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 infantum
UniProt:
A4HRL9_LEIIN
TriTrypDb:
LINF_020006700
Length:
817

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)

Annotations by Jardim et al.

Glycosylation, Phosphoglycan beta 1,3 galactosyltransferase SCGR6

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. yes 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

A4HRL9
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HRL9

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 62 66 PF00656 0.630
CLV_NRD_NRD_1 12 14 PF00675 0.452
CLV_NRD_NRD_1 314 316 PF00675 0.560
CLV_NRD_NRD_1 369 371 PF00675 0.644
CLV_NRD_NRD_1 411 413 PF00675 0.701
CLV_NRD_NRD_1 416 418 PF00675 0.674
CLV_NRD_NRD_1 435 437 PF00675 0.574
CLV_NRD_NRD_1 494 496 PF00675 0.715
CLV_NRD_NRD_1 667 669 PF00675 0.547
CLV_NRD_NRD_1 733 735 PF00675 0.561
CLV_NRD_NRD_1 754 756 PF00675 0.573
CLV_NRD_NRD_1 93 95 PF00675 0.494
CLV_PCSK_KEX2_1 11 13 PF00082 0.457
CLV_PCSK_KEX2_1 314 316 PF00082 0.552
CLV_PCSK_KEX2_1 369 371 PF00082 0.659
CLV_PCSK_KEX2_1 411 413 PF00082 0.699
CLV_PCSK_KEX2_1 416 418 PF00082 0.672
CLV_PCSK_KEX2_1 435 437 PF00082 0.574
CLV_PCSK_KEX2_1 494 496 PF00082 0.644
CLV_PCSK_KEX2_1 564 566 PF00082 0.595
CLV_PCSK_KEX2_1 667 669 PF00082 0.561
CLV_PCSK_KEX2_1 733 735 PF00082 0.628
CLV_PCSK_KEX2_1 753 755 PF00082 0.557
CLV_PCSK_KEX2_1 777 779 PF00082 0.570
CLV_PCSK_KEX2_1 93 95 PF00082 0.503
CLV_PCSK_PC1ET2_1 11 13 PF00082 0.452
CLV_PCSK_PC1ET2_1 564 566 PF00082 0.559
CLV_PCSK_PC1ET2_1 733 735 PF00082 0.628
CLV_PCSK_PC1ET2_1 753 755 PF00082 0.536
CLV_PCSK_PC1ET2_1 777 779 PF00082 0.567
CLV_PCSK_PC7_1 310 316 PF00082 0.540
CLV_PCSK_PC7_1 412 418 PF00082 0.563
CLV_PCSK_PC7_1 663 669 PF00082 0.523
CLV_PCSK_SKI1_1 306 310 PF00082 0.593
CLV_PCSK_SKI1_1 384 388 PF00082 0.605
CLV_PCSK_SKI1_1 435 439 PF00082 0.569
CLV_PCSK_SKI1_1 519 523 PF00082 0.610
CLV_PCSK_SKI1_1 595 599 PF00082 0.554
DEG_APCC_DBOX_1 138 146 PF00400 0.398
DEG_APCC_DBOX_1 369 377 PF00400 0.417
DEG_SCF_FBW7_1 455 462 PF00400 0.500
DEG_SCF_FBW7_2 424 431 PF00400 0.326
DOC_CKS1_1 288 293 PF01111 0.362
DOC_CKS1_1 456 461 PF01111 0.504
DOC_CYCLIN_yCln2_LP_2 183 189 PF00134 0.395
DOC_CYCLIN_yCln2_LP_2 4 10 PF00134 0.642
DOC_CYCLIN_yCln2_LP_2 453 459 PF00134 0.546
DOC_MAPK_gen_1 84 92 PF00069 0.643
DOC_MAPK_MEF2A_6 110 119 PF00069 0.385
DOC_MAPK_MEF2A_6 240 248 PF00069 0.379
DOC_MAPK_MEF2A_6 483 490 PF00069 0.452
DOC_MAPK_MEF2A_6 507 516 PF00069 0.356
