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: 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: E9B366
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 | 0.458 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.357 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 347 | 349 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 443 | 445 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.395 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.675 |
DEG_MDM2_SWIB_1 | 272 | 280 | PF02201 | 0.276 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.657 |
DEG_SCF_TRCP1_1 | 488 | 494 | PF00400 | 0.542 |
DOC_CKS1_1 | 280 | 285 | PF01111 | 0.341 |
DOC_CYCLIN_RxL_1 | 355 | 363 | PF00134 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 470 | 476 | PF00134 | 0.525 |
DOC_CYCLIN_yCln2_LP_2 | 89 | 95 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 70 | 77 | PF00069 | 0.580 |
DOC_MAPK_MEF2A_6 | 221 | 228 | PF00069 | 0.703 |
DOC_MAPK_MEF2A_6 | 464 | 472 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.581 |
DOC_PP1_RVXF_1 | 135 | 142 | PF00149 | 0.393 |
DOC_PP4_FxxP_1 | 403 | 406 | PF00568 | 0.241 |
DOC_PP4_FxxP_1 | 453 | 456 | PF00568 | 0.510 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.202 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.371 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.557 |
DOC_USP7_UBL2_3 | 70 | 74 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.743 |
LIG_14-3-3_CanoR_1 | 480 | 486 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 492 | 496 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.626 |
LIG_Actin_WH2_2 | 430 | 445 | PF00022 | 0.282 |
LIG_Clathr_ClatBox_1 | 156 | 160 | PF01394 | 0.341 |
LIG_Clathr_ClatBox_1 | 78 | 82 | PF01394 | 0.664 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.313 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.228 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.636 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.654 |
LIG_GSK3_LRP6_1 | 107 | 112 | PF00069 | 0.637 |
LIG_LIR_Apic_2 | 121 | 126 | PF02991 | 0.615 |
LIG_LIR_Apic_2 | 450 | 456 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 131 | 139 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 412 | 423 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 390 | 394 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.259 |
LIG_NRBOX | 437 | 443 | PF00104 | 0.189 |
LIG_PDZ_Class_2 | 493 | 498 | PF00595 | 0.568 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.276 |
LIG_Pex14_2 | 396 | 400 | PF04695 | 0.252 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.281 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.599 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.660 |
LIG_SH3_1 | 105 | 111 | PF00018 | 0.690 |
LIG_SH3_1 | 123 | 129 | PF00018 | 0.611 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.621 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.668 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.606 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.384 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.758 |
LIG_SUMO_SIM_par_1 | 155 | 160 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 167 | 172 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 28 | 35 | PF11976 | 0.177 |
LIG_UBA3_1 | 437 | 443 | PF00899 | 0.276 |
LIG_WRC_WIRS_1 | 53 | 58 | PF05994 | 0.357 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.608 |
MOD_CDC14_SPxK_1 | 372 | 375 | PF00782 | 0.442 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.613 |
MOD_CDK_SPxK_1 | 369 | 375 | PF00069 | 0.442 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.506 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.562 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.767 |
MOD_CMANNOS | 397 | 400 | PF00535 | 0.177 |
MOD_DYRK1A_RPxSP_1 | 369 | 373 | PF00069 | 0.510 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.452 |
MOD_GlcNHglycan | 230 | 234 | PF01048 | 0.463 |
MOD_GlcNHglycan | 352 | 356 | PF01048 | 0.320 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.515 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.475 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.687 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.683 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.442 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.464 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.712 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.325 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.372 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.436 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.260 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.174 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.725 |
MOD_NEK2_2 | 52 | 57 | PF00069 | 0.203 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.726 |
MOD_PKA_1 | 186 | 192 | PF00069 | 0.551 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.601 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.577 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.560 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.739 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.543 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.657 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.300 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.234 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.365 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.635 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.767 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.666 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.428 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.571 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.412 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.741 |
MOD_SUMO_for_1 | 179 | 182 | PF00179 | 0.594 |
MOD_SUMO_for_1 | 234 | 237 | PF00179 | 0.723 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.325 |
TRG_DiLeu_BaEn_1 | 352 | 357 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.298 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.596 |
TRG_NLS_MonoExtN_4 | 345 | 350 | PF00514 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC8 | Leptomonas seymouri | 64% | 100% |
A0A1X0NT53 | Trypanosomatidae | 31% | 100% |
A0A3Q8IDC1 | Leishmania donovani | 89% | 100% |
A0A422NZP0 | Trypanosoma rangeli | 32% | 100% |
A4HKS8 | Leishmania braziliensis | 68% | 96% |
E9AHM2 | Leishmania infantum | 89% | 100% |
Q4Q4Y8 | Leishmania major | 86% | 98% |
V5AXY5 | Trypanosoma cruzi | 32% | 100% |