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 infantum
UniProt:
E9AGT3_LEIIN
TriTrypDb:
LINF_190019600
Length:
777

Annotations

LeishMANIAdb annotations

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

Annotations by Jardim et al.

Transporters, glycerol uptake

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

E9AGT3
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AGT3

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_Caspase3-7 302 306 PF00656 0.374
CLV_C14_Caspase3-7 721 725 PF00656 0.412
CLV_NRD_NRD_1 228 230 PF00675 0.416
CLV_NRD_NRD_1 459 461 PF00675 0.332
CLV_NRD_NRD_1 541 543 PF00675 0.296
CLV_NRD_NRD_1 629 631 PF00675 0.404
CLV_NRD_NRD_1 657 659 PF00675 0.439
CLV_NRD_NRD_1 670 672 PF00675 0.368
CLV_PCSK_KEX2_1 227 229 PF00082 0.392
CLV_PCSK_KEX2_1 541 543 PF00082 0.296
CLV_PCSK_KEX2_1 629 631 PF00082 0.404
CLV_PCSK_KEX2_1 657 659 PF00082 0.440
CLV_PCSK_KEX2_1 670 672 PF00082 0.389
CLV_PCSK_PC7_1 666 672 PF00082 0.424
CLV_PCSK_SKI1_1 107 111 PF00082 0.576
CLV_PCSK_SKI1_1 164 168 PF00082 0.407
CLV_PCSK_SKI1_1 464 468 PF00082 0.331
CLV_PCSK_SKI1_1 578 582 PF00082 0.457
CLV_PCSK_SKI1_1 658 662 PF00082 0.427
CLV_PCSK_SKI1_1 730 734 PF00082 0.570
DEG_APCC_DBOX_1 577 585 PF00400 0.554
DEG_APCC_DBOX_1 657 665 PF00400 0.631
DEG_MDM2_SWIB_1 110 117 PF02201 0.334
DEG_Nend_UBRbox_2 1 3 PF02207 0.670
DEG_SCF_FBW7_1 736 741 PF00400 0.349
DEG_SPOP_SBC_1 452 456 PF00917 0.561
DOC_CDC14_PxL_1 482 490 PF14671 0.418
DOC_CYCLIN_RxL_1 161 171 PF00134 0.420
DOC_CYCLIN_yCln2_LP_2 430 436 PF00134 0.407
DOC_MAPK_DCC_7 578 588 PF00069 0.341
DOC_MAPK_gen_1 337 346 PF00069 0.420
DOC_MAPK_gen_1 576 583 PF00069 0.487
DOC_MAPK_MEF2A_6 576 583 PF00069 0.571
DOC_PP1_RVXF_1 320 326 PF00149 0.458
DOC_PP1_RVXF_1 350 357 PF00149 0.302
DOC_PP1_RVXF_1 52 58 PF00149 0.666
DOC_PP1_SILK_1 467 472 PF00149 0.374
DOC_PP2B_LxvP_1 430 433 PF13499 0.407
DOC_PP4_FxxP_1 260 263 PF00568 0.364
DOC_PP4_FxxP_1 57 60 PF00568 0.642
DOC_USP7_MATH_1 176 180 PF00917 0.802
DOC_USP7_MATH_1 187 191 PF00917 0.644
DOC_USP7_MATH_1 37 41 PF00917 0.651
DOC_USP7_MATH_1 439 443 PF00917 0.343
DOC_USP7_MATH_1 445 449 PF00917 0.498
DOC_USP7_MATH_1 453 457 PF00917 0.498
DOC_USP7_MATH_1 656 660 PF00917 0.639
DOC_WW_Pin1_4 172 177 PF00397 0.669
DOC_WW_Pin1_4 183 188 PF00397 0.635
DOC_WW_Pin1_4 19 24 PF00397 0.785
DOC_WW_Pin1_4 219 224 PF00397 0.641
DOC_WW_Pin1_4 33 38 PF00397 0.778
DOC_WW_Pin1_4 56 61 PF00397 0.724
DOC_WW_Pin1_4 670 675 PF00397 0.658
DOC_WW_Pin1_4 734 739 PF00397 0.446
LIG_14-3-3_CanoR_1 164 170 PF00244 0.608
LIG_14-3-3_CanoR_1 216 221 PF00244 0.780
LIG_14-3-3_CanoR_1 347 352 PF00244 0.350
LIG_14-3-3_CanoR_1 451 459 PF00244 0.580
LIG_14-3-3_CanoR_1 471 480 PF00244 0.252
LIG_14-3-3_CanoR_1 497 501 PF00244 0.320
LIG_14-3-3_CanoR_1 578 584 PF00244 0.440
LIG_14-3-3_CanoR_1 657 661 PF00244 0.619
LIG_14-3-3_CanoR_1 666 674 PF00244 0.703
LIG_14-3-3_CanoR_1 763 769 PF00244 0.536
LIG_Actin_WH2_2 337 354 PF00022 0.334
LIG_Actin_WH2_2 503 519 PF00022 0.330
LIG_BRCT_BRCA1_1 489 493 PF00533 0.309
LIG_BRCT_BRCA1_1 524 528 PF00533 0.599
LIG_BRCT_BRCA1_1 617 621 PF00533 0.422
LIG_CSL_BTD_1 203 206 PF09270 0.624
LIG_CtBP_PxDLS_1 537 541 PF00389 0.498
LIG_deltaCOP1_diTrp_1 136 142 PF00928 0.350
LIG_deltaCOP1_diTrp_1 556 564 PF00928 0.502
LIG_EH_1 119 123 PF12763 0.340
LIG_eIF4E_1 425 431 PF01652 0.432
LIG_FHA_1 229 235 PF00498 0.695
LIG_FHA_1 308 314 PF00498 0.494
LIG_FHA_1 348 354 PF00498 0.371
LIG_FHA_1 378 384 PF00498 0.371
LIG_FHA_1 545 551 PF00498 0.490
LIG_FHA_1 59 65 PF00498 0.690
LIG_FHA_1 636 642 PF00498 0.658
LIG_FHA_1 689 695 PF00498 0.376
LIG_FHA_1 739 745 PF00498 0.479
LIG_FHA_2 12 18 PF00498 0.646
LIG_FHA_2 497 503 PF00498 0.320
LIG_FHA_2 60 66 PF00498 0.728
LIG_FHA_2 721 727 PF00498 0.431
LIG_Integrin_isoDGR_2 648 650 PF01839 0.485
LIG_LIR_Apic_2 237 241 PF02991 0.312
LIG_LIR_Gen_1 111 122 PF02991 0.428
LIG_LIR_Gen_1 144 154 PF02991 0.319
LIG_LIR_Gen_1 419 428 PF02991 0.301
LIG_LIR_Gen_1 441 450 PF02991 0.373
LIG_LIR_Gen_1 475 485 PF02991 0.421
LIG_LIR_Gen_1 490 501 PF02991 0.287
LIG_LIR_Gen_1 525 536 PF02991 0.563
LIG_LIR_Gen_1 70 78 PF02991 0.688
LIG_LIR_Gen_1 767 775 PF02991 0.528
LIG_LIR_Nem_3 103 109 PF02991 0.369
LIG_LIR_Nem_3 111 117 PF02991 0.401
LIG_LIR_Nem_3 136 142 PF02991 0.339
LIG_LIR_Nem_3 144 149 PF02991 0.321
LIG_LIR_Nem_3 160 166 PF02991 0.465
LIG_LIR_Nem_3 310 315 PF02991 0.396
LIG_LIR_Nem_3 419 425 PF02991 0.310
LIG_LIR_Nem_3 441 446 PF02991 0.379
LIG_LIR_Nem_3 475 480 PF02991 0.409
LIG_LIR_Nem_3 490 496 PF02991 0.248
LIG_LIR_Nem_3 525 531 PF02991 0.583
LIG_LIR_Nem_3 678 684 PF02991 0.608
LIG_LIR_Nem_3 70 74 PF02991 0.646
LIG_LIR_Nem_3 767 771 PF02991 0.577
LIG_LYPXL_S_1 74 78 PF13949 0.474
LIG_LYPXL_yS_3 75 78 PF13949 0.591
LIG_MYND_1 33 37 PF01753 0.639
LIG_NRBOX 151 157 PF00104 0.430
LIG_PAM2_1 670 682 PF00658 0.557
LIG_Pex14_1 312 316 PF04695 0.426
LIG_Pex14_1 342 346 PF04695 0.328
LIG_Pex14_1 557 561 PF04695 0.496
LIG_Pex14_1 564 568 PF04695 0.496
LIG_Pex14_2 110 114 PF04695 0.338
LIG_Pex14_2 518 522 PF04695 0.350
LIG_Pex14_2 553 557 PF04695 0.498
LIG_Pex14_2 589 593 PF04695 0.349
LIG_PTB_Apo_2 117 124 PF02174 0.352
LIG_REV1ctd_RIR_1 120 129 PF16727 0.354
LIG_SH2_CRK 163 167 PF00017 0.533
LIG_SH2_CRK 244 248 PF00017 0.350
LIG_SH2_CRK 420 424 PF00017 0.301
LIG_SH2_CRK 477 481 PF00017 0.453
LIG_SH2_CRK 491 495 PF00017 0.328
LIG_SH2_CRK 568 572 PF00017 0.496
LIG_SH2_CRK 71 75 PF00017 0.692
LIG_SH2_NCK_1 244 248 PF00017 0.370
LIG_SH2_NCK_1 71 75 PF00017 0.643
LIG_SH2_SRC 131 134 PF00017 0.329
LIG_SH2_STAP1 131 135 PF00017 0.373
LIG_SH2_STAP1 425 429 PF00017 0.374
LIG_SH2_STAP1 491 495 PF00017 0.314
LIG_SH2_STAP1 71 75 PF00017 0.727
LIG_SH2_STAP1 749 753 PF00017 0.314
LIG_SH2_STAT3 311 314 PF00017 0.413
LIG_SH2_STAT5 244 247 PF00017 0.369
LIG_SH2_STAT5 271 274 PF00017 0.433
LIG_SH2_STAT5 299 302 PF00017 0.487
LIG_SH2_STAT5 315 318 PF00017 0.401
LIG_SH2_STAT5 428 431 PF00017 0.356
LIG_SH2_STAT5 435 438 PF00017 0.343
LIG_SH2_STAT5 473 476 PF00017 0.356
LIG_SH2_STAT5 477 480 PF00017 0.359
LIG_SH2_STAT5 513 516 PF00017 0.416
LIG_SH2_STAT5 570 573 PF00017 0.496
LIG_SH2_STAT5 768 771 PF00017 0.540
LIG_SH2_STAT5 83 86 PF00017 0.336
LIG_SH3_3 12 18 PF00018 0.660
LIG_SH3_3 200 206 PF00018 0.663
LIG_SH3_3 252 258 PF00018 0.472
LIG_SH3_3 328 334 PF00018 0.536
LIG_SH3_3 38 44 PF00018 0.782
LIG_SH3_3 426 432 PF00018 0.451
LIG_SH3_3 480 486 PF00018 0.418
LIG_SUMO_SIM_par_1 299 305 PF11976 0.526
LIG_TRFH_1 428 432 PF08558 0.456
LIG_TYR_ITIM 511 516 PF00017 0.429
LIG_TYR_ITIM 566 571 PF00017 0.338
LIG_UBA3_1 510 517 PF00899 0.374
LIG_UBA3_1 771 776 PF00899 0.519
LIG_WRC_WIRS_1 101 106 PF05994 0.386
LIG_WRC_WIRS_1 440 445 PF05994 0.363
LIG_WW_1 432 435 PF00397 0.407
LIG_WW_3 205 209 PF00397 0.450
LIG_WW_3 43 47 PF00397 0.542
MOD_CK1_1 168 174 PF00069 0.571
MOD_CK1_1 179 185 PF00069 0.580
MOD_CK1_1 188 194 PF00069 0.522
MOD_CK1_1 19 25 PF00069 0.691
MOD_CK1_1 36 42 PF00069 0.761
MOD_CK1_1 59 65 PF00069 0.679
MOD_CK1_1 720 726 PF00069 0.660
MOD_CK2_1 496 502 PF00069 0.445
MOD_CK2_1 529 535 PF00069 0.365
MOD_CMANNOS 554 557 PF00535 0.343
MOD_GlcNHglycan 159 162 PF01048 0.447
MOD_GlcNHglycan 172 175 PF01048 0.591
MOD_GlcNHglycan 187 190 PF01048 0.751
MOD_GlcNHglycan 192 196 PF01048 0.613
MOD_GlcNHglycan 223 226 PF01048 0.701
MOD_GlcNHglycan 29 32 PF01048 0.715
MOD_GlcNHglycan 394 397 PF01048 0.493
MOD_GlcNHglycan 531 534 PF01048 0.432
MOD_GlcNHglycan 617 620 PF01048 0.355
MOD_GlcNHglycan 667 670 PF01048 0.475
MOD_GlcNHglycan 720 723 PF01048 0.688
MOD_GlcNHglycan 751 754 PF01048 0.369
MOD_GSK3_1 165 172 PF00069 0.598
MOD_GSK3_1 179 186 PF00069 0.714
MOD_GSK3_1 187 194 PF00069 0.759
MOD_GSK3_1 212 219 PF00069 0.540
MOD_GSK3_1 33 40 PF00069 0.770
MOD_GSK3_1 635 642 PF00069 0.532
MOD_GSK3_1 734 741 PF00069 0.531
MOD_GSK3_1 86 93 PF00069 0.492
MOD_LATS_1 449 455 PF00433 0.317
MOD_NEK2_1 167 172 PF00069 0.538
MOD_NEK2_1 234 239 PF00069 0.492
MOD_NEK2_1 27 32 PF00069 0.782
MOD_NEK2_1 307 312 PF00069 0.538
MOD_NEK2_1 346 351 PF00069 0.373
MOD_NEK2_1 496 501 PF00069 0.361
MOD_NEK2_1 516 521 PF00069 0.238
MOD_NEK2_1 544 549 PF00069 0.357
MOD_NEK2_1 675 680 PF00069 0.513
MOD_NEK2_1 747 752 PF00069 0.380
MOD_NEK2_2 49 54 PF00069 0.518
MOD_PIKK_1 39 45 PF00454 0.721
MOD_PK_1 77 83 PF00069 0.534
MOD_PKA_1 228 234 PF00069 0.436
MOD_PKA_2 228 234 PF00069 0.492
MOD_PKA_2 346 352 PF00069 0.444
MOD_PKA_2 496 502 PF00069 0.374
MOD_PKA_2 649 655 PF00069 0.574
MOD_PKA_2 656 662 PF00069 0.478
MOD_PKA_2 665 671 PF00069 0.577
MOD_PKB_1 214 222 PF00069 0.477
MOD_Plk_1 11 17 PF00069 0.547
MOD_Plk_1 131 137 PF00069 0.426
MOD_Plk_1 307 313 PF00069 0.417
MOD_Plk_1 475 481 PF00069 0.501
MOD_Plk_1 69 75 PF00069 0.517
MOD_Plk_4 16 22 PF00069 0.555
MOD_Plk_4 242 248 PF00069 0.450
MOD_Plk_4 293 299 PF00069 0.379
MOD_Plk_4 307 313 PF00069 0.489
MOD_Plk_4 475 481 PF00069 0.444
MOD_Plk_4 496 502 PF00069 0.408
MOD_Plk_4 579 585 PF00069 0.418
MOD_Plk_4 675 681 PF00069 0.568
MOD_Plk_4 689 695 PF00069 0.326
MOD_Plk_4 70 76 PF00069 0.683
MOD_Plk_4 764 770 PF00069 0.392
MOD_Plk_4 90 96 PF00069 0.270
MOD_ProDKin_1 172 178 PF00069 0.586
MOD_ProDKin_1 183 189 PF00069 0.536
MOD_ProDKin_1 19 25 PF00069 0.744
MOD_ProDKin_1 219 225 PF00069 0.540
MOD_ProDKin_1 33 39 PF00069 0.737
MOD_ProDKin_1 56 62 PF00069 0.668
MOD_ProDKin_1 670 676 PF00069 0.564
MOD_ProDKin_1 734 740 PF00069 0.542
TRG_DiLeu_BaEn_2 501 507 PF01217 0.422
TRG_DiLeu_BaLyEn_6 260 265 PF01217 0.427
TRG_DiLeu_BaLyEn_6 30 35 PF01217 0.537
TRG_DiLeu_BaLyEn_6 349 354 PF01217 0.454
TRG_ENDOCYTIC_2 106 109 PF00928 0.520
TRG_ENDOCYTIC_2 146 149 PF00928 0.390
TRG_ENDOCYTIC_2 163 166 PF00928 0.282
TRG_ENDOCYTIC_2 244 247 PF00928 0.354
TRG_ENDOCYTIC_2 271 274 PF00928 0.362
TRG_ENDOCYTIC_2 283 286 PF00928 0.326
TRG_ENDOCYTIC_2 420 423 PF00928 0.346
TRG_ENDOCYTIC_2 428 431 PF00928 0.342
TRG_ENDOCYTIC_2 477 480 PF00928 0.374
TRG_ENDOCYTIC_2 491 494 PF00928 0.357
TRG_ENDOCYTIC_2 513 516 PF00928 0.396
TRG_ENDOCYTIC_2 568 571 PF00928 0.341
TRG_ENDOCYTIC_2 681 684 PF00928 0.367
TRG_ENDOCYTIC_2 71 74 PF00928 0.555
TRG_ENDOCYTIC_2 75 78 PF00928 0.516
TRG_ENDOCYTIC_2 768 771 PF00928 0.451
TRG_ER_diArg_1 213 216 PF00400 0.535
TRG_ER_diArg_1 227 229 PF00400 0.422
TRG_ER_diArg_1 339 342 PF00400 0.454
TRG_ER_diArg_1 540 542 PF00400 0.341
TRG_ER_diArg_1 576 579 PF00400 0.365
TRG_ER_diArg_1 628 630 PF00400 0.488
TRG_ER_diArg_1 656 658 PF00400 0.567
TRG_ER_diArg_1 670 672 PF00400 0.434

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0S4IRP6 Bodo saltans 35% 100%
A0A1X0P614 Trypanosomatidae 34% 100%
A0A1X0P616 Trypanosomatidae 41% 100%
A0A3Q8IAC1 Leishmania donovani 97% 100%
A0A3Q8IBC3 Leishmania donovani 86% 100%
A0A3Q8IBE0 Leishmania donovani 74% 93%
A0A3Q8IDD7 Leishmania donovani 97% 100%
A0A3S5H769 Leishmania donovani 96% 100%
A0A3S5IRW9 Trypanosoma rangeli 35% 100%
A0A3S7WVJ2 Leishmania donovani 74% 92%
A0A3S7WVK4 Leishmania donovani 99% 100%
A4HA75 Leishmania braziliensis 62% 99%
A4HA76 Leishmania braziliensis 62% 100%
A4HA77 Leishmania braziliensis 64% 100%
A4HA80 Leishmania braziliensis 58% 100%
A4HA81 Leishmania braziliensis 66% 100%
A4HA82 Leishmania braziliensis 68% 100%
D0A0T4 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 37% 100%
E8NHJ2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 89% 100%
E9AGT0 Leishmania infantum 74% 100%
E9AGT1 Leishmania infantum 99% 100%
E9AGT2 Leishmania infantum 96% 100%
E9AGT4 Leishmania infantum 97% 100%
E9AS85 Leishmania mexicana (strain MHOM/GT/2001/U1103) 89% 100%
E9AS86 Leishmania mexicana (strain MHOM/GT/2001/U1103) 31% 100%
Q4QD78 Leishmania major 90% 100%
Q4QD79 Leishmania major 91% 100%
Q4QD80 Leishmania major 91% 100%
Q4QD81 Leishmania major 71% 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