DOC_PP1_RVXF_1 481 488 PF00149 0.354
DOC_PP1_RVXF_1 517 524 PF00149 0.448
DOC_PP2B_LxvP_1 453 456 PF13499 0.550
DOC_PP4_FxxP_1 461 464 PF00568 0.384
DOC_USP7_MATH_1 14 18 PF00917 0.631
DOC_USP7_MATH_1 232 236 PF00917 0.528
DOC_USP7_MATH_1 247 251 PF00917 0.368
DOC_USP7_MATH_1 349 353 PF00917 0.504
DOC_USP7_MATH_1 441 445 PF00917 0.419
DOC_WW_Pin1_4 182 187 PF00397 0.419
DOC_WW_Pin1_4 287 292 PF00397 0.401
DOC_WW_Pin1_4 3 8 PF00397 0.650
DOC_WW_Pin1_4 424 429 PF00397 0.517
DOC_WW_Pin1_4 455 460 PF00397 0.505
DOC_WW_Pin1_4 707 712 PF00397 0.326
DOC_WW_Pin1_4 75 80 PF00397 0.662
DOC_WW_Pin1_4 776 781 PF00397 0.365
LIG_14-3-3_CanoR_1 110 115 PF00244 0.234
LIG_14-3-3_CanoR_1 12 19 PF00244 0.664
LIG_14-3-3_CanoR_1 212 219 PF00244 0.459
LIG_14-3-3_CanoR_1 314 318 PF00244 0.496
LIG_14-3-3_CanoR_1 360 368 PF00244 0.474
LIG_14-3-3_CanoR_1 370 378 PF00244 0.407
LIG_14-3-3_CanoR_1 435 440 PF00244 0.448
LIG_14-3-3_CanoR_1 754 762 PF00244 0.375
LIG_14-3-3_CanoR_1 803 808 PF00244 0.333
LIG_14-3-3_CanoR_1 84 92 PF00244 0.667
LIG_Actin_WH2_2 175 190 PF00022 0.394
LIG_Actin_WH2_2 254 270 PF00022 0.399
LIG_Actin_WH2_2 653 669 PF00022 0.299
LIG_BIR_II_1 1 5 PF00653 0.639
LIG_EH1_1 607 615 PF00400 0.272
LIG_FHA_1 14 20 PF00498 0.635
LIG_FHA_1 174 180 PF00498 0.396
LIG_FHA_1 196 202 PF00498 0.546
LIG_FHA_1 250 256 PF00498 0.520
LIG_FHA_1 288 294 PF00498 0.362
LIG_FHA_1 3 9 PF00498 0.665
LIG_FHA_1 385 391 PF00498 0.401
LIG_FHA_1 441 447 PF00498 0.437
LIG_FHA_1 605 611 PF00498 0.306
LIG_FHA_1 71 77 PF00498 0.678
LIG_FHA_1 802 808 PF00498 0.335
LIG_FHA_2 317 323 PF00498 0.432
LIG_FHA_2 377 383 PF00498 0.519
LIG_FHA_2 499 505 PF00498 0.374
LIG_FHA_2 708 714 PF00498 0.313
LIG_FHA_2 755 761 PF00498 0.356
LIG_FHA_2 764 770 PF00498 0.326
LIG_FHA_2 803 809 PF00498 0.350
LIG_LIR_Apic_2 458 464 PF02991 0.391
LIG_LIR_Apic_2 505 511 PF02991 0.482
LIG_LIR_Gen_1 290 299 PF02991 0.357
LIG_LIR_Gen_1 319 324 PF02991 0.348
LIG_LIR_Gen_1 525 536 PF02991 0.379
LIG_LIR_Gen_1 542 552 PF02991 0.376
LIG_LIR_Gen_1 683 691 PF02991 0.360
LIG_LIR_Gen_1 698 706 PF02991 0.402
LIG_LIR_Nem_3 290 295 PF02991 0.366
LIG_LIR_Nem_3 316 320 PF02991 0.495
LIG_LIR_Nem_3 525 531 PF02991 0.427
LIG_LIR_Nem_3 542 548 PF02991 0.340
LIG_LIR_Nem_3 683 688 PF02991 0.359
LIG_LIR_Nem_3 698 704 PF02991 0.407
LIG_LIR_Nem_3 713 717 PF02991 0.303
LIG_LIR_Nem_3 808 814 PF02991 0.350
LIG_NRBOX 656 662 PF00104 0.300
LIG_Pex14_2 193 197 PF04695 0.364
LIG_PTB_Apo_2 596 603 PF02174 0.283
