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: E9B0Q7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 558 | 562 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 658 | 660 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 680 | 682 | PF00675 | 0.592 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 680 | 682 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.525 |
CLV_Separin_Metazoa | 180 | 184 | PF03568 | 0.419 |
CLV_Separin_Metazoa | 666 | 670 | PF03568 | 0.600 |
DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.422 |
DEG_APCC_DBOX_1 | 267 | 275 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.417 |
DEG_APCC_DBOX_1 | 515 | 523 | PF00400 | 0.575 |
DOC_CYCLIN_RxL_1 | 297 | 305 | PF00134 | 0.450 |
DOC_CYCLIN_RxL_1 | 432 | 442 | PF00134 | 0.417 |
DOC_MAPK_gen_1 | 696 | 704 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 696 | 704 | PF00069 | 0.372 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 48 | 51 | PF13499 | 0.442 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.472 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 668 | 673 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 137 | 146 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 261 | 266 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 385 | 395 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 530 | 540 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 606 | 611 | PF00244 | 0.555 |
LIG_Actin_WH2_2 | 33 | 49 | PF00022 | 0.466 |
LIG_Actin_WH2_2 | 432 | 449 | PF00022 | 0.321 |
LIG_APCC_ABBA_1 | 591 | 596 | PF00400 | 0.524 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.762 |
LIG_CaM_IQ_9 | 278 | 294 | PF13499 | 0.510 |
LIG_EH1_1 | 42 | 50 | PF00400 | 0.413 |
LIG_EH1_1 | 83 | 91 | PF00400 | 0.344 |
LIG_eIF4E_1 | 632 | 638 | PF01652 | 0.557 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.467 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.419 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.534 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.473 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.555 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.626 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.553 |
LIG_FHA_1 | 688 | 694 | PF00498 | 0.540 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.410 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.473 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.585 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.583 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.570 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.553 |
LIG_LIR_Gen_1 | 31 | 41 | PF02991 | 0.353 |
LIG_LIR_LC3C_4 | 147 | 152 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 633 | 637 | PF02991 | 0.537 |
LIG_NRBOX | 624 | 630 | PF00104 | 0.549 |
LIG_PCNA_yPIPBox_3 | 164 | 178 | PF02747 | 0.498 |
LIG_PCNA_yPIPBox_3 | 489 | 502 | PF02747 | 0.477 |
LIG_PCNA_yPIPBox_3 | 620 | 629 | PF02747 | 0.337 |
LIG_PCNA_yPIPBox_3 | 678 | 692 | PF02747 | 0.585 |
LIG_PDZ_Class_2 | 699 | 704 | PF00595 | 0.382 |
LIG_PTB_Apo_2 | 259 | 266 | PF02174 | 0.536 |
LIG_PTB_Phospho_1 | 259 | 265 | PF10480 | 0.535 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.455 |
LIG_SH2_CRK | 634 | 638 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.455 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.496 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.747 |
LIG_SUMO_SIM_anti_2 | 147 | 152 | PF11976 | 0.286 |
LIG_SUMO_SIM_anti_2 | 434 | 440 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 577 | 582 | PF11976 | 0.522 |
LIG_SUMO_SIM_anti_2 | 662 | 669 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 149 | 154 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 434 | 440 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 468 | 474 | PF11976 | 0.563 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.485 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.503 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.611 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.435 |
LIG_TRAF2_1 | 582 | 585 | PF00917 | 0.586 |
LIG_TRFH_1 | 185 | 189 | PF08558 | 0.468 |
LIG_TRFH_1 | 235 | 239 | PF08558 | 0.475 |
MOD_CDK_SPxxK_3 | 597 | 604 | PF00069 | 0.587 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.616 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.649 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.318 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.545 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.594 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.698 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.641 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.511 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.435 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.584 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.532 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.562 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.738 |
MOD_DYRK1A_RPxSP_1 | 210 | 214 | PF00069 | 0.476 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.380 |
MOD_GlcNHglycan | 126 | 131 | PF01048 | 0.633 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.367 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.609 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.773 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.662 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.639 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.552 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.705 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.498 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.518 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.540 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.711 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.603 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.530 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.654 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.560 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.589 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.708 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.607 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.493 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.562 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.519 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.582 |
MOD_N-GLC_2 | 85 | 87 | PF02516 | 0.396 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.561 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.576 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.670 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.554 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.658 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.472 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.525 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.528 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.376 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.502 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.491 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.514 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.365 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.569 |
MOD_PKB_1 | 384 | 392 | PF00069 | 0.549 |
MOD_PKB_1 | 604 | 612 | PF00069 | 0.513 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.531 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.464 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.505 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.580 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.656 |
MOD_Plk_2-3 | 584 | 590 | PF00069 | 0.591 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.399 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.493 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.656 |
MOD_Plk_4 | 624 | 630 | PF00069 | 0.439 |
MOD_Plk_4 | 641 | 647 | PF00069 | 0.447 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.417 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.579 |
MOD_Plk_4 | 687 | 693 | PF00069 | 0.577 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.731 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.682 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.781 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.567 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.514 |
MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.671 |
MOD_ProDKin_1 | 668 | 674 | PF00069 | 0.679 |
MOD_SUMO_for_1 | 396 | 399 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 161 | 166 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 270 | 276 | PF00179 | 0.397 |
MOD_SUMO_rev_2 | 288 | 294 | PF00179 | 0.423 |
TRG_DiLeu_BaEn_3 | 662 | 668 | PF01217 | 0.543 |
TRG_DiLeu_BaEn_4 | 584 | 590 | PF01217 | 0.591 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 657 | 659 | PF00400 | 0.653 |
TRG_NES_CRM1_1 | 413 | 426 | PF08389 | 0.561 |
TRG_NES_CRM1_1 | 430 | 444 | PF08389 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 300 | 305 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 435 | 440 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 469 | 474 | PF00026 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 635 | 640 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P981 | Leptomonas seymouri | 57% | 95% |
A0A1X0P283 | Trypanosomatidae | 29% | 100% |
A0A3Q8IFR6 | Leishmania donovani | 91% | 100% |
A0A3R7NW91 | Trypanosoma rangeli | 31% | 100% |
A4HI80 | Leishmania braziliensis | 77% | 100% |
A4I5F9 | Leishmania infantum | 91% | 100% |
Q4Q7H6 | Leishmania major | 90% | 100% |
V5DQP9 | Trypanosoma cruzi | 32% | 100% |