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.
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q4Y8
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0006644 | phospholipid metabolic process | 4 | 8 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0008610 | lipid biosynthetic process | 4 | 8 |
GO:0008654 | phospholipid biosynthetic process | 5 | 8 |
GO:0009058 | biosynthetic process | 2 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016024 | CDP-diacylglycerol biosynthetic process | 6 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044249 | cellular biosynthetic process | 3 | 8 |
GO:0044255 | cellular lipid metabolic process | 3 | 8 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 8 |
GO:0046341 | CDP-diacylglycerol metabolic process | 6 | 8 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 8 |
GO:0046486 | glycerolipid metabolic process | 4 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090407 | organophosphate biosynthetic process | 4 | 8 |
GO:1901576 | organic substance biosynthetic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004605 | phosphatidate cytidylyltransferase activity | 6 | 9 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016779 | nucleotidyltransferase activity | 4 | 11 |
GO:0070567 | cytidylyltransferase activity | 5 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.482 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.390 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 337 | 339 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 433 | 435 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.150 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.336 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.705 |
DEG_MDM2_SWIB_1 | 262 | 270 | PF02201 | 0.335 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.744 |
DEG_SCF_TRCP1_1 | 478 | 484 | PF00400 | 0.579 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.480 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.746 |
DOC_CYCLIN_RxL_1 | 345 | 353 | PF00134 | 0.668 |
DOC_CYCLIN_yCln2_LP_2 | 460 | 466 | PF00134 | 0.562 |
DOC_MAPK_DCC_7 | 88 | 98 | PF00069 | 0.615 |
DOC_MAPK_gen_1 | 70 | 77 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 454 | 462 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 5 | 14 | PF00069 | 0.600 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.542 |
DOC_PP1_RVXF_1 | 135 | 142 | PF00149 | 0.447 |
DOC_PP4_FxxP_1 | 393 | 396 | PF00568 | 0.302 |
DOC_PP4_FxxP_1 | 443 | 446 | PF00568 | 0.553 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.487 |
DOC_USP7_UBL2_3 | 337 | 341 | PF12436 | 0.636 |
DOC_USP7_UBL2_3 | 70 | 74 | PF12436 | 0.545 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.741 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 470 | 476 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 482 | 486 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.150 |
LIG_Actin_WH2_2 | 420 | 435 | PF00022 | 0.344 |
LIG_BRCT_BRCA1_1 | 270 | 274 | PF00533 | 0.246 |
LIG_Clathr_ClatBox_1 | 156 | 160 | PF01394 | 0.480 |
LIG_Clathr_ClatBox_1 | 78 | 82 | PF01394 | 0.649 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.340 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.380 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.714 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.735 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.701 |
LIG_GSK3_LRP6_1 | 107 | 112 | PF00069 | 0.709 |
LIG_LIR_Apic_2 | 121 | 126 | PF02991 | 0.621 |
LIG_LIR_Apic_2 | 2 | 7 | PF02991 | 0.629 |
LIG_LIR_Apic_2 | 440 | 446 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 131 | 139 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 251 | 262 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 402 | 413 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 235 | 239 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.315 |
LIG_NRBOX | 409 | 415 | PF00104 | 0.430 |
LIG_NRBOX | 427 | 433 | PF00104 | 0.225 |
LIG_PDZ_Class_2 | 483 | 488 | PF00595 | 0.758 |
LIG_Pex14_2 | 262 | 266 | PF04695 | 0.335 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.359 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.498 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.275 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.661 |
LIG_SH3_1 | 105 | 111 | PF00018 | 0.735 |
LIG_SH3_1 | 123 | 129 | PF00018 | 0.644 |
LIG_SH3_1 | 211 | 217 | PF00018 | 0.622 |
LIG_SH3_1 | 4 | 10 | PF00018 | 0.628 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.600 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.703 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.618 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.682 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.397 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.362 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.701 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.798 |
LIG_SUMO_SIM_anti_2 | 307 | 313 | PF11976 | 0.557 |
LIG_SUMO_SIM_par_1 | 155 | 160 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 167 | 172 | PF11976 | 0.389 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.660 |
LIG_UBA3_1 | 427 | 433 | PF00899 | 0.335 |
LIG_WRC_WIRS_1 | 53 | 58 | PF05994 | 0.428 |
MOD_CDC14_SPxK_1 | 362 | 365 | PF00782 | 0.482 |
MOD_CDK_SPxK_1 | 359 | 365 | PF00069 | 0.482 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.762 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.400 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.669 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.631 |
MOD_DYRK1A_RPxSP_1 | 359 | 363 | PF00069 | 0.553 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.548 |
MOD_GlcNHglycan | 342 | 346 | PF01048 | 0.354 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.519 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.521 |
MOD_GlcNHglycan | 65 | 69 | PF01048 | 0.340 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.676 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.482 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.381 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.664 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.334 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.426 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.594 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.354 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.294 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.247 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.716 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.712 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.717 |
MOD_PKA_1 | 186 | 192 | PF00069 | 0.598 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.614 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.723 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.740 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.534 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.751 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.358 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.398 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.283 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.419 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.452 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.722 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.775 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.466 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.788 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.602 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.445 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.737 |
MOD_SUMO_for_1 | 179 | 182 | PF00179 | 0.656 |
MOD_SUMO_for_1 | 224 | 227 | PF00179 | 0.739 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.335 |
TRG_DiLeu_BaEn_1 | 342 | 347 | PF01217 | 0.614 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.643 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 389 | 392 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.723 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.674 |
TRG_NLS_MonoExtN_4 | 335 | 340 | PF00514 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 338 | 342 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC8 | Leptomonas seymouri | 63% | 100% |
A0A0S4IRI0 | Bodo saltans | 31% | 100% |
A0A1X0NT53 | Trypanosomatidae | 31% | 100% |
A0A3Q8IDC1 | Leishmania donovani | 89% | 99% |
A0A422NZP0 | Trypanosoma rangeli | 34% | 100% |
A4HKS8 | Leishmania braziliensis | 67% | 100% |
E9AHM2 | Leishmania infantum | 89% | 99% |
E9B366 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 98% |
V5AXY5 | Trypanosoma cruzi | 33% | 100% |