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 mexicana
UniProt:
E9B3H7_LEIMU
TriTrypDb:
LmxM.31.3990
Length:
588

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: 16
NetGPI no yes: 0, no: 16
Cellular components
Term Name Level Count
GO:0016020 membrane 2 10
GO:0110165 cellular anatomical entity 1 10
GO:0005886 plasma membrane 3 1

Expansion

Sequence features

E9B3H7
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9B3H7

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 17
GO:0016740 transferase activity 2 17
GO:0016757 glycosyltransferase activity 3 6

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 292 296 PF00656 0.384
CLV_MEL_PAP_1 223 229 PF00089 0.466
CLV_NRD_NRD_1 1 3 PF00675 0.492
CLV_NRD_NRD_1 14 16 PF00675 0.527
CLV_NRD_NRD_1 154 156 PF00675 0.575
CLV_NRD_NRD_1 225 227 PF00675 0.466
CLV_NRD_NRD_1 376 378 PF00675 0.527
CLV_NRD_NRD_1 475 477 PF00675 0.608
CLV_NRD_NRD_1 534 536 PF00675 0.642
CLV_PCSK_KEX2_1 14 16 PF00082 0.519
CLV_PCSK_KEX2_1 225 227 PF00082 0.466
CLV_PCSK_KEX2_1 375 377 PF00082 0.546
CLV_PCSK_KEX2_1 475 477 PF00082 0.608
CLV_PCSK_KEX2_1 534 536 PF00082 0.640
CLV_PCSK_SKI1_1 15 19 PF00082 0.346
CLV_PCSK_SKI1_1 168 172 PF00082 0.523
CLV_PCSK_SKI1_1 283 287 PF00082 0.410
CLV_PCSK_SKI1_1 329 333 PF00082 0.649
CLV_PCSK_SKI1_1 376 380 PF00082 0.535
CLV_PCSK_SKI1_1 400 404 PF00082 0.567
CLV_PCSK_SKI1_1 475 479 PF00082 0.650
CLV_PCSK_SKI1_1 50 54 PF00082 0.699
CLV_PCSK_SKI1_1 535 539 PF00082 0.554
CLV_PCSK_SKI1_1 577 581 PF00082 0.569
DEG_APCC_DBOX_1 399 407 PF00400 0.345
DEG_Nend_UBRbox_1 1 4 PF02207 0.711
DEG_SPOP_SBC_1 80 84 PF00917 0.502
DOC_CKS1_1 180 185 PF01111 0.316
DOC_CYCLIN_RxL_1 153 161 PF00134 0.274
DOC_MAPK_DCC_7 20 28 PF00069 0.297
DOC_MAPK_gen_1 11 19 PF00069 0.759
DOC_MAPK_HePTP_8 17 29 PF00069 0.317
DOC_MAPK_MEF2A_6 20 29 PF00069 0.357
DOC_MAPK_MEF2A_6 335 343 PF00069 0.474
DOC_PP4_FxxP_1 48 51 PF00568 0.434
DOC_USP7_MATH_1 101 105 PF00917 0.440
DOC_USP7_MATH_1 114 118 PF00917 0.461
DOC_USP7_MATH_1 43 47 PF00917 0.413
DOC_USP7_MATH_1 71 75 PF00917 0.469
DOC_USP7_MATH_1 86 90 PF00917 0.442
DOC_USP7_UBL2_3 584 588 PF12436 0.374
DOC_WW_Pin1_4 116 121 PF00397 0.462
DOC_WW_Pin1_4 125 130 PF00397 0.466
DOC_WW_Pin1_4 179 184 PF00397 0.312
DOC_WW_Pin1_4 384 389 PF00397 0.349
DOC_WW_Pin1_4 41 46 PF00397 0.454
DOC_WW_Pin1_4 454 459 PF00397 0.426
LIG_14-3-3_CanoR_1 14 20 PF00244 0.508
LIG_14-3-3_CanoR_1 2 8 PF00244 0.735
LIG_14-3-3_CanoR_1 327 332 PF00244 0.451
LIG_14-3-3_CanoR_1 400 409 PF00244 0.303
LIG_14-3-3_CanoR_1 539 543 PF00244 0.397
LIG_14-3-3_CanoR_1 553 558 PF00244 0.363
LIG_14-3-3_CanoR_1 72 76 PF00244 0.510
LIG_14-3-3_CanoR_1 88 95 PF00244 0.523
LIG_BIR_III_2 175 179 PF00653 0.314
LIG_deltaCOP1_diTrp_1 262 268 PF00928 0.334
LIG_deltaCOP1_diTrp_1 422 432 PF00928 0.391
LIG_DLG_GKlike_1 327 334 PF00625 0.303
LIG_FHA_1 100 106 PF00498 0.454
LIG_FHA_1 172 178 PF00498 0.336
LIG_FHA_1 183 189 PF00498 0.387
LIG_FHA_1 214 220 PF00498 0.341
LIG_FHA_1 345 351 PF00498 0.374
LIG_FHA_1 393 399 PF00498 0.373
LIG_FHA_1 52 58 PF00498 0.436
LIG_FHA_1 524 530 PF00498 0.402
LIG_FHA_2 110 116 PF00498 0.554
LIG_FHA_2 258 264 PF00498 0.380
LIG_FHA_2 272 278 PF00498 0.267
LIG_FHA_2 290 296 PF00498 0.316
LIG_FHA_2 559 565 PF00498 0.448
LIG_Integrin_RGD_1 293 295 PF01839 0.545
LIG_LIR_Apic_2 46 51 PF02991 0.420
LIG_LIR_Gen_1 139 147 PF02991 0.502
LIG_LIR_Gen_1 434 443 PF02991 0.342
LIG_LIR_Gen_1 511 522 PF02991 0.454
LIG_LIR_Nem_3 187 193 PF02991 0.374
LIG_LIR_Nem_3 315 321 PF02991 0.376
LIG_LIR_Nem_3 336 341 PF02991 0.484
LIG_LIR_Nem_3 411 417 PF02991 0.405
LIG_LIR_Nem_3 422 428 PF02991 0.378
LIG_LIR_Nem_3 434 439 PF02991 0.403
LIG_LIR_Nem_3 444 449 PF02991 0.444
LIG_LIR_Nem_3 511 517 PF02991 0.493
LIG_LYPXL_yS_3 338 341 PF13949 0.400
LIG_Pex14_2 190 194 PF04695 0.318
LIG_Pex14_2 428 432 PF04695 0.472
LIG_SH2_CRK 204 208 PF00017 0.311
LIG_SH2_CRK 489 493 PF00017 0.411
LIG_SH2_NCK_1 449 453 PF00017 0.373
LIG_SH2_STAP1 321 325 PF00017 0.375
LIG_SH2_STAP1 544 548 PF00017 0.482
LIG_SH2_STAT3 206 209 PF00017 0.380
LIG_SH2_STAT3 544 547 PF00017 0.449
LIG_SH2_STAT5 193 196 PF00017 0.319
LIG_SH2_STAT5 206 209 PF00017 0.409
LIG_SH2_STAT5 382 385 PF00017 0.432
LIG_SH2_STAT5 408 411 PF00017 0.442
LIG_SH2_STAT5 413 416 PF00017 0.457
LIG_SH2_STAT5 481 484 PF00017 0.501
LIG_SH3_1 346 352 PF00018 0.330
LIG_SH3_2 349 354 PF14604 0.369
LIG_SH3_3 102 108 PF00018 0.472
LIG_SH3_3 336 342 PF00018 0.411
LIG_SH3_3 346 352 PF00018 0.322
LIG_SH3_3 65 71 PF00018 0.504
LIG_SH3_3 74 80 PF00018 0.472
LIG_SUMO_SIM_par_1 177 182 PF11976 0.392
LIG_SUMO_SIM_par_1 36 41 PF11976 0.353
LIG_SUMO_SIM_par_1 394 399 PF11976 0.323
LIG_SxIP_EBH_1 72 82 PF03271 0.438
LIG_TRAF2_1 260 263 PF00917 0.322
LIG_TRAF2_1 506 509 PF00917 0.368
LIG_TRAF2_1 561 564 PF00917 0.434
LIG_TRAF2_1 90 93 PF00917 0.435
LIG_TYR_ITIM 202 207 PF00017 0.344
LIG_UBA3_1 180 189 PF00899 0.354
LIG_UBA3_1 280 286 PF00899 0.224
MOD_CK1_1 214 220 PF00069 0.215
MOD_CK1_1 575 581 PF00069 0.366
MOD_CK1_1 96 102 PF00069 0.431
MOD_CK2_1 109 115 PF00069 0.582
MOD_CK2_1 257 263 PF00069 0.428
MOD_CK2_1 271 277 PF00069 0.187
MOD_CK2_1 316 322 PF00069 0.379
MOD_CK2_1 43 49 PF00069 0.416
MOD_CK2_1 558 564 PF00069 0.444
MOD_CK2_1 56 62 PF00069 0.490
MOD_CK2_1 575 581 PF00069 0.330
MOD_CK2_1 86 92 PF00069 0.499
MOD_GlcNHglycan 109 112 PF01048 0.691
MOD_GlcNHglycan 229 232 PF01048 0.522
MOD_GlcNHglycan 244 247 PF01048 0.522
MOD_GlcNHglycan 3 6 PF01048 0.406
MOD_GlcNHglycan 335 338 PF01048 0.626
MOD_GlcNHglycan 365 368 PF01048 0.772
MOD_GlcNHglycan 45 48 PF01048 0.655
MOD_GlcNHglycan 563 567 PF01048 0.677
MOD_GlcNHglycan 95 98 PF01048 0.673
MOD_GSK3_1 392 399 PF00069 0.359
MOD_GSK3_1 52 59 PF00069 0.498
MOD_GSK3_1 558 565 PF00069 0.420
MOD_GSK3_1 80 87 PF00069 0.478
