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: A0A3Q8IF78
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 | 217 | 221 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.494 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.578 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.557 |
DOC_CYCLIN_RxL_1 | 186 | 195 | PF00134 | 0.555 |
DOC_CYCLIN_RxL_1 | 85 | 93 | PF00134 | 0.563 |
DOC_CYCLIN_yCln2_LP_2 | 177 | 183 | PF00134 | 0.615 |
DOC_CYCLIN_yCln2_LP_2 | 187 | 193 | PF00134 | 0.442 |
DOC_MAPK_MEF2A_6 | 127 | 136 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 291 | 299 | PF00069 | 0.366 |
DOC_PP1_RVXF_1 | 187 | 194 | PF00149 | 0.565 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.411 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.692 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.646 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 252 | 257 | PF00244 | 0.565 |
LIG_Actin_WH2_2 | 207 | 225 | PF00022 | 0.454 |
LIG_APCC_ABBA_1 | 147 | 152 | PF00400 | 0.372 |
LIG_BIR_III_4 | 93 | 97 | PF00653 | 0.470 |
LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.592 |
LIG_CaM_NSCaTE_8 | 230 | 237 | PF13499 | 0.461 |
LIG_Clathr_ClatBox_1 | 211 | 215 | PF01394 | 0.446 |
LIG_Clathr_ClatBox_1 | 309 | 313 | PF01394 | 0.450 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.427 |
LIG_eIF4E_1 | 42 | 48 | PF01652 | 0.538 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.607 |
LIG_HCF-1_HBM_1 | 203 | 206 | PF13415 | 0.436 |
LIG_LIR_Gen_1 | 152 | 159 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.521 |
LIG_MYND_1 | 349 | 353 | PF01753 | 0.543 |
LIG_NRBOX | 207 | 213 | PF00104 | 0.443 |
LIG_NRBOX | 86 | 92 | PF00104 | 0.507 |
LIG_Pex14_1 | 202 | 206 | PF04695 | 0.356 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.556 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 42 | 46 | PF00017 | 0.694 |
LIG_SH2_STAT3 | 78 | 81 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.538 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.571 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.549 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.673 |
LIG_SUMO_SIM_par_1 | 307 | 314 | PF11976 | 0.439 |
LIG_SxIP_EBH_1 | 329 | 339 | PF03271 | 0.466 |
MOD_CDC14_SPxK_1 | 179 | 182 | PF00782 | 0.579 |
MOD_CDK_SPK_2 | 349 | 354 | PF00069 | 0.479 |
MOD_CDK_SPxK_1 | 176 | 182 | PF00069 | 0.581 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.574 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.692 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.546 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.633 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.620 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.423 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.730 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.687 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.682 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.619 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.686 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.712 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.560 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.616 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.473 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.687 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.726 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.733 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.710 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.485 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.440 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.470 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.703 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.679 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.492 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.623 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.509 |
MOD_PKB_1 | 275 | 283 | PF00069 | 0.461 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.470 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.682 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.693 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.582 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.743 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.699 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.642 |
MOD_SUMO_for_1 | 243 | 246 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 20 | 25 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 189 | 194 | PF00026 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 88 | 93 | PF00026 | 0.586 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1T2 | Leptomonas seymouri | 34% | 99% |
A0A3R7K7C7 | Trypanosoma rangeli | 30% | 100% |
A4HE11 | Leishmania braziliensis | 70% | 98% |
A4I1B8 | Leishmania infantum | 97% | 98% |
D0A5L2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AXF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
Q4QA18 | Leishmania major | 90% | 98% |