LeishMANIAdb
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Putative GIPL galf transferase

Quick info Annotations Function or PPIs Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Putative GIPL galf transferase
Gene product:
GIPL galf transferase, putative
Species:
Leishmania braziliensis
UniProt:
A4HL36_LEIBR
TriTrypDb:
LbrM.32.4230 , LBRM2903_320052400 *
Length:
577

Annotations

LeishMANIAdb annotations

A large family of glycosyltransferases expanded in parazitic kinetoplastids (and even more in T cruzi). Localization: ER (by homology)

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: 13
NetGPI no yes: 0, no: 13
Cellular components
Term Name Level Count
GO:0005886 plasma membrane 3 1
GO:0016020 membrane 2 7
GO:0110165 cellular anatomical entity 1 7

Expansion

Sequence features

A4HL36
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HL36

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 14
GO:0016740 transferase activity 2 14
GO:0016757 glycosyltransferase activity 3 6

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 282 286 PF00656 0.361
CLV_NRD_NRD_1 13 15 PF00675 0.519
CLV_NRD_NRD_1 145 147 PF00675 0.563
CLV_NRD_NRD_1 354 356 PF00675 0.609
CLV_PCSK_FUR_1 473 477 PF00082 0.541
CLV_PCSK_KEX2_1 13 15 PF00082 0.490
CLV_PCSK_KEX2_1 145 147 PF00082 0.571
CLV_PCSK_KEX2_1 354 356 PF00082 0.590
CLV_PCSK_KEX2_1 475 477 PF00082 0.579
CLV_PCSK_PC1ET2_1 475 477 PF00082 0.544
CLV_PCSK_SKI1_1 22 26 PF00082 0.359
CLV_PCSK_SKI1_1 268 272 PF00082 0.505
CLV_PCSK_SKI1_1 319 323 PF00082 0.611
CLV_PCSK_SKI1_1 390 394 PF00082 0.592
CLV_PCSK_SKI1_1 464 468 PF00082 0.673
DEG_APCC_DBOX_1 267 275 PF00400 0.286
DEG_APCC_DBOX_1 389 397 PF00400 0.327
DEG_SCF_FBW7_2 50 57 PF00400 0.415
DOC_CKS1_1 170 175 PF01111 0.330
DOC_CKS1_1 51 56 PF01111 0.414
DOC_CYCLIN_RxL_1 143 152 PF00134 0.276
DOC_CYCLIN_RxL_1 265 273 PF00134 0.219
DOC_MAPK_MEF2A_6 325 333 PF00069 0.422
DOC_PP1_RVXF_1 462 468 PF00149 0.341
DOC_PP4_FxxP_1 43 46 PF00568 0.380
DOC_USP7_MATH_1 460 464 PF00917 0.431
DOC_WW_Pin1_4 122 127 PF00397 0.422
DOC_WW_Pin1_4 169 174 PF00397 0.327
DOC_WW_Pin1_4 374 379 PF00397 0.363
DOC_WW_Pin1_4 444 449 PF00397 0.434
DOC_WW_Pin1_4 50 55 PF00397 0.436
DOC_WW_Pin1_4 80 85 PF00397 0.467
LIG_14-3-3_CanoR_1 14 20 PF00244 0.672
LIG_14-3-3_CanoR_1 202 210 PF00244 0.269
LIG_14-3-3_CanoR_1 390 396 PF00244 0.328
LIG_14-3-3_CanoR_1 528 534 PF00244 0.382
LIG_APCC_ABBA_1 40 45 PF00400 0.370
LIG_APCC_ABBAyCdc20_2 118 124 PF00400 0.441
LIG_BIR_II_1 1 5 PF00653 0.665
LIG_deltaCOP1_diTrp_1 251 258 PF00928 0.300
LIG_deltaCOP1_diTrp_1 409 418 PF00928 0.400
LIG_eIF4E_1 19 25 PF01652 0.589
LIG_eIF4E_1 483 489 PF01652 0.347
LIG_FHA_1 139 145 PF00498 0.300
LIG_FHA_1 173 179 PF00498 0.325
LIG_FHA_1 19 25 PF00498 0.563
LIG_FHA_1 204 210 PF00498 0.366
LIG_FHA_1 335 341 PF00498 0.402
