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:
A4HJ20_LEIBR
TriTrypDb:
LbrM.31.0570 , LBRM2903_020006500
Length:
812

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

A4HJ20
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HJ20

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_NRD_NRD_1 121 123 PF00675 0.574
CLV_NRD_NRD_1 307 309 PF00675 0.547
CLV_NRD_NRD_1 319 321 PF00675 0.519
CLV_NRD_NRD_1 34 36 PF00675 0.409
CLV_NRD_NRD_1 405 407 PF00675 0.772
CLV_NRD_NRD_1 410 412 PF00675 0.757
CLV_NRD_NRD_1 489 491 PF00675 0.675
CLV_NRD_NRD_1 662 664 PF00675 0.534
CLV_NRD_NRD_1 731 733 PF00675 0.504
CLV_NRD_NRD_1 749 751 PF00675 0.517
CLV_PCSK_KEX2_1 120 122 PF00082 0.597
CLV_PCSK_KEX2_1 319 321 PF00082 0.530
CLV_PCSK_KEX2_1 34 36 PF00082 0.409
CLV_PCSK_KEX2_1 405 407 PF00082 0.770
CLV_PCSK_KEX2_1 410 412 PF00082 0.755
CLV_PCSK_KEX2_1 489 491 PF00082 0.607
CLV_PCSK_KEX2_1 57 59 PF00082 0.482
CLV_PCSK_KEX2_1 662 664 PF00082 0.584
CLV_PCSK_KEX2_1 730 732 PF00082 0.570
CLV_PCSK_KEX2_1 749 751 PF00082 0.528
CLV_PCSK_KEX2_1 772 774 PF00082 0.614
CLV_PCSK_PC1ET2_1 57 59 PF00082 0.472
CLV_PCSK_PC1ET2_1 730 732 PF00082 0.570
CLV_PCSK_PC1ET2_1 772 774 PF00082 0.597
CLV_PCSK_PC7_1 406 412 PF00082 0.645
CLV_PCSK_PC7_1 658 664 PF00082 0.498
CLV_PCSK_SKI1_1 156 160 PF00082 0.542
CLV_PCSK_SKI1_1 300 304 PF00082 0.570
CLV_PCSK_SKI1_1 352 356 PF00082 0.603
CLV_PCSK_SKI1_1 406 410 PF00082 0.691
CLV_PCSK_SKI1_1 478 482 PF00082 0.471
CLV_PCSK_SKI1_1 514 518 PF00082 0.581
CLV_PCSK_SKI1_1 611 615 PF00082 0.491
CLV_PCSK_SKI1_1 658 662 PF00082 0.497
CLV_PCSK_SKI1_1 769 773 PF00082 0.540
DEG_SCF_FBW7_1 450 457 PF00400 0.512
DEG_SCF_FBW7_1 8 14 PF00400 0.621
DOC_CKS1_1 451 456 PF01111 0.517
DOC_CKS1_1 8 13 PF01111 0.621
DOC_CYCLIN_yCln2_LP_2 137 143 PF00134 0.376
DOC_CYCLIN_yCln2_LP_2 448 454 PF00134 0.553
DOC_MAPK_JIP1_4 94 100 PF00069 0.566
DOC_MAPK_MEF2A_6 234 242 PF00069 0.373
DOC_MAPK_MEF2A_6 478 485 PF00069 0.444
DOC_MAPK_MEF2A_6 92 100 PF00069 0.679
DOC_PP1_RVXF_1 476 483 PF00149 0.338
DOC_PP1_RVXF_1 512 519 PF00149 0.436
DOC_PP1_RVXF_1 670 676 PF00149 0.262
DOC_PP2B_LxvP_1 448 451 PF13499 0.556
DOC_PP4_FxxP_1 21 24 PF00568 0.595
DOC_PP4_FxxP_1 456 459 PF00568 0.400
DOC_USP7_MATH_1 165 169 PF00917 0.329
DOC_USP7_MATH_1 241 245 PF00917 0.400
DOC_USP7_MATH_1 276 280 PF00917 0.438
