LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase

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

Quick info

Protein:
Phosphoglycan beta 1,3 galactosyltransferase
Gene product:
phosphoglycan beta 1,3 galactosyltransferase
Species:
Leishmania braziliensis
UniProt:
A4H3B8_LEIBR
TriTrypDb:
LbrM.02.0250 , LBRM2903_020007600 * , LBRM2903_020007700
Length:
828

Annotations

LeishMANIAdb annotations

Phosphoglycan beta 1,3 galactosyltransferase (required for proper protective coat formation). Probably part of a much larger group. Expanded in Leishmaniids. Localization: Golgi (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: 60
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: 16
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 53
NetGPI no yes: 0, no: 53
Cellular components
Term Name Level Count
GO:0016020 membrane 2 54
GO:0110165 cellular anatomical entity 1 54
GO:0000139 Golgi membrane 5 14
GO:0031090 organelle membrane 3 14
GO:0098588 bounding membrane of organelle 4 14

Expansion

Sequence features

A4H3B8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4H3B8

Function

Biological processes
Term Name Level Count
GO:0006486 protein glycosylation 4 54
GO:0006807 nitrogen compound metabolic process 2 54
GO:0008152 metabolic process 1 54
GO:0019538 protein metabolic process 3 54
GO:0036211 protein modification process 4 54
GO:0043170 macromolecule metabolic process 3 54
GO:0043412 macromolecule modification 4 54
GO:0043413 macromolecule glycosylation 3 54
GO:0044238 primary metabolic process 2 54
GO:0070085 glycosylation 2 54
GO:0071704 organic substance metabolic process 2 54
GO:1901564 organonitrogen compound metabolic process 3 54
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 54
GO:0016740 transferase activity 2 54
GO:0016757 glycosyltransferase activity 3 54
GO:0016758 hexosyltransferase activity 4 54
GO:0008194 UDP-glycosyltransferase activity 4 14

