LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase 4

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 4
Gene product:
phosphoglycan beta 1,3 galactosyltransferase 4 (fragment)
Species:
Leishmania donovani
UniProt:
A0A451EJD9_LEIDO
TriTrypDb:
LdBPK_360010.1 , LdCL_020005000 , LDHU3_31.5600
Length:
815

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

A0A451EJD9
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A451EJD9

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 0.402
CLV_C14_Caspase3-7 435 439 PF00656 0.360
CLV_C14_Caspase3-7 71 75 PF00656 0.630
CLV_C14_Caspase3-7 742 746 PF00656 0.316
CLV_NRD_NRD_1 106 108 PF00675 0.439
CLV_NRD_NRD_1 148 150 PF00675 0.689
CLV_NRD_NRD_1 284 286 PF00675 0.594
CLV_NRD_NRD_1 400 402 PF00675 0.677
CLV_NRD_NRD_1 490 492 PF00675 0.654
CLV_NRD_NRD_1 611 613 PF00675 0.559
CLV_NRD_NRD_1 93 95 PF00675 0.475
CLV_PCSK_KEX2_1 105 107 PF00082 0.465
CLV_PCSK_KEX2_1 284 286 PF00082 0.588
CLV_PCSK_KEX2_1 314 316 PF00082 0.543
CLV_PCSK_KEX2_1 400 402 PF00082 0.675
CLV_PCSK_KEX2_1 611 613 PF00082 0.548
CLV_PCSK_KEX2_1 673 675 PF00082 0.631
CLV_PCSK_KEX2_1 768 770 PF00082 0.584
CLV_PCSK_KEX2_1 93 95 PF00082 0.475
CLV_PCSK_PC1ET2_1 105 107 PF00082 0.417
CLV_PCSK_PC1ET2_1 314 316 PF00082 0.517
CLV_PCSK_PC1ET2_1 673 675 PF00082 0.576
CLV_PCSK_PC1ET2_1 768 770 PF00082 0.580
CLV_PCSK_PC7_1 101 107 PF00082 0.387
CLV_PCSK_PC7_1 89 95 PF00082 0.410
CLV_PCSK_SKI1_1 106 110 PF00082 0.261
CLV_PCSK_SKI1_1 401 405 PF00082 0.593
CLV_PCSK_SKI1_1 563 567 PF00082 0.544
CLV_PCSK_SKI1_1 732 736 PF00082 0.540
CLV_Separin_Metazoa 269 273 PF03568 0.337
DEG_APCC_DBOX_1 105 113 PF00400 0.434
DEG_Nend_UBRbox_1 1 4 PF02207 0.684
DEG_SCF_FBW7_1 452 459 PF00400 0.477
DOC_CKS1_1 453 458 PF01111 0.482
DOC_CYCLIN_yCln2_LP_2 249 255 PF00134 0.337
DOC_CYCLIN_yCln2_LP_2 450 456 PF00134 0.522
DOC_CYCLIN_yCln2_LP_2 632 638 PF00134 0.329
DOC_MAPK_DCC_7 572 581 PF00069 0.345
DOC_MAPK_gen_1 105 114 PF00069 0.537
DOC_MAPK_gen_1 298 307 PF00069 0.387
DOC_MAPK_HePTP_8 102 114 PF00069 0.440
DOC_MAPK_JIP1_4 298 304 PF00069 0.366
DOC_MAPK_MEF2A_6 105 114 PF00069 0.566
DOC_MAPK_MEF2A_6 480 487 PF00069 0.436
DOC_MAPK_MEF2A_6 572 581 PF00069 0.345
DOC_MAPK_MEF2A_6 658 667 PF00069 0.277
DOC_MAPK_NFAT4_5 480 488 PF00069 0.338
DOC_PP1_RVXF_1 514 521 PF00149 0.445
DOC_PP1_RVXF_1 588 594 PF00149 0.301
DOC_PP2B_LxvP_1 450 453 PF13499 0.520
DOC_PP2B_LxvP_1 543 546 PF13499 0.310
DOC_PP2B_LxvP_1 632 635 PF13499 0.309
DOC_PP4_FxxP_1 153 156 PF00568 0.431
DOC_USP7_MATH_1 148 152 PF00917 0.439
