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:
A4HA81_LEIBR
TriTrypDb:
LbrM.19.1580 , LBRM2903_190022100
Length:
655

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: 27
NetGPI no yes: 0, no: 27
Cellular components
Term Name Level Count
GO:0016020 membrane 2 28
GO:0110165 cellular anatomical entity 1 28
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

A4HA81
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HA81

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_1 137 139 PF00675 0.286
CLV_NRD_NRD_1 432 434 PF00675 0.394
CLV_NRD_NRD_1 514 516 PF00675 0.371
CLV_NRD_NRD_1 602 604 PF00675 0.456
CLV_PCSK_KEX2_1 514 516 PF00082 0.371
CLV_PCSK_KEX2_1 602 604 PF00082 0.456
CLV_PCSK_SKI1_1 138 142 PF00082 0.338
CLV_PCSK_SKI1_1 434 438 PF00082 0.363
CLV_PCSK_SKI1_1 551 555 PF00082 0.449
CLV_PCSK_SKI1_1 575 579 PF00082 0.466
DEG_APCC_DBOX_1 550 558 PF00400 0.449
DEG_Nend_UBRbox_1 1 4 PF02207 0.620
DEG_SPOP_SBC_1 16 20 PF00917 0.617
DEG_SPOP_SBC_1 425 429 PF00917 0.584
DOC_CDC14_PxL_1 455 463 PF14671 0.444
DOC_CYCLIN_RxL_1 136 145 PF00134 0.422
DOC_CYCLIN_yCln2_LP_2 12 15 PF00134 0.631
DOC_CYCLIN_yCln2_LP_2 403 409 PF00134 0.457
DOC_MAPK_DCC_7 551 561 PF00069 0.490
DOC_MAPK_MEF2A_6 575 584 PF00069 0.240
DOC_PP1_RVXF_1 323 330 PF00149 0.421
DOC_PP2B_LxvP_1 12 15 PF13499 0.635
DOC_PP2B_LxvP_1 403 406 PF13499 0.457
DOC_PP4_FxxP_1 234 237 PF00568 0.405
DOC_USP7_MATH_1 146 150 PF00917 0.643
DOC_USP7_MATH_1 170 174 PF00917 0.636
DOC_USP7_MATH_1 374 378 PF00917 0.324
DOC_USP7_MATH_1 412 416 PF00917 0.501
DOC_USP7_MATH_1 418 422 PF00917 0.550
DOC_USP7_MATH_1 426 430 PF00917 0.464
DOC_USP7_MATH_1 462 466 PF00917 0.273
DOC_USP7_MATH_1 637 641 PF00917 0.589
DOC_WW_Pin1_4 155 160 PF00397 0.631
DOC_WW_Pin1_4 177 182 PF00397 0.659
DOC_WW_Pin1_4 30 35 PF00397 0.624
DOC_WW_Pin1_4 640 645 PF00397 0.716
LIG_14-3-3_CanoR_1 143 150 PF00244 0.640
LIG_14-3-3_CanoR_1 176 181 PF00244 0.622
LIG_14-3-3_CanoR_1 314 320 PF00244 0.397
LIG_14-3-3_CanoR_1 325 330 PF00244 0.335
LIG_14-3-3_CanoR_1 424 432 PF00244 0.584
LIG_14-3-3_CanoR_1 433 439 PF00244 0.506
LIG_14-3-3_CanoR_1 444 453 PF00244 0.216
LIG_14-3-3_CanoR_1 551 557 PF00244 0.465
LIG_14-3-3_CanoR_1 611 618 PF00244 0.599
LIG_14-3-3_CanoR_1 625 630 PF00244 0.635
LIG_14-3-3_CanoR_1 646 652 PF00244 0.664
LIG_Actin_WH2_2 310 327 PF00022 0.414
LIG_BRCT_BRCA1_1 497 501 PF00533 0.565
LIG_BRCT_BRCA1_1 590 594 PF00533 0.449
LIG_CtBP_PxDLS_1 510 514 PF00389 0.578
LIG_deltaCOP1_diTrp_1 110 116 PF00928 0.414
LIG_deltaCOP1_diTrp_1 525 534 PF00928 0.585
LIG_DLG_GKlike_1 625 632 PF00625 0.534
LIG_eIF4E_1 398 404 PF01652 0.457
LIG_eIF4E_1 446 452 PF01652 0.265
LIG_eIF4E_1 70 76 PF01652 0.231
LIG_EVH1_1 13 17 PF00568 0.628
LIG_FHA_1 177 183 PF00498 0.606
LIG_FHA_1 203 209 PF00498 0.669
LIG_FHA_1 219 225 PF00498 0.258
LIG_FHA_1 282 288 PF00498 0.453
LIG_FHA_1 321 327 PF00498 0.395
LIG_FHA_1 33 39 PF00498 0.668
LIG_FHA_1 446 452 PF00498 0.278
LIG_FHA_1 518 524 PF00498 0.584
LIG_FHA_1 61 67 PF00498 0.237
LIG_FHA_1 7 13 PF00498 0.648
LIG_FHA_2 106 112 PF00498 0.315
LIG_FHA_2 290 296 PF00498 0.374
LIG_FHA_2 34 40 PF00498 0.661
LIG_FHA_2 352 358 PF00498 0.332
LIG_FHA_2 520 526 PF00498 0.465
LIG_FHA_2 611 617 PF00498 0.584
LIG_LIR_Apic_2 54 60 PF02991 0.418
LIG_LIR_Apic_2 650 654 PF02991 0.592
LIG_LIR_Gen_1 117 128 PF02991 0.284
LIG_LIR_Gen_1 221 229 PF02991 0.263
LIG_LIR_Gen_1 392 401 PF02991 0.384
LIG_LIR_Gen_1 414 423 PF02991 0.457
LIG_LIR_Gen_1 437 447 PF02991 0.508
LIG_LIR_Gen_1 44 52 PF02991 0.643
LIG_LIR_Gen_1 483 494 PF02991 0.313
LIG_LIR_Gen_1 498 509 PF02991 0.530
LIG_LIR_Nem_3 110 116 PF02991 0.391
LIG_LIR_Nem_3 117 123 PF02991 0.337
LIG_LIR_Nem_3 134 140 PF02991 0.298
LIG_LIR_Nem_3 216 220 PF02991 0.268
LIG_LIR_Nem_3 221 226 PF02991 0.261
LIG_LIR_Nem_3 284 289 PF02991 0.460
LIG_LIR_Nem_3 392 398 PF02991 0.409
LIG_LIR_Nem_3 402 407 PF02991 0.359
LIG_LIR_Nem_3 414 419 PF02991 0.422
LIG_LIR_Nem_3 421 425 PF02991 0.512
LIG_LIR_Nem_3 437 443 PF02991 0.467
LIG_LIR_Nem_3 44 48 PF02991 0.665
LIG_LIR_Nem_3 477 482 PF02991 0.246
LIG_LIR_Nem_3 483 489 PF02991 0.330
LIG_LIR_Nem_3 498 504 PF02991 0.547
LIG_LIR_Nem_3 80 86 PF02991 0.334
LIG_Pex14_1 286 290 PF04695 0.480
LIG_Pex14_1 315 319 PF04695 0.440
LIG_Pex14_1 530 534 PF04695 0.609
LIG_Pex14_1 537 541 PF04695 0.536
LIG_Pex14_2 136 140 PF04695 0.299
LIG_Pex14_2 491 495 PF04695 0.496
LIG_Pex14_2 526 530 PF04695 0.615
LIG_Pex14_2 562 566 PF04695 0.476
LIG_SH2_CRK 120 124 PF00017 0.239
LIG_SH2_CRK 393 397 PF00017 0.384
LIG_SH2_CRK 422 426 PF00017 0.484
LIG_SH2_CRK 45 49 PF00017 0.655
LIG_SH2_CRK 541 545 PF00017 0.609
LIG_SH2_GRB2like 105 108 PF00017 0.364
LIG_SH2_NCK_1 45 49 PF00017 0.655
LIG_SH2_NCK_1 482 486 PF00017 0.217
LIG_SH2_STAP1 105 109 PF00017 0.410
LIG_SH2_STAP1 438 442 PF00017 0.484
LIG_SH2_STAP1 446 450 PF00017 0.270
LIG_SH2_STAP1 45 49 PF00017 0.618
LIG_SH2_STAP1 482 486 PF00017 0.235
LIG_SH2_STAT3 285 288 PF00017 0.456
LIG_SH2_STAT5 218 221 PF00017 0.422
LIG_SH2_STAT5 245 248 PF00017 0.464
LIG_SH2_STAT5 273 276 PF00017 0.522
LIG_SH2_STAT5 289 292 PF00017 0.371
LIG_SH2_STAT5 401 404 PF00017 0.495
LIG_SH2_STAT5 408 411 PF00017 0.389
LIG_SH2_STAT5 466 469 PF00017 0.246
LIG_SH2_STAT5 479 482 PF00017 0.313
LIG_SH2_STAT5 486 489 PF00017 0.339
LIG_SH2_STAT5 543 546 PF00017 0.609
LIG_SH2_STAT5 57 60 PF00017 0.399
LIG_SH3_3 11 17 PF00018 0.670
LIG_SH3_3 226 232 PF00018 0.461
LIG_SH3_3 384 390 PF00018 0.281
LIG_SH3_3 453 459 PF00018 0.444
LIG_SUMO_SIM_anti_2 158 166 PF11976 0.586
LIG_SUMO_SIM_anti_2 448 454 PF11976 0.265
LIG_SUMO_SIM_par_1 158 166 PF11976 0.586
LIG_SUMO_SIM_par_1 519 525 PF11976 0.452
LIG_TRAF2_1 472 475 PF00917 0.246
LIG_TRFH_1 401 405 PF08558 0.457
LIG_TYR_ITIM 420 425 PF00017 0.487
LIG_TYR_ITIM 484 489 PF00017 0.457
LIG_TYR_ITIM 539 544 PF00017 0.603
LIG_UBA3_1 96 103 PF00899 0.299
LIG_WRC_WIRS_1 214 219 PF05994 0.226
LIG_WRC_WIRS_1 326 331 PF05994 0.285
LIG_WRC_WIRS_1 413 418 PF05994 0.501
LIG_WRC_WIRS_1 75 80 PF05994 0.336
LIG_WW_1 405 408 PF00397 0.457
MOD_CDK_SPxK_1 640 646 PF00069 0.559
MOD_CK1_1 114 120 PF00069 0.267
MOD_CK1_1 149 155 PF00069 0.660
MOD_CK1_1 19 25 PF00069 0.627
MOD_CK1_1 33 39 PF00069 0.653
MOD_CK1_1 640 646 PF00069 0.593
MOD_CK2_1 290 296 PF00069 0.374
MOD_CK2_1 351 357 PF00069 0.363
MOD_CK2_1 469 475 PF00069 0.393
MOD_CK2_1 502 508 PF00069 0.540
MOD_CK2_1 610 616 PF00069 0.583
MOD_CK2_1 639 645 PF00069 0.552
MOD_CMANNOS 527 530 PF00535 0.415
MOD_GlcNHglycan 113 116 PF01048 0.470
MOD_GlcNHglycan 133 136 PF01048 0.377
MOD_GlcNHglycan 152 155 PF01048 0.366
MOD_GlcNHglycan 165 170 PF01048 0.422
MOD_GlcNHglycan 197 200 PF01048 0.496
MOD_GlcNHglycan 292 295 PF01048 0.573
MOD_GlcNHglycan 504 507 PF01048 0.384
MOD_GlcNHglycan 590 593 PF01048 0.383
MOD_GlcNHglycan 613 616 PF01048 0.433
MOD_GlcNHglycan 639 642 PF01048 0.441
MOD_GSK3_1 111 118 PF00069 0.309
MOD_GSK3_1 142 149 PF00069 0.675
MOD_GSK3_1 15 22 PF00069 0.658
MOD_GSK3_1 260 267 PF00069 0.325
MOD_GSK3_1 315 322 PF00069 0.277
MOD_GSK3_1 43 50 PF00069 0.576
MOD_GSK3_1 434 441 PF00069 0.425
MOD_GSK3_1 462 469 PF00069 0.265
MOD_GSK3_1 621 628 PF00069 0.590
MOD_N-GLC_1 81 86 PF02516 0.466
MOD_N-GLC_1 88 93 PF02516 0.482
MOD_NEK2_1 142 147 PF00069 0.636
MOD_NEK2_1 21 26 PF00069 0.596
MOD_NEK2_1 260 265 PF00069 0.362
MOD_NEK2_1 281 286 PF00069 0.412
MOD_NEK2_1 308 313 PF00069 0.377
MOD_NEK2_1 319 324 PF00069 0.364
MOD_NEK2_1 480 485 PF00069 0.321
MOD_NEK2_1 517 522 PF00069 0.596
MOD_NEK2_1 546 551 PF00069 0.471
MOD_NEK2_1 639 644 PF00069 0.617
MOD_NEK2_1 65 70 PF00069 0.219
MOD_NEK2_2 315 320 PF00069 0.274
MOD_NEK2_2 399 404 PF00069 0.265
MOD_NEK2_2 438 443 PF00069 0.418
MOD_PK_1 51 57 PF00069 0.555
MOD_PKA_2 142 148 PF00069 0.545
MOD_PKA_2 150 156 PF00069 0.579
MOD_PKA_2 319 325 PF00069 0.379
MOD_PKA_2 345 351 PF00069 0.367
MOD_PKA_2 6 12 PF00069 0.633
MOD_PKA_2 610 616 PF00069 0.614
MOD_PKB_1 174 182 PF00069 0.607
MOD_Plk_1 105 111 PF00069 0.390
MOD_Plk_1 351 357 PF00069 0.357
MOD_Plk_1 43 49 PF00069 0.634
MOD_Plk_1 469 475 PF00069 0.246
MOD_Plk_1 81 87 PF00069 0.270
MOD_Plk_4 119 125 PF00069 0.256
MOD_Plk_4 213 219 PF00069 0.366
MOD_Plk_4 260 266 PF00069 0.399
MOD_Plk_4 281 287 PF00069 0.417
MOD_Plk_4 399 405 PF00069 0.268
MOD_Plk_4 418 424 PF00069 0.439
MOD_Plk_4 44 50 PF00069 0.658
MOD_Plk_4 446 452 PF00069 0.462
MOD_Plk_4 462 468 PF00069 0.254
MOD_Plk_4 552 558 PF00069 0.492
MOD_Plk_4 65 71 PF00069 0.311
MOD_ProDKin_1 155 161 PF00069 0.632
MOD_ProDKin_1 177 183 PF00069 0.660
MOD_ProDKin_1 30 36 PF00069 0.634
MOD_ProDKin_1 640 646 PF00069 0.722
TRG_DiLeu_BaEn_1 296 301 PF01217 0.385
TRG_DiLeu_BaLyEn_6 156 161 PF01217 0.590
TRG_DiLeu_BaLyEn_6 234 239 PF01217 0.422
TRG_DiLeu_BaLyEn_6 322 327 PF01217 0.400
TRG_DiLeu_LyEn_5 92 97 PF01217 0.295
TRG_ENDOCYTIC_2 120 123 PF00928 0.334
TRG_ENDOCYTIC_2 137 140 PF00928 0.471
TRG_ENDOCYTIC_2 245 248 PF00928 0.434
TRG_ENDOCYTIC_2 257 260 PF00928 0.302
TRG_ENDOCYTIC_2 393 396 PF00928 0.398
TRG_ENDOCYTIC_2 401 404 PF00928 0.391
TRG_ENDOCYTIC_2 422 425 PF00928 0.487
TRG_ENDOCYTIC_2 45 48 PF00928 0.658
TRG_ENDOCYTIC_2 481 484 PF00928 0.290
TRG_ENDOCYTIC_2 486 489 PF00928 0.453
TRG_ENDOCYTIC_2 49 52 PF00928 0.599
TRG_ENDOCYTIC_2 541 544 PF00928 0.609
TRG_ER_diArg_1 189 192 PF00400 0.684
TRG_ER_diArg_1 513 515 PF00400 0.571
TRG_ER_diArg_1 601 603 PF00400 0.645
TRG_NES_CRM1_1 511 525 PF08389 0.466

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IAC1 Leishmania donovani 65% 84%
A0A3Q8IBC3 Leishmania donovani 65% 100%
A0A3Q8IBE0 Leishmania donovani 61% 78%
A0A3Q8IDD7 Leishmania donovani 65% 84%
A0A3S5H769 Leishmania donovani 66% 96%
A0A3S7WVJ2 Leishmania donovani 61% 78%
A0A3S7WVK4 Leishmania donovani 65% 84%
A4HA75 Leishmania braziliensis 74% 100%
A4HA76 Leishmania braziliensis 77% 98%
A4HA77 Leishmania braziliensis 96% 100%
A4HA79 Leishmania braziliensis 91% 100%
A4HA80 Leishmania braziliensis 71% 100%
A4HA82 Leishmania braziliensis 96% 88%
E8NHJ2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 69% 100%
E9AGT0 Leishmania infantum 61% 78%
E9AGT1 Leishmania infantum 67% 100%
E9AGT2 Leishmania infantum 68% 100%
E9AGT3 Leishmania infantum 66% 84%
E9AGT4 Leishmania infantum 65% 84%
E9AS84 Leishmania mexicana (strain MHOM/GT/2001/U1103) 72% 100%
E9AS85 Leishmania mexicana (strain MHOM/GT/2001/U1103) 66% 85%
E9AS86 Leishmania mexicana (strain MHOM/GT/2001/U1103) 30% 87%
Q4QD78 Leishmania major 65% 100%
Q4QD79 Leishmania major 65% 100%
Q4QD80 Leishmania major 66% 100%
Q4QD81 Leishmania major 63% 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