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: E9AMV2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.279 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.364 |
DEG_APCC_DBOX_1 | 29 | 37 | PF00400 | 0.297 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.588 |
DOC_CYCLIN_RxL_1 | 177 | 187 | PF00134 | 0.457 |
DOC_MAPK_gen_1 | 30 | 38 | PF00069 | 0.279 |
DOC_MAPK_HePTP_8 | 28 | 40 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 31 | 40 | PF00069 | 0.357 |
DOC_PP1_RVXF_1 | 269 | 276 | PF00149 | 0.511 |
DOC_PP4_FxxP_1 | 40 | 43 | PF00568 | 0.410 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.739 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.543 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.410 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.334 |
LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.617 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.410 |
LIG_BRCT_BRCA1_2 | 265 | 271 | PF00533 | 0.621 |
LIG_BRCT_BRCA1_2 | 72 | 78 | PF00533 | 0.246 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.614 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.446 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.536 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.584 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.407 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.277 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.421 |
LIG_HCF-1_HBM_1 | 255 | 258 | PF13415 | 0.469 |
LIG_Integrin_isoDGR_2 | 283 | 285 | PF01839 | 0.652 |
LIG_LIR_Apic_2 | 39 | 43 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 68 | 76 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 8 | 18 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 8 | 13 | PF02991 | 0.522 |
LIG_NRBOX | 32 | 38 | PF00104 | 0.357 |
LIG_PDZ_Class_2 | 306 | 311 | PF00595 | 0.398 |
LIG_PTB_Apo_2 | 189 | 196 | PF02174 | 0.431 |
LIG_PTB_Apo_2 | 39 | 46 | PF02174 | 0.378 |
LIG_REV1ctd_RIR_1 | 192 | 202 | PF16727 | 0.482 |
LIG_SH2_CRK | 260 | 264 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.446 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.467 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.619 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.393 |
LIG_UBA3_1 | 70 | 78 | PF00899 | 0.266 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.355 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.693 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.389 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.737 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.489 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.588 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.405 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.395 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.530 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.514 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.277 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.422 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.479 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.378 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.273 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.653 |
MOD_PK_1 | 198 | 204 | PF00069 | 0.420 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.427 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.391 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.531 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.505 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.517 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.497 |
MOD_SUMO_rev_2 | 288 | 296 | PF00179 | 0.367 |
TRG_DiLeu_BaEn_1 | 282 | 287 | PF01217 | 0.596 |
TRG_DiLeu_BaEn_4 | 8 | 14 | PF01217 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 28 | 33 | PF01217 | 0.297 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.517 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 144 | 149 | PF00026 | 0.649 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBQ0 | Leptomonas seymouri | 59% | 99% |
A0A1X0NI65 | Trypanosomatidae | 40% | 100% |
A0A3S7WQS2 | Leishmania donovani | 89% | 100% |
A0A422N3Q8 | Trypanosoma rangeli | 39% | 100% |
A4H5S8 | Leishmania braziliensis | 74% | 100% |
A4HU22 | Leishmania infantum | 90% | 100% |
D0A9J2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
Q4QHS4 | Leishmania major | 91% | 100% |
V5D6M9 | Trypanosoma cruzi | 41% | 100% |