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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9ASB0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.201 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.413 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.201 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.413 |
CLV_PCSK_PC7_1 | 243 | 249 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.422 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.707 |
DOC_CDC14_PxL_1 | 75 | 83 | PF14671 | 0.293 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.422 |
DOC_CKS1_1 | 7 | 12 | PF01111 | 0.497 |
DOC_MAPK_gen_1 | 282 | 290 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.415 |
DOC_PP1_RVXF_1 | 139 | 145 | PF00149 | 0.438 |
DOC_PP1_RVXF_1 | 301 | 307 | PF00149 | 0.465 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.597 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 119 | 126 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 218 | 223 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 264 | 271 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 279 | 288 | PF00244 | 0.378 |
LIG_APCC_ABBA_1 | 102 | 107 | PF00400 | 0.273 |
LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.438 |
LIG_deltaCOP1_diTrp_1 | 160 | 167 | PF00928 | 0.357 |
LIG_eIF4E_1 | 76 | 82 | PF01652 | 0.521 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.408 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.391 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.457 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.724 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.556 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.528 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.359 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.607 |
LIG_IRF3_LxIS_1 | 219 | 226 | PF10401 | 0.201 |
LIG_LIR_Apic_2 | 115 | 120 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 74 | 79 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 196 | 206 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 295 | 306 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.430 |
LIG_NRBOX | 218 | 224 | PF00104 | 0.326 |
LIG_NRBOX | 300 | 306 | PF00104 | 0.465 |
LIG_PCNA_yPIPBox_3 | 285 | 298 | PF02747 | 0.422 |
LIG_PDZ_Class_1 | 313 | 318 | PF00595 | 0.478 |
LIG_SH2_CRK | 117 | 121 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 77 | 80 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.521 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.552 |
LIG_SUMO_SIM_anti_2 | 128 | 133 | PF11976 | 0.425 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.424 |
MOD_CAAXbox | 315 | 318 | PF01239 | 0.484 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.486 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.801 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.565 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.489 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.483 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.488 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.457 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.415 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.405 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.373 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.722 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.623 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.438 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.422 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.376 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.681 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.445 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.649 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.500 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.357 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.503 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.438 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.369 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.206 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.430 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.517 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.288 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.485 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.365 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.330 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.492 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.582 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.396 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.388 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.528 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.371 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.551 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.477 |
TRG_DiLeu_BaEn_1 | 313 | 318 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 271 | 276 | PF01217 | 0.438 |
TRG_DiLeu_LyEn_5 | 300 | 305 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.197 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.423 |
TRG_NES_CRM1_1 | 93 | 107 | PF08389 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9A9 | Leptomonas seymouri | 53% | 85% |
A0A0S4IWN1 | Bodo saltans | 33% | 93% |
A0A1X0P699 | Trypanosomatidae | 40% | 100% |
A0A3S7WVN6 | Leishmania donovani | 94% | 100% |
A4HAA6 | Leishmania braziliensis | 71% | 100% |
A4HYI6 | Leishmania infantum | 94% | 100% |
Q4QD52 | Leishmania major | 89% | 100% |