LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase 7

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 7
Gene product:
phosphoglycan beta 1,3 galactosyltransferase 6
Species:
Leishmania infantum
UniProt:
A4IAQ2_LEIIN
TriTrypDb:
LINF_020005000 *
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

A4IAQ2
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4IAQ2

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_Caspase3-7 434 438 PF00656 0.342
CLV_C14_Caspase3-7 740 744 PF00656 0.306
CLV_NRD_NRD_1 283 285 PF00675 0.637
CLV_NRD_NRD_1 399 401 PF00675 0.677
CLV_NRD_NRD_1 489 491 PF00675 0.644
CLV_NRD_NRD_1 565 567 PF00675 0.451
CLV_NRD_NRD_1 576 578 PF00675 0.410
CLV_NRD_NRD_1 609 611 PF00675 0.541
CLV_NRD_NRD_1 70 72 PF00675 0.449
CLV_NRD_NRD_1 779 781 PF00675 0.523
CLV_NRD_NRD_1 92 94 PF00675 0.483
CLV_PCSK_KEX2_1 105 107 PF00082 0.456
CLV_PCSK_KEX2_1 283 285 PF00082 0.627
CLV_PCSK_KEX2_1 313 315 PF00082 0.536
CLV_PCSK_KEX2_1 399 401 PF00082 0.675
CLV_PCSK_KEX2_1 565 567 PF00082 0.469
CLV_PCSK_KEX2_1 576 578 PF00082 0.410
CLV_PCSK_KEX2_1 609 611 PF00082 0.530
CLV_PCSK_KEX2_1 671 673 PF00082 0.648
CLV_PCSK_KEX2_1 766 768 PF00082 0.578
CLV_PCSK_KEX2_1 779 781 PF00082 0.556
CLV_PCSK_KEX2_1 92 94 PF00082 0.483
CLV_PCSK_PC1ET2_1 105 107 PF00082 0.419
CLV_PCSK_PC1ET2_1 313 315 PF00082 0.510
CLV_PCSK_PC1ET2_1 671 673 PF00082 0.592
CLV_PCSK_PC1ET2_1 766 768 PF00082 0.574
CLV_PCSK_PC7_1 775 781 PF00082 0.530
CLV_PCSK_PC7_1 88 94 PF00082 0.413
CLV_PCSK_SKI1_1 105 109 PF00082 0.261
CLV_PCSK_SKI1_1 400 404 PF00082 0.595
CLV_PCSK_SKI1_1 730 734 PF00082 0.540
CLV_Separin_Metazoa 268 272 PF03568 0.349
DEG_Nend_UBRbox_1 1 4 PF02207 0.677
DEG_SCF_FBW7_1 451 458 PF00400 0.483
DOC_CKS1_1 452 457 PF01111 0.481
DOC_CYCLIN_yCln2_LP_2 248 254 PF00134 0.346
DOC_CYCLIN_yCln2_LP_2 449 455 PF00134 0.535
DOC_CYCLIN_yCln2_LP_2 630 636 PF00134 0.333
DOC_MAPK_gen_1 105 113 PF00069 0.533
DOC_MAPK_gen_1 297 306 PF00069 0.396
DOC_MAPK_HePTP_8 103 115 PF00069 0.438
DOC_MAPK_JIP1_4 297 303 PF00069 0.376
DOC_MAPK_MEF2A_6 105 113 PF00069 0.574
DOC_MAPK_MEF2A_6 479 486 PF00069 0.441
DOC_MAPK_MEF2A_6 656 665 PF00069 0.298
DOC_MAPK_NFAT4_5 479 487 PF00069 0.341
DOC_PP1_RVXF_1 513 520 PF00149 0.419
DOC_PP2B_LxvP_1 449 452 PF13499 0.543
DOC_PP2B_LxvP_1 542 545 PF13499 0.297
DOC_PP2B_LxvP_1 630 633 PF13499 0.316
DOC_PP4_FxxP_1 152 155 PF00568 0.412
DOC_SPAK_OSR1_1 106 110 PF12202 0.413
DOC_USP7_MATH_1 221 225 PF00917 0.453
DOC_USP7_MATH_1 240 244 PF00917 0.506
DOC_USP7_MATH_1 255 259 PF00917 0.360
DOC_USP7_MATH_1 288 292 PF00917 0.479
DOC_USP7_MATH_1 36 40 PF00917 0.708
DOC_USP7_MATH_1 370 374 PF00917 0.382
DOC_USP7_MATH_1 690 694 PF00917 0.396
DOC_USP7_MATH_1 808 812 PF00917 0.309
DOC_USP7_MATH_1 91 95 PF00917 0.675
DOC_USP7_UBL2_3 491 495 PF12436 0.353
DOC_USP7_UBL2_3 730 734 PF12436 0.335
DOC_WW_Pin1_4 123 128 PF00397 0.434
DOC_WW_Pin1_4 151 156 PF00397 0.446
DOC_WW_Pin1_4 417 422 PF00397 0.489
DOC_WW_Pin1_4 437 442 PF00397 0.415
DOC_WW_Pin1_4 451 456 PF00397 0.457
LIG_14-3-3_CanoR_1 148 156 PF00244 0.440
LIG_14-3-3_CanoR_1 322 326 PF00244 0.466
LIG_14-3-3_CanoR_1 426 430 PF00244 0.412
LIG_14-3-3_CanoR_1 432 436 PF00244 0.367
LIG_14-3-3_CanoR_1 479 483 PF00244 0.317
LIG_14-3-3_CanoR_1 656 662 PF00244 0.308
LIG_14-3-3_CanoR_1 675 682 PF00244 0.301
LIG_14-3-3_CanoR_1 800 805 PF00244 0.334
LIG_14-3-3_CanoR_1 92 100 PF00244 0.682
LIG_Actin_WH2_2 661 677 PF00022 0.330
LIG_Actin_WH2_2 751 768 PF00022 0.324
LIG_APCC_ABBA_1 619 624 PF00400 0.307
LIG_Clathr_ClatBox_1 184 188 PF01394 0.393
LIG_FHA_1 194 200 PF00498 0.539
LIG_FHA_1 258 264 PF00498 0.490
LIG_FHA_1 337 343 PF00498 0.356
LIG_FHA_1 360 366 PF00498 0.412
LIG_FHA_1 425 431 PF00498 0.351
LIG_FHA_1 437 443 PF00498 0.404
LIG_FHA_1 511 517 PF00498 0.231
LIG_FHA_1 568 574 PF00498 0.412
LIG_FHA_1 616 622 PF00498 0.330
LIG_FHA_1 800 806 PF00498 0.342
LIG_FHA_2 325 331 PF00498 0.411
LIG_FHA_2 369 375 PF00498 0.483
LIG_FHA_2 382 388 PF00498 0.385
LIG_FHA_2 759 765 PF00498 0.336
LIG_FHA_2 801 807 PF00498 0.359
LIG_Integrin_RGD_1 775 777 PF01839 0.570
LIG_LIR_Apic_2 150 155 PF02991 0.419
LIG_LIR_Apic_2 415 421 PF02991 0.347
LIG_LIR_Apic_2 503 507 PF02991 0.436
LIG_LIR_Gen_1 154 160 PF02991 0.483
LIG_LIR_Gen_1 205 216 PF02991 0.379
LIG_LIR_Gen_1 481 487 PF02991 0.377
LIG_LIR_Gen_1 538 548 PF02991 0.431
LIG_LIR_Gen_1 618 627 PF02991 0.316
LIG_LIR_Gen_1 640 647 PF02991 0.373
LIG_LIR_Gen_1 696 707 PF02991 0.374
LIG_LIR_Nem_3 154 159 PF02991 0.484
LIG_LIR_Nem_3 164 169 PF02991 0.394
LIG_LIR_Nem_3 205 211 PF02991 0.391
LIG_LIR_Nem_3 324 328 PF02991 0.469
LIG_LIR_Nem_3 405 410 PF02991 0.428
LIG_LIR_Nem_3 481 486 PF02991 0.340
LIG_LIR_Nem_3 525 530 PF02991 0.346
LIG_LIR_Nem_3 538 544 PF02991 0.367
LIG_LIR_Nem_3 618 622 PF02991 0.337
LIG_LIR_Nem_3 640 645 PF02991 0.393
LIG_LIR_Nem_3 696 702 PF02991 0.377
LIG_NRBOX 110 116 PF00104 0.308
LIG_NRBOX 625 631 PF00104 0.343
LIG_Pex14_2 152 156 PF04695 0.413
LIG_Pex14_2 719 723 PF04695 0.267
LIG_PTB_Apo_2 207 214 PF02174 0.386
LIG_PTB_Apo_2 636 643 PF02174 0.299
LIG_PTB_Phospho_1 207 213 PF10480 0.384
LIG_PTB_Phospho_1 636 642 PF10480 0.272
