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: 8 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QA18
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 3 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009056 | catabolic process | 2 | 3 |
GO:0009057 | macromolecule catabolic process | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0019538 | protein metabolic process | 3 | 3 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044248 | cellular catabolic process | 3 | 3 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 3 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 3 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
GO:1901575 | organic substance catabolic process | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.449 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 269 | 271 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.600 |
DEG_SPOP_SBC_1 | 59 | 63 | PF00917 | 0.548 |
DOC_CYCLIN_RxL_1 | 179 | 188 | PF00134 | 0.571 |
DOC_CYCLIN_RxL_1 | 85 | 93 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 170 | 176 | PF00134 | 0.589 |
DOC_CYCLIN_yCln2_LP_2 | 180 | 186 | PF00134 | 0.442 |
DOC_MAPK_HePTP_8 | 117 | 129 | PF00069 | 0.625 |
DOC_MAPK_MEF2A_6 | 120 | 129 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 180 | 187 | PF00149 | 0.582 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.406 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.697 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 120 | 124 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 246 | 251 | PF00244 | 0.531 |
LIG_Actin_WH2_2 | 200 | 218 | PF00022 | 0.427 |
LIG_APCC_ABBA_1 | 140 | 145 | PF00400 | 0.314 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.489 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.586 |
LIG_CaM_NSCaTE_8 | 223 | 230 | PF13499 | 0.476 |
LIG_Clathr_ClatBox_1 | 204 | 208 | PF01394 | 0.422 |
LIG_Clathr_ClatBox_1 | 303 | 307 | PF01394 | 0.435 |
LIG_eIF4E_1 | 199 | 205 | PF01652 | 0.396 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.673 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.468 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.662 |
LIG_HCF-1_HBM_1 | 196 | 199 | PF13415 | 0.403 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 145 | 152 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 44 | 54 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 145 | 150 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.555 |
LIG_MYND_1 | 343 | 347 | PF01753 | 0.526 |
LIG_NRBOX | 200 | 206 | PF00104 | 0.440 |
LIG_NRBOX | 86 | 92 | PF00104 | 0.499 |
LIG_Pex14_1 | 195 | 199 | PF04695 | 0.326 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.495 |
LIG_SH2_SRC | 143 | 146 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 42 | 46 | PF00017 | 0.631 |
LIG_SH2_STAT3 | 78 | 81 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.498 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.484 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.530 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.621 |
LIG_SUMO_SIM_par_1 | 115 | 123 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 301 | 308 | PF11976 | 0.424 |
MOD_CDC14_SPxK_1 | 172 | 175 | PF00782 | 0.547 |
MOD_CDK_SPK_2 | 343 | 348 | PF00069 | 0.465 |
MOD_CDK_SPxK_1 | 169 | 175 | PF00069 | 0.557 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.656 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.674 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.655 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.473 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.604 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.363 |
MOD_DYRK1A_RPxSP_1 | 120 | 124 | PF00069 | 0.452 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.698 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.600 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.597 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.599 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.685 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.546 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.542 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.447 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.701 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.743 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.635 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.456 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.648 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.483 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.376 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.443 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.621 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.641 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.279 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.297 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.446 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.619 |
MOD_PKB_1 | 269 | 277 | PF00069 | 0.467 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.458 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.588 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.705 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.546 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.659 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.657 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.729 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.661 |
MOD_SUMO_for_1 | 236 | 239 | PF00179 | 0.597 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.396 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 182 | 187 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 88 | 93 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1T2 | Leptomonas seymouri | 36% | 98% |
A0A1X0P4E3 | Trypanosomatidae | 27% | 100% |
A0A3Q8IF78 | Leishmania donovani | 90% | 98% |
A0A3R7K7C7 | Trypanosoma rangeli | 30% | 100% |
A4HE11 | Leishmania braziliensis | 71% | 99% |
A4I1B8 | Leishmania infantum | 92% | 100% |
D0A5L2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AXF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |