 32% | 84% |
Q01989 | Drosophila melanogaster | 32% | 84% |
Q04439 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 86% |
Q0CEX5 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 32% | 84% |
Q0WPU1 | Arabidopsis thaliana | 34% | 69% |
Q12965 | Homo sapiens | 31% | 95% |
Q17R14 | Bos taurus | 31% | 100% |
Q1DLP2 | Coccidioides immitis (strain RS) | 32% | 84% |
Q1EG27 | Mus musculus | 29% | 80% |
Q29122 | Sus scrofa | 32% | 84% |
Q2HDI2 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 31% | 86% |
Q2US45 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 32% | 83% |
Q39160 | Arabidopsis thaliana | 34% | 69% |
Q4WC55 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 33% | 84% |
Q59MQ0 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 80% |
Q5SV80 | Mus musculus | 30% | 100% |
Q5SYD0 | Mus musculus | 31% | 100% |
Q5ZMC2 | Gallus gallus | 31% | 100% |
Q63356 | Rattus norvegicus | 30% | 95% |
Q63357 | Rattus norvegicus | 32% | 100% |
Q64331 | Mus musculus | 30% | 83% |
Q6BUQ2 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 30% | 81% |
Q6CVE9 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 83% |
Q6FMJ3 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 29% | 84% |
Q6FN18 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 30% | 86% |
Q6GPA1 | Xenopus laevis | 31% | 100% |
Q758Q9 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 30% | 81% |
Q7RQ71 | Plasmodium yoelii yoelii | 30% | 100% |
Q7SDM3 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 30% | 85% |
Q7Z8J6 | Ustilago maydis (strain 521 / FGSC 9021) | 30% | 82% |
Q875Q8 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 32% | 68% |
Q875X3 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 33% | 67% |
Q875X4 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 32% | 74% |
Q876G9 | Saccharomyces uvarum (strain ATCC 76518 / CBS 7001 / CLIB 283 / NBRC 10550 / MCYC 623 / NCYC 2669 / NRRL Y-11845) | 34% | 67% |
Q8N1T3 | Homo sapiens | 32% | 100% |
Q8WXR4 | Homo sapiens | 31% | 78% |
Q9I8D1 | Gallus gallus | 30% | 82% |
Q9LHE9 | Arabidopsis thaliana | 34% | 90% |
Q9LKB9 | Arabidopsis thaliana | 33% | 70% |
Q9M2K0 | Arabidopsis thaliana | 32% | 85% |
Q9UBC5 | Homo sapiens | 31% | 100% |
Q9UM54 | Homo sapiens | 32% | 81% |
Q9USI6 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 69% |
V5B459 | Trypanosoma cruzi | 35% | 100% |
V5BB96 | Trypanosoma cruzi | 33% | 71% |
V5BI08 | Trypanosoma cruzi | 58% | 99% |
V5BII5 | Trypanosoma cruzi | 30% | 86% |
V5BXI5 | Trypanosoma cruzi | 28% | 86% |
V5DLJ9 | Trypanosoma cruzi | 34% | 90% |