LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase 1

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 1
Gene product:
phosphoglycan beta 1,3 galactosyltransferase 1
Species:
Leishmania braziliensis
UniProt:
A4H4W8_LEIBR
TriTrypDb:
LbrM.07.0240 , LBRM2903_020007700 , LBRM2903_350005100
Length:
813

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: 52
NetGPI no yes: 0, no: 52
Cellular components
Term Name Level Count
GO:0016020 membrane 2 53
GO:0110165 cellular anatomical entity 1 53
GO:0000139 Golgi membrane 5 14
GO:0031090 organelle membrane 3 14
GO:0098588 bounding membrane of organelle 4 14

Expansion

Sequence features

A4H4W8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4H4W8

Function

Biological processes
Term Name Level Count
GO:0006486 protein glycosylation 4 53
GO:0006807 nitrogen compound metabolic process 2 53
GO:0008152 metabolic process 1 53
GO:0019538 protein metabolic process 3 53
GO:0036211 protein modification process 4 53
GO:0043170 macromolecule metabolic process 3 53
GO:0043412 macromolecule modification 4 53
GO:0043413 macromolecule glycosylation 3 53
GO:0044238 primary metabolic process 2 53
GO:0070085 glycosylation 2 53
GO:0071704 organic substance metabolic process 2 53
GO:1901564 organonitrogen compound metabolic process 3 53
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 53
GO:0016740 transferase activity 2 53
GO:0016757 glycosyltransferase activity 3 53
GO:0016758 hexosyltransferase activity 4 53
GO:0008194 UDP-glycosyltransferase activity 4 14

