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: A4HKS8
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 | 444 | 448 | PF00656 | 0.458 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.288 |
DEG_COP1_1 | 4 | 12 | PF00400 | 0.585 |
DEG_MDM2_SWIB_1 | 253 | 261 | PF02201 | 0.276 |
DEG_SPOP_SBC_1 | 84 | 88 | PF00917 | 0.586 |
DOC_CKS1_1 | 261 | 266 | PF01111 | 0.341 |
DOC_CYCLIN_RxL_1 | 336 | 344 | PF00134 | 0.573 |
DOC_CYCLIN_yCln2_LP_2 | 261 | 267 | PF00134 | 0.349 |
DOC_CYCLIN_yCln2_LP_2 | 451 | 457 | PF00134 | 0.525 |
DOC_MAPK_gen_1 | 428 | 436 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 70 | 77 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 445 | 453 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 116 | 123 | PF00149 | 0.393 |
DOC_PP4_FxxP_1 | 384 | 387 | PF00568 | 0.241 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.202 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.607 |
DOC_USP7_UBL2_3 | 70 | 74 | PF12436 | 0.488 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.698 |
LIG_14-3-3_CanoR_1 | 329 | 338 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 82 | 92 | PF00244 | 0.520 |
LIG_Actin_WH2_2 | 411 | 426 | PF00022 | 0.282 |
LIG_Clathr_ClatBox_1 | 137 | 141 | PF01394 | 0.341 |
LIG_EH1_1 | 146 | 154 | PF00400 | 0.285 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.228 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.308 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.637 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.400 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.638 |
LIG_LIR_Apic_2 | 102 | 107 | PF02991 | 0.528 |
LIG_LIR_Apic_2 | 382 | 387 | PF02991 | 0.186 |
LIG_LIR_Gen_1 | 112 | 120 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 133 | 144 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 289 | 299 | PF02991 | 0.199 |
LIG_LIR_Gen_1 | 335 | 345 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 112 | 117 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.626 |
LIG_LYPXL_S_1 | 348 | 352 | PF13949 | 0.186 |
LIG_LYPXL_S_1 | 99 | 103 | PF13949 | 0.259 |
LIG_LYPXL_SIV_4 | 395 | 403 | PF13949 | 0.186 |
LIG_LYPXL_yS_3 | 100 | 103 | PF13949 | 0.464 |
LIG_LYPXL_yS_3 | 349 | 352 | PF13949 | 0.386 |
LIG_MAD2 | 339 | 347 | PF02301 | 0.471 |
LIG_NRBOX | 400 | 406 | PF00104 | 0.444 |
LIG_NRBOX | 418 | 424 | PF00104 | 0.380 |
LIG_PDZ_Class_1 | 465 | 470 | PF00595 | 0.475 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.276 |
LIG_PTB_Apo_2 | 285 | 292 | PF02174 | 0.199 |
LIG_PTB_Apo_2 | 390 | 397 | PF02174 | 0.274 |
LIG_PTB_Phospho_1 | 390 | 396 | PF10480 | 0.186 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.504 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.279 |
LIG_SH2_CRK | 306 | 310 | PF00017 | 0.581 |
LIG_SH2_CRK | 380 | 384 | PF00017 | 0.225 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.169 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.205 |
LIG_SH3_1 | 104 | 110 | PF00018 | 0.528 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.523 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.339 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.386 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.386 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.578 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.455 |
LIG_UBA3_1 | 418 | 424 | PF00899 | 0.442 |
MOD_CDC14_SPxK_1 | 353 | 356 | PF00782 | 0.442 |
MOD_CDK_SPxK_1 | 350 | 356 | PF00069 | 0.442 |
MOD_Cter_Amidation | 326 | 329 | PF01082 | 0.382 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.431 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.464 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.392 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.199 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.442 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.625 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.683 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.313 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.325 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.266 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.593 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.214 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.430 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.459 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.646 |
MOD_NEK2_2 | 44 | 49 | PF00069 | 0.302 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.533 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.507 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.469 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.710 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.571 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.543 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.517 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.231 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.300 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.411 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.414 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.636 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.428 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.560 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.412 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.689 |
MOD_SUMO_rev_2 | 208 | 218 | PF00179 | 0.574 |
TRG_DiLeu_BaEn_1 | 133 | 138 | PF01217 | 0.325 |
TRG_DiLeu_BaEn_1 | 141 | 146 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_2 | 332 | 338 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.210 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 329 | 333 | PF00026 | 0.421 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC8 | Leptomonas seymouri | 56% | 99% |
A0A1X0NT53 | Trypanosomatidae | 33% | 100% |
A0A3Q8IDC1 | Leishmania donovani | 69% | 95% |
A0A422NZP0 | Trypanosoma rangeli | 36% | 100% |
E9AHM2 | Leishmania infantum | 69% | 95% |
E9B366 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 94% |
Q4Q4Y8 | Leishmania major | 67% | 100% |
V5AXY5 | Trypanosoma cruzi | 33% | 100% |