LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase 2

Quick info Annotations Function or PPIs Localization Phosphorylation 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 4
Species:
Leishmania infantum
UniProt:
A4HZM0_LEIIN
TriTrypDb:
LINF_310041000 *
Length:
816

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

Phosphorylation

Amastigote: 27

Expansion

Sequence features

A4HZM0
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HZM0

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_Caspase3-7 180 184 PF00656 0.410
CLV_C14_Caspase3-7 435 439 PF00656 0.333
CLV_C14_Caspase3-7 743 747 PF00656 0.298
CLV_NRD_NRD_1 149 151 PF00675 0.631
CLV_NRD_NRD_1 284 286 PF00675 0.593
CLV_NRD_NRD_1 400 402 PF00675 0.602
CLV_NRD_NRD_1 490 492 PF00675 0.595
CLV_NRD_NRD_1 612 614 PF00675 0.519
CLV_NRD_NRD_1 93 95 PF00675 0.435
CLV_PCSK_KEX2_1 106 108 PF00082 0.403
CLV_PCSK_KEX2_1 138 140 PF00082 0.662
CLV_PCSK_KEX2_1 149 151 PF00082 0.604
CLV_PCSK_KEX2_1 284 286 PF00082 0.587
CLV_PCSK_KEX2_1 314 316 PF00082 0.521
CLV_PCSK_KEX2_1 400 402 PF00082 0.601
CLV_PCSK_KEX2_1 612 614 PF00082 0.511
CLV_PCSK_KEX2_1 674 676 PF00082 0.586
CLV_PCSK_KEX2_1 769 771 PF00082 0.546
CLV_PCSK_KEX2_1 93 95 PF00082 0.435
CLV_PCSK_PC1ET2_1 106 108 PF00082 0.377
CLV_PCSK_PC1ET2_1 138 140 PF00082 0.637
CLV_PCSK_PC1ET2_1 314 316 PF00082 0.503
CLV_PCSK_PC1ET2_1 674 676 PF00082 0.545
CLV_PCSK_PC1ET2_1 769 771 PF00082 0.543
CLV_PCSK_SKI1_1 106 110 PF00082 0.241
CLV_PCSK_SKI1_1 401 405 PF00082 0.549
CLV_PCSK_SKI1_1 563 567 PF00082 0.555
CLV_PCSK_SKI1_1 733 737 PF00082 0.514
CLV_Separin_Metazoa 269 273 PF03568 0.318
DEG_Nend_UBRbox_1 1 4 PF02207 0.657
DEG_SCF_FBW7_1 452 459 PF00400 0.414
DEG_SPOP_SBC_1 239 243 PF00917 0.347
DOC_CKS1_1 453 458 PF01111 0.413
DOC_CYCLIN_yCln2_LP_2 249 255 PF00134 0.321
DOC_CYCLIN_yCln2_LP_2 450 456 PF00134 0.447
DOC_CYCLIN_yCln2_LP_2 633 639 PF00134 0.312
DOC_MAPK_DCC_7 572 581 PF00069 0.329
DOC_MAPK_gen_1 106 114 PF00069 0.490
DOC_MAPK_gen_1 298 307 PF00069 0.353
DOC_MAPK_gen_1 496 503 PF00069 0.341
DOC_MAPK_HePTP_8 104 116 PF00069 0.426
DOC_MAPK_JIP1_4 298 304 PF00069 0.341
DOC_MAPK_MEF2A_6 106 114 PF00069 0.517
DOC_MAPK_MEF2A_6 480 487 PF00069 0.374
DOC_MAPK_MEF2A_6 572 581 PF00069 0.320
DOC_MAPK_MEF2A_6 628 635 PF00069 0.329
DOC_MAPK_MEF2A_6 659 668 PF00069 0.270
DOC_MAPK_NFAT4_5 480 488 PF00069 0.308
DOC_MAPK_NFAT4_5 628 636 PF00069 0.285
DOC_PP1_RVXF_1 500 506 PF00149 0.351
DOC_PP1_RVXF_1 514 521 PF00149 0.367
DOC_PP1_RVXF_1 588 594 PF00149 0.277
DOC_PP2B_LxvP_1 450 453 PF13499 0.452
DOC_PP2B_LxvP_1 543 546 PF13499 0.283
DOC_PP2B_LxvP_1 633 636 PF13499 0.301
DOC_PP4_FxxP_1 153 156 PF00568 0.409
DOC_SPAK_OSR1_1 107 111 PF12202 0.409
DOC_SPAK_OSR1_1 128 132 PF12202 0.362
DOC_USP7_MATH_1 148 152 PF00917 0.410
DOC_USP7_MATH_1 222 226 PF00917 0.451
DOC_USP7_MATH_1 256 260 PF00917 0.324
DOC_USP7_MATH_1 37 41 PF00917 0.665
DOC_USP7_MATH_1 371 375 PF00917 0.366
DOC_USP7_MATH_1 693 697 PF00917 0.380
DOC_USP7_MATH_1 811 815 PF00917 0.278
DOC_USP7_MATH_1 92 96 PF00917 0.628
DOC_USP7_UBL2_3 492 496 PF12436 0.329
DOC_USP7_UBL2_3 723 727 PF12436 0.293
DOC_USP7_UBL2_3 733 737 PF12436 0.311
DOC_WW_Pin1_4 152 157 PF00397 0.434
DOC_WW_Pin1_4 24 29 PF00397 0.627
DOC_WW_Pin1_4 286 291 PF00397 0.402
DOC_WW_Pin1_4 418 423 PF00397 0.412
DOC_WW_Pin1_4 438 443 PF00397 0.385
DOC_WW_Pin1_4 452 457 PF00397 0.395
LIG_14-3-3_CanoR_1 149 157 PF00244 0.426
LIG_14-3-3_CanoR_1 169 177 PF00244 0.433
LIG_14-3-3_CanoR_1 427 431 PF00244 0.429
LIG_14-3-3_CanoR_1 480 484 PF00244 0.282
LIG_14-3-3_CanoR_1 502 506 PF00244 0.307
LIG_14-3-3_CanoR_1 563 570 PF00244 0.364
LIG_14-3-3_CanoR_1 659 665 PF00244 0.281
LIG_14-3-3_CanoR_1 678 685 PF00244 0.273
LIG_14-3-3_CanoR_1 803 808 PF00244 0.303
LIG_14-3-3_CanoR_1 93 100 PF00244 0.639
LIG_Actin_WH2_2 664 680 PF00022 0.298
LIG_Actin_WH2_2 754 771 PF00022 0.310
LIG_APCC_ABBA_1 159 164 PF00400 0.360
LIG_BRCT_BRCA1_1 84 88 PF00533 0.610
LIG_Clathr_ClatBox_1 185 189 PF01394 0.401
LIG_EH_1 619 623 PF12763 0.332
LIG_FHA_1 128 134 PF00498 0.427
LIG_FHA_1 180 186 PF00498 0.437
LIG_FHA_1 195 201 PF00498 0.478
LIG_FHA_1 259 265 PF00498 0.415
LIG_FHA_1 338 344 PF00498 0.315
LIG_FHA_1 361 367 PF00498 0.350
LIG_FHA_1 426 432 PF00498 0.341
LIG_FHA_1 438 444 PF00498 0.417
LIG_FHA_1 512 518 PF00498 0.314
LIG_FHA_1 564 570 PF00498 0.318
LIG_FHA_1 576 582 PF00498 0.369
LIG_FHA_1 781 787 PF00498 0.311
LIG_FHA_1 803 809 PF00498 0.310
LIG_FHA_2 163 169 PF00498 0.371
LIG_FHA_2 370 376 PF00498 0.432
LIG_FHA_2 762 768 PF00498 0.322
LIG_FHA_2 804 810 PF00498 0.320
LIG_Integrin_RGD_1 778 780 PF01839 0.536
LIG_LIR_Apic_2 151 156 PF02991 0.409
LIG_LIR_Apic_2 416 422 PF02991 0.321
LIG_LIR_Apic_2 504 508 PF02991 0.376
LIG_LIR_Gen_1 155 161 PF02991 0.440
LIG_LIR_Gen_1 206 217 PF02991 0.383
LIG_LIR_Gen_1 482 488 PF02991 0.336
LIG_LIR_Gen_1 539 549 PF02991 0.314
LIG_LIR_Gen_1 634 645 PF02991 0.312
LIG_LIR_Gen_1 699 710 PF02991 0.328
LIG_LIR_Nem_3 155 160 PF02991 0.444
LIG_LIR_Nem_3 206 212 PF02991 0.388
LIG_LIR_Nem_3 325 329 PF02991 0.399
LIG_LIR_Nem_3 406 411 PF02991 0.344
LIG_LIR_Nem_3 482 487 PF02991 0.353
LIG_LIR_Nem_3 526 531 PF02991 0.354
LIG_LIR_Nem_3 539 545 PF02991 0.336
LIG_LIR_Nem_3 643 648 PF02991 0.417
LIG_LIR_Nem_3 699 705 PF02991 0.332
LIG_NRBOX 111 117 PF00104 0.273
LIG_NRBOX 628 634 PF00104 0.317
LIG_Pex14_2 153 157 PF04695 0.412
LIG_Pex14_2 722 726 PF04695 0.252
LIG_PTB_Apo_2 208 215 PF02174 0.388
LIG_PTB_Apo_2 639 646 PF02174 0.286
LIG_PTB_Phospho_1 208 214 PF10480 0.386
