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. | yes | yes: 20 |
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 | yes | yes: 10, no: 9 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9B246
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 20 |
GO:0008152 | metabolic process | 1 | 20 |
GO:0044238 | primary metabolic process | 2 | 20 |
GO:0071704 | organic substance metabolic process | 2 | 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004806 | triglyceride lipase activity | 5 | 10 |
GO:0016298 | lipase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 11 |
GO:0004620 | phospholipase activity | 5 | 1 |
GO:0008970 | phospholipase A1 activity | 5 | 1 |
GO:0052739 | phosphatidylserine 1-acylhydrolase activity | 5 | 1 |
GO:0052740 | 1-acyl-2-lysophosphatidylserine acylhydrolase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.304 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.261 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.208 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.380 |
DOC_CYCLIN_RxL_1 | 52 | 60 | PF00134 | 0.209 |
DOC_MAPK_gen_1 | 110 | 116 | PF00069 | 0.370 |
DOC_MAPK_HePTP_8 | 211 | 223 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.260 |
DOC_PP1_RVXF_1 | 53 | 60 | PF00149 | 0.302 |
DOC_PP1_RVXF_1 | 6 | 13 | PF00149 | 0.456 |
DOC_PP4_FxxP_1 | 231 | 234 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.383 |
DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.317 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.256 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.341 |
LIG_14-3-3_CanoR_1 | 148 | 157 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 252 | 256 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 270 | 275 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 47 | 57 | PF00244 | 0.486 |
LIG_deltaCOP1_diTrp_1 | 52 | 59 | PF00928 | 0.281 |
LIG_eIF4E_1 | 172 | 178 | PF01652 | 0.413 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.502 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.444 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.308 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.281 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.413 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.547 |
LIG_GBD_Chelix_1 | 15 | 23 | PF00786 | 0.432 |
LIG_LIR_Apic_2 | 135 | 139 | PF02991 | 0.320 |
LIG_LIR_Apic_2 | 230 | 234 | PF02991 | 0.337 |
LIG_LIR_Apic_2 | 338 | 342 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 152 | 162 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 271 | 281 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 344 | 354 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.494 |
LIG_NRP_CendR_1 | 362 | 363 | PF00754 | 0.504 |
LIG_PCNA_yPIPBox_3 | 8 | 20 | PF02747 | 0.371 |
LIG_Pex14_1 | 54 | 58 | PF04695 | 0.213 |
LIG_PTB_Apo_2 | 125 | 132 | PF02174 | 0.296 |
LIG_PTB_Apo_2 | 235 | 242 | PF02174 | 0.334 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.458 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 92 | 95 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 339 | 343 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.340 |
LIG_SH3_2 | 265 | 270 | PF14604 | 0.413 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.520 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.313 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.382 |
LIG_SUMO_SIM_anti_2 | 164 | 169 | PF11976 | 0.284 |
LIG_SUMO_SIM_anti_2 | 245 | 250 | PF11976 | 0.257 |
LIG_SUMO_SIM_anti_2 | 33 | 42 | PF11976 | 0.590 |
LIG_SUMO_SIM_par_1 | 224 | 230 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 347 | 353 | PF11976 | 0.530 |
LIG_TRFH_1 | 339 | 343 | PF08558 | 0.516 |
LIG_TYR_ITIM | 317 | 322 | PF00017 | 0.372 |
LIG_WRC_WIRS_1 | 228 | 233 | PF05994 | 0.350 |
LIG_WW_3 | 267 | 271 | PF00397 | 0.413 |
MOD_CDK_SPxxK_3 | 80 | 87 | PF00069 | 0.272 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.348 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.403 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.213 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.382 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.476 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.423 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.505 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.407 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.434 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.291 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.380 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.642 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.452 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.556 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.432 |
MOD_N-GLC_1 | 358 | 363 | PF02516 | 0.678 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.462 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.394 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.335 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.343 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.376 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.364 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.408 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.364 |
MOD_NEK2_2 | 153 | 158 | PF00069 | 0.378 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.428 |
MOD_NEK2_2 | 251 | 256 | PF00069 | 0.298 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.395 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.251 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.334 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.324 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.341 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.275 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.402 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.276 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.187 |
MOD_Plk_2-3 | 335 | 341 | PF00069 | 0.422 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.580 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.454 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.640 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.321 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.461 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.400 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.287 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.336 |
MOD_SUMO_rev_2 | 29 | 39 | PF00179 | 0.367 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.314 |
TRG_NES_CRM1_1 | 340 | 353 | PF08389 | 0.354 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0D0 | Leptomonas seymouri | 54% | 100% |
A0A0S4IJE8 | Bodo saltans | 38% | 100% |
A0A0S4J5D7 | Bodo saltans | 38% | 100% |
A0A0S4JTA1 | Bodo saltans | 38% | 100% |
A0A1X0NZH3 | Trypanosomatidae | 38% | 86% |
A0A1X0P001 | Trypanosomatidae | 36% | 100% |
A0A3Q8IFI3 | Leishmania donovani | 77% | 99% |
A0A3Q8IG97 | Leishmania donovani | 33% | 100% |
A0A422NPJ5 | Trypanosoma rangeli | 37% | 73% |
A2QSY5 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 28% | 100% |
A4HJN0 | Leishmania braziliensis | 58% | 100% |
A4HLK7 | Leishmania braziliensis | 37% | 100% |
A4I6H7 | Leishmania infantum | 33% | 100% |
A4I752 | Leishmania infantum | 77% | 99% |
C9ZME7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 99% |
O42807 | Aspergillus niger | 28% | 100% |
O59952 | Thermomyces lanuginosus | 30% | 100% |
P61869 | Penicillium cyclopium | 30% | 100% |
P61870 | Penicillium camembertii | 30% | 100% |
P61871 | Rhizopus niveus | 31% | 93% |
P61872 | Rhizopus oryzae | 31% | 93% |
Q4Q615 | Leishmania major | 74% | 100% |
Q4Q6I0 | Leishmania major | 32% | 100% |
Q9BHD5 | Leishmania major | 39% | 100% |
Q9XTR8 | Caenorhabditis elegans | 28% | 100% |
V5B761 | Trypanosoma cruzi | 41% | 100% |