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:0005789 | endoplasmic reticulum membrane | 4 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4H7U0
Term | Name | Level | Count |
---|---|---|---|
GO:0006575 | cellular modified amino acid metabolic process | 3 | 12 |
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006644 | phospholipid metabolic process | 4 | 12 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 12 |
GO:0006658 | phosphatidylserine metabolic process | 4 | 12 |
GO:0006659 | phosphatidylserine biosynthetic process | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 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:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0042398 | cellular modified amino acid biosynthetic process | 4 | 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: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:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003882 | CDP-diacylglycerol-serine O-phosphatidyltransferase activity | 6 | 5 |
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 | 5 |
GO:0106245 | L-serine-phosphatidylethanolamine phosphatidyltransferase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.345 |
CLV_PCSK_FUR_1 | 406 | 410 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 254 | 256 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.296 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.353 |
DEG_MDM2_SWIB_1 | 203 | 211 | PF02201 | 0.243 |
DOC_CDC14_PxL_1 | 433 | 441 | PF14671 | 0.430 |
DOC_CDC14_PxL_1 | 49 | 57 | PF14671 | 0.355 |
DOC_CYCLIN_RxL_1 | 169 | 178 | PF00134 | 0.353 |
DOC_MAPK_gen_1 | 177 | 187 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 408 | 417 | PF00069 | 0.589 |
DOC_MAPK_HePTP_8 | 45 | 57 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 180 | 189 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 410 | 419 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 48 | 57 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 94 | 101 | PF00069 | 0.311 |
DOC_PP1_RVXF_1 | 17 | 24 | PF00149 | 0.624 |
DOC_PP1_RVXF_1 | 60 | 66 | PF00149 | 0.264 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.190 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.391 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.514 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.643 |
LIG_14-3-3_CanoR_1 | 143 | 151 | PF00244 | 0.237 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.296 |
LIG_AP2alpha_2 | 149 | 151 | PF02296 | 0.320 |
LIG_APCC_ABBA_1 | 109 | 114 | PF00400 | 0.416 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.538 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.296 |
LIG_deltaCOP1_diTrp_1 | 148 | 158 | PF00928 | 0.328 |
LIG_EH1_1 | 168 | 176 | PF00400 | 0.330 |
LIG_EH1_1 | 279 | 287 | PF00400 | 0.382 |
LIG_EH1_1 | 296 | 304 | PF00400 | 0.197 |
LIG_eIF4E_1 | 124 | 130 | PF01652 | 0.327 |
LIG_eIF4E_1 | 169 | 175 | PF01652 | 0.353 |
LIG_eIF4E_1 | 369 | 375 | PF01652 | 0.237 |
LIG_eIF4E_1 | 414 | 420 | PF01652 | 0.362 |
LIG_eIF4E_1 | 52 | 58 | PF01652 | 0.249 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.416 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.298 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.273 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.258 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.319 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.287 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.268 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.243 |
LIG_GBD_Chelix_1 | 282 | 290 | PF00786 | 0.325 |
LIG_GBD_Chelix_1 | 388 | 396 | PF00786 | 0.190 |
LIG_HCF-1_HBM_1 | 25 | 28 | PF13415 | 0.474 |
LIG_LIR_Gen_1 | 108 | 116 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 156 | 164 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 186 | 196 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.112 |
LIG_LIR_Gen_1 | 32 | 41 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 329 | 339 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 344 | 355 | PF02991 | 0.210 |
LIG_LIR_Gen_1 | 390 | 401 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 69 | 78 | PF02991 | 0.237 |
LIG_LIR_LC3C_4 | 308 | 313 | PF02991 | 0.168 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.157 |
LIG_LIR_Nem_3 | 178 | 182 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.112 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 32 | 37 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 69 | 75 | PF02991 | 0.237 |
LIG_LYPXL_yS_3 | 52 | 55 | PF13949 | 0.376 |
LIG_NRBOX | 286 | 292 | PF00104 | 0.361 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.416 |