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 387 391 PF00656 0.365
CLV_NRD_NRD_1 16 18 PF00675 0.418
CLV_NRD_NRD_1 302 304 PF00675 0.540
CLV_NRD_NRD_1 314 316 PF00675 0.509
CLV_NRD_NRD_1 400 402 PF00675 0.693
CLV_NRD_NRD_1 405 407 PF00675 0.660
CLV_NRD_NRD_1 483 485 PF00675 0.684
CLV_NRD_NRD_1 561 563 PF00675 0.663
CLV_NRD_NRD_1 619 621 PF00675 0.566
CLV_NRD_NRD_1 654 656 PF00675 0.494
CLV_NRD_NRD_1 789 791 PF00675 0.526
CLV_NRD_NRD_1 79 81 PF00675 0.440
CLV_NRD_NRD_1 88 90 PF00675 0.507
CLV_PCSK_KEX2_1 15 17 PF00082 0.421
CLV_PCSK_KEX2_1 314 316 PF00082 0.521
CLV_PCSK_KEX2_1 400 402 PF00082 0.691
CLV_PCSK_KEX2_1 405 407 PF00082 0.658
CLV_PCSK_KEX2_1 483 485 PF00082 0.613
CLV_PCSK_KEX2_1 54 56 PF00082 0.404
CLV_PCSK_KEX2_1 561 563 PF00082 0.678
CLV_PCSK_KEX2_1 619 621 PF00082 0.554
CLV_PCSK_KEX2_1 648 650 PF00082 0.516
CLV_PCSK_KEX2_1 654 656 PF00082 0.493
CLV_PCSK_KEX2_1 755 757 PF00082 0.507
CLV_PCSK_KEX2_1 789 791 PF00082 0.563
CLV_PCSK_KEX2_1 79 81 PF00082 0.448
CLV_PCSK_KEX2_1 88 90 PF00082 0.508
CLV_PCSK_PC1ET2_1 15 17 PF00082 0.421
CLV_PCSK_PC1ET2_1 54 56 PF00082 0.399
CLV_PCSK_PC1ET2_1 648 650 PF00082 0.481
CLV_PCSK_PC1ET2_1 755 757 PF00082 0.493
CLV_PCSK_PC7_1 401 407 PF00082 0.547
CLV_PCSK_SKI1_1 122 126 PF00082 0.593
CLV_PCSK_SKI1_1 17 21 PF00082 0.402
CLV_PCSK_SKI1_1 295 299 PF00082 0.570
CLV_PCSK_SKI1_1 363 367 PF00082 0.596
CLV_PCSK_SKI1_1 373 377 PF00082 0.598
CLV_PCSK_SKI1_1 472 476 PF00082 0.467
CLV_PCSK_SKI1_1 508 512 PF00082 0.592
CLV_PCSK_SKI1_1 655 659 PF00082 0.481
CLV_PCSK_SKI1_1 69 73 PF00082 0.387
CLV_PCSK_SKI1_1 742 746 PF00082 0.574
CLV_PCSK_SKI1_1 88 92 PF00082 0.422
DEG_APCC_DBOX_1 358 366 PF00400 0.396
DEG_SCF_FBW7_1 444 451 PF00400 0.501
DOC_CKS1_1 445 450 PF01111 0.509
DOC_CYCLIN_RxL_1 359 369 PF00134 0.344
DOC_CYCLIN_yCln2_LP_2 172 178 PF00134 0.363
DOC_CYCLIN_yCln2_LP_2 442 448 PF00134 0.536
DOC_MAPK_gen_1 359 366 PF00069 0.347
DOC_MAPK_MEF2A_6 229 237 PF00069 0.354
DOC_MAPK_MEF2A_6 359 366 PF00069 0.354
DOC_MAPK_MEF2A_6 472 479 PF00069 0.448
DOC_MAPK_MEF2A_6 496 505 PF00069 0.339
DOC_MAPK_MEF2A_6 629 637 PF00069 0.322
DOC_MAPK_MEF2A_6 69 78 PF00069 0.610
DOC_MAPK_NFAT4_5 69 77 PF00069 0.578
DOC_PP1_RVXF_1 155 161 PF00149 0.354
DOC_PP1_RVXF_1 470 477 PF00149 0.336
DOC_PP1_RVXF_1 506 513 PF00149 0.434
DOC_PP1_RVXF_1 652 659 PF00149 0.261
DOC_PP2B_LxvP_1 442 445 PF13499 0.540
DOC_PP4_FxxP_1 450 453 PF00568 0.389
DOC_USP7_MATH_1 236 240 PF00917 0.368
DOC_USP7_MATH_1 271 275 PF00917 0.422
DOC_USP7_MATH_1 430 434 PF00917 0.416
DOC_USP7_MATH_1 736 740 PF00917 0.301
DOC_WW_Pin1_4 353 358 PF00397 0.375
DOC_WW_Pin1_4 413 418 PF00397 0.501
DOC_WW_Pin1_4 444 449 PF00397 0.472
LIG_14-3-3_CanoR_1 122 131 PF00244 0.368
LIG_14-3-3_CanoR_1 142 148 PF00244 0.428
LIG_14-3-3_CanoR_1 303 307 PF00244 0.470
LIG_14-3-3_CanoR_1 577 583 PF00244 0.356
LIG_14-3-3_CanoR_1 69 75 PF00244 0.607
LIG_14-3-3_CanoR_1 7 11 PF00244 0.634
LIG_14-3-3_CanoR_1 79 86 PF00244 0.610
LIG_14-3-3_CanoR_1 790 796 PF00244 0.348
LIG_Actin_WH2_2 243 259 PF00022 0.374
LIG_Actin_WH2_2 626 641 PF00022 0.290
LIG_deltaCOP1_diTrp_1 690 695 PF00928 0.242
LIG_FHA_1 112 118 PF00498 0.339
LIG_FHA_1 185 191 PF00498 0.535
LIG_FHA_1 239 245 PF00498 0.503
LIG_FHA_1 318 324 PF00498 0.353
