LeishMANIAdb
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CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase

Quick info Annotations Function or PPIs Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase
Gene product:
phosphatidylglycerolphosphate synthase - mitochondrial - putative
Species:
Leishmania infantum
UniProt:
A4HT38_LEIIN
TriTrypDb:
LINF_070007200
Length:
755

Annotations

LeishMANIAdb annotations

Overall very similar to animal mitochondrial PGS1 enzymes, with one key difference: instead a a transit signal, the Kinetoplastid variant has membrane anchor.

Annotations by Jardim et al.

Phospholipid biosynthesis, phosphatidylglycerophosphate synthase

Localization

Secreted promastigote
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
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 9
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 7
NetGPI no yes: 0, no: 7
Cellular components
Term Name Level Count
GO:0005739 mitochondrion 5 8
GO:0043226 organelle 2 8
GO:0043227 membrane-bounded organelle 3 8
GO:0043229 intracellular organelle 3 8
GO:0043231 intracellular membrane-bounded organelle 4 8
GO:0110165 cellular anatomical entity 1 8

Expansion

Sequence features

A4HT38
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HT38

Function

Biological processes
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:0006655 phosphatidylglycerol biosynthetic process 6 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:0019637 organophosphate metabolic process 3 8
GO:0032048 cardiolipin metabolic process 7 8
GO:0032049 cardiolipin biosynthetic process 7 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:0046471 phosphatidylglycerol 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
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 8
GO:0003824 catalytic activity 1 8
GO:0005488 binding 1 8
GO:0005524 ATP binding 5 8
GO:0008444 CDP-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase activity 6 8
GO:0016740 transferase activity 2 8
GO:0016772 transferase activity, transferring phosphorus-containing groups 3 8
GO:0016780 phosphotransferase activity, for other substituted phosphate groups 4 8
GO:0017076 purine nucleotide binding 4 8
GO:0017169 CDP-alcohol phosphatidyltransferase activity 5 8
GO:0030554 adenyl nucleotide binding 5 8
GO:0032553 ribonucleotide binding 3 8
GO:0032555 purine ribonucleotide binding 4 8
GO:0032559 adenyl ribonucleotide binding 5 8
GO:0035639 purine ribonucleoside triphosphate binding 4 8
GO:0036094 small molecule binding 2 8
GO:0043167 ion binding 2 8
GO:0043168 anion binding 3 8
GO:0097159 organic cyclic compound binding 2 8
GO:0097367 carbohydrate derivative binding 2 8
GO:1901265 nucleoside phosphate binding 3 8
GO:1901363 heterocyclic compound binding 2 8

