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: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9ARI1
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0006644 | phospholipid metabolic process | 4 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044255 | cellular lipid metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0008195 | phosphatidate phosphatase activity | 6 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016791 | phosphatase activity | 5 | 8 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.594 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.378 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.433 |
DEG_ODPH_VHL_1 | 334 | 345 | PF01847 | 0.217 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.695 |
DOC_CYCLIN_yCln2_LP_2 | 337 | 343 | PF00134 | 0.507 |
DOC_MAPK_DCC_7 | 329 | 339 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 321 | 327 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 150 | 158 | PF00069 | 0.659 |
DOC_PP1_RVXF_1 | 289 | 295 | PF00149 | 0.294 |
DOC_PP2B_LxvP_1 | 337 | 340 | PF13499 | 0.507 |
DOC_PP4_FxxP_1 | 137 | 140 | PF00568 | 0.639 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.217 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.217 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.333 |
LIG_14-3-3_CanoR_1 | 160 | 167 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 218 | 223 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 291 | 295 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 322 | 328 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 42 | 47 | PF00244 | 0.340 |
LIG_BRCT_BRCA1_1 | 242 | 246 | PF00533 | 0.334 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.294 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.357 |
LIG_BRCT_BRCA1_1 | 57 | 61 | PF00533 | 0.347 |
LIG_EH1_1 | 310 | 318 | PF00400 | 0.217 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.702 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.208 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.438 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.612 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.449 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.333 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.277 |
LIG_IRF3_LxIS_1 | 29 | 35 | PF10401 | 0.217 |
LIG_LIR_Apic_2 | 136 | 140 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 45 | 49 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 103 | 113 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 282 | 287 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 300 | 311 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 63 | 72 | PF02991 | 0.217 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.217 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.578 |
LIG_Pex14_2 | 242 | 246 | PF04695 | 0.315 |
LIG_PTB_Apo_2 | 348 | 355 | PF02174 | 0.208 |
LIG_PTB_Phospho_1 | 348 | 354 | PF10480 | 0.208 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.455 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.645 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.333 |
LIG_SUMO_SIM_anti_2 | 153 | 158 | PF11976 | 0.656 |
LIG_SUMO_SIM_anti_2 | 65 | 70 | PF11976 | 0.214 |
LIG_SUMO_SIM_par_1 | 155 | 161 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 341 | 346 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 368 | 374 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 63 | 70 | PF11976 | 0.217 |
LIG_UBA3_1 | 250 | 255 | PF00899 | 0.217 |
LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.408 |
MOD_CDC14_SPxK_1 | 211 | 214 | PF00782 | 0.670 |
MOD_CDK_SPxK_1 | 208 | 214 | PF00069 | 0.676 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.718 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.672 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.712 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.246 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.578 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.658 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.274 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.486 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.451 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.442 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.494 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.337 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.195 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.508 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.375 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.278 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.668 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.443 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.347 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.333 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.294 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.344 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.296 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.452 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.627 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.281 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.354 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.516 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.441 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.526 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.392 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.294 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.578 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.266 |
MOD_PKB_1 | 216 | 224 | PF00069 | 0.576 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.299 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.584 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.398 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.683 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.747 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.676 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.333 |
MOD_SUMO_rev_2 | 99 | 107 | PF00179 | 0.622 |
TRG_DiLeu_BaEn_1 | 103 | 108 | PF01217 | 0.576 |
TRG_DiLeu_BaEn_1 | 153 | 158 | PF01217 | 0.681 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.294 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WUU8 | Leishmania donovani | 68% | 94% |
A4H9E7 | Leishmania braziliensis | 50% | 97% |
A4H9F0 | Leishmania braziliensis | 49% | 97% |
A4HXR9 | Leishmania infantum | 69% | 94% |
D0A051 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4QDZ8 | Leishmania major | 66% | 100% |