LeishMANIAdb
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Putative glycerol uptake protein

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

Quick info

Protein:
Putative glycerol uptake protein
Gene product:
glycerol uptake protein, putative
Species:
Leishmania mexicana
UniProt:
E9AS85_LEIMU
TriTrypDb:
LmxM.19.1345 *
Length:
775

Annotations

LeishMANIAdb annotations

Membrane-bound O-acyltransferase involved in the remodeling of glycosylphosphatidylinositol (GPI) anchors. Related to fungal GUP1 proteins.

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: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 30
NetGPI no yes: 0, no: 30
Cellular components
Term Name Level Count
GO:0016020 membrane 2 31
GO:0110165 cellular anatomical entity 1 31
GO:0005737 cytoplasm 2 4
GO:0005783 endoplasmic reticulum 5 4
GO:0043226 organelle 2 4
GO:0043227 membrane-bounded organelle 3 4
GO:0043229 intracellular organelle 3 4
GO:0043231 intracellular membrane-bounded organelle 4 4

Expansion

Sequence features

E9AS85
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AS85

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 5
GO:0016740 transferase activity 2 5
GO:0016746 acyltransferase activity 3 5

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 719 723 PF00656 0.420
CLV_NRD_NRD_1 226 228 PF00675 0.403
CLV_NRD_NRD_1 457 459 PF00675 0.332
CLV_NRD_NRD_1 539 541 PF00675 0.296
CLV_NRD_NRD_1 627 629 PF00675 0.414
CLV_NRD_NRD_1 655 657 PF00675 0.428
CLV_NRD_NRD_1 668 670 PF00675 0.375
CLV_PCSK_KEX2_1 145 147 PF00082 0.243
CLV_PCSK_KEX2_1 226 228 PF00082 0.374
CLV_PCSK_KEX2_1 539 541 PF00082 0.296
CLV_PCSK_KEX2_1 627 629 PF00082 0.414
CLV_PCSK_KEX2_1 655 657 PF00082 0.430
CLV_PCSK_KEX2_1 668 670 PF00082 0.396
CLV_PCSK_PC1ET2_1 145 147 PF00082 0.235
CLV_PCSK_PC7_1 664 670 PF00082 0.426
CLV_PCSK_SKI1_1 105 109 PF00082 0.582
CLV_PCSK_SKI1_1 145 149 PF00082 0.276
CLV_PCSK_SKI1_1 162 166 PF00082 0.417
CLV_PCSK_SKI1_1 462 466 PF00082 0.331
CLV_PCSK_SKI1_1 576 580 PF00082 0.457
CLV_PCSK_SKI1_1 656 660 PF00082 0.426
CLV_PCSK_SKI1_1 728 732 PF00082 0.590
DEG_APCC_DBOX_1 49 57 PF00400 0.572
DEG_APCC_DBOX_1 575 583 PF00400 0.422
DEG_APCC_DBOX_1 655 663 PF00400 0.632
DEG_MDM2_SWIB_1 108 115 PF02201 0.336
DEG_SCF_FBW7_1 734 739 PF00400 0.375
DEG_SPOP_SBC_1 450 454 PF00917 0.561
DOC_CDC14_PxL_1 480 488 PF14671 0.418
DOC_CKS1_1 167 172 PF01111 0.563
DOC_CKS1_1 58 63 PF01111 0.530
DOC_CYCLIN_RxL_1 159 169 PF00134 0.438
DOC_CYCLIN_yCln2_LP_2 18 21 PF00134 0.592
DOC_CYCLIN_yCln2_LP_2 428 434 PF00134 0.407
DOC_MAPK_DCC_7 576 586 PF00069 0.341
DOC_MAPK_gen_1 145 152 PF00069 0.237
DOC_MAPK_gen_1 337 344 PF00069 0.406
DOC_MAPK_gen_1 574 581 PF00069 0.487
DOC_MAPK_MEF2A_6 145 154 PF00069 0.418
DOC_MAPK_MEF2A_6 574 581 PF00069 0.571
DOC_MAPK_NFAT4_5 145 153 PF00069 0.264
DOC_PP1_RVXF_1 348 355 PF00149 0.303
DOC_PP1_RVXF_1 50 56 PF00149 0.675
DOC_PP1_SILK_1 465 470 PF00149 0.374
DOC_PP2B_LxvP_1 18 21 PF13499 0.592
DOC_PP2B_LxvP_1 428 431 PF13499 0.407
DOC_PP4_FxxP_1 55 58 PF00568 0.636
DOC_USP7_MATH_1 174 178 PF00917 0.805
DOC_USP7_MATH_1 181 185 PF00917 0.673
DOC_USP7_MATH_1 25 29 PF00917 0.769
DOC_USP7_MATH_1 35 39 PF00917 0.668
DOC_USP7_MATH_1 399 403 PF00917 0.388
DOC_USP7_MATH_1 437 441 PF00917 0.343
DOC_USP7_MATH_1 443 447 PF00917 0.498
DOC_USP7_MATH_1 451 455 PF00917 0.498
DOC_USP7_MATH_1 643 647 PF00917 0.615
DOC_USP7_MATH_1 654 658 PF00917 0.630
DOC_USP7_MATH_1 730 734 PF00917 0.350
DOC_USP7_UBL2_3 206 210 PF12436 0.562
DOC_USP7_UBL2_3 3 7 PF12436 0.604
DOC_WW_Pin1_4 166 171 PF00397 0.636
DOC_WW_Pin1_4 19 24 PF00397 0.685
DOC_WW_Pin1_4 217 222 PF00397 0.626
DOC_WW_Pin1_4 31 36 PF00397 0.802
DOC_WW_Pin1_4 54 59 PF00397 0.717
DOC_WW_Pin1_4 668 673 PF00397 0.668
DOC_WW_Pin1_4 732 737 PF00397 0.473
LIG_14-3-3_CanoR_1 105 111 PF00244 0.263
LIG_14-3-3_CanoR_1 162 168 PF00244 0.620
LIG_14-3-3_CanoR_1 337 343 PF00244 0.374
LIG_14-3-3_CanoR_1 345 350 PF00244 0.353
LIG_14-3-3_CanoR_1 449 457 PF00244 0.580
LIG_14-3-3_CanoR_1 469 478 PF00244 0.252
LIG_14-3-3_CanoR_1 495 499 PF00244 0.320
LIG_14-3-3_CanoR_1 576 582 PF00244 0.440
LIG_14-3-3_CanoR_1 655 659 PF00244 0.614
LIG_14-3-3_CanoR_1 664 672 PF00244 0.707
LIG_14-3-3_CanoR_1 761 767 PF00244 0.559
LIG_Actin_WH2_2 335 352 PF00022 0.337
LIG_Actin_WH2_2 501 517 PF00022 0.330
LIG_BRCT_BRCA1_1 340 344 PF00533 0.315
LIG_BRCT_BRCA1_1 487 491 PF00533 0.309
LIG_BRCT_BRCA1_1 615 619 PF00533 0.422
LIG_CtBP_PxDLS_1 535 539 PF00389 0.498
LIG_deltaCOP1_diTrp_1 134 140 PF00928 0.365
LIG_deltaCOP1_diTrp_1 550 559 PF00928 0.493
LIG_EH_1 117 121 PF12763 0.340
LIG_eIF4E_1 423 429 PF01652 0.432
LIG_EVH1_2 20 24 PF00568 0.587
LIG_FHA_1 227 233 PF00498 0.692
LIG_FHA_1 306 312 PF00498 0.510
LIG_FHA_1 313 319 PF00498 0.390
LIG_FHA_1 321 327 PF00498 0.340
LIG_FHA_1 346 352 PF00498 0.373
LIG_FHA_1 543 549 PF00498 0.490
LIG_FHA_1 57 63 PF00498 0.667
LIG_FHA_1 634 640 PF00498 0.648
LIG_FHA_1 737 743 PF00498 0.479
LIG_FHA_1 762 768 PF00498 0.618
LIG_FHA_1 8 14 PF00498 0.615
LIG_FHA_2 10 16 PF00498 0.653
LIG_FHA_2 495 501 PF00498 0.320
LIG_FHA_2 545 551 PF00498 0.441
LIG_FHA_2 58 64 PF00498 0.709
LIG_FHA_2 719 725 PF00498 0.441
LIG_LIR_Apic_2 166 170 PF02991 0.535
LIG_LIR_Apic_2 235 239 PF02991 0.312
LIG_LIR_Gen_1 109 120 PF02991 0.429
LIG_LIR_Gen_1 417 426 PF02991 0.301
LIG_LIR_Gen_1 439 448 PF02991 0.373
LIG_LIR_Gen_1 473 483 PF02991 0.421
LIG_LIR_Gen_1 488 499 PF02991 0.287
LIG_LIR_Gen_1 764 773 PF02991 0.541
LIG_LIR_Nem_3 101 107 PF02991 0.380
LIG_LIR_Nem_3 109 115 PF02991 0.403
LIG_LIR_Nem_3 134 140 PF02991 0.353
LIG_LIR_Nem_3 142 147 PF02991 0.275
LIG_LIR_Nem_3 158 164 PF02991 0.476
LIG_LIR_Nem_3 308 313 PF02991 0.420
LIG_LIR_Nem_3 417 423 PF02991 0.310
LIG_LIR_Nem_3 439 444 PF02991 0.379
LIG_LIR_Nem_3 473 478 PF02991 0.409
LIG_LIR_Nem_3 488 494 PF02991 0.248
LIG_LIR_Nem_3 689 695 PF02991 0.381
LIG_LIR_Nem_3 70 76 PF02991 0.652
LIG_LIR_Nem_3 764 769 PF02991 0.593
LIG_LYPXL_S_1 72 76 PF13949 0.499
LIG_LYPXL_yS_3 73 76 PF13949 0.617
LIG_MYND_1 16 20 PF01753 0.592
LIG_MYND_1 31 35 PF01753 0.665
LIG_NRBOX 149 155 PF00104 0.430
LIG_PAM2_1 668 680 PF00658 0.569
LIG_Pex14_1 340 344 PF04695 0.332
LIG_Pex14_1 555 559 PF04695 0.496
LIG_Pex14_1 562 566 PF04695 0.496
LIG_Pex14_2 108 112 PF04695 0.342
LIG_Pex14_2 516 520 PF04695 0.350
LIG_Pex14_2 551 555 PF04695 0.498
LIG_Pex14_2 587 591 PF04695 0.349
LIG_PTB_Apo_2 115 122 PF02174 0.349
LIG_REV1ctd_RIR_1 118 127 PF16727 0.353
LIG_SH2_CRK 161 165 PF00017 0.541
LIG_SH2_CRK 167 171 PF00017 0.590
LIG_SH2_CRK 313 317 PF00017 0.312
LIG_SH2_CRK 418 422 PF00017 0.301
LIG_SH2_CRK 475 479 PF00017 0.453
LIG_SH2_CRK 489 493 PF00017 0.328
LIG_SH2_CRK 566 570 PF00017 0.496
LIG_SH2_CRK 69 73 PF00017 0.725
LIG_SH2_GRB2like 129 132 PF00017 0.334
LIG_SH2_NCK_1 167 171 PF00017 0.561
LIG_SH2_NCK_1 242 246 PF00017 0.370
LIG_SH2_NCK_1 69 73 PF00017 0.677
LIG_SH2_SRC 129 132 PF00017 0.341
LIG_SH2_STAP1 129 133 PF00017 0.383
LIG_SH2_STAP1 423 427 PF00017 0.374
LIG_SH2_STAP1 489 493 PF00017 0.314
LIG_SH2_STAP1 69 73 PF00017 0.761
LIG_SH2_STAP1 747 751 PF00017 0.314
LIG_SH2_STAT3 309 312 PF00017 0.430
LIG_SH2_STAT5 167 170 PF00017 0.570
LIG_SH2_STAT5 242 245 PF00017 0.369
LIG_SH2_STAT5 269 272 PF00017 0.433
LIG_SH2_STAT5 297 300 PF00017 0.497
LIG_SH2_STAT5 313 316 PF00017 0.413
LIG_SH2_STAT5 426 429 PF00017 0.356
LIG_SH2_STAT5 433 436 PF00017 0.343
LIG_SH2_STAT5 471 474 PF00017 0.356
LIG_SH2_STAT5 475 478 PF00017 0.359
LIG_SH2_STAT5 511 514 PF00017 0.416
LIG_SH2_STAT5 568 571 PF00017 0.496
LIG_SH2_STAT5 766 769 PF00017 0.554
LIG_SH2_STAT5 81 84 PF00017 0.336
LIG_SH3_3 10 16 PF00018 0.667
LIG_SH3_3 17 23 PF00018 0.597
LIG_SH3_3 198 204 PF00018 0.662
LIG_SH3_3 250 256 PF00018 0.479
LIG_SH3_3 36 42 PF00018 0.794
LIG_SH3_3 424 430 PF00018 0.451
LIG_SH3_3 478 484 PF00018 0.418
LIG_SH3_3 55 61 PF00018 0.532
LIG_SUMO_SIM_anti_2 290 297 PF11976 0.313
LIG_SUMO_SIM_anti_2 315 321 PF11976 0.308
LIG_SUMO_SIM_par_1 297 303 PF11976 0.535
LIG_SUMO_SIM_par_1 314 321 PF11976 0.514
LIG_SUMO_SIM_par_1 544 550 PF11976 0.449
LIG_TRFH_1 426 430 PF08558 0.456
LIG_TYR_ITIM 311 316 PF00017 0.356
LIG_TYR_ITIM 509 514 PF00017 0.429
LIG_TYR_ITIM 564 569 PF00017 0.338
LIG_UBA3_1 508 515 PF00899 0.374
LIG_UBA3_1 769 774 PF00899 0.528
LIG_WRC_WIRS_1 438 443 PF05994 0.363
LIG_WRC_WIRS_1 99 104 PF05994 0.405
LIG_WW_1 430 433 PF00397 0.407
LIG_WW_3 41 45 PF00397 0.553
MOD_CK1_1 166 172 PF00069 0.597
MOD_CK1_1 177 183 PF00069 0.576
MOD_CK1_1 186 192 PF00069 0.504
MOD_CK1_1 317 323 PF00069 0.508
MOD_CK1_1 34 40 PF00069 0.783
MOD_CK1_1 57 63 PF00069 0.648
MOD_CK1_1 718 724 PF00069 0.678
MOD_CK1_1 9 15 PF00069 0.495
MOD_CK2_1 494 500 PF00069 0.445
MOD_CK2_1 527 533 PF00069 0.365
MOD_CMANNOS 552 555 PF00535 0.343
MOD_GlcNHglycan 157 160 PF01048 0.447
MOD_GlcNHglycan 170 173 PF01048 0.612
MOD_GlcNHglycan 185 188 PF01048 0.741
MOD_GlcNHglycan 221 224 PF01048 0.676
MOD_GlcNHglycan 27 30 PF01048 0.742
MOD_GlcNHglycan 392 395 PF01048 0.519
MOD_GlcNHglycan 529 532 PF01048 0.432
MOD_GlcNHglycan 645 648 PF01048 0.494
MOD_GlcNHglycan 665 668 PF01048 0.473
MOD_GlcNHglycan 718 721 PF01048 0.709
MOD_GlcNHglycan 749 752 PF01048 0.369
MOD_GSK3_1 166 173 PF00069 0.663
MOD_GSK3_1 177 184 PF00069 0.709
MOD_GSK3_1 185 192 PF00069 0.745
MOD_GSK3_1 31 38 PF00069 0.802
MOD_GSK3_1 314 321 PF00069 0.670
MOD_GSK3_1 633 640 PF00069 0.522
MOD_GSK3_1 732 739 PF00069 0.569
MOD_GSK3_1 84 91 PF00069 0.492
MOD_LATS_1 447 453 PF00433 0.317
MOD_NEK2_1 165 170 PF00069 0.562
MOD_NEK2_1 185 190 PF00069 0.681
MOD_NEK2_1 232 237 PF00069 0.497
MOD_NEK2_1 288 293 PF00069 0.342
MOD_NEK2_1 305 310 PF00069 0.550
MOD_NEK2_1 338 343 PF00069 0.394
MOD_NEK2_1 344 349 PF00069 0.378
MOD_NEK2_1 494 499 PF00069 0.361
MOD_NEK2_1 514 519 PF00069 0.238
MOD_NEK2_1 542 547 PF00069 0.357
MOD_NEK2_1 673 678 PF00069 0.527
MOD_NEK2_1 745 750 PF00069 0.380
MOD_NEK2_2 687 692 PF00069 0.306
MOD_PIKK_1 123 129 PF00454 0.371
MOD_PK_1 75 81 PF00069 0.556
MOD_PKA_1 226 232 PF00069 0.427
MOD_PKA_2 226 232 PF00069 0.484
MOD_PKA_2 338 344 PF00069 0.442
MOD_PKA_2 370 376 PF00069 0.450
MOD_PKA_2 494 500 PF00069 0.374
MOD_PKA_2 654 660 PF00069 0.471
MOD_PKA_2 663 669 PF00069 0.579
MOD_Plk_1 129 135 PF00069 0.449
MOD_Plk_1 305 311 PF00069 0.433
MOD_Plk_1 473 479 PF00069 0.501
MOD_Plk_4 14 20 PF00069 0.564
MOD_Plk_4 305 311 PF00069 0.505
MOD_Plk_4 314 320 PF00069 0.547
MOD_Plk_4 473 479 PF00069 0.444
MOD_Plk_4 494 500 PF00069 0.408
MOD_Plk_4 577 583 PF00069 0.418
MOD_Plk_4 673 679 PF00069 0.586
MOD_Plk_4 68 74 PF00069 0.725
MOD_Plk_4 687 693 PF00069 0.326
MOD_Plk_4 762 768 PF00069 0.420
MOD_Plk_4 88 94 PF00069 0.270
MOD_ProDKin_1 166 172 PF00069 0.542
MOD_ProDKin_1 19 25 PF00069 0.604
MOD_ProDKin_1 217 223 PF00069 0.520
MOD_ProDKin_1 31 37 PF00069 0.771
MOD_ProDKin_1 54 60 PF00069 0.655
MOD_ProDKin_1 668 674 PF00069 0.579
MOD_ProDKin_1 732 738 PF00069 0.580
TRG_DiLeu_BaEn_2 499 505 PF01217 0.422
TRG_DiLeu_BaLyEn_6 258 263 PF01217 0.427
TRG_DiLeu_BaLyEn_6 28 33 PF01217 0.570
TRG_DiLeu_BaLyEn_6 347 352 PF01217 0.457
TRG_DiLeu_BaLyEn_6 521 526 PF01217 0.234
TRG_ENDOCYTIC_2 104 107 PF00928 0.542
TRG_ENDOCYTIC_2 144 147 PF00928 0.390
TRG_ENDOCYTIC_2 161 164 PF00928 0.292
TRG_ENDOCYTIC_2 269 272 PF00928 0.362
TRG_ENDOCYTIC_2 281 284 PF00928 0.326
TRG_ENDOCYTIC_2 313 316 PF00928 0.482
TRG_ENDOCYTIC_2 418 421 PF00928 0.346
TRG_ENDOCYTIC_2 426 429 PF00928 0.342
TRG_ENDOCYTIC_2 475 478 PF00928 0.374
TRG_ENDOCYTIC_2 489 492 PF00928 0.357
TRG_ENDOCYTIC_2 511 514 PF00928 0.396
TRG_ENDOCYTIC_2 566 569 PF00928 0.341
TRG_ENDOCYTIC_2 69 72 PF00928 0.599
TRG_ENDOCYTIC_2 73 76 PF00928 0.552
TRG_ENDOCYTIC_2 766 769 PF00928 0.470
TRG_ER_diArg_1 211 214 PF00400 0.545
TRG_ER_diArg_1 337 340 PF00400 0.452
TRG_ER_diArg_1 49 52 PF00400 0.490
TRG_ER_diArg_1 538 540 PF00400 0.341
TRG_ER_diArg_1 574 577 PF00400 0.365
TRG_ER_diArg_1 626 628 PF00400 0.507
TRG_ER_diArg_1 654 656 PF00400 0.549
TRG_ER_diArg_1 668 670 PF00400 0.444
TRG_NES_CRM1_1 536 550 PF08389 0.270

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0S4IRP6 Bodo saltans 35% 100%
A0A1X0P614 Trypanosomatidae 34% 100%
A0A1X0P616 Trypanosomatidae 41% 100%
A0A3Q8IAC1 Leishmania donovani 89% 100%
A0A3Q8IBC3 Leishmania donovani 83% 100%
A0A3Q8IBE0 Leishmania donovani 66% 93%
A0A3Q8IDD7 Leishmania donovani 89% 100%
A0A3S5H769 Leishmania donovani 91% 100%
A0A3S5IRW9 Trypanosoma rangeli 35% 100%
A0A3S7WVJ2 Leishmania donovani 66% 92%
A0A3S7WVK4 Leishmania donovani 89% 100%
A4HA75 Leishmania braziliensis 61% 100%
A4HA76 Leishmania braziliensis 60% 100%
A4HA77 Leishmania braziliensis 64% 100%
A4HA80 Leishmania braziliensis 56% 100%
A4HA81 Leishmania braziliensis 66% 100%
A4HA82 Leishmania braziliensis 67% 100%
D0A0T4 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 38% 100%
E8NHJ2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 98% 100%
E9AGT0 Leishmania infantum 66% 92%
E9AGT1 Leishmania infantum 89% 100%
E9AGT2 Leishmania infantum 90% 100%
E9AGT3 Leishmania infantum 89% 100%
E9AGT4 Leishmania infantum 90% 100%
E9AS86 Leishmania mexicana (strain MHOM/GT/2001/U1103) 31% 100%
Q4QD78 Leishmania major 88% 100%
Q4QD79 Leishmania major 87% 100%
Q4QD80 Leishmania major 86% 100%
Q4QD81 Leishmania major 68% 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