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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 11 |
GO:0042995 | cell projection | 2 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 11 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
GO:0005743 | mitochondrial inner membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0019866 | organelle inner membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
Related structures:
AlphaFold database: E9B4G8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 4 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 3 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 3 |
GO:0016310 | phosphorylation | 5 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016301 | kinase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.302 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.350 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.373 |
DEG_APCC_DBOX_1 | 98 | 106 | PF00400 | 0.427 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.384 |
DEG_ODPH_VHL_1 | 127 | 139 | PF01847 | 0.348 |
DEG_SCF_FBW7_1 | 232 | 239 | PF00400 | 0.316 |
DOC_CYCLIN_RxL_1 | 179 | 189 | PF00134 | 0.313 |
DOC_CYCLIN_RxL_1 | 226 | 235 | PF00134 | 0.379 |
DOC_CYCLIN_RxL_1 | 272 | 283 | PF00134 | 0.444 |
DOC_MAPK_gen_1 | 214 | 221 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 247 | 256 | PF00069 | 0.207 |
DOC_MAPK_MEF2A_6 | 317 | 326 | PF00069 | 0.283 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.373 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.248 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.312 |
LIG_14-3-3_CanoR_1 | 355 | 362 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 369 | 374 | PF00244 | 0.209 |
LIG_BIR_III_4 | 379 | 383 | PF00653 | 0.319 |
LIG_BRCT_BRCA1_1 | 162 | 166 | PF00533 | 0.329 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.408 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.468 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.492 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.328 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.354 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.499 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.372 |
LIG_GBD_Chelix_1 | 318 | 326 | PF00786 | 0.315 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 367 | 378 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.457 |
LIG_NRBOX | 226 | 232 | PF00104 | 0.316 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.331 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.623 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.558 |
LIG_SUMO_SIM_anti_2 | 207 | 212 | PF11976 | 0.305 |
LIG_SUMO_SIM_anti_2 | 344 | 352 | PF11976 | 0.267 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.326 |
LIG_Vh1_VBS_1 | 339 | 357 | PF01044 | 0.472 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.409 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.451 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.295 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.370 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.434 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.374 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.339 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.363 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.316 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.253 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.507 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.424 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.432 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.388 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.408 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.375 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.546 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.594 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.341 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.365 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.471 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.377 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.459 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.461 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.640 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.400 |
MOD_N-GLC_2 | 140 | 142 | PF02516 | 0.223 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.683 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.458 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.422 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.336 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.322 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.348 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.521 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.288 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.422 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.509 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.335 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.417 |
MOD_NEK2_2 | 364 | 369 | PF00069 | 0.327 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.363 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.442 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.373 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.515 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.397 |
MOD_Plk_2-3 | 86 | 92 | PF00069 | 0.398 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.309 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.327 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.321 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.241 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.496 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.322 |
TRG_DiLeu_BaEn_1 | 226 | 231 | PF01217 | 0.245 |
TRG_DiLeu_LyEn_5 | 226 | 231 | PF01217 | 0.245 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.229 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 182 | 187 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 99 | 103 | PF00026 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRL6 | Bodo saltans | 27% | 100% |
A0A0S4ITQ8 | Bodo saltans | 23% | 86% |
A0A0S4KN43 | Bodo saltans | 27% | 72% |
A0A3S7X7D2 | Leishmania donovani | 87% | 94% |
A4I9H0 | Leishmania infantum | 87% | 94% |
C9ZRQ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 79% |
C9ZXN7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 86% |
Q4Q3K7 | Leishmania major | 87% | 100% |
V5BMQ2 | Trypanosoma cruzi | 23% | 75% |