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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0031207 | Sec62/Sec63 complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9B6I8
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006613 | cotranslational protein targeting to membrane | 6 | 1 |
GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 1 |
GO:0006620 | post-translational protein targeting to endoplasmic reticulum membrane | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0045047 | protein targeting to ER | 6 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0008320 | protein transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0022884 | macromolecule transmembrane transporter activity | 3 | 1 |
GO:0140318 | protein transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.339 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.571 |
CLV_PCSK_FUR_1 | 133 | 137 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 279 | 281 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.603 |
CLV_PCSK_PC1ET2_1 | 45 | 47 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.637 |
DEG_APCC_DBOX_1 | 141 | 149 | PF00400 | 0.587 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.414 |
DEG_APCC_DBOX_1 | 2 | 10 | PF00400 | 0.673 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.661 |
DOC_CKS1_1 | 29 | 34 | PF01111 | 0.457 |
DOC_CKS1_1 | 308 | 313 | PF01111 | 0.254 |
DOC_CYCLIN_RxL_1 | 362 | 372 | PF00134 | 0.398 |
DOC_CYCLIN_yCln2_LP_2 | 196 | 202 | PF00134 | 0.415 |
DOC_PP1_RVXF_1 | 363 | 370 | PF00149 | 0.390 |
DOC_PP2B_LxvP_1 | 196 | 199 | PF13499 | 0.416 |
DOC_PP2B_LxvP_1 | 419 | 422 | PF13499 | 0.374 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.502 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 174 | 179 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 235 | 242 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 260 | 269 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 309 | 315 | PF00244 | 0.224 |
LIG_BRCT_BRCA1_1 | 263 | 267 | PF00533 | 0.404 |
LIG_EH1_1 | 175 | 183 | PF00400 | 0.421 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.389 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.363 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.498 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.325 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.549 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.273 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.348 |
LIG_LIR_Apic_2 | 310 | 315 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 173 | 183 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 210 | 218 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 247 | 256 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 268 | 277 | PF02991 | 0.226 |
LIG_LIR_Gen_1 | 31 | 41 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 338 | 349 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.226 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.289 |
LIG_NRBOX | 144 | 150 | PF00104 | 0.446 |
LIG_PTB_Apo_2 | 363 | 370 | PF02174 | 0.287 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.351 |
LIG_SH2_CRK | 212 | 216 | PF00017 | 0.477 |
LIG_SH2_CRK | 269 | 273 | PF00017 | 0.282 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.354 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.431 |
LIG_SH2_SRC | 269 | 272 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.393 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.612 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.401 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.314 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.451 |
LIG_SUMO_SIM_anti_2 | 163 | 169 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 165 | 171 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 200 | 205 | PF11976 | 0.436 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.658 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.546 |
MOD_CDK_SPxxK_3 | 28 | 35 | PF00069 | 0.360 |
MOD_CDK_SPxxK_3 | 86 | 93 | PF00069 | 0.666 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.683 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.411 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.480 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.310 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.613 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.727 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.318 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.540 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.272 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.354 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.560 |
MOD_GlcNHglycan | 14 | 18 | PF01048 | 0.492 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.492 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.618 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.552 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.322 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.406 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.318 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.653 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.457 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.557 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.517 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.754 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.418 |
MOD_NEK2_2 | 422 | 427 | PF00069 | 0.525 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.360 |
MOD_PK_1 | 417 | 423 | PF00069 | 0.336 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.705 |
MOD_PKA_1 | 235 | 241 | PF00069 | 0.360 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.630 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.714 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.360 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.320 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.587 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.660 |
MOD_PKB_1 | 133 | 141 | PF00069 | 0.595 |
MOD_PKB_1 | 227 | 235 | PF00069 | 0.434 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.365 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.436 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.345 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.356 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.279 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.458 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.291 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.305 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.664 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.740 |
MOD_SUMO_for_1 | 272 | 275 | PF00179 | 0.231 |
TRG_DiLeu_BaEn_2 | 146 | 152 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 226 | 229 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.522 |
TRG_NLS_MonoExtN_4 | 136 | 143 | PF00514 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 67 | 72 | PF00026 | 0.320 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P559 | Leptomonas seymouri | 66% | 99% |
A0A0S4JM78 | Bodo saltans | 29% | 100% |
A0A1X0P5J7 | Trypanosomatidae | 49% | 97% |
A0A3Q8IJK4 | Leishmania donovani | 92% | 100% |
A0A422MXB6 | Trypanosoma rangeli | 47% | 100% |
A4HMX6 | Leishmania braziliensis | 80% | 100% |
A4IBK0 | Leishmania infantum | 92% | 100% |
C9ZZ44 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AFD3 | Leishmania major | 90% | 100% |
V5DUR2 | Trypanosoma cruzi | 45% | 100% |