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:
A4HA76_LEIBR
TriTrypDb:
LbrM.19.1520 , LBRM2903_190022100
Length:
632

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

A4HA76
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HA76

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 0.602
CLV_NRD_NRD_1 409 411 PF00675 0.394
CLV_NRD_NRD_1 491 493 PF00675 0.371
CLV_NRD_NRD_1 579 581 PF00675 0.462
CLV_NRD_NRD_1 73 75 PF00675 0.501
CLV_PCSK_KEX2_1 491 493 PF00082 0.371
CLV_PCSK_KEX2_1 579 581 PF00082 0.462
CLV_PCSK_KEX2_1 73 75 PF00082 0.501
CLV_PCSK_SKI1_1 411 415 PF00082 0.363
CLV_PCSK_SKI1_1 528 532 PF00082 0.449
CLV_PCSK_SKI1_1 552 556 PF00082 0.466
CLV_PCSK_SKI1_1 63 67 PF00082 0.580
DEG_APCC_DBOX_1 527 535 PF00400 0.449
DEG_SPOP_SBC_1 115 119 PF00917 0.532
DEG_SPOP_SBC_1 402 406 PF00917 0.584
DOC_ANK_TNKS_1 73 80 PF00023 0.287
DOC_CDC14_PxL_1 432 440 PF14671 0.444
DOC_CYCLIN_RxL_1 2 12 PF00134 0.549
DOC_CYCLIN_yCln2_LP_2 380 386 PF00134 0.457
DOC_MAPK_DCC_7 528 538 PF00069 0.490
DOC_MAPK_JIP1_4 171 177 PF00069 0.519
DOC_MAPK_MEF2A_6 171 179 PF00069 0.540
DOC_MAPK_MEF2A_6 552 561 PF00069 0.240
DOC_PP1_RVXF_1 3 10 PF00149 0.622
DOC_PP1_RVXF_1 300 307 PF00149 0.421
DOC_PP2B_LxvP_1 380 383 PF13499 0.457
DOC_PP2B_LxvP_1 65 68 PF13499 0.323
DOC_PP4_FxxP_1 210 213 PF00568 0.405
DOC_USP7_MATH_1 159 163 PF00917 0.631
DOC_USP7_MATH_1 184 188 PF00917 0.490
DOC_USP7_MATH_1 351 355 PF00917 0.324
DOC_USP7_MATH_1 389 393 PF00917 0.501
DOC_USP7_MATH_1 395 399 PF00917 0.550
DOC_USP7_MATH_1 403 407 PF00917 0.464
DOC_USP7_MATH_1 439 443 PF00917 0.273
DOC_USP7_MATH_1 614 618 PF00917 0.593
DOC_WW_Pin1_4 617 622 PF00397 0.731
LIG_14-3-3_CanoR_1 113 120 PF00244 0.632
LIG_14-3-3_CanoR_1 122 130 PF00244 0.651
LIG_14-3-3_CanoR_1 291 297 PF00244 0.395
LIG_14-3-3_CanoR_1 302 307 PF00244 0.335
LIG_14-3-3_CanoR_1 401 409 PF00244 0.584
LIG_14-3-3_CanoR_1 410 416 PF00244 0.506
LIG_14-3-3_CanoR_1 421 430 PF00244 0.216
LIG_14-3-3_CanoR_1 5 10 PF00244 0.556
LIG_14-3-3_CanoR_1 528 534 PF00244 0.465
LIG_14-3-3_CanoR_1 588 595 PF00244 0.602
LIG_14-3-3_CanoR_1 602 607 PF00244 0.647
LIG_14-3-3_CanoR_1 623 629 PF00244 0.670
LIG_14-3-3_CanoR_1 90 98 PF00244 0.272
LIG_Actin_WH2_2 287 304 PF00022 0.412
LIG_BRCT_BRCA1_1 474 478 PF00533 0.565
LIG_BRCT_BRCA1_1 567 571 PF00533 0.449
LIG_CtBP_PxDLS_1 172 176 PF00389 0.514
LIG_CtBP_PxDLS_1 487 491 PF00389 0.578
LIG_deltaCOP1_diTrp_1 502 511 PF00928 0.585
LIG_deltaCOP1_diTrp_1 85 91 PF00928 0.410
