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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HDW9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.480 |
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.485 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.463 |
CLV_PCSK_FUR_1 | 237 | 241 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.711 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 629 | 631 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.411 |
CLV_Separin_Metazoa | 304 | 308 | PF03568 | 0.507 |
DEG_APCC_DBOX_1 | 237 | 245 | PF00400 | 0.573 |
DEG_APCC_DBOX_1 | 36 | 44 | PF00400 | 0.325 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.502 |
DOC_CYCLIN_RxL_1 | 444 | 454 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 143 | 153 | PF00069 | 0.679 |
DOC_MAPK_gen_1 | 313 | 321 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 634 | 643 | PF00069 | 0.643 |
DOC_MAPK_gen_1 | 64 | 72 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 104 | 111 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 314 | 323 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 564 | 572 | PF00069 | 0.558 |
DOC_PP2B_LxvP_1 | 303 | 306 | PF13499 | 0.523 |
DOC_PP4_FxxP_1 | 559 | 562 | PF00568 | 0.546 |
DOC_PP4_FxxP_1 | 609 | 612 | PF00568 | 0.595 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.539 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 143 | 153 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 173 | 181 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 343 | 348 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 418 | 427 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 550 | 558 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 569 | 573 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 634 | 639 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 91 | 99 | PF00244 | 0.552 |
LIG_Actin_RPEL_3 | 526 | 545 | PF02755 | 0.520 |
LIG_AP_GAE_1 | 596 | 602 | PF02883 | 0.643 |
LIG_APCC_ABBA_1 | 524 | 529 | PF00400 | 0.505 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.478 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 366 | 370 | PF00533 | 0.571 |
LIG_deltaCOP1_diTrp_1 | 94 | 99 | PF00928 | 0.452 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.633 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.516 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.462 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.412 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.548 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.587 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.513 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.535 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.590 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.566 |
LIG_LIR_Apic_2 | 608 | 612 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 361 | 370 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 657 | 666 | PF02991 | 0.706 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 355 | 359 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 361 | 365 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 482 | 488 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 575 | 579 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 657 | 662 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.448 |
LIG_MAD2 | 554 | 562 | PF02301 | 0.412 |
LIG_Pex14_2 | 620 | 624 | PF04695 | 0.619 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.623 |
LIG_SH2_STAT3 | 707 | 710 | PF00017 | 0.556 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.622 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.587 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.502 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 114 | 120 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 336 | 342 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 98 | 106 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 448 | 454 | PF11976 | 0.586 |
LIG_SUMO_SIM_par_1 | 611 | 618 | PF11976 | 0.587 |
LIG_UBA3_1 | 119 | 128 | PF00899 | 0.597 |
LIG_WW_3 | 561 | 565 | PF00397 | 0.553 |
MOD_CDK_SPxxK_3 | 364 | 371 | PF00069 | 0.605 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.549 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.605 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.739 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.527 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.701 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.586 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.615 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.634 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.612 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.580 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.763 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.741 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.573 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.576 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.743 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.774 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.476 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.549 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.579 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.690 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.602 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.756 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.743 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.428 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.521 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.500 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.458 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.424 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.429 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.637 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.645 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.465 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.301 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.537 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.736 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.442 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.610 |
MOD_PIKK_1 | 649 | 655 | PF00454 | 0.606 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.624 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.678 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.565 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.643 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.435 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.489 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.541 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.585 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.566 |
MOD_PKB_1 | 263 | 271 | PF00069 | 0.698 |
MOD_PKB_1 | 476 | 484 | PF00069 | 0.613 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.679 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.615 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.545 |
MOD_Plk_1 | 516 | 522 | PF00069 | 0.483 |
MOD_Plk_2-3 | 590 | 596 | PF00069 | 0.620 |
MOD_Plk_2-3 | 597 | 603 | PF00069 | 0.626 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.395 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.638 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.464 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.579 |
MOD_SUMO_rev_2 | 125 | 129 | PF00179 | 0.680 |
MOD_SUMO_rev_2 | 172 | 180 | PF00179 | 0.711 |
MOD_SUMO_rev_2 | 625 | 631 | PF00179 | 0.585 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_2 | 574 | 580 | PF01217 | 0.466 |
TRG_DiLeu_BaEn_2 | 94 | 100 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.685 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 474 | 476 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 684 | 687 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 709 | 712 | PF00400 | 0.772 |
TRG_NES_CRM1_1 | 113 | 126 | PF08389 | 0.614 |
TRG_NLS_MonoExtC_3 | 237 | 242 | PF00514 | 0.567 |
TRG_NLS_MonoExtC_3 | 261 | 267 | PF00514 | 0.716 |
TRG_NLS_MonoExtN_4 | 140 | 147 | PF00514 | 0.508 |
TRG_NLS_MonoExtN_4 | 237 | 242 | PF00514 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 645 | 650 | PF00026 | 0.637 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I765 | Leptomonas seymouri | 79% | 100% |
A0A0S4JHQ3 | Bodo saltans | 41% | 82% |
A0A1X0P4I5 | Trypanosomatidae | 59% | 100% |
A0A3S7WYX6 | Leishmania donovani | 88% | 100% |
A0A422NF47 | Trypanosoma rangeli | 59% | 100% |
A4I164 | Leishmania infantum | 88% | 100% |
D0A5F0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AX98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QA74 | Leishmania major | 88% | 100% |
V5DPB1 | Trypanosoma cruzi | 58% | 100% |