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 257 261 PF00656 0.665
CLV_C14_Caspase3-7 704 708 PF00656 0.598
CLV_NRD_NRD_1 190 192 PF00675 0.417
CLV_NRD_NRD_1 367 369 PF00675 0.432
CLV_NRD_NRD_1 451 453 PF00675 0.449
CLV_NRD_NRD_1 490 492 PF00675 0.412
CLV_NRD_NRD_1 606 608 PF00675 0.443
CLV_NRD_NRD_1 630 632 PF00675 0.501
CLV_NRD_NRD_1 69 71 PF00675 0.548
CLV_PCSK_KEX2_1 134 136 PF00082 0.368
CLV_PCSK_KEX2_1 490 492 PF00082 0.393
CLV_PCSK_KEX2_1 606 608 PF00082 0.443
CLV_PCSK_KEX2_1 630 632 PF00082 0.504
CLV_PCSK_PC1ET2_1 134 136 PF00082 0.368
CLV_PCSK_SKI1_1 141 145 PF00082 0.367
CLV_PCSK_SKI1_1 280 284 PF00082 0.411
CLV_PCSK_SKI1_1 301 305 PF00082 0.383
CLV_PCSK_SKI1_1 349 353 PF00082 0.392
CLV_PCSK_SKI1_1 526 530 PF00082 0.354
CLV_PCSK_SKI1_1 616 620 PF00082 0.416
DEG_APCC_DBOX_1 190 198 PF00400 0.626
DEG_APCC_DBOX_1 582 590 PF00400 0.599
DEG_APCC_DBOX_1 713 721 PF00400 0.553
DEG_SPOP_SBC_1 264 268 PF00917 0.785
DOC_CYCLIN_RxL_1 520 533 PF00134 0.578
DOC_CYCLIN_yCln2_LP_2 122 128 PF00134 0.588
DOC_MAPK_FxFP_2 506 509 PF00069 0.563
DOC_MAPK_gen_1 191 197 PF00069 0.586
DOC_MAPK_gen_1 299 306 PF00069 0.592
DOC_MAPK_gen_1 452 459 PF00069 0.615
DOC_MAPK_MEF2A_6 739 746 PF00069 0.629
DOC_PP1_RVXF_1 164 170 PF00149 0.598
DOC_PP1_RVXF_1 495 501 PF00149 0.546
DOC_PP1_RVXF_1 614 621 PF00149 0.617
DOC_PP4_FxxP_1 506 509 PF00568 0.563
DOC_USP7_MATH_1 113 117 PF00917 0.546
DOC_USP7_MATH_1 139 143 PF00917 0.598
DOC_USP7_MATH_1 220 224 PF00917 0.729
DOC_USP7_MATH_1 271 275 PF00917 0.769
DOC_USP7_MATH_1 387 391 PF00917 0.721
DOC_USP7_MATH_1 410 414 PF00917 0.750
DOC_USP7_MATH_1 436 440 PF00917 0.759
DOC_USP7_MATH_1 44 48 PF00917 0.785
DOC_USP7_MATH_1 681 685 PF00917 0.522
DOC_USP7_MATH_1 69 73 PF00917 0.777
DOC_USP7_MATH_2 670 676 PF00917 0.627
DOC_WW_Pin1_4 223 228 PF00397 0.755
DOC_WW_Pin1_4 383 388 PF00397 0.787
DOC_WW_Pin1_4 40 45 PF00397 0.720
DOC_WW_Pin1_4 417 422 PF00397 0.758
DOC_WW_Pin1_4 431 436 PF00397 0.664
DOC_WW_Pin1_4 444 449 PF00397 0.602
DOC_WW_Pin1_4 539 544 PF00397 0.531
DOC_WW_Pin1_4 639 644 PF00397 0.759
LIG_14-3-3_CanoR_1 141 146 PF00244 0.530
LIG_14-3-3_CanoR_1 230 236 PF00244 0.791
LIG_14-3-3_CanoR_1 360 364 PF00244 0.616
LIG_14-3-3_CanoR_1 452 459 PF00244 0.571
LIG_14-3-3_CanoR_1 530 539 PF00244 0.546
LIG_14-3-3_CanoR_1 70 76 PF00244 0.728
LIG_Actin_WH2_2 591 608 PF00022 0.645
LIG_APCC_ABBA_1 19 24 PF00400 0.644
LIG_APCC_ABBAyCdc20_2 515 521 PF00400 0.542
LIG_BRCT_BRCA1_1 155 159 PF00533 0.535
LIG_BRCT_BRCA1_1 237 241 PF00533 0.731
LIG_BRCT_BRCA1_1 396 400 PF00533 0.643
LIG_CaM_NSCaTE_8 488 495 PF13499 0.521
LIG_deltaCOP1_diTrp_1 499 506 PF00928 0.591
LIG_EH1_1 176 184 PF00400 0.589
LIG_FHA_1 1 7 PF00498 0.344
LIG_FHA_1 116 122 PF00498 0.574
LIG_FHA_1 16 22 PF00498 0.356
LIG_FHA_1 178 184 PF00498 0.532
LIG_FHA_1 208 214 PF00498 0.754
LIG_FHA_1 350 356 PF00498 0.606
LIG_FHA_1 436 442 PF00498 0.791
LIG_FHA_1 49 55 PF00498 0.718
LIG_FHA_1 557 563 PF00498 0.577
LIG_FHA_1 564 570 PF00498 0.551
LIG_FHA_2 197 203 PF00498 0.603
LIG_FHA_2 331 337 PF00498 0.587
LIG_FHA_2 531 537 PF00498 0.586
