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:
A4HA79_LEIBR
TriTrypDb:
LbrM.19.1550 , LBRM2903_190022100
Length:
490

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: 21
NetGPI no yes: 0, no: 21
Cellular components
Term Name Level Count
GO:0016020 membrane 2 22
GO:0110165 cellular anatomical entity 1 22
GO:0005737 cytoplasm 2 2
GO:0005783 endoplasmic reticulum 5 2
GO:0043226 organelle 2 2
GO:0043227 membrane-bounded organelle 3 2
GO:0043229 intracellular organelle 3 2
GO:0043231 intracellular membrane-bounded organelle 4 2

Expansion

Sequence features

A4HA79
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HA79

Function

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

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_NRD_NRD_1 173 175 PF00675 0.295
CLV_NRD_NRD_1 255 257 PF00675 0.273
CLV_NRD_NRD_1 344 346 PF00675 0.375
CLV_NRD_NRD_1 373 375 PF00675 0.492
CLV_NRD_NRD_1 385 387 PF00675 0.418
CLV_PCSK_KEX2_1 255 257 PF00082 0.273
CLV_PCSK_KEX2_1 344 346 PF00082 0.375
CLV_PCSK_KEX2_1 372 374 PF00082 0.350
CLV_PCSK_KEX2_1 385 387 PF00082 0.422
CLV_PCSK_KEX2_1 484 486 PF00082 0.280
CLV_PCSK_PC1ET2_1 484 486 PF00082 0.349
CLV_PCSK_PC7_1 381 387 PF00082 0.372
CLV_PCSK_SKI1_1 175 179 PF00082 0.289
CLV_PCSK_SKI1_1 293 297 PF00082 0.457
CLV_PCSK_SKI1_1 317 321 PF00082 0.405
CLV_PCSK_SKI1_1 373 377 PF00082 0.349
CLV_PCSK_SKI1_1 473 477 PF00082 0.280
DEG_APCC_DBOX_1 292 300 PF00400 0.534
DEG_APCC_DBOX_1 372 380 PF00400 0.553
DEG_SCF_FBW7_1 448 455 PF00400 0.333
DEG_SPOP_SBC_1 166 170 PF00917 0.542
DOC_CDC14_PxL_1 196 204 PF14671 0.396
DOC_CYCLIN_yCln2_LP_2 144 150 PF00134 0.374
DOC_MAPK_DCC_7 293 303 PF00069 0.307
DOC_MAPK_MEF2A_6 317 326 PF00069 0.297
DOC_PP1_RVXF_1 64 71 PF00149 0.289
DOC_PP2B_LxvP_1 144 147 PF13499 0.357
DOC_USP7_MATH_1 115 119 PF00917 0.380
DOC_USP7_MATH_1 153 157 PF00917 0.315
DOC_USP7_MATH_1 159 163 PF00917 0.481
DOC_USP7_MATH_1 167 171 PF00917 0.468
DOC_USP7_MATH_1 203 207 PF00917 0.215
DOC_USP7_MATH_1 259 263 PF00917 0.374
DOC_USP7_MATH_1 403 407 PF00917 0.199
DOC_USP7_MATH_1 446 450 PF00917 0.316
DOC_WW_Pin1_4 362 367 PF00397 0.535
DOC_WW_Pin1_4 385 390 PF00397 0.668
DOC_WW_Pin1_4 448 453 PF00397 0.396
LIG_14-3-3_CanoR_1 165 173 PF00244 0.597
LIG_14-3-3_CanoR_1 174 180 PF00244 0.453
LIG_14-3-3_CanoR_1 185 194 PF00244 0.445
LIG_14-3-3_CanoR_1 293 299 PF00244 0.401
LIG_14-3-3_CanoR_1 390 395 PF00244 0.566
LIG_14-3-3_CanoR_1 55 61 PF00244 0.370
LIG_14-3-3_CanoR_1 66 71 PF00244 0.369
LIG_Actin_WH2_2 51 68 PF00022 0.345
LIG_BIR_II_1 1 5 PF00653 0.378
LIG_BRCT_BRCA1_1 238 242 PF00533 0.579
LIG_BRCT_BRCA1_1 332 336 PF00533 0.401
LIG_BRCT_BRCA1_1 405 409 PF00533 0.219
LIG_BRCT_BRCA1_1 415 419 PF00533 0.191
LIG_CtBP_PxDLS_1 251 255 PF00389 0.474