LIG_FHA_1 374 380 PF00498 0.395
LIG_FHA_1 430 436 PF00498 0.430
LIG_FHA_1 570 576 PF00498 0.413
LIG_FHA_1 591 597 PF00498 0.262
LIG_FHA_1 612 618 PF00498 0.293
LIG_FHA_1 62 68 PF00498 0.599
LIG_FHA_1 630 636 PF00498 0.340
LIG_FHA_1 680 686 PF00498 0.245
LIG_FHA_1 701 707 PF00498 0.285
LIG_FHA_1 71 77 PF00498 0.620
LIG_FHA_2 366 372 PF00498 0.519
LIG_FHA_2 743 749 PF00498 0.355
LIG_FHA_2 792 798 PF00498 0.352
LIG_LIR_Apic_2 447 453 PF02991 0.393
LIG_LIR_Apic_2 495 500 PF02991 0.446
LIG_LIR_Gen_1 531 541 PF02991 0.358
LIG_LIR_Gen_1 690 700 PF02991 0.339
LIG_LIR_Gen_1 707 713 PF02991 0.363
LIG_LIR_Gen_1 720 728 PF02991 0.277
LIG_LIR_Nem_3 262 267 PF02991 0.371
LIG_LIR_Nem_3 305 309 PF02991 0.469
LIG_LIR_Nem_3 531 537 PF02991 0.321
LIG_LIR_Nem_3 650 656 PF02991 0.398
LIG_LIR_Nem_3 690 695 PF02991 0.330
LIG_LIR_Nem_3 707 711 PF02991 0.366
LIG_LIR_Nem_3 720 726 PF02991 0.279
LIG_LIR_Nem_3 820 825 PF02991 0.308
LIG_MAD2 620 628 PF02301 0.247
LIG_MYND_1 336 340 PF01753 0.387
LIG_Pex14_1 691 695 PF04695 0.243
LIG_Pex14_2 182 186 PF04695 0.349
LIG_PTB_Apo_2 40 47 PF02174 0.581
LIG_RPA_C_Fungi 401 413 PF08784 0.340
LIG_RPA_C_Fungi 614 626 PF08784 0.294
LIG_SH2_CRK 653 657 PF00017 0.342
LIG_SH2_CRK 822 826 PF00017 0.353
LIG_SH2_GRB2like 804 807 PF00017 0.342
LIG_SH2_PTP2 534 537 PF00017 0.361
LIG_SH2_SRC 309 312 PF00017 0.399
LIG_SH2_SRC 515 518 PF00017 0.434
LIG_SH2_STAP1 204 208 PF00017 0.548
LIG_SH2_STAP1 515 519 PF00017 0.559
LIG_SH2_STAP1 804 808 PF00017 0.457
LIG_SH2_STAT5 123 126 PF00017 0.439
LIG_SH2_STAT5 281 284 PF00017 0.468
LIG_SH2_STAT5 327 330 PF00017 0.503
LIG_SH2_STAT5 437 440 PF00017 0.466
LIG_SH2_STAT5 456 459 PF00017 0.385
LIG_SH2_STAT5 534 537 PF00017 0.397
LIG_SH2_STAT5 546 549 PF00017 0.457
LIG_SH2_STAT5 687 690 PF00017 0.401
LIG_SH2_STAT5 723 726 PF00017 0.541
LIG_SH2_STAT5 727 730 PF00017 0.462
LIG_SH3_3 16 22 PF00018 0.520
LIG_SH3_3 274 280 PF00018 0.531
LIG_SH3_3 361 367 PF00018 0.397
LIG_SH3_3 442 448 PF00018 0.632
LIG_SH3_3 53 59 PF00018 0.504
LIG_SH3_3 532 538 PF00018 0.370
LIG_SH3_3 552 558 PF00018 0.457
LIG_SH3_3 7 13 PF00018 0.515
LIG_SUMO_SIM_par_1 108 114 PF11976 0.241
LIG_TRAF2_1 308 311 PF00917 0.404
LIG_TRAF2_1 579 582 PF00917 0.412
LIG_TRAF2_1 744 747 PF00917 0.422
LIG_TYR_ITIM 307 312 PF00017 0.545
LIG_TYR_ITIM 651 656 PF00017 0.297
LIG_WW_3 275 279 PF00397 0.402
MOD_CDC14_SPxK_1 356 359 PF00782 0.400
MOD_CDK_SPxK_1 353 359 PF00069 0.427
MOD_CK1_1 341 347 PF00069 0.671
MOD_CK1_1 350 356 PF00069 0.477
MOD_CK1_1 423 429 PF00069 0.519
MOD_CK1_1 433 439 PF00069 0.441
MOD_CK1_1 48 54 PF00069 0.527
MOD_CK1_1 82 88 PF00069 0.503
MOD_CK2_1 203 209 PF00069 0.487
MOD_CK2_1 365 371 PF00069 0.679
MOD_CK2_1 449 455 PF00069 0.464
MOD_CK2_1 576 582 PF00069 0.423
MOD_CK2_1 585 591 PF00069 0.412
MOD_CK2_1 742 748 PF00069 0.503
MOD_CK2_1 791 797 PF00069 0.386
MOD_Cter_Amidation 86 89 PF01082 0.482
MOD_GlcNHglycan 205 208 PF01048 0.597
MOD_GlcNHglycan 222 225 PF01048 0.613
MOD_GlcNHglycan 261 264 PF01048 0.372
MOD_GlcNHglycan 273 276 PF01048 0.439
MOD_GlcNHglycan 339 343 PF01048 0.567
MOD_GlcNHglycan 349 352 PF01048 0.595
MOD_GlcNHglycan 432 435 PF01048 0.563
MOD_GlcNHglycan 438 441 PF01048 0.546
MOD_GlcNHglycan 461 464 PF01048 0.559
MOD_GlcNHglycan 565 568 PF01048 0.554
