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: A0A3S7X5I4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.622 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.535 |
CLV_PCSK_FUR_1 | 229 | 233 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.555 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.450 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.544 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.483 |
DOC_CYCLIN_RxL_1 | 228 | 238 | PF00134 | 0.488 |
DOC_MAPK_DCC_7 | 95 | 105 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 173 | 181 | PF00069 | 0.435 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.469 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.582 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.389 |
LIG_APCC_ABBA_1 | 120 | 125 | PF00400 | 0.508 |
LIG_Clathr_ClatBox_1 | 106 | 110 | PF01394 | 0.311 |
LIG_eIF4E_1 | 123 | 129 | PF01652 | 0.402 |
LIG_eIF4E_1 | 228 | 234 | PF01652 | 0.505 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.471 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.411 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.567 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.493 |
LIG_LIR_Gen_1 | 175 | 181 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 4 | 15 | PF02991 | 0.651 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 89 | 98 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.443 |
LIG_LYPXL_yS_3 | 123 | 126 | PF13949 | 0.331 |
LIG_PDZ_Class_1 | 286 | 291 | PF00595 | 0.490 |
LIG_Pex14_2 | 138 | 142 | PF04695 | 0.377 |
LIG_Pex14_2 | 262 | 266 | PF04695 | 0.348 |
LIG_PTB_Apo_2 | 108 | 115 | PF02174 | 0.354 |
LIG_PTB_Apo_2 | 222 | 229 | PF02174 | 0.390 |
LIG_PTB_Phospho_1 | 222 | 228 | PF10480 | 0.383 |
LIG_SH3_1 | 118 | 124 | PF00018 | 0.326 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.432 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.537 |
LIG_SUMO_SIM_anti_2 | 101 | 108 | PF11976 | 0.310 |
LIG_SUMO_SIM_anti_2 | 125 | 130 | PF11976 | 0.467 |
LIG_SUMO_SIM_anti_2 | 247 | 254 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 101 | 108 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 213 | 218 | PF11976 | 0.331 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.515 |
LIG_UBA3_1 | 233 | 237 | PF00899 | 0.570 |
LIG_WRC_WIRS_1 | 134 | 139 | PF05994 | 0.420 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.683 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.431 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.480 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.455 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.486 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.447 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.606 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.441 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.615 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.431 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.513 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.655 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.552 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.522 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.341 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.422 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.413 |
MOD_PK_1 | 162 | 168 | PF00069 | 0.620 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.434 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.391 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.432 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.598 |
MOD_Plk_2-3 | 3 | 9 | PF00069 | 0.415 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.472 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.535 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.346 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.402 |
TRG_DiLeu_BaEn_1 | 18 | 23 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_3 | 45 | 51 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 229 | 234 | PF01217 | 0.642 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.528 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.450 |
TRG_NES_CRM1_1 | 207 | 220 | PF08389 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMW3 | Leptomonas seymouri | 68% | 98% |
A0A1X0NUU9 | Trypanosomatidae | 47% | 94% |
A0A422NL68 | Trypanosoma rangeli | 40% | 100% |
A4HKE8 | Leishmania braziliensis | 80% | 100% |
A4I7X6 | Leishmania infantum | 100% | 100% |
D0AA41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 93% |
E9B2T7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q5C0 | Leishmania major | 96% | 100% |
V5BF01 | Trypanosoma cruzi | 39% | 100% |