DOC_USP7_MATH_1 569 573 PF00917 0.388
DOC_USP7_MATH_1 61 65 PF00917 0.650
DOC_WW_Pin1_4 169 174 PF00397 0.347
DOC_WW_Pin1_4 181 186 PF00397 0.398
DOC_WW_Pin1_4 363 368 PF00397 0.419
DOC_WW_Pin1_4 417 422 PF00397 0.540
DOC_WW_Pin1_4 42 47 PF00397 0.634
DOC_WW_Pin1_4 450 455 PF00397 0.488
DOC_WW_Pin1_4 50 55 PF00397 0.664
DOC_WW_Pin1_4 7 12 PF00397 0.623
DOC_WW_Pin1_4 702 707 PF00397 0.300
DOC_WW_Pin1_4 771 776 PF00397 0.366
LIG_14-3-3_CanoR_1 122 130 PF00244 0.346
LIG_14-3-3_CanoR_1 166 174 PF00244 0.348
LIG_14-3-3_CanoR_1 308 312 PF00244 0.455
LIG_14-3-3_CanoR_1 352 357 PF00244 0.426
LIG_14-3-3_CanoR_1 411 421 PF00244 0.443
LIG_14-3-3_CanoR_1 571 578 PF00244 0.391
LIG_14-3-3_CanoR_1 593 598 PF00244 0.272
LIG_14-3-3_CanoR_1 749 753 PF00244 0.336
LIG_Actin_WH2_2 248 264 PF00022 0.399
LIG_Actin_WH2_2 648 664 PF00022 0.282
LIG_BIR_II_1 1 5 PF00653 0.622
LIG_BIR_III_2 760 764 PF00653 0.280
LIG_BIR_III_4 60 64 PF00653 0.620
LIG_BRCT_BRCA1_1 364 368 PF00533 0.412
LIG_CtBP_PxDLS_1 342 346 PF00389 0.401
LIG_FHA_1 105 111 PF00498 0.276
LIG_FHA_1 190 196 PF00498 0.542
LIG_FHA_1 244 250 PF00498 0.537
LIG_FHA_1 323 329 PF00498 0.357
LIG_FHA_1 369 375 PF00498 0.435
LIG_FHA_1 436 442 PF00498 0.464
LIG_FHA_1 571 577 PF00498 0.389
LIG_FHA_1 600 606 PF00498 0.281
LIG_FHA_2 391 397 PF00498 0.401
LIG_FHA_2 629 635 PF00498 0.288
LIG_FHA_2 703 709 PF00498 0.286
LIG_FHA_2 798 804 PF00498 0.314
LIG_Integrin_RGD_1 58 60 PF01839 0.434
LIG_Integrin_RGD_1 688 690 PF01839 0.505
LIG_LIR_Apic_2 453 459 PF02991 0.406
LIG_LIR_Apic_2 804 810 PF02991 0.259
LIG_LIR_Gen_1 138 145 PF02991 0.461
LIG_LIR_Gen_1 537 547 PF02991 0.345
LIG_LIR_Gen_1 690 699 PF02991 0.385
LIG_LIR_Gen_1 719 725 PF02991 0.271
LIG_LIR_LC3C_4 107 110 PF02991 0.204
LIG_LIR_Nem_3 138 144 PF02991 0.463
LIG_LIR_Nem_3 267 272 PF02991 0.394
LIG_LIR_Nem_3 310 314 PF02991 0.458
LIG_LIR_Nem_3 37 42 PF02991 0.595
LIG_LIR_Nem_3 537 543 PF02991 0.310
LIG_LIR_Nem_3 638 644 PF02991 0.393
LIG_LIR_Nem_3 690 694 PF02991 0.405
LIG_LIR_Nem_3 695 699 PF02991 0.354
LIG_LIR_Nem_3 719 724 PF02991 0.296
LIG_NRBOX 129 135 PF00104 0.333
LIG_NRBOX 604 610 PF00104 0.234
LIG_NRBOX 651 657 PF00104 0.267
LIG_Pex14_1 795 799 PF04695 0.277
LIG_REV1ctd_RIR_1 37 45 PF16727 0.596
LIG_REV1ctd_RIR_1 713 722 PF16727 0.277
LIG_SH2_CRK 540 544 PF00017 0.240
