Phospholipid biosynthesis, phospholipid:diacylglycerol acyltransferase
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0016020 | membrane | 2 | 9 |
Related structures:
AlphaFold database: A4HU26
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008080 | N-acetyltransferase activity | 6 | 7 |
GO:0008374 | O-acyltransferase activity | 5 | 12 |
GO:0016407 | acetyltransferase activity | 5 | 7 |
GO:0016410 | N-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 12 |
GO:0046027 | phospholipid:diacylglycerol acyltransferase activity | 7 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 5 | 9 | PF00656 | 0.708 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.638 |
DEG_APCC_DBOX_1 | 122 | 130 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 309 | 317 | PF00400 | 0.255 |
DEG_Kelch_Keap1_1 | 621 | 626 | PF01344 | 0.480 |
DEG_SCF_TRCP1_1 | 252 | 257 | PF00400 | 0.325 |
DOC_CDC14_PxL_1 | 469 | 477 | PF14671 | 0.255 |
DOC_CKS1_1 | 508 | 513 | PF01111 | 0.203 |
DOC_CYCLIN_yClb1_LxF_4 | 310 | 316 | PF00134 | 0.325 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 645 | 654 | PF00134 | 0.335 |
DOC_MAPK_gen_1 | 121 | 130 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 176 | 182 | PF00069 | 0.262 |
DOC_MAPK_gen_1 | 319 | 327 | PF00069 | 0.293 |
DOC_MAPK_gen_1 | 93 | 104 | PF00069 | 0.662 |
DOC_MAPK_HePTP_8 | 119 | 131 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 176 | 183 | PF00069 | 0.346 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.564 |
DOC_PP4_FxxP_1 | 79 | 82 | PF00568 | 0.644 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 579 | 583 | PF12436 | 0.323 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.241 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 158 | 164 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 202 | 207 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 24 | 31 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 310 | 314 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 408 | 417 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 528 | 536 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 61 | 66 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 637 | 646 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.630 |
LIG_Actin_WH2_2 | 560 | 578 | PF00022 | 0.323 |
LIG_APCC_Cbox_2 | 352 | 358 | PF00515 | 0.325 |
LIG_BIR_III_2 | 156 | 160 | PF00653 | 0.356 |
LIG_BRCT_BRCA1_1 | 311 | 315 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 515 | 519 | PF00533 | 0.323 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.656 |
LIG_EH1_1 | 124 | 132 | PF00400 | 0.362 |
LIG_EH1_1 | 590 | 598 | PF00400 | 0.304 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.314 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.257 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.268 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.332 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.318 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.245 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.432 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.414 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.230 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.704 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.381 |
LIG_FHA_2 | 618 | 624 | PF00498 | 0.418 |
LIG_FXI_DFP_1 | 72 | 76 | PF00024 | 0.449 |
LIG_GBD_Chelix_1 | 126 | 134 | PF00786 | 0.365 |
LIG_HP1_1 | 179 | 183 | PF01393 | 0.291 |
LIG_Integrin_RGD_1 | 169 | 171 | PF01839 | 0.570 |
LIG_LIR_Apic_2 | 257 | 263 | PF02991 | 0.307 |
LIG_LIR_Apic_2 | 76 | 82 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 252 | 263 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 407 | 418 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 636 | 646 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 70 | 80 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 205 | 210 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 407 | 413 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 636 | 642 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.691 |
LIG_OCRL_FandH_1 | 349 | 361 | PF00620 | 0.325 |
LIG_Pex14_1 | 230 | 234 | PF04695 | 0.325 |
LIG_Pex14_2 | 206 | 210 | PF04695 | 0.363 |
LIG_Pex14_2 | 75 | 79 | PF04695 | 0.721 |
LIG_REV1ctd_RIR_1 | 161 | 170 | PF16727 | 0.385 |
LIG_REV1ctd_RIR_1 | 337 | 345 | PF16727 | 0.325 |
LIG_SH2_GRB2like | 358 | 361 | PF00017 | 0.316 |
LIG_SH2_GRB2like | 619 | 622 | PF00017 | 0.375 |
LIG_SH2_NCK_1 | 619 | 623 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 639 | 643 | PF00017 | 0.225 |
LIG_SH2_PTP2 | 358 | 361 | PF00017 | 0.325 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.713 |
LIG_SH2_SRC | 358 | 361 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.230 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.233 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.418 |
LIG_SH3_1 | 657 | 663 | PF00018 | 0.407 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.453 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.723 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.328 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.231 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.222 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.419 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.407 |
LIG_SUMO_SIM_anti_2 | 592 | 598 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 14 | 19 | PF11976 | 0.753 |
LIG_UBA3_1 | 233 | 239 | PF00899 | 0.255 |
LIG_UBA3_1 | 593 | 599 | PF00899 | 0.277 |
LIG_WRC_WIRS_1 | 394 | 399 | PF05994 | 0.316 |
LIG_WRC_WIRS_1 | 462 | 467 | PF05994 | 0.381 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.621 |
MOD_CDC14_SPxK_1 | 295 | 298 | PF00782 | 0.255 |
MOD_CDK_SPxK_1 | 292 | 298 | PF00069 | 0.255 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.355 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.280 |
MOD_CK1_1 | 676 | 682 | PF00069 | 0.512 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.414 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.317 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.302 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.613 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.534 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.485 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.506 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.432 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.503 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.489 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.452 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.412 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.470 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.693 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.514 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.300 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.272 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.325 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.345 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.350 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.323 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.414 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.325 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.495 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.646 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.642 |
MOD_LATS_1 | 635 | 641 | PF00433 | 0.357 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.508 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.413 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.490 |
MOD_N-GLC_1 | 520 | 525 | PF02516 | 0.504 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.534 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.518 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.250 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.265 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.764 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.323 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.474 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.465 |
MOD_NEK2_2 | 159 | 164 | PF00069 | 0.366 |
MOD_NEK2_2 | 514 | 519 | PF00069 | 0.301 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.325 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.664 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.698 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.316 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.255 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.323 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.337 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.325 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.629 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.376 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.667 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.191 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.290 |
MOD_Plk_1 | 532 | 538 | PF00069 | 0.325 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.303 |
MOD_Plk_1 | 625 | 631 | PF00069 | 0.365 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.631 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.342 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.398 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.361 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.316 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.300 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.290 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.355 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.325 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.705 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.241 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.323 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 243 | 249 | PF00179 | 0.343 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 591 | 594 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 551 | 553 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 60 | 63 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 632 | 634 | PF00400 | 0.382 |
TRG_NLS_MonoExtC_3 | 654 | 659 | PF00514 | 0.409 |
TRG_NLS_MonoExtN_4 | 319 | 325 | PF00514 | 0.315 |
TRG_NLS_MonoExtN_4 | 655 | 660 | PF00514 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.486 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU70 | Leptomonas seymouri | 67% | 90% |
A0A0S4J6G5 | Bodo saltans | 37% | 100% |
A0A1X0NHY0 | Trypanosomatidae | 46% | 86% |
A0A3R7KCW2 | Trypanosoma rangeli | 43% | 100% |
A0A3S7WQS8 | Leishmania donovani | 100% | 100% |
A4H5T3 | Leishmania braziliensis | 85% | 100% |
D0A9K5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AMV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O94680 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P40345 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
Q4QHS0 | Leishmania major | 95% | 100% |
V5BDI6 | Trypanosoma cruzi | 43% | 100% |