Phospholipid biosynthesis, cholinephosphate cytidylyltransferase A
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
Related structures:
AlphaFold database: A4HY04
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006644 | phospholipid metabolic process | 4 | 12 |
GO:0006646 | phosphatidylethanolamine biosynthetic process | 6 | 12 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 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: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:0046337 | phosphatidylethanolamine metabolic process | 6 | 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:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004306 | ethanolamine-phosphate cytidylyltransferase activity | 6 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 12 |
GO:0070567 | cytidylyltransferase activity | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 584 | 588 | PF00656 | 0.713 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.491 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.306 |
DEG_APCC_DBOX_1 | 302 | 310 | PF00400 | 0.409 |
DEG_SCF_FBW7_1 | 550 | 557 | PF00400 | 0.634 |
DOC_CKS1_1 | 431 | 436 | PF01111 | 0.626 |
DOC_CKS1_1 | 530 | 535 | PF01111 | 0.562 |
DOC_CKS1_1 | 551 | 556 | PF01111 | 0.642 |
DOC_MAPK_gen_1 | 332 | 342 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 388 | 396 | PF00069 | 0.554 |
DOC_MAPK_HePTP_8 | 236 | 248 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 220 | 227 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 239 | 248 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 303 | 310 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 338 | 345 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 460 | 469 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 517 | 525 | PF00069 | 0.459 |
DOC_MAPK_NFAT4_5 | 220 | 228 | PF00069 | 0.449 |
DOC_MAPK_NFAT4_5 | 338 | 346 | PF00069 | 0.484 |
DOC_MAPK_RevD_3 | 373 | 389 | PF00069 | 0.372 |
DOC_PP1_RVXF_1 | 27 | 34 | PF00149 | 0.636 |
DOC_PP1_SILK_1 | 544 | 549 | PF00149 | 0.521 |
DOC_PP2B_LxvP_1 | 156 | 159 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 427 | 430 | PF13499 | 0.533 |
DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.606 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.684 |
DOC_USP7_UBL2_3 | 265 | 269 | PF12436 | 0.657 |
DOC_USP7_UBL2_3 | 334 | 338 | PF12436 | 0.555 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 171 | 181 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 44 | 53 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 566 | 573 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 578 | 585 | PF00244 | 0.545 |
LIG_Actin_WH2_2 | 91 | 106 | PF00022 | 0.707 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.649 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.552 |
LIG_Clathr_ClatBox_1 | 375 | 379 | PF01394 | 0.344 |
LIG_EH1_1 | 285 | 293 | PF00400 | 0.449 |
LIG_EH1_1 | 414 | 422 | PF00400 | 0.520 |
LIG_eIF4E_1 | 337 | 343 | PF01652 | 0.581 |
LIG_eIF4E_1 | 415 | 421 | PF01652 | 0.547 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.491 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.242 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.601 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.395 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.535 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.555 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.537 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.363 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.473 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.541 |
LIG_FHA_2 | 582 | 588 | PF00498 | 0.679 |
LIG_IRF3_LxIS_1 | 181 | 187 | PF10401 | 0.451 |
LIG_LIR_Apic_2 | 477 | 481 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 528 | 533 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 535 | 541 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 160 | 167 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 324 | 333 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 359 | 367 | PF02991 | 0.353 |
LIG_LIR_LC3C_4 | 319 | 322 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.589 |
LIG_NRBOX | 178 | 184 | PF00104 | 0.363 |
LIG_NRBOX | 286 | 292 | PF00104 | 0.475 |
LIG_NRBOX | 398 | 404 | PF00104 | 0.630 |
LIG_NRBOX | 60 | 66 | PF00104 | 0.592 |
LIG_PDZ_Class_3 | 584 | 589 | PF00595 | 0.674 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.567 |
LIG_PTB_Apo_2 | 267 | 274 | PF02174 | 0.653 |
LIG_PTB_Apo_2 | 72 | 79 | PF02174 | 0.639 |
LIG_PTB_Phospho_1 | 267 | 273 | PF10480 | 0.651 |
LIG_PTB_Phospho_1 | 72 | 78 | PF10480 | 0.631 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.343 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.587 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.324 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.562 |
LIG_SH2_CRK | 530 | 534 | PF00017 | 0.501 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.499 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.526 |
LIG_SH2_GRB2like | 518 | 521 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 530 | 534 | PF00017 | 0.476 |
LIG_SH2_SRC | 415 | 418 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.562 |
LIG_SH3_1 | 548 | 554 | PF00018 | 0.625 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.501 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.637 |
LIG_SH3_5 | 159 | 163 | PF00018 | 0.520 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 285 | 291 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 327 | 332 | PF11976 | 0.451 |
LIG_SUMO_SIM_anti_2 | 362 | 369 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 181 | 187 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 247 | 253 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 318 | 324 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 374 | 379 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 419 | 424 | PF11976 | 0.512 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.648 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.469 |
LIG_TRFH_1 | 353 | 357 | PF08558 | 0.413 |
LIG_TYR_ITIM | 315 | 320 | PF00017 | 0.475 |
LIG_TYR_ITIM | 516 | 521 | PF00017 | 0.562 |
LIG_UBA3_1 | 305 | 312 | PF00899 | 0.431 |
LIG_UBA3_1 | 330 | 338 | PF00899 | 0.551 |
LIG_WRC_WIRS_1 | 322 | 327 | PF05994 | 0.344 |
MOD_CDK_SPxK_1 | 430 | 436 | PF00069 | 0.626 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.398 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.551 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.328 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.557 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.283 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.487 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.640 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.363 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.458 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.546 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.562 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.464 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.328 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.470 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.533 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.581 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.522 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.578 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.568 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.562 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.410 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.542 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.660 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.407 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.393 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.324 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.514 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.637 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.518 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.517 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.450 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.476 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.578 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.674 |
MOD_PKB_1 | 200 | 208 | PF00069 | 0.599 |
MOD_PKB_1 | 564 | 572 | PF00069 | 0.589 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.770 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.414 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.343 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.517 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.570 |
MOD_Plk_1 | 569 | 575 | PF00069 | 0.687 |
MOD_Plk_2-3 | 581 | 587 | PF00069 | 0.680 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.770 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.320 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.339 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.344 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.348 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.563 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.351 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.291 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.525 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.508 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.570 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.565 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.534 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.620 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.627 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.476 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.562 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.623 |
MOD_SUMO_rev_2 | 571 | 580 | PF00179 | 0.693 |
TRG_DiLeu_BaEn_1 | 14 | 19 | PF01217 | 0.640 |
TRG_DiLeu_BaEn_1 | 283 | 288 | PF01217 | 0.363 |
TRG_DiLeu_BaLyEn_6 | 461 | 466 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 199 | 202 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I259 | Leptomonas seymouri | 78% | 100% |
A0A0S4JNN5 | Bodo saltans | 47% | 100% |
A0A1X0P717 | Trypanosomatidae | 62% | 100% |
A0A3Q8IA23 | Leishmania donovani | 100% | 100% |
A0A422P0J5 | Trypanosoma rangeli | 61% | 100% |
A4H9L4 | Leishmania braziliensis | 92% | 99% |
D0A5A2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9ARR7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4QDQ6 | Leishmania major | 96% | 100% |
V5BEI8 | Trypanosoma cruzi | 59% | 100% |