| 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: A4HCJ6
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.465 |
| CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.568 |
| CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.741 |
| CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.682 |
| CLV_PCSK_FUR_1 | 150 | 154 | PF00082 | 0.568 |
| CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.571 |
| CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.744 |
| CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.728 |
| CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.725 |
| CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.445 |
| CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.582 |
| CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.470 |
| CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.580 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.545 |
| DEG_SPOP_SBC_1 | 309 | 313 | PF00917 | 0.631 |
| DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.614 |
| DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.483 |
| DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.480 |
| DOC_CYCLIN_RxL_1 | 146 | 159 | PF00134 | 0.493 |
| DOC_CYCLIN_RxL_1 | 28 | 42 | PF00134 | 0.676 |
| DOC_CYCLIN_yCln2_LP_2 | 27 | 33 | PF00134 | 0.428 |
| DOC_MAPK_gen_1 | 129 | 136 | PF00069 | 0.500 |
| DOC_PP2B_LxvP_1 | 277 | 280 | PF13499 | 0.590 |
| DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.621 |
| DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.578 |
| DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.644 |
| DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.612 |
| DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.616 |
| DOC_USP7_UBL2_3 | 65 | 69 | PF12436 | 0.722 |
| DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.693 |
| DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.573 |
| DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.638 |
| DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.687 |
| LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.722 |
| LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.467 |
| LIG_14-3-3_CanoR_1 | 292 | 299 | PF00244 | 0.522 |
| LIG_14-3-3_CanoR_1 | 324 | 334 | PF00244 | 0.742 |
| LIG_APCC_ABBA_1 | 362 | 367 | PF00400 | 0.450 |
| LIG_FHA_1 | 16 | 22 | PF00498 | 0.559 |
| LIG_FHA_1 | 315 | 321 | PF00498 | 0.541 |
| LIG_FHA_1 | 359 | 365 | PF00498 | 0.451 |
| LIG_FHA_2 | 104 | 110 | PF00498 | 0.613 |
| LIG_FHA_2 | 327 | 333 | PF00498 | 0.588 |
| LIG_IBAR_NPY_1 | 186 | 188 | PF08397 | 0.524 |
| LIG_LIR_Gen_1 | 240 | 246 | PF02991 | 0.586 |
| LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.523 |
| LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.428 |
| LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.587 |
| LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.434 |
| LIG_PDZ_Class_2 | 370 | 375 | PF00595 | 0.647 |
| LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.639 |
| LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.633 |
| LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.622 |
| LIG_SUMO_SIM_par_1 | 359 | 368 | PF11976 | 0.537 |
| LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.543 |
| LIG_TRAF2_1 | 294 | 297 | PF00917 | 0.442 |
| LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.612 |
| LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.545 |
| LIG_UBA3_1 | 176 | 185 | PF00899 | 0.579 |
| LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.640 |
| MOD_CDK_SPK_2 | 76 | 81 | PF00069 | 0.623 |
