LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase 2

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 2
Gene product:
phosphoglycan beta 1,3 galactosyltransferase 2
Species:
Leishmania braziliensis
UniProt:
E9AIP8_LEIBR
TriTrypDb:
LbrM.21.0010 , LBRM2903_020007700 * , LBRM2903_350005100
Length:
790

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

E9AIP8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AIP8

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_Caspase3-7 365 369 PF00656 0.349
CLV_C14_Caspase3-7 390 394 PF00656 0.307
CLV_NRD_NRD_1 123 125 PF00675 0.691
CLV_NRD_NRD_1 269 271 PF00675 0.623
CLV_NRD_NRD_1 332 334 PF00675 0.553
CLV_NRD_NRD_1 378 380 PF00675 0.667
CLV_NRD_NRD_1 589 591 PF00675 0.549
CLV_NRD_NRD_1 652 654 PF00675 0.542
CLV_NRD_NRD_1 86 88 PF00675 0.423
CLV_PCSK_FUR_1 82 86 PF00082 0.414
CLV_PCSK_KEX2_1 332 334 PF00082 0.553
CLV_PCSK_KEX2_1 378 380 PF00082 0.665
CLV_PCSK_KEX2_1 589 591 PF00082 0.539
CLV_PCSK_KEX2_1 652 654 PF00082 0.600
CLV_PCSK_KEX2_1 708 710 PF00082 0.545
CLV_PCSK_KEX2_1 84 86 PF00082 0.464
CLV_PCSK_PC1ET2_1 708 710 PF00082 0.545
CLV_PCSK_PC7_1 82 88 PF00082 0.382
CLV_PCSK_SKI1_1 125 129 PF00082 0.617
CLV_PCSK_SKI1_1 361 365 PF00082 0.556
CLV_PCSK_SKI1_1 379 383 PF00082 0.589
CLV_PCSK_SKI1_1 541 545 PF00082 0.546
CLV_PCSK_SKI1_1 608 612 PF00082 0.520
CLV_PCSK_SKI1_1 636 640 PF00082 0.483
CLV_PCSK_SKI1_1 776 780 PF00082 0.508
DEG_APCC_DBOX_1 84 92 PF00400 0.432
DEG_SCF_FBW7_1 430 437 PF00400 0.470
DOC_CDC14_PxL_1 505 513 PF14671 0.241
DOC_CDC14_PxL_1 91 99 PF14671 0.208
DOC_CKS1_1 431 436 PF01111 0.471
DOC_CYCLIN_yCln2_LP_2 227 233 PF00134 0.326
DOC_CYCLIN_yCln2_LP_2 428 434 PF00134 0.515
DOC_CYCLIN_yCln2_LP_2 61 67 PF00134 0.598
DOC_MAPK_gen_1 82 91 PF00069 0.680
DOC_MAPK_MEF2A_6 458 465 PF00069 0.428
DOC_MAPK_MEF2A_6 513 522 PF00069 0.295
DOC_MAPK_MEF2A_6 84 93 PF00069 0.538
DOC_MAPK_NFAT4_5 458 466 PF00069 0.337
DOC_PP1_RVXF_1 491 498 PF00149 0.418
DOC_PP1_RVXF_1 672 678 PF00149 0.318
DOC_PP2B_LxvP_1 428 431 PF13499 0.521
DOC_PP2B_LxvP_1 520 523 PF13499 0.301
DOC_PP2B_LxvP_1 61 64 PF13499 0.599
DOC_PP2B_PxIxI_1 399 405 PF00149 0.271
DOC_PP4_FxxP_1 684 687 PF00568 0.271
DOC_USP7_MATH_1 108 112 PF00917 0.387
DOC_USP7_MATH_1 127 131 PF00917 0.418
DOC_USP7_MATH_1 18 22 PF00917 0.682
DOC_USP7_MATH_1 219 223 PF00917 0.490
DOC_USP7_MATH_1 234 238 PF00917 0.340
DOC_USP7_MATH_1 252 256 PF00917 0.263
DOC_USP7_MATH_1 265 269 PF00917 0.399
DOC_USP7_MATH_1 355 359 PF00917 0.357
DOC_USP7_MATH_1 435 439 PF00917 0.295
DOC_USP7_MATH_1 598 602 PF00917 0.328
DOC_USP7_MATH_1 613 617 PF00917 0.285
DOC_USP7_MATH_1 670 674 PF00917 0.369
DOC_USP7_MATH_1 78 82 PF00917 0.616
DOC_USP7_UBL2_3 698 702 PF12436 0.319
DOC_WW_Pin1_4 334 339 PF00397 0.414
DOC_WW_Pin1_4 396 401 PF00397 0.458
DOC_WW_Pin1_4 407 412 PF00397 0.381
DOC_WW_Pin1_4 430 435 PF00397 0.439
LIG_14-3-3_CanoR_1 114 122 PF00244 0.438
LIG_14-3-3_CanoR_1 124 130 PF00244 0.441
LIG_14-3-3_CanoR_1 147 155 PF00244 0.434
LIG_14-3-3_CanoR_1 165 174 PF00244 0.400
LIG_14-3-3_CanoR_1 189 193 PF00244 0.405
LIG_14-3-3_CanoR_1 270 280 PF00244 0.344
LIG_14-3-3_CanoR_1 3 8 PF00244 0.652
LIG_14-3-3_CanoR_1 301 305 PF00244 0.448
LIG_14-3-3_CanoR_1 332 338 PF00244 0.374
LIG_14-3-3_CanoR_1 458 462 PF00244 0.311
LIG_14-3-3_CanoR_1 541 548 PF00244 0.360
LIG_14-3-3_CanoR_1 674 678 PF00244 0.300
LIG_14-3-3_CanoR_1 757 761 PF00244 0.357
LIG_Actin_WH2_2 686 704 PF00022 0.243
LIG_BRCT_BRCA1_1 61 65 PF00533 0.607
LIG_EH_1 596 600 PF12763 0.338
LIG_FHA_1 132 138 PF00498 0.430
LIG_FHA_1 173 179 PF00498 0.540
LIG_FHA_1 237 243 PF00498 0.460
LIG_FHA_1 316 322 PF00498 0.340
LIG_FHA_1 34 40 PF00498 0.664
LIG_FHA_1 342 348 PF00498 0.379
LIG_FHA_1 542 548 PF00498 0.338
LIG_FHA_1 554 560 PF00498 0.369
LIG_FHA_1 756 762 PF00498 0.338
LIG_FHA_2 126 132 PF00498 0.406
LIG_FHA_2 304 310 PF00498 0.390
LIG_FHA_2 348 354 PF00498 0.481
LIG_LIR_Apic_2 479 485 PF02991 0.467
LIG_LIR_Apic_2 682 687 PF02991 0.252
LIG_LIR_Gen_1 133 139 PF02991 0.468
LIG_LIR_Gen_1 460 466 PF02991 0.370
LIG_LIR_Gen_1 516 526 PF02991 0.347
LIG_LIR_Gen_1 621 629 PF02991 0.351
LIG_LIR_Gen_1 676 684 PF02991 0.350
LIG_LIR_Nem_3 133 138 PF02991 0.474
LIG_LIR_Nem_3 303 307 PF02991 0.447
LIG_LIR_Nem_3 384 389 PF02991 0.365
LIG_LIR_Nem_3 460 465 PF02991 0.335
LIG_LIR_Nem_3 503 508 PF02991 0.392
LIG_LIR_Nem_3 516 522 PF02991 0.314
LIG_LIR_Nem_3 616 622 PF02991 0.369
LIG_LIR_Nem_3 676 680 PF02991 0.355
LIG_NRBOX 605 611 PF00104 0.340
LIG_Pex14_1 570 574 PF04695 0.301
LIG_SH2_NCK_1 354 358 PF00017 0.390
LIG_SH2_SRC 629 632 PF00017 0.255
LIG_SH2_STAP1 500 504 PF00017 0.438
LIG_SH2_STAP1 629 633 PF00017 0.289
LIG_SH2_STAP1 771 775 PF00017 0.366
LIG_SH2_STAT3 258 261 PF00017 0.357
LIG_SH2_STAT5 103 106 PF00017 0.243
LIG_SH2_STAT5 325 328 PF00017 0.410
LIG_SH2_STAT5 502 505 PF00017 0.344
LIG_SH2_STAT5 510 513 PF00017 0.322
LIG_SH2_STAT5 519 522 PF00017 0.329
LIG_SH2_STAT5 525 528 PF00017 0.327
LIG_SH2_STAT5 585 588 PF00017 0.264
LIG_SH2_STAT5 622 625 PF00017 0.337
LIG_SH2_STAT5 692 695 PF00017 0.426
LIG_SH2_STAT5 760 763 PF00017 0.373
LIG_SH3_3 246 252 PF00018 0.256
LIG_SH3_3 405 411 PF00018 0.317
LIG_SH3_3 428 434 PF00018 0.487
LIG_SH3_3 503 509 PF00018 0.373
LIG_SH3_3 684 690 PF00018 0.298
LIG_SUMO_SIM_anti_2 621 627 PF11976 0.250
LIG_SUMO_SIM_par_1 745 750 PF11976 0.272
LIG_SUMO_SIM_par_1 95 100 PF11976 0.244
LIG_TRAF2_1 208 211 PF00917 0.407
LIG_TYR_ITIM 305 310 PF00017 0.513
LIG_TYR_ITIM 572 577 PF00017 0.308
MOD_CDK_SPK_2 334 339 PF00069 0.461
MOD_CK1_1 106 112 PF00069 0.529
MOD_CK1_1 272 278 PF00069 0.501
MOD_CK1_1 334 340 PF00069 0.628
MOD_CK1_1 407 413 PF00069 0.461
MOD_CK1_1 419 425 PF00069 0.423
MOD_CK1_1 426 432 PF00069 0.453
MOD_CK1_1 6 12 PF00069 0.521
MOD_CK1_1 673 679 PF00069 0.345
MOD_CK2_1 115 121 PF00069 0.586
MOD_CK2_1 26 32 PF00069 0.546
MOD_CK2_1 303 309 PF00069 0.462
MOD_CK2_1 347 353 PF00069 0.625
MOD_Cter_Amidation 650 653 PF01082 0.366
MOD_GlcNHglycan 142 145 PF01048 0.522
MOD_GlcNHglycan 149 152 PF01048 0.498
MOD_GlcNHglycan 221 224 PF01048 0.604
MOD_GlcNHglycan 425 428 PF01048 0.532
MOD_GlcNHglycan 437 440 PF01048 0.377
MOD_GSK3_1 127 134 PF00069 0.571
MOD_GSK3_1 20 27 PF00069 0.582
MOD_GSK3_1 265 272 PF00069 0.530
MOD_GSK3_1 334 341 PF00069 0.625
MOD_GSK3_1 419 426 PF00069 0.389
MOD_GSK3_1 430 437 PF00069 0.418
MOD_GSK3_1 6 13 PF00069 0.532
MOD_N-GLC_1 10 15 PF02516 0.499
MOD_N-GLC_1 115 120 PF02516 0.535
MOD_N-GLC_1 24 29 PF02516 0.531
MOD_N-GLC_1 265 270 PF02516 0.447
MOD_N-GLC_1 315 320 PF02516 0.379
MOD_N-GLC_1 541 546 PF02516 0.410
MOD_N-GLC_1 614 619 PF02516 0.327
MOD_N-GLC_1 722 727 PF02516 0.404
MOD_NEK2_1 218 223 PF00069 0.547
MOD_NEK2_1 269 274 PF00069 0.483
MOD_NEK2_1 476 481 PF00069 0.529
MOD_NEK2_1 543 548 PF00069 0.412
MOD_NEK2_1 599 604 PF00069 0.408
MOD_NEK2_1 747 752 PF00069 0.315
MOD_NEK2_1 97 102 PF00069 0.350
MOD_NEK2_2 172 177 PF00069 0.686
MOD_NEK2_2 265 270 PF00069 0.455
MOD_NEK2_2 614 619 PF00069 0.324
MOD_OFUCOSY 17 24 PF10250 0.498
MOD_PIKK_1 272 278 PF00454 0.416
MOD_PIKK_1 488 494 PF00454 0.529
MOD_PIKK_1 6 12 PF00454 0.545
MOD_PIKK_1 731 737 PF00454 0.371
MOD_PKA_2 131 137 PF00069 0.510
MOD_PKA_2 188 194 PF00069 0.512
MOD_PKA_2 269 275 PF00069 0.566
MOD_PKA_2 300 306 PF00069 0.548
MOD_PKA_2 331 337 PF00069 0.490
MOD_PKA_2 338 344 PF00069 0.466
MOD_PKA_2 457 463 PF00069 0.430
MOD_PKA_2 659 665 PF00069 0.325
MOD_PKA_2 673 679 PF00069 0.297
MOD_PKA_2 756 762 PF00069 0.358
MOD_PKB_1 539 547 PF00069 0.318
MOD_Plk_1 10 16 PF00069 0.498
MOD_Plk_1 115 121 PF00069 0.545
MOD_Plk_1 265 271 PF00069 0.447
MOD_Plk_1 33 39 PF00069 0.532
MOD_Plk_1 416 422 PF00069 0.412
MOD_Plk_1 614 620 PF00069 0.333
MOD_Plk_1 747 753 PF00069 0.347
MOD_Plk_2-3 331 337 PF00069 0.491
MOD_Plk_2-3 45 51 PF00069 0.512
MOD_Plk_4 10 16 PF00069 0.506
MOD_Plk_4 3 9 PF00069 0.519
MOD_Plk_4 300 306 PF00069 0.473
MOD_Plk_4 404 410 PF00069 0.435
MOD_Plk_4 457 463 PF00069 0.369
MOD_Plk_4 614 620 PF00069 0.369
MOD_Plk_4 621 627 PF00069 0.336
MOD_Plk_4 676 682 PF00069 0.487
MOD_Plk_4 736 742 PF00069 0.369
MOD_Plk_4 747 753 PF00069 0.346
MOD_Plk_4 756 762 PF00069 0.358
MOD_Plk_4 97 103 PF00069 0.336
MOD_ProDKin_1 334 340 PF00069 0.500
MOD_ProDKin_1 396 402 PF00069 0.568
MOD_ProDKin_1 407 413 PF00069 0.466
MOD_ProDKin_1 430 436 PF00069 0.529
MOD_SUMO_rev_2 156 164 PF00179 0.471
MOD_SUMO_rev_2 209 215 PF00179 0.474
MOD_SUMO_rev_2 700 710 PF00179 0.342
TRG_DiLeu_BaEn_1 621 626 PF01217 0.280
TRG_DiLeu_BaEn_1 706 711 PF01217 0.357
TRG_DiLeu_BaLyEn_6 34 39 PF01217 0.526
TRG_DiLeu_LyEn_5 706 711 PF01217 0.355
TRG_ENDOCYTIC_2 200 203 PF00928 0.462
TRG_ENDOCYTIC_2 307 310 PF00928 0.548
TRG_ENDOCYTIC_2 502 505 PF00928 0.551
TRG_ENDOCYTIC_2 519 522 PF00928 0.264
TRG_ENDOCYTIC_2 574 577 PF00928 0.300
TRG_ENDOCYTIC_2 622 625 PF00928 0.451
TRG_ENDOCYTIC_2 629 632 PF00928 0.373
TRG_ER_diArg_1 164 167 PF00400 0.472
TRG_ER_diArg_1 378 380 PF00400 0.565
TRG_ER_diArg_1 589 591 PF00400 0.386
TRG_ER_diArg_1 652 654 PF00400 0.407
TRG_ER_diArg_1 82 85 PF00400 0.531
TRG_ER_diArg_1 86 88 PF00400 0.500
TRG_Pf-PMV_PEXEL_1 589 593 PF00026 0.430
TRG_Pf-PMV_PEXEL_1 608 612 PF00026 0.331
TRG_Pf-PMV_PEXEL_1 708 712 PF00026 0.370

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 64% 97%
A0A3S5H4Y6 Leishmania donovani 38% 98%
A0A3S5H4Y9 Leishmania donovani 32% 80%
A0A3S7WT86 Leishmania donovani 35% 77%
A0A3S7WWA6 Leishmania donovani 64% 97%
A0A451EJD9 Leishmania donovani 57% 97%
A0A451EJF4 Leishmania donovani 40% 97%
A0A451EJF6 Leishmania donovani 41% 100%
A0A451EJF8 Leishmania donovani 36% 100%
A0A451EJF9 Leishmania donovani 41% 92%
A4H3A9 Leishmania braziliensis 40% 100%
A4H3B4 Leishmania braziliensis 39% 97%
A4H3B5 Leishmania braziliensis 41% 100%
A4H3B6 Leishmania braziliensis 38% 100%
A4H3B8 Leishmania braziliensis 39% 95%
A4H3B9 Leishmania braziliensis 36% 89%
A4H4W8 Leishmania braziliensis 90% 97%
A4HJ20 Leishmania braziliensis 38% 97%
A4HNK3 Leishmania braziliensis 95% 100%
A4HNK6 Leishmania braziliensis 94% 100%
A4HRL9 Leishmania infantum 38% 97%
A4HRM0 Leishmania infantum 38% 100%
A4HRM1 Leishmania infantum 40% 100%
A4HRS1 Leishmania infantum 38% 92%
A4HRS3 Leishmania infantum 32% 80%
A4HRS5 Leishmania infantum 36% 100%
A4HZM0 Leishmania infantum 57% 97%
A4I7C7 Leishmania infantum 58% 97%
A4IAQ2 Leishmania infantum 54% 97%
E9AC91 Leishmania major 37% 100%
E9AC92 Leishmania major 39% 100%
E9AC94 Leishmania major 31% 100%
E9AC95 Leishmania major 36% 100%
E9AC96 Leishmania major 39% 100%
E9AC98 Leishmania major 31% 100%
E9AEH8 Leishmania major 58% 100%
E9AHA6 Leishmania infantum 57% 97%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 41% 97%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 99%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 36% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 32% 80%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 68% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 59% 97%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 59% 97%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 65% 97%
Q4Q5T6 Leishmania major 58% 100%
Q4QCL8 Leishmania major 64% 100%
Q4QFJ3 Leishmania major 37% 77%
Q4QIG9 Leishmania major 64% 100%
Q7YXU9 Leishmania major 64% 100%
Q7YXV1 Leishmania major 64% 100%
Q7YXV2 Leishmania major 63% 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