LeishMANIAdb
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Putative 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:
Putative phosphoglycan beta 1,3 galactosyltransferase
Gene product:
phosphoglycan beta 1,3 galactosyltransferase, putative
Species:
Leishmania major
UniProt:
Q4QFJ3_LEIMA
TriTrypDb:
LmjF.14.1400 * , LMJLV39_140021900 * , LMJSD75_140021600 *
Length:
1029

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:0000139 Golgi membrane 5 15
GO:0016020 membrane 2 51
GO:0031090 organelle membrane 3 15
GO:0098588 bounding membrane of organelle 4 15
GO:0110165 cellular anatomical entity 1 51

Expansion

Sequence features

Q4QFJ3
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QFJ3

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:0008194 UDP-glycosyltransferase activity 4 15
GO:0016740 transferase activity 2 51
GO:0016757 glycosyltransferase activity 3 51
GO:0016758 hexosyltransferase activity 4 51

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 10 14 PF00656 0.639
CLV_C14_Caspase3-7 652 656 PF00656 0.254
CLV_C14_Caspase3-7 998 1002 PF00656 0.313
CLV_NRD_NRD_1 127 129 PF00675 0.439
CLV_NRD_NRD_1 147 149 PF00675 0.425
CLV_NRD_NRD_1 19 21 PF00675 0.434
CLV_NRD_NRD_1 227 229 PF00675 0.616
CLV_NRD_NRD_1 32 34 PF00675 0.417
CLV_NRD_NRD_1 389 391 PF00675 0.511
CLV_NRD_NRD_1 403 405 PF00675 0.676
CLV_NRD_NRD_1 577 579 PF00675 0.679
CLV_NRD_NRD_1 653 655 PF00675 0.526
CLV_NRD_NRD_1 665 667 PF00675 0.686
CLV_NRD_NRD_1 732 734 PF00675 0.585
CLV_NRD_NRD_1 769 771 PF00675 0.511
CLV_NRD_NRD_1 787 789 PF00675 0.554
CLV_NRD_NRD_1 839 841 PF00675 0.538
CLV_NRD_NRD_1 850 852 PF00675 0.522
CLV_NRD_NRD_1 87 89 PF00675 0.450
CLV_NRD_NRD_1 958 960 PF00675 0.603
CLV_PCSK_FUR_1 575 579 PF00082 0.528
CLV_PCSK_FUR_1 85 89 PF00082 0.430
CLV_PCSK_KEX2_1 126 128 PF00082 0.438
CLV_PCSK_KEX2_1 147 149 PF00082 0.434
CLV_PCSK_KEX2_1 19 21 PF00082 0.435
CLV_PCSK_KEX2_1 227 229 PF00082 0.616
CLV_PCSK_KEX2_1 32 34 PF00082 0.416
CLV_PCSK_KEX2_1 575 577 PF00082 0.678
CLV_PCSK_KEX2_1 653 655 PF00082 0.493
CLV_PCSK_KEX2_1 665 667 PF00082 0.618
CLV_PCSK_KEX2_1 769 771 PF00082 0.517
CLV_PCSK_KEX2_1 787 789 PF00082 0.544
CLV_PCSK_KEX2_1 839 841 PF00082 0.583
CLV_PCSK_KEX2_1 85 87 PF00082 0.463
CLV_PCSK_KEX2_1 850 852 PF00082 0.583
CLV_PCSK_SKI1_1 118 122 PF00082 0.383
CLV_PCSK_SKI1_1 154 158 PF00082 0.274
CLV_PCSK_SKI1_1 286 290 PF00082 0.592
CLV_PCSK_SKI1_1 294 298 PF00082 0.518
CLV_PCSK_SKI1_1 437 441 PF00082 0.576
CLV_PCSK_SKI1_1 546 550 PF00082 0.528
CLV_PCSK_SKI1_1 577 581 PF00082 0.609
CLV_PCSK_SKI1_1 666 670 PF00082 0.570
CLV_PCSK_SKI1_1 690 694 PF00082 0.578