LIG_SH2_CRK 642 646 PF00017 0.293
LIG_SH2_CRK 721 725 PF00017 0.286
LIG_SH2_CRK 807 811 PF00017 0.317
LIG_SH2_NCK_1 381 385 PF00017 0.438
LIG_SH2_NCK_1 777 781 PF00017 0.357
LIG_SH2_NCK_1 807 811 PF00017 0.283
LIG_SH2_SRC 314 317 PF00017 0.331
LIG_SH2_SRC 521 524 PF00017 0.360
LIG_SH2_SRC 711 714 PF00017 0.265
LIG_SH2_STAP1 209 213 PF00017 0.459
LIG_SH2_STAP1 521 525 PF00017 0.445
LIG_SH2_STAP1 721 725 PF00017 0.282
LIG_SH2_STAT5 286 289 PF00017 0.378
LIG_SH2_STAT5 332 335 PF00017 0.411
LIG_SH2_STAT5 443 446 PF00017 0.413
LIG_SH2_STAT5 462 465 PF00017 0.362
LIG_SH2_STAT5 552 555 PF00017 0.367
LIG_SH2_STAT5 711 714 PF00017 0.429
LIG_SH3_3 279 285 PF00018 0.455
LIG_SH3_3 336 342 PF00018 0.335
LIG_SH3_3 416 422 PF00018 0.400
LIG_SH3_3 448 454 PF00018 0.527
LIG_SH3_3 48 54 PF00018 0.641
LIG_SH3_3 556 562 PF00018 0.368
LIG_SH3_3 610 616 PF00018 0.323
LIG_SH3_5 706 710 PF00018 0.219
LIG_SUMO_SIM_anti_2 107 113 PF11976 0.266
LIG_SUMO_SIM_anti_2 155 162 PF11976 0.333
LIG_SUMO_SIM_par_1 155 162 PF11976 0.337
LIG_SUMO_SIM_par_1 179 184 PF11976 0.345
LIG_SUMO_SIM_par_1 341 349 PF11976 0.399
LIG_TRAF2_1 313 316 PF00917 0.341
LIG_TYR_ITIM 312 317 PF00017 0.525
LIG_TYR_ITIM 640 645 PF00017 0.281
LIG_UBA3_1 133 139 PF00899 0.430
LIG_WW_3 280 284 PF00397 0.421
MOD_CDK_SPK_2 50 55 PF00069 0.511
MOD_CDK_SPxxK_3 50 57 PF00069 0.523
MOD_CK1_1 14 20 PF00069 0.588
MOD_CK1_1 169 175 PF00069 0.401
MOD_CK1_1 2 8 PF00069 0.542
MOD_CK1_1 27 33 PF00069 0.512
MOD_CK1_1 430 436 PF00069 0.580
MOD_CK1_1 439 445 PF00069 0.492
MOD_CK2_1 208 214 PF00069 0.506
MOD_CK2_1 374 380 PF00069 0.680
MOD_CK2_1 455 461 PF00069 0.485
MOD_CMANNOS 795 798 PF00535 0.289
MOD_Cter_Amidation 728 731 PF01082 0.367
MOD_GlcNHglycan 16 19 PF01048 0.625
MOD_GlcNHglycan 21 24 PF01048 0.567
MOD_GlcNHglycan 210 213 PF01048 0.626
MOD_GlcNHglycan 227 230 PF01048 0.583
MOD_GlcNHglycan 266 269 PF01048 0.401
MOD_GlcNHglycan 278 281 PF01048 0.421
MOD_GlcNHglycan 352 355 PF01048 0.572
MOD_GlcNHglycan 42 45 PF01048 0.581
MOD_GlcNHglycan 429 432 PF01048 0.519
MOD_GlcNHglycan 438 441 PF01048 0.617
MOD_GlcNHglycan 467 470 PF01048 0.589
MOD_GlcNHglycan 726 729 PF01048 0.445
MOD_GSK3_1 135 142 PF00069 0.557
MOD_GSK3_1 165 172 PF00069 0.413
MOD_GSK3_1 201 208 PF00069 0.550
MOD_GSK3_1 24 31 PF00069 0.521
MOD_GSK3_1 3 10 PF00069 0.544
