| 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: E9AXQ5
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.399 |
| CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.359 |
| CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.533 |
| CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.633 |
| CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.359 |
| CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.633 |
| CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.690 |
| CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.515 |
| CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.503 |
| CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.739 |
| CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.501 |
| DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.516 |
| DEG_SPOP_SBC_1 | 227 | 231 | PF00917 | 0.522 |
| DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.790 |
| DOC_CKS1_1 | 70 | 75 | PF01111 | 0.561 |
| DOC_PP2B_LxvP_1 | 145 | 148 | PF13499 | 0.417 |
| DOC_PP4_FxxP_1 | 52 | 55 | PF00568 | 0.527 |
| DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.464 |
| DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.687 |
| DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.458 |
| DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.720 |
| DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.657 |
| DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.644 |
| DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.657 |
| DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.740 |
| LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.616 |
| LIG_14-3-3_CanoR_1 | 298 | 304 | PF00244 | 0.369 |
| LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.299 |
| LIG_CtBP_PxDLS_1 | 73 | 77 | PF00389 | 0.559 |
| LIG_deltaCOP1_diTrp_1 | 247 | 251 | PF00928 | 0.367 |
| LIG_FHA_1 | 113 | 119 | PF00498 | 0.473 |
| LIG_FHA_1 | 228 | 234 | PF00498 | 0.614 |
| LIG_FHA_2 | 230 | 236 | PF00498 | 0.545 |
| LIG_IRF3_LxIS_1 | 251 | 257 | PF10401 | 0.495 |
| LIG_LIR_Apic_2 | 195 | 200 | PF02991 | 0.549 |
| LIG_LIR_Apic_2 | 50 | 55 | PF02991 | 0.680 |
| LIG_LIR_Gen_1 | 247 | 256 | PF02991 | 0.383 |
| LIG_LIR_Gen_1 | 33 | 44 | PF02991 | 0.663 |
| LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.406 |
| LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.367 |
| LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.657 |
| LIG_LYPXL_yS_3 | 267 | 270 | PF13949 | 0.541 |
| LIG_MAD2 | 131 | 139 | PF02301 | 0.540 |
| LIG_MYND_1 | 99 | 103 | PF01753 | 0.568 |
| LIG_MYND_3 | 191 | 195 | PF01753 | 0.530 |
| LIG_REV1ctd_RIR_1 | 280 | 290 | PF16727 | 0.506 |
| LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.337 |
| LIG_SH3_3 | 166 | 172 | PF00018 | 0.525 |
| LIG_SH3_3 | 64 | 70 | PF00018 | 0.619 |
| LIG_SUMO_SIM_par_1 | 102 | 107 | PF11976 | 0.537 |
| LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.520 |
| LIG_UBA3_1 | 181 | 189 | PF00899 | 0.401 |
| MOD_CDC14_SPxK_1 | 92 | 95 | PF00782 | 0.484 |
| MOD_CDK_SPK_2 | 214 | 219 | PF00069 | 0.438 |
| MOD_CDK_SPxK_1 | 89 | 95 | PF00069 | 0.488 |
| MOD_CDK_SPxxK_3 | 123 | 130 | PF00069 | 0.427 |
| MOD_CK1_1 | 126 | 132 | PF00069 | 0.422 |
| MOD_CK1_1 | 229 | 235 | PF00069 | 0.460 |
| MOD_CK1_1 | 77 | 83 | PF00069 | 0.720 |
| MOD_CK1_1 | 85 | 91 | PF00069 | 0.554 |
| MOD_CK2_1 | 229 | 235 | PF00069 | 0.587 |
| MOD_CK2_1 | 72 | 78 | PF00069 | 0.759 |
| MOD_DYRK1A_RPxSP_1 | 123 | 127 | PF00069 | 0.454 |
| MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.559 |
| MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.690 |
| MOD_GSK3_1 | 156 | 163 | PF00069 | 0.563 |
| MOD_GSK3_1 | 250 | 257 | PF00069 | 0.492 |
| MOD_GSK3_1 | 28 | 35 | PF00069 | 0.651 |
| MOD_GSK3_1 | 65 | 72 | PF00069 | 0.672 |
| MOD_GSK3_1 | 79 | 86 | PF00069 | 0.601 |
| MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.502 |
| MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.475 |
| MOD_NEK2_1 | 156 | 161 | PF00069 | 0.481 |
| MOD_NEK2_1 | 174 | 179 | PF00069 | 0.344 |
| MOD_NEK2_1 | 226 | 231 | PF00069 | 0.646 |
| MOD_NEK2_1 | 30 | 35 | PF00069 | 0.725 |
| MOD_NEK2_1 | 307 | 312 | PF00069 | 0.539 |
| MOD_NEK2_1 | 38 | 43 | PF00069 | 0.544 |
| MOD_PKA_2 | 39 | 45 | PF00069 | 0.615 |
| MOD_Plk_4 | 239 | 245 | PF00069 | 0.378 |
| MOD_Plk_4 | 291 | 297 | PF00069 | 0.443 |
| MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.451 |
| MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.720 |
| MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.652 |
| MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.645 |
| MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.739 |
| MOD_SUMO_rev_2 | 253 | 262 | PF00179 | 0.510 |
| TRG_DiLeu_BaEn_1 | 107 | 112 | PF01217 | 0.526 |
| TRG_DiLeu_BaLyEn_6 | 52 | 57 | PF01217 | 0.676 |
| TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.535 |
| TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.314 |
| TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.356 |
| TRG_NES_CRM1_1 | 107 | 120 | PF08389 | 0.460 |
| TRG_Pf-PMV_PEXEL_1 | 299 | 304 | PF00026 | 0.420 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IMC8 | Leptomonas seymouri | 56% | 97% |
| A0A1X0NY85 | Trypanosomatidae | 35% | 100% |
| A0A3S7WZA0 | Leishmania donovani | 82% | 98% |
| A0A422NGK2 | Trypanosoma rangeli | 35% | 100% |
| A4HEG9 | Leishmania braziliensis | 66% | 100% |
| A4I1M1 | Leishmania infantum | 82% | 98% |
| C9ZK64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 96% |
| Q4Q9R6 | Leishmania major | 83% | 100% |
| V5BHV8 | Trypanosoma cruzi | 35% | 100% |