CLV_PCSK_SKI1_1 871 875 PF00082 0.495
CLV_PCSK_SKI1_1 94 98 PF00082 0.369
CLV_PCSK_SKI1_1 944 948 PF00082 0.567
DEG_MDM2_SWIB_1 166 173 PF02201 0.224
DEG_SPOP_SBC_1 74 78 PF00917 0.639
DOC_ANK_TNKS_1 492 499 PF00023 0.439
DOC_CKS1_1 487 492 PF01111 0.460
DOC_CKS1_1 991 996 PF01111 0.357
DOC_CYCLIN_RxL_1 115 125 PF00134 0.580
DOC_CYCLIN_RxL_1 148 159 PF00134 0.539
DOC_CYCLIN_RxL_1 88 99 PF00134 0.584
DOC_CYCLIN_yCln2_LP_2 624 630 PF00134 0.486
DOC_MAPK_gen_1 126 133 PF00069 0.635
DOC_MAPK_gen_1 152 160 PF00069 0.520
DOC_MAPK_gen_1 575 581 PF00069 0.299
DOC_MAPK_gen_1 653 659 PF00069 0.257
DOC_MAPK_gen_1 769 777 PF00069 0.298
DOC_MAPK_MEF2A_6 152 160 PF00069 0.508
DOC_MAPK_MEF2A_6 368 376 PF00069 0.354
DOC_MAPK_MEF2A_6 524 533 PF00069 0.291
DOC_MAPK_MEF2A_6 653 661 PF00069 0.416
DOC_MAPK_MEF2A_6 678 687 PF00069 0.339
DOC_PP1_RVXF_1 100 106 PF00149 0.536
DOC_PP1_RVXF_1 284 290 PF00149 0.382
DOC_PP1_RVXF_1 688 695 PF00149 0.414
DOC_PP1_RVXF_1 869 876 PF00149 0.331
DOC_PP2B_LxvP_1 203 206 PF13499 0.372
DOC_PP2B_LxvP_1 217 220 PF13499 0.326
DOC_PP2B_LxvP_1 427 430 PF13499 0.274
DOC_PP2B_LxvP_1 531 534 PF13499 0.280
DOC_PP2B_LxvP_1 567 570 PF13499 0.381
DOC_PP2B_LxvP_1 624 627 PF13499 0.495
DOC_USP7_MATH_1 179 183 PF00917 0.345
DOC_USP7_MATH_1 222 226 PF00917 0.333
DOC_USP7_MATH_1 246 250 PF00917 0.392
DOC_USP7_MATH_1 349 353 PF00917 0.409
DOC_USP7_MATH_1 375 379 PF00917 0.350
DOC_USP7_MATH_1 411 415 PF00917 0.497
DOC_USP7_MATH_1 516 520 PF00917 0.304
DOC_USP7_MATH_1 908 912 PF00917 0.412
DOC_USP7_MATH_1 934 938 PF00917 0.299
DOC_USP7_UBL2_3 505 509 PF12436 0.431
DOC_WW_Pin1_4 334 339 PF00397 0.406
DOC_WW_Pin1_4 404 409 PF00397 0.451
DOC_WW_Pin1_4 486 491 PF00397 0.478
DOC_WW_Pin1_4 590 595 PF00397 0.507
DOC_WW_Pin1_4 608 613 PF00397 0.363
DOC_WW_Pin1_4 990 995 PF00397 0.407
LIG_14-3-3_CanoR_1 102 108 PF00244 0.622
LIG_14-3-3_CanoR_1 126 132 PF00244 0.627
LIG_14-3-3_CanoR_1 147 151 PF00244 0.555
LIG_14-3-3_CanoR_1 19 28 PF00244 0.639
LIG_14-3-3_CanoR_1 227 232 PF00244 0.465
LIG_14-3-3_CanoR_1 265 273 PF00244 0.312
LIG_14-3-3_CanoR_1 277 287 PF00244 0.332
LIG_14-3-3_CanoR_1 291 297 PF00244 0.332
LIG_14-3-3_CanoR_1 445 449 PF00244 0.463
LIG_14-3-3_CanoR_1 45 50 PF00244 0.597
LIG_14-3-3_CanoR_1 52 58 PF00244 0.602
LIG_14-3-3_CanoR_1 524 529 PF00244 0.326
LIG_14-3-3_CanoR_1 546 551 PF00244 0.289
LIG_14-3-3_CanoR_1 576 582 PF00244 0.349
LIG_14-3-3_CanoR_1 604 612 PF00244 0.447
LIG_14-3-3_CanoR_1 788 794 PF00244 0.235
LIG_14-3-3_CanoR_1 871 876 PF00244 0.319
LIG_14-3-3_CanoR_1 88 97 PF00244 0.629
LIG_Actin_WH2_2 532 548 PF00022 0.288
