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: 15 |
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: 9, no: 9 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HJN0
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 19 |
GO:0008152 | metabolic process | 1 | 19 |
GO:0044238 | primary metabolic process | 2 | 19 |
GO:0071704 | organic substance metabolic process | 2 | 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004806 | triglyceride lipase activity | 5 | 9 |
GO:0016298 | lipase activity | 4 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 10 |
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 | 112 | 116 | PF00656 | 0.172 |
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.143 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.309 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.408 |
DOC_MAPK_DCC_7 | 229 | 238 | PF00069 | 0.143 |
DOC_PP1_RVXF_1 | 62 | 69 | PF00149 | 0.224 |
DOC_PP4_FxxP_1 | 241 | 244 | PF00568 | 0.231 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.171 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.282 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.314 |
DOC_USP7_MATH_2 | 352 | 358 | PF00917 | 0.345 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.260 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.216 |
LIG_14-3-3_CanoR_1 | 266 | 274 | PF00244 | 0.227 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.596 |
LIG_Clathr_ClatBox_1 | 358 | 362 | PF01394 | 0.274 |
LIG_EH1_1 | 172 | 180 | PF00400 | 0.143 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.318 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.216 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.322 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.236 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.285 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.390 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.295 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.395 |
LIG_GBD_Chelix_1 | 3 | 11 | PF00786 | 0.308 |
LIG_LIR_Apic_2 | 139 | 144 | PF02991 | 0.226 |
LIG_LIR_Apic_2 | 240 | 244 | PF02991 | 0.239 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 184 | 189 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 354 | 364 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 184 | 188 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.353 |
LIG_LYPXL_SIV_4 | 163 | 171 | PF13949 | 0.143 |
LIG_MYND_1 | 275 | 279 | PF01753 | 0.160 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.298 |
LIG_Pex14_1 | 141 | 145 | PF04695 | 0.194 |
LIG_PTB_Apo_2 | 245 | 252 | PF02174 | 0.238 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.327 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.328 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.253 |
LIG_SH2_CRK | 356 | 360 | PF00017 | 0.263 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.321 |
LIG_SH2_GRB2like | 101 | 104 | PF00017 | 0.327 |
LIG_SH2_PTP2 | 284 | 287 | PF00017 | 0.270 |
LIG_SH2_SRC | 284 | 287 | PF00017 | 0.225 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.244 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.242 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.222 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.261 |
LIG_SUMO_SIM_par_1 | 23 | 28 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 234 | 240 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.363 |
LIG_TRFH_1 | 349 | 353 | PF08558 | 0.372 |
LIG_TYR_ITIM | 167 | 172 | PF00017 | 0.170 |
LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.265 |
LIG_UBA3_1 | 37 | 44 | PF00899 | 0.306 |
LIG_WRC_WIRS_1 | 238 | 243 | PF05994 | 0.249 |
MOD_CDK_SPxxK_3 | 89 | 96 | PF00069 | 0.205 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.654 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.276 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.275 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.152 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.274 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.319 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.345 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.244 |
MOD_Cter_Amidation | 61 | 64 | PF01082 | 0.377 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.508 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.398 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.425 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.506 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.585 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.310 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.209 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.167 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.265 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.326 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.441 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.473 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.509 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.455 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.533 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.498 |
MOD_N-GLC_2 | 152 | 154 | PF02516 | 0.507 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.251 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.268 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.261 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.192 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.277 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.291 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.308 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.306 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.266 |
MOD_NEK2_2 | 163 | 168 | PF00069 | 0.271 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.306 |
MOD_NEK2_2 | 314 | 319 | PF00069 | 0.286 |
MOD_PK_1 | 44 | 50 | PF00069 | 0.299 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.230 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.225 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.288 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.298 |
MOD_Plk_2-3 | 174 | 180 | PF00069 | 0.143 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.231 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.325 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.350 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.230 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.289 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.234 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.498 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.279 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.254 |
TRG_DiLeu_BaEn_1 | 354 | 359 | PF01217 | 0.194 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.270 |
TRG_ER_diArg_1 | 367 | 370 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0D0 | Leptomonas seymouri | 55% | 100% |
A0A0S4IJE8 | Bodo saltans | 33% | 100% |
A0A0S4J5D7 | Bodo saltans | 38% | 100% |
A0A0S4JTA1 | Bodo saltans | 38% | 100% |
A0A1X0NZH3 | Trypanosomatidae | 37% | 88% |
A0A1X0P001 | Trypanosomatidae | 36% | 100% |
A0A3Q8IFI3 | Leishmania donovani | 60% | 100% |
A0A3Q8IG97 | Leishmania donovani | 32% | 100% |
A0A422NPJ5 | Trypanosoma rangeli | 34% | 75% |
A4HLK7 | Leishmania braziliensis | 35% | 100% |
A4I6H7 | Leishmania infantum | 32% | 100% |
A4I752 | Leishmania infantum | 60% | 100% |
C9ZME7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9B246 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
P19515 | Rhizomucor miehei | 33% | 100% |
P61871 | Rhizopus niveus | 31% | 95% |
P61872 | Rhizopus oryzae | 31% | 95% |
Q4Q615 | Leishmania major | 59% | 100% |
Q4Q6I0 | Leishmania major | 34% | 100% |
Q9BHD5 | Leishmania major | 39% | 100% |
Q9XTR8 | Caenorhabditis elegans | 25% | 100% |
V5B761 | Trypanosoma cruzi | 38% | 100% |