LIG_FHA_1 383 389 PF00498 0.377
LIG_FHA_1 513 519 PF00498 0.396
LIG_FHA_1 80 86 PF00498 0.618
LIG_FHA_1 87 93 PF00498 0.438
LIG_FHA_2 248 254 PF00498 0.330
LIG_FHA_2 280 286 PF00498 0.382
LIG_FHA_2 358 364 PF00498 0.368
LIG_FHA_2 548 554 PF00498 0.449
LIG_Integrin_RGD_1 283 285 PF01839 0.567
LIG_LIR_Apic_2 424 429 PF02991 0.289
LIG_LIR_Apic_2 535 541 PF02991 0.403
LIG_LIR_Apic_2 93 99 PF02991 0.479
LIG_LIR_Gen_1 27 38 PF02991 0.236
LIG_LIR_Gen_1 500 511 PF02991 0.421
LIG_LIR_Nem_3 177 183 PF02991 0.462
LIG_LIR_Nem_3 305 311 PF02991 0.398
LIG_LIR_Nem_3 326 331 PF02991 0.403
LIG_LIR_Nem_3 401 407 PF02991 0.499
LIG_LIR_Nem_3 412 418 PF02991 0.345
LIG_LIR_Nem_3 451 456 PF02991 0.389
LIG_LIR_Nem_3 500 506 PF02991 0.508
LIG_LYPXL_yS_3 328 331 PF13949 0.439
LIG_Pex14_2 180 184 PF04695 0.316
LIG_Pex14_2 418 422 PF04695 0.358
LIG_SH2_CRK 194 198 PF00017 0.332
LIG_SH2_CRK 426 430 PF00017 0.306
LIG_SH2_CRK 478 482 PF00017 0.396
LIG_SH2_GRB2like 505 508 PF00017 0.337
LIG_SH2_NCK_1 426 430 PF00017 0.311
LIG_SH2_NCK_1 439 443 PF00017 0.388
LIG_SH2_NCK_1 87 91 PF00017 0.417
LIG_SH2_STAP1 158 162 PF00017 0.299
LIG_SH2_STAP1 311 315 PF00017 0.405
LIG_SH2_STAP1 456 460 PF00017 0.461
LIG_SH2_STAT3 196 199 PF00017 0.406
LIG_SH2_STAT3 533 536 PF00017 0.506
LIG_SH2_STAT5 196 199 PF00017 0.402
LIG_SH2_STAT5 372 375 PF00017 0.414
LIG_SH2_STAT5 398 401 PF00017 0.393
LIG_SH2_STAT5 403 406 PF00017 0.417
LIG_SH2_STAT5 453 456 PF00017 0.462
LIG_SH2_STAT5 470 473 PF00017 0.420
LIG_SH2_STAT5 503 506 PF00017 0.336
LIG_SH3_1 336 342 PF00018 0.360
LIG_SH3_1 426 432 PF00018 0.314
LIG_SH3_2 339 344 PF14604 0.358
LIG_SH3_3 326 332 PF00018 0.424
LIG_SH3_3 336 342 PF00018 0.308
LIG_SH3_3 426 432 PF00018 0.314
LIG_SUMO_SIM_par_1 167 172 PF11976 0.375
LIG_SUMO_SIM_par_1 384 389 PF11976 0.340
LIG_TRAF2_1 250 253 PF00917 0.305
LIG_TRAF2_1 495 498 PF00917 0.388
LIG_TRAF2_1 550 553 PF00917 0.448
LIG_TYR_ITIM 192 197 PF00017 0.325
LIG_Vh1_VBS_1 24 42 PF01044 0.220
MOD_CK1_1 204 210 PF00069 0.229
MOD_CK1_1 532 538 PF00069 0.376
MOD_CK1_1 75 81 PF00069 0.511
MOD_CK2_1 247 253 PF00069 0.298
MOD_CK2_1 306 312 PF00069 0.391
MOD_CK2_1 357 363 PF00069 0.387
MOD_CK2_1 492 498 PF00069 0.351
MOD_CK2_1 547 553 PF00069 0.458
MOD_CK2_1 569 575 PF00069 0.406
MOD_GlcNHglycan 219 222 PF01048 0.515
MOD_GlcNHglycan 234 237 PF01048 0.478
MOD_GlcNHglycan 325 328 PF01048 0.602
MOD_GlcNHglycan 355 358 PF01048 0.687
MOD_GlcNHglycan 519 523 PF01048 0.534
MOD_GlcNHglycan 552 556 PF01048 0.656
MOD_GlcNHglycan 72 75 PF01048 0.649
MOD_GSK3_1 20 27 PF00069 0.426
MOD_GSK3_1 353 360 PF00069 0.357
MOD_GSK3_1 382 389 PF00069 0.451
MOD_GSK3_1 46 53 PF00069 0.473
MOD_GSK3_1 547 554 PF00069 0.472
MOD_GSK3_1 57 64 PF00069 0.595
MOD_GSK3_1 68 75 PF00069 0.577
MOD_GSK3_1 86 93 PF00069 0.435
MOD_N-GLC_1 122 127 PF02516 0.624
MOD_N-GLC_1 306 311 PF02516 0.598