LIG_PTB_Phospho_1 639 645 PF10480 0.269
LIG_SH2_CRK 645 649 PF00017 0.279
LIG_SH2_CRK 709 713 PF00017 0.261
LIG_SH2_GRB2like 595 598 PF00017 0.294
LIG_SH2_NCK_1 376 380 PF00017 0.366
LIG_SH2_NCK_1 709 713 PF00017 0.261
LIG_SH2_NCK_1 796 800 PF00017 0.292
LIG_SH2_SRC 595 598 PF00017 0.287
LIG_SH2_SRC 796 799 PF00017 0.275
LIG_SH2_STAP1 214 218 PF00017 0.405
LIG_SH2_STAP1 523 527 PF00017 0.389
LIG_SH2_STAP1 637 641 PF00017 0.330
LIG_SH2_STAP1 645 649 PF00017 0.306
LIG_SH2_STAP1 796 800 PF00017 0.331
LIG_SH2_STAT3 280 283 PF00017 0.353
LIG_SH2_STAT5 347 350 PF00017 0.364
LIG_SH2_STAT5 397 400 PF00017 0.331
LIG_SH2_STAT5 464 467 PF00017 0.298
LIG_SH2_STAT5 525 528 PF00017 0.321
LIG_SH2_STAT5 533 536 PF00017 0.296
LIG_SH2_STAT5 542 545 PF00017 0.293
LIG_SH2_STAT5 548 551 PF00017 0.286
LIG_SH2_STAT5 637 640 PF00017 0.328
LIG_SH2_STAT5 679 682 PF00017 0.394
LIG_SH2_STAT5 716 719 PF00017 0.364
LIG_SH2_STAT5 721 724 PF00017 0.337
LIG_SH2_STAT5 785 788 PF00017 0.334
LIG_SH3_1 709 715 PF00018 0.257
LIG_SH3_3 284 290 PF00018 0.389
LIG_SH3_3 450 456 PF00018 0.428
LIG_SH3_3 526 532 PF00018 0.401
LIG_SH3_3 571 577 PF00018 0.354
LIG_SH3_3 615 621 PF00018 0.301
LIG_SH3_3 687 693 PF00018 0.321
LIG_SH3_3 709 715 PF00018 0.279
LIG_SH3_4 492 499 PF00018 0.332
LIG_SUMO_SIM_par_1 628 634 PF11976 0.311
MOD_CDC14_SPxK_1 27 30 PF00782 0.619
MOD_CDK_SPxK_1 24 30 PF00069 0.622
MOD_CDK_SPxxK_3 286 293 PF00069 0.379
MOD_CK1_1 127 133 PF00069 0.396
MOD_CK1_1 155 161 PF00069 0.410
MOD_CK1_1 241 247 PF00069 0.346
MOD_CK1_1 289 295 PF00069 0.441
MOD_CK1_1 356 362 PF00069 0.467
MOD_CK1_1 393 399 PF00069 0.299
MOD_CK1_1 429 435 PF00069 0.350
MOD_CK1_1 65 71 PF00069 0.668
MOD_CK1_1 696 702 PF00069 0.308
MOD_CK2_1 162 168 PF00069 0.387
MOD_CK2_1 33 39 PF00069 0.640
MOD_CK2_1 369 375 PF00069 0.444
MOD_CK2_1 53 59 PF00069 0.637
MOD_CK2_1 678 684 PF00069 0.335
MOD_CK2_1 803 809 PF00069 0.293
MOD_GlcNHglycan 215 218 PF01048 0.635
MOD_GlcNHglycan 243 246 PF01048 0.669
MOD_GlcNHglycan 35 38 PF01048 0.531
MOD_GlcNHglycan 39 42 PF01048 0.524
MOD_GlcNHglycan 392 395 PF01048 0.524
MOD_GlcNHglycan 446 449 PF01048 0.595
MOD_GlcNHglycan 468 471 PF01048 0.567
MOD_GlcNHglycan 59 63 PF01048 0.475
MOD_GlcNHglycan 65 68 PF01048 0.463
MOD_GlcNHglycan 741 745 PF01048 0.513
MOD_GlcNHglycan 813 816 PF01048 0.513
MOD_GlcNHglycan 94 97 PF01048 0.431
MOD_GSK3_1 137 144 PF00069 0.441
MOD_GSK3_1 148 155 PF00069 0.454
MOD_GSK3_1 177 184 PF00069 0.457
MOD_GSK3_1 222 229 PF00069 0.469
MOD_GSK3_1 33 40 PF00069 0.735
MOD_GSK3_1 353 360 PF00069 0.436
MOD_GSK3_1 425 432 PF00069 0.378
MOD_GSK3_1 444 451 PF00069 0.385
MOD_GSK3_1 452 459 PF00069 0.341
MOD_GSK3_1 54 61 PF00069 0.677
MOD_GSK3_1 62 69 PF00069 0.692
MOD_GSK3_1 631 638 PF00069 0.296
MOD_GSK3_1 640 647 PF00069 0.290