LIG_deltaCOP1_diTrp_1 267 276 PF00928 0.463
LIG_eIF4E_1 139 145 PF01652 0.407
LIG_eIF4E_1 187 193 PF01652 0.322
LIG_FHA_1 187 193 PF00498 0.302
LIG_FHA_1 22 28 PF00498 0.455
LIG_FHA_1 351 357 PF00498 0.619
LIG_FHA_1 366 372 PF00498 0.506
LIG_FHA_1 451 457 PF00498 0.337
LIG_FHA_1 478 484 PF00498 0.606
LIG_FHA_1 62 68 PF00498 0.393
LIG_FHA_2 262 268 PF00498 0.525
LIG_FHA_2 31 37 PF00498 0.500
LIG_FHA_2 93 99 PF00498 0.390
LIG_LIR_Gen_1 133 142 PF02991 0.278
LIG_LIR_Gen_1 155 164 PF02991 0.338
LIG_LIR_Gen_1 178 188 PF02991 0.563
LIG_LIR_Gen_1 224 235 PF02991 0.232
LIG_LIR_Gen_1 239 250 PF02991 0.548
LIG_LIR_Nem_3 133 139 PF02991 0.278
LIG_LIR_Nem_3 143 148 PF02991 0.312
LIG_LIR_Nem_3 155 160 PF02991 0.375
LIG_LIR_Nem_3 162 166 PF02991 0.452
LIG_LIR_Nem_3 178 184 PF02991 0.563
LIG_LIR_Nem_3 224 230 PF02991 0.280
LIG_LIR_Nem_3 239 245 PF02991 0.559
LIG_LIR_Nem_3 24 29 PF02991 0.432
LIG_LIR_Nem_3 393 399 PF02991 0.586
LIG_Pex14_1 26 30 PF04695 0.434
LIG_Pex14_1 272 276 PF04695 0.466
LIG_Pex14_1 279 283 PF04695 0.466
LIG_Pex14_1 56 60 PF04695 0.357
LIG_Pex14_2 232 236 PF04695 0.321
LIG_Pex14_2 268 272 PF04695 0.468
LIG_Pex14_2 304 308 PF04695 0.323
LIG_PTB_Apo_2 257 264 PF02174 0.374
LIG_PTB_Phospho_1 257 263 PF10480 0.374
LIG_SH2_CRK 134 138 PF00017 0.277
LIG_SH2_CRK 163 167 PF00017 0.577
LIG_SH2_CRK 283 287 PF00017 0.466
LIG_SH2_CRK 396 400 PF00017 0.457
LIG_SH2_NCK_1 223 227 PF00017 0.211
LIG_SH2_NCK_1 436 440 PF00017 0.309
LIG_SH2_SRC 436 439 PF00017 0.309
LIG_SH2_STAP1 179 183 PF00017 0.465
LIG_SH2_STAP1 187 191 PF00017 0.347
LIG_SH2_STAP1 223 227 PF00017 0.238
LIG_SH2_STAT3 25 28 PF00017 0.420
LIG_SH2_STAT5 13 16 PF00017 0.429
LIG_SH2_STAT5 142 145 PF00017 0.321
LIG_SH2_STAT5 149 152 PF00017 0.314
LIG_SH2_STAT5 207 210 PF00017 0.314
LIG_SH2_STAT5 220 223 PF00017 0.313
LIG_SH2_STAT5 227 230 PF00017 0.353
LIG_SH2_STAT5 263 266 PF00017 0.374
LIG_SH2_STAT5 285 288 PF00017 0.466
LIG_SH2_STAT5 29 32 PF00017 0.434
LIG_SH2_STAT5 487 490 PF00017 0.513
LIG_SH3_3 125 131 PF00018 0.345
LIG_SH3_3 194 200 PF00018 0.396
LIG_SUMO_SIM_anti_2 189 195 PF11976 0.226
LIG_SUMO_SIM_anti_2 466 472 PF11976 0.389
LIG_TRAF2_1 213 216 PF00917 0.209
LIG_TRFH_1 142 146 PF08558 0.456
LIG_TYR_ITIM 161 166 PF00017 0.456
LIG_TYR_ITIM 225 230 PF00017 0.405
LIG_TYR_ITIM 281 286 PF00017 0.303
LIG_WRC_WIRS_1 154 159 PF05994 0.322
LIG_WRC_WIRS_1 391 396 PF05994 0.360
LIG_WRC_WIRS_1 67 72 PF05994 0.390
LIG_WW_1 146 149 PF00397 0.413
MOD_CDK_SPK_2 385 390 PF00069 0.342
MOD_CK1_1 365 371 PF00069 0.399
MOD_CK1_1 464 470 PF00069 0.297
MOD_CK2_1 210 216 PF00069 0.456
MOD_CK2_1 243 249 PF00069 0.336
MOD_CK2_1 261 267 PF00069 0.183
MOD_CK2_1 31 37 PF00069 0.667
MOD_CK2_1 92 98 PF00069 0.494
MOD_CMANNOS 269 272 PF00535 0.309
MOD_GlcNHglycan 245 248 PF01048 0.407