DOC_USP7_MATH_1 222 226 PF00917 0.477
DOC_USP7_MATH_1 241 245 PF00917 0.504
DOC_USP7_MATH_1 256 260 PF00917 0.353
DOC_USP7_MATH_1 37 41 PF00917 0.732
DOC_USP7_MATH_1 371 375 PF00917 0.385
DOC_USP7_MATH_1 692 696 PF00917 0.396
DOC_USP7_MATH_1 810 814 PF00917 0.297
DOC_USP7_MATH_1 92 96 PF00917 0.655
DOC_USP7_UBL2_3 492 496 PF12436 0.355
DOC_USP7_UBL2_3 732 736 PF12436 0.336
DOC_WW_Pin1_4 152 157 PF00397 0.464
DOC_WW_Pin1_4 24 29 PF00397 0.644
DOC_WW_Pin1_4 286 291 PF00397 0.415
DOC_WW_Pin1_4 418 423 PF00397 0.482
DOC_WW_Pin1_4 438 443 PF00397 0.429
DOC_WW_Pin1_4 452 457 PF00397 0.453
LIG_14-3-3_CanoR_1 149 157 PF00244 0.460
LIG_14-3-3_CanoR_1 169 177 PF00244 0.461
LIG_14-3-3_CanoR_1 323 327 PF00244 0.465
LIG_14-3-3_CanoR_1 427 431 PF00244 0.408
LIG_14-3-3_CanoR_1 433 437 PF00244 0.410
LIG_14-3-3_CanoR_1 480 484 PF00244 0.312
LIG_14-3-3_CanoR_1 563 570 PF00244 0.359
LIG_14-3-3_CanoR_1 658 664 PF00244 0.296
LIG_14-3-3_CanoR_1 677 684 PF00244 0.279
LIG_14-3-3_CanoR_1 802 807 PF00244 0.316
LIG_14-3-3_CanoR_1 93 100 PF00244 0.694
LIG_Actin_WH2_2 663 679 PF00022 0.314
LIG_Actin_WH2_2 753 770 PF00022 0.334
LIG_APCC_ABBA_1 159 164 PF00400 0.386
LIG_APCC_ABBA_1 621 626 PF00400 0.296
LIG_BIR_III_2 74 78 PF00653 0.622
LIG_BRCT_BRCA1_1 503 507 PF00533 0.277
LIG_Clathr_ClatBox_1 185 189 PF01394 0.376
LIG_deltaCOP1_diTrp_1 696 701 PF00928 0.275
LIG_EH1_1 77 85 PF00400 0.619
LIG_FHA_1 128 134 PF00498 0.472
LIG_FHA_1 195 201 PF00498 0.534
LIG_FHA_1 259 265 PF00498 0.483
LIG_FHA_1 338 344 PF00498 0.352
LIG_FHA_1 361 367 PF00498 0.359
LIG_FHA_1 438 444 PF00498 0.428
LIG_FHA_1 512 518 PF00498 0.249
LIG_FHA_1 564 570 PF00498 0.338
LIG_FHA_1 576 582 PF00498 0.378
LIG_FHA_1 618 624 PF00498 0.310
LIG_FHA_1 802 808 PF00498 0.323
LIG_FHA_2 163 169 PF00498 0.392
LIG_FHA_2 326 332 PF00498 0.409
LIG_FHA_2 370 376 PF00498 0.481
LIG_FHA_2 761 767 PF00498 0.352
LIG_FHA_2 803 809 PF00498 0.339
LIG_Integrin_RGD_1 777 779 PF01839 0.573
LIG_LIR_Apic_2 151 156 PF02991 0.434
LIG_LIR_Apic_2 416 422 PF02991 0.343
LIG_LIR_Apic_2 504 508 PF02991 0.421
LIG_LIR_Gen_1 155 161 PF02991 0.495
LIG_LIR_Gen_1 206 217 PF02991 0.411
LIG_LIR_Gen_1 482 488 PF02991 0.375
LIG_LIR_Gen_1 539 549 PF02991 0.444
LIG_LIR_Gen_1 595 601 PF02991 0.253
LIG_LIR_Gen_1 620 629 PF02991 0.292
LIG_LIR_Gen_1 642 649 PF02991 0.365
LIG_LIR_Gen_1 698 709 PF02991 0.374
LIG_LIR_Nem_3 155 160 PF02991 0.499
LIG_LIR_Nem_3 206 212 PF02991 0.413
LIG_LIR_Nem_3 325 329 PF02991 0.466
LIG_LIR_Nem_3 406 411 PF02991 0.372
LIG_LIR_Nem_3 482 487 PF02991 0.338
LIG_LIR_Nem_3 526 531 PF02991 0.396
