Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 99 |
NetGPI | no | yes: 0, no: 100 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3S7X438
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 101 |
GO:0006807 | nitrogen compound metabolic process | 2 | 101 |
GO:0008152 | metabolic process | 1 | 101 |
GO:0019538 | protein metabolic process | 3 | 101 |
GO:0043170 | macromolecule metabolic process | 3 | 101 |
GO:0044238 | primary metabolic process | 2 | 101 |
GO:0071704 | organic substance metabolic process | 2 | 101 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 101 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 101 |
GO:0004175 | endopeptidase activity | 4 | 101 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 101 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 101 |
GO:0008233 | peptidase activity | 3 | 101 |
GO:0008234 | cysteine-type peptidase activity | 4 | 101 |
GO:0016787 | hydrolase activity | 2 | 101 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 101 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 14 | 18 | PF00656 | 0.682 |
CLV_C14_Caspase3-7 | 520 | 524 | PF00656 | 0.377 |
CLV_MEL_PAP_1 | 305 | 311 | PF00089 | 0.168 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 905 | 907 | PF00675 | 0.593 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 905 | 907 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 742 | 746 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 870 | 874 | PF00082 | 0.445 |
DEG_APCC_DBOX_1 | 623 | 631 | PF00400 | 0.584 |
DEG_APCC_DBOX_1 | 867 | 875 | PF00400 | 0.268 |
DEG_MDM2_SWIB_1 | 584 | 592 | PF02201 | 0.422 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.695 |
DEG_SPOP_SBC_1 | 67 | 71 | PF00917 | 0.469 |
DOC_CKS1_1 | 254 | 259 | PF01111 | 0.457 |
DOC_CKS1_1 | 516 | 521 | PF01111 | 0.491 |
DOC_CKS1_1 | 54 | 59 | PF01111 | 0.438 |
DOC_CKS1_1 | 829 | 834 | PF01111 | 0.465 |
DOC_CYCLIN_RxL_1 | 786 | 800 | PF00134 | 0.531 |
DOC_MAPK_gen_1 | 421 | 429 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 789 | 798 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 868 | 876 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 887 | 895 | PF00069 | 0.514 |
DOC_MAPK_JIP1_4 | 792 | 798 | PF00069 | 0.252 |
DOC_MAPK_MEF2A_6 | 624 | 632 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 789 | 798 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 842 | 850 | PF00069 | 0.496 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.729 |
DOC_PP2B_LxvP_1 | 24 | 27 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 630 | 633 | PF13499 | 0.469 |
DOC_PP4_FxxP_1 | 23 | 26 | PF00568 | 0.461 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.313 |
DOC_PP4_FxxP_1 | 407 | 410 | PF00568 | 0.527 |
DOC_PP4_FxxP_1 | 489 | 492 | PF00568 | 0.485 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 896 | 900 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 917 | 921 | PF00917 | 0.475 |
DOC_USP7_UBL2_3 | 148 | 152 | PF12436 | 0.565 |
DOC_USP7_UBL2_3 | 552 | 556 | PF12436 | 0.480 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 828 | 833 | PF00397 | 0.497 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 490 | 499 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 508 | 517 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 537 | 545 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 599 | 606 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 822 | 832 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 847 | 851 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 905 | 913 | PF00244 | 0.504 |
LIG_Actin_WH2_2 | 641 | 659 | PF00022 | 0.524 |
LIG_Actin_WH2_2 | 832 | 849 | PF00022 | 0.512 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.597 |
LIG_BRCT_BRCA1_1 | 272 | 276 | PF00533 | 0.355 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.710 |
LIG_BRCT_BRCA1_1 | 898 | 902 | PF00533 | 0.486 |
LIG_CSL_BTD_1 | 516 | 519 | PF09270 | 0.536 |
LIG_deltaCOP1_diTrp_1 | 271 | 276 | PF00928 | 0.249 |
LIG_deltaCOP1_diTrp_1 | 715 | 723 | PF00928 | 0.484 |
LIG_DLG_GKlike_1 | 660 | 667 | PF00625 | 0.365 |
LIG_EH1_1 | 652 | 660 | PF00400 | 0.487 |
LIG_eIF4E_1 | 653 | 659 | PF01652 | 0.508 |
LIG_EVH1_2 | 26 | 30 | PF00568 | 0.451 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.512 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.351 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.448 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.482 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.465 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.516 |
LIG_FHA_1 | 831 | 837 | PF00498 | 0.525 |
LIG_FHA_1 | 883 | 889 | PF00498 | 0.486 |