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 385 389 PF00656 0.416
CLV_C14_Caspase3-7 410 414 PF00656 0.315
CLV_NRD_NRD_1 106 108 PF00675 0.465
CLV_NRD_NRD_1 143 145 PF00675 0.654
CLV_NRD_NRD_1 21 23 PF00675 0.421
CLV_NRD_NRD_1 289 291 PF00675 0.676
CLV_NRD_NRD_1 352 354 PF00675 0.562
CLV_NRD_NRD_1 398 400 PF00675 0.682
CLV_NRD_NRD_1 611 613 PF00675 0.563
CLV_NRD_NRD_1 674 676 PF00675 0.624
CLV_NRD_NRD_1 801 803 PF00675 0.564
CLV_NRD_NRD_1 9 11 PF00675 0.418
CLV_PCSK_FUR_1 796 800 PF00082 0.475
CLV_PCSK_KEX2_1 105 107 PF00082 0.487
CLV_PCSK_KEX2_1 21 23 PF00082 0.413
CLV_PCSK_KEX2_1 352 354 PF00082 0.557
CLV_PCSK_KEX2_1 398 400 PF00082 0.625
CLV_PCSK_KEX2_1 611 613 PF00082 0.556
CLV_PCSK_KEX2_1 674 676 PF00082 0.661
CLV_PCSK_KEX2_1 730 732 PF00082 0.545
CLV_PCSK_KEX2_1 798 800 PF00082 0.535
CLV_PCSK_KEX2_1 801 803 PF00082 0.583
CLV_PCSK_KEX2_1 9 11 PF00082 0.424
CLV_PCSK_PC1ET2_1 730 732 PF00082 0.545
CLV_PCSK_PC1ET2_1 798 800 PF00082 0.491
CLV_PCSK_PC7_1 102 108 PF00082 0.391
CLV_PCSK_PC7_1 5 11 PF00082 0.408
CLV_PCSK_SKI1_1 399 403 PF00082 0.595
CLV_PCSK_SKI1_1 630 634 PF00082 0.513
CLV_PCSK_SKI1_1 658 662 PF00082 0.485
CLV_PCSK_SKI1_1 802 806 PF00082 0.534
DEG_APCC_DBOX_1 104 112 PF00400 0.438
DEG_Nend_UBRbox_1 1 4 PF02207 0.640
DEG_SCF_FBW7_1 450 457 PF00400 0.481
DEG_SPOP_SBC_1 239 243 PF00917 0.338
DOC_ANK_TNKS_1 380 387 PF00023 0.322
DOC_CDC14_PxL_1 526 534 PF14671 0.244
DOC_CKS1_1 451 456 PF01111 0.484
DOC_CYCLIN_yCln2_LP_2 247 253 PF00134 0.341
DOC_CYCLIN_yCln2_LP_2 448 454 PF00134 0.528
DOC_CYCLIN_yCln2_LP_2 81 87 PF00134 0.595
DOC_MAPK_gen_1 102 111 PF00069 0.677
DOC_MAPK_MEF2A_6 105 113 PF00069 0.574
DOC_MAPK_MEF2A_6 478 485 PF00069 0.438
DOC_MAPK_MEF2A_6 534 543 PF00069 0.303
DOC_MAPK_NFAT4_5 478 486 PF00069 0.339
DOC_PP1_RVXF_1 512 519 PF00149 0.436
DOC_PP1_RVXF_1 694 700 PF00149 0.321
DOC_PP2B_LxvP_1 448 451 PF13499 0.533
DOC_PP2B_LxvP_1 541 544 PF13499 0.313
DOC_PP2B_LxvP_1 81 84 PF13499 0.591
DOC_PP2B_PxIxI_1 419 425 PF00149 0.276
DOC_PP4_FxxP_1 706 709 PF00568 0.270
DOC_USP7_MATH_1 130 134 PF00917 0.394
DOC_USP7_MATH_1 239 243 PF00917 0.506
DOC_USP7_MATH_1 254 258 PF00917 0.356
DOC_USP7_MATH_1 285 289 PF00917 0.430
DOC_USP7_MATH_1 38 42 PF00917 0.692
DOC_USP7_MATH_1 455 459 PF00917 0.301
DOC_USP7_MATH_1 620 624 PF00917 0.344
DOC_USP7_MATH_1 635 639 PF00917 0.320
DOC_USP7_MATH_1 692 696 PF00917 0.373
DOC_USP7_MATH_1 98 102 PF00917 0.634
DOC_USP7_UBL2_3 720 724 PF12436 0.327
DOC_WW_Pin1_4 240 245 PF00397 0.341
DOC_WW_Pin1_4 354 359 PF00397 0.429
DOC_WW_Pin1_4 416 421 PF00397 0.481
DOC_WW_Pin1_4 427 432 PF00397 0.388
DOC_WW_Pin1_4 450 455 PF00397 0.455
LIG_14-3-3_CanoR_1 134 142 PF00244 0.409
LIG_14-3-3_CanoR_1 144 150 PF00244 0.411
LIG_14-3-3_CanoR_1 152 158 PF00244 0.420
LIG_14-3-3_CanoR_1 167 175 PF00244 0.446
LIG_14-3-3_CanoR_1 185 194 PF00244 0.377
LIG_14-3-3_CanoR_1 209 213 PF00244 0.399
LIG_14-3-3_CanoR_1 21 27 PF00244 0.640
LIG_14-3-3_CanoR_1 290 300 PF00244 0.380
LIG_14-3-3_CanoR_1 321 325 PF00244 0.467
LIG_14-3-3_CanoR_1 352 358 PF00244 0.387
LIG_14-3-3_CanoR_1 478 482 PF00244 0.316
LIG_14-3-3_CanoR_1 551 558 PF00244 0.338
LIG_14-3-3_CanoR_1 560 565 PF00244 0.366
LIG_14-3-3_CanoR_1 630 635 PF00244 0.292
LIG_14-3-3_CanoR_1 696 700 PF00244 0.316