LIG_LIR_Nem_3 539 545 PF02991 0.364
LIG_LIR_Nem_3 595 599 PF02991 0.265
LIG_LIR_Nem_3 620 624 PF02991 0.306
LIG_LIR_Nem_3 642 647 PF02991 0.386
LIG_LIR_Nem_3 698 704 PF02991 0.379
LIG_NRBOX 111 117 PF00104 0.297
LIG_NRBOX 627 633 PF00104 0.335
LIG_Pex14_1 592 596 PF04695 0.271
LIG_Pex14_2 153 157 PF04695 0.432
LIG_Pex14_2 721 725 PF04695 0.266
LIG_PTB_Apo_2 208 215 PF02174 0.424
LIG_PTB_Apo_2 638 645 PF02174 0.296
LIG_PTB_Phospho_1 208 214 PF10480 0.422
LIG_PTB_Phospho_1 638 644 PF10480 0.271
LIG_SH2_CRK 644 648 PF00017 0.292
LIG_SH2_CRK 708 712 PF00017 0.273
LIG_SH2_NCK_1 376 380 PF00017 0.422
LIG_SH2_NCK_1 708 712 PF00017 0.273
LIG_SH2_NCK_1 795 799 PF00017 0.320
LIG_SH2_SRC 795 798 PF00017 0.293
LIG_SH2_STAP1 214 218 PF00017 0.456
LIG_SH2_STAP1 523 527 PF00017 0.455
LIG_SH2_STAP1 636 640 PF00017 0.359
LIG_SH2_STAP1 644 648 PF00017 0.331
LIG_SH2_STAP1 795 799 PF00017 0.376
LIG_SH2_STAT3 280 283 PF00017 0.364
LIG_SH2_STAT5 347 350 PF00017 0.425
LIG_SH2_STAT5 397 400 PF00017 0.372
LIG_SH2_STAT5 464 467 PF00017 0.321
LIG_SH2_STAT5 525 528 PF00017 0.338
LIG_SH2_STAT5 533 536 PF00017 0.311
LIG_SH2_STAT5 542 545 PF00017 0.381
LIG_SH2_STAT5 548 551 PF00017 0.333
LIG_SH2_STAT5 636 639 PF00017 0.356
LIG_SH2_STAT5 678 681 PF00017 0.358
LIG_SH2_STAT5 715 718 PF00017 0.436
LIG_SH2_STAT5 720 723 PF00017 0.390
LIG_SH2_STAT5 784 787 PF00017 0.372
LIG_SH3_1 708 714 PF00018 0.269
LIG_SH3_3 284 290 PF00018 0.393
LIG_SH3_3 450 456 PF00018 0.494
LIG_SH3_3 526 532 PF00018 0.373
LIG_SH3_3 571 577 PF00018 0.384
LIG_SH3_3 686 692 PF00018 0.332
LIG_SH3_3 708 714 PF00018 0.302
LIG_SH3_4 492 499 PF00018 0.353
LIG_SUMO_SIM_anti_2 626 631 PF11976 0.307
LIG_TRAF2_1 680 683 PF00917 0.262
LIG_TYR_ITIM 327 332 PF00017 0.442
LIG_WRC_WIRS_1 618 623 PF05994 0.276
MOD_CDC14_SPxK_1 27 30 PF00782 0.626
MOD_CDK_SPxK_1 24 30 PF00069 0.626
MOD_CDK_SPxxK_3 286 293 PF00069 0.388
MOD_CK1_1 127 133 PF00069 0.437
MOD_CK1_1 140 146 PF00069 0.452
MOD_CK1_1 155 161 PF00069 0.446
MOD_CK1_1 289 295 PF00069 0.452
MOD_CK1_1 356 362 PF00069 0.517
MOD_CK1_1 429 435 PF00069 0.392
MOD_CK1_1 65 71 PF00069 0.682
MOD_CK1_1 695 701 PF00069 0.339
MOD_CK2_1 140 146 PF00069 0.442
MOD_CK2_1 162 168 PF00069 0.420
MOD_CK2_1 325 331 PF00069 0.406
MOD_CK2_1 33 39 PF00069 0.675
MOD_CK2_1 369 375 PF00069 0.499
MOD_CK2_1 53 59 PF00069 0.652
MOD_CK2_1 677 683 PF00069 0.316
MOD_CK2_1 802 808 PF00069 0.298
MOD_GlcNHglycan 215 218 PF01048 0.698
MOD_GlcNHglycan 243 246 PF01048 0.695
MOD_GlcNHglycan 35 38 PF01048 0.530
MOD_GlcNHglycan 39 42 PF01048 0.524
MOD_GlcNHglycan 446 449 PF01048 0.641