LIG_BIR_III_2 919 923 PF00653 0.383
LIG_EH1_1 207 215 PF00400 0.347
LIG_FHA_1 115 121 PF00498 0.565
LIG_FHA_1 176 182 PF00498 0.412
LIG_FHA_1 303 309 PF00498 0.480
LIG_FHA_1 378 384 PF00498 0.470
LIG_FHA_1 520 526 PF00498 0.300
LIG_FHA_1 538 544 PF00498 0.336
LIG_FHA_1 545 551 PF00498 0.328
LIG_FHA_2 20 26 PF00498 0.614
LIG_FHA_2 338 344 PF00498 0.437
LIG_FHA_2 448 454 PF00498 0.422
LIG_FHA_2 457 463 PF00498 0.359
LIG_FHA_2 699 705 PF00498 0.266
LIG_FHA_2 790 796 PF00498 0.243
LIG_FHA_2 8 14 PF00498 0.629
LIG_FHA_2 965 971 PF00498 0.386
LIG_HCF-1_HBM_1 898 901 PF13415 0.292
LIG_Integrin_RGD_1 33 35 PF01839 0.407
LIG_LIR_Apic_2 475 479 PF02991 0.326
LIG_LIR_Apic_2 61 65 PF02991 0.608
LIG_LIR_Gen_1 162 171 PF02991 0.232
LIG_LIR_Gen_1 420 430 PF02991 0.336
LIG_LIR_Gen_1 450 455 PF02991 0.324
LIG_LIR_Gen_1 514 525 PF02991 0.304
LIG_LIR_Gen_1 655 662 PF02991 0.363
LIG_LIR_Gen_1 713 723 PF02991 0.357
LIG_LIR_Gen_1 819 825 PF02991 0.367
LIG_LIR_Gen_1 874 880 PF02991 0.367
LIG_LIR_Nem_3 1007 1013 PF02991 0.296
LIG_LIR_Nem_3 162 167 PF02991 0.241
LIG_LIR_Nem_3 420 426 PF02991 0.340
LIG_LIR_Nem_3 447 451 PF02991 0.459
LIG_LIR_Nem_3 514 520 PF02991 0.320
LIG_LIR_Nem_3 701 705 PF02991 0.409
LIG_LIR_Nem_3 713 719 PF02991 0.318
LIG_LIR_Nem_3 874 878 PF02991 0.372
LIG_LIR_Nem_3 887 893 PF02991 0.292
LIG_NRBOX 49 55 PF00104 0.587
LIG_NRBOX 831 837 PF00104 0.290
LIG_PDZ_Class_2 1024 1029 PF00595 0.322
LIG_Pex14_2 105 109 PF04695 0.544
LIG_Pex14_2 166 170 PF04695 0.224
LIG_Pex14_2 849 853 PF04695 0.273
LIG_REV1ctd_RIR_1 286 295 PF16727 0.347
LIG_SH2_NCK_1 812 816 PF00017 0.307
LIG_SH2_PTP2 164 167 PF00017 0.211
LIG_SH2_PTP2 196 199 PF00017 0.392
LIG_SH2_PTP2 517 520 PF00017 0.290
LIG_SH2_PTP2 716 719 PF00017 0.315
LIG_SH2_SRC 322 325 PF00017 0.355
LIG_SH2_SRC 816 819 PF00017 0.290
LIG_SH2_STAP1 322 326 PF00017 0.423
LIG_SH2_STAP1 641 645 PF00017 0.244
LIG_SH2_STAP1 812 816 PF00017 0.370
LIG_SH2_STAP1 821 825 PF00017 0.334
LIG_SH2_STAT5 1010 1013 PF00017 0.305
LIG_SH2_STAT5 164 167 PF00017 0.266
LIG_SH2_STAT5 196 199 PF00017 0.424
LIG_SH2_STAT5 280 283 PF00017 0.325
LIG_SH2_STAT5 423 426 PF00017 0.374
LIG_SH2_STAT5 469 472 PF00017 0.408
LIG_SH2_STAT5 517 520 PF00017 0.290
LIG_SH2_STAT5 699 702 PF00017 0.355
LIG_SH2_STAT5 716 719 PF00017 0.345
LIG_SH2_STAT5 722 725 PF00017 0.348
LIG_SH2_STAT5 728 731 PF00017 0.373
LIG_SH2_STAT5 776 779 PF00017 0.273
LIG_SH2_STAT5 806 809 PF00017 0.305
LIG_SH2_STAT5 854 857 PF00017 0.348
LIG_SH2_STAT5 890 893 PF00017 0.447
LIG_SH2_STAT5 996 999 PF00017 0.424
LIG_SH3_1 405 411 PF00018 0.425
LIG_SH3_3 168 174 PF00018 0.240