LIG_14-3-3_CanoR_1 779 783 PF00244 0.366
LIG_Actin_WH2_2 536 553 PF00022 0.282
LIG_Actin_WH2_2 708 726 PF00022 0.246
LIG_BRCT_BRCA1_1 81 85 PF00533 0.603
LIG_EH_1 618 622 PF12763 0.356
LIG_FHA_1 152 158 PF00498 0.437
LIG_FHA_1 193 199 PF00498 0.538
LIG_FHA_1 257 263 PF00498 0.484
LIG_FHA_1 336 342 PF00498 0.388
LIG_FHA_1 362 368 PF00498 0.383
LIG_FHA_1 54 60 PF00498 0.642
LIG_FHA_1 575 581 PF00498 0.379
LIG_FHA_1 753 759 PF00498 0.276
LIG_FHA_1 778 784 PF00498 0.346
LIG_FHA_1 803 809 PF00498 0.317
LIG_FHA_2 146 152 PF00498 0.389
LIG_FHA_2 324 330 PF00498 0.408
LIG_FHA_2 368 374 PF00498 0.409
LIG_LIR_Apic_2 500 506 PF02991 0.457
LIG_LIR_Apic_2 557 561 PF02991 0.318
LIG_LIR_Apic_2 704 709 PF02991 0.252
LIG_LIR_Gen_1 154 159 PF02991 0.467
LIG_LIR_Gen_1 204 215 PF02991 0.384
LIG_LIR_Gen_1 480 487 PF02991 0.377
LIG_LIR_Gen_1 537 547 PF02991 0.359
LIG_LIR_Gen_1 643 651 PF02991 0.356
LIG_LIR_Gen_1 698 706 PF02991 0.362
LIG_LIR_Nem_3 154 158 PF02991 0.469
LIG_LIR_Nem_3 204 210 PF02991 0.393
LIG_LIR_Nem_3 323 327 PF02991 0.359
LIG_LIR_Nem_3 404 409 PF02991 0.386
LIG_LIR_Nem_3 480 485 PF02991 0.336
LIG_LIR_Nem_3 524 529 PF02991 0.416
LIG_LIR_Nem_3 537 543 PF02991 0.321
LIG_LIR_Nem_3 643 647 PF02991 0.370
LIG_LIR_Nem_3 698 702 PF02991 0.365
LIG_NRBOX 145 151 PF00104 0.378
LIG_NRBOX 627 633 PF00104 0.349
LIG_PCNA_yPIPBox_3 143 152 PF02747 0.376
LIG_Pex14_1 591 595 PF04695 0.268
LIG_SH2_NCK_1 374 378 PF00017 0.403
LIG_SH2_SRC 651 654 PF00017 0.254
LIG_SH2_STAP1 521 525 PF00017 0.361
LIG_SH2_STAP1 651 655 PF00017 0.427
LIG_SH2_STAP1 793 797 PF00017 0.374
LIG_SH2_STAT3 278 281 PF00017 0.378
LIG_SH2_STAT3 552 555 PF00017 0.276
LIG_SH2_STAT5 123 126 PF00017 0.256
LIG_SH2_STAT5 345 348 PF00017 0.456
LIG_SH2_STAT5 395 398 PF00017 0.365
LIG_SH2_STAT5 523 526 PF00017 0.366
LIG_SH2_STAT5 531 534 PF00017 0.334
LIG_SH2_STAT5 540 543 PF00017 0.341
LIG_SH2_STAT5 546 549 PF00017 0.343
LIG_SH2_STAT5 552 555 PF00017 0.374
LIG_SH2_STAT5 607 610 PF00017 0.270
LIG_SH2_STAT5 644 647 PF00017 0.341
LIG_SH2_STAT5 714 717 PF00017 0.450
LIG_SH2_STAT5 782 785 PF00017 0.386
LIG_SH2_STAT5 803 806 PF00017 0.331
LIG_SH3_1 10 16 PF00018 0.602
LIG_SH3_3 10 16 PF00018 0.631
LIG_SH3_3 425 431 PF00018 0.342
LIG_SH3_3 448 454 PF00018 0.487
LIG_SH3_3 524 530 PF00018 0.396
LIG_SH3_3 706 712 PF00018 0.307
LIG_SUMO_SIM_anti_2 623 630 PF11976 0.317
LIG_SUMO_SIM_anti_2 643 649 PF11976 0.258
LIG_SUMO_SIM_par_1 767 772 PF11976 0.294
LIG_TRAF2_1 228 231 PF00917 0.415
LIG_TYR_ITIM 325 330 PF00017 0.539
LIG_WRC_WIRS_1 124 129 PF05994 0.410
MOD_CDK_SPK_2 354 359 PF00069 0.478
MOD_CK1_1 126 132 PF00069 0.528
MOD_CK1_1 133 139 PF00069 0.539
MOD_CK1_1 25 31 PF00069 0.592
MOD_CK1_1 272 278 PF00069 0.336
MOD_CK1_1 292 298 PF00069 0.496
MOD_CK1_1 32 38 PF00069 0.561
MOD_CK1_1 354 360 PF00069 0.778
MOD_CK1_1 427 433 PF00069 0.468
MOD_CK1_1 446 452 PF00069 0.443
MOD_CK1_1 695 701 PF00069 0.349
MOD_CK2_1 323 329 PF00069 0.488
MOD_CK2_1 367 373 PF00069 0.638
MOD_CK2_1 764 770 PF00069 0.386
MOD_Cter_Amidation 672 675 PF01082 0.371
MOD_GlcNHglycan 162 165 PF01048 0.490
MOD_GlcNHglycan 169 172 PF01048 0.497
MOD_GlcNHglycan 34 37 PF01048 0.617
MOD_GlcNHglycan 445 448 PF01048 0.543
MOD_GlcNHglycan 457 460 PF01048 0.448
MOD_GlcNHglycan 810 813 PF01048 0.381
