LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase

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
Gene product:
phosphoglycan beta 1,3 galactosyltransferase
Species:
Leishmania donovani
UniProt:
A0A3S5H4Y9_LEIDO
TriTrypDb:
LdBPK_020200.1 * , LdCL_020007400 , LDHU3_02.0300
Length:
993

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: 55
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: 49
NetGPI no yes: 0, no: 49
Cellular components
Term Name Level Count
GO:0016020 membrane 2 50
GO:0110165 cellular anatomical entity 1 50
GO:0000139 Golgi membrane 5 14
GO:0031090 organelle membrane 3 14
GO:0098588 bounding membrane of organelle 4 14

Expansion

Sequence features

A0A3S5H4Y9
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3S5H4Y9

Function

Biological processes
Term Name Level Count
GO:0006486 protein glycosylation 4 50
GO:0006807 nitrogen compound metabolic process 2 50
GO:0008152 metabolic process 1 50
GO:0019538 protein metabolic process 3 50
GO:0036211 protein modification process 4 50
GO:0043170 macromolecule metabolic process 3 50
GO:0043412 macromolecule modification 4 50
GO:0043413 macromolecule glycosylation 3 50
GO:0044238 primary metabolic process 2 50
GO:0070085 glycosylation 2 50
GO:0071704 organic substance metabolic process 2 50
GO:1901564 organonitrogen compound metabolic process 3 50
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 50
GO:0016740 transferase activity 2 50
GO:0016757 glycosyltransferase activity 3 50
GO:0016758 hexosyltransferase activity 4 50
GO:0008194 UDP-glycosyltransferase activity 4 14

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 158 162 PF00656 0.632
CLV_C14_Caspase3-7 430 434 PF00656 0.291
CLV_C14_Caspase3-7 547 551 PF00656 0.285
CLV_C14_Caspase3-7 62 66 PF00656 0.642
CLV_C14_Caspase3-7 669 673 PF00656 0.402
CLV_NRD_NRD_1 151 153 PF00675 0.470
CLV_NRD_NRD_1 191 193 PF00675 0.451
CLV_NRD_NRD_1 220 222 PF00675 0.430
CLV_NRD_NRD_1 238 240 PF00675 0.458
CLV_NRD_NRD_1 241 243 PF00675 0.493
CLV_NRD_NRD_1 270 272 PF00675 0.593
CLV_NRD_NRD_1 273 275 PF00675 0.615
CLV_NRD_NRD_1 295 297 PF00675 0.553
CLV_NRD_NRD_1 302 304 PF00675 0.537
CLV_NRD_NRD_1 577 579 PF00675 0.676
CLV_NRD_NRD_1 662 664 PF00675 0.711
CLV_NRD_NRD_1 729 731 PF00675 0.557
CLV_NRD_NRD_1 800 802 PF00675 0.595
CLV_NRD_NRD_1 858 860 PF00675 0.571
CLV_NRD_NRD_1 869 871 PF00675 0.569
CLV_NRD_NRD_1 885 887 PF00675 0.536
CLV_PCSK_FUR_1 239 243 PF00082 0.417