MOD_GlcNHglycan 468 471 PF01048 0.634
MOD_GlcNHglycan 65 68 PF01048 0.473
MOD_GlcNHglycan 740 744 PF01048 0.537
MOD_GlcNHglycan 812 815 PF01048 0.544
MOD_GlcNHglycan 94 97 PF01048 0.467
MOD_GSK3_1 124 131 PF00069 0.495
MOD_GSK3_1 137 144 PF00069 0.486
MOD_GSK3_1 148 155 PF00069 0.516
MOD_GSK3_1 177 184 PF00069 0.449
MOD_GSK3_1 222 229 PF00069 0.506
MOD_GSK3_1 235 242 PF00069 0.430
MOD_GSK3_1 33 40 PF00069 0.728
MOD_GSK3_1 353 360 PF00069 0.484
MOD_GSK3_1 444 451 PF00069 0.425
MOD_GSK3_1 452 459 PF00069 0.372
MOD_GSK3_1 62 69 PF00069 0.667
MOD_GSK3_1 639 646 PF00069 0.302
MOD_GSK3_1 695 702 PF00069 0.343
MOD_GSK3_1 755 762 PF00069 0.363
MOD_N-GLC_1 181 186 PF02516 0.603
MOD_N-GLC_1 210 215 PF02516 0.639
MOD_N-GLC_1 337 342 PF02516 0.541
MOD_N-GLC_1 563 568 PF02516 0.546
MOD_N-GLC_1 746 751 PF02516 0.570
MOD_N-GLC_1 771 776 PF02516 0.527
MOD_N-GLC_1 802 807 PF02516 0.511
MOD_NEK2_1 170 175 PF00069 0.487
MOD_NEK2_1 240 245 PF00069 0.461
MOD_NEK2_1 565 570 PF00069 0.355
MOD_NEK2_1 639 644 PF00069 0.294
MOD_NEK2_2 194 199 PF00069 0.531
MOD_PIKK_1 124 130 PF00454 0.462
MOD_PIKK_1 132 138 PF00454 0.462
MOD_PIKK_1 170 176 PF00454 0.415
MOD_PIKK_1 511 517 PF00454 0.446
MOD_PIKK_1 746 752 PF00454 0.354
MOD_PIKK_1 755 761 PF00454 0.343
MOD_PIKK_1 78 84 PF00454 0.635
MOD_PK_1 235 241 PF00069 0.411
MOD_PKA_1 491 497 PF00069 0.478
MOD_PKA_2 13 19 PF00069 0.699
MOD_PKA_2 141 147 PF00069 0.473
MOD_PKA_2 148 154 PF00069 0.455
MOD_PKA_2 168 174 PF00069 0.460
MOD_PKA_2 223 229 PF00069 0.499
MOD_PKA_2 292 298 PF00069 0.467
MOD_PKA_2 322 328 PF00069 0.467
MOD_PKA_2 353 359 PF00069 0.417
MOD_PKA_2 426 432 PF00069 0.419
MOD_PKA_2 479 485 PF00069 0.371
MOD_PKA_2 801 807 PF00069 0.334
MOD_PKA_2 92 98 PF00069 0.683
MOD_PKB_1 800 808 PF00069 0.304
MOD_Plk_1 181 187 PF00069 0.398
MOD_Plk_1 203 209 PF00069 0.422
MOD_Plk_1 210 216 PF00069 0.417
MOD_Plk_1 538 544 PF00069 0.320
MOD_Plk_1 695 701 PF00069 0.375
MOD_Plk_1 739 745 PF00069 0.315
MOD_Plk_1 771 777 PF00069 0.332
MOD_Plk_1 802 808 PF00069 0.317
MOD_Plk_2-3 353 359 PF00069 0.415
MOD_Plk_4 181 187 PF00069 0.434
MOD_Plk_4 235 241 PF00069 0.431
MOD_Plk_4 322 328 PF00069 0.409
MOD_Plk_4 426 432 PF00069 0.382
MOD_Plk_4 479 485 PF00069 0.324
MOD_Plk_4 538 544 PF00069 0.320
MOD_Plk_4 634 640 PF00069 0.325
MOD_Plk_4 643 649 PF00069 0.305
MOD_Plk_4 700 706 PF00069 0.412
MOD_Plk_4 771 777 PF00069 0.344
MOD_Plk_4 802 808 PF00069 0.333
MOD_ProDKin_1 152 158 PF00069 0.462
MOD_ProDKin_1 24 30 PF00069 0.644
MOD_ProDKin_1 286 292 PF00069 0.418
MOD_ProDKin_1 418 424 PF00069 0.486
MOD_ProDKin_1 438 444 PF00069 0.425
MOD_ProDKin_1 452 458 PF00069 0.448
MOD_SUMO_for_1 721 724 PF00179 0.266
MOD_SUMO_rev_2 486 494 PF00179 0.350
TRG_DiLeu_BaEn_1 181 186 PF01217 0.393
TRG_DiLeu_BaLyEn_6 104 109 PF01217 0.529
TRG_DiLeu_BaLyEn_6 609 614 PF01217 0.345
TRG_ENDOCYTIC_2 329 332 PF00928 0.473
TRG_ENDOCYTIC_2 525 528 PF00928 0.467
TRG_ENDOCYTIC_2 542 545 PF00928 0.437
TRG_ENDOCYTIC_2 636 639 PF00928 0.370
TRG_ENDOCYTIC_2 644 647 PF00928 0.390
TRG_ER_diArg_1 106 108 PF00400 0.638
TRG_ER_diArg_1 284 286 PF00400 0.391
TRG_ER_diArg_1 400 402 PF00400 0.470
TRG_ER_diArg_1 611 613 PF00400 0.343
TRG_ER_diArg_1 799 802 PF00400 0.318
TRG_ER_diArg_1 92 94 PF00400 0.669
TRG_NLS_Bipartite_1 93 109 PF00514 0.565
TRG_NLS_MonoExtC_3 495 501 PF00514 0.333
TRG_NLS_MonoExtN_4 493 500 PF00514 0.370
TRG_Pf-PMV_PEXEL_1 199 203 PF00026 0.612
TRG_Pf-PMV_PEXEL_1 611 615 PF00026 0.576

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 81% 100%
A0A3S5H4Y6 Leishmania donovani 40% 100%
A0A3S5H4Y9 Leishmania donovani 31% 100%
A0A3S7WT86 Leishmania donovani 37% 79%
A0A3S7WWA6 Leishmania donovani 81% 100%
A0A451EJF4 Leishmania donovani 38% 100%
A0A451EJF6 Leishmania donovani 41% 100%
A0A451EJF8 Leishmania donovani 37% 100%
A0A451EJF9 Leishmania donovani 41% 94%
A4H3A9 Leishmania braziliensis 40% 100%
A4H3B4 Leishmania braziliensis 40% 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 41% 100%
A4HRM0 Leishmania infantum 39% 100%
A4HRM1 Leishmania infantum 42% 98%
A4HRS1 Leishmania infantum 42% 100%
A4HRS3 Leishmania infantum 31% 100%
A4HRS5 Leishmania infantum 39% 100%
A4HZM0 Leishmania infantum 91% 100%
A4I7C7 Leishmania infantum 92% 100%
A4IAQ2 Leishmania infantum 89% 100%
E9AC91 Leishmania major 41% 100%
E9AC92 Leishmania major 41% 100%
E9AC94 Leishmania major 31% 69%
E9AC95 Leishmania major 38% 100%
E9AC96 Leishmania major 41% 100%
E9AC98 Leishmania major 32% 100%
E9AEH8 Leishmania major 82% 100%
E9AHA6 Leishmania infantum 97% 100%
E9AIP8 Leishmania braziliensis 57% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 100%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 100%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 38% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 33% 82%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 80% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 80% 100%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
Q4Q5T6 Leishmania major 82% 100%
Q4QCL8 Leishmania major 73% 100%
Q4QFJ3 Leishmania major 37% 79%
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