LIG_REV1ctd_RIR_1 718 727 PF16727 0.304
LIG_SH2_CRK 122 126 PF00017 0.266
LIG_SH2_CRK 545 549 PF00017 0.268
LIG_SH2_CRK 811 815 PF00017 0.348
LIG_SH2_GRB2like 793 796 PF00017 0.322
LIG_SH2_NCK_1 122 126 PF00017 0.246
LIG_SH2_SRC 320 323 PF00017 0.361
LIG_SH2_SRC 526 529 PF00017 0.380
LIG_SH2_SRC 716 719 PF00017 0.289
LIG_SH2_STAP1 122 126 PF00017 0.266
LIG_SH2_STAP1 50 54 PF00017 0.628
LIG_SH2_STAP1 526 530 PF00017 0.470
LIG_SH2_STAP1 579 583 PF00017 0.328
LIG_SH2_STAP1 797 801 PF00017 0.394
LIG_SH2_STAT5 144 147 PF00017 0.428
LIG_SH2_STAT5 292 295 PF00017 0.411
LIG_SH2_STAT5 338 341 PF00017 0.440
LIG_SH2_STAT5 448 451 PF00017 0.389
LIG_SH2_STAT5 467 470 PF00017 0.442
LIG_SH2_STAT5 557 560 PF00017 0.389
LIG_SH2_STAT5 680 683 PF00017 0.370
LIG_SH2_STAT5 716 719 PF00017 0.462
LIG_SH3_3 285 291 PF00018 0.469
LIG_SH3_3 453 459 PF00018 0.546
LIG_SH3_3 563 569 PF00018 0.369
LIG_SH3_3 615 621 PF00018 0.340
LIG_SUMO_SIM_anti_2 113 119 PF11976 0.290
LIG_TRAF2_1 319 322 PF00917 0.375
LIG_TYR_ITIM 318 323 PF00017 0.468
LIG_TYR_ITSM 288 295 PF00017 0.358
LIG_UBA3_1 145 149 PF00899 0.421
LIG_WW_3 78 82 PF00397 0.636
MOD_CDC14_SPxK_1 185 188 PF00782 0.403
MOD_CDC14_SPxK_1 78 81 PF00782 0.635
MOD_CDK_SPxK_1 182 188 PF00069 0.401
MOD_CDK_SPxK_1 75 81 PF00069 0.638
MOD_CK1_1 2 8 PF00069 0.669
MOD_CK1_1 352 358 PF00069 0.576
MOD_CK1_1 39 45 PF00069 0.698
MOD_CK1_1 444 450 PF00069 0.375
MOD_CK1_1 59 65 PF00069 0.664
MOD_CK2_1 214 220 PF00069 0.445
MOD_CK2_1 316 322 PF00069 0.432
MOD_CK2_1 361 367 PF00069 0.500
MOD_CK2_1 376 382 PF00069 0.540
MOD_CK2_1 460 466 PF00069 0.391
MOD_CK2_1 733 739 PF00069 0.411
MOD_CK2_1 754 760 PF00069 0.341
MOD_CK2_1 763 769 PF00069 0.331
MOD_GlcNHglycan 100 103 PF01048 0.423
MOD_GlcNHglycan 216 219 PF01048 0.728
MOD_GlcNHglycan 234 237 PF01048 0.743
MOD_GlcNHglycan 355 358 PF01048 0.735
MOD_GlcNHglycan 363 366 PF01048 0.676
MOD_GlcNHglycan 37 41 PF01048 0.528
MOD_GlcNHglycan 373 376 PF01048 0.615
MOD_GlcNHglycan 442 446 PF01048 0.609
MOD_GlcNHglycan 449 452 PF01048 0.650
MOD_GlcNHglycan 472 475 PF01048 0.670
MOD_GlcNHglycan 559 562 PF01048 0.542
MOD_GlcNHglycan 576 579 PF01048 0.591
MOD_GlcNHglycan 58 61 PF01048 0.468
MOD_GlcNHglycan 86 89 PF01048 0.468
MOD_GSK3_1 169 176 PF00069 0.416
MOD_GSK3_1 178 185 PF00069 0.413
MOD_GSK3_1 207 214 PF00069 0.452
MOD_GSK3_1 349 356 PF00069 0.577
MOD_GSK3_1 431 438 PF00069 0.468
MOD_GSK3_1 440 447 PF00069 0.416
MOD_GSK3_1 451 458 PF00069 0.430