LIG_SH3_3 194 200 PF00018 0.412
LIG_SH3_3 203 209 PF00018 0.378
LIG_SH3_3 405 411 PF00018 0.476
LIG_SH3_3 471 477 PF00018 0.295
LIG_SH3_3 484 490 PF00018 0.453
LIG_SH3_3 610 616 PF00018 0.413
LIG_SH3_3 624 630 PF00018 0.452
LIG_SH3_3 700 706 PF00018 0.414
LIG_SH3_3 734 740 PF00018 0.374
LIG_SH3_3 988 994 PF00018 0.369
LIG_SUMO_SIM_anti_2 1014 1021 PF11976 0.271
LIG_SUMO_SIM_anti_2 46 51 PF11976 0.578
LIG_SUMO_SIM_par_1 178 188 PF11976 0.351
LIG_SUMO_SIM_par_1 792 799 PF11976 0.287
LIG_TRAF2_1 65 68 PF00917 0.625
LIG_TRAF2_1 758 761 PF00917 0.308
LIG_TRAF2_1 968 971 PF00917 0.371
LIG_TYR_ITIM 194 199 PF00017 0.373
LIG_ULM_U2AF65_1 390 395 PF00076 0.283
LIG_WRC_WIRS_1 157 162 PF05994 0.227
MOD_CDK_SPK_2 334 339 PF00069 0.406
MOD_CDK_SPK_2 404 409 PF00069 0.420
MOD_CDK_SPxxK_3 486 493 PF00069 0.442
MOD_CK1_1 292 298 PF00069 0.318
MOD_CK1_1 337 343 PF00069 0.426
MOD_CK1_1 48 54 PF00069 0.611
MOD_CK1_1 519 525 PF00069 0.286
MOD_CK1_1 590 596 PF00069 0.352
MOD_CK1_1 63 69 PF00069 0.662
MOD_CK1_1 990 996 PF00069 0.358
MOD_CK2_1 179 185 PF00069 0.360
MOD_CK2_1 19 25 PF00069 0.625
MOD_CK2_1 447 453 PF00069 0.417
MOD_CK2_1 456 462 PF00069 0.349
MOD_CK2_1 698 704 PF00069 0.265
MOD_CK2_1 755 761 PF00069 0.370
MOD_CK2_1 789 795 PF00069 0.232
MOD_CK2_1 964 970 PF00069 0.391
MOD_CMANNOS 853 856 PF00535 0.442
MOD_Cter_Amidation 731 734 PF01082 0.544
MOD_GlcNHglycan 161 164 PF01048 0.235
MOD_GlcNHglycan 267 270 PF01048 0.522
MOD_GlcNHglycan 490 493 PF01048 0.710
MOD_GlcNHglycan 608 611 PF01048 0.685
MOD_GlcNHglycan 62 65 PF01048 0.498
MOD_GlcNHglycan 643 646 PF01048 0.651
MOD_GlcNHglycan 777 780 PF01048 0.452
MOD_GlcNHglycan 811 815 PF01048 0.492
MOD_GlcNHglycan 901 904 PF01048 0.601
MOD_GlcNHglycan 909 913 PF01048 0.670
MOD_GlcNHglycan 949 952 PF01048 0.569
MOD_GSK3_1 175 182 PF00069 0.379
MOD_GSK3_1 246 253 PF00069 0.392
MOD_GSK3_1 290 297 PF00069 0.404
MOD_GSK3_1 333 340 PF00069 0.478
MOD_GSK3_1 477 484 PF00069 0.511
MOD_GSK3_1 519 526 PF00069 0.283
MOD_GSK3_1 577 584 PF00069 0.330
MOD_GSK3_1 599 606 PF00069 0.452
MOD_GSK3_1 742 749 PF00069 0.421
MOD_GSK3_1 75 82 PF00069 0.690
MOD_GSK3_1 816 823 PF00069 0.316
MOD_LATS_1 17 23 PF00433 0.618
MOD_N-GLC_1 871 876 PF02516 0.519
MOD_NEK2_1 121 126 PF00069 0.601
MOD_NEK2_1 156 161 PF00069 0.357
MOD_NEK2_1 175 180 PF00069 0.365
MOD_NEK2_1 18 23 PF00069 0.647
MOD_NEK2_1 252 257 PF00069 0.356
MOD_NEK2_1 276 281 PF00069 0.348
MOD_NEK2_1 289 294 PF00069 0.411
MOD_NEK2_1 296 301 PF00069 0.321
MOD_NEK2_1 333 338 PF00069 0.396
MOD_NEK2_1 359 364 PF00069 0.437
MOD_NEK2_1 53 58 PF00069 0.646
MOD_NEK2_1 60 65 PF00069 0.646
MOD_NEK2_1 789 794 PF00069 0.271
