LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase-like protein

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-like protein
Gene product:
phosphoglycan beta 1,3 galactosyltransferase-like protein
Species:
Leishmania mexicana
UniProt:
E9AJI5_LEIMU
TriTrypDb:
LmxM.02.0200 *
Length:
773

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. 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: 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 13
GO:0031090 organelle membrane 3 13
GO:0098588 bounding membrane of organelle 4 13

Expansion

Sequence features

E9AJI5
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AJI5

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 13

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 196 200 PF00656 0.421
CLV_NRD_NRD_1 11 13 PF00675 0.501
CLV_NRD_NRD_1 15 17 PF00675 0.519
CLV_NRD_NRD_1 332 334 PF00675 0.740
CLV_NRD_NRD_1 337 339 PF00675 0.719
CLV_NRD_NRD_1 416 418 PF00675 0.733
CLV_NRD_NRD_1 494 496 PF00675 0.670
CLV_NRD_NRD_1 56 58 PF00675 0.634
CLV_NRD_NRD_1 566 568 PF00675 0.622
CLV_NRD_NRD_1 580 582 PF00675 0.554
CLV_NRD_NRD_1 596 598 PF00675 0.548
CLV_NRD_NRD_1 601 603 PF00675 0.542
CLV_NRD_NRD_1 734 736 PF00675 0.558
CLV_PCSK_KEX2_1 10 12 PF00082 0.514
CLV_PCSK_KEX2_1 17 19 PF00082 0.523
CLV_PCSK_KEX2_1 283 285 PF00082 0.696
CLV_PCSK_KEX2_1 331 333 PF00082 0.746
CLV_PCSK_KEX2_1 337 339 PF00082 0.717
CLV_PCSK_KEX2_1 416 418 PF00082 0.662
CLV_PCSK_KEX2_1 44 46 PF00082 0.641
CLV_PCSK_KEX2_1 493 495 PF00082 0.687
CLV_PCSK_KEX2_1 56 58 PF00082 0.603
CLV_PCSK_KEX2_1 566 568 PF00082 0.611
CLV_PCSK_KEX2_1 579 581 PF00082 0.622
CLV_PCSK_KEX2_1 595 597 PF00082 0.561
CLV_PCSK_KEX2_1 601 603 PF00082 0.541
CLV_PCSK_KEX2_1 734 736 PF00082 0.597
CLV_PCSK_PC1ET2_1 17 19 PF00082 0.469
CLV_PCSK_PC1ET2_1 283 285 PF00082 0.687
CLV_PCSK_PC1ET2_1 44 46 PF00082 0.617
CLV_PCSK_PC1ET2_1 595 597 PF00082 0.527
CLV_PCSK_PC7_1 333 339 PF00082 0.601
CLV_PCSK_PC7_1 597 603 PF00082 0.504
CLV_PCSK_PC7_1 7 13 PF00082 0.468
CLV_PCSK_PC7_1 730 736 PF00082 0.566
CLV_PCSK_SKI1_1 225 229 PF00082 0.619
CLV_PCSK_SKI1_1 298 302 PF00082 0.609
CLV_PCSK_SKI1_1 333 337 PF00082 0.657
CLV_PCSK_SKI1_1 41 45 PF00082 0.595
CLV_PCSK_SKI1_1 441 445 PF00082 0.643
CLV_PCSK_SKI1_1 596 600 PF00082 0.549
CLV_PCSK_SKI1_1 602 606 PF00082 0.531
CLV_PCSK_SKI1_1 687 691 PF00082 0.605
DEG_APCC_DBOX_1 578 586 PF00400 0.355
DEG_Nend_UBRbox_1 1 4 PF02207 0.641
DEG_SCF_FBW7_1 377 384 PF00400 0.536
DEG_SPOP_SBC_1 317 321 PF00917 0.414
DOC_ANK_TNKS_1 493 500 PF00023 0.437
DOC_CKS1_1 150 155 PF01111 0.397
DOC_CKS1_1 207 212 PF01111 0.400
DOC_CKS1_1 268 273 PF01111 0.496
DOC_CKS1_1 275 280 PF01111 0.502