MOD_GSK3_1 126 133 PF00069 0.516
MOD_GSK3_1 25 32 PF00069 0.586
MOD_GSK3_1 285 292 PF00069 0.540
MOD_GSK3_1 354 361 PF00069 0.649
MOD_GSK3_1 387 394 PF00069 0.392
MOD_GSK3_1 439 446 PF00069 0.464
MOD_GSK3_1 450 457 PF00069 0.444
MOD_GSK3_1 560 567 PF00069 0.365
MOD_N-GLC_1 201 206 PF02516 0.478
MOD_N-GLC_1 22 27 PF02516 0.507
MOD_N-GLC_1 285 290 PF02516 0.455
MOD_N-GLC_1 29 34 PF02516 0.519
MOD_N-GLC_1 335 340 PF02516 0.397
MOD_N-GLC_1 38 43 PF02516 0.495
MOD_N-GLC_1 636 641 PF02516 0.330
MOD_N-GLC_1 744 749 PF02516 0.425
MOD_N-GLC_2 42 44 PF02516 0.494
MOD_NEK2_1 238 243 PF00069 0.561
MOD_NEK2_1 289 294 PF00069 0.492
MOD_NEK2_1 497 502 PF00069 0.485
MOD_NEK2_1 550 555 PF00069 0.364
MOD_NEK2_1 564 569 PF00069 0.414
MOD_NEK2_1 621 626 PF00069 0.433
MOD_NEK2_2 192 197 PF00069 0.681
MOD_NEK2_2 285 290 PF00069 0.449
MOD_NEK2_2 636 641 PF00069 0.327
MOD_PIKK_1 100 106 PF00454 0.508
MOD_PIKK_1 25 31 PF00454 0.565
MOD_PIKK_1 292 298 PF00454 0.486
MOD_PIKK_1 509 515 PF00454 0.553
MOD_PIKK_1 550 556 PF00454 0.457
MOD_PIKK_1 753 759 PF00454 0.389
MOD_PKA_1 144 150 PF00069 0.439
MOD_PKA_2 133 139 PF00069 0.513
MOD_PKA_2 151 157 PF00069 0.514
MOD_PKA_2 208 214 PF00069 0.513
MOD_PKA_2 289 295 PF00069 0.570
MOD_PKA_2 320 326 PF00069 0.473
MOD_PKA_2 351 357 PF00069 0.516
MOD_PKA_2 358 364 PF00069 0.553
MOD_PKA_2 477 483 PF00069 0.444
MOD_PKA_2 550 556 PF00069 0.322
MOD_PKA_2 695 701 PF00069 0.295
MOD_PKA_2 778 784 PF00069 0.365
MOD_Plk_1 201 207 PF00069 0.503
MOD_Plk_1 22 28 PF00069 0.515
MOD_Plk_1 285 291 PF00069 0.453
MOD_Plk_1 29 35 PF00069 0.512
MOD_Plk_1 53 59 PF00069 0.526
MOD_Plk_1 636 642 PF00069 0.337
MOD_Plk_2-3 65 71 PF00069 0.510
MOD_Plk_4 117 123 PF00069 0.335
MOD_Plk_4 145 151 PF00069 0.465
MOD_Plk_4 22 28 PF00069 0.560
MOD_Plk_4 29 35 PF00069 0.549
MOD_Plk_4 320 326 PF00069 0.421
MOD_Plk_4 391 397 PF00069 0.402
MOD_Plk_4 424 430 PF00069 0.429
MOD_Plk_4 477 483 PF00069 0.378
MOD_Plk_4 643 649 PF00069 0.335
MOD_Plk_4 698 704 PF00069 0.508
MOD_Plk_4 758 764 PF00069 0.426
MOD_Plk_4 778 784 PF00069 0.368
MOD_ProDKin_1 240 246 PF00069 0.392
MOD_ProDKin_1 354 360 PF00069 0.522
MOD_ProDKin_1 416 422 PF00069 0.601
MOD_ProDKin_1 427 433 PF00069 0.473
MOD_ProDKin_1 450 456 PF00069 0.552
MOD_SUMO_rev_2 176 184 PF00179 0.486
MOD_SUMO_rev_2 229 235 PF00179 0.481
MOD_SUMO_rev_2 722 732 PF00179 0.345
TRG_DiLeu_BaEn_1 643 648 PF01217 0.286
TRG_DiLeu_BaEn_1 728 733 PF01217 0.358
TRG_DiLeu_BaLyEn_6 54 59 PF01217 0.577
TRG_DiLeu_BaLyEn_6 627 632 PF01217 0.313
TRG_DiLeu_LyEn_5 728 733 PF01217 0.355
TRG_ENDOCYTIC_2 220 223 PF00928 0.481
TRG_ENDOCYTIC_2 327 330 PF00928 0.580
TRG_ENDOCYTIC_2 523 526 PF00928 0.594
TRG_ENDOCYTIC_2 540 543 PF00928 0.269
TRG_ENDOCYTIC_2 644 647 PF00928 0.464
TRG_ENDOCYTIC_2 651 654 PF00928 0.370
TRG_ER_diArg_1 105 107 PF00400 0.579
TRG_ER_diArg_1 20 22 PF00400 0.493
TRG_ER_diArg_1 398 400 PF00400 0.585
TRG_ER_diArg_1 611 613 PF00400 0.403
TRG_ER_diArg_1 674 676 PF00400 0.487
TRG_ER_diArg_1 799 802 PF00400 0.416
TRG_ER_diArg_1 8 10 PF00400 0.499
TRG_NLS_MonoExtC_3 797 802 PF00514 0.308
TRG_NLS_MonoExtN_4 796 802 PF00514 0.322
TRG_Pf-PMV_PEXEL_1 611 615 PF00026 0.450
TRG_Pf-PMV_PEXEL_1 630 634 PF00026 0.318
TRG_Pf-PMV_PEXEL_1 730 734 PF00026 0.371