LIG_NRP_CendR_1 | 461 | 463 | PF00754 | 0.500 |
LIG_Pex14_1 | 393 | 397 | PF04695 | 0.296 |
LIG_Pex14_2 | 203 | 207 | PF04695 | 0.243 |
LIG_PTB_Apo_2 | 415 | 422 | PF02174 | 0.330 |
LIG_REV1ctd_RIR_1 | 456 | 463 | PF16727 | 0.384 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.248 |
LIG_SH2_SRC | 125 | 128 | PF00017 | 0.197 |
LIG_SH2_STAP1 | 422 | 426 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.330 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.659 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.320 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.416 |
LIG_SUMO_SIM_anti_2 | 284 | 290 | PF11976 | 0.414 |
LIG_SUMO_SIM_anti_2 | 42 | 48 | PF11976 | 0.373 |
LIG_SUMO_SIM_anti_2 | 54 | 59 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 190 | 195 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 399 | 404 | PF11976 | 0.526 |
LIG_TYR_ITIM | 395 | 400 | PF00017 | 0.381 |
LIG_UBA3_1 | 229 | 236 | PF00899 | 0.381 |
LIG_UBA3_1 | 302 | 306 | PF00899 | 0.197 |
LIG_WRC_WIRS_1 | 106 | 111 | PF05994 | 0.298 |
MOD_CDC14_SPxK_1 | 275 | 278 | PF00782 | 0.504 |
MOD_CDK_SPxK_1 | 272 | 278 | PF00069 | 0.504 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.227 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.280 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.325 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.456 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.190 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.596 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.337 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.359 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.390 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.382 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.267 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.553 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.243 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.291 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.406 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.422 |
MOD_NEK2_2 | 323 | 328 | PF00069 | 0.190 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.268 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.280 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.296 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.368 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.270 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.346 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.276 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.306 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.487 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.311 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.277 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.291 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.265 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.519 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.497 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.642 |
TRG_DiLeu_BaEn_2 | 328 | 334 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 460 | 463 | PF00400 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.242 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIC0 | Leptomonas seymouri | 77% | 88% |
A0A0S4ILR0 | Bodo saltans | 47% | 100% |
A0A1X0NNG6 | Trypanosomatidae | 57% | 91% |
A0A3R7N202 | Trypanosoma rangeli | 57% | 91% |
A0A3S7WT59 | Leishmania donovani | 87% | 87% |
A4HW66 | Leishmania infantum | 87% | 87% |
B1H3H9 | Xenopus tropicalis | 33% | 100% |
B2GV22 | Rattus norvegicus | 35% | 98% |
C9ZSV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 91% |
E1BYA3 | Gallus gallus | 36% | 100% |
E7EY42 | Danio rerio | 35% | 100% |
E9APW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 87% |
F4HXY7 | Arabidopsis thaliana | 37% | 100% |
O08888 | Cricetulus griseus | 36% | 98% |
P48651 | Homo sapiens | 33% | 98% |
Q00576 | Cricetulus griseus | 33% | 98% |
Q08D11 | Xenopus tropicalis | 36% | 98% |
Q0JR55 | Oryza sativa subsp. japonica | 37% | 100% |
Q2KHY9 | Bos taurus | 33% | 98% |
Q4QFL4 | Leishmania major | 86% | 100% |
Q5N8Q3 | Oryza sativa subsp. japonica | 39% | 100% |
Q5PQL5 | Rattus norvegicus | 34% | 98% |
Q5ZM65 | Gallus gallus | 33% | 98% |
Q6I628 | Oryza sativa subsp. japonica | 35% | 100% |
Q803C9 | Danio rerio | 33% | 100% |
Q99LH2 | Mus musculus | 34% | 98% |
Q9BVG9 | Homo sapiens | 39% | 95% |
Q9VPD3 | Drosophila melanogaster | 35% | 93% |
Q9Z1X2 | Mus musculus | 36% | 98% |
V5DC50 | Trypanosoma cruzi | 57% | 91% |