LIG_FHA_2 60 66 PF00498 0.813
LIG_FHA_2 702 708 PF00498 0.599
LIG_Integrin_RGD_1 255 257 PF01839 0.485
LIG_LIR_Apic_2 504 509 PF02991 0.566
LIG_LIR_Gen_1 18 25 PF02991 0.575
LIG_LIR_Gen_1 184 190 PF02991 0.567
LIG_LIR_Gen_1 336 346 PF02991 0.541
LIG_LIR_Gen_1 542 552 PF02991 0.530
LIG_LIR_Nem_3 18 22 PF02991 0.432
LIG_LIR_Nem_3 288 293 PF02991 0.610
LIG_LIR_Nem_3 336 341 PF02991 0.515
LIG_LIR_Nem_3 499 503 PF02991 0.574
LIG_LIR_Nem_3 505 511 PF02991 0.510
LIG_LIR_Nem_3 592 598 PF02991 0.550
LIG_NRBOX 716 722 PF00104 0.558
LIG_OCRL_FandH_1 313 325 PF00620 0.556
LIG_PALB2_WD40_1 346 354 PF16756 0.580
LIG_PCNA_PIPBox_1 98 107 PF02747 0.591
LIG_PCNA_yPIPBox_3 337 351 PF02747 0.554
LIG_PCNA_yPIPBox_3 91 105 PF02747 0.640
LIG_PDZ_Class_3 750 755 PF00595 0.677
LIG_Pex14_1 290 294 PF04695 0.639
LIG_RPA_C_Fungi 486 498 PF08784 0.383
LIG_RPA_C_Fungi 626 638 PF08784 0.433
LIG_SH2_CRK 284 288 PF00017 0.466
LIG_SH2_CRK 338 342 PF00017 0.326
LIG_SH2_CRK 602 606 PF00017 0.501
LIG_SH2_CRK 689 693 PF00017 0.487
LIG_SH2_GRB2like 284 287 PF00017 0.465
LIG_SH2_GRB2like 544 547 PF00017 0.422
LIG_SH2_SRC 284 287 PF00017 0.465
LIG_SH2_STAP1 503 507 PF00017 0.451
LIG_SH2_STAT5 149 152 PF00017 0.403
LIG_SH2_STAT5 330 333 PF00017 0.430
LIG_SH2_STAT5 544 547 PF00017 0.422
LIG_SH2_STAT5 561 564 PF00017 0.405
LIG_SH2_STAT5 588 591 PF00017 0.430
LIG_SH2_STAT5 597 600 PF00017 0.433
LIG_SH2_STAT5 678 681 PF00017 0.455
LIG_SH2_STAT5 7 10 PF00017 0.515
LIG_SH3_3 290 296 PF00018 0.422
LIG_SH3_3 430 436 PF00018 0.592
LIG_SH3_3 665 671 PF00018 0.613
LIG_SUMO_SIM_anti_2 178 184 PF11976 0.416
LIG_SUMO_SIM_anti_2 454 460 PF11976 0.406
LIG_SUMO_SIM_par_1 178 184 PF11976 0.469
LIG_SUMO_SIM_par_1 193 199 PF11976 0.514
LIG_TYR_ITIM 127 132 PF00017 0.457
LIG_TYR_ITIM 5 10 PF00017 0.501
LIG_TYR_ITIM 586 591 PF00017 0.481
LIG_WRC_WIRS_1 101 106 PF05994 0.464
LIG_WRC_WIRS_1 503 508 PF05994 0.449
MOD_CDC14_SPxK_1 420 423 PF00782 0.617
MOD_CDK_SPxK_1 383 389 PF00069 0.772
MOD_CDK_SPxK_1 417 423 PF00069 0.628
MOD_CDK_SPxxK_3 223 230 PF00069 0.614
MOD_CDK_SPxxK_3 639 646 PF00069 0.650
MOD_CK1_1 196 202 PF00069 0.561
MOD_CK1_1 223 229 PF00069 0.750
MOD_CK1_1 231 237 PF00069 0.756
MOD_CK1_1 263 269 PF00069 0.796
MOD_CK1_1 439 445 PF00069 0.674
MOD_CK1_1 468 474 PF00069 0.516
MOD_CK1_1 47 53 PF00069 0.754
MOD_CK1_1 568 574 PF00069 0.471
MOD_CK2_1 196 202 PF00069 0.502
MOD_CK2_1 410 416 PF00069 0.704
MOD_CK2_1 439 445 PF00069 0.707
MOD_CK2_1 529 535 PF00069 0.431
MOD_Cter_Amidation 628 631 PF01082 0.576
MOD_DYRK1A_RPxSP_1 431 435 PF00069 0.737
MOD_GlcNHglycan 145 148 PF01048 0.381
MOD_GlcNHglycan 222 225 PF01048 0.708
MOD_GlcNHglycan 257 260 PF01048 0.814
MOD_GlcNHglycan 262 265 PF01048 0.769
MOD_GlcNHglycan 376 379 PF01048 0.505
MOD_GlcNHglycan 389 392 PF01048 0.594
MOD_GlcNHglycan 396 399 PF01048 0.616
MOD_GlcNHglycan 412 415 PF01048 0.537
MOD_GlcNHglycan 46 49 PF01048 0.669
MOD_GlcNHglycan 633 636 PF01048 0.646
MOD_GlcNHglycan 674 677 PF01048 0.458
MOD_GlcNHglycan 78 82 PF01048 0.605
MOD_GSK3_1 139 146 PF00069 0.478
MOD_GSK3_1 222 229 PF00069 0.795
MOD_GSK3_1 230 237 PF00069 0.766
