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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 19 |
GO:0042995 | cell projection | 2 | 19 |
GO:0043226 | organelle | 2 | 19 |
GO:0043227 | membrane-bounded organelle | 3 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 19 |
GO:0005743 | mitochondrial inner membrane | 5 | 1 |
GO:0016020 | membrane | 2 | 2 |
GO:0019866 | organelle inner membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031966 | mitochondrial membrane | 4 | 1 |
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 |
Related structures:
AlphaFold database: Q4QFY4
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 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
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 | 1 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.376 |
CLV_Separin_Metazoa | 406 | 410 | PF03568 | 0.395 |
DEG_APCC_DBOX_1 | 134 | 142 | PF00400 | 0.280 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.619 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.545 |
DOC_CDC14_PxL_1 | 199 | 207 | PF14671 | 0.385 |
DOC_CDC14_PxL_1 | 332 | 340 | PF14671 | 0.438 |
DOC_CDC14_PxL_1 | 377 | 385 | PF14671 | 0.332 |
DOC_CDC14_PxL_1 | 422 | 430 | PF14671 | 0.465 |
DOC_CYCLIN_RxL_1 | 133 | 144 | PF00134 | 0.257 |
DOC_CYCLIN_RxL_1 | 277 | 286 | PF00134 | 0.332 |
DOC_CYCLIN_RxL_1 | 72 | 83 | PF00134 | 0.377 |
DOC_MAPK_DCC_7 | 148 | 156 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 72 | 81 | PF00069 | 0.419 |
DOC_MAPK_HePTP_8 | 69 | 81 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 139 | 147 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 148 | 156 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.461 |
DOC_PP1_RVXF_1 | 315 | 321 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 442 | 445 | PF13499 | 0.283 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.398 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 190 | 199 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 252 | 261 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 369 | 377 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 9 | 15 | PF00244 | 0.457 |
LIG_Actin_WH2_2 | 325 | 341 | PF00022 | 0.457 |
LIG_Actin_WH2_2 | 36 | 54 | PF00022 | 0.490 |
LIG_Clathr_ClatBox_1 | 157 | 161 | PF01394 | 0.281 |
LIG_CtBP_PxDLS_1 | 444 | 448 | PF00389 | 0.283 |
LIG_DLG_GKlike_1 | 139 | 146 | PF00625 | 0.317 |
LIG_DLG_GKlike_1 | 280 | 287 | PF00625 | 0.320 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.331 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.513 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.515 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.323 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.338 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.473 |
LIG_GBD_Chelix_1 | 65 | 73 | PF00786 | 0.379 |
LIG_Integrin_RGD_1 | 120 | 122 | PF01839 | 0.351 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 387 | 396 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.449 |
LIG_MYND_1 | 445 | 449 | PF01753 | 0.304 |
LIG_NRBOX | 64 | 70 | PF00104 | 0.374 |
LIG_NRBOX | 76 | 82 | PF00104 | 0.337 |
LIG_RPA_C_Fungi | 185 | 197 | PF08784 | 0.288 |
LIG_RPA_C_Fungi | 5 | 17 | PF08784 | 0.330 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.416 |
LIG_SH2_PTP2 | 430 | 433 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.268 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.302 |
LIG_SUMO_SIM_anti_2 | 142 | 147 | PF11976 | 0.330 |
LIG_SUMO_SIM_anti_2 | 254 | 262 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 272 | 277 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 404 | 409 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 279 | 286 | PF11976 | 0.462 |
LIG_TYR_ITIM | 428 | 433 | PF00017 | 0.272 |
MOD_CDK_SPK_2 | 445 | 450 | PF00069 | 0.338 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.396 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.507 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.373 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.420 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.313 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.428 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.485 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.503 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.640 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.427 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.276 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.388 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.487 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.314 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.386 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.464 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.454 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.426 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.405 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.311 |
MOD_LATS_1 | 250 | 256 | PF00433 | 0.283 |
MOD_LATS_1 | 292 | 298 | PF00433 | 0.375 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.490 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.463 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.394 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.388 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.549 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.323 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.634 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.607 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.318 |
MOD_PK_1 | 206 | 212 | PF00069 | 0.253 |
MOD_PK_1 | 294 | 300 | PF00069 | 0.310 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.490 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.582 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.490 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.437 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.618 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.383 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.413 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.393 |
MOD_Plk_2-3 | 316 | 322 | PF00069 | 0.391 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.472 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.420 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.301 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.282 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.463 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.499 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.445 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.400 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.354 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.509 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.530 |
MOD_SUMO_rev_2 | 209 | 214 | PF00179 | 0.334 |
TRG_DiLeu_BaLyEn_6 | 27 | 32 | PF01217 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 277 | 282 | PF01217 | 0.327 |
TRG_DiLeu_BaLyEn_6 | 60 | 65 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 75 | 80 | PF01217 | 0.486 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.268 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.303 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.349 |
TRG_NES_CRM1_1 | 201 | 211 | PF08389 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.248 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 78 | 82 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F9 | Leptomonas seymouri | 35% | 87% |
A0A0N0P8N9 | Leptomonas seymouri | 32% | 69% |
A0A0N1I0W0 | Leptomonas seymouri | 27% | 89% |
A0A0N1I1E8 | Leptomonas seymouri | 27% | 100% |
A0A1X0NEN5 | Trypanosomatidae | 27% | 78% |
A0A1X0P4M6 | Trypanosomatidae | 25% | 79% |
A0A3Q8I8N4 | Leishmania donovani | 94% | 100% |
A0A3S5H5M6 | Leishmania donovani | 24% | 85% |
A4H3R1 | Leishmania braziliensis | 30% | 66% |
A4H7G0 | Leishmania braziliensis | 78% | 99% |
A4HCY0 | Leishmania braziliensis | 28% | 98% |
A4HSP5 | Leishmania infantum | 24% | 85% |
E9AGK6 | Leishmania infantum | 94% | 100% |
E9AKN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 85% |
E9APJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
E9B1R3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 73% |
Q4QB46 | Leishmania major | 25% | 94% |