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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9B0T6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.420 |
CLV_MEL_PAP_1 | 635 | 641 | PF00089 | 0.475 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.728 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 33 | 35 | PF00082 | 0.666 |
CLV_PCSK_PC1ET2_1 | 605 | 607 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.567 |
CLV_Separin_Metazoa | 656 | 660 | PF03568 | 0.612 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.577 |
DEG_APCC_DBOX_1 | 251 | 259 | PF00400 | 0.406 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 605 | 613 | PF00400 | 0.709 |
DEG_MDM2_SWIB_1 | 463 | 471 | PF02201 | 0.491 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.701 |
DEG_SCF_FBW7_1 | 54 | 61 | PF00400 | 0.440 |
DEG_SPOP_SBC_1 | 441 | 445 | PF00917 | 0.677 |
DOC_CKS1_1 | 415 | 420 | PF01111 | 0.479 |
DOC_CKS1_1 | 447 | 452 | PF01111 | 0.449 |
DOC_CYCLIN_RxL_1 | 591 | 604 | PF00134 | 0.528 |
DOC_MAPK_FxFP_2 | 294 | 297 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 194 | 202 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 605 | 612 | PF00069 | 0.655 |
DOC_MAPK_gen_1 | 8 | 17 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 464 | 473 | PF00069 | 0.455 |
DOC_PP1_RVXF_1 | 172 | 179 | PF00149 | 0.505 |
DOC_PP1_RVXF_1 | 404 | 410 | PF00149 | 0.575 |
DOC_PP1_RVXF_1 | 462 | 468 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.511 |
DOC_PP4_FxxP_1 | 277 | 280 | PF00568 | 0.762 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.441 |
DOC_PP4_FxxP_1 | 514 | 517 | PF00568 | 0.742 |
DOC_SPAK_OSR1_1 | 573 | 577 | PF12202 | 0.487 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 652 | 656 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.771 |
DOC_USP7_MATH_2 | 297 | 303 | PF00917 | 0.446 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 680 | 685 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 160 | 170 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 194 | 200 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 252 | 260 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 348 | 356 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 390 | 398 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 431 | 435 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 464 | 468 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 622 | 628 | PF00244 | 0.693 |
LIG_Actin_WH2_2 | 374 | 392 | PF00022 | 0.404 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.508 |
LIG_CSL_BTD_1 | 408 | 411 | PF09270 | 0.567 |
LIG_deltaCOP1_diTrp_1 | 570 | 574 | PF00928 | 0.500 |
LIG_eIF4E_1 | 457 | 463 | PF01652 | 0.531 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.414 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.369 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.488 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.388 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.546 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.743 |
LIG_LIR_Apic_2 | 275 | 280 | PF02991 | 0.739 |
LIG_LIR_Apic_2 | 291 | 297 | PF02991 | 0.654 |
LIG_LIR_Apic_2 | 513 | 517 | PF02991 | 0.648 |
LIG_LIR_Apic_2 | 666 | 671 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 482 | 492 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.425 |
LIG_MYND_1 | 584 | 588 | PF01753 | 0.531 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.487 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.477 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.538 |
LIG_SH2_CRK | 484 | 488 | PF00017 | 0.496 |
LIG_SH2_SRC | 228 | 231 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.241 |
LIG_SH2_STAP1 | 672 | 676 | PF00017 | 0.487 |
LIG_SH2_STAT3 | 412 | 415 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.688 |
LIG_SH3_2 | 447 | 452 | PF14604 | 0.449 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.470 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.505 |
LIG_SH3_3 | 678 | 684 | PF00018 | 0.603 |
LIG_SUMO_SIM_anti_2 | 245 | 250 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 311 | 317 | PF11976 | 0.387 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.469 |
LIG_WRC_WIRS_1 | 154 | 159 | PF05994 | 0.477 |
LIG_WRC_WIRS_1 | 511 | 516 | PF05994 | 0.522 |
MOD_CDK_SPK_2 | 682 | 687 | PF00069 | 0.483 |
MOD_CDK_SPxK_1 | 446 | 452 | PF00069 | 0.453 |
MOD_CDK_SPxxK_3 | 680 | 687 | PF00069 | 0.663 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.433 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.552 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.490 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.474 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.777 |
MOD_CK2_1 | 650 | 656 | PF00069 | 0.542 |
MOD_Cter_Amidation | 635 | 638 | PF01082 | 0.470 |
MOD_DYRK1A_RPxSP_1 | 680 | 684 | PF00069 | 0.585 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.586 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.381 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.431 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.489 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.666 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.394 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.370 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.705 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.525 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.416 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.668 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.521 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.538 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.592 |
MOD_GlcNHglycan | 647 | 651 | PF01048 | 0.710 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.608 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.718 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.628 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.336 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.508 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.448 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.464 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.657 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.524 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.661 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.560 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.626 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.640 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.657 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.741 |
MOD_GSK3_1 | 646 | 653 | PF00069 | 0.616 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.742 |
MOD_LATS_1 | 317 | 323 | PF00433 | 0.583 |
MOD_LATS_1 | 346 | 352 | PF00433 | 0.535 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.480 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.425 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.673 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.245 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.481 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.502 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.496 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.524 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.524 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.652 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.628 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.530 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.629 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.495 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.556 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.472 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.717 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.648 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.517 |
MOD_PKB_1 | 135 | 143 | PF00069 | 0.616 |
MOD_PKB_1 | 279 | 287 | PF00069 | 0.448 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.756 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.497 |
MOD_Plk_2-3 | 430 | 436 | PF00069 | 0.481 |
MOD_Plk_2-3 | 510 | 516 | PF00069 | 0.455 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.555 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.411 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.512 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.561 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.561 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.637 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.778 |
MOD_ProDKin_1 | 680 | 686 | PF00069 | 0.711 |
MOD_SUMO_for_1 | 507 | 510 | PF00179 | 0.676 |
TRG_DiLeu_BaEn_1 | 369 | 374 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 591 | 593 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 637 | 639 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 679 | 682 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 690 | 693 | PF00400 | 0.656 |
TRG_NES_CRM1_1 | 27 | 40 | PF08389 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 659 | 663 | PF00026 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 66 | 70 | PF00026 | 0.680 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA41 | Leptomonas seymouri | 47% | 95% |
A0A1X0P203 | Trypanosomatidae | 25% | 100% |
A0A422P4Y6 | Trypanosoma rangeli | 25% | 100% |
A4HIA7 | Leishmania braziliensis | 74% | 100% |
A4I5J1 | Leishmania infantum | 88% | 100% |
C9ZQS6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
Q4Q7E2 | Leishmania major | 87% | 100% |
V5BU74 | Trypanosoma cruzi | 25% | 100% |