CLV_PCSK_FUR_1 271 275 PF00082 0.576
CLV_PCSK_FUR_1 575 579 PF00082 0.507
CLV_PCSK_KEX2_1 151 153 PF00082 0.470
CLV_PCSK_KEX2_1 191 193 PF00082 0.454
CLV_PCSK_KEX2_1 220 222 PF00082 0.428
CLV_PCSK_KEX2_1 238 240 PF00082 0.475
CLV_PCSK_KEX2_1 241 243 PF00082 0.516
CLV_PCSK_KEX2_1 270 272 PF00082 0.635
CLV_PCSK_KEX2_1 273 275 PF00082 0.578
CLV_PCSK_KEX2_1 295 297 PF00082 0.553
CLV_PCSK_KEX2_1 577 579 PF00082 0.674
CLV_PCSK_KEX2_1 662 664 PF00082 0.637
CLV_PCSK_KEX2_1 729 731 PF00082 0.572
CLV_PCSK_KEX2_1 790 792 PF00082 0.643
CLV_PCSK_KEX2_1 858 860 PF00082 0.620
CLV_PCSK_KEX2_1 869 871 PF00082 0.635
CLV_PCSK_KEX2_1 885 887 PF00082 0.534
CLV_PCSK_PC1ET2_1 241 243 PF00082 0.445
CLV_PCSK_PC1ET2_1 790 792 PF00082 0.567
CLV_PCSK_SKI1_1 247 251 PF00082 0.304
CLV_PCSK_SKI1_1 303 307 PF00082 0.520
CLV_PCSK_SKI1_1 429 433 PF00082 0.467
CLV_PCSK_SKI1_1 686 690 PF00082 0.597
CLV_PCSK_SKI1_1 790 794 PF00082 0.609
CLV_PCSK_SKI1_1 805 809 PF00082 0.501
CLV_PCSK_SKI1_1 869 873 PF00082 0.529
CLV_Separin_Metazoa 440 444 PF03568 0.363
DEG_APCC_DBOX_1 610 618 PF00400 0.317
DOC_CYCLIN_yCln2_LP_2 621 627 PF00134 0.491
DOC_CYCLIN_yCln2_LP_2 964 970 PF00134 0.348
DOC_MAPK_DCC_7 457 467 PF00069 0.302
DOC_MAPK_gen_1 198 206 PF00069 0.593
DOC_MAPK_gen_1 238 246 PF00069 0.694
DOC_MAPK_gen_1 303 310 PF00069 0.310
DOC_MAPK_gen_1 457 467 PF00069 0.389
DOC_MAPK_gen_1 801 808 PF00069 0.288
DOC_MAPK_MEF2A_6 200 208 PF00069 0.588
DOC_MAPK_MEF2A_6 247 254 PF00069 0.427
DOC_MAPK_MEF2A_6 460 467 PF00069 0.334
DOC_MAPK_MEF2A_6 706 715 PF00069 0.300
DOC_PP1_RVXF_1 301 308 PF00149 0.340
DOC_PP1_RVXF_1 684 691 PF00149 0.436
DOC_PP2B_LxvP_1 167 170 PF13499 0.611
DOC_PP2B_LxvP_1 357 360 PF13499 0.414
DOC_PP2B_LxvP_1 621 624 PF13499 0.497
DOC_PP2B_LxvP_1 771 774 PF13499 0.389
DOC_PP2B_LxvP_1 94 97 PF13499 0.662
DOC_PP2B_LxvP_1 964 967 PF13499 0.336
DOC_PP2B_PxIxI_1 462 468 PF00149 0.280
DOC_PP4_FxxP_1 540 543 PF00568 0.323
DOC_USP7_MATH_1 123 127 PF00917 0.645
DOC_USP7_MATH_1 427 431 PF00917 0.353
DOC_USP7_MATH_1 46 50 PF00917 0.647
DOC_USP7_MATH_1 484 488 PF00917 0.279
DOC_USP7_MATH_1 764 768 PF00917 0.442
DOC_WW_Pin1_4 113 118 PF00397 0.647
DOC_WW_Pin1_4 590 595 PF00397 0.502
DOC_WW_Pin1_4 606 611 PF00397 0.355
DOC_WW_Pin1_4 773 778 PF00397 0.378
DOC_WW_Pin1_4 900 905 PF00397 0.324
DOC_WW_Pin1_4 923 928 PF00397 0.393
LIG_14-3-3_CanoR_1 198 208 PF00244 0.632
LIG_14-3-3_CanoR_1 429 437 PF00244 0.280
LIG_14-3-3_CanoR_1 486 490 PF00244 0.459