MOD_NEK2_1 947 952 PF00069 0.374
MOD_NEK2_2 222 227 PF00069 0.341
MOD_NEK2_2 302 307 PF00069 0.486
MOD_NEK2_2 411 416 PF00069 0.429
MOD_NEK2_2 496 501 PF00069 0.449
MOD_NEK2_2 764 769 PF00069 0.283
MOD_PIKK_1 278 284 PF00454 0.313
MOD_PIKK_1 296 302 PF00454 0.297
MOD_PIKK_1 349 355 PF00454 0.393
MOD_PIKK_1 519 525 PF00454 0.286
MOD_PIKK_1 570 576 PF00454 0.329
MOD_PIKK_1 63 69 PF00454 0.637
MOD_PIKK_1 685 691 PF00454 0.433
MOD_PK_1 127 133 PF00069 0.607
MOD_PK_1 227 233 PF00069 0.396
MOD_PK_1 43 49 PF00069 0.603
MOD_PK_1 987 993 PF00069 0.369
MOD_PKA_1 127 133 PF00069 0.619
MOD_PKA_1 19 25 PF00069 0.625
MOD_PKA_1 227 233 PF00069 0.395
MOD_PKA_1 577 583 PF00069 0.337
MOD_PKA_1 653 659 PF00069 0.321
MOD_PKA_2 127 133 PF00069 0.623
MOD_PKA_2 146 152 PF00069 0.561
MOD_PKA_2 18 24 PF00069 0.638
MOD_PKA_2 227 233 PF00069 0.460
MOD_PKA_2 276 282 PF00069 0.330
MOD_PKA_2 290 296 PF00069 0.336
MOD_PKA_2 398 404 PF00069 0.416
MOD_PKA_2 411 417 PF00069 0.497
MOD_PKA_2 444 450 PF00069 0.472
MOD_PKA_2 523 529 PF00069 0.344
MOD_PKA_2 577 583 PF00069 0.358
MOD_PKA_2 588 594 PF00069 0.364
MOD_PKA_2 603 609 PF00069 0.428
MOD_PKA_2 653 659 PF00069 0.374
MOD_PKA_2 732 738 PF00069 0.342
MOD_PKA_2 899 905 PF00069 0.373
MOD_PKB_1 263 271 PF00069 0.331
MOD_PKB_1 575 583 PF00069 0.336
MOD_PKB_1 869 877 PF00069 0.284
MOD_Plk_1 342 348 PF00069 0.424
MOD_Plk_1 599 605 PF00069 0.331
MOD_Plk_1 712 718 PF00069 0.326
MOD_Plk_1 871 877 PF00069 0.360
MOD_Plk_1 987 993 PF00069 0.393
MOD_Plk_2-3 746 752 PF00069 0.412
MOD_Plk_4 127 133 PF00069 0.617
MOD_Plk_4 179 185 PF00069 0.358
MOD_Plk_4 227 233 PF00069 0.393
MOD_Plk_4 444 450 PF00069 0.410
MOD_Plk_4 45 51 PF00069 0.600
MOD_Plk_4 527 533 PF00069 0.296
MOD_Plk_4 653 659 PF00069 0.332
MOD_Plk_4 712 718 PF00069 0.326
MOD_Plk_4 789 795 PF00069 0.265
MOD_Plk_4 816 822 PF00069 0.332
MOD_Plk_4 934 940 PF00069 0.323
MOD_ProDKin_1 334 340 PF00069 0.408
MOD_ProDKin_1 404 410 PF00069 0.452
MOD_ProDKin_1 486 492 PF00069 0.478
MOD_ProDKin_1 590 596 PF00069 0.507
MOD_ProDKin_1 608 614 PF00069 0.361
MOD_ProDKin_1 990 996 PF00069 0.399
TRG_DiLeu_BaEn_1 140 145 PF01217 0.549
TRG_DiLeu_BaEn_1 751 756 PF01217 0.387
TRG_DiLeu_BaLyEn_6 49 54 PF01217 0.608
TRG_DiLeu_BaLyEn_6 562 567 PF01217 0.393
TRG_DiLeu_BaLyEn_6 613 618 PF01217 0.302
TRG_ENDOCYTIC_2 1010 1013 PF00928 0.283
TRG_ENDOCYTIC_2 164 167 PF00928 0.243
TRG_ENDOCYTIC_2 196 199 PF00928 0.392
TRG_ENDOCYTIC_2 423 426 PF00928 0.374
TRG_ENDOCYTIC_2 451 454 PF00928 0.469
TRG_ENDOCYTIC_2 517 520 PF00928 0.290
TRG_ENDOCYTIC_2 699 702 PF00928 0.455
TRG_ENDOCYTIC_2 716 719 PF00928 0.248