MOD_GSK3_1 344 351 PF00069 0.666
MOD_GSK3_1 387 394 PF00069 0.456
MOD_GSK3_1 413 420 PF00069 0.523
MOD_GSK3_1 42 49 PF00069 0.579
MOD_GSK3_1 426 433 PF00069 0.631
MOD_GSK3_1 435 442 PF00069 0.547
MOD_GSK3_1 446 453 PF00069 0.560
MOD_GSK3_1 720 727 PF00069 0.388
MOD_N-GLC_1 362 367 PF02516 0.558
MOD_N-GLC_1 391 396 PF02516 0.439
MOD_N-GLC_1 46 51 PF02516 0.506
MOD_N-GLC_1 569 574 PF02516 0.510
MOD_NEK2_1 104 109 PF00069 0.374
MOD_NEK2_1 225 230 PF00069 0.535
MOD_NEK2_1 368 373 PF00069 0.496
MOD_NEK2_1 40 45 PF00069 0.526
MOD_NEK2_1 427 432 PF00069 0.477
MOD_NEK2_1 724 729 PF00069 0.399
MOD_NEK2_2 189 194 PF00069 0.670
MOD_PIKK_1 509 515 PF00454 0.527
MOD_PK_1 139 145 PF00069 0.409
MOD_PKA_1 34 40 PF00069 0.465
MOD_PKA_1 489 495 PF00069 0.607
MOD_PKA_2 152 158 PF00069 0.505
MOD_PKA_2 165 171 PF00069 0.401
MOD_PKA_2 307 313 PF00069 0.559
MOD_PKA_2 34 40 PF00069 0.473
MOD_PKA_2 427 433 PF00069 0.631
MOD_PKA_2 489 495 PF00069 0.559
MOD_PKA_2 570 576 PF00069 0.430
MOD_PKA_2 748 754 PF00069 0.376
MOD_Plk_1 692 698 PF00069 0.388
MOD_Plk_2-3 344 350 PF00069 0.553
MOD_Plk_4 104 110 PF00069 0.320
MOD_Plk_4 307 313 PF00069 0.482
MOD_Plk_4 439 445 PF00069 0.476
MOD_Plk_4 599 605 PF00069 0.313
MOD_Plk_4 695 701 PF00069 0.485
MOD_ProDKin_1 169 175 PF00069 0.410
MOD_ProDKin_1 181 187 PF00069 0.470
MOD_ProDKin_1 363 369 PF00069 0.507
MOD_ProDKin_1 417 423 PF00069 0.672
MOD_ProDKin_1 42 48 PF00069 0.529
MOD_ProDKin_1 450 456 PF00069 0.601
MOD_ProDKin_1 50 56 PF00069 0.572
MOD_ProDKin_1 7 13 PF00069 0.512
MOD_ProDKin_1 702 708 PF00069 0.336
MOD_ProDKin_1 771 777 PF00069 0.425
TRG_DiLeu_BaLyEn_6 129 134 PF01217 0.385
TRG_DiLeu_BaLyEn_6 177 182 PF01217 0.405
TRG_DiLeu_BaLyEn_6 21 26 PF01217 0.487
TRG_DiLeu_BaLyEn_6 604 609 PF01217 0.392
TRG_DiLeu_BaLyEn_6 84 89 PF01217 0.399
TRG_ENDOCYTIC_2 286 289 PF00928 0.450
TRG_ENDOCYTIC_2 314 317 PF00928 0.563
TRG_ENDOCYTIC_2 523 526 PF00928 0.559
TRG_ENDOCYTIC_2 540 543 PF00928 0.260
TRG_ENDOCYTIC_2 641 644 PF00928 0.474
TRG_ENDOCYTIC_2 691 694 PF00928 0.324
TRG_ENDOCYTIC_2 721 724 PF00928 0.327
TRG_ER_diArg_1 120 122 PF00400 0.441
TRG_ER_diArg_1 33 35 PF00400 0.456
TRG_ER_diArg_1 404 406 PF00400 0.703
TRG_ER_diArg_1 409 411 PF00400 0.670
TRG_ER_diArg_1 489 491 PF00400 0.465
TRG_ER_diArg_1 592 595 PF00400 0.368
TRG_ER_diArg_1 661 663 PF00400 0.414
TRG_ER_diArg_1 76 79 PF00400 0.461
TRG_NLS_MonoExtC_3 493 499 PF00514 0.403
TRG_NLS_MonoExtN_4 491 498 PF00514 0.459
TRG_Pf-PMV_PEXEL_1 495 499 PF00026 0.417

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 41% 100%
A0A3S5H4Y6 Leishmania donovani 60% 100%
A0A3S5H4Y9 Leishmania donovani 39% 82%
A0A3S7WT86 Leishmania donovani 40% 79%
A0A3S7WWA6 Leishmania donovani 41% 100%
A0A451EJD9 Leishmania donovani 39% 100%
A0A451EJF4 Leishmania donovani 63% 99%
A0A451EJF6 Leishmania donovani 55% 100%
A0A451EJF8 Leishmania donovani 57% 100%
A0A451EJF9 Leishmania donovani 50% 94%
A4H3A9 Leishmania braziliensis 86% 99%
A4H3B4 Leishmania braziliensis 70% 100%
A4H3B6 Leishmania braziliensis 94% 100%
A4H3B8 Leishmania braziliensis 59% 100%
A4H3B9 Leishmania braziliensis 38% 100%
A4H4W8 Leishmania braziliensis 37% 100%
A4HNK3 Leishmania braziliensis 41% 100%
A4HNK6 Leishmania braziliensis 38% 100%
A4HRL9 Leishmania infantum 61% 99%
A4HRM0 Leishmania infantum 65% 100%
A4HRM1 Leishmania infantum 55% 100%
A4HRS1 Leishmania infantum 50% 94%
A4HRS3 Leishmania infantum 39% 82%
A4HRS5 Leishmania infantum 57% 100%
A4HZM0 Leishmania infantum 39% 100%
A4I7C7 Leishmania infantum 40% 100%
A4IAQ2 Leishmania infantum 39% 100%
E9AC91 Leishmania major 62% 100%
E9AC92 Leishmania major 58% 100%
E9AC94 Leishmania major 38% 69%
E9AC95 Leishmania major 55% 100%
E9AC96 Leishmania major 50% 100%
E9AC98 Leishmania major 38% 82%
E9AEH8 Leishmania major 38% 100%
E9AHA6 Leishmania infantum 39% 100%
E9AIP8 Leishmania braziliensis 38% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 64% 99%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 59% 100%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 59% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 36% 82%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 38% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 38% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 37% 100%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 39% 100%
Q4Q5T6 Leishmania major 39% 100%
Q4QCL8 Leishmania major 39% 100%
Q4QFJ3 Leishmania major 40% 79%
Q4QIG9 Leishmania major 39% 100%
Q7YXU9 Leishmania major 39% 100%
Q7YXV1 Leishmania major 39% 100%
Q7YXV2 Leishmania major 39% 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