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: 9 |
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:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HF17
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006644 | phospholipid metabolic process | 4 | 12 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0008654 | phospholipid biosynthetic process | 5 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016024 | CDP-diacylglycerol biosynthetic process | 6 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 12 |
GO:0046341 | CDP-diacylglycerol metabolic process | 6 | 12 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 12 |
GO:0046486 | glycerolipid metabolic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090407 | organophosphate biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:0006655 | phosphatidylglycerol biosynthetic process | 6 | 1 |
GO:0046471 | phosphatidylglycerol metabolic process | 6 | 1 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004605 | phosphatidate cytidylyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0070567 | cytidylyltransferase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.739 |
CLV_MEL_PAP_1 | 84 | 90 | PF00089 | 0.528 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.333 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.446 |
DEG_APCC_DBOX_1 | 239 | 247 | PF00400 | 0.442 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.703 |
DEG_APCC_DBOX_1 | 86 | 94 | PF00400 | 0.441 |
DEG_SPOP_SBC_1 | 46 | 50 | PF00917 | 0.581 |
DOC_CYCLIN_RxL_1 | 236 | 247 | PF00134 | 0.453 |
DOC_MAPK_DCC_7 | 112 | 122 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 112 | 122 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 240 | 246 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 3 | 12 | PF00069 | 0.682 |
DOC_MAPK_MEF2A_6 | 113 | 122 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 5 | 14 | PF00069 | 0.702 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.415 |
DOC_MAPK_NFAT4_5 | 87 | 95 | PF00069 | 0.415 |
DOC_MAPK_RevD_3 | 166 | 179 | PF00069 | 0.301 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.294 |
DOC_PP4_FxxP_1 | 217 | 220 | PF00568 | 0.294 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.718 |
DOC_USP7_UBL2_3 | 353 | 357 | PF12436 | 0.442 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.326 |
LIG_14-3-3_CanoR_1 | 417 | 421 | PF00244 | 0.569 |
LIG_Actin_WH2_2 | 163 | 180 | PF00022 | 0.294 |
LIG_APCC_ABBA_1 | 98 | 103 | PF00400 | 0.264 |
LIG_APCC_ABBAyCdc20_2 | 390 | 396 | PF00400 | 0.573 |
LIG_BRCT_BRCA1_1 | 118 | 122 | PF00533 | 0.528 |
LIG_BRCT_BRCA1_1 | 130 | 134 | PF00533 | 0.234 |
LIG_BRCT_BRCA1_1 | 265 | 269 | PF00533 | 0.379 |
LIG_BRCT_BRCA1_2 | 118 | 124 | PF00533 | 0.528 |
LIG_Clathr_ClatBox_1 | 93 | 97 | PF01394 | 0.441 |
LIG_deltaCOP1_diTrp_1 | 228 | 234 | PF00928 | 0.294 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.220 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.323 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.322 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.714 |
LIG_GBD_Chelix_1 | 420 | 428 | PF00786 | 0.411 |
LIG_LIR_Gen_1 | 131 | 137 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 147 | 155 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 190 | 198 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 336 | 344 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 68 | 78 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 147 | 151 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 336 | 340 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 360 | 364 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 68 | 73 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.315 |
LIG_MAD2 | 8 | 16 | PF02301 | 0.694 |
LIG_PCNA_yPIPBox_3 | 226 | 240 | PF02747 | 0.415 |
LIG_PCNA_yPIPBox_3 | 415 | 425 | PF02747 | 0.580 |
LIG_PDZ_Class_2 | 425 | 430 | PF00595 | 0.636 |
LIG_Pex14_1 | 230 | 234 | PF04695 | 0.294 |
LIG_Pex14_1 | 265 | 269 | PF04695 | 0.296 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.442 |
LIG_Pex14_2 | 255 | 259 | PF04695 | 0.294 |
LIG_Pex14_2 | 261 | 265 | PF04695 | 0.294 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.294 |
LIG_Pex14_2 | 344 | 348 | PF04695 | 0.294 |
LIG_PTB_Apo_2 | 294 | 301 | PF02174 | 0.328 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.347 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.466 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.556 |
LIG_SH2_PTP2 | 132 | 135 | PF00017 | 0.402 |
LIG_SH2_PTP2 | 76 | 79 | PF00017 | 0.329 |
LIG_SH2_STAT3 | 182 | 185 | PF00017 | 0.442 |
