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: Q4QA74
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.411 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.505 |
CLV_PCSK_FUR_1 | 237 | 241 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 475 | 477 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 629 | 631 | PF00082 | 0.559 |
CLV_PCSK_PC7_1 | 258 | 264 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.465 |
DEG_APCC_DBOX_1 | 237 | 245 | PF00400 | 0.509 |
DEG_APCC_DBOX_1 | 257 | 265 | PF00400 | 0.381 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.468 |
DEG_APCC_DBOX_1 | 76 | 84 | PF00400 | 0.348 |
DOC_CYCLIN_RxL_1 | 444 | 454 | PF00134 | 0.424 |
DOC_MAPK_gen_1 | 144 | 153 | PF00069 | 0.666 |
DOC_MAPK_gen_1 | 313 | 321 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 634 | 643 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 104 | 111 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 314 | 323 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 564 | 572 | PF00069 | 0.542 |
DOC_PP4_FxxP_1 | 559 | 562 | PF00568 | 0.511 |
DOC_PP4_FxxP_1 | 609 | 612 | PF00568 | 0.548 |
DOC_PP4_FxxP_1 | 707 | 710 | PF00568 | 0.571 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.542 |
DOC_USP7_UBL2_3 | 134 | 138 | PF12436 | 0.626 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.561 |
LIG_14-3-3_CanoR_1 | 146 | 153 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 343 | 348 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 418 | 427 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 550 | 558 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 569 | 573 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 634 | 639 | PF00244 | 0.595 |
LIG_Actin_RPEL_3 | 526 | 545 | PF02755 | 0.467 |
LIG_AP_GAE_1 | 596 | 602 | PF02883 | 0.582 |
LIG_APCC_ABBA_1 | 524 | 529 | PF00400 | 0.467 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.419 |
LIG_BIR_III_4 | 432 | 436 | PF00653 | 0.564 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 366 | 370 | PF00533 | 0.543 |
LIG_deltaCOP1_diTrp_1 | 94 | 99 | PF00928 | 0.392 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.577 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.415 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.367 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.486 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.537 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.466 |
LIG_FHA_2 | 652 | 658 | PF00498 | 0.538 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.545 |
LIG_LIR_Apic_2 | 608 | 612 | PF02991 | 0.576 |
LIG_LIR_Apic_2 | 706 | 710 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 295 | 303 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 361 | 370 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 355 | 359 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 361 | 365 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 482 | 488 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 575 | 579 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 656 | 662 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.388 |
LIG_Pex14_2 | 620 | 624 | PF04695 | 0.561 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.305 |
LIG_SH2_SRC | 198 | 201 | PF00017 | 0.528 |
LIG_SH2_SRC | 233 | 236 | PF00017 | 0.604 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.295 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.538 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.551 |
LIG_SH3_3 | 552 | 558 | PF00018 | 0.444 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.480 |
LIG_Sin3_3 | 509 | 516 | PF02671 | 0.326 |
LIG_SUMO_SIM_anti_2 | 114 | 120 | PF11976 | 0.374 |
LIG_SUMO_SIM_anti_2 | 336 | 341 | PF11976 | 0.400 |
LIG_SUMO_SIM_anti_2 | 98 | 106 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 448 | 454 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 611 | 618 | PF11976 | 0.538 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.545 |
LIG_WW_3 | 561 | 565 | PF00397 | 0.519 |
MOD_CDK_SPxxK_3 | 364 | 371 | PF00069 | 0.475 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.507 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.608 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.700 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.682 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.675 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.652 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.761 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.461 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.568 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.569 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.560 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.562 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.698 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.714 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.722 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.589 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.576 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.558 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.698 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.725 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.452 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.521 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.692 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.556 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.756 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.709 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.494 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.614 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.570 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.470 |
MOD_N-GLC_1 | 681 | 686 | PF02516 | 0.626 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.400 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.383 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.437 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.597 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.593 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.409 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.462 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.706 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.569 |
MOD_PIKK_1 | 649 | 655 | PF00454 | 0.556 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.526 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.677 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.522 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.587 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.421 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.561 |
MOD_PKA_2 | 625 | 631 | PF00069 | 0.535 |
MOD_PKB_1 | 263 | 271 | PF00069 | 0.657 |
MOD_PKB_1 | 476 | 484 | PF00069 | 0.575 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.584 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.523 |
MOD_Plk_1 | 516 | 522 | PF00069 | 0.433 |
MOD_Plk_2-3 | 590 | 596 | PF00069 | 0.573 |
MOD_Plk_2-3 | 597 | 603 | PF00069 | 0.562 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.428 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.501 |
MOD_Plk_4 | 615 | 621 | PF00069 | 0.594 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.475 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.419 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.553 |
MOD_SUMO_rev_2 | 172 | 180 | PF00179 | 0.700 |
MOD_SUMO_rev_2 | 625 | 631 | PF00179 | 0.535 |
TRG_DiLeu_BaEn_1 | 336 | 341 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_2 | 574 | 580 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_2 | 94 | 100 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.639 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 708 | 711 | PF00400 | 0.714 |
TRG_NES_CRM1_1 | 113 | 126 | PF08389 | 0.601 |
TRG_NLS_MonoExtC_3 | 237 | 242 | PF00514 | 0.504 |
TRG_NLS_MonoExtC_3 | 261 | 267 | PF00514 | 0.569 |
TRG_NLS_MonoExtN_4 | 237 | 242 | PF00514 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 645 | 650 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I765 | Leptomonas seymouri | 81% | 100% |
A0A0S4JHQ3 | Bodo saltans | 41% | 82% |
A0A1X0P4I5 | Trypanosomatidae | 59% | 100% |
A0A3S7WYX6 | Leishmania donovani | 95% | 100% |
A0A422NF47 | Trypanosoma rangeli | 59% | 100% |
A4HDW9 | Leishmania braziliensis | 88% | 100% |
A4I164 | Leishmania infantum | 95% | 100% |
D0A5F0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AX98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5DPB1 | Trypanosoma cruzi | 58% | 100% |