MOD_GlcNHglycan 33 36 PF01048 0.406
MOD_GlcNHglycan 332 335 PF01048 0.341
MOD_GlcNHglycan 406 409 PF01048 0.318
MOD_GlcNHglycan 433 436 PF01048 0.643
MOD_GlcNHglycan 463 466 PF01048 0.368
MOD_GSK3_1 203 210 PF00069 0.373
MOD_GSK3_1 413 420 PF00069 0.269
MOD_GSK3_1 446 453 PF00069 0.530
MOD_GSK3_1 473 480 PF00069 0.514
MOD_GSK3_1 56 63 PF00069 0.482
MOD_N-GLC_1 259 264 PF02516 0.177
MOD_NEK2_1 21 26 PF00069 0.556
MOD_NEK2_1 221 226 PF00069 0.294
MOD_NEK2_1 288 293 PF00069 0.349
MOD_NEK2_1 30 35 PF00069 0.594
MOD_NEK2_1 4 9 PF00069 0.317
MOD_NEK2_1 425 430 PF00069 0.529
MOD_NEK2_1 461 466 PF00069 0.346
MOD_NEK2_1 49 54 PF00069 0.468
MOD_NEK2_1 60 65 PF00069 0.397
MOD_NEK2_2 140 145 PF00069 0.226
MOD_NEK2_2 261 266 PF00069 0.182
MOD_NEK2_2 56 61 PF00069 0.336
MOD_PKA_2 60 66 PF00069 0.480
MOD_PKA_2 86 92 PF00069 0.473
MOD_Plk_1 210 216 PF00069 0.387
MOD_Plk_1 259 265 PF00069 0.187
MOD_Plk_1 357 363 PF00069 0.424
MOD_Plk_1 92 98 PF00069 0.484
MOD_Plk_4 140 146 PF00069 0.243
MOD_Plk_4 159 165 PF00069 0.326
MOD_Plk_4 187 193 PF00069 0.418
MOD_Plk_4 203 209 PF00069 0.345
MOD_Plk_4 21 27 PF00069 0.554
MOD_Plk_4 294 300 PF00069 0.412
MOD_Plk_4 390 396 PF00069 0.567
MOD_ProDKin_1 362 368 PF00069 0.402
MOD_ProDKin_1 385 391 PF00069 0.583
MOD_ProDKin_1 448 454 PF00069 0.482
TRG_DiLeu_BaEn_1 37 42 PF01217 0.414
TRG_DiLeu_BaLyEn_6 371 376 PF01217 0.320
TRG_DiLeu_BaLyEn_6 63 68 PF01217 0.440
TRG_ENDOCYTIC_2 134 137 PF00928 0.316
TRG_ENDOCYTIC_2 142 145 PF00928 0.304
TRG_ENDOCYTIC_2 163 166 PF00928 0.437
TRG_ENDOCYTIC_2 222 225 PF00928 0.284
TRG_ENDOCYTIC_2 227 230 PF00928 0.361
TRG_ENDOCYTIC_2 283 286 PF00928 0.307
TRG_ENDOCYTIC_2 396 399 PF00928 0.348
TRG_ER_diArg_1 254 256 PF00400 0.316
TRG_ER_diArg_1 343 345 PF00400 0.459
TRG_ER_diArg_1 371 374 PF00400 0.641
TRG_ER_diArg_1 385 387 PF00400 0.509

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0S4IRP6 Bodo saltans 36% 82%
A0A1X0P614 Trypanosomatidae 33% 79%
A0A1X0P616 Trypanosomatidae 39% 80%
A0A1X0P718 Trypanosomatidae 41% 76%
A0A3Q8IBC3 Leishmania donovani 67% 81%
A0A3R7NNW7 Trypanosoma rangeli 41% 100%
A0A3S5H769 Leishmania donovani 70% 72%
A0A3S5IRW9 Trypanosoma rangeli 35% 79%
A0A3S7WVS3 Leishmania donovani 68% 100%
A4HA75 Leishmania braziliensis 97% 100%
A4HA76 Leishmania braziliensis 92% 78%
A4HA81 Leishmania braziliensis 91% 75%
D0A0T4 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 42% 80%
E8NHJ2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 69% 82%
E9AGS9 Leishmania infantum 67% 100%
E9AGT1 Leishmania infantum 76% 85%
E9AGT2 Leishmania infantum 74% 89%
E9AS84 Leishmania mexicana (strain MHOM/GT/2001/U1103) 70% 100%
Q4QD81 Leishmania major 68% 100%
Q4QD82 Leishmania major 77% 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