LIG_SH2_STAT3 | 275 | 278 | PF00017 | 0.196 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.230 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.298 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.259 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.578 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.628 |
LIG_SUMO_SIM_anti_2 | 7 | 13 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 192 | 199 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 242 | 247 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 94 | 99 | PF11976 | 0.266 |
LIG_TRFH_1 | 155 | 159 | PF08558 | 0.347 |
LIG_TYR_ITAM | 58 | 79 | PF00017 | 0.366 |
LIG_TYR_ITIM | 130 | 135 | PF00017 | 0.409 |
LIG_TYR_ITIM | 59 | 64 | PF00017 | 0.642 |
LIG_UBA3_1 | 172 | 179 | PF00899 | 0.394 |
LIG_UBA3_1 | 243 | 250 | PF00899 | 0.449 |
LIG_WRC_WIRS_1 | 264 | 269 | PF05994 | 0.415 |
LIG_WRC_WIRS_1 | 319 | 324 | PF05994 | 0.309 |
LIG_WRC_WIRS_1 | 334 | 339 | PF05994 | 0.221 |
MOD_CDC14_SPxK_1 | 247 | 250 | PF00782 | 0.442 |
MOD_CDK_SPK_2 | 244 | 249 | PF00069 | 0.442 |
MOD_CDK_SPxK_1 | 244 | 250 | PF00069 | 0.442 |
MOD_CDK_SPxxK_3 | 322 | 329 | PF00069 | 0.328 |
MOD_CMANNOS | 265 | 268 | PF00535 | 0.310 |
MOD_Cter_Amidation | 238 | 241 | PF01082 | 0.347 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.528 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.294 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.538 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.663 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.448 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.294 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.282 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.740 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.676 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.535 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.310 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.180 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.283 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.291 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.342 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.291 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.310 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.309 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.280 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.541 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.298 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.194 |
MOD_PIKK_1 | 419 | 425 | PF00454 | 0.525 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.542 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.757 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.310 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.339 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.453 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.250 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.200 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.264 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.317 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.111 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.605 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.667 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.442 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.326 |
MOD_SUMO_rev_2 | 50 | 59 | PF00179 | 0.713 |
TRG_DiLeu_BaEn_1 | 7 | 12 | PF01217 | 0.572 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.730 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.237 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P387 | Leptomonas seymouri | 82% | 100% |
A0A0S4JNH9 | Bodo saltans | 49% | 100% |
A0A1X0NS18 | Trypanosomatidae | 59% | 100% |
A0A3S7WZX3 | Leishmania donovani | 88% | 100% |
A0A422N205 | Trypanosoma rangeli | 55% | 100% |
A0JNC1 | Bos taurus | 34% | 97% |
A4I295 | Leishmania infantum | 88% | 100% |
C9ZRP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AYE1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O04928 | Arabidopsis thaliana | 37% | 100% |
O04940 | Solanum tuberosum | 40% | 100% |
O35052 | Rattus norvegicus | 38% | 93% |
O49639 | Arabidopsis thaliana | 37% | 100% |
O95674 | Homo sapiens | 35% | 97% |
P38221 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 94% |
P53439 | Caenorhabditis elegans | 35% | 92% |
P56079 | Drosophila melanogaster | 34% | 96% |
P98191 | Mus musculus | 38% | 93% |
Q1PE48 | Arabidopsis thaliana | 37% | 91% |
Q4Q932 | Leishmania major | 88% | 100% |
Q55D90 | Dictyostelium discoideum | 39% | 90% |
Q91XU8 | Rattus norvegicus | 34% | 97% |
Q92903 | Homo sapiens | 35% | 93% |
Q99L43 | Mus musculus | 35% | 97% |
Q9P381 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 98% |
V5D1I7 | Trypanosoma cruzi | 56% | 100% |