Phospholipid biosynthesis, phosphatidylserine synthase
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: A4HW66
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 | 15 | 17 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.348 |
CLV_PCSK_FUR_1 | 408 | 412 | PF00082 | 0.294 |
CLV_PCSK_FUR_1 | 476 | 480 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.339 |
CLV_PCSK_PC1ET2_1 | 324 | 326 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 410 | 412 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.523 |
DEG_APCC_DBOX_1 | 384 | 392 | PF00400 | 0.354 |
DEG_MDM2_SWIB_1 | 273 | 281 | PF02201 | 0.244 |
DEG_SCF_FBW7_1 | 28 | 33 | PF00400 | 0.622 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.663 |
DOC_CDC14_PxL_1 | 503 | 511 | PF14671 | 0.432 |
DOC_CYCLIN_RxL_1 | 239 | 248 | PF00134 | 0.354 |
DOC_CYCLIN_RxL_1 | 320 | 328 | PF00134 | 0.397 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.664 |
DOC_MAPK_gen_1 | 247 | 257 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 478 | 487 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 164 | 171 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 250 | 259 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 480 | 489 | PF00069 | 0.549 |
DOC_MAPK_MEF2A_6 | 55 | 63 | PF00069 | 0.674 |
DOC_MAPK_NFAT4_5 | 164 | 172 | PF00069 | 0.364 |
DOC_PP1_RVXF_1 | 87 | 94 | PF00149 | 0.637 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.602 |
DOC_PP4_FxxP_1 | 343 | 346 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.658 |
DOC_USP7_MATH_2 | 67 | 73 | PF00917 | 0.667 |
DOC_USP7_UBL2_3 | 320 | 324 | PF12436 | 0.516 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 250 | 259 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 411 | 421 | PF00244 | 0.470 |
LIG_AP2alpha_2 | 219 | 221 | PF02296 | 0.321 |
LIG_APCC_ABBA_1 | 179 | 184 | PF00400 | 0.417 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.297 |
LIG_deltaCOP1_diTrp_1 | 217 | 228 | PF00928 | 0.332 |
LIG_EH1_1 | 238 | 246 | PF00400 | 0.331 |
LIG_EH1_1 | 349 | 357 | PF00400 | 0.384 |
LIG_EH1_1 | 366 | 374 | PF00400 | 0.198 |
LIG_eIF4E_1 | 194 | 200 | PF01652 | 0.328 |
LIG_eIF4E_1 | 239 | 245 | PF01652 | 0.354 |
LIG_eIF4E_1 | 484 | 490 | PF01652 | 0.363 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.300 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.417 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.392 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.274 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.259 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.321 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.288 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.689 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.269 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.244 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.626 |
LIG_LIR_Gen_1 | 102 | 111 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 178 | 185 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 226 | 234 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 275 | 286 | PF02991 | 0.113 |
LIG_LIR_Gen_1 | 399 | 409 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 414 | 425 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 178 | 182 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.158 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.113 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 524 | 529 | PF02991 | 0.367 |
LIG_LYPXL_yS_3 | 122 | 125 | PF13949 | 0.355 |
LIG_NRBOX | 356 | 362 | PF00104 | 0.362 |
LIG_NRBOX | 387 | 393 | PF00104 | 0.417 |
LIG_Pex14_1 | 463 | 467 | PF04695 | 0.297 |
LIG_Pex14_2 | 273 | 277 | PF04695 | 0.244 |
LIG_PTB_Apo_2 | 485 | 492 | PF02174 | 0.331 |
LIG_SH2_PTP2 | 526 | 529 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 492 | 496 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.568 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.417 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.681 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.322 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.659 |
LIG_SUMO_SIM_anti_2 | 112 | 117 | PF11976 | 0.374 |
LIG_SUMO_SIM_anti_2 | 353 | 359 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 242 | 248 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 260 | 265 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 469 | 474 | PF11976 | 0.530 |
LIG_TRAF2_1 | 215 | 218 | PF00917 | 0.324 |
LIG_TYR_ITIM | 465 | 470 | PF00017 | 0.382 |
LIG_UBA3_1 | 181 | 190 | PF00899 | 0.394 |
LIG_UBA3_1 | 299 | 306 | PF00899 | 0.382 |
LIG_WRC_WIRS_1 | 176 | 181 | PF05994 | 0.299 |
MOD_CDC14_SPxK_1 | 345 | 348 | PF00782 | 0.505 |
MOD_CDK_SPxK_1 | 342 | 348 | PF00069 | 0.505 |
MOD_CDK_SPxxK_3 | 82 | 89 | PF00069 | 0.653 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.746 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.701 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.281 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.757 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.629 |
MOD_DYRK1A_RPxSP_1 | 96 | 100 | PF00069 | 0.603 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.338 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.597 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.392 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.724 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.384 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.666 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.424 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.244 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.293 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.350 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.407 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.269 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.299 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.282 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.297 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.278 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.518 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.347 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.278 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.313 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.488 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.707 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.499 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.629 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.543 |
TRG_DiLeu_BaEn_2 | 523 | 529 | PF01217 | 0.305 |
TRG_DiLeu_BaLyEn_6 | 322 | 327 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 76 | 81 | PF01217 | 0.668 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.375 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 398 | 402 | PF00026 | 0.330 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIC0 | Leptomonas seymouri | 74% | 100% |
A0A0S4ILR0 | Bodo saltans | 48% | 100% |
A0A1X0NNG6 | Trypanosomatidae | 56% | 100% |
A0A3R7N202 | Trypanosoma rangeli | 53% | 100% |
A0A3S7WT59 | Leishmania donovani | 100% | 100% |
A4H7U0 | Leishmania braziliensis | 87% | 100% |
B2GV22 | Rattus norvegicus | 34% | 100% |
C9ZSV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E1BYA3 | Gallus gallus | 35% | 100% |
E7EY42 | Danio rerio | 35% | 100% |
E9APW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O08888 | Cricetulus griseus | 35% | 100% |
P48651 | Homo sapiens | 32% | 100% |
Q00576 | Cricetulus griseus | 32% | 100% |
Q08D11 | Xenopus tropicalis | 35% | 100% |
Q2KHY9 | Bos taurus | 32% | 100% |
Q4QFL4 | Leishmania major | 94% | 100% |
Q5PQL5 | Rattus norvegicus | 32% | 100% |
Q5ZM65 | Gallus gallus | 32% | 100% |
Q6I628 | Oryza sativa subsp. japonica | 35% | 100% |
Q803C9 | Danio rerio | 32% | 100% |
Q99LH2 | Mus musculus | 32% | 100% |
Q9VPD3 | Drosophila melanogaster | 32% | 100% |
Q9Z1X2 | Mus musculus | 35% | 100% |
V5DC50 | Trypanosoma cruzi | 57% | 100% |