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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8IHE5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.743 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.599 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 12 | 14 | PF00082 | 0.680 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.433 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.675 |
DEG_APCC_DBOX_1 | 257 | 265 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 442 | 450 | PF00400 | 0.473 |
DOC_CKS1_1 | 24 | 29 | PF01111 | 0.584 |
DOC_CYCLIN_RxL_1 | 77 | 86 | PF00134 | 0.452 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 469 | 478 | PF00134 | 0.501 |
DOC_MAPK_MEF2A_6 | 243 | 251 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 258 | 265 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 270 | 277 | PF00069 | 0.361 |
DOC_MAPK_NFAT4_5 | 270 | 278 | PF00069 | 0.403 |
DOC_PP2B_LxvP_1 | 19 | 22 | PF13499 | 0.683 |
DOC_PP2B_LxvP_1 | 561 | 564 | PF13499 | 0.457 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.668 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.536 |
DOC_USP7_UBL2_3 | 361 | 365 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.753 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.739 |
LIG_14-3-3_CanoR_1 | 184 | 194 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 198 | 206 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 343 | 348 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 405 | 414 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 431 | 435 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 443 | 447 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 506 | 512 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.580 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_BRCT_BRCA1_1 | 522 | 526 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 608 | 612 | PF00533 | 0.434 |
LIG_eIF4E_1 | 272 | 278 | PF01652 | 0.440 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.492 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.356 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.490 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.433 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.634 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.440 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.556 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.592 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.519 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.475 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.595 |
LIG_LIR_Apic_2 | 14 | 18 | PF02991 | 0.668 |
LIG_LIR_Apic_2 | 181 | 186 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 215 | 223 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 433 | 442 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 508 | 517 | PF02991 | 0.713 |
LIG_LIR_Gen_1 | 523 | 534 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 433 | 437 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 608 | 613 | PF02991 | 0.515 |
LIG_NRBOX | 276 | 282 | PF00104 | 0.307 |
LIG_Pex14_2 | 213 | 217 | PF04695 | 0.363 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.473 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 288 | 292 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 613 | 617 | PF00017 | 0.499 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 633 | 636 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.229 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.741 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.505 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.543 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.392 |
LIG_SUMO_SIM_anti_2 | 305 | 311 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 68 | 77 | PF11976 | 0.417 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.637 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.503 |
LIG_TRAF2_2 | 627 | 632 | PF00917 | 0.343 |
LIG_TRFH_1 | 509 | 513 | PF08558 | 0.501 |
LIG_UBA3_1 | 261 | 270 | PF00899 | 0.394 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.650 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.757 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.516 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.539 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.709 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.612 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.593 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.512 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.459 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.493 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.416 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.613 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.661 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.715 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.686 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.494 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.610 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.504 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.614 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.433 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.655 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.525 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.423 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.396 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.602 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.497 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.682 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.553 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.320 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.469 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.383 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.439 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.436 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.492 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.420 |
MOD_NEK2_2 | 507 | 512 | PF00069 | 0.554 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.412 |
MOD_PIKK_1 | 556 | 562 | PF00454 | 0.440 |
MOD_PKA_1 | 360 | 366 | PF00069 | 0.543 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.553 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.442 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.422 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.551 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.597 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.441 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.470 |
MOD_Plk_2-3 | 229 | 235 | PF00069 | 0.497 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.679 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.397 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.292 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.447 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.393 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.354 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.740 |
MOD_SUMO_rev_2 | 84 | 89 | PF00179 | 0.517 |
TRG_DiLeu_BaEn_1 | 545 | 550 | PF01217 | 0.380 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_3 | 68 | 74 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_3 | 76 | 82 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 516 | 521 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 551 | 556 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 621 | 626 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 447 | 450 | PF00400 | 0.288 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK53 | Leptomonas seymouri | 61% | 99% |
A0A1X0NRY3 | Trypanosomatidae | 28% | 100% |
A0A422P2Z2 | Trypanosoma rangeli | 27% | 100% |
A4HKZ1 | Leishmania braziliensis | 74% | 100% |
A4I8H2 | Leishmania infantum | 99% | 100% |
D0AAP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9B3D2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q4S4 | Leishmania major | 94% | 100% |
V5BQY9 | Trypanosoma cruzi | 25% | 100% |