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: A4HE11
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 | 214 | 218 | PF00656 | 0.435 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.484 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.524 |
DEG_SCF_FBW7_1 | 22 | 29 | PF00400 | 0.493 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.450 |
DOC_CYCLIN_RxL_1 | 183 | 192 | PF00134 | 0.511 |
DOC_CYCLIN_RxL_1 | 87 | 95 | PF00134 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 184 | 190 | PF00134 | 0.395 |
DOC_PP1_RVXF_1 | 184 | 191 | PF00149 | 0.516 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.574 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 287 | 296 | PF00244 | 0.366 |
LIG_Actin_WH2_2 | 204 | 222 | PF00022 | 0.516 |
LIG_BIR_III_4 | 309 | 313 | PF00653 | 0.326 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.622 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.452 |
LIG_CaM_NSCaTE_8 | 227 | 234 | PF13499 | 0.435 |
LIG_Clathr_ClatBox_1 | 208 | 212 | PF01394 | 0.394 |
LIG_Clathr_ClatBox_1 | 305 | 309 | PF01394 | 0.421 |
LIG_eIF4E_1 | 203 | 209 | PF01652 | 0.364 |
LIG_eIF4E_1 | 44 | 50 | PF01652 | 0.398 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.399 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.413 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.475 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.457 |
LIG_HCF-1_HBM_1 | 200 | 203 | PF13415 | 0.366 |
LIG_LIR_Gen_1 | 124 | 135 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 145 | 149 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.513 |
LIG_MYND_1 | 345 | 349 | PF01753 | 0.504 |
LIG_NRBOX | 204 | 210 | PF00104 | 0.403 |
LIG_NRBOX | 88 | 94 | PF00104 | 0.411 |
LIG_OCRL_FandH_1 | 8 | 20 | PF00620 | 0.332 |
LIG_Pex14_1 | 199 | 203 | PF04695 | 0.302 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 80 | 83 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.427 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.411 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.468 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.395 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.524 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.430 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.354 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.261 |
LIG_SUMO_SIM_par_1 | 304 | 309 | PF11976 | 0.405 |
LIG_Vh1_VBS_1 | 281 | 299 | PF01044 | 0.254 |
MOD_CDC14_SPxK_1 | 64 | 67 | PF00782 | 0.575 |
MOD_CDK_SPxK_1 | 22 | 28 | PF00069 | 0.486 |
MOD_CDK_SPxK_1 | 61 | 67 | PF00069 | 0.582 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.629 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.532 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.478 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.671 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.498 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.338 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.343 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.664 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.440 |
MOD_GlcNHglycan | 318 | 322 | PF01048 | 0.557 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.578 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.749 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.519 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.560 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.493 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.627 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.677 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.474 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.468 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.632 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.479 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.465 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.663 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.446 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.342 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.359 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.384 |
MOD_NEK2_2 | 289 | 294 | PF00069 | 0.264 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.432 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.646 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.285 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.651 |
MOD_PKB_1 | 271 | 279 | PF00069 | 0.441 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.373 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.482 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.225 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.637 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.469 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.660 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.709 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.375 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.486 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.655 |
MOD_SUMO_for_1 | 240 | 243 | PF00179 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.406 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.448 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 186 | 191 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 90 | 95 | PF00026 | 0.493 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1T2 | Leptomonas seymouri | 38% | 98% |
A0A3Q8IF78 | Leishmania donovani | 70% | 99% |
A0A3R7K7C7 | Trypanosoma rangeli | 30% | 100% |
A4I1B8 | Leishmania infantum | 71% | 100% |
D0A5L2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AXF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QA18 | Leishmania major | 71% | 99% |