LIG_FHA_1 | 908 | 914 | PF00498 | 0.438 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.547 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.464 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.488 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.375 |
LIG_FHA_2 | 758 | 764 | PF00498 | 0.509 |
LIG_FHA_2 | 825 | 831 | PF00498 | 0.485 |
LIG_HCF-1_HBM_1 | 854 | 857 | PF13415 | 0.469 |
LIG_Integrin_RGD_1 | 864 | 866 | PF01839 | 0.308 |
LIG_LIR_Apic_2 | 21 | 26 | PF02991 | 0.461 |
LIG_LIR_Apic_2 | 228 | 234 | PF02991 | 0.589 |
LIG_LIR_Apic_2 | 346 | 351 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 431 | 437 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 135 | 145 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 551 | 562 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 611 | 621 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 652 | 659 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 769 | 778 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 560 | 564 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 577 | 582 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 604 | 609 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 611 | 617 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 652 | 656 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 663 | 667 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 769 | 774 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 854 | 860 | PF02991 | 0.373 |
LIG_LYPXL_yS_3 | 547 | 550 | PF13949 | 0.548 |
LIG_MYND_1 | 230 | 234 | PF01753 | 0.378 |
LIG_PCNA_PIPBox_1 | 248 | 257 | PF02747 | 0.181 |
LIG_PCNA_yPIPBox_3 | 245 | 255 | PF02747 | 0.198 |
LIG_Pex14_2 | 584 | 588 | PF04695 | 0.474 |
LIG_Pex14_2 | 872 | 876 | PF04695 | 0.475 |
LIG_PTB_Apo_2 | 866 | 873 | PF02174 | 0.482 |
LIG_REV1ctd_RIR_1 | 742 | 749 | PF16727 | 0.248 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.520 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.377 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.238 |
LIG_SH2_CRK | 348 | 352 | PF00017 | 0.540 |
LIG_SH2_CRK | 554 | 558 | PF00017 | 0.477 |
LIG_SH2_CRK | 561 | 565 | PF00017 | 0.476 |
LIG_SH2_CRK | 606 | 610 | PF00017 | 0.529 |
LIG_SH2_CRK | 653 | 657 | PF00017 | 0.494 |
LIG_SH2_CRK | 771 | 775 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 348 | 351 | PF00017 | 0.528 |
LIG_SH2_NCK_1 | 255 | 259 | PF00017 | 0.424 |
LIG_SH2_NCK_1 | 561 | 565 | PF00017 | 0.499 |
LIG_SH2_PTP2 | 858 | 861 | PF00017 | 0.430 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.567 |
LIG_SH2_SRC | 440 | 443 | PF00017 | 0.493 |
LIG_SH2_SRC | 525 | 528 | PF00017 | 0.496 |
LIG_SH2_SRC | 858 | 861 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 585 | 589 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.592 |
LIG_SH2_STAT3 | 313 | 316 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 771 | 774 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 838 | 841 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 858 | 861 | PF00017 | 0.391 |
LIG_SH3_2 | 784 | 789 | PF14604 | 0.572 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.450 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.526 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.444 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.680 |
LIG_SH3_3 | 781 | 787 | PF00018 | 0.571 |
LIG_SH3_3 | 826 | 832 | PF00018 | 0.563 |
LIG_SH3_3 | 890 | 896 | PF00018 | 0.448 |
LIG_SUMO_SIM_anti_2 | 323 | 330 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 751 | 757 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 792 | 797 | PF11976 | 0.404 |
LIG_TRAF2_1 | 616 | 619 | PF00917 | 0.375 |
LIG_TYR_ITIM | 263 | 268 | PF00017 | 0.349 |
LIG_TYR_ITIM | 545 | 550 | PF00017 | 0.548 |
LIG_UBA3_1 | 613 | 620 | PF00899 | 0.486 |
LIG_WRC_WIRS_1 | 579 | 584 | PF05994 | 0.525 |
LIG_WRC_WIRS_1 | 749 | 754 | PF05994 | 0.484 |
MOD_CDK_SPxxK_3 | 253 | 260 | PF00069 | 0.389 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.593 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.631 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.317 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.504 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.560 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.486 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.543 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.476 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.712 |
MOD_CK1_1 | 757 | 763 | PF00069 | 0.505 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.612 |
MOD_CK1_1 | 797 | 803 | PF00069 | 0.416 |
MOD_CK1_1 | 907 | 913 | PF00069 | 0.491 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.512 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.519 |
MOD_CK2_1 | 757 | 763 | PF00069 | 0.486 |
MOD_CK2_1 | 828 | 834 | PF00069 | 0.432 |
MOD_CMANNOS | 713 | 716 | PF00535 | 0.276 |
MOD_GlcNHglycan | 119 | 123 | PF01048 | 0.511 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.619 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.618 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.343 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.498 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.458 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.509 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.408 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.469 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.274 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.295 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.283 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.265 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.742 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.338 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.316 |
MOD_GlcNHglycan | 759 | 763 | PF01048 | 0.631 |
MOD_GlcNHglycan | 814 | 818 | PF01048 | 0.538 |
MOD_GlcNHglycan | 898 | 901 | PF01048 | 0.419 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.624 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.635 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.689 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.660 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.350 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.454 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.498 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.454 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.524 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.476 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.491 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.617 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.457 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.404 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.402 |
MOD_GSK3_1 | 876 | 883 | PF00069 | 0.464 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.516 |
MOD_N-GLC_1 | 277 | 282 | PF02516 | 0.328 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.420 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.462 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.477 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.574 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.589 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.323 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.708 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.704 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.423 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.488 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.489 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.459 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.349 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.413 |
MOD_NEK2_1 | 876 | 881 | PF00069 | 0.429 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.671 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.510 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.544 |
MOD_PIKK_1 | 480 | 486 | PF00454 | 0.599 |
MOD_PIKK_1 | 772 | 778 | PF00454 | 0.391 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.504 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.405 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.539 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.487 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.503 |
MOD_PKA_2 | 841 | 847 | PF00069 | 0.413 |
MOD_PKA_2 | 904 | 910 | PF00069 | 0.496 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.447 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.463 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.384 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.543 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.555 |
MOD_Plk_1 | 754 | 760 | PF00069 | 0.386 |
MOD_Plk_2-3 | 11 | 17 | PF00069 | 0.632 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.387 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.348 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.251 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.341 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.498 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.503 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.490 |
MOD_Plk_4 | 748 | 754 | PF00069 | 0.394 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.596 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.768 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.661 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.353 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.458 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.585 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.548 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.469 |
MOD_ProDKin_1 | 828 | 834 | PF00069 | 0.505 |
MOD_SUMO_rev_2 | 616 | 621 | PF00179 | 0.547 |
TRG_DiLeu_BaEn_1 | 323 | 328 | PF01217 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 545 | 550 | PF01217 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 662 | 667 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 547 | 550 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 653 | 656 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 771 | 774 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 857 | 860 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 861 | 864 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 888 | 891 | PF00400 | 0.485 |
TRG_NES_CRM1_1 | 747 | 759 | PF08389 | 0.481 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 30% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 54% | 95% |
A0A0N1IGQ2 | Leptomonas seymouri | 29% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 30% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 33% | 100% |
A0A0N1P9P1 | Leptomonas seymouri | 30% | 100% |
A0A0N1PCA9 | Leptomonas seymouri | 29% | 100% |
A0A0N1PE91 | Leptomonas seymouri | 28% | 100% |
A0A0N1PFI4 | Leptomonas seymouri | 31% | 100% |
A0A0S4JS70 | Bodo saltans | 25% | 100% |
A0A0S4KGT2 | Bodo saltans | 36% | 100% |
A0A0S4KKP7 | Bodo saltans | 24% | 100% |
A0A1X0NJ19 | Trypanosomatidae | 28% | 77% |
A0A1X0NJK2 | Trypanosomatidae | 29% | 100% |
A0A1X0NJX8 | Trypanosomatidae | 34% | 100% |
A0A1X0NKT7 | Trypanosomatidae | 39% | 100% |
A0A1X0NKX8 | Trypanosomatidae | 28% | 100% |
A0A1X0NMT3 | Trypanosomatidae | 29% | 100% |
A0A1X0NW84 | Trypanosomatidae | 30% | 100% |
A0A1X0NW85 | Trypanosomatidae | 30% | 100% |
A0A1X0NW89 | Trypanosomatidae | 28% | 100% |
A0A1X0NWA6 | Trypanosomatidae | 26% | 100% |
A0A1X0NWW1 | Trypanosomatidae | 30% | 100% |
A0A3Q8IBS3 | Leishmania donovani | 30% | 100% |
A0A3Q8IDD4 | Leishmania donovani | 29% | 98% |
A0A3Q8IJT4 | Leishmania donovani | 27% | 97% |
A0A3S5H5A5 | Leishmania donovani | 32% | 100% |
A0A3S5ISG2 | Trypanosoma rangeli | 31% | 100% |
A0A3S7WW18 | Leishmania donovani | 30% | 100% |
A0A3S7WW41 | Leishmania donovani | 29% | 94% |
A0A3S7WW71 | Leishmania donovani | 30% | 94% |
A0A3S7X430 | Leishmania donovani | 33% | 100% |
A0A3S7X460 | Leishmania donovani | 31% | 100% |
A0A3S7X463 | Leishmania donovani | 29% | 100% |
A0A3S7X470 | Leishmania donovani | 32% | 100% |
A0A422MYU1 | Trypanosoma rangeli | 29% | 100% |
A0A422MYX0 | Trypanosoma rangeli | 30% | 100% |
A4H3W4 | Leishmania braziliensis | 33% | 100% |
A4HE81 | Leishmania braziliensis | 28% | 97% |
A4HJ14 | Leishmania braziliensis | 33% | 100% |
A4HJ21 | Leishmania braziliensis | 28% | 100% |
A4HJ22 | Leishmania braziliensis | 72% | 100% |
A4HJ24 | Leishmania braziliensis | 30% | 99% |
A4HS39 | Leishmania infantum | 32% | 100% |
A4HYN0 | Leishmania infantum | 30% | 100% |
A4HYW1 | Leishmania infantum | 30% | 100% |
A4HYW2 | Leishmania infantum | 30% | 94% |
A4HYW3 | Leishmania infantum | 29% | 94% |
A4I1J4 | Leishmania infantum | 28% | 98% |
A4I6E4 | Leishmania infantum | 32% | 100% |
A4I6E6 | Leishmania infantum | 31% | 100% |
A4I6F0 | Leishmania infantum | 99% | 100% |
A4I6K4 | Leishmania infantum | 33% | 100% |
A4I6K5 | Leishmania infantum | 28% | 100% |
A4I6K6 | Leishmania infantum | 27% | 97% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 87% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 97% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 97% |
E9AIH1 | Leishmania braziliensis | 29% | 100% |
E9AIH3 | Leishmania braziliensis | 30% | 94% |
E9AIH4 | Leishmania braziliensis | 29% | 96% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 94% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 96% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 97% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 97% |
Q4Q6L7 | Leishmania major | 31% | 100% |
Q4Q6L9 | Leishmania major | 31% | 100% |
Q4Q6M0 | Leishmania major | 90% | 100% |
Q4Q6M2 | Leishmania major | 28% | 97% |
Q4Q6M3 | Leishmania major | 28% | 100% |
Q4Q6M4 | Leishmania major | 33% | 100% |
Q4Q9U3 | Leishmania major | 28% | 98% |
Q4QCS6 | Leishmania major | 29% | 94% |
Q4QCS7 | Leishmania major | 30% | 95% |
Q4QCS8 | Leishmania major | 30% | 100% |
Q4QCS9 | Leishmania major | 30% | 100% |
Q9U0T9 | Leishmania major | 33% | 100% |
V5AYJ1 | Trypanosoma cruzi | 30% | 100% |
V5B5I4 | Trypanosoma cruzi | 30% | 100% |
V5BA05 | Trypanosoma cruzi | 32% | 100% |
V5BEL3 | Trypanosoma cruzi | 30% | 100% |
V5BII7 | Trypanosoma cruzi | 28% | 76% |
V5BN20 | Trypanosoma cruzi | 32% | 100% |
V5D9Y2 | Trypanosoma cruzi | 31% | 100% |
V5DES7 | Trypanosoma cruzi | 29% | 100% |