DOC_CKS1_1 378 383 PF01111 0.543
DOC_CYCLIN_yCln2_LP_2 375 381 PF00134 0.575
DOC_MAPK_gen_1 16 22 PF00069 0.728
DOC_MAPK_gen_1 576 584 PF00069 0.392
DOC_MAPK_gen_1 734 742 PF00069 0.330
DOC_MAPK_JIP1_4 18 24 PF00069 0.625
DOC_MAPK_MEF2A_6 159 167 PF00069 0.414
DOC_MAPK_MEF2A_6 16 24 PF00069 0.745
DOC_MAPK_MEF2A_6 405 412 PF00069 0.497
DOC_MAPK_MEF2A_6 429 438 PF00069 0.386
DOC_MAPK_MEF2A_6 90 99 PF00069 0.421
DOC_MAPK_RevD_3 324 338 PF00069 0.364
DOC_PP1_RVXF_1 403 410 PF00149 0.391
DOC_PP1_RVXF_1 439 446 PF00149 0.486
DOC_PP1_RVXF_1 599 606 PF00149 0.308
DOC_PP2B_LxvP_1 375 378 PF13499 0.574
DOC_PP4_FxxP_1 383 386 PF00568 0.445
DOC_USP7_MATH_1 166 170 PF00917 0.422
DOC_USP7_MATH_1 231 235 PF00917 0.335
DOC_USP7_MATH_1 264 268 PF00917 0.483
DOC_USP7_MATH_1 288 292 PF00917 0.421
DOC_USP7_MATH_1 316 320 PF00917 0.457
DOC_USP7_MATH_1 575 579 PF00917 0.417
DOC_USP7_MATH_1 665 669 PF00917 0.288
DOC_WW_Pin1_4 106 111 PF00397 0.425
DOC_WW_Pin1_4 149 154 PF00397 0.401
DOC_WW_Pin1_4 206 211 PF00397 0.434
DOC_WW_Pin1_4 267 272 PF00397 0.514
DOC_WW_Pin1_4 274 279 PF00397 0.519
DOC_WW_Pin1_4 345 350 PF00397 0.555
DOC_WW_Pin1_4 377 382 PF00397 0.509
LIG_14-3-3_CanoR_1 131 138 PF00244 0.469
LIG_14-3-3_CanoR_1 233 237 PF00244 0.520
LIG_14-3-3_CanoR_1 337 341 PF00244 0.418
LIG_14-3-3_CanoR_1 532 537 PF00244 0.369
LIG_14-3-3_CanoR_1 596 601 PF00244 0.365
LIG_14-3-3_CanoR_1 735 741 PF00244 0.389
LIG_14-3-3_CanoR_1 77 83 PF00244 0.455
LIG_14-3-3_CanoR_1 98 106 PF00244 0.418
LIG_Actin_WH2_2 173 189 PF00022 0.428
LIG_Actin_WH2_2 29 46 PF00022 0.266
LIG_Actin_WH2_2 322 339 PF00022 0.391
LIG_deltaCOP1_diTrp_1 637 642 PF00928 0.303
LIG_eIF4E_1 29 35 PF01652 0.292
LIG_eIF4E_1 296 302 PF01652 0.375
LIG_FHA_1 115 121 PF00498 0.579
LIG_FHA_1 169 175 PF00498 0.559
LIG_FHA_1 207 213 PF00498 0.400
LIG_FHA_1 319 325 PF00498 0.470
LIG_FHA_1 648 654 PF00498 0.344
LIG_FHA_1 737 743 PF00498 0.373
LIG_FHA_1 78 84 PF00498 0.427
LIG_FHA_1 94 100 PF00498 0.419
LIG_FHA_2 194 200 PF00498 0.396
LIG_FHA_2 236 242 PF00498 0.467
LIG_FHA_2 275 281 PF00498 0.508
LIG_FHA_2 304 310 PF00498 0.528
LIG_FHA_2 688 694 PF00498 0.387
LIG_FHA_2 80 86 PF00498 0.391
LIG_Integrin_isoDGR_2 629 631 PF01839 0.534
LIG_LIR_Apic_2 380 386 PF02991 0.443
LIG_LIR_Apic_2 427 433 PF02991 0.503
LIG_LIR_Gen_1 209 218 PF02991 0.383
LIG_LIR_Gen_1 238 243 PF02991 0.381
LIG_LIR_Gen_1 447 458 PF02991 0.404
LIG_LIR_Gen_1 464 474 PF02991 0.413
LIG_LIR_Gen_1 637 647 PF02991 0.400
LIG_LIR_Gen_1 654 660 PF02991 0.419
LIG_LIR_LC3C_4 321 326 PF02991 0.430
LIG_LIR_Nem_3 152 157 PF02991 0.382
LIG_LIR_Nem_3 192 197 PF02991 0.430
LIG_LIR_Nem_3 209 214 PF02991 0.394
LIG_LIR_Nem_3 234 239 PF02991 0.521
LIG_LIR_Nem_3 304 308 PF02991 0.385
LIG_LIR_Nem_3 447 453 PF02991 0.453
LIG_LIR_Nem_3 464 470 PF02991 0.375
LIG_LIR_Nem_3 521 527 PF02991 0.466
LIG_LIR_Nem_3 599 603 PF02991 0.432
LIG_LIR_Nem_3 637 642 PF02991 0.391
LIG_LIR_Nem_3 654 658 PF02991 0.422
LIG_LIR_Nem_3 667 673 PF02991 0.331
LIG_LIR_Nem_3 717 723 PF02991 0.342
LIG_LIR_Nem_3 765 770 PF02991 0.358
LIG_Pex14_1 638 642 PF04695 0.305
LIG_RPA_C_Fungi 561 573 PF08784 0.355
LIG_SH2_CRK 150 154 PF00017 0.453
LIG_SH2_CRK 467 471 PF00017 0.317
LIG_SH2_CRK 524 528 PF00017 0.561
LIG_SH2_CRK 600 604 PF00017 0.389
LIG_SH2_CRK 617 621 PF00017 0.332
LIG_SH2_CRK 767 771 PF00017 0.421
LIG_SH2_GRB2like 749 752 PF00017 0.401
LIG_SH2_NCK_1 150 154 PF00017 0.453
LIG_SH2_NCK_1 308 312 PF00017 0.565
LIG_SH2_SRC 239 242 PF00017 0.459
LIG_SH2_SRC 448 451 PF00017 0.479
LIG_SH2_STAP1 448 452 PF00017 0.604
LIG_SH2_STAP1 749 753 PF00017 0.515
LIG_SH2_STAT5 211 214 PF00017 0.516
LIG_SH2_STAT5 257 260 PF00017 0.554
LIG_SH2_STAT5 29 32 PF00017 0.315
LIG_SH2_STAT5 370 373 PF00017 0.510
LIG_SH2_STAT5 389 392 PF00017 0.433
LIG_SH2_STAT5 479 482 PF00017 0.511
LIG_SH2_STAT5 634 637 PF00017 0.457
LIG_SH2_STAT5 670 673 PF00017 0.595
LIG_SH2_STAT5 674 677 PF00017 0.525
LIG_SH3_1 150 156 PF00018 0.444
LIG_SH3_2 278 283 PF14604 0.577
LIG_SH3_3 104 110 PF00018 0.433
LIG_SH3_3 150 156 PF00018 0.458
LIG_SH3_3 204 210 PF00018 0.597
LIG_SH3_3 275 281 PF00018 0.589
LIG_SH3_3 343 349 PF00018 0.442
LIG_SH3_3 375 381 PF00018 0.668
LIG_SH3_3 524 530 PF00018 0.520
LIG_SUMO_SIM_anti_2 31 37 PF11976 0.321
LIG_SUMO_SIM_par_1 502 508 PF11976 0.534
LIG_SUMO_SIM_par_1 738 744 PF11976 0.384
LIG_TRAF2_1 238 241 PF00917 0.466
LIG_TRAF2_1 689 692 PF00917 0.469
LIG_TRAF2_1 82 85 PF00917 0.427
LIG_TYR_ITIM 237 242 PF00017 0.603
LIG_TYR_ITIM 598 603 PF00017 0.340
LIG_TYR_ITSM 207 214 PF00017 0.449
LIG_UBA3_1 39 44 PF00899 0.432
LIG_WRC_WIRS_1 302 307 PF05994 0.412
LIG_WW_3 205 209 PF00397 0.486
LIG_WW_3 490 494 PF00397 0.498
MOD_CDK_SPxxK_3 345 352 PF00069 0.400
MOD_CK1_1 175 181 PF00069 0.387
MOD_CK1_1 267 273 PF00069 0.752
MOD_CK1_1 369 375 PF00069 0.453
MOD_CK1_1 79 85 PF00069 0.456
MOD_CK1_1 93 99 PF00069 0.481
MOD_CK2_1 133 139 PF00069 0.544
MOD_CK2_1 235 241 PF00069 0.549
MOD_CK2_1 274 280 PF00069 0.628
MOD_CK2_1 301 307 PF00069 0.689
MOD_CK2_1 354 360 PF00069 0.458
MOD_CK2_1 382 388 PF00069 0.518
MOD_CK2_1 532 538 PF00069 0.452
MOD_CK2_1 687 693 PF00069 0.527
MOD_CK2_1 79 85 PF00069 0.465
MOD_GlcNHglycan 135 138 PF01048 0.652
MOD_GlcNHglycan 272 275 PF01048 0.680
MOD_GlcNHglycan 298 301 PF01048 0.504
MOD_GlcNHglycan 371 374 PF01048 0.583
MOD_GlcNHglycan 394 397 PF01048 0.604
MOD_GlcNHglycan 720 723 PF01048 0.378
MOD_GlcNHglycan 92 95 PF01048 0.515
MOD_GlcNHglycan 99 102 PF01048 0.528
MOD_GSK3_1 102 109 PF00069 0.545
MOD_GSK3_1 126 133 PF00069 0.577
MOD_GSK3_1 168 175 PF00069 0.380
MOD_GSK3_1 231 238 PF00069 0.333
MOD_GSK3_1 270 277 PF00069 0.766
MOD_GSK3_1 369 376 PF00069 0.570
MOD_GSK3_1 377 384 PF00069 0.505
MOD_GSK3_1 43 50 PF00069 0.495
MOD_GSK3_1 514 521 PF00069 0.533
MOD_GSK3_1 647 654 PF00069 0.451
MOD_GSK3_1 73 80 PF00069 0.502
MOD_GSK3_1 754 761 PF00069 0.383
MOD_GSK3_1 93 100 PF00069 0.542
MOD_N-GLC_1 102 107 PF02516 0.481
MOD_N-GLC_1 296 301 PF02516 0.449
MOD_N-GLC_1 651 656 PF02516 0.393
MOD_N-GLC_1 718 723 PF02516 0.399
MOD_N-GLC_1 730 735 PF02516 0.428
MOD_NEK2_1 165 170 PF00069 0.481
MOD_NEK2_1 28 33 PF00069 0.408
MOD_NEK2_1 336 341 PF00069 0.414
MOD_NEK2_1 43 48 PF00069 0.471
MOD_NEK2_1 481 486 PF00069 0.511
MOD_NEK2_1 718 723 PF00069 0.396
MOD_NEK2_2 114 119 PF00069 0.723
MOD_NEK2_2 544 549 PF00069 0.360
MOD_PIKK_1 309 315 PF00454 0.454
MOD_PIKK_1 354 360 PF00454 0.444
MOD_PIKK_1 436 442 PF00454 0.602
MOD_PIKK_1 481 487 PF00454 0.444
MOD_PIKK_1 551 557 PF00454 0.365
MOD_PKA_1 10 16 PF00069 0.494
MOD_PKA_1 416 422 PF00069 0.670
MOD_PKA_1 596 602 PF00069 0.338
MOD_PKA_2 10 16 PF00069 0.531
MOD_PKA_2 130 136 PF00069 0.585
MOD_PKA_2 232 238 PF00069 0.631
MOD_PKA_2 336 342 PF00069 0.467
MOD_PKA_2 354 360 PF00069 0.639
MOD_PKA_2 416 422 PF00069 0.620
MOD_PKA_2 596 602 PF00069 0.379
MOD_PKA_2 663 669 PF00069 0.320
MOD_PKA_2 76 82 PF00069 0.541
MOD_PKA_2 97 103 PF00069 0.476
MOD_Plk_1 102 108 PF00069 0.481
MOD_Plk_1 172 178 PF00069 0.390
MOD_Plk_1 296 302 PF00069 0.446
MOD_Plk_1 590 596 PF00069 0.390
MOD_Plk_1 651 657 PF00069 0.459
MOD_Plk_4 102 108 PF00069 0.536
MOD_Plk_4 232 238 PF00069 0.549
MOD_Plk_4 366 372 PF00069 0.472
MOD_Plk_4 558 564 PF00069 0.395
MOD_Plk_4 654 660 PF00069 0.568
MOD_Plk_4 665 671 PF00069 0.385
MOD_ProDKin_1 106 112 PF00069 0.490
MOD_ProDKin_1 149 155 PF00069 0.457
MOD_ProDKin_1 206 212 PF00069 0.496
MOD_ProDKin_1 267 273 PF00069 0.623
MOD_ProDKin_1 274 280 PF00069 0.627
MOD_ProDKin_1 345 351 PF00069 0.680
MOD_ProDKin_1 377 383 PF00069 0.613
TRG_ENDOCYTIC_2 211 214 PF00928 0.516
TRG_ENDOCYTIC_2 239 242 PF00928 0.645
TRG_ENDOCYTIC_2 450 453 PF00928 0.619
TRG_ENDOCYTIC_2 467 470 PF00928 0.318
TRG_ENDOCYTIC_2 524 527 PF00928 0.573
TRG_ENDOCYTIC_2 600 603 PF00928 0.530
TRG_ENDOCYTIC_2 617 620 PF00928 0.349
TRG_ENDOCYTIC_2 639 642 PF00928 0.356
TRG_ENDOCYTIC_2 767 770 PF00928 0.395
TRG_ER_diArg_1 15 18 PF00400 0.612
TRG_ER_diArg_1 331 333 PF00400 0.664
TRG_ER_diArg_1 336 338 PF00400 0.613
TRG_ER_diArg_1 416 418 PF00400 0.523
TRG_ER_diArg_1 492 495 PF00400 0.566
TRG_ER_diArg_1 531 534 PF00400 0.465
TRG_ER_diArg_1 55 57 PF00400 0.448
TRG_ER_diArg_1 566 568 PF00400 0.466
TRG_ER_diArg_1 579 581 PF00400 0.489
TRG_ER_diArg_1 596 598 PF00400 0.372
TRG_ER_diArg_1 600 602 PF00400 0.377
TRG_ER_diArg_1 662 665 PF00400 0.366
TRG_ER_diArg_1 734 736 PF00400 0.401
TRG_ER_diArg_1 9 12 PF00400 0.609
TRG_NLS_Bipartite_1 579 599 PF00514 0.351
TRG_Pf-PMV_PEXEL_1 422 426 PF00026 0.489
TRG_Pf-PMV_PEXEL_1 534 538 PF00026 0.386
TRG_Pf-PMV_PEXEL_1 768 772 PF00026 0.400
TRG_Pf-PMV_PEXEL_1 81 85 PF00026 0.469

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 38% 95%
A0A3S5H4Y6 Leishmania donovani 62% 96%
A0A3S5H4Y9 Leishmania donovani 33% 78%
A0A3S7WT86 Leishmania donovani 40% 75%
A0A3S7WWA6 Leishmania donovani 38% 95%
A0A451EJD9 Leishmania donovani 38% 95%
A0A451EJF4 Leishmania donovani 59% 95%
A0A451EJF6 Leishmania donovani 59% 100%
A0A451EJF8 Leishmania donovani 87% 100%
A0A451EJF9 Leishmania donovani 54% 90%
A4H3A9 Leishmania braziliensis 57% 100%
A4H3B4 Leishmania braziliensis 55% 100%
A4H3B5 Leishmania braziliensis 55% 95%
A4H3B6 Leishmania braziliensis 60% 95%
A4H3B7 Leishmania braziliensis 42% 100%
A4H3B8 Leishmania braziliensis 66% 100%
A4H3B9 Leishmania braziliensis 38% 100%
A4H4W8 Leishmania braziliensis 37% 100%
A4HJ20 Leishmania braziliensis 59% 100%
A4HNK3 Leishmania braziliensis 38% 95%
A4HNK6 Leishmania braziliensis 36% 100%
A4HRL9 Leishmania infantum 56% 95%
A4HRM0 Leishmania infantum 69% 100%
A4HRM1 Leishmania infantum 60% 100%
A4HRS1 Leishmania infantum 54% 90%
A4HRS3 Leishmania infantum 33% 78%
A4HRS5 Leishmania infantum 87% 100%
A4HZM0 Leishmania infantum 38% 95%
A4I7C7 Leishmania infantum 39% 95%
A4IAQ2 Leishmania infantum 38% 95%
E9AC91 Leishmania major 54% 100%
E9AC92 Leishmania major 54% 100%
E9AC95 Leishmania major 84% 100%
E9AC96 Leishmania major 54% 100%
E9AC98 Leishmania major 35% 100%
E9AEH8 Leishmania major 39% 100%
E9AHA6 Leishmania infantum 38% 95%
E9AIP8 Leishmania braziliensis 36% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 60% 100%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 62% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 34% 100%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 36% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 37% 95%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 38% 95%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 38% 95%
Q4Q5T6 Leishmania major 39% 100%
Q4QCL8 Leishmania major 37% 100%
Q4QFJ3 Leishmania major 40% 100%
Q4QIG9 Leishmania major 38% 100%
Q7YXU9 Leishmania major 38% 100%
Q7YXV1 Leishmania major 36% 100%
Q7YXV2 Leishmania major 39% 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