MOD_GlcNHglycan 578 581 PF01048 0.423
MOD_GlcNHglycan 585 588 PF01048 0.404
MOD_GlcNHglycan 609 612 PF01048 0.284
MOD_GlcNHglycan 643 648 PF01048 0.334
MOD_GlcNHglycan 738 741 PF01048 0.435
MOD_GlcNHglycan 775 778 PF01048 0.348
MOD_GlcNHglycan 81 84 PF01048 0.488
MOD_GlcNHglycan 96 99 PF01048 0.473
MOD_GSK3_1 1 8 PF00069 0.525
MOD_GSK3_1 111 118 PF00069 0.292
MOD_GSK3_1 123 130 PF00069 0.478
MOD_GSK3_1 196 203 PF00069 0.553
MOD_GSK3_1 349 356 PF00069 0.553
MOD_GSK3_1 429 436 PF00069 0.501
MOD_GSK3_1 44 51 PF00069 0.478
MOD_GSK3_1 440 447 PF00069 0.507
MOD_GSK3_1 607 614 PF00069 0.248
MOD_GSK3_1 643 650 PF00069 0.381
MOD_GSK3_1 70 77 PF00069 0.565
MOD_GSK3_1 700 707 PF00069 0.387
MOD_GSK3_1 738 745 PF00069 0.421
MOD_GSK3_1 78 85 PF00069 0.514
MOD_GSK3_1 785 792 PF00069 0.380
MOD_GSK3_1 94 101 PF00069 0.421
MOD_N-GLC_1 158 163 PF02516 0.466
MOD_N-GLC_1 569 574 PF02516 0.466
MOD_N-GLC_1 704 709 PF02516 0.332
MOD_N-GLC_1 773 778 PF02516 0.364
MOD_NEK2_1 1 6 PF00069 0.505
MOD_NEK2_1 111 116 PF00069 0.337
MOD_NEK2_1 158 163 PF00069 0.562
MOD_NEK2_1 220 225 PF00069 0.562
MOD_NEK2_1 45 50 PF00069 0.490
MOD_NEK2_1 571 576 PF00069 0.454
MOD_NEK2_1 583 588 PF00069 0.394
MOD_NEK2_1 61 66 PF00069 0.532
MOD_NEK2_1 679 684 PF00069 0.283
MOD_NEK2_1 74 79 PF00069 0.502
MOD_NEK2_1 773 778 PF00069 0.362
MOD_NEK2_2 184 189 PF00069 0.684
MOD_NEK2_2 597 602 PF00069 0.300
MOD_PIKK_1 373 379 PF00454 0.412
MOD_PIKK_1 503 509 PF00454 0.549
MOD_PIKK_1 604 610 PF00454 0.307
MOD_PIKK_1 755 761 PF00454 0.411
MOD_PK_1 406 412 PF00069 0.363
MOD_PKA_1 483 489 PF00069 0.628
MOD_PKA_1 755 761 PF00069 0.334
MOD_PKA_1 789 795 PF00069 0.330
MOD_PKA_1 79 85 PF00069 0.478
MOD_PKA_2 302 308 PF00069 0.579
MOD_PKA_2 483 489 PF00069 0.577
MOD_PKA_2 576 582 PF00069 0.420
MOD_PKA_2 6 12 PF00069 0.529
MOD_PKA_2 755 761 PF00069 0.349
MOD_PKA_2 78 84 PF00069 0.512
MOD_PKA_2 789 795 PF00069 0.356
MOD_PKB_1 165 173 PF00069 0.442
MOD_Plk_1 127 133 PF00069 0.446
MOD_Plk_1 704 710 PF00069 0.394
MOD_Plk_4 167 173 PF00069 0.456
MOD_Plk_4 302 308 PF00069 0.497
MOD_Plk_4 433 439 PF00069 0.423
MOD_Plk_4 45 51 PF00069 0.463
MOD_Plk_4 611 617 PF00069 0.330
MOD_Plk_4 707 713 PF00069 0.507
MOD_ProDKin_1 353 359 PF00069 0.443
MOD_ProDKin_1 413 419 PF00069 0.624
MOD_ProDKin_1 444 450 PF00069 0.585
MOD_SUMO_rev_2 25 32 PF00179 0.475
TRG_ENDOCYTIC_2 281 284 PF00928 0.468
TRG_ENDOCYTIC_2 309 312 PF00928 0.588
TRG_ENDOCYTIC_2 517 520 PF00928 0.576
TRG_ENDOCYTIC_2 534 537 PF00928 0.265
TRG_ENDOCYTIC_2 653 656 PF00928 0.483
TRG_ENDOCYTIC_2 670 673 PF00928 0.293
TRG_ENDOCYTIC_2 692 695 PF00928 0.288
TRG_ENDOCYTIC_2 723 726 PF00928 0.285
TRG_ENDOCYTIC_2 822 825 PF00928 0.337
TRG_ER_diArg_1 165 168 PF00400 0.461
TRG_ER_diArg_1 359 362 PF00400 0.415
TRG_ER_diArg_1 400 402 PF00400 0.600
TRG_ER_diArg_1 404 406 PF00400 0.549
TRG_ER_diArg_1 483 485 PF00400 0.472
TRG_ER_diArg_1 619 621 PF00400 0.407
TRG_ER_diArg_1 653 655 PF00400 0.331
TRG_ER_diArg_1 715 718 PF00400 0.315
TRG_ER_diArg_1 78 80 PF00400 0.539
TRG_ER_diArg_1 789 791 PF00400 0.377
TRG_ER_diArg_1 88 90 PF00400 0.629
TRG_NLS_MonoExtC_3 487 493 PF00514 0.418
TRG_NLS_MonoExtN_4 13 19 PF00514 0.478
TRG_NLS_MonoExtN_4 485 492 PF00514 0.473
TRG_Pf-PMV_PEXEL_1 489 493 PF00026 0.442
TRG_Pf-PMV_PEXEL_1 823 827 PF00026 0.330

