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: 7 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AXF4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.529 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.420 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.537 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.480 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.540 |
DOC_AGCK_PIF_2 | 149 | 154 | PF00069 | 0.342 |
DOC_CKS1_1 | 332 | 337 | PF01111 | 0.371 |
DOC_CYCLIN_RxL_1 | 181 | 190 | PF00134 | 0.532 |
DOC_CYCLIN_RxL_1 | 87 | 95 | PF00134 | 0.500 |
DOC_CYCLIN_yCln2_LP_2 | 182 | 188 | PF00134 | 0.415 |
DOC_MAPK_HePTP_8 | 119 | 131 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 122 | 131 | PF00069 | 0.670 |
DOC_MAPK_MEF2A_6 | 288 | 296 | PF00069 | 0.339 |
DOC_PP1_RVXF_1 | 182 | 189 | PF00149 | 0.536 |
DOC_PP2B_LxvP_1 | 289 | 292 | PF13499 | 0.385 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 122 | 126 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.519 |
LIG_Actin_WH2_2 | 202 | 220 | PF00022 | 0.531 |
LIG_APCC_ABBA_1 | 142 | 147 | PF00400 | 0.340 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.547 |
LIG_CaM_NSCaTE_8 | 225 | 232 | PF13499 | 0.437 |
LIG_Clathr_ClatBox_1 | 206 | 210 | PF01394 | 0.405 |
LIG_Clathr_ClatBox_1 | 306 | 310 | PF01394 | 0.431 |
LIG_eIF4E_1 | 201 | 207 | PF01652 | 0.383 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.493 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.525 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.439 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.591 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.472 |
LIG_HCF-1_HBM_1 | 198 | 201 | PF13415 | 0.388 |
LIG_LIR_Gen_1 | 137 | 146 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 147 | 154 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.507 |
LIG_MYND_1 | 346 | 350 | PF01753 | 0.506 |
LIG_MYND_3 | 235 | 239 | PF01753 | 0.406 |
LIG_NRBOX | 202 | 208 | PF00104 | 0.420 |
LIG_NRBOX | 88 | 94 | PF00104 | 0.462 |
LIG_Pex14_1 | 197 | 201 | PF04695 | 0.326 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.518 |
LIG_SH2_SRC | 145 | 148 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.562 |
LIG_SH2_STAT3 | 80 | 83 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.512 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.467 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.450 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.511 |
LIG_SUMO_SIM_par_1 | 304 | 311 | PF11976 | 0.420 |
MOD_CDK_SPxxK_3 | 331 | 338 | PF00069 | 0.409 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.500 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.669 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.581 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.360 |
MOD_DYRK1A_RPxSP_1 | 122 | 126 | PF00069 | 0.458 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.664 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.693 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.532 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.584 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.679 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.557 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.508 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.663 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.295 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.475 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.660 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.695 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.506 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.715 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.471 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.464 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.579 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.377 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.449 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.678 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.655 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.290 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.450 |
MOD_PKB_1 | 272 | 280 | PF00069 | 0.445 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.499 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.628 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.498 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.708 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.677 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.414 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.599 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.378 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 90 | 95 | PF00026 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1T2 | Leptomonas seymouri | 34% | 99% |
A0A3Q8IF78 | Leishmania donovani | 85% | 99% |
A0A3R7K7C7 | Trypanosoma rangeli | 31% | 100% |
A4HE11 | Leishmania braziliensis | 71% | 99% |
A4I1B8 | Leishmania infantum | 87% | 100% |
D0A5L2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
Q4QA18 | Leishmania major | 88% | 99% |