MOD_GSK3_1 93 100 PF00069 0.468
MOD_LATS_1 13 19 PF00433 0.424
MOD_N-GLC_1 316 321 PF02516 0.620
MOD_N-GLC_1 471 476 PF02516 0.634
MOD_N-GLC_1 517 522 PF02516 0.641
MOD_N-GLC_1 553 558 PF02516 0.693
MOD_NEK2_1 1 6 PF00069 0.676
MOD_NEK2_1 227 232 PF00069 0.335
MOD_NEK2_1 401 406 PF00069 0.331
MOD_NEK2_1 517 522 PF00069 0.452
MOD_NEK2_1 538 543 PF00069 0.432
MOD_NEK2_1 562 567 PF00069 0.538
MOD_NEK2_2 271 276 PF00069 0.196
MOD_NEK2_2 431 436 PF00069 0.306
MOD_PIKK_1 168 174 PF00454 0.290
MOD_PIKK_1 517 523 PF00454 0.292
MOD_PKA_2 1 7 PF00069 0.659
MOD_PKA_2 139 145 PF00069 0.523
MOD_PKA_2 211 217 PF00069 0.215
MOD_PKA_2 363 369 PF00069 0.440
MOD_PKA_2 538 544 PF00069 0.409
MOD_PKA_2 57 63 PF00069 0.457
MOD_PKA_2 71 77 PF00069 0.499
MOD_PKA_2 87 93 PF00069 0.482
MOD_PKB_1 551 559 PF00069 0.357
MOD_Plk_1 114 120 PF00069 0.600
MOD_Plk_1 168 174 PF00069 0.290
MOD_Plk_1 214 220 PF00069 0.344
MOD_Plk_1 316 322 PF00069 0.390
MOD_Plk_1 517 523 PF00069 0.440
MOD_Plk_1 553 559 PF00069 0.466
MOD_Plk_4 271 277 PF00069 0.223
MOD_Plk_4 316 322 PF00069 0.379
MOD_Plk_4 431 437 PF00069 0.334
MOD_Plk_4 523 529 PF00069 0.337
MOD_Plk_4 575 581 PF00069 0.324
MOD_Plk_4 71 77 PF00069 0.450
MOD_ProDKin_1 116 122 PF00069 0.463
MOD_ProDKin_1 125 131 PF00069 0.464
MOD_ProDKin_1 179 185 PF00069 0.316
MOD_ProDKin_1 384 390 PF00069 0.352
MOD_ProDKin_1 41 47 PF00069 0.456
MOD_ProDKin_1 454 460 PF00069 0.428
MOD_SUMO_rev_2 505 515 PF00179 0.461
TRG_DiLeu_BaEn_4 563 569 PF01217 0.426
TRG_DiLeu_BaLyEn_6 175 180 PF01217 0.329
TRG_DiLeu_BaLyEn_6 229 234 PF01217 0.289
TRG_DiLeu_BaLyEn_6 346 351 PF01217 0.312
TRG_ENDOCYTIC_2 204 207 PF00928 0.364
TRG_ENDOCYTIC_2 338 341 PF00928 0.486
TRG_ENDOCYTIC_2 436 439 PF00928 0.313
TRG_ENDOCYTIC_2 489 492 PF00928 0.433
TRG_ENDOCYTIC_2 514 517 PF00928 0.411
TRG_ENDOCYTIC_2 576 579 PF00928 0.376
TRG_ER_diArg_1 14 16 PF00400 0.720
TRG_ER_diArg_1 225 227 PF00400 0.272
TRG_ER_diArg_1 236 239 PF00400 0.233
TRG_ER_diArg_1 326 329 PF00400 0.403
TRG_ER_diArg_1 354 357 PF00400 0.391
TRG_ER_diArg_1 374 377 PF00400 0.295
TRG_NES_CRM1_1 149 161 PF08389 0.325
TRG_Pf-PMV_PEXEL_1 560 564 PF00026 0.751

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1PES8 Leptomonas seymouri 26% 100%
A0A1X0NWK3 Trypanosomatidae 31% 100%
A0A3Q8IHI5 Leishmania donovani 78% 89%
A0A3S5H7D9 Leishmania donovani 28% 100%
A0A3S7X6F1 Leishmania donovani 30% 100%
A4HDU8 Leishmania braziliensis 26% 100%
A4HL36 Leishmania braziliensis 64% 98%
A4I143 Leishmania infantum 28% 100%
A4I8P7 Leishmania infantum 30% 100%
E9AHM5 Leishmania infantum 78% 99%
E9AXX9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 28% 100%
E9B3L0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 30% 100%
Q05889 Leishmania donovani 28% 100%
Q4QD44 Leishmania major 75% 100%
Q6XFB5 Leishmania major 31% 100%
Q9NC61 Leishmania major 27% 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