LIG_DLG_GKlike_1 602 609 PF00625 0.544
LIG_eIF4E_1 375 381 PF01652 0.457
LIG_eIF4E_1 423 429 PF01652 0.265
LIG_FHA_1 106 112 PF00498 0.214
LIG_FHA_1 195 201 PF00498 0.258
LIG_FHA_1 258 264 PF00498 0.447
LIG_FHA_1 298 304 PF00498 0.395
LIG_FHA_1 423 429 PF00498 0.278
LIG_FHA_1 47 53 PF00498 0.289
LIG_FHA_1 495 501 PF00498 0.584
LIG_FHA_1 8 14 PF00498 0.660
LIG_FHA_1 94 100 PF00498 0.218
LIG_FHA_2 267 273 PF00498 0.355
LIG_FHA_2 329 335 PF00498 0.337
LIG_FHA_2 497 503 PF00498 0.465
LIG_FHA_2 588 594 PF00498 0.586
LIG_FHA_2 95 101 PF00498 0.231
LIG_LIR_Apic_2 187 191 PF02991 0.317
LIG_LIR_Apic_2 627 631 PF02991 0.596
LIG_LIR_Gen_1 18 27 PF02991 0.629
LIG_LIR_Gen_1 197 205 PF02991 0.263
LIG_LIR_Gen_1 369 378 PF02991 0.384
LIG_LIR_Gen_1 391 400 PF02991 0.457
LIG_LIR_Gen_1 414 424 PF02991 0.508
LIG_LIR_Gen_1 460 471 PF02991 0.313
LIG_LIR_Gen_1 475 486 PF02991 0.530
LIG_LIR_Gen_1 92 103 PF02991 0.284
LIG_LIR_Nem_3 18 23 PF02991 0.642
LIG_LIR_Nem_3 197 202 PF02991 0.261
LIG_LIR_Nem_3 260 265 PF02991 0.455
LIG_LIR_Nem_3 369 375 PF02991 0.409
LIG_LIR_Nem_3 379 384 PF02991 0.359
LIG_LIR_Nem_3 391 396 PF02991 0.422
LIG_LIR_Nem_3 398 402 PF02991 0.512
LIG_LIR_Nem_3 414 420 PF02991 0.467
LIG_LIR_Nem_3 460 466 PF02991 0.330
LIG_LIR_Nem_3 475 481 PF02991 0.547
LIG_LIR_Nem_3 85 91 PF02991 0.388
LIG_LIR_Nem_3 92 98 PF02991 0.339
LIG_LYPXL_S_1 23 27 PF13949 0.385
LIG_LYPXL_yS_3 24 27 PF13949 0.586
LIG_NRBOX 61 67 PF00104 0.304
LIG_Pex14_1 262 266 PF04695 0.473
LIG_Pex14_1 292 296 PF04695 0.438
LIG_Pex14_1 507 511 PF04695 0.609
LIG_Pex14_1 514 518 PF04695 0.536
LIG_Pex14_2 468 472 PF04695 0.496
LIG_Pex14_2 503 507 PF04695 0.615
LIG_Pex14_2 539 543 PF04695 0.476
LIG_PTB_Apo_2 18 25 PF02174 0.532
LIG_PTB_Phospho_1 18 24 PF10480 0.534
LIG_SH2_CRK 20 24 PF00017 0.634
LIG_SH2_CRK 370 374 PF00017 0.384
LIG_SH2_CRK 399 403 PF00017 0.484
LIG_SH2_CRK 518 522 PF00017 0.609
LIG_SH2_CRK 75 79 PF00017 0.299
LIG_SH2_CRK 95 99 PF00017 0.239
LIG_SH2_NCK_1 20 24 PF00017 0.634
LIG_SH2_NCK_1 75 79 PF00017 0.285
LIG_SH2_SRC 133 136 PF00017 0.605
LIG_SH2_STAP1 415 419 PF00017 0.484
LIG_SH2_STAP1 423 427 PF00017 0.270
LIG_SH2_STAP1 80 84 PF00017 0.395
LIG_SH2_STAP1 95 99 PF00017 0.240
LIG_SH2_STAT3 261 264 PF00017 0.452
LIG_SH2_STAT5 194 197 PF00017 0.422
LIG_SH2_STAT5 221 224 PF00017 0.464
LIG_SH2_STAT5 249 252 PF00017 0.521
LIG_SH2_STAT5 265 268 PF00017 0.359
LIG_SH2_STAT5 32 35 PF00017 0.399
LIG_SH2_STAT5 378 381 PF00017 0.495
LIG_SH2_STAT5 385 388 PF00017 0.389