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 64% 100%
A0A3S5H4Y6 Leishmania donovani 37% 100%
A0A3S5H4Y9 Leishmania donovani 33% 82%
A0A3S7WT86 Leishmania donovani 36% 79%
A0A3S7WWA6 Leishmania donovani 64% 100%
A0A451EJD9 Leishmania donovani 57% 100%
A0A451EJF4 Leishmania donovani 38% 100%
A0A451EJF6 Leishmania donovani 39% 100%
A0A451EJF8 Leishmania donovani 36% 100%
A0A451EJF9 Leishmania donovani 40% 94%
A4H3A9 Leishmania braziliensis 40% 100%
A4H3B4 Leishmania braziliensis 38% 100%
A4H3B6 Leishmania braziliensis 39% 100%
A4H3B8 Leishmania braziliensis 40% 100%
A4H3B9 Leishmania braziliensis 33% 100%
A4HJ20 Leishmania braziliensis 37% 100%
A4HNK3 Leishmania braziliensis 95% 100%
A4HNK6 Leishmania braziliensis 93% 100%
A4HRL9 Leishmania infantum 38% 100%
A4HRM0 Leishmania infantum 36% 100%
A4HRM1 Leishmania infantum 40% 100%
A4HRS1 Leishmania infantum 40% 94%
A4HRS3 Leishmania infantum 33% 82%
A4HRS5 Leishmania infantum 36% 100%
A4HZM0 Leishmania infantum 57% 100%
A4I7C7 Leishmania infantum 58% 100%
A4IAQ2 Leishmania infantum 55% 100%
E9AC91 Leishmania major 37% 100%
E9AC92 Leishmania major 39% 100%
E9AC94 Leishmania major 33% 100%
E9AC95 Leishmania major 35% 100%
E9AC96 Leishmania major 40% 100%
E9AC98 Leishmania major 33% 100%
E9AEH8 Leishmania major 58% 100%
E9AHA6 Leishmania infantum 57% 100%
E9AIP8 Leishmania braziliensis 90% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 99%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 38% 100%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 37% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 33% 82%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 66% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 59% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 59% 100%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 64% 100%
Q4Q5T6 Leishmania major 58% 100%
Q4QCL8 Leishmania major 62% 100%
Q4QFJ3 Leishmania major 36% 79%
Q4QIG9 Leishmania major 62% 100%
Q7YXU9 Leishmania major 63% 100%
Q7YXV1 Leishmania major 63% 100%
Q7YXV2 Leishmania major 62% 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