LIG_14-3-3_CanoR_1 491 495 PF00244 0.422
LIG_14-3-3_CanoR_1 577 582 PF00244 0.326
LIG_14-3-3_CanoR_1 68 75 PF00244 0.667
LIG_14-3-3_CanoR_1 889 895 PF00244 0.322
LIG_Actin_WH2_2 301 318 PF00022 0.307
LIG_Actin_WH2_2 434 450 PF00022 0.381
LIG_Actin_WH2_2 745 762 PF00022 0.417
LIG_BIR_II_1 1 5 PF00653 0.654
LIG_BIR_III_2 974 978 PF00653 0.350
LIG_BIR_III_4 370 374 PF00653 0.420
LIG_BIR_III_4 887 891 PF00653 0.325
LIG_BRCT_BRCA1_1 486 490 PF00533 0.254
LIG_CSL_BTD_1 964 967 PF09270 0.322
LIG_EVH1_1 94 98 PF00568 0.654
LIG_EVH1_2 180 184 PF00568 0.614
LIG_FHA_1 281 287 PF00498 0.410
LIG_FHA_1 312 318 PF00498 0.465
LIG_FHA_1 328 334 PF00498 0.334
LIG_FHA_1 392 398 PF00498 0.349
LIG_FHA_1 430 436 PF00498 0.493
LIG_FHA_1 51 57 PF00498 0.643
LIG_FHA_1 585 591 PF00498 0.328
LIG_FHA_1 766 772 PF00498 0.408
LIG_FHA_1 798 804 PF00498 0.325
LIG_FHA_1 815 821 PF00498 0.349
LIG_FHA_1 91 97 PF00498 0.679
LIG_FHA_2 224 230 PF00498 0.575
LIG_FHA_2 542 548 PF00498 0.457
LIG_FHA_2 60 66 PF00498 0.644
LIG_FHA_2 843 849 PF00498 0.307
LIG_FHA_2 870 876 PF00498 0.318
LIG_FHA_2 901 907 PF00498 0.311
LIG_FHA_2 924 930 PF00498 0.397
LIG_Integrin_isoDGR_2 727 729 PF01839 0.483
LIG_Integrin_RGD_1 670 672 PF01839 0.600
LIG_LIR_Apic_2 539 543 PF02991 0.331
LIG_LIR_Gen_1 202 212 PF02991 0.566
LIG_LIR_Gen_1 652 660 PF02991 0.353
LIG_LIR_Gen_1 692 703 PF02991 0.355
LIG_LIR_Gen_1 707 716 PF02991 0.361
LIG_LIR_Gen_1 720 726 PF02991 0.338
LIG_LIR_Gen_1 837 844 PF02991 0.390
LIG_LIR_Gen_1 879 888 PF02991 0.410
LIG_LIR_Gen_1 893 899 PF02991 0.379
LIG_LIR_Nem_3 129 134 PF02991 0.642
LIG_LIR_Nem_3 487 492 PF02991 0.467
LIG_LIR_Nem_3 552 558 PF02991 0.304
LIG_LIR_Nem_3 687 693 PF02991 0.373
LIG_LIR_Nem_3 707 711 PF02991 0.300
LIG_LIR_Nem_3 720 725 PF02991 0.335
LIG_LIR_Nem_3 830 834 PF02991 0.381
LIG_LIR_Nem_3 837 842 PF02991 0.415
LIG_LIR_Nem_3 879 884 PF02991 0.396
LIG_LIR_Nem_3 893 897 PF02991 0.384
LIG_NRBOX 396 402 PF00104 0.324
LIG_PDZ_Class_2 988 993 PF00595 0.294
LIG_Pex14_2 831 835 PF04695 0.292
LIG_PTAP_UEV_1 169 174 PF05743 0.605
LIG_PTB_Apo_2 829 836 PF02174 0.305
LIG_SH2_CRK 265 269 PF00017 0.338
LIG_SH2_CRK 492 496 PF00017 0.275
LIG_SH2_CRK 555 559 PF00017 0.296
LIG_SH2_NCK_1 492 496 PF00017 0.275
LIG_SH2_NCK_1 708 712 PF00017 0.252
LIG_SH2_NCK_1 839 843 PF00017 0.302
LIG_SH2_PTP2 464 467 PF00017 0.270
LIG_SH2_PTP2 712 715 PF00017 0.318
LIG_SH2_SRC 331 334 PF00017 0.321
LIG_SH2_SRC 510 513 PF00017 0.246
LIG_SH2_SRC 693 696 PF00017 0.360
LIG_SH2_SRC 708 711 PF00017 0.260
LIG_SH2_STAP1 265 269 PF00017 0.338
LIG_SH2_STAP1 301 305 PF00017 0.338
LIG_SH2_STAP1 408 412 PF00017 0.307
LIG_SH2_STAP1 492 496 PF00017 0.275
LIG_SH2_STAP1 693 697 PF00017 0.448
LIG_SH2_STAP1 708 712 PF00017 0.279
LIG_SH2_STAP1 839 843 PF00017 0.362
LIG_SH2_STAT5 331 334 PF00017 0.331
LIG_SH2_STAT5 464 467 PF00017 0.373
LIG_SH2_STAT5 492 495 PF00017 0.305
LIG_SH2_STAT5 510 513 PF00017 0.423
LIG_SH2_STAT5 712 715 PF00017 0.343
LIG_SH2_STAT5 724 727 PF00017 0.358
LIG_SH2_STAT5 839 842 PF00017 0.375
LIG_SH2_STAT5 909 912 PF00017 0.474
LIG_SH2_STAT5 914 917 PF00017 0.426
LIG_SH3_2 117 122 PF14604 0.615
LIG_SH3_3 114 120 PF00018 0.633
LIG_SH3_3 167 173 PF00018 0.627
LIG_SH3_3 272 278 PF00018 0.409
LIG_SH3_3 456 462 PF00018 0.448
LIG_SH3_3 607 613 PF00018 0.425
LIG_SH3_3 621 627 PF00018 0.461
LIG_SH3_3 696 702 PF00018 0.392
LIG_SH3_3 771 777 PF00018 0.383
LIG_SH3_3 89 95 PF00018 0.671
LIG_SUMO_SIM_anti_2 13 19 PF11976 0.636
LIG_SUMO_SIM_anti_2 283 288 PF11976 0.345
LIG_SUMO_SIM_anti_2 822 827 PF11976 0.302
LIG_TRAF2_1 513 516 PF00917 0.284
LIG_TRAF2_1 544 547 PF00917 0.306
LIG_TRAF2_1 936 939 PF00917 0.360
LIG_UBA3_1 103 108 PF00899 0.635
LIG_ULM_U2AF65_1 303 308 PF00076 0.317
LIG_WW_1 461 464 PF00397 0.292
MOD_CDK_SPK_2 606 611 PF00069 0.367
MOD_CK1_1 126 132 PF00069 0.677
MOD_CK1_1 171 177 PF00069 0.663
MOD_CK1_1 451 457 PF00069 0.370
MOD_CK1_1 472 478 PF00069 0.312
MOD_CK1_1 49 55 PF00069 0.657
MOD_CK1_1 561 567 PF00069 0.357
MOD_CK1_1 588 594 PF00069 0.329
MOD_CK1_1 606 612 PF00069 0.435
MOD_CK1_1 776 782 PF00069 0.353
MOD_CK1_1 84 90 PF00069 0.673
MOD_CK1_1 922 928 PF00069 0.399
MOD_CK2_1 541 547 PF00069 0.486
MOD_CK2_1 869 875 PF00069 0.359
MOD_CK2_1 923 929 PF00069 0.450
MOD_Cter_Amidation 727 730 PF01082 0.520
MOD_Cter_Amidation 856 859 PF01082 0.510
MOD_GlcNHglycan 170 173 PF01048 0.473
MOD_GlcNHglycan 209 212 PF01048 0.443
MOD_GlcNHglycan 375 378 PF01048 0.624
MOD_GlcNHglycan 471 474 PF01048 0.478
MOD_GlcNHglycan 49 52 PF01048 0.456
MOD_GlcNHglycan 563 566 PF01048 0.584
MOD_GlcNHglycan 605 608 PF01048 0.675
MOD_GlcNHglycan 640 643 PF01048 0.646
MOD_GlcNHglycan 75 78 PF01048 0.463
MOD_GlcNHglycan 752 755 PF01048 0.672
MOD_GlcNHglycan 83 86 PF01048 0.456
MOD_GlcNHglycan 89 92 PF01048 0.448
MOD_GlcNHglycan 921 924 PF01048 0.628
MOD_GlcNHglycan 968 971 PF01048 0.594
MOD_GSK3_1 108 115 PF00069 0.672
MOD_GSK3_1 180 187 PF00069 0.697
MOD_GSK3_1 207 214 PF00069 0.594
MOD_GSK3_1 276 283 PF00069 0.476
MOD_GSK3_1 46 53 PF00069 0.647
MOD_GSK3_1 584 591 PF00069 0.355
MOD_GSK3_1 599 606 PF00069 0.440
MOD_GSK3_1 69 76 PF00069 0.651
MOD_GSK3_1 77 84 PF00069 0.662
MOD_GSK3_1 919 926 PF00069 0.411
MOD_N-GLC_1 280 285 PF02516 0.574
MOD_N-GLC_1 949 954 PF02516 0.591
MOD_NEK2_1 184 189 PF00069 0.645
MOD_NEK2_1 250 255 PF00069 0.370
MOD_NEK2_1 299 304 PF00069 0.411
MOD_NEK2_1 47 52 PF00069 0.659
MOD_NEK2_1 490 495 PF00069 0.288
MOD_NEK2_1 558 563 PF00069 0.356
MOD_NEK2_1 765 770 PF00069 0.415
MOD_NEK2_1 850 855 PF00069 0.298
MOD_NEK2_2 311 316 PF00069 0.474
MOD_NEK2_2 755 760 PF00069 0.435
MOD_NEK2_2 824 829 PF00069 0.281
MOD_PIKK_1 199 205 PF00454 0.575
MOD_PIKK_1 50 56 PF00454 0.642
MOD_PIKK_1 681 687 PF00454 0.459
MOD_PIKK_1 69 75 PF00454 0.652
MOD_PIKK_1 766 772 PF00454 0.431
MOD_PIKK_1 77 83 PF00454 0.657
MOD_PK_1 108 114 PF00069 0.643
MOD_PK_1 448 454 PF00069 0.313
MOD_PKA_1 577 583 PF00069 0.307
MOD_PKA_1 662 668 PF00069 0.551
MOD_PKA_1 869 875 PF00069 0.318
MOD_PKA_2 184 190 PF00069 0.679
MOD_PKA_2 199 205 PF00069 0.636
MOD_PKA_2 223 229 PF00069 0.607
MOD_PKA_2 485 491 PF00069 0.465
MOD_PKA_2 541 547 PF00069 0.341
MOD_PKA_2 577 583 PF00069 0.327
MOD_PKA_2 662 668 PF00069 0.511
MOD_PKA_2 77 83 PF00069 0.663
MOD_PKA_2 869 875 PF00069 0.338
MOD_PKA_2 919 925 PF00069 0.390
MOD_PKB_1 575 583 PF00069 0.306
MOD_Plk_1 874 880 PF00069 0.344
MOD_Plk_1 949 955 PF00069 0.365
MOD_Plk_4 126 132 PF00069 0.662
MOD_Plk_4 250 256 PF00069 0.334
MOD_Plk_4 282 288 PF00069 0.359
MOD_Plk_4 327 333 PF00069 0.317
MOD_Plk_4 485 491 PF00069 0.410
MOD_Plk_4 52 58 PF00069 0.660
MOD_Plk_4 521 527 PF00069 0.422
MOD_Plk_4 850 856 PF00069 0.325
MOD_ProDKin_1 113 119 PF00069 0.641
MOD_ProDKin_1 590 596 PF00069 0.506
MOD_ProDKin_1 606 612 PF00069 0.343
MOD_ProDKin_1 773 779 PF00069 0.373
MOD_ProDKin_1 900 906 PF00069 0.322
MOD_ProDKin_1 923 929 PF00069 0.392
MOD_SUMO_for_1 666 669 PF00179 0.417
MOD_SUMO_rev_2 969 977 PF00179 0.370
TRG_DiLeu_BaEn_2 845 851 PF01217 0.292
TRG_DiLeu_BaLyEn_6 160 165 PF01217 0.640
TRG_ENDOCYTIC_2 265 268 PF00928 0.346
TRG_ENDOCYTIC_2 408 411 PF00928 0.308
TRG_ENDOCYTIC_2 464 467 PF00928 0.373
TRG_ENDOCYTIC_2 492 495 PF00928 0.477
TRG_ENDOCYTIC_2 555 558 PF00928 0.296
TRG_ENDOCYTIC_2 695 698 PF00928 0.458
TRG_ENDOCYTIC_2 708 711 PF00928 0.307
TRG_ENDOCYTIC_2 712 715 PF00928 0.248
TRG_ENDOCYTIC_2 839 842 PF00928 0.420
TRG_ER_diArg_1 191 193 PF00400 0.663
TRG_ER_diArg_1 197 200 PF00400 0.630