LIG_SH2_STAT5 41 44 PF00017 0.301
LIG_SH2_STAT5 443 446 PF00017 0.246
LIG_SH2_STAT5 463 466 PF00017 0.339
LIG_SH2_STAT5 520 523 PF00017 0.609
LIG_SH2_STAT5 61 64 PF00017 0.303
LIG_SH2_STAT5 95 98 PF00017 0.242
LIG_SH3_3 202 208 PF00018 0.460
LIG_SH3_3 361 367 PF00018 0.281
LIG_SH3_3 430 436 PF00018 0.444
LIG_SUMO_SIM_anti_2 425 431 PF11976 0.265
LIG_SUMO_SIM_par_1 496 502 PF11976 0.452
LIG_SUMO_SIM_par_1 96 102 PF11976 0.226
LIG_TRAF2_1 449 452 PF00917 0.246
LIG_TRFH_1 378 382 PF08558 0.457
LIG_TYR_ITIM 397 402 PF00017 0.487
LIG_TYR_ITIM 461 466 PF00017 0.457
LIG_TYR_ITIM 516 521 PF00017 0.603
LIG_WRC_WIRS_1 303 308 PF05994 0.285
LIG_WRC_WIRS_1 390 395 PF05994 0.501
LIG_WRC_WIRS_1 6 11 PF05994 0.547
LIG_WW_1 382 385 PF00397 0.457
MOD_CDK_SPxK_1 617 623 PF00069 0.570
MOD_CK1_1 116 122 PF00069 0.671
MOD_CK1_1 129 135 PF00069 0.637
MOD_CK1_1 162 168 PF00069 0.614
MOD_CK1_1 617 623 PF00069 0.605
MOD_CK1_1 8 14 PF00069 0.646
MOD_CK2_1 267 273 PF00069 0.355
MOD_CK2_1 328 334 PF00069 0.368
MOD_CK2_1 446 452 PF00069 0.393
MOD_CK2_1 479 485 PF00069 0.540
MOD_CK2_1 587 593 PF00069 0.586
MOD_CK2_1 616 622 PF00069 0.565
MOD_CK2_1 94 100 PF00069 0.218
MOD_CMANNOS 504 507 PF00535 0.415
MOD_GlcNHglycan 100 104 PF01048 0.333
MOD_GlcNHglycan 161 165 PF01048 0.463
MOD_GlcNHglycan 269 272 PF01048 0.553
MOD_GlcNHglycan 481 484 PF01048 0.384
MOD_GlcNHglycan 567 570 PF01048 0.383
MOD_GlcNHglycan 590 593 PF01048 0.437
MOD_GlcNHglycan 616 619 PF01048 0.452
MOD_GSK3_1 114 121 PF00069 0.674
MOD_GSK3_1 122 129 PF00069 0.678
MOD_GSK3_1 146 153 PF00069 0.659
MOD_GSK3_1 15 22 PF00069 0.564
MOD_GSK3_1 167 174 PF00069 0.643
MOD_GSK3_1 236 243 PF00069 0.325
MOD_GSK3_1 292 299 PF00069 0.275
MOD_GSK3_1 439 446 PF00069 0.265
MOD_GSK3_1 598 605 PF00069 0.604
MOD_GSK3_1 89 96 PF00069 0.307
MOD_NEK2_1 105 110 PF00069 0.328
MOD_NEK2_1 140 145 PF00069 0.623
MOD_NEK2_1 236 241 PF00069 0.362
MOD_NEK2_1 257 262 PF00069 0.410
MOD_NEK2_1 266 271 PF00069 0.410
MOD_NEK2_1 285 290 PF00069 0.381
MOD_NEK2_1 296 301 PF00069 0.362
MOD_NEK2_1 494 499 PF00069 0.596
MOD_NEK2_1 523 528 PF00069 0.471
MOD_NEK2_1 616 621 PF00069 0.630
MOD_NEK2_2 292 297 PF00069 0.272
MOD_NEK2_2 376 381 PF00069 0.265
MOD_NEK2_2 46 51 PF00069 0.226
MOD_PIKK_1 133 139 PF00454 0.612
MOD_PIKK_1 83 89 PF00454 0.284
MOD_PKA_2 296 302 PF00069 0.378
MOD_PKA_2 322 328 PF00069 0.370
MOD_PKA_2 587 593 PF00069 0.616
MOD_PKA_2 89 95 PF00069 0.272
MOD_PKB_1 3 11 PF00069 0.549
MOD_Plk_1 328 334 PF00069 0.362
