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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8IF64
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 447 | 451 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.674 |
CLV_PCSK_FUR_1 | 500 | 504 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.681 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.624 |
DEG_ODPH_VHL_1 | 402 | 414 | PF01847 | 0.533 |
DEG_SCF_TRCP1_1 | 120 | 126 | PF00400 | 0.661 |
DEG_SPOP_SBC_1 | 345 | 349 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 376 | 380 | PF00917 | 0.631 |
DOC_CYCLIN_RxL_1 | 312 | 325 | PF00134 | 0.707 |
DOC_MAPK_MEF2A_6 | 222 | 229 | PF00069 | 0.495 |
DOC_MAPK_NFAT4_5 | 222 | 230 | PF00069 | 0.626 |
DOC_MIT_MIM_1 | 573 | 583 | PF04212 | 0.607 |
DOC_PP1_RVXF_1 | 202 | 208 | PF00149 | 0.542 |
DOC_PP1_RVXF_1 | 490 | 497 | PF00149 | 0.482 |
DOC_PP1_RVXF_1 | 568 | 574 | PF00149 | 0.571 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.506 |
DOC_PP4_FxxP_1 | 342 | 345 | PF00568 | 0.635 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.479 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 154 | 163 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 16 | 22 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 290 | 296 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 383 | 391 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 491 | 495 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 80 | 89 | PF00244 | 0.693 |
LIG_Actin_WH2_2 | 422 | 438 | PF00022 | 0.609 |
LIG_AP2alpha_2 | 139 | 141 | PF02296 | 0.710 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.635 |
LIG_BIR_III_2 | 355 | 359 | PF00653 | 0.676 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.567 |
LIG_BRCT_BRCA1_1 | 295 | 299 | PF00533 | 0.525 |
LIG_BRCT_BRCA1_1 | 492 | 496 | PF00533 | 0.593 |
LIG_deltaCOP1_diTrp_1 | 137 | 143 | PF00928 | 0.735 |
LIG_deltaCOP1_diTrp_1 | 187 | 195 | PF00928 | 0.584 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.760 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.528 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.698 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.669 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.598 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.520 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.315 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.580 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.571 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.398 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.517 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.646 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.660 |
LIG_LIR_Apic_2 | 20 | 25 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 406 | 416 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 493 | 501 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 572 | 581 | PF02991 | 0.677 |
LIG_LIR_LC3C_4 | 409 | 413 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 493 | 499 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 572 | 576 | PF02991 | 0.670 |
LIG_LYPXL_yS_3 | 337 | 340 | PF13949 | 0.727 |
LIG_MLH1_MIPbox_1 | 295 | 299 | PF16413 | 0.525 |
LIG_MYND_1 | 372 | 376 | PF01753 | 0.644 |
LIG_NRBOX | 33 | 39 | PF00104 | 0.604 |
LIG_NRBOX | 444 | 450 | PF00104 | 0.449 |
LIG_Pex14_1 | 156 | 160 | PF04695 | 0.534 |
LIG_PTB_Apo_2 | 336 | 343 | PF02174 | 0.589 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.664 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.700 |
LIG_SH2_GRB2like | 201 | 204 | PF00017 | 0.554 |
LIG_SH2_GRB2like | 471 | 474 | PF00017 | 0.591 |
LIG_SH2_SRC | 305 | 308 | PF00017 | 0.549 |
LIG_SH2_SRC | 534 | 537 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 295 | 299 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.523 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.740 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.644 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.478 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.538 |
LIG_SUMO_SIM_anti_2 | 167 | 173 | PF11976 | 0.637 |
LIG_SUMO_SIM_anti_2 | 409 | 415 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 409 | 415 | PF11976 | 0.522 |
LIG_TRAF2_1 | 518 | 521 | PF00917 | 0.504 |
LIG_TYR_ITIM | 38 | 43 | PF00017 | 0.567 |
LIG_WRC_WIRS_1 | 295 | 300 | PF05994 | 0.552 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.758 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.691 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.635 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.531 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.620 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.650 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.505 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.655 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.649 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.504 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.748 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.781 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.646 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.647 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.682 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.633 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.608 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.465 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.619 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.528 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.770 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.536 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.662 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.714 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.587 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.563 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.731 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.584 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.474 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.655 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.543 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.560 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.607 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.527 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.668 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.524 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.614 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.565 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.625 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.684 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.497 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.527 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.521 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.536 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.577 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.664 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.638 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.650 |
MOD_PIKK_1 | 424 | 430 | PF00454 | 0.539 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.681 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.681 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.691 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.718 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.556 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.765 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.766 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.593 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.431 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.681 |
MOD_PKB_1 | 85 | 93 | PF00069 | 0.705 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.502 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.590 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.583 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.628 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.598 |
MOD_Plk_2-3 | 444 | 450 | PF00069 | 0.541 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.657 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.559 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.630 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.489 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.513 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.403 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.713 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.622 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.478 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.599 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.714 |
MOD_SUMO_for_1 | 561 | 564 | PF00179 | 0.733 |
MOD_SUMO_rev_2 | 555 | 563 | PF00179 | 0.733 |
TRG_DiLeu_BaEn_1 | 167 | 172 | PF01217 | 0.636 |
TRG_DiLeu_BaEn_1 | 444 | 449 | PF01217 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.673 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.714 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.727 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 85 | 88 | PF00400 | 0.616 |
TRG_NLS_Bipartite_1 | 68 | 83 | PF00514 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 470 | 475 | PF00026 | 0.644 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.719 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEU5 | Leptomonas seymouri | 42% | 99% |
A4HAC5 | Leishmania braziliensis | 78% | 100% |
A4I9H8 | Leishmania infantum | 100% | 100% |
E9B4H6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q3J9 | Leishmania major | 93% | 100% |