MOD_GSK3_1 494 501 PF00069 0.363
MOD_GSK3_1 59 66 PF00069 0.694
MOD_GSK3_1 70 77 PF00069 0.725
MOD_GSK3_1 725 732 PF00069 0.359
MOD_GSK3_1 84 91 PF00069 0.671
MOD_GSK3_1 94 101 PF00069 0.623
MOD_N-GLC_1 169 174 PF02516 0.609
MOD_N-GLC_1 349 354 PF02516 0.658
MOD_N-GLC_1 360 365 PF02516 0.709
MOD_N-GLC_1 498 503 PF02516 0.571
MOD_N-GLC_1 583 588 PF02516 0.497
MOD_NEK2_1 124 129 PF00069 0.467
MOD_NEK2_1 169 174 PF00069 0.493
MOD_NEK2_1 246 251 PF00069 0.363
MOD_NEK2_1 36 41 PF00069 0.681
MOD_NEK2_1 391 396 PF00069 0.389
MOD_NEK2_1 48 53 PF00069 0.653
MOD_NEK2_1 502 507 PF00069 0.436
MOD_NEK2_1 63 68 PF00069 0.653
MOD_NEK2_1 638 643 PF00069 0.325
MOD_NEK2_1 725 730 PF00069 0.335
MOD_NEK2_2 173 178 PF00069 0.390
MOD_NEK2_2 195 200 PF00069 0.551
MOD_NEK2_2 590 595 PF00069 0.298
MOD_NEK2_2 88 93 PF00069 0.639
MOD_PIKK_1 124 130 PF00454 0.456
MOD_PIKK_1 514 520 PF00454 0.472
MOD_PK_1 110 116 PF00069 0.234
MOD_PK_1 803 809 PF00069 0.295
MOD_PKA_1 12 18 PF00069 0.641
MOD_PKA_1 435 441 PF00069 0.366
MOD_PKA_1 494 500 PF00069 0.528
MOD_PKA_1 733 739 PF00069 0.339
MOD_PKA_1 753 759 PF00069 0.355
MOD_PKA_2 12 18 PF00069 0.664
MOD_PKA_2 211 217 PF00069 0.486
MOD_PKA_2 313 319 PF00069 0.498
MOD_PKA_2 371 377 PF00069 0.422
MOD_PKA_2 435 441 PF00069 0.458
MOD_PKA_2 494 500 PF00069 0.466
MOD_PKA_2 662 668 PF00069 0.302
MOD_PKA_2 733 739 PF00069 0.362
MOD_PKA_2 753 759 PF00069 0.365
MOD_PKA_2 802 808 PF00069 0.348
MOD_PKB_1 84 92 PF00069 0.645
MOD_Plk_1 441 447 PF00069 0.379
MOD_Plk_1 498 504 PF00069 0.369
MOD_Plk_1 541 547 PF00069 0.340
MOD_Plk_1 638 644 PF00069 0.325
MOD_Plk_1 697 703 PF00069 0.365
MOD_Plk_4 110 116 PF00069 0.335
MOD_Plk_4 178 184 PF00069 0.416
MOD_Plk_4 444 450 PF00069 0.366
MOD_Plk_4 541 547 PF00069 0.343
MOD_Plk_4 604 610 PF00069 0.304
MOD_Plk_4 700 706 PF00069 0.439
MOD_ProDKin_1 182 188 PF00069 0.420
MOD_ProDKin_1 287 293 PF00069 0.394
MOD_ProDKin_1 3 9 PF00069 0.652
MOD_ProDKin_1 424 430 PF00069 0.518
MOD_ProDKin_1 455 461 PF00069 0.502
MOD_ProDKin_1 707 713 PF00069 0.324
MOD_ProDKin_1 75 81 PF00069 0.662
MOD_ProDKin_1 776 782 PF00069 0.362
TRG_DiLeu_BaLyEn_6 609 614 PF01217 0.364
TRG_ENDOCYTIC_2 122 125 PF00928 0.269
TRG_ENDOCYTIC_2 292 295 PF00928 0.411
TRG_ENDOCYTIC_2 320 323 PF00928 0.496
TRG_ENDOCYTIC_2 528 531 PF00928 0.481
TRG_ENDOCYTIC_2 545 548 PF00928 0.269
TRG_ENDOCYTIC_2 714 717 PF00928 0.280
TRG_ENDOCYTIC_2 811 814 PF00928 0.335
TRG_ER_diArg_1 368 370 PF00400 0.443
