Related to bacterial cytidyltransferase enzymes. Relatively conserved architecture, with the expection of an insertion of 2 helices.. Might have been acquired by horizontal gene transfer in the ancestors of Kinetoplastids.
Phospholipid biosynthesis, Phosphatidate cytidylyltransferase
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AHM2
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006644 | phospholipid metabolic process | 4 | 7 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008610 | lipid biosynthetic process | 4 | 7 |
GO:0008654 | phospholipid biosynthetic process | 5 | 7 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016024 | CDP-diacylglycerol biosynthetic process | 6 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 7 |
GO:0046341 | CDP-diacylglycerol metabolic process | 6 | 7 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 7 |
GO:0046486 | glycerolipid metabolic process | 4 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090407 | organophosphate biosynthetic process | 4 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004605 | phosphatidate cytidylyltransferase activity | 6 | 8 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016779 | nucleotidyltransferase activity | 4 | 10 |
GO:0070567 | cytidylyltransferase activity | 5 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 463 | 467 | PF00656 | 0.421 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.381 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 347 | 349 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.221 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.248 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.601 |
DEG_MDM2_SWIB_1 | 272 | 280 | PF02201 | 0.248 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.623 |
DOC_CKS1_1 | 280 | 285 | PF01111 | 0.281 |
DOC_CYCLIN_RxL_1 | 355 | 363 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 470 | 476 | PF00134 | 0.503 |
DOC_MAPK_gen_1 | 70 | 77 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 464 | 472 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.456 |
DOC_PP1_RVXF_1 | 135 | 142 | PF00149 | 0.362 |
DOC_PP4_FxxP_1 | 453 | 456 | PF00568 | 0.486 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.426 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.537 |
DOC_USP7_UBL2_3 | 70 | 74 | PF12436 | 0.473 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.654 |
LIG_14-3-3_CanoR_1 | 316 | 321 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 480 | 486 | PF00244 | 0.489 |
LIG_Actin_WH2_2 | 430 | 445 | PF00022 | 0.253 |
LIG_Clathr_ClatBox_1 | 156 | 160 | PF01394 | 0.281 |
LIG_Clathr_ClatBox_1 | 78 | 82 | PF01394 | 0.559 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.382 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.301 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.621 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.577 |
LIG_GSK3_LRP6_1 | 107 | 112 | PF00069 | 0.523 |
LIG_LIR_Apic_2 | 121 | 126 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 450 | 456 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 131 | 139 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 412 | 423 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.233 |
LIG_NRBOX | 419 | 425 | PF00104 | 0.422 |
LIG_NRBOX | 437 | 443 | PF00104 | 0.179 |
LIG_NRP_CendR_1 | 492 | 493 | PF00754 | 0.352 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.248 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.252 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.488 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.423 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.250 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.557 |
LIG_SH3_1 | 105 | 111 | PF00018 | 0.576 |
LIG_SH3_1 | 123 | 129 | PF00018 | 0.472 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.497 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.520 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.487 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.344 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.303 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.734 |
LIG_SUMO_SIM_par_1 | 154 | 160 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 167 | 172 | PF11976 | 0.280 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.572 |
LIG_UBA3_1 | 437 | 443 | PF00899 | 0.248 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.348 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.564 |
MOD_CDC14_SPxK_1 | 372 | 375 | PF00782 | 0.421 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.576 |
MOD_CDK_SPxK_1 | 369 | 375 | PF00069 | 0.421 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.563 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.386 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.595 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.542 |
MOD_DYRK1A_RPxSP_1 | 369 | 373 | PF00069 | 0.486 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.591 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.457 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.469 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.406 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.337 |
MOD_GlcNHglycan | 65 | 69 | PF01048 | 0.237 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.428 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.597 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.421 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.611 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.303 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.339 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.454 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.267 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.234 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.548 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.186 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.633 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.609 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.619 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.228 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.650 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.503 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.559 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.247 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.290 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.504 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.289 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.213 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.372 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.532 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.650 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.611 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.402 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.533 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.396 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.650 |
MOD_SUMO_for_1 | 179 | 182 | PF00179 | 0.531 |
MOD_SUMO_for_1 | 234 | 237 | PF00179 | 0.660 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.303 |
TRG_DiLeu_BaEn_1 | 352 | 357 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.639 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.571 |
TRG_NLS_MonoExtN_4 | 345 | 350 | PF00514 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC8 | Leptomonas seymouri | 61% | 100% |
A0A1X0NT53 | Trypanosomatidae | 31% | 100% |
A0A3Q8IDC1 | Leishmania donovani | 100% | 100% |
A0A422NZP0 | Trypanosoma rangeli | 33% | 100% |
A4HKS8 | Leishmania braziliensis | 69% | 96% |
E9B366 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q4Y8 | Leishmania major | 89% | 99% |
V5AXY5 | Trypanosoma cruzi | 32% | 100% |