MOD_GSK3_1 696 703 PF00069 0.348
MOD_GSK3_1 756 763 PF00069 0.328
MOD_N-GLC_1 210 215 PF02516 0.599
MOD_N-GLC_1 230 235 PF02516 0.608
MOD_N-GLC_1 337 342 PF02516 0.510
MOD_N-GLC_1 563 568 PF02516 0.525
MOD_N-GLC_1 747 752 PF02516 0.536
MOD_N-GLC_1 772 777 PF02516 0.502
MOD_N-GLC_1 803 808 PF02516 0.500
MOD_NEK2_1 170 175 PF00069 0.463
MOD_NEK2_1 240 245 PF00069 0.432
MOD_NEK2_1 501 506 PF00069 0.352
MOD_NEK2_1 565 570 PF00069 0.360
MOD_NEK2_1 622 627 PF00069 0.392
MOD_NEK2_1 631 636 PF00069 0.330
MOD_NEK2_1 640 645 PF00069 0.286
MOD_NEK2_2 194 199 PF00069 0.482
MOD_PIKK_1 132 138 PF00454 0.426
MOD_PIKK_1 170 176 PF00454 0.423
MOD_PIKK_1 511 517 PF00454 0.377
MOD_PIKK_1 747 753 PF00454 0.324
MOD_PIKK_1 756 762 PF00454 0.313
MOD_PIKK_1 99 105 PF00454 0.578
MOD_PKA_1 491 497 PF00069 0.414
MOD_PKA_2 127 133 PF00069 0.371
MOD_PKA_2 13 19 PF00069 0.656
MOD_PKA_2 141 147 PF00069 0.434
MOD_PKA_2 148 154 PF00069 0.421
MOD_PKA_2 168 174 PF00069 0.420
MOD_PKA_2 223 229 PF00069 0.465
MOD_PKA_2 292 298 PF00069 0.436
MOD_PKA_2 353 359 PF00069 0.389
MOD_PKA_2 426 432 PF00069 0.373
MOD_PKA_2 479 485 PF00069 0.322
MOD_PKA_2 501 507 PF00069 0.347
MOD_PKA_2 802 808 PF00069 0.316
MOD_PKA_2 92 98 PF00069 0.623
MOD_PKB_1 801 809 PF00069 0.297
MOD_Plk_1 203 209 PF00069 0.401
MOD_Plk_1 210 216 PF00069 0.383
MOD_Plk_1 230 236 PF00069 0.406
MOD_Plk_1 538 544 PF00069 0.291
MOD_Plk_1 740 746 PF00069 0.302
MOD_Plk_1 772 778 PF00069 0.304
MOD_Plk_1 803 809 PF00069 0.306
MOD_Plk_2-3 353 359 PF00069 0.388
MOD_Plk_4 181 187 PF00069 0.440
MOD_Plk_4 393 399 PF00069 0.322
MOD_Plk_4 426 432 PF00069 0.418
MOD_Plk_4 479 485 PF00069 0.291
MOD_Plk_4 538 544 PF00069 0.291
MOD_Plk_4 635 641 PF00069 0.356
MOD_Plk_4 644 650 PF00069 0.301
MOD_Plk_4 701 707 PF00069 0.353
MOD_Plk_4 772 778 PF00069 0.312
MOD_Plk_4 803 809 PF00069 0.317
MOD_ProDKin_1 152 158 PF00069 0.430
MOD_ProDKin_1 24 30 PF00069 0.627
MOD_ProDKin_1 286 292 PF00069 0.403
MOD_ProDKin_1 418 424 PF00069 0.416
MOD_ProDKin_1 438 444 PF00069 0.382
MOD_ProDKin_1 452 458 PF00069 0.392
MOD_SUMO_for_1 722 725 PF00179 0.253
MOD_SUMO_rev_2 486 494 PF00179 0.326
TRG_DiLeu_BaEn_1 181 186 PF01217 0.406
TRG_DiLeu_BaLyEn_6 610 615 PF01217 0.308
TRG_DiLeu_BaLyEn_6 625 630 PF01217 0.284
TRG_ENDOCYTIC_2 329 332 PF00928 0.405
TRG_ENDOCYTIC_2 525 528 PF00928 0.400
TRG_ENDOCYTIC_2 542 545 PF00928 0.286
TRG_ENDOCYTIC_2 637 640 PF00928 0.337
TRG_ENDOCYTIC_2 645 648 PF00928 0.348
TRG_ER_diArg_1 284 286 PF00400 0.388
TRG_ER_diArg_1 400 402 PF00400 0.398
TRG_ER_diArg_1 612 614 PF00400 0.306
TRG_ER_diArg_1 800 803 PF00400 0.300
TRG_ER_diArg_1 92 94 PF00400 0.631
TRG_NLS_MonoExtN_4 493 500 PF00514 0.344
TRG_Pf-PMV_PEXEL_1 199 203 PF00026 0.605
TRG_Pf-PMV_PEXEL_1 612 616 PF00026 0.536

