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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HQA8
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 9 |
GO:0006644 | phospholipid metabolic process | 4 | 9 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0008610 | lipid biosynthetic process | 4 | 9 |
GO:0008654 | phospholipid biosynthetic process | 5 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0019637 | organophosphate metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 9 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046337 | phosphatidylethanolamine metabolic process | 6 | 1 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090407 | organophosphate biosynthetic process | 4 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004142 | diacylglycerol cholinephosphotransferase activity | 6 | 4 |
GO:0004307 | ethanolaminephosphotransferase activity | 6 | 8 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 12 |
GO:0017169 | CDP-alcohol phosphatidyltransferase activity | 5 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.431 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.340 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.299 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.347 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.588 |
DOC_AGCK_PIF_1 | 102 | 107 | PF00069 | 0.166 |
DOC_CDC14_PxL_1 | 282 | 290 | PF14671 | 0.220 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.247 |
DOC_CKS1_1 | 152 | 157 | PF01111 | 0.247 |
DOC_CKS1_1 | 212 | 217 | PF01111 | 0.280 |
DOC_MAPK_MEF2A_6 | 245 | 252 | PF00069 | 0.349 |
DOC_MAPK_NFAT4_5 | 245 | 253 | PF00069 | 0.220 |
DOC_PP1_RVXF_1 | 243 | 250 | PF00149 | 0.330 |
DOC_PP1_RVXF_1 | 303 | 309 | PF00149 | 0.186 |
DOC_PP1_RVXF_1 | 370 | 377 | PF00149 | 0.234 |
DOC_PP4_FxxP_1 | 138 | 141 | PF00568 | 0.262 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.175 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.247 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.361 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 326 | 330 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 331 | 335 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.570 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.281 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.423 |
LIG_deltaCOP1_diTrp_1 | 157 | 167 | PF00928 | 0.166 |
LIG_eIF4E_1 | 99 | 105 | PF01652 | 0.247 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.248 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.476 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.336 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.357 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.405 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.218 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.279 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.299 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.410 |
LIG_IRF3_LxIS_1 | 400 | 407 | PF10401 | 0.536 |
LIG_LIR_Apic_2 | 136 | 141 | PF02991 | 0.421 |
LIG_LIR_Apic_2 | 151 | 155 | PF02991 | 0.262 |
LIG_LIR_Apic_2 | 16 | 22 | PF02991 | 0.581 |
LIG_LIR_Apic_2 | 209 | 215 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 163 | 172 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 246 | 257 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 339 | 350 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 35 | 46 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 382 | 392 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 96 | 107 | PF02991 | 0.190 |
LIG_LIR_Nem_3 | 101 | 105 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.204 |
LIG_LIR_Nem_3 | 163 | 167 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 382 | 387 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.390 |
LIG_LYPXL_SIV_4 | 223 | 231 | PF13949 | 0.223 |
LIG_PCNA_PIPBox_1 | 153 | 162 | PF02747 | 0.264 |
LIG_PCNA_yPIPBox_3 | 146 | 158 | PF02747 | 0.323 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.180 |
LIG_Pex14_1 | 95 | 99 | PF04695 | 0.247 |
LIG_Pex14_2 | 138 | 142 | PF04695 | 0.367 |
LIG_Pex14_2 | 170 | 174 | PF04695 | 0.262 |
LIG_Rb_pABgroove_1 | 125 | 133 | PF01858 | 0.410 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.262 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.358 |
LIG_SH2_GRB2like | 186 | 189 | PF00017 | 0.533 |
LIG_SH2_GRB2like | 403 | 406 | PF00017 | 0.480 |
LIG_SH2_GRB2like | 49 | 52 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.379 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.556 |
LIG_SH2_SRC | 186 | 189 | PF00017 | 0.533 |
LIG_SH2_SRC | 19 | 22 | PF00017 | 0.556 |
LIG_SH2_SRC | 403 | 406 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 99 | 103 | PF00017 | 0.262 |
LIG_SH2_STAT3 | 44 | 47 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.237 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.593 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.313 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.504 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.340 |
LIG_SUMO_SIM_anti_2 | 76 | 83 | PF11976 | 0.167 |
LIG_SUMO_SIM_par_1 | 318 | 323 | PF11976 | 0.276 |
LIG_UBA3_1 | 408 | 415 | PF00899 | 0.536 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.166 |
LIG_WRC_WIRS_1 | 99 | 104 | PF05994 | 0.430 |
LIG_WW_1 | 21 | 24 | PF00397 | 0.511 |
MOD_CDK_SPxxK_3 | 151 | 158 | PF00069 | 0.238 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.374 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.237 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.320 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.468 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.484 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.442 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.489 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.299 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.351 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.454 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.503 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.276 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.458 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.282 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.585 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.244 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.251 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.513 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.359 |
MOD_N-GLC_1 | 361 | 366 | PF02516 | 0.427 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.280 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.441 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.243 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.276 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.219 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.296 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.248 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.409 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.288 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.467 |
MOD_NEK2_2 | 93 | 98 | PF00069 | 0.169 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.437 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.591 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.438 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.549 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.272 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.582 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.403 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.214 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.476 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.345 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.441 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.375 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.320 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.337 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.457 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.330 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.348 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.452 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.175 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.247 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.363 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.442 |
MOD_SUMO_rev_2 | 111 | 118 | PF00179 | 0.410 |
TRG_DiLeu_BaEn_1 | 157 | 162 | PF01217 | 0.190 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.162 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.259 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.277 |
TRG_ER_diLys_1 | 412 | 417 | PF00400 | 0.621 |
TRG_NLS_MonoExtN_4 | 26 | 33 | PF00514 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I260 | Leptomonas seymouri | 63% | 100% |
A0A0S4JA45 | Bodo saltans | 37% | 95% |
A0A1X0NLI0 | Trypanosomatidae | 51% | 92% |
A0A3Q8IRT0 | Leishmania donovani | 80% | 100% |
A0A3R7NAX1 | Trypanosoma rangeli | 47% | 97% |
A4IE03 | Leishmania infantum | 80% | 100% |
D0A400 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 97% |
E9AU25 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
O82567 | Arabidopsis thaliana | 31% | 100% |
O82568 | Arabidopsis thaliana | 31% | 100% |
P17898 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q17QM4 | Bos taurus | 27% | 100% |
Q4Q0H0 | Leishmania major | 81% | 100% |
Q550W1 | Dictyostelium discoideum | 29% | 100% |
Q55AQ3 | Dictyostelium discoideum | 28% | 100% |
Q7ZW02 | Danio rerio | 27% | 100% |
V5B3K4 | Trypanosoma cruzi | 49% | 96% |