TRG_ENDOCYTIC_2 821 824 PF00928 0.397
TRG_ER_diArg_1 126 128 PF00400 0.620
TRG_ER_diArg_1 146 148 PF00400 0.630
TRG_ER_diArg_1 18 20 PF00400 0.624
TRG_ER_diArg_1 226 228 PF00400 0.405
TRG_ER_diArg_1 264 267 PF00400 0.341
TRG_ER_diArg_1 575 578 PF00400 0.477
TRG_ER_diArg_1 665 667 PF00400 0.405
TRG_ER_diArg_1 768 770 PF00400 0.286
TRG_ER_diArg_1 787 789 PF00400 0.349
TRG_ER_diArg_1 839 841 PF00400 0.351
TRG_ER_diArg_1 849 851 PF00400 0.348
TRG_ER_diArg_1 85 88 PF00400 0.649
TRG_ER_diArg_1 867 870 PF00400 0.334
TRG_ER_diArg_1 882 885 PF00400 0.281
TRG_ER_diArg_1 942 945 PF00400 0.333
TRG_NLS_MonoExtN_4 731 737 PF00514 0.324
TRG_Pf-PMV_PEXEL_1 119 123 PF00026 0.386
TRG_Pf-PMV_PEXEL_1 787 791 PF00026 0.561
TRG_Pf-PMV_PEXEL_1 834 838 PF00026 0.471
TRG_Pf-PMV_PEXEL_1 94 99 PF00026 0.365

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 37% 100%
A0A3S5H4Y6 Leishmania donovani 44% 100%
A0A3S5H4Y9 Leishmania donovani 37% 100%
A0A3S7WT86 Leishmania donovani 90% 100%
A0A3S7WWA6 Leishmania donovani 37% 100%
A0A451EJD9 Leishmania donovani 37% 100%
A0A451EJF4 Leishmania donovani 43% 100%
A0A451EJF8 Leishmania donovani 42% 100%
A0A451EJF9 Leishmania donovani 42% 100%
A4H3A9 Leishmania braziliensis 40% 100%
A4H3B4 Leishmania braziliensis 40% 100%
A4H3B6 Leishmania braziliensis 39% 100%
A4H3B8 Leishmania braziliensis 40% 100%
A4H3B9 Leishmania braziliensis 36% 100%
A4H4W8 Leishmania braziliensis 36% 100%
A4HJ20 Leishmania braziliensis 40% 100%
A4HNK6 Leishmania braziliensis 36% 100%
A4HRL9 Leishmania infantum 43% 100%
A4HRM0 Leishmania infantum 44% 100%
A4HRS1 Leishmania infantum 42% 100%
A4HRS3 Leishmania infantum 37% 100%
A4HRS5 Leishmania infantum 42% 100%
A4HW87 Leishmania infantum 90% 76%
A4HZM0 Leishmania infantum 36% 100%
A4I7C7 Leishmania infantum 36% 100%
A4IAQ2 Leishmania infantum 37% 100%
E9AC91 Leishmania major 41% 100%
E9AC92 Leishmania major 41% 100%
E9AC94 Leishmania major 37% 87%
E9AC95 Leishmania major 40% 100%
E9AC96 Leishmania major 41% 100%
E9AC98 Leishmania major 37% 100%
E9AEH8 Leishmania major 36% 100%
E9AHA6 Leishmania infantum 37% 100%
E9AIP8 Leishmania braziliensis 37% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 42% 100%
E9AJI4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 43% 100%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 36% 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) 35% 100%
Q4Q5T6 Leishmania major 36% 100%
Q4QCL8 Leishmania major 36% 100%
Q4QIG9 Leishmania major 36% 100%
Q7YXU9 Leishmania major 37% 100%
Q7YXV1 Leishmania major 37% 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