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 braziliensis
UniProt:
A4HA82_LEIBR
TriTrypDb:
LbrM.19.1590 , LBRM2903_190022100
Length:
748

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: 29
NetGPI no yes: 0, no: 29
Cellular components
Term Name Level Count
GO:0016020 membrane 2 30
GO:0110165 cellular anatomical entity 1 30
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

A4HA82
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HA82

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_NRD_NRD_1 432 434 PF00675 0.321
CLV_NRD_NRD_1 514 516 PF00675 0.302
CLV_NRD_NRD_1 602 604 PF00675 0.400
CLV_NRD_NRD_1 631 633 PF00675 0.413
CLV_NRD_NRD_1 643 645 PF00675 0.377
CLV_PCSK_KEX2_1 514 516 PF00082 0.302
CLV_PCSK_KEX2_1 602 604 PF00082 0.400
CLV_PCSK_KEX2_1 630 632 PF00082 0.422
CLV_PCSK_KEX2_1 643 645 PF00082 0.398
CLV_PCSK_KEX2_1 742 744 PF00082 0.299
CLV_PCSK_PC1ET2_1 742 744 PF00082 0.344
CLV_PCSK_PC7_1 639 645 PF00082 0.433
CLV_PCSK_SKI1_1 138 142 PF00082 0.333
CLV_PCSK_SKI1_1 434 438 PF00082 0.311
CLV_PCSK_SKI1_1 551 555 PF00082 0.445
CLV_PCSK_SKI1_1 575 579 PF00082 0.449
CLV_PCSK_SKI1_1 623 627 PF00082 0.416
CLV_PCSK_SKI1_1 631 635 PF00082 0.423
CLV_PCSK_SKI1_1 731 735 PF00082 0.289
DEG_APCC_DBOX_1 550 558 PF00400 0.425
DEG_APCC_DBOX_1 630 638 PF00400 0.627
DEG_Nend_UBRbox_1 1 4 PF02207 0.609
DEG_SCF_FBW7_1 706 713 PF00400 0.352
DEG_SPOP_SBC_1 16 20 PF00917 0.605
DEG_SPOP_SBC_1 425 429 PF00917 0.564
DOC_CDC14_PxL_1 455 463 PF14671 0.421
DOC_CYCLIN_yCln2_LP_2 12 15 PF00134 0.620
DOC_CYCLIN_yCln2_LP_2 403 409 PF00134 0.445
DOC_MAPK_DCC_7 551 561 PF00069 0.344
DOC_MAPK_MEF2A_6 575 584 PF00069 0.220
DOC_PP1_RVXF_1 323 330 PF00149 0.306
DOC_PP2B_LxvP_1 12 15 PF13499 0.632
DOC_PP2B_LxvP_1 403 406 PF13499 0.445
DOC_PP4_FxxP_1 234 237 PF00568 0.382
DOC_USP7_MATH_1 146 150 PF00917 0.748
DOC_USP7_MATH_1 170 174 PF00917 0.635
DOC_USP7_MATH_1 374 378 PF00917 0.382
DOC_USP7_MATH_1 412 416 PF00917 0.346
DOC_USP7_MATH_1 418 422 PF00917 0.500
DOC_USP7_MATH_1 426 430 PF00917 0.500
DOC_USP7_MATH_1 462 466 PF00917 0.256
DOC_USP7_MATH_1 661 665 PF00917 0.205
DOC_USP7_MATH_1 704 708 PF00917 0.329
DOC_WW_Pin1_4 155 160 PF00397 0.625
DOC_WW_Pin1_4 177 182 PF00397 0.653
DOC_WW_Pin1_4 30 35 PF00397 0.678
DOC_WW_Pin1_4 643 648 PF00397 0.675
DOC_WW_Pin1_4 706 711 PF00397 0.436
LIG_14-3-3_CanoR_1 143 150 PF00244 0.647
LIG_14-3-3_CanoR_1 176 181 PF00244 0.667
LIG_14-3-3_CanoR_1 314 320 PF00244 0.364
LIG_14-3-3_CanoR_1 325 330 PF00244 0.372
LIG_14-3-3_CanoR_1 424 432 PF00244 0.573
LIG_14-3-3_CanoR_1 433 439 PF00244 0.523
LIG_14-3-3_CanoR_1 444 453 PF00244 0.243
LIG_14-3-3_CanoR_1 551 557 PF00244 0.443
LIG_14-3-3_CanoR_1 623 628 PF00244 0.603
LIG_14-3-3_CanoR_1 648 653 PF00244 0.604
LIG_Actin_WH2_2 310 327 PF00022 0.341
LIG_BRCT_BRCA1_1 23 27 PF00533 0.579
LIG_BRCT_BRCA1_1 497 501 PF00533 0.613
LIG_BRCT_BRCA1_1 590 594 PF00533 0.425
LIG_BRCT_BRCA1_1 663 667 PF00533 0.252
LIG_BRCT_BRCA1_1 673 677 PF00533 0.218
LIG_CtBP_PxDLS_1 510 514 PF00389 0.505
LIG_deltaCOP1_diTrp_1 110 116 PF00928 0.371
LIG_deltaCOP1_diTrp_1 525 534 PF00928 0.497
LIG_eIF4E_1 398 404 PF01652 0.435
LIG_eIF4E_1 446 452 PF01652 0.292
LIG_eIF4E_1 70 76 PF01652 0.352
LIG_EVH1_1 13 17 PF00568 0.616
LIG_FHA_1 177 183 PF00498 0.594
LIG_FHA_1 203 209 PF00498 0.721
LIG_FHA_1 219 225 PF00498 0.361
LIG_FHA_1 282 288 PF00498 0.516
LIG_FHA_1 321 327 PF00498 0.375
LIG_FHA_1 33 39 PF00498 0.662
LIG_FHA_1 446 452 PF00498 0.318
LIG_FHA_1 518 524 PF00498 0.493
LIG_FHA_1 609 615 PF00498 0.648
LIG_FHA_1 61 67 PF00498 0.235
LIG_FHA_1 624 630 PF00498 0.537
LIG_FHA_1 7 13 PF00498 0.798
LIG_FHA_1 709 715 PF00498 0.409
LIG_FHA_1 736 742 PF00498 0.636
LIG_FHA_2 106 112 PF00498 0.297
LIG_FHA_2 290 296 PF00498 0.414
LIG_FHA_2 34 40 PF00498 0.683
LIG_FHA_2 352 358 PF00498 0.389
LIG_FHA_2 520 526 PF00498 0.444
LIG_LIR_Apic_2 54 60 PF02991 0.406
LIG_LIR_Gen_1 117 128 PF02991 0.335
LIG_LIR_Gen_1 221 229 PF02991 0.465
LIG_LIR_Gen_1 392 401 PF02991 0.308
LIG_LIR_Gen_1 414 423 PF02991 0.391
LIG_LIR_Gen_1 437 447 PF02991 0.544
LIG_LIR_Gen_1 44 52 PF02991 0.685
LIG_LIR_Gen_1 483 494 PF02991 0.287
LIG_LIR_Gen_1 498 509 PF02991 0.569
LIG_LIR_Nem_3 110 116 PF02991 0.361
LIG_LIR_Nem_3 117 123 PF02991 0.329
LIG_LIR_Nem_3 134 140 PF02991 0.509
LIG_LIR_Nem_3 216 220 PF02991 0.484
LIG_LIR_Nem_3 221 226 PF02991 0.383
LIG_LIR_Nem_3 284 289 PF02991 0.415
LIG_LIR_Nem_3 392 398 PF02991 0.317
LIG_LIR_Nem_3 402 407 PF02991 0.359
LIG_LIR_Nem_3 414 419 PF02991 0.368
LIG_LIR_Nem_3 421 425 PF02991 0.488
LIG_LIR_Nem_3 437 443 PF02991 0.518
LIG_LIR_Nem_3 44 48 PF02991 0.678
LIG_LIR_Nem_3 483 489 PF02991 0.331
LIG_LIR_Nem_3 498 504 PF02991 0.592
LIG_LIR_Nem_3 651 657 PF02991 0.676
LIG_LIR_Nem_3 664 670 PF02991 0.392
LIG_Pex14_1 286 290 PF04695 0.462
LIG_Pex14_1 315 319 PF04695 0.334
LIG_Pex14_1 530 534 PF04695 0.498
LIG_Pex14_1 537 541 PF04695 0.498
LIG_Pex14_2 136 140 PF04695 0.330
LIG_Pex14_2 491 495 PF04695 0.355
LIG_Pex14_2 526 530 PF04695 0.500
LIG_Pex14_2 562 566 PF04695 0.356
LIG_PTB_Apo_2 136 143 PF02174 0.291
LIG_PTB_Apo_2 77 84 PF02174 0.266
LIG_SH2_CRK 120 124 PF00017 0.229
LIG_SH2_CRK 393 397 PF00017 0.307
LIG_SH2_CRK 422 426 PF00017 0.468
LIG_SH2_CRK 45 49 PF00017 0.665
LIG_SH2_CRK 541 545 PF00017 0.498
LIG_SH2_CRK 654 658 PF00017 0.474
LIG_SH2_GRB2like 105 108 PF00017 0.340
LIG_SH2_NCK_1 45 49 PF00017 0.665
LIG_SH2_STAP1 105 109 PF00017 0.389
LIG_SH2_STAP1 438 442 PF00017 0.485
LIG_SH2_STAP1 446 450 PF00017 0.339
LIG_SH2_STAP1 45 49 PF00017 0.743
LIG_SH2_STAT3 285 288 PF00017 0.445
LIG_SH2_STAT5 218 221 PF00017 0.387
LIG_SH2_STAT5 245 248 PF00017 0.478
LIG_SH2_STAT5 273 276 PF00017 0.480
LIG_SH2_STAT5 289 292 PF00017 0.425
LIG_SH2_STAT5 401 404 PF00017 0.354
LIG_SH2_STAT5 408 411 PF00017 0.360
LIG_SH2_STAT5 466 469 PF00017 0.313
LIG_SH2_STAT5 486 489 PF00017 0.401
LIG_SH2_STAT5 543 546 PF00017 0.498
LIG_SH2_STAT5 57 60 PF00017 0.320
LIG_SH2_STAT5 745 748 PF00017 0.531
LIG_SH3_3 11 17 PF00018 0.663
LIG_SH3_3 226 232 PF00018 0.469
LIG_SH3_3 384 390 PF00018 0.322
LIG_SH3_3 453 459 PF00018 0.421
LIG_SUMO_SIM_anti_2 158 166 PF11976 0.568
LIG_SUMO_SIM_anti_2 448 454 PF11976 0.243
LIG_SUMO_SIM_anti_2 63 69 PF11976 0.426
LIG_SUMO_SIM_anti_2 724 730 PF11976 0.396
LIG_SUMO_SIM_par_1 158 166 PF11976 0.568
LIG_SUMO_SIM_par_1 519 525 PF11976 0.461
LIG_TRAF2_1 472 475 PF00917 0.227
LIG_TRFH_1 401 405 PF08558 0.435
LIG_TYR_ITIM 420 425 PF00017 0.473
LIG_TYR_ITIM 484 489 PF00017 0.415
LIG_TYR_ITIM 539 544 PF00017 0.340
LIG_UBA3_1 96 103 PF00899 0.322
LIG_WRC_WIRS_1 214 219 PF05994 0.214
LIG_WRC_WIRS_1 326 331 PF05994 0.300
LIG_WRC_WIRS_1 413 418 PF05994 0.372
LIG_WRC_WIRS_1 649 654 PF05994 0.395
LIG_WRC_WIRS_1 75 80 PF05994 0.394
LIG_WW_1 405 408 PF00397 0.445
MOD_CDK_SPK_2 643 648 PF00069 0.401
MOD_CK1_1 114 120 PF00069 0.288
MOD_CK1_1 149 155 PF00069 0.581
MOD_CK1_1 19 25 PF00069 0.653
MOD_CK1_1 33 39 PF00069 0.624
MOD_CK1_1 722 728 PF00069 0.259
MOD_CK2_1 290 296 PF00069 0.648
MOD_CK2_1 351 357 PF00069 0.462
MOD_CK2_1 469 475 PF00069 0.448
MOD_CK2_1 502 508 PF00069 0.368
MOD_CMANNOS 527 530 PF00535 0.346
MOD_GlcNHglycan 113 116 PF01048 0.393
MOD_GlcNHglycan 133 136 PF01048 0.488
MOD_GlcNHglycan 152 155 PF01048 0.536
MOD_GlcNHglycan 165 170 PF01048 0.507
MOD_GlcNHglycan 197 200 PF01048 0.731
MOD_GlcNHglycan 292 295 PF01048 0.424
MOD_GlcNHglycan 504 507 PF01048 0.435
MOD_GlcNHglycan 590 593 PF01048 0.358
MOD_GSK3_1 111 118 PF00069 0.562
MOD_GSK3_1 142 149 PF00069 0.620
MOD_GSK3_1 15 22 PF00069 0.723
MOD_GSK3_1 260 267 PF00069 0.352
MOD_GSK3_1 315 322 PF00069 0.288
MOD_GSK3_1 43 50 PF00069 0.536
MOD_GSK3_1 434 441 PF00069 0.309
MOD_GSK3_1 462 469 PF00069 0.364
MOD_GSK3_1 671 678 PF00069 0.386
MOD_GSK3_1 704 711 PF00069 0.541
MOD_GSK3_1 731 738 PF00069 0.516
MOD_N-GLC_1 81 86 PF02516 0.281
MOD_N-GLC_1 88 93 PF02516 0.495
MOD_NEK2_1 142 147 PF00069 0.550
MOD_NEK2_1 21 26 PF00069 0.584
MOD_NEK2_1 259 264 PF00069 0.346
MOD_NEK2_1 281 286 PF00069 0.564
MOD_NEK2_1 308 313 PF00069 0.480
MOD_NEK2_1 319 324 PF00069 0.394
MOD_NEK2_1 517 522 PF00069 0.340
MOD_NEK2_1 546 551 PF00069 0.368
MOD_NEK2_1 683 688 PF00069 0.609
MOD_NEK2_1 719 724 PF00069 0.380
MOD_NEK2_2 315 320 PF00069 0.284
MOD_NEK2_2 399 404 PF00069 0.243
MOD_NEK2_2 438 443 PF00069 0.276
MOD_NEK2_2 662 667 PF00069 0.349
MOD_PK_1 51 57 PF00069 0.510
MOD_PKA_2 142 148 PF00069 0.492
MOD_PKA_2 150 156 PF00069 0.550
MOD_PKA_2 319 325 PF00069 0.433
MOD_PKA_2 345 351 PF00069 0.482
MOD_PKA_2 6 12 PF00069 0.514
MOD_PKB_1 174 182 PF00069 0.488
MOD_PKB_1 621 629 PF00069 0.389
MOD_Plk_1 105 111 PF00069 0.453
MOD_Plk_1 351 357 PF00069 0.462
MOD_Plk_1 43 49 PF00069 0.545
MOD_Plk_1 469 475 PF00069 0.243
MOD_Plk_1 615 621 PF00069 0.455
MOD_Plk_1 81 87 PF00069 0.375
MOD_Plk_4 119 125 PF00069 0.435
MOD_Plk_4 213 219 PF00069 0.461
MOD_Plk_4 260 266 PF00069 0.375
MOD_Plk_4 281 287 PF00069 0.530
MOD_Plk_4 399 405 PF00069 0.268
MOD_Plk_4 418 424 PF00069 0.289
MOD_Plk_4 44 50 PF00069 0.698
MOD_Plk_4 446 452 PF00069 0.519
MOD_Plk_4 462 468 PF00069 0.352
MOD_Plk_4 552 558 PF00069 0.403
MOD_Plk_4 648 654 PF00069 0.609
MOD_Plk_4 662 668 PF00069 0.370
MOD_ProDKin_1 155 161 PF00069 0.521
MOD_ProDKin_1 177 183 PF00069 0.563
MOD_ProDKin_1 30 36 PF00069 0.600
MOD_ProDKin_1 643 649 PF00069 0.587
MOD_ProDKin_1 706 712 PF00069 0.528
TRG_DiLeu_BaEn_1 296 301 PF01217 0.423
TRG_DiLeu_BaEn_2 474 480 PF01217 0.425
TRG_DiLeu_BaLyEn_6 156 161 PF01217 0.455
TRG_DiLeu_BaLyEn_6 234 239 PF01217 0.430
TRG_DiLeu_BaLyEn_6 322 327 PF01217 0.459
TRG_DiLeu_BaLyEn_6 629 634 PF01217 0.359
TRG_DiLeu_LyEn_5 92 97 PF01217 0.315
TRG_ENDOCYTIC_2 120 123 PF00928 0.393
TRG_ENDOCYTIC_2 137 140 PF00928 0.294
TRG_ENDOCYTIC_2 245 248 PF00928 0.375
TRG_ENDOCYTIC_2 257 260 PF00928 0.325
TRG_ENDOCYTIC_2 393 396 PF00928 0.351
TRG_ENDOCYTIC_2 401 404 PF00928 0.343
TRG_ENDOCYTIC_2 422 425 PF00928 0.456
TRG_ENDOCYTIC_2 45 48 PF00928 0.599
TRG_ENDOCYTIC_2 486 489 PF00928 0.414
TRG_ENDOCYTIC_2 49 52 PF00928 0.536
TRG_ENDOCYTIC_2 541 544 PF00928 0.344
TRG_ENDOCYTIC_2 654 657 PF00928 0.393
TRG_ER_diArg_1 189 192 PF00400 0.719
TRG_ER_diArg_1 513 515 PF00400 0.349
TRG_ER_diArg_1 601 603 PF00400 0.487
TRG_ER_diArg_1 629 632 PF00400 0.512
TRG_ER_diArg_1 643 645 PF00400 0.445
TRG_NES_CRM1_1 511 525 PF08389 0.259
TRG_Pf-PMV_PEXEL_1 623 627 PF00026 0.390

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0S4IRP6 Bodo saltans 36% 100%
A0A1X0P614 Trypanosomatidae 33% 100%
A0A1X0P616 Trypanosomatidae 40% 100%
A0A3Q8IAC1 Leishmania donovani 67% 96%
A0A3Q8IBC3 Leishmania donovani 63% 100%
A0A3Q8IBE0 Leishmania donovani 62% 89%
A0A3Q8IDD7 Leishmania donovani 67% 96%
A0A3S5H769 Leishmania donovani 66% 100%
A0A3S5IRW9 Trypanosoma rangeli 36% 100%
A0A3S7WVJ2 Leishmania donovani 62% 89%
A0A3S7WVK4 Leishmania donovani 67% 96%
A4HA75 Leishmania braziliensis 80% 100%
A4HA76 Leishmania braziliensis 75% 100%
A4HA77 Leishmania braziliensis 98% 100%
A4HA80 Leishmania braziliensis 69% 100%
A4HA81 Leishmania braziliensis 96% 100%
E8NHJ2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 70% 100%
E9AGT0 Leishmania infantum 62% 89%
E9AGT1 Leishmania infantum 69% 100%
E9AGT2 Leishmania infantum 68% 100%
E9AGT3 Leishmania infantum 68% 96%
E9AGT4 Leishmania infantum 67% 96%
E9AS85 Leishmania mexicana (strain MHOM/GT/2001/U1103) 67% 97%
E9AS86 Leishmania mexicana (strain MHOM/GT/2001/U1103) 28% 99%
Q4QD78 Leishmania major 65% 100%
Q4QD79 Leishmania major 65% 100%
Q4QD80 Leishmania major 66% 100%
Q4QD81 Leishmania major 61% 99%

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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