TRG_ER_diArg_1 411 413 PF00400 0.494
TRG_ER_diArg_1 415 417 PF00400 0.465
TRG_ER_diArg_1 435 437 PF00400 0.374
TRG_ER_diArg_1 494 496 PF00400 0.420
TRG_ER_diArg_1 666 668 PF00400 0.366
TRG_ER_diArg_1 92 94 PF00400 0.701
TRG_NES_CRM1_1 136 152 PF08389 0.407
TRG_NLS_MonoExtC_3 732 737 PF00514 0.355
TRG_NLS_MonoExtN_4 733 738 PF00514 0.345
TRG_Pf-PMV_PEXEL_1 612 616 PF00026 0.598
TRG_Pf-PMV_PEXEL_1 812 816 PF00026 0.532

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 42% 100%
A0A3S5H4Y6 Leishmania donovani 84% 100%
A0A3S5H4Y9 Leishmania donovani 34% 82%
A0A3S7WT86 Leishmania donovani 43% 79%
A0A3S7WWA6 Leishmania donovani 42% 100%
A0A451EJD9 Leishmania donovani 41% 100%
A0A451EJF4 Leishmania donovani 98% 100%
A0A451EJF6 Leishmania donovani 75% 100%
A0A451EJF8 Leishmania donovani 60% 100%
A0A451EJF9 Leishmania donovani 66% 95%
A4H3A9 Leishmania braziliensis 65% 100%
A4H3B4 Leishmania braziliensis 68% 100%
A4H3B6 Leishmania braziliensis 64% 100%
A4H3B8 Leishmania braziliensis 59% 100%
A4H3B9 Leishmania braziliensis 40% 100%
A4H4W8 Leishmania braziliensis 38% 100%
A4HJ20 Leishmania braziliensis 61% 100%
A4HNK3 Leishmania braziliensis 41% 100%
A4HNK6 Leishmania braziliensis 38% 100%
A4HRM0 Leishmania infantum 74% 100%
A4HRM1 Leishmania infantum 74% 100%
A4HRS1 Leishmania infantum 62% 95%
A4HRS3 Leishmania infantum 34% 82%
A4HRS5 Leishmania infantum 59% 100%
A4HZM0 Leishmania infantum 38% 100%
A4I7C7 Leishmania infantum 41% 100%
A4IAQ2 Leishmania infantum 37% 100%
E9AC91 Leishmania major 88% 100%
E9AC92 Leishmania major 80% 100%
E9AC94 Leishmania major 34% 100%
E9AC95 Leishmania major 60% 100%
E9AC96 Leishmania major 68% 100%
E9AC98 Leishmania major 34% 100%
E9AEH8 Leishmania major 41% 100%
E9AHA6 Leishmania infantum 40% 100%
E9AIP8 Leishmania braziliensis 38% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 86% 100%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 71% 100%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 56% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 34% 100%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 39% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 100%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 41% 100%
Q4Q5T6 Leishmania major 41% 100%
Q4QCL8 Leishmania major 41% 100%
Q4QFJ3 Leishmania major 43% 100%
Q4QIG9 Leishmania major 41% 100%
Q7YXU9 Leishmania major 40% 100%
Q7YXV1 Leishmania major 42% 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