MOD_GSK3_1 260 267 PF00069 0.751
MOD_GSK3_1 374 381 PF00069 0.547
MOD_GSK3_1 38 45 PF00069 0.597
MOD_GSK3_1 383 390 PF00069 0.612
MOD_GSK3_1 406 413 PF00069 0.689
MOD_GSK3_1 431 438 PF00069 0.675
MOD_GSK3_1 50 57 PF00069 0.735
MOD_GSK3_1 721 728 PF00069 0.429
MOD_LATS_1 609 615 PF00433 0.415
MOD_N-GLC_1 324 329 PF02516 0.376
MOD_N-GLC_1 387 392 PF02516 0.567
MOD_N-GLC_1 410 415 PF02516 0.714
MOD_NEK2_1 177 182 PF00069 0.415
MOD_NEK2_1 235 240 PF00069 0.767
MOD_NEK2_1 354 359 PF00069 0.468
MOD_NEK2_1 38 43 PF00069 0.518
MOD_NEK2_1 393 398 PF00069 0.697
MOD_NEK2_1 400 405 PF00069 0.600
MOD_NEK2_1 529 534 PF00069 0.467
MOD_NEK2_1 547 552 PF00069 0.268
MOD_NEK2_1 556 561 PF00069 0.380
MOD_NEK2_1 591 596 PF00069 0.416
MOD_NEK2_1 701 706 PF00069 0.424
MOD_NEK2_1 709 714 PF00069 0.430
MOD_NEK2_1 721 726 PF00069 0.246
MOD_NEK2_1 732 737 PF00069 0.599
MOD_NEK2_2 236 241 PF00069 0.662
MOD_NEK2_2 688 693 PF00069 0.432
MOD_PIKK_1 349 355 PF00454 0.484
MOD_PIKK_1 439 445 PF00454 0.707
MOD_PK_1 611 617 PF00069 0.494
MOD_PKA_2 316 322 PF00069 0.430
MOD_PKA_2 359 365 PF00069 0.490
MOD_PKA_2 451 457 PF00069 0.523
MOD_PKA_2 529 535 PF00069 0.441
MOD_PKA_2 69 75 PF00069 0.683
MOD_PKA_2 709 715 PF00069 0.522
MOD_Plk_1 591 597 PF00069 0.419
MOD_Plk_1 611 617 PF00069 0.235
MOD_Plk_4 196 202 PF00069 0.499
MOD_Plk_4 236 242 PF00069 0.760
MOD_Plk_4 316 322 PF00069 0.430
MOD_Plk_4 436 442 PF00069 0.751
MOD_Plk_4 502 508 PF00069 0.404
MOD_Plk_4 519 525 PF00069 0.399
MOD_Plk_4 547 553 PF00069 0.476
MOD_Plk_4 557 563 PF00069 0.478
MOD_Plk_4 84 90 PF00069 0.498
MOD_ProDKin_1 223 229 PF00069 0.710
MOD_ProDKin_1 383 389 PF00069 0.753
MOD_ProDKin_1 40 46 PF00069 0.669
MOD_ProDKin_1 417 423 PF00069 0.711
MOD_ProDKin_1 431 437 PF00069 0.588
MOD_ProDKin_1 444 450 PF00069 0.484
MOD_ProDKin_1 539 545 PF00069 0.398
MOD_ProDKin_1 639 645 PF00069 0.716
MOD_SUMO_rev_2 184 194 PF00179 0.511
MOD_SUMO_rev_2 53 62 PF00179 0.610
TRG_DiLeu_BaEn_1 716 721 PF01217 0.423
TRG_DiLeu_BaEn_2 534 540 PF01217 0.464
TRG_DiLeu_BaEn_2 696 702 PF01217 0.410
TRG_DiLeu_BaEn_2 99 105 PF01217 0.476
TRG_ENDOCYTIC_2 129 132 PF00928 0.426
TRG_ENDOCYTIC_2 185 188 PF00928 0.434
TRG_ENDOCYTIC_2 338 341 PF00928 0.393
TRG_ENDOCYTIC_2 503 506 PF00928 0.454
TRG_ENDOCYTIC_2 544 547 PF00928 0.386
TRG_ENDOCYTIC_2 588 591 PF00928 0.430
TRG_ENDOCYTIC_2 596 599 PF00928 0.421
TRG_ENDOCYTIC_2 602 605 PF00928 0.439
TRG_ENDOCYTIC_2 689 692 PF00928 0.489
TRG_ENDOCYTIC_2 7 10 PF00928 0.447
TRG_ER_diArg_1 166 169 PF00400 0.575
TRG_ER_diArg_1 277 280 PF00400 0.534
TRG_ER_diArg_1 490 492 PF00400 0.480
TRG_ER_diArg_1 605 607 PF00400 0.564
TRG_NES_CRM1_1 455 466 PF08389 0.438
TRG_NES_CRM1_1 715 729 PF08389 0.480
TRG_Pf-PMV_PEXEL_1 198 202 PF00026 0.460

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1ILX1 Leptomonas seymouri 62% 100%
A0A0S4JQL9 Bodo saltans 36% 100%
A0A3S5H5W5 Leishmania donovani 99% 100%
A4H4W4 Leishmania braziliensis 78% 99%
E9AL30 Leishmania mexicana (strain MHOM/GT/2001/U1103) 90% 99%
Q4QIS4 Leishmania major 92% 100%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS