LeishMANIAdb
  • Home
  • Browse
  • Manual
  • FAQ
  • Download

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:
A4HA75_LEIBR
TriTrypDb:
LbrM.19.1510 , LBRM2903_190022100 *
Length:
724

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: 31
NetGPI no yes: 0, no: 31
Cellular components
Term Name Level Count
GO:0016020 membrane 2 32
GO:0110165 cellular anatomical entity 1 32
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

A4HA75
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HA75

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_Caspase3-7 125 129 PF00656 0.588
CLV_NRD_NRD_1 408 410 PF00675 0.314
CLV_NRD_NRD_1 490 492 PF00675 0.296
CLV_NRD_NRD_1 578 580 PF00675 0.399
CLV_NRD_NRD_1 607 609 PF00675 0.415
CLV_NRD_NRD_1 619 621 PF00675 0.396
CLV_NRD_NRD_1 73 75 PF00675 0.487
CLV_PCSK_KEX2_1 490 492 PF00082 0.296
CLV_PCSK_KEX2_1 578 580 PF00082 0.402
CLV_PCSK_KEX2_1 606 608 PF00082 0.427
CLV_PCSK_KEX2_1 619 621 PF00082 0.412
CLV_PCSK_KEX2_1 718 720 PF00082 0.302
CLV_PCSK_KEX2_1 73 75 PF00082 0.487
CLV_PCSK_PC1ET2_1 718 720 PF00082 0.350
CLV_PCSK_PC7_1 615 621 PF00082 0.446
CLV_PCSK_SKI1_1 410 414 PF00082 0.304
CLV_PCSK_SKI1_1 527 531 PF00082 0.438
CLV_PCSK_SKI1_1 551 555 PF00082 0.444
CLV_PCSK_SKI1_1 607 611 PF00082 0.406
CLV_PCSK_SKI1_1 63 67 PF00082 0.534
CLV_PCSK_SKI1_1 707 711 PF00082 0.315
DEG_APCC_DBOX_1 526 534 PF00400 0.399
DEG_APCC_DBOX_1 606 614 PF00400 0.609
DEG_SCF_FBW7_1 682 689 PF00400 0.345
DEG_SPOP_SBC_1 115 119 PF00917 0.518
DEG_SPOP_SBC_1 401 405 PF00917 0.543
DOC_ANK_TNKS_1 73 80 PF00023 0.274
DOC_CDC14_PxL_1 431 439 PF14671 0.395
DOC_CYCLIN_RxL_1 2 12 PF00134 0.521
DOC_CYCLIN_yCln2_LP_2 379 385 PF00134 0.437
DOC_MAPK_DCC_7 527 537 PF00069 0.333
DOC_MAPK_gen_1 168 177 PF00069 0.572
DOC_MAPK_JIP1_4 171 177 PF00069 0.509
DOC_MAPK_MEF2A_6 168 177 PF00069 0.713
DOC_MAPK_MEF2A_6 551 560 PF00069 0.221
DOC_PP1_RVXF_1 299 306 PF00149 0.298
DOC_PP1_RVXF_1 3 10 PF00149 0.583
DOC_PP2B_LxvP_1 379 382 PF13499 0.437
DOC_PP2B_LxvP_1 65 68 PF13499 0.347
DOC_PP4_FxxP_1 210 213 PF00568 0.362
DOC_USP7_MATH_1 159 163 PF00917 0.615
DOC_USP7_MATH_1 184 188 PF00917 0.478
DOC_USP7_MATH_1 350 354 PF00917 0.430
DOC_USP7_MATH_1 388 392 PF00917 0.335
DOC_USP7_MATH_1 394 398 PF00917 0.492
DOC_USP7_MATH_1 402 406 PF00917 0.492
DOC_USP7_MATH_1 438 442 PF00917 0.249
DOC_USP7_MATH_1 637 641 PF00917 0.212
DOC_USP7_MATH_1 680 684 PF00917 0.325
DOC_WW_Pin1_4 596 601 PF00397 0.577
DOC_WW_Pin1_4 619 624 PF00397 0.643
DOC_WW_Pin1_4 682 687 PF00397 0.430
LIG_14-3-3_CanoR_1 113 120 PF00244 0.603
LIG_14-3-3_CanoR_1 122 130 PF00244 0.636
LIG_14-3-3_CanoR_1 290 296 PF00244 0.354
LIG_14-3-3_CanoR_1 301 306 PF00244 0.358
LIG_14-3-3_CanoR_1 400 408 PF00244 0.568
LIG_14-3-3_CanoR_1 409 415 PF00244 0.516
LIG_14-3-3_CanoR_1 420 429 PF00244 0.233
LIG_14-3-3_CanoR_1 5 10 PF00244 0.520
LIG_14-3-3_CanoR_1 527 533 PF00244 0.413
LIG_14-3-3_CanoR_1 624 629 PF00244 0.589
LIG_14-3-3_CanoR_1 90 98 PF00244 0.257
LIG_Actin_WH2_2 286 303 PF00022 0.333
LIG_BRCT_BRCA1_1 473 477 PF00533 0.613
LIG_BRCT_BRCA1_1 566 570 PF00533 0.399
LIG_BRCT_BRCA1_1 639 643 PF00533 0.249
LIG_BRCT_BRCA1_1 649 653 PF00533 0.217
LIG_CtBP_PxDLS_1 172 176 PF00389 0.504
LIG_CtBP_PxDLS_1 486 490 PF00389 0.498
LIG_deltaCOP1_diTrp_1 501 510 PF00928 0.490
LIG_deltaCOP1_diTrp_1 85 91 PF00928 0.348
LIG_eIF4E_1 374 380 PF01652 0.406
LIG_eIF4E_1 422 428 PF01652 0.291
LIG_FHA_1 106 112 PF00498 0.333
LIG_FHA_1 195 201 PF00498 0.347
LIG_FHA_1 258 264 PF00498 0.507
LIG_FHA_1 297 303 PF00498 0.355
LIG_FHA_1 422 428 PF00498 0.313
LIG_FHA_1 47 53 PF00498 0.321
LIG_FHA_1 494 500 PF00498 0.484
LIG_FHA_1 585 591 PF00498 0.674
LIG_FHA_1 600 606 PF00498 0.562
LIG_FHA_1 685 691 PF00498 0.412
LIG_FHA_1 712 718 PF00498 0.663
LIG_FHA_1 8 14 PF00498 0.602
LIG_FHA_1 94 100 PF00498 0.247
LIG_FHA_2 266 272 PF00498 0.401
LIG_FHA_2 328 334 PF00498 0.387
LIG_FHA_2 496 502 PF00498 0.442
LIG_FHA_2 95 101 PF00498 0.214
LIG_LIR_Apic_2 187 191 PF02991 0.287
LIG_LIR_Gen_1 18 27 PF02991 0.668
LIG_LIR_Gen_1 197 205 PF02991 0.450
LIG_LIR_Gen_1 368 377 PF02991 0.301
LIG_LIR_Gen_1 390 399 PF02991 0.381
LIG_LIR_Gen_1 413 423 PF02991 0.539
LIG_LIR_Gen_1 459 470 PF02991 0.283
LIG_LIR_Gen_1 474 485 PF02991 0.566
LIG_LIR_Gen_1 92 103 PF02991 0.320
LIG_LIR_Nem_3 18 23 PF02991 0.653
LIG_LIR_Nem_3 197 202 PF02991 0.362
LIG_LIR_Nem_3 260 265 PF02991 0.395
LIG_LIR_Nem_3 368 374 PF02991 0.309
LIG_LIR_Nem_3 378 383 PF02991 0.346
LIG_LIR_Nem_3 390 395 PF02991 0.356
LIG_LIR_Nem_3 397 401 PF02991 0.479
LIG_LIR_Nem_3 413 419 PF02991 0.510
LIG_LIR_Nem_3 459 465 PF02991 0.325
LIG_LIR_Nem_3 474 480 PF02991 0.589
LIG_LIR_Nem_3 627 633 PF02991 0.666
LIG_LIR_Nem_3 85 91 PF02991 0.339
LIG_LIR_Nem_3 92 98 PF02991 0.318
LIG_LYPXL_S_1 23 27 PF13949 0.445
LIG_LYPXL_yS_3 24 27 PF13949 0.571
LIG_NRBOX 61 67 PF00104 0.268
LIG_Pex14_1 262 266 PF04695 0.421
LIG_Pex14_1 291 295 PF04695 0.323
LIG_Pex14_1 506 510 PF04695 0.491
LIG_Pex14_1 513 517 PF04695 0.491
LIG_Pex14_2 467 471 PF04695 0.343
LIG_Pex14_2 502 506 PF04695 0.492
LIG_Pex14_2 538 542 PF04695 0.345
LIG_PTB_Apo_2 18 25 PF02174 0.532
LIG_PTB_Phospho_1 18 24 PF10480 0.531
LIG_SH2_CRK 20 24 PF00017 0.614
LIG_SH2_CRK 369 373 PF00017 0.300
LIG_SH2_CRK 398 402 PF00017 0.458
LIG_SH2_CRK 517 521 PF00017 0.491
LIG_SH2_CRK 630 634 PF00017 0.471
LIG_SH2_CRK 75 79 PF00017 0.283
LIG_SH2_CRK 95 99 PF00017 0.220
LIG_SH2_NCK_1 20 24 PF00017 0.614
LIG_SH2_NCK_1 670 674 PF00017 0.325
LIG_SH2_NCK_1 75 79 PF00017 0.271
LIG_SH2_SRC 133 136 PF00017 0.593
LIG_SH2_SRC 670 673 PF00017 0.325
LIG_SH2_STAP1 414 418 PF00017 0.478
LIG_SH2_STAP1 422 426 PF00017 0.329
LIG_SH2_STAP1 80 84 PF00017 0.371
LIG_SH2_STAP1 95 99 PF00017 0.221
LIG_SH2_STAT3 261 264 PF00017 0.411
LIG_SH2_STAT5 194 197 PF00017 0.380
LIG_SH2_STAT5 221 224 PF00017 0.466
LIG_SH2_STAT5 249 252 PF00017 0.467
LIG_SH2_STAT5 265 268 PF00017 0.396
LIG_SH2_STAT5 32 35 PF00017 0.301
LIG_SH2_STAT5 377 380 PF00017 0.343
LIG_SH2_STAT5 384 387 PF00017 0.348
LIG_SH2_STAT5 41 44 PF00017 0.295
LIG_SH2_STAT5 442 445 PF00017 0.307
LIG_SH2_STAT5 462 465 PF00017 0.393
LIG_SH2_STAT5 519 522 PF00017 0.501
LIG_SH2_STAT5 61 64 PF00017 0.251
LIG_SH2_STAT5 721 724 PF00017 0.526
LIG_SH2_STAT5 95 98 PF00017 0.361
LIG_SH3_3 202 208 PF00018 0.419
LIG_SH3_3 360 366 PF00018 0.318
LIG_SH3_3 429 435 PF00018 0.395
LIG_SUMO_SIM_anti_2 424 430 PF11976 0.242
LIG_SUMO_SIM_anti_2 700 706 PF11976 0.392
LIG_SUMO_SIM_par_1 495 501 PF11976 0.437
LIG_SUMO_SIM_par_1 96 102 PF11976 0.209
LIG_TRAF2_1 448 451 PF00917 0.226
LIG_TRFH_1 377 381 PF08558 0.406
LIG_TYR_ITIM 396 401 PF00017 0.466
LIG_TYR_ITIM 460 465 PF00017 0.405
LIG_TYR_ITIM 515 520 PF00017 0.329
LIG_WRC_WIRS_1 302 307 PF05994 0.288
LIG_WRC_WIRS_1 389 394 PF05994 0.359
LIG_WRC_WIRS_1 6 11 PF05994 0.354
LIG_WRC_WIRS_1 625 630 PF05994 0.407
LIG_WW_1 381 384 PF00397 0.437
MOD_CDK_SPK_2 619 624 PF00069 0.391
MOD_CK1_1 116 122 PF00069 0.547
MOD_CK1_1 129 135 PF00069 0.519
MOD_CK1_1 162 168 PF00069 0.478
MOD_CK1_1 599 605 PF00069 0.420
MOD_CK1_1 698 704 PF00069 0.316
MOD_CK1_1 8 14 PF00069 0.565
MOD_CK2_1 266 272 PF00069 0.630
MOD_CK2_1 327 333 PF00069 0.453
MOD_CK2_1 445 451 PF00069 0.417
MOD_CK2_1 478 484 PF00069 0.381
MOD_CK2_1 94 100 PF00069 0.209
MOD_CMANNOS 503 506 PF00535 0.335
MOD_GlcNHglycan 100 104 PF01048 0.511
MOD_GlcNHglycan 161 165 PF01048 0.541
MOD_GlcNHglycan 268 271 PF01048 0.407
MOD_GlcNHglycan 480 483 PF01048 0.406
MOD_GlcNHglycan 566 569 PF01048 0.369
MOD_GlcNHglycan 640 643 PF01048 0.415
MOD_GlcNHglycan 667 670 PF01048 0.674
MOD_GlcNHglycan 697 700 PF01048 0.396
MOD_GSK3_1 114 121 PF00069 0.544
MOD_GSK3_1 122 129 PF00069 0.570
MOD_GSK3_1 146 153 PF00069 0.548
MOD_GSK3_1 15 22 PF00069 0.476
MOD_GSK3_1 167 174 PF00069 0.665
MOD_GSK3_1 236 243 PF00069 0.331
MOD_GSK3_1 291 298 PF00069 0.284
MOD_GSK3_1 410 417 PF00069 0.291
MOD_GSK3_1 438 445 PF00069 0.356
MOD_GSK3_1 647 654 PF00069 0.379
MOD_GSK3_1 680 687 PF00069 0.539
MOD_GSK3_1 707 714 PF00069 0.585
MOD_GSK3_1 89 96 PF00069 0.592
MOD_NEK2_1 105 110 PF00069 0.297
MOD_NEK2_1 140 145 PF00069 0.494
MOD_NEK2_1 236 241 PF00069 0.333
MOD_NEK2_1 257 262 PF00069 0.546
MOD_NEK2_1 284 289 PF00069 0.475
MOD_NEK2_1 295 300 PF00069 0.380
MOD_NEK2_1 493 498 PF00069 0.327
MOD_NEK2_1 522 527 PF00069 0.359
MOD_NEK2_1 659 664 PF00069 0.610
MOD_NEK2_1 695 700 PF00069 0.372
MOD_NEK2_2 291 296 PF00069 0.281
MOD_NEK2_2 375 380 PF00069 0.242
MOD_NEK2_2 414 419 PF00069 0.260
MOD_NEK2_2 46 51 PF00069 0.209
MOD_PIKK_1 133 139 PF00454 0.483
MOD_PIKK_1 83 89 PF00454 0.330
MOD_PKA_2 167 173 PF00069 0.693
MOD_PKA_2 295 301 PF00069 0.422
MOD_PKA_2 321 327 PF00069 0.471
MOD_PKA_2 89 95 PF00069 0.285
MOD_PKB_1 3 11 PF00069 0.371
MOD_Plk_1 327 333 PF00069 0.453
MOD_Plk_1 445 451 PF00069 0.242
MOD_Plk_1 591 597 PF00069 0.467
MOD_Plk_1 99 105 PF00069 0.215
MOD_Plk_4 106 112 PF00069 0.282
MOD_Plk_4 15 21 PF00069 0.665
MOD_Plk_4 236 242 PF00069 0.356
MOD_Plk_4 257 263 PF00069 0.512
MOD_Plk_4 375 381 PF00069 0.266
MOD_Plk_4 394 400 PF00069 0.273
MOD_Plk_4 422 428 PF00069 0.517
MOD_Plk_4 438 444 PF00069 0.340
MOD_Plk_4 528 534 PF00069 0.392
MOD_Plk_4 624 630 PF00069 0.595
MOD_Plk_4 67 73 PF00069 0.376
MOD_Plk_4 94 100 PF00069 0.398
MOD_ProDKin_1 596 602 PF00069 0.451
MOD_ProDKin_1 619 625 PF00069 0.542
MOD_ProDKin_1 682 688 PF00069 0.520