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 42% 100%
A0A3S5H4Y6 Leishmania donovani 59% 100%
A0A3S5H4Y9 Leishmania donovani 40% 83%
A0A3S7WT86 Leishmania donovani 41% 81%
A0A3S7WWA6 Leishmania donovani 42% 100%
A0A451EJD9 Leishmania donovani 42% 100%
A0A451EJF4 Leishmania donovani 61% 100%
A0A451EJF6 Leishmania donovani 62% 100%
A0A451EJF8 Leishmania donovani 66% 100%
A0A451EJF9 Leishmania donovani 60% 96%
A4H3A9 Leishmania braziliensis 62% 100%
A4H3B4 Leishmania braziliensis 72% 100%
A4H3B6 Leishmania braziliensis 61% 100%
A4H3B7 Leishmania braziliensis 45% 100%
A4H3B9 Leishmania braziliensis 39% 93%
A4H4W8 Leishmania braziliensis 40% 100%
A4HJ20 Leishmania braziliensis 59% 100%
A4HNK3 Leishmania braziliensis 41% 100%
A4HNK6 Leishmania braziliensis 40% 100%
A4HRL9 Leishmania infantum 59% 100%
A4HRM0 Leishmania infantum 54% 100%
A4HRM1 Leishmania infantum 62% 100%
A4HRS1 Leishmania infantum 60% 96%
A4HRS3 Leishmania infantum 40% 83%
A4HRS5 Leishmania infantum 66% 100%
A4HZM0 Leishmania infantum 42% 100%
A4I7C7 Leishmania infantum 43% 100%
A4IAQ2 Leishmania infantum 41% 100%
E9AC91 Leishmania major 60% 100%
E9AC92 Leishmania major 60% 100%
E9AC94 Leishmania major 40% 70%
E9AC95 Leishmania major 66% 100%
E9AC96 Leishmania major 60% 100%
E9AC98 Leishmania major 40% 83%
E9AEH8 Leishmania major 40% 100%
E9AHA6 Leishmania infantum 42% 100%
E9AIP8 Leishmania braziliensis 39% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 62% 100%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 61% 100%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 66% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 38% 84%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 41% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 42% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 41% 100%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 42% 100%
Q4Q5T6 Leishmania major 40% 100%
Q4QCL8 Leishmania major 40% 100%
Q4QFJ3 Leishmania major 40% 100%
Q4QIG9 Leishmania major 41% 100%
Q7YXU9 Leishmania major 40% 100%
Q7YXV1 Leishmania major 40% 100%
Q7YXV2 Leishmania major 41% 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