LIG_SH2_CRK 642 646 PF00017 0.300
LIG_SH2_CRK 706 710 PF00017 0.271
LIG_SH2_NCK_1 375 379 PF00017 0.396
LIG_SH2_NCK_1 706 710 PF00017 0.271
LIG_SH2_NCK_1 793 797 PF00017 0.319
LIG_SH2_SRC 793 796 PF00017 0.289
LIG_SH2_STAP1 213 217 PF00017 0.412
LIG_SH2_STAP1 522 526 PF00017 0.423
LIG_SH2_STAP1 634 638 PF00017 0.381
LIG_SH2_STAP1 642 646 PF00017 0.324
LIG_SH2_STAP1 793 797 PF00017 0.376
LIG_SH2_STAT3 279 282 PF00017 0.395
LIG_SH2_STAT5 346 349 PF00017 0.429
LIG_SH2_STAT5 396 399 PF00017 0.360
LIG_SH2_STAT5 463 466 PF00017 0.328
LIG_SH2_STAT5 524 527 PF00017 0.317
LIG_SH2_STAT5 532 535 PF00017 0.318
LIG_SH2_STAT5 541 544 PF00017 0.326
LIG_SH2_STAT5 547 550 PF00017 0.318
LIG_SH2_STAT5 634 637 PF00017 0.355
LIG_SH2_STAT5 676 679 PF00017 0.384
LIG_SH2_STAT5 713 716 PF00017 0.435
LIG_SH2_STAT5 718 721 PF00017 0.392
LIG_SH2_STAT5 782 785 PF00017 0.383
LIG_SH3_1 706 712 PF00018 0.268
LIG_SH3_3 449 455 PF00018 0.512
LIG_SH3_3 525 531 PF00018 0.354
LIG_SH3_3 684 690 PF00018 0.378
LIG_SH3_3 706 712 PF00018 0.301
LIG_SH3_4 491 498 PF00018 0.355
LIG_SUMO_SIM_anti_2 624 629 PF11976 0.311
LIG_TYR_ITIM 326 331 PF00017 0.444
LIG_WRC_WIRS_1 616 621 PF05994 0.294
MOD_CK1_1 126 132 PF00069 0.467
MOD_CK1_1 154 160 PF00069 0.440
MOD_CK1_1 291 297 PF00069 0.458
MOD_CK1_1 355 361 PF00069 0.508
MOD_CK1_1 392 398 PF00069 0.306
MOD_CK1_1 428 434 PF00069 0.378
MOD_CK1_1 64 70 PF00069 0.708
MOD_CK1_1 693 699 PF00069 0.325
MOD_CK2_1 161 167 PF00069 0.400
MOD_CK2_1 32 38 PF00069 0.667
MOD_CK2_1 324 330 PF00069 0.477
MOD_CK2_1 368 374 PF00069 0.504
MOD_CK2_1 675 681 PF00069 0.339
MOD_GlcNHglycan 131 134 PF01048 0.639
MOD_GlcNHglycan 163 166 PF01048 0.591
MOD_GlcNHglycan 214 217 PF01048 0.654
MOD_GlcNHglycan 242 245 PF01048 0.714
MOD_GlcNHglycan 34 37 PF01048 0.506
MOD_GlcNHglycan 38 41 PF01048 0.497
MOD_GlcNHglycan 391 394 PF01048 0.533
MOD_GlcNHglycan 445 448 PF01048 0.660
MOD_GlcNHglycan 467 470 PF01048 0.638
MOD_GlcNHglycan 59 62 PF01048 0.510
MOD_GlcNHglycan 64 67 PF01048 0.497
MOD_GlcNHglycan 738 742 PF01048 0.528
MOD_GlcNHglycan 810 813 PF01048 0.552
MOD_GlcNHglycan 93 96 PF01048 0.476
MOD_GSK3_1 123 130 PF00069 0.528
MOD_GSK3_1 147 154 PF00069 0.485
MOD_GSK3_1 221 228 PF00069 0.485
MOD_GSK3_1 234 241 PF00069 0.399
MOD_GSK3_1 32 39 PF00069 0.712
MOD_GSK3_1 352 359 PF00069 0.457
MOD_GSK3_1 424 431 PF00069 0.426
MOD_GSK3_1 443 450 PF00069 0.444
MOD_GSK3_1 451 458 PF00069 0.376
MOD_GSK3_1 53 60 PF00069 0.712
MOD_GSK3_1 567 574 PF00069 0.236
MOD_GSK3_1 61 68 PF00069 0.679
MOD_GSK3_1 637 644 PF00069 0.297
MOD_GSK3_1 693 700 PF00069 0.332
MOD_GSK3_1 73 80 PF00069 0.659
MOD_GSK3_1 753 760 PF00069 0.352
MOD_LATS_1 569 575 PF00433 0.201
MOD_N-GLC_1 127 132 PF02516 0.617
MOD_N-GLC_1 209 214 PF02516 0.593
MOD_N-GLC_1 336 341 PF02516 0.545
MOD_N-GLC_1 693 698 PF02516 0.522
MOD_N-GLC_1 744 749 PF02516 0.569
MOD_N-GLC_1 769 774 PF02516 0.515
MOD_N-GLC_1 800 805 PF02516 0.530
MOD_N-GLC_2 585 587 PF02516 0.401
MOD_NEK2_1 169 174 PF00069 0.453
MOD_NEK2_1 23 28 PF00069 0.640
MOD_NEK2_1 239 244 PF00069 0.456
MOD_NEK2_1 637 642 PF00069 0.387
MOD_NEK2_2 193 198 PF00069 0.550
MOD_PIKK_1 131 137 PF00454 0.481
MOD_PIKK_1 169 175 PF00454 0.393
MOD_PIKK_1 24 30 PF00454 0.662
MOD_PIKK_1 286 292 PF00454 0.472
MOD_PIKK_1 510 516 PF00454 0.430
MOD_PIKK_1 579 585 PF00454 0.215
MOD_PIKK_1 744 750 PF00454 0.353
MOD_PIKK_1 753 759 PF00454 0.333
MOD_PIKK_1 77 83 PF00454 0.626
MOD_PIKK_1 98 104 PF00454 0.599
MOD_PK_1 234 240 PF00069 0.380
MOD_PKA_1 490 496 PF00069 0.481
MOD_PKA_2 12 18 PF00069 0.684
MOD_PKA_2 147 153 PF00069 0.439
MOD_PKA_2 222 228 PF00069 0.479
MOD_PKA_2 291 297 PF00069 0.465
MOD_PKA_2 321 327 PF00069 0.468
MOD_PKA_2 352 358 PF00069 0.415
MOD_PKA_2 425 431 PF00069 0.423
MOD_PKA_2 478 484 PF00069 0.375
MOD_PKA_2 799 805 PF00069 0.353
MOD_PKA_2 91 97 PF00069 0.665
MOD_PKB_1 798 806 PF00069 0.321
MOD_Plk_1 202 208 PF00069 0.417
MOD_Plk_1 209 215 PF00069 0.370
MOD_Plk_1 537 543 PF00069 0.302
MOD_Plk_1 693 699 PF00069 0.362
MOD_Plk_1 737 743 PF00069 0.307
MOD_Plk_1 769 775 PF00069 0.326
MOD_Plk_1 800 806 PF00069 0.336
MOD_Plk_2-3 352 358 PF00069 0.413
MOD_Plk_4 180 186 PF00069 0.444
MOD_Plk_4 234 240 PF00069 0.400
MOD_Plk_4 321 327 PF00069 0.409
MOD_Plk_4 392 398 PF00069 0.340
MOD_Plk_4 425 431 PF00069 0.376
MOD_Plk_4 478 484 PF00069 0.327
MOD_Plk_4 537 543 PF00069 0.302
MOD_Plk_4 632 638 PF00069 0.340
MOD_Plk_4 641 647 PF00069 0.295
MOD_Plk_4 698 704 PF00069 0.413
MOD_Plk_4 769 775 PF00069 0.342
MOD_Plk_4 800 806 PF00069 0.353
MOD_ProDKin_1 123 129 PF00069 0.443
MOD_ProDKin_1 151 157 PF00069 0.446
MOD_ProDKin_1 417 423 PF00069 0.493
MOD_ProDKin_1 437 443 PF00069 0.412
MOD_ProDKin_1 451 457 PF00069 0.452
MOD_SUMO_for_1 719 722 PF00179 0.267
MOD_SUMO_rev_2 485 493 PF00179 0.370
TRG_DiLeu_BaLyEn_6 135 140 PF01217 0.439
TRG_DiLeu_BaLyEn_6 607 612 PF01217 0.327
TRG_ENDOCYTIC_2 328 331 PF00928 0.476
TRG_ENDOCYTIC_2 524 527 PF00928 0.432
TRG_ENDOCYTIC_2 541 544 PF00928 0.234
TRG_ENDOCYTIC_2 634 637 PF00928 0.369
TRG_ENDOCYTIC_2 642 645 PF00928 0.399
TRG_ER_diArg_1 283 285 PF00400 0.428
TRG_ER_diArg_1 399 401 PF00400 0.470
TRG_ER_diArg_1 564 566 PF00400 0.255
TRG_ER_diArg_1 576 578 PF00400 0.217
TRG_ER_diArg_1 609 611 PF00400 0.322
TRG_ER_diArg_1 778 780 PF00400 0.338
TRG_ER_diArg_1 797 800 PF00400 0.329
TRG_ER_diArg_1 91 93 PF00400 0.681
TRG_NLS_MonoExtC_3 494 500 PF00514 0.335
TRG_NLS_MonoExtN_4 492 499 PF00514 0.372
TRG_Pf-PMV_PEXEL_1 137 141 PF00026 0.632
TRG_Pf-PMV_PEXEL_1 198 202 PF00026 0.612
TRG_Pf-PMV_PEXEL_1 609 613 PF00026 0.549

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 77% 100%
A0A3S5H4Y6 Leishmania donovani 39% 100%
A0A3S5H4Y9 Leishmania donovani 32% 82%
A0A3S7WT86 Leishmania donovani 36% 79%
A0A3S7WWA6 Leishmania donovani 77% 100%
A0A451EJD9 Leishmania donovani 89% 100%
A0A451EJF4 Leishmania donovani 37% 100%
A0A451EJF6 Leishmania donovani 41% 100%
A0A451EJF8 Leishmania donovani 38% 100%
A0A451EJF9 Leishmania donovani 39% 94%
A4H3A9 Leishmania braziliensis 40% 100%
A4H3B4 Leishmania braziliensis 40% 100%
A4H3B6 Leishmania braziliensis 38% 100%
A4H3B8 Leishmania braziliensis 41% 100%
A4H3B9 Leishmania braziliensis 33% 100%
A4H4W8 Leishmania braziliensis 55% 100%
A4HJ20 Leishmania braziliensis 39% 100%
A4HNK3 Leishmania braziliensis 60% 99%
A4HNK6 Leishmania braziliensis 55% 99%
A4HRL9 Leishmania infantum 37% 100%
A4HRM0 Leishmania infantum 38% 100%
A4HRM1 Leishmania infantum 41% 100%
A4HRS1 Leishmania infantum 39% 94%
A4HRS3 Leishmania infantum 31% 82%
A4HRS5 Leishmania infantum 38% 100%
A4HZM0 Leishmania infantum 87% 100%
A4I7C7 Leishmania infantum 89% 100%
E9AC91 Leishmania major 40% 100%
E9AC92 Leishmania major 41% 100%
E9AC94 Leishmania major 32% 69%
E9AC95 Leishmania major 37% 100%
E9AC96 Leishmania major 42% 100%
E9AC98 Leishmania major 32% 82%
E9AEH8 Leishmania major 80% 100%
E9AHA6 Leishmania infantum 90% 100%
E9AIP8 Leishmania braziliensis 54% 98%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 39% 100%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 39% 100%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 38% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 32% 82%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 70% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 78% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 77% 100%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 70% 100%
Q4Q5T6 Leishmania major 80% 100%
Q4QCL8 Leishmania major 71% 100%
Q4QFJ3 Leishmania major 37% 79%
Q4QIG9 Leishmania major 71% 100%
Q7YXU9 Leishmania major 70% 100%
Q7YXV1 Leishmania major 72% 100%
Q7YXV2 Leishmania major 71% 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