MOD_Plk_1 446 452 PF00069 0.246
MOD_Plk_1 99 105 PF00069 0.233
MOD_Plk_4 106 112 PF00069 0.235
MOD_Plk_4 15 21 PF00069 0.637
MOD_Plk_4 236 242 PF00069 0.399
MOD_Plk_4 257 263 PF00069 0.415
MOD_Plk_4 376 382 PF00069 0.268
MOD_Plk_4 395 401 PF00069 0.439
MOD_Plk_4 423 429 PF00069 0.462
MOD_Plk_4 439 445 PF00069 0.254
MOD_Plk_4 529 535 PF00069 0.492
MOD_Plk_4 67 73 PF00069 0.286
MOD_Plk_4 94 100 PF00069 0.256
MOD_ProDKin_1 617 623 PF00069 0.733
TRG_DiLeu_BaEn_1 273 278 PF01217 0.360
TRG_DiLeu_BaEn_2 451 457 PF01217 0.371
TRG_DiLeu_BaEn_2 99 105 PF01217 0.226
TRG_DiLeu_BaLyEn_6 2 7 PF01217 0.548
TRG_DiLeu_BaLyEn_6 210 215 PF01217 0.422
TRG_DiLeu_BaLyEn_6 299 304 PF01217 0.400
TRG_ENDOCYTIC_2 20 23 PF00928 0.639
TRG_ENDOCYTIC_2 221 224 PF00928 0.434
TRG_ENDOCYTIC_2 233 236 PF00928 0.302
TRG_ENDOCYTIC_2 24 27 PF00928 0.601
TRG_ENDOCYTIC_2 370 373 PF00928 0.398
TRG_ENDOCYTIC_2 378 381 PF00928 0.391
TRG_ENDOCYTIC_2 399 402 PF00928 0.487
TRG_ENDOCYTIC_2 463 466 PF00928 0.453
TRG_ENDOCYTIC_2 518 521 PF00928 0.609
TRG_ENDOCYTIC_2 75 78 PF00928 0.330
TRG_ENDOCYTIC_2 95 98 PF00928 0.334
TRG_ER_diArg_1 2 5 PF00400 0.561
TRG_ER_diArg_1 490 492 PF00400 0.571
TRG_ER_diArg_1 578 580 PF00400 0.654
TRG_ER_diArg_1 72 74 PF00400 0.286
TRG_NES_CRM1_1 488 502 PF08389 0.466

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IAC1 Leishmania donovani 61% 81%
A0A3Q8IBC3 Leishmania donovani 61% 100%
A0A3Q8IBE0 Leishmania donovani 63% 76%
A0A3Q8IDD7 Leishmania donovani 61% 81%
A0A3S5H769 Leishmania donovani 62% 92%
A0A3S7WVJ2 Leishmania donovani 63% 75%
A0A3S7WVK4 Leishmania donovani 61% 81%
A4HA75 Leishmania braziliensis 95% 100%
A4HA77 Leishmania braziliensis 73% 100%
A4HA79 Leishmania braziliensis 92% 100%
A4HA80 Leishmania braziliensis 99% 68%
A4HA81 Leishmania braziliensis 77% 96%
A4HA82 Leishmania braziliensis 75% 84%
E8NHJ2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 72% 100%
E9AGT0 Leishmania infantum 63% 75%
E9AGT1 Leishmania infantum 63% 100%
E9AGT2 Leishmania infantum 62% 100%
E9AGT3 Leishmania infantum 62% 81%
E9AGT4 Leishmania infantum 60% 81%
E9AS84 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
E9AS85 Leishmania mexicana (strain MHOM/GT/2001/U1103) 60% 82%
E9AS86 Leishmania mexicana (strain MHOM/GT/2001/U1103) 31% 84%
Q4QD78 Leishmania major 59% 100%
Q4QD79 Leishmania major 60% 100%
Q4QD80 Leishmania major 60% 100%
Q4QD81 Leishmania major 64% 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