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 86% 100%
A0A3S5H4Y6 Leishmania donovani 37% 100%
A0A3S5H4Y9 Leishmania donovani 31% 82%
A0A3S7WT86 Leishmania donovani 37% 79%
A0A3S7WWA6 Leishmania donovani 86% 100%
A0A451EJD9 Leishmania donovani 91% 100%
A0A451EJF4 Leishmania donovani 38% 100%
A0A451EJF6 Leishmania donovani 40% 100%
A0A451EJF8 Leishmania donovani 38% 100%
A0A451EJF9 Leishmania donovani 40% 95%
A4H3A9 Leishmania braziliensis 40% 100%
A4H3B4 Leishmania braziliensis 41% 100%
A4H3B6 Leishmania braziliensis 39% 100%
A4H3B8 Leishmania braziliensis 42% 100%
A4H3B9 Leishmania braziliensis 34% 100%
A4H4W8 Leishmania braziliensis 57% 100%
A4HJ20 Leishmania braziliensis 39% 100%
A4HNK3 Leishmania braziliensis 64% 100%
A4HNK6 Leishmania braziliensis 57% 100%
A4HRL9 Leishmania infantum 38% 100%
A4HRM0 Leishmania infantum 38% 100%
A4HRM1 Leishmania infantum 40% 100%
A4HRS1 Leishmania infantum 40% 95%
A4HRS3 Leishmania infantum 31% 82%
A4HRS5 Leishmania infantum 37% 100%
A4I7C7 Leishmania infantum 97% 100%
A4IAQ2 Leishmania infantum 87% 100%
E9AC91 Leishmania major 41% 100%
E9AC92 Leishmania major 41% 100%
E9AC94 Leishmania major 32% 69%
E9AC95 Leishmania major 37% 100%
E9AC96 Leishmania major 41% 100%
E9AC98 Leishmania major 32% 100%
E9AEH8 Leishmania major 84% 100%
E9AHA6 Leishmania infantum 91% 100%
E9AIP8 Leishmania braziliensis 57% 99%
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) 30% 100%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 81% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 81% 100%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
Q4Q5T6 Leishmania major 84% 100%
Q4QCL8 Leishmania major 73% 100%
Q4QFJ3 Leishmania major 36% 100%
Q4QIG9 Leishmania major 74% 100%
Q7YXU9 Leishmania major 72% 100%
Q7YXV1 Leishmania major 74% 100%
Q7YXV2 Leishmania major 73% 100%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2024 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS