LeishMANIAdb
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Phosphoglycan beta 1,3 galactosyltransferase, putative

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, putative
Gene product:
phosphoglycan beta 1,3 galactosyltransferase, putative
Species:
Leishmania donovani
UniProt:
A0A3S7WT86_LEIDO
TriTrypDb:
LdBPK_141500.1 * , LdCL_140020800 , LDHU3_14.1870
Length:
1028

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: 50
NetGPI no yes: 0, no: 50
Cellular components
Term Name Level Count
GO:0016020 membrane 2 51
GO:0110165 cellular anatomical entity 1 51
GO:0000139 Golgi membrane 5 14
GO:0031090 organelle membrane 3 14
GO:0098588 bounding membrane of organelle 4 14

Expansion

Sequence features

A0A3S7WT86
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3S7WT86

Function

Biological processes
Term Name Level Count
GO:0006486 protein glycosylation 4 51
GO:0006807 nitrogen compound metabolic process 2 51
GO:0008152 metabolic process 1 51
GO:0019538 protein metabolic process 3 51
GO:0036211 protein modification process 4 51
GO:0043170 macromolecule metabolic process 3 51
GO:0043412 macromolecule modification 4 51
GO:0043413 macromolecule glycosylation 3 51
GO:0044238 primary metabolic process 2 51
GO:0070085 glycosylation 2 51
GO:0071704 organic substance metabolic process 2 51
GO:1901564 organonitrogen compound metabolic process 3 51
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 51
GO:0016740 transferase activity 2 51
GO:0016757 glycosyltransferase activity 3 51
GO:0016758 hexosyltransferase activity 4 51
GO:0008194 UDP-glycosyltransferase activity 4 14

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 10 14 PF00656 0.643
CLV_C14_Caspase3-7 651 655 PF00656 0.253
CLV_C14_Caspase3-7 997 1001 PF00656 0.318
CLV_NRD_NRD_1 126 128 PF00675 0.447
CLV_NRD_NRD_1 146 148 PF00675 0.451
CLV_NRD_NRD_1 226 228 PF00675 0.593
CLV_NRD_NRD_1 388 390 PF00675 0.512
CLV_NRD_NRD_1 576 578 PF00675 0.689
CLV_NRD_NRD_1 652 654 PF00675 0.523
CLV_NRD_NRD_1 664 666 PF00675 0.682
CLV_NRD_NRD_1 731 733 PF00675 0.575
CLV_NRD_NRD_1 768 770 PF00675 0.515
CLV_NRD_NRD_1 786 788 PF00675 0.554
CLV_NRD_NRD_1 838 840 PF00675 0.531
CLV_NRD_NRD_1 849 851 PF00675 0.518
CLV_NRD_NRD_1 86 88 PF00675 0.441
CLV_NRD_NRD_1 957 959 PF00675 0.624
CLV_PCSK_FUR_1 574 578 PF00082 0.528
CLV_PCSK_FUR_1 83 87 PF00082 0.433
CLV_PCSK_KEX2_1 125 127 PF00082 0.451
CLV_PCSK_KEX2_1 146 148 PF00082 0.448
CLV_PCSK_KEX2_1 226 228 PF00082 0.593
CLV_PCSK_KEX2_1 574 576 PF00082 0.691
CLV_PCSK_KEX2_1 652 654 PF00082 0.491
CLV_PCSK_KEX2_1 664 666 PF00082 0.623
CLV_PCSK_KEX2_1 768 770 PF00082 0.524
CLV_PCSK_KEX2_1 786 788 PF00082 0.544
CLV_PCSK_KEX2_1 83 85 PF00082 0.449
CLV_PCSK_KEX2_1 838 840 PF00082 0.568
CLV_PCSK_KEX2_1 849 851 PF00082 0.583
CLV_PCSK_KEX2_1 86 88 PF00082 0.440
CLV_PCSK_SKI1_1 117 121 PF00082 0.368
CLV_PCSK_SKI1_1 153 157 PF00082 0.271
CLV_PCSK_SKI1_1 253 257 PF00082 0.525
CLV_PCSK_SKI1_1 285 289 PF00082 0.562
CLV_PCSK_SKI1_1 293 297 PF00082 0.501
CLV_PCSK_SKI1_1 436 440 PF00082 0.590
CLV_PCSK_SKI1_1 545 549 PF00082 0.528
CLV_PCSK_SKI1_1 576 580 PF00082 0.612
CLV_PCSK_SKI1_1 665 669 PF00082 0.579
CLV_PCSK_SKI1_1 689 693 PF00082 0.581
CLV_PCSK_SKI1_1 870 874 PF00082 0.508
CLV_PCSK_SKI1_1 93 97 PF00082 0.366
CLV_PCSK_SKI1_1 943 947 PF00082 0.567
DEG_MDM2_SWIB_1 165 172 PF02201 0.224
DEG_SPOP_SBC_1 74 78 PF00917 0.639
DOC_CKS1_1 990 995 PF01111 0.372
DOC_CYCLIN_RxL_1 114 124 PF00134 0.571
DOC_CYCLIN_RxL_1 147 158 PF00134 0.527
DOC_CYCLIN_RxL_1 253 261 PF00134 0.310
DOC_CYCLIN_RxL_1 87 98 PF00134 0.581
DOC_CYCLIN_yCln2_LP_2 623 629 PF00134 0.478
DOC_MAPK_gen_1 125 132 PF00069 0.635
DOC_MAPK_gen_1 151 159 PF00069 0.449
DOC_MAPK_gen_1 574 580 PF00069 0.299
DOC_MAPK_gen_1 652 658 PF00069 0.254
DOC_MAPK_gen_1 768 776 PF00069 0.304
DOC_MAPK_MEF2A_6 151 159 PF00069 0.417
DOC_MAPK_MEF2A_6 192 200 PF00069 0.377
DOC_MAPK_MEF2A_6 367 375 PF00069 0.330
DOC_MAPK_MEF2A_6 523 532 PF00069 0.286
DOC_MAPK_MEF2A_6 652 660 PF00069 0.409
DOC_MAPK_MEF2A_6 677 686 PF00069 0.341
DOC_MAPK_RevD_3 211 227 PF00069 0.335
DOC_PP1_RVXF_1 283 289 PF00149 0.364
DOC_PP1_RVXF_1 687 694 PF00149 0.420
DOC_PP1_RVXF_1 868 875 PF00149 0.336
DOC_PP2B_LxvP_1 202 205 PF13499 0.375
DOC_PP2B_LxvP_1 426 429 PF13499 0.275
DOC_PP2B_LxvP_1 530 533 PF13499 0.272
DOC_PP2B_LxvP_1 566 569 PF13499 0.361
DOC_PP2B_LxvP_1 623 626 PF13499 0.484
DOC_USP7_MATH_1 348 352 PF00917 0.403
DOC_USP7_MATH_1 374 378 PF00917 0.347
DOC_USP7_MATH_1 410 414 PF00917 0.488
DOC_USP7_MATH_1 515 519 PF00917 0.300
DOC_USP7_MATH_1 526 530 PF00917 0.343
DOC_USP7_MATH_1 907 911 PF00917 0.398
DOC_USP7_MATH_1 933 937 PF00917 0.312
DOC_USP7_UBL2_3 504 508 PF12436 0.431
DOC_WW_Pin1_4 333 338 PF00397 0.419
DOC_WW_Pin1_4 403 408 PF00397 0.456
DOC_WW_Pin1_4 417 422 PF00397 0.411
DOC_WW_Pin1_4 589 594 PF00397 0.482
DOC_WW_Pin1_4 607 612 PF00397 0.421
DOC_WW_Pin1_4 989 994 PF00397 0.416
LIG_14-3-3_CanoR_1 101 107 PF00244 0.564
LIG_14-3-3_CanoR_1 125 131 PF00244 0.627
LIG_14-3-3_CanoR_1 18 26 PF00244 0.646
LIG_14-3-3_CanoR_1 226 231 PF00244 0.448
LIG_14-3-3_CanoR_1 264 272 PF00244 0.316
LIG_14-3-3_CanoR_1 27 31 PF00244 0.640
LIG_14-3-3_CanoR_1 276 280 PF00244 0.331
LIG_14-3-3_CanoR_1 293 301 PF00244 0.299
LIG_14-3-3_CanoR_1 444 448 PF00244 0.451
LIG_14-3-3_CanoR_1 45 54 PF00244 0.585
LIG_14-3-3_CanoR_1 523 531 PF00244 0.318
LIG_14-3-3_CanoR_1 545 550 PF00244 0.291
LIG_14-3-3_CanoR_1 575 581 PF00244 0.346
LIG_14-3-3_CanoR_1 60 65 PF00244 0.628
LIG_14-3-3_CanoR_1 603 607 PF00244 0.422
LIG_14-3-3_CanoR_1 622 626 PF00244 0.295
LIG_14-3-3_CanoR_1 787 793 PF00244 0.237
LIG_14-3-3_CanoR_1 87 96 PF00244 0.624
LIG_14-3-3_CanoR_1 870 875 PF00244 0.329
LIG_14-3-3_CanoR_1 941 946 PF00244 0.370
LIG_14-3-3_CterR_2 1025 1028 PF00244 0.387
LIG_Actin_WH2_2 531 547 PF00022 0.280
LIG_EH1_1 206 214 PF00400 0.336
LIG_FHA_1 103 109 PF00498 0.550
LIG_FHA_1 114 120 PF00498 0.565
LIG_FHA_1 127 133 PF00498 0.628
LIG_FHA_1 156 162 PF00498 0.255
LIG_FHA_1 206 212 PF00498 0.394
LIG_FHA_1 302 308 PF00498 0.474
LIG_FHA_1 311 317 PF00498 0.431
LIG_FHA_1 377 383 PF00498 0.476
LIG_FHA_1 418 424 PF00498 0.358
LIG_FHA_1 544 550 PF00498 0.331
LIG_FHA_2 20 26 PF00498 0.643
LIG_FHA_2 337 343 PF00498 0.430
LIG_FHA_2 456 462 PF00498 0.272
LIG_FHA_2 698 704 PF00498 0.279
LIG_FHA_2 789 795 PF00498 0.258
LIG_FHA_2 8 14 PF00498 0.640
LIG_FHA_2 964 970 PF00498 0.387
LIG_GBD_Chelix_1 938 946 PF00786 0.512
LIG_LIR_Gen_1 419 429 PF02991 0.341
LIG_LIR_Gen_1 513 524 PF02991 0.300
LIG_LIR_Gen_1 654 661 PF02991 0.356
LIG_LIR_Gen_1 712 722 PF02991 0.357
LIG_LIR_Gen_1 818 824 PF02991 0.365
LIG_LIR_Gen_1 873 879 PF02991 0.417
LIG_LIR_Gen_1 971 981 PF02991 0.355
LIG_LIR_Nem_3 1006 1012 PF02991 0.318
LIG_LIR_Nem_3 419 425 PF02991 0.361
LIG_LIR_Nem_3 446 450 PF02991 0.468
LIG_LIR_Nem_3 474 478 PF02991 0.333
LIG_LIR_Nem_3 513 519 PF02991 0.317
LIG_LIR_Nem_3 700 704 PF02991 0.409
LIG_LIR_Nem_3 712 718 PF02991 0.320
LIG_LIR_Nem_3 873 877 PF02991 0.424
LIG_LIR_Nem_3 886 892 PF02991 0.288
LIG_LIR_Nem_3 971 977 PF02991 0.362
LIG_NRBOX 49 55 PF00104 0.580
LIG_NRBOX 830 836 PF00104 0.289
LIG_Pex14_2 165 169 PF04695 0.224
LIG_Pex14_2 848 852 PF04695 0.276
LIG_Rb_LxCxE_1 916 936 PF01857 0.316
LIG_Rb_pABgroove_1 254 262 PF01858 0.308
LIG_SH2_NCK_1 811 815 PF00017 0.292
LIG_SH2_PTP2 195 198 PF00017 0.389
LIG_SH2_PTP2 516 519 PF00017 0.290
LIG_SH2_PTP2 715 718 PF00017 0.313
LIG_SH2_SRC 321 324 PF00017 0.349
LIG_SH2_SRC 815 818 PF00017 0.284
LIG_SH2_STAP1 321 325 PF00017 0.415
LIG_SH2_STAP1 640 644 PF00017 0.247
LIG_SH2_STAP1 811 815 PF00017 0.346
LIG_SH2_STAP1 820 824 PF00017 0.333
LIG_SH2_STAT5 1009 1012 PF00017 0.297
LIG_SH2_STAT5 195 198 PF00017 0.405
LIG_SH2_STAT5 422 425 PF00017 0.377
LIG_SH2_STAT5 468 471 PF00017 0.397
LIG_SH2_STAT5 5 8 PF00017 0.615
LIG_SH2_STAT5 516 519 PF00017 0.290
LIG_SH2_STAT5 698 701 PF00017 0.350
LIG_SH2_STAT5 715 718 PF00017 0.341
LIG_SH2_STAT5 721 724 PF00017 0.350
LIG_SH2_STAT5 727 730 PF00017 0.361
LIG_SH2_STAT5 775 778 PF00017 0.282
LIG_SH2_STAT5 805 808 PF00017 0.283
LIG_SH2_STAT5 853 856 PF00017 0.365
LIG_SH2_STAT5 889 892 PF00017 0.446
LIG_SH2_STAT5 995 998 PF00017 0.437
LIG_SH3_1 404 410 PF00018 0.447
LIG_SH3_3 167 173 PF00018 0.239
LIG_SH3_3 193 199 PF00018 0.421
LIG_SH3_3 213 219 PF00018 0.335
LIG_SH3_3 404 410 PF00018 0.459
LIG_SH3_3 470 476 PF00018 0.284
LIG_SH3_3 483 489 PF00018 0.438
LIG_SH3_3 609 615 PF00018 0.400
LIG_SH3_3 623 629 PF00018 0.452
LIG_SH3_3 699 705 PF00018 0.417
LIG_SH3_3 733 739 PF00018 0.433
LIG_SH3_3 987 993 PF00018 0.403
LIG_SUMO_SIM_anti_2 1013 1020 PF11976 0.323
LIG_SUMO_SIM_par_1 128 135 PF11976 0.599
LIG_SUMO_SIM_par_1 791 798 PF11976 0.274
LIG_TRAF2_1 65 68 PF00917 0.629
LIG_TRAF2_1 757 760 PF00917 0.312
LIG_TRAF2_1 967 970 PF00917 0.369
LIG_TYR_ITSM 418 425 PF00017 0.349
LIG_ULM_U2AF65_1 389 394 PF00076 0.287
LIG_WRC_WIRS_1 156 161 PF05994 0.227
MOD_CDK_SPK_2 333 338 PF00069 0.411
MOD_CDK_SPK_2 403 408 PF00069 0.442
MOD_CK1_1 291 297 PF00069 0.301
MOD_CK1_1 336 342 PF00069 0.419
MOD_CK1_1 48 54 PF00069 0.603
MOD_CK1_1 518 524 PF00069 0.280
MOD_CK1_1 589 595 PF00069 0.336
MOD_CK1_1 63 69 PF00069 0.647
MOD_CK1_1 989 995 PF00069 0.373
MOD_CK2_1 19 25 PF00069 0.637
MOD_CK2_1 697 703 PF00069 0.274
MOD_CK2_1 754 760 PF00069 0.382
MOD_CK2_1 788 794 PF00069 0.251
MOD_CK2_1 963 969 PF00069 0.391
MOD_CMANNOS 852 855 PF00535 0.461
MOD_Cter_Amidation 730 733 PF01082 0.547
MOD_GlcNHglycan 236 239 PF01048 0.598
MOD_GlcNHglycan 266 269 PF01048 0.522
MOD_GlcNHglycan 47 50 PF01048 0.391
MOD_GlcNHglycan 524 527 PF01048 0.514
MOD_GlcNHglycan 607 610 PF01048 0.669
MOD_GlcNHglycan 62 65 PF01048 0.433
MOD_GlcNHglycan 642 645 PF01048 0.632
MOD_GlcNHglycan 776 779 PF01048 0.471
MOD_GlcNHglycan 810 814 PF01048 0.489
MOD_GlcNHglycan 900 903 PF01048 0.578
MOD_GlcNHglycan 908 912 PF01048 0.628
MOD_GSK3_1 131 138 PF00069 0.629
MOD_GSK3_1 214 221 PF00069 0.387
MOD_GSK3_1 289 296 PF00069 0.376
MOD_GSK3_1 332 339 PF00069 0.478
MOD_GSK3_1 411 418 PF00069 0.442
MOD_GSK3_1 476 483 PF00069 0.523
MOD_GSK3_1 518 525 PF00069 0.278
MOD_GSK3_1 576 583 PF00069 0.334
MOD_GSK3_1 598 605 PF00069 0.462
MOD_GSK3_1 741 748 PF00069 0.429
MOD_GSK3_1 75 82 PF00069 0.720
MOD_GSK3_1 815 822 PF00069 0.313
MOD_N-GLC_1 135 140 PF02516 0.355
MOD_N-GLC_1 343 348 PF02516 0.640
MOD_N-GLC_1 870 875 PF02516 0.523
MOD_NEK2_1 120 125 PF00069 0.591
MOD_NEK2_1 155 160 PF00069 0.355
MOD_NEK2_1 251 256 PF00069 0.334
MOD_NEK2_1 275 280 PF00069 0.356
MOD_NEK2_1 288 293 PF00069 0.380
MOD_NEK2_1 295 300 PF00069 0.306
MOD_NEK2_1 332 337 PF00069 0.401
MOD_NEK2_1 358 363 PF00069 0.408
MOD_NEK2_1 53 58 PF00069 0.636
MOD_NEK2_1 788 793 PF00069 0.271
MOD_NEK2_2 301 306 PF00069 0.469
MOD_NEK2_2 495 500 PF00069 0.451
MOD_NEK2_2 763 768 PF00069 0.288
MOD_PIKK_1 295 301 PF00454 0.280
MOD_PIKK_1 348 354 PF00454 0.394
MOD_PIKK_1 518 524 PF00454 0.281
MOD_PIKK_1 569 575 PF00454 0.328
MOD_PIKK_1 63 69 PF00454 0.626
MOD_PIKK_1 684 690 PF00454 0.426
MOD_PK_1 226 232 PF00069 0.382
MOD_PK_1 43 49 PF00069 0.595
MOD_PK_1 941 947 PF00069 0.328
MOD_PK_1 986 992 PF00069 0.387
MOD_PKA_1 126 132 PF00069 0.632
MOD_PKA_1 226 232 PF00069 0.382
MOD_PKA_1 576 582 PF00069 0.334
MOD_PKA_1 652 658 PF00069 0.317
MOD_PKA_2 126 132 PF00069 0.670
MOD_PKA_2 19 25 PF00069 0.650
MOD_PKA_2 226 232 PF00069 0.445
MOD_PKA_2 26 32 PF00069 0.639
MOD_PKA_2 275 281 PF00069 0.333
MOD_PKA_2 397 403 PF00069 0.412
MOD_PKA_2 410 416 PF00069 0.505
MOD_PKA_2 443 449 PF00069 0.458
MOD_PKA_2 522 528 PF00069 0.331
MOD_PKA_2 576 582 PF00069 0.352
MOD_PKA_2 587 593 PF00069 0.338
MOD_PKA_2 602 608 PF00069 0.426
MOD_PKA_2 621 627 PF00069 0.304
MOD_PKA_2 652 658 PF00069 0.370
MOD_PKA_2 731 737 PF00069 0.340
MOD_PKA_2 898 904 PF00069 0.364
MOD_PKB_1 262 270 PF00069 0.326
MOD_PKB_1 574 582 PF00069 0.335
MOD_PKB_1 868 876 PF00069 0.301
MOD_Plk_1 495 501 PF00069 0.443
MOD_Plk_1 598 604 PF00069 0.324
MOD_Plk_1 711 717 PF00069 0.332
MOD_Plk_1 870 876 PF00069 0.357
MOD_Plk_1 986 992 PF00069 0.410
MOD_Plk_2-3 7 13 PF00069 0.625
MOD_Plk_2-3 745 751 PF00069 0.425
MOD_Plk_4 126 132 PF00069 0.620
MOD_Plk_4 218 224 PF00069 0.348
MOD_Plk_4 226 232 PF00069 0.379
MOD_Plk_4 251 257 PF00069 0.327
MOD_Plk_4 443 449 PF00069 0.405
MOD_Plk_4 526 532 PF00069 0.289
MOD_Plk_4 53 59 PF00069 0.585
MOD_Plk_4 652 658 PF00069 0.328
MOD_Plk_4 711 717 PF00069 0.343
MOD_Plk_4 788 794 PF00069 0.265
MOD_Plk_4 815 821 PF00069 0.310
MOD_Plk_4 933 939 PF00069 0.300
MOD_ProDKin_1 333 339 PF00069 0.418
MOD_ProDKin_1 403 409 PF00069 0.457
MOD_ProDKin_1 417 423 PF00069 0.398
MOD_ProDKin_1 589 595 PF00069 0.484
MOD_ProDKin_1 607 613 PF00069 0.419
MOD_ProDKin_1 989 995 PF00069 0.410
TRG_DiLeu_BaEn_2 138 144 PF01217 0.547
TRG_DiLeu_BaLyEn_6 49 54 PF01217 0.600
TRG_DiLeu_BaLyEn_6 561 566 PF01217 0.389
TRG_DiLeu_BaLyEn_6 612 617 PF01217 0.305
TRG_ENDOCYTIC_2 1009 1012 PF00928 0.304
TRG_ENDOCYTIC_2 195 198 PF00928 0.389
TRG_ENDOCYTIC_2 422 425 PF00928 0.377
TRG_ENDOCYTIC_2 450 453 PF00928 0.481
TRG_ENDOCYTIC_2 516 519 PF00928 0.290
TRG_ENDOCYTIC_2 698 701 PF00928 0.462
TRG_ENDOCYTIC_2 715 718 PF00928 0.247
TRG_ENDOCYTIC_2 820 823 PF00928 0.417
TRG_ER_diArg_1 125 127 PF00400 0.624
TRG_ER_diArg_1 145 147 PF00400 0.632
TRG_ER_diArg_1 225 227 PF00400 0.389
TRG_ER_diArg_1 263 266 PF00400 0.331
TRG_ER_diArg_1 574 577 PF00400 0.489
TRG_ER_diArg_1 664 666 PF00400 0.403
TRG_ER_diArg_1 729 732 PF00400 0.343
TRG_ER_diArg_1 767 769 PF00400 0.290
TRG_ER_diArg_1 786 788 PF00400 0.336
TRG_ER_diArg_1 83 86 PF00400 0.650
TRG_ER_diArg_1 838 840 PF00400 0.343
TRG_ER_diArg_1 848 850 PF00400 0.342
TRG_ER_diArg_1 866 869 PF00400 0.360
TRG_ER_diArg_1 881 884 PF00400 0.282
TRG_NLS_MonoExtN_4 730 736 PF00514 0.326
TRG_Pf-PMV_PEXEL_1 118 122 PF00026 0.371
TRG_Pf-PMV_PEXEL_1 257 261 PF00026 0.525
TRG_Pf-PMV_PEXEL_1 786 790 PF00026 0.561
TRG_Pf-PMV_PEXEL_1 833 837 PF00026 0.471
TRG_Pf-PMV_PEXEL_1 93 98 PF00026 0.361

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 37% 100%
A0A3S5H4Y6 Leishmania donovani 44% 100%
A0A3S5H4Y9 Leishmania donovani 36% 100%
A0A3S7WWA6 Leishmania donovani 37% 100%
A0A451EJD9 Leishmania donovani 37% 100%
A0A451EJF4 Leishmania donovani 44% 100%
A0A451EJF8 Leishmania donovani 42% 100%
A0A451EJF9 Leishmania donovani 47% 100%
A4H3A9 Leishmania braziliensis 40% 95%
A4H3B4 Leishmania braziliensis 40% 100%
A4H3B6 Leishmania braziliensis 39% 99%
A4H3B8 Leishmania braziliensis 41% 100%
A4H3B9 Leishmania braziliensis 36% 100%
A4H4W8 Leishmania braziliensis 36% 100%
A4HJ20 Leishmania braziliensis 40% 100%
A4HNK6 Leishmania braziliensis 37% 100%
A4HRL9 Leishmania infantum 43% 100%
A4HRM0 Leishmania infantum 43% 100%
A4HRS1 Leishmania infantum 47% 100%
A4HRS3 Leishmania infantum 36% 100%
A4HRS5 Leishmania infantum 41% 100%
A4HW87 Leishmania infantum 99% 100%
A4HZM0 Leishmania infantum 37% 100%
A4I7C7 Leishmania infantum 37% 100%
A4IAQ2 Leishmania infantum 36% 100%
E9AC91 Leishmania major 41% 100%
E9AC92 Leishmania major 41% 100%
E9AC94 Leishmania major 36% 87%
E9AC95 Leishmania major 40% 100%
E9AC96 Leishmania major 41% 100%
E9AC98 Leishmania major 36% 100%
E9AEH8 Leishmania major 35% 100%
E9AHA6 Leishmania infantum 37% 100%
E9AIP8 Leishmania braziliensis 35% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 42% 100%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 42% 100%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 99%
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) 36% 100%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 36% 100%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 36% 100%
Q4Q5T6 Leishmania major 35% 100%
Q4QCL8 Leishmania major 35% 100%
Q4QFJ3 Leishmania major 90% 100%
Q4QIG9 Leishmania major 36% 100%
Q7YXU9 Leishmania major 37% 100%
Q7YXV1 Leishmania major 36% 100%
Q7YXV2 Leishmania major 36% 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