MOD_N-GLC_1 460 465 PF02516 0.637
MOD_N-GLC_1 501 506 PF02516 0.629
MOD_N-GLC_1 569 574 PF02516 0.573
MOD_N-GLC_1 65 70 PF02516 0.646
MOD_N-GLC_1 75 80 PF02516 0.623
MOD_NEK2_1 217 222 PF00069 0.305
MOD_NEK2_1 24 29 PF00069 0.303
MOD_NEK2_1 270 275 PF00069 0.246
MOD_NEK2_1 391 396 PF00069 0.412
MOD_NEK2_1 506 511 PF00069 0.466
MOD_NEK2_1 518 523 PF00069 0.514
MOD_NEK2_1 527 532 PF00069 0.447
MOD_NEK2_1 551 556 PF00069 0.479
MOD_NEK2_1 70 75 PF00069 0.477
MOD_NEK2_1 79 84 PF00069 0.423
MOD_NEK2_2 20 25 PF00069 0.589
MOD_NEK2_2 421 426 PF00069 0.326
MOD_PIKK_1 465 471 PF00454 0.337
MOD_PIKK_1 532 538 PF00454 0.421
MOD_PIKK_1 65 71 PF00454 0.444
MOD_PKA_2 201 207 PF00069 0.229
MOD_PKA_2 353 359 PF00069 0.431
MOD_PKA_2 527 533 PF00069 0.397
MOD_Plk_1 138 144 PF00069 0.305
MOD_Plk_1 204 210 PF00069 0.375
MOD_Plk_1 284 290 PF00069 0.298
MOD_Plk_1 306 312 PF00069 0.402
MOD_Plk_1 460 466 PF00069 0.353
MOD_Plk_1 501 507 PF00069 0.403
MOD_Plk_1 65 71 PF00069 0.454
MOD_Plk_1 75 81 PF00069 0.423
MOD_Plk_1 90 96 PF00069 0.437
MOD_Plk_4 25 31 PF00069 0.385
MOD_Plk_4 270 276 PF00069 0.325
MOD_Plk_4 284 290 PF00069 0.330
MOD_Plk_4 306 312 PF00069 0.400
MOD_Plk_4 391 397 PF00069 0.264
MOD_Plk_4 421 427 PF00069 0.293
MOD_Plk_4 501 507 PF00069 0.418
MOD_Plk_4 512 518 PF00069 0.358
MOD_Plk_4 75 81 PF00069 0.481
MOD_Plk_4 91 97 PF00069 0.439
MOD_ProDKin_1 122 128 PF00069 0.419
MOD_ProDKin_1 169 175 PF00069 0.329
MOD_ProDKin_1 374 380 PF00069 0.367
MOD_ProDKin_1 444 450 PF00069 0.438
MOD_ProDKin_1 50 56 PF00069 0.439
MOD_ProDKin_1 80 86 PF00069 0.466
TRG_DiLeu_BaEn_1 219 224 PF01217 0.232
TRG_DiLeu_BaEn_4 552 558 PF01217 0.439
TRG_DiLeu_BaLyEn_6 165 170 PF01217 0.337
TRG_DiLeu_LyEn_5 219 224 PF01217 0.219
TRG_ENDOCYTIC_2 194 197 PF00928 0.408
TRG_ENDOCYTIC_2 328 331 PF00928 0.404
TRG_ENDOCYTIC_2 478 481 PF00928 0.428
TRG_ENDOCYTIC_2 503 506 PF00928 0.435
TRG_ENDOCYTIC_2 565 568 PF00928 0.424
TRG_ER_diArg_1 13 15 PF00400 0.673
TRG_ER_diArg_1 144 146 PF00400 0.326
TRG_ER_diArg_1 226 229 PF00400 0.249
TRG_ER_diArg_1 316 319 PF00400 0.436
TRG_ER_diArg_1 344 347 PF00400 0.496
TRG_NLS_MonoExtN_4 130 136 PF00514 0.340
TRG_Pf-PMV_PEXEL_1 146 151 PF00026 0.549
TRG_Pf-PMV_PEXEL_1 549 553 PF00026 0.655

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IHI5 Leishmania donovani 63% 87%
A0A3S5H7D9 Leishmania donovani 29% 100%
A0A3S7X6F1 Leishmania donovani 33% 100%
A4I143 Leishmania infantum 29% 100%
A4I8P7 Leishmania infantum 33% 100%
E9AHM5 Leishmania infantum 64% 97%
E9AXX9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 29% 100%
E9B3H7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 64% 98%
E9B3L0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 33% 100%
Q4QD44 Leishmania major 62% 99%
Q6XFB5 Leishmania major 30% 100%
Q9NC61 Leishmania major 26% 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