TRG_ER_diArg_1 219 221 PF00400 0.630
TRG_ER_diArg_1 269 271 PF00400 0.371
TRG_ER_diArg_1 272 274 PF00400 0.397
TRG_ER_diArg_1 294 296 PF00400 0.358
TRG_ER_diArg_1 574 577 PF00400 0.459
TRG_ER_diArg_1 729 732 PF00400 0.346
TRG_ER_diArg_1 858 861 PF00400 0.386
TRG_ER_diArg_1 869 871 PF00400 0.375
TRG_ER_diArg_1 884 886 PF00400 0.332
TRG_NLS_MonoExtN_4 238 245 PF00514 0.585
TRG_Pf-PMV_PEXEL_1 634 638 PF00026 0.472
TRG_Pf-PMV_PEXEL_1 791 796 PF00026 0.587

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 31% 100%
A0A3S5H4Y6 Leishmania donovani 35% 99%
A0A3S7WT86 Leishmania donovani 36% 100%
A0A3S7WWA6 Leishmania donovani 31% 100%
A0A451EJD9 Leishmania donovani 31% 100%
A0A451EJF4 Leishmania donovani 34% 100%
A0A451EJF8 Leishmania donovani 34% 100%
A0A451EJF9 Leishmania donovani 38% 100%
A4H3A9 Leishmania braziliensis 38% 100%
A4H3B4 Leishmania braziliensis 39% 100%
A4H3B6 Leishmania braziliensis 38% 100%
A4H3B7 Leishmania braziliensis 38% 93%
A4H3B8 Leishmania braziliensis 40% 100%
A4H3B9 Leishmania braziliensis 65% 100%
A4H4W8 Leishmania braziliensis 33% 100%
A4HJ20 Leishmania braziliensis 39% 100%
A4HNK6 Leishmania braziliensis 33% 100%
A4HRL9 Leishmania infantum 34% 99%
A4HRM0 Leishmania infantum 35% 90%
A4HRS1 Leishmania infantum 38% 100%
A4HRS3 Leishmania infantum 99% 100%
A4HRS5 Leishmania infantum 33% 95%
A4HZM0 Leishmania infantum 31% 100%
A4I7C7 Leishmania infantum 31% 100%
A4IAQ2 Leishmania infantum 32% 100%
E9AC91 Leishmania major 38% 100%
E9AC92 Leishmania major 38% 100%
E9AC94 Leishmania major 91% 100%
E9AC95 Leishmania major 34% 95%
E9AC96 Leishmania major 38% 100%
E9AC98 Leishmania major 91% 100%
E9AEH8 Leishmania major 32% 100%
E9AHA6 Leishmania infantum 31% 100%
E9AIP8 Leishmania braziliensis 32% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 35% 100%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 35% 98%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 33% 94%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 80% 99%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 33% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 34% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 34% 100%
Q4Q5T6 Leishmania major 32% 100%
Q4QCL8 Leishmania major 32% 100%
Q4QFJ3 Leishmania major 37% 100%
Q4QIG9 Leishmania major 32% 100%
Q7YXU9 Leishmania major 33% 100%
Q7YXV1 Leishmania major 33% 100%
Q7YXV2 Leishmania major 31% 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