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: 1, no: 22 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 2 |
GO:0031514 | motile cilium | 5 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
GO:0005819 | spindle | 5 | 2 |
GO:0005930 | axoneme | 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:0072686 | mitotic spindle | 6 | 2 |
Related structures:
AlphaFold database: A4HE78
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |
GO:0000281 | mitotic cytokinesis | 4 | 2 |
GO:0000910 | cytokinesis | 3 | 2 |
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007010 | cytoskeleton organization | 5 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0007051 | spindle organization | 3 | 2 |
GO:0007052 | mitotic spindle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0048870 | cell motility | 2 | 2 |
GO:0060285 | cilium-dependent cell motility | 4 | 2 |
GO:0061640 | cytoskeleton-dependent cytokinesis | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 10 |
GO:0005509 | calcium ion binding | 5 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 2 |
GO:0043014 | alpha-tubulin binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.486 |
CLV_C14_Caspase3-7 | 545 | 549 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 765 | 769 | PF00656 | 0.357 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.391 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.222 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.206 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 697 | 699 | PF00675 | 0.405 |
CLV_PCSK_FUR_1 | 198 | 202 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 496 | 498 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 688 | 692 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 720 | 724 | PF00082 | 0.274 |
DEG_APCC_DBOX_1 | 683 | 691 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 723 | 731 | PF00400 | 0.373 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.617 |
DEG_ODPH_VHL_1 | 592 | 603 | PF01847 | 0.414 |
DOC_CYCLIN_yCln2_LP_2 | 465 | 471 | PF00134 | 0.451 |
DOC_MAPK_gen_1 | 121 | 129 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 163 | 173 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 392 | 399 | PF00069 | 0.364 |
DOC_MAPK_gen_1 | 42 | 49 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 430 | 439 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 566 | 574 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 683 | 693 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 717 | 727 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 123 | 131 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 566 | 574 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 575 | 582 | PF00069 | 0.350 |
DOC_MAPK_NFAT4_5 | 575 | 583 | PF00069 | 0.403 |
DOC_PP2B_LxvP_1 | 215 | 218 | PF13499 | 0.372 |
DOC_PP4_FxxP_1 | 418 | 421 | PF00568 | 0.410 |
DOC_PP4_FxxP_1 | 492 | 495 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 269 | 273 | PF12436 | 0.492 |
DOC_USP7_UBL2_3 | 681 | 685 | PF12436 | 0.509 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.356 |
LIG_14-3-3_CanoR_1 | 236 | 243 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 38 | 42 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 414 | 418 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 457 | 462 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 584 | 592 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 724 | 728 | PF00244 | 0.328 |
LIG_Actin_WH2_2 | 567 | 583 | PF00022 | 0.488 |
LIG_Actin_WH2_2 | 656 | 674 | PF00022 | 0.502 |
LIG_APCC_ABBA_1 | 301 | 306 | PF00400 | 0.437 |
LIG_BRCT_BRCA1_1 | 382 | 386 | PF00533 | 0.406 |
LIG_BRCT_BRCA1_1 | 474 | 478 | PF00533 | 0.406 |
LIG_BRCT_BRCA1_1 | 585 | 589 | PF00533 | 0.282 |
LIG_BRCT_BRCA1_1 | 744 | 748 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_2 | 90 | 96 | PF00533 | 0.412 |
LIG_deltaCOP1_diTrp_1 | 81 | 90 | PF00928 | 0.473 |
LIG_eIF4E_1 | 538 | 544 | PF01652 | 0.523 |
LIG_EVH1_1 | 419 | 423 | PF00568 | 0.466 |
LIG_EVH1_2 | 422 | 426 | PF00568 | 0.479 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.474 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.398 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.559 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.446 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.422 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.495 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.439 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.400 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.435 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.544 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.314 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.338 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.457 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.408 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.393 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.699 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.413 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.495 |
LIG_FHA_2 | 674 | 680 | PF00498 | 0.397 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.622 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.504 |
LIG_GBD_Chelix_1 | 570 | 578 | PF00786 | 0.336 |
LIG_LIR_Apic_2 | 320 | 326 | PF02991 | 0.409 |
LIG_LIR_Apic_2 | 358 | 362 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 415 | 421 | PF02991 | 0.581 |
LIG_LIR_Apic_2 | 536 | 541 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 281 | 288 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 295 | 305 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 393 | 403 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 597 | 607 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 635 | 643 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 745 | 754 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 393 | 398 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 586 | 592 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 635 | 639 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 704 | 709 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 745 | 751 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 757 | 763 | PF02991 | 0.261 |
LIG_MAD2 | 154 | 162 | PF02301 | 0.492 |
LIG_NRBOX | 569 | 575 | PF00104 | 0.436 |
LIG_NRBOX | 742 | 748 | PF00104 | 0.411 |
LIG_Pex14_1 | 86 | 90 | PF04695 | 0.544 |
LIG_Pex14_2 | 478 | 482 | PF04695 | 0.426 |
LIG_Pex14_2 | 90 | 94 | PF04695 | 0.599 |
LIG_PTB_Apo_2 | 84 | 91 | PF02174 | 0.658 |
LIG_Rb_pABgroove_1 | 742 | 750 | PF01858 | 0.368 |
LIG_REV1ctd_RIR_1 | 129 | 138 | PF16727 | 0.406 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.523 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.532 |
LIG_SH2_CRK | 374 | 378 | PF00017 | 0.469 |
LIG_SH2_CRK | 395 | 399 | PF00017 | 0.429 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.523 |
LIG_SH2_NCK_1 | 14 | 18 | PF00017 | 0.581 |
LIG_SH2_PTP2 | 600 | 603 | PF00017 | 0.393 |
LIG_SH2_SRC | 14 | 17 | PF00017 | 0.584 |
LIG_SH2_SRC | 55 | 58 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.413 |
LIG_SH2_STAT3 | 63 | 66 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.570 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.436 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.501 |
LIG_SUMO_SIM_anti_2 | 615 | 624 | PF11976 | 0.319 |
LIG_SUMO_SIM_anti_2 | 738 | 749 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 308 | 314 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 641 | 649 | PF11976 | 0.579 |
LIG_TRAF2_1 | 615 | 618 | PF00917 | 0.326 |
LIG_TRAF2_1 | 701 | 704 | PF00917 | 0.422 |
LIG_TYR_ITIM | 280 | 285 | PF00017 | 0.517 |
LIG_TYR_ITIM | 296 | 301 | PF00017 | 0.411 |
LIG_TYR_ITIM | 598 | 603 | PF00017 | 0.359 |
LIG_WRC_WIRS_1 | 458 | 463 | PF05994 | 0.338 |
LIG_WRC_WIRS_1 | 479 | 484 | PF05994 | 0.437 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.476 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.438 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.349 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.463 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.490 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.454 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.286 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.433 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.436 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.431 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.700 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.360 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.556 |
MOD_CK2_1 | 673 | 679 | PF00069 | 0.438 |
MOD_CK2_1 | 698 | 704 | PF00069 | 0.466 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.566 |
MOD_CMANNOS | 86 | 89 | PF00535 | 0.646 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.293 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.223 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.639 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.274 |
MOD_GlcNHglycan | 318 | 322 | PF01048 | 0.203 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.147 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.310 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.270 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.226 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.274 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.698 |
MOD_GlcNHglycan | 711 | 715 | PF01048 | 0.519 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.565 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.460 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.428 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.388 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.341 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.437 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.497 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.514 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.489 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.494 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.406 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.506 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.427 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.385 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.446 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.474 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.284 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.152 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.643 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.292 |
MOD_N-GLC_1 | 612 | 617 | PF02516 | 0.438 |
MOD_N-GLC_1 | 624 | 629 | PF02516 | 0.415 |
MOD_N-GLC_1 | 663 | 668 | PF02516 | 0.463 |
MOD_N-GLC_1 | 733 | 738 | PF02516 | 0.321 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.547 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.559 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.464 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.445 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.521 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.454 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.343 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.530 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.365 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.485 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.348 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.509 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.533 |
MOD_PIKK_1 | 548 | 554 | PF00454 | 0.582 |
MOD_PK_1 | 413 | 419 | PF00069 | 0.602 |
MOD_PK_1 | 698 | 704 | PF00069 | 0.528 |
MOD_PKA_1 | 413 | 419 | PF00069 | 0.600 |
MOD_PKA_1 | 496 | 502 | PF00069 | 0.512 |
MOD_PKA_1 | 698 | 704 | PF00069 | 0.438 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.588 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.491 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.614 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.493 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.393 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.385 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.411 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.481 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.462 |
MOD_PKA_2 | 723 | 729 | PF00069 | 0.349 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.437 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.402 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.473 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.437 |
MOD_Plk_1 | 739 | 745 | PF00069 | 0.433 |
MOD_Plk_1 | 756 | 762 | PF00069 | 0.245 |
MOD_Plk_2-3 | 136 | 142 | PF00069 | 0.460 |
MOD_Plk_2-3 | 306 | 312 | PF00069 | 0.426 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.458 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.427 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.447 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.600 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.545 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.424 |
MOD_Plk_4 | 739 | 745 | PF00069 | 0.293 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.358 |
MOD_SUMO_rev_2 | 148 | 156 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 240 | 248 | PF00179 | 0.424 |
MOD_SUMO_rev_2 | 44 | 53 | PF00179 | 0.640 |
MOD_SUMO_rev_2 | 481 | 489 | PF00179 | 0.375 |
MOD_SUMO_rev_2 | 673 | 682 | PF00179 | 0.342 |
TRG_DiLeu_BaEn_1 | 617 | 622 | PF01217 | 0.336 |
TRG_DiLeu_BaEn_1 | 704 | 709 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_2 | 473 | 479 | PF01217 | 0.444 |
TRG_DiLeu_LyEn_5 | 704 | 709 | PF01217 | 0.377 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 636 | 639 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 760 | 763 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 682 | 684 | PF00400 | 0.425 |
TRG_NES_CRM1_1 | 170 | 181 | PF08389 | 0.522 |
TRG_NES_CRM1_1 | 295 | 306 | PF08389 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 707 | 711 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H4 | Leptomonas seymouri | 26% | 92% |
A0A0N1HZ98 | Leptomonas seymouri | 73% | 100% |
A0A0N1I3M2 | Leptomonas seymouri | 27% | 100% |
A0A0N1PBW1 | Leptomonas seymouri | 26% | 100% |
A0A0S4IJW8 | Bodo saltans | 25% | 94% |
A0A0S4IQM0 | Bodo saltans | 25% | 100% |
A0A0S4J8J7 | Bodo saltans | 41% | 84% |
A0A1X0NEV8 | Trypanosomatidae | 24% | 97% |
A0A1X0NLI2 | Trypanosomatidae | 26% | 100% |
A0A1X0NMQ3 | Trypanosomatidae | 56% | 99% |
A0A1X0P419 | Trypanosomatidae | 27% | 100% |
A0A3Q8IDH4 | Leishmania donovani | 90% | 100% |
A0A3Q8IPU3 | Leishmania donovani | 26% | 100% |
A0A3R7KM50 | Trypanosoma rangeli | 27% | 97% |
A0A3R7L048 | Trypanosoma rangeli | 28% | 100% |
A0A3S5H688 | Leishmania donovani | 22% | 89% |
A0A3S7XC76 | Leishmania donovani | 27% | 100% |
A0A422N0Z6 | Trypanosoma rangeli | 55% | 99% |
A0A422NK00 | Trypanosoma rangeli | 24% | 100% |
A4HFK9 | Leishmania braziliensis | 26% | 100% |
A4HQF8 | Leishmania braziliensis | 29% | 100% |
A4HTP5 | Leishmania infantum | 22% | 89% |
A4I1J2 | Leishmania infantum | 90% | 100% |
A4IC94 | Leishmania infantum | 27% | 100% |
C9ZJX4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 96% |
C9ZPE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 99% |
D0A3K7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
D0A5T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AD64 | Leishmania major | 26% | 100% |
E9AHF6 | Leishmania infantum | 26% | 100% |
E9AI34 | Leishmania braziliensis | 24% | 90% |
E9AMI2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 90% |
E9AU74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AXM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AYY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q32TF8 | Danio rerio | 26% | 100% |
Q32TG3 | Gallus gallus | 26% | 100% |
Q4Q0C0 | Leishmania major | 26% | 100% |
Q4Q9U5 | Leishmania major | 88% | 100% |
Q4QI57 | Leishmania major | 23% | 100% |
Q5JVL4 | Homo sapiens | 26% | 100% |
V5ASV2 | Trypanosoma cruzi | 24% | 100% |
V5D3X9 | Trypanosoma cruzi | 55% | 99% |
V5DA42 | Trypanosoma cruzi | 27% | 100% |