TRG_DiLeu_BaEn_1 272 277 PF01217 0.411
TRG_DiLeu_BaEn_2 450 456 PF01217 0.391
TRG_DiLeu_BaEn_2 99 105 PF01217 0.209
TRG_DiLeu_BaLyEn_6 2 7 PF01217 0.390
TRG_DiLeu_BaLyEn_6 210 215 PF01217 0.376
TRG_DiLeu_BaLyEn_6 298 303 PF01217 0.427
TRG_DiLeu_BaLyEn_6 605 610 PF01217 0.367
TRG_ENDOCYTIC_2 20 23 PF00928 0.559
TRG_ENDOCYTIC_2 221 224 PF00928 0.354
TRG_ENDOCYTIC_2 233 236 PF00928 0.306
TRG_ENDOCYTIC_2 24 27 PF00928 0.513
TRG_ENDOCYTIC_2 369 372 PF00928 0.340
TRG_ENDOCYTIC_2 377 380 PF00928 0.331
TRG_ENDOCYTIC_2 398 401 PF00928 0.448
TRG_ENDOCYTIC_2 462 465 PF00928 0.404
TRG_ENDOCYTIC_2 517 520 PF00928 0.332
TRG_ENDOCYTIC_2 630 633 PF00928 0.372
TRG_ENDOCYTIC_2 75 78 PF00928 0.601
TRG_ENDOCYTIC_2 95 98 PF00928 0.348
TRG_ER_diArg_1 2 5 PF00400 0.412
TRG_ER_diArg_1 489 491 PF00400 0.340
TRG_ER_diArg_1 577 579 PF00400 0.527
TRG_ER_diArg_1 605 608 PF00400 0.509
TRG_ER_diArg_1 619 621 PF00400 0.471
TRG_ER_diArg_1 72 74 PF00400 0.303
TRG_NES_CRM1_1 487 501 PF08389 0.250

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0S4IRP6 Bodo saltans 36% 100%
A0A1X0P614 Trypanosomatidae 33% 100%
A0A1X0P616 Trypanosomatidae 40% 100%
A0A3Q8IAC1 Leishmania donovani 62% 93%
A0A3Q8IBC3 Leishmania donovani 59% 100%
A0A3Q8IBE0 Leishmania donovani 61% 87%
A0A3Q8IDD7 Leishmania donovani 62% 93%
A0A3S5H769 Leishmania donovani 62% 100%
A0A3S5IRW9 Trypanosoma rangeli 35% 100%
A0A3S7WVJ2 Leishmania donovani 61% 86%
A0A3S7WVK4 Leishmania donovani 62% 93%
A4HA76 Leishmania braziliensis 95% 100%
A4HA77 Leishmania braziliensis 72% 100%
A4HA79 Leishmania braziliensis 97% 100%
A4HA80 Leishmania braziliensis 89% 78%
A4HA81 Leishmania braziliensis 74% 100%
A4HA82 Leishmania braziliensis 80% 97%
E8NHJ2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 71% 100%
E9AGT0 Leishmania infantum 61% 86%
E9AGT1 Leishmania infantum 64% 100%
E9AGT2 Leishmania infantum 62% 100%
E9AGT3 Leishmania infantum 62% 93%
E9AGT4 Leishmania infantum 61% 93%
E9AS84 Leishmania mexicana (strain MHOM/GT/2001/U1103) 72% 100%
E9AS85 Leishmania mexicana (strain MHOM/GT/2001/U1103) 61% 93%
E9AS86 Leishmania mexicana (strain MHOM/GT/2001/U1103) 29% 96%
Q4QD78 Leishmania major 60% 100%
Q4QD79 Leishmania major 61% 100%
Q4QD80 Leishmania major 61% 100%
Q4QD81 Leishmania major 61% 100%

Download

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