| MOD_CK1_1 | 120 | 126 | PF00069 | 0.550 |
| MOD_CK1_1 | 193 | 199 | PF00069 | 0.599 |
| MOD_CK1_1 | 311 | 317 | PF00069 | 0.674 |
| MOD_CK1_1 | 51 | 57 | PF00069 | 0.636 |
| MOD_CK1_1 | 6 | 12 | PF00069 | 0.612 |
| MOD_CK1_1 | 60 | 66 | PF00069 | 0.719 |
| MOD_CK1_1 | 68 | 74 | PF00069 | 0.587 |
| MOD_CK1_1 | 79 | 85 | PF00069 | 0.648 |
| MOD_CK1_1 | 93 | 99 | PF00069 | 0.555 |
| MOD_CK2_1 | 241 | 247 | PF00069 | 0.686 |
| MOD_CK2_1 | 254 | 260 | PF00069 | 0.446 |
| MOD_CK2_1 | 291 | 297 | PF00069 | 0.609 |
| MOD_CK2_1 | 85 | 91 | PF00069 | 0.697 |
| MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.429 |
| MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.514 |
| MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.722 |
| MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.476 |
| MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.547 |
| MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.579 |
| MOD_GlcNHglycan | 91 | 95 | PF01048 | 0.488 |
| MOD_GSK3_1 | 113 | 120 | PF00069 | 0.513 |
| MOD_GSK3_1 | 15 | 22 | PF00069 | 0.551 |
| MOD_GSK3_1 | 189 | 196 | PF00069 | 0.685 |
| MOD_GSK3_1 | 233 | 240 | PF00069 | 0.656 |
| MOD_GSK3_1 | 246 | 253 | PF00069 | 0.660 |
| MOD_GSK3_1 | 304 | 311 | PF00069 | 0.594 |
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.579 |
| MOD_GSK3_1 | 48 | 55 | PF00069 | 0.487 |
| MOD_GSK3_1 | 68 | 75 | PF00069 | 0.668 |
| MOD_GSK3_1 | 86 | 93 | PF00069 | 0.631 |
| MOD_LATS_1 | 32 | 38 | PF00433 | 0.555 |
| MOD_NEK2_1 | 213 | 218 | PF00069 | 0.619 |
| MOD_NEK2_1 | 325 | 330 | PF00069 | 0.560 |
| MOD_NEK2_1 | 36 | 41 | PF00069 | 0.640 |
| MOD_NEK2_2 | 280 | 285 | PF00069 | 0.600 |
| MOD_PIKK_1 | 19 | 25 | PF00454 | 0.523 |
| MOD_PIKK_1 | 213 | 219 | PF00454 | 0.639 |
| MOD_PIKK_1 | 86 | 92 | PF00454 | 0.461 |
| MOD_PKA_1 | 65 | 71 | PF00069 | 0.496 |
| MOD_PKA_2 | 193 | 199 | PF00069 | 0.647 |
| MOD_PKA_2 | 291 | 297 | PF00069 | 0.482 |
| MOD_PKA_2 | 52 | 58 | PF00069 | 0.665 |
| MOD_PKA_2 | 65 | 71 | PF00069 | 0.593 |
| MOD_Plk_1 | 15 | 21 | PF00069 | 0.429 |
| MOD_Plk_1 | 158 | 164 | PF00069 | 0.553 |
| MOD_Plk_1 | 280 | 286 | PF00069 | 0.467 |
| MOD_Plk_1 | 358 | 364 | PF00069 | 0.586 |
| MOD_Plk_2-3 | 241 | 247 | PF00069 | 0.619 |
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.642 |
| MOD_Plk_4 | 280 | 286 | PF00069 | 0.564 |
| MOD_Plk_4 | 93 | 99 | PF00069 | 0.496 |
| MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.695 |
| MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.573 |
| MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.639 |
| MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.687 |
| TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.639 |
| TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.679 |
| TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.586 |
| TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.526 |
| TRG_NLS_MonoExtC_3 | 64 | 69 | PF00514 | 0.741 |
| TRG_NLS_MonoExtN_4 | 65 | 70 | PF00514 | 0.750 |
| TRG_Pf-PMV_PEXEL_1 | 152 | 156 | PF00026 | 0.619 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I4X3 | Leptomonas seymouri | 36% | 100% |
| A0A1X0NTI1 | Trypanosomatidae | 31% | 100% |
| A0A3Q8IAT9 | Leishmania donovani | 74% | 100% |
| A0A422N4X5 | Trypanosoma rangeli | 28% | 100% |
| A4I016 | Leishmania infantum | 74% | 100% |
| C9ZQ77 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
| E9AVY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
| Q4QBJ0 | Leishmania major | 71% | 99% |
| V5ARZ4 | Trypanosoma cruzi | 29% | 100% |