LeishMANIAdb
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Stealth_CR3 domain-containing protein

Quick info Annotations Function or PPIs Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Stealth_CR3 domain-containing protein
Gene product:
Protein of unknown function (DUF3184), putative
Species:
Leishmania mexicana
UniProt:
E9AQR1_LEIMU
TriTrypDb:
LmxM.16.1015
Length:
929

Annotations

LeishMANIAdb annotations

N-acetylglucosamine-1-phosphotransferase homologous protein. Assumed to be a type II TM protein like its distant relatives.. Signal-anchored glycan biogenesis protein essential for mannose 6-P generation (lysosomal signal for the Metazoan hosts). Family only expended 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: 120
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: 32
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 36
NetGPI no yes: 0, no: 36
Cellular components
Term Name Level Count
GO:0016020 membrane 2 19
GO:0110165 cellular anatomical entity 1 26
GO:0005794 Golgi apparatus 5 9
GO:0043226 organelle 2 9
GO:0043227 membrane-bounded organelle 3 9
GO:0043229 intracellular organelle 3 9
GO:0043231 intracellular membrane-bounded organelle 4 9

Expansion

Sequence features

E9AQR1
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AQR1

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 35
GO:0016740 transferase activity 2 35
GO:0016772 transferase activity, transferring phosphorus-containing groups 3 16

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 332 336 PF00656 0.466
CLV_C14_Caspase3-7 499 503 PF00656 0.353
CLV_C14_Caspase3-7 611 615 PF00656 0.374
CLV_C14_Caspase3-7 687 691 PF00656 0.436
CLV_MEL_PAP_1 202 208 PF00089 0.641
CLV_NRD_NRD_1 158 160 PF00675 0.707
CLV_NRD_NRD_1 194 196 PF00675 0.707
CLV_NRD_NRD_1 225 227 PF00675 0.604
CLV_NRD_NRD_1 39 41 PF00675 0.570
CLV_NRD_NRD_1 432 434 PF00675 0.569
CLV_NRD_NRD_1 519 521 PF00675 0.699
CLV_NRD_NRD_1 522 524 PF00675 0.663
CLV_NRD_NRD_1 595 597 PF00675 0.714
CLV_NRD_NRD_1 714 716 PF00675 0.528
CLV_NRD_NRD_1 808 810 PF00675 0.730
CLV_PCSK_FUR_1 520 524 PF00082 0.668
CLV_PCSK_FUR_1 593 597 PF00082 0.686
CLV_PCSK_KEX2_1 158 160 PF00082 0.706
CLV_PCSK_KEX2_1 194 196 PF00082 0.697
CLV_PCSK_KEX2_1 38 40 PF00082 0.573
CLV_PCSK_KEX2_1 45 47 PF00082 0.552
CLV_PCSK_KEX2_1 519 521 PF00082 0.699
CLV_PCSK_KEX2_1 522 524 PF00082 0.621
CLV_PCSK_KEX2_1 595 597 PF00082 0.708
CLV_PCSK_KEX2_1 714 716 PF00082 0.528
CLV_PCSK_KEX2_1 808 810 PF00082 0.730
CLV_PCSK_PC1ET2_1 45 47 PF00082 0.546
CLV_PCSK_PC7_1 34 40 PF00082 0.502
CLV_PCSK_SKI1_1 195 199 PF00082 0.661
CLV_PCSK_SKI1_1 338 342 PF00082 0.678
CLV_PCSK_SKI1_1 34 38 PF00082 0.481
CLV_PCSK_SKI1_1 392 396 PF00082 0.586
CLV_PCSK_SKI1_1 429 433 PF00082 0.646
CLV_PCSK_SKI1_1 434 438 PF00082 0.604
CLV_PCSK_SKI1_1 523 527 PF00082 0.679
CLV_PCSK_SKI1_1 561 565 PF00082 0.562
CLV_PCSK_SKI1_1 673 677 PF00082 0.682
CLV_PCSK_SKI1_1 714 718 PF00082 0.654
CLV_PCSK_SKI1_1 770 774 PF00082 0.721
CLV_PCSK_SKI1_1 854 858 PF00082 0.698
DEG_APCC_DBOX_1 304 312 PF00400 0.446
DEG_SCF_FBW7_1 116 123 PF00400 0.485
DEG_SCF_FBW7_1 129 134 PF00400 0.486
DOC_CKS1_1 128 133 PF01111 0.495
DOC_CKS1_1 680 685 PF01111 0.490
DOC_CYCLIN_RxL_1 711 719 PF00134 0.328
DOC_CYCLIN_yCln2_LP_2 563 569 PF00134 0.361
DOC_MAPK_DCC_7 648 657 PF00069 0.438
DOC_MAPK_gen_1 354 362 PF00069 0.279
DOC_MAPK_gen_1 390 399 PF00069 0.386
DOC_MAPK_gen_1 45 55 PF00069 0.592
DOC_MAPK_gen_1 556 565 PF00069 0.471
DOC_MAPK_gen_1 648 657 PF00069 0.459
DOC_MAPK_HePTP_8 676 688 PF00069 0.487
DOC_MAPK_MEF2A_6 392 401 PF00069 0.386
DOC_MAPK_MEF2A_6 48 57 PF00069 0.468
DOC_MAPK_MEF2A_6 558 567 PF00069 0.472
DOC_MAPK_MEF2A_6 679 688 PF00069 0.488
DOC_MAPK_MEF2A_6 751 758 PF00069 0.532
DOC_PP1_RVXF_1 891 898 PF00149 0.403
DOC_PP1_SILK_1 429 434 PF00149 0.348
DOC_PP2B_LxvP_1 437 440 PF13499 0.351
DOC_PP2B_LxvP_1 563 566 PF13499 0.472
DOC_PP2B_LxvP_1 857 860 PF13499 0.447
DOC_PP4_FxxP_1 115 118 PF00568 0.480
DOC_PP4_FxxP_1 680 683 PF00568 0.441
DOC_USP7_MATH_1 124 128 PF00917 0.527
DOC_USP7_MATH_1 254 258 PF00917 0.396
DOC_USP7_MATH_1 352 356 PF00917 0.415
DOC_USP7_MATH_1 549 553 PF00917 0.301
DOC_USP7_MATH_1 846 850 PF00917 0.490
DOC_USP7_MATH_1 901 905 PF00917 0.521
DOC_WW_Pin1_4 114 119 PF00397 0.530
DOC_WW_Pin1_4 120 125 PF00397 0.546
DOC_WW_Pin1_4 127 132 PF00397 0.544
DOC_WW_Pin1_4 141 146 PF00397 0.498
DOC_WW_Pin1_4 195 200 PF00397 0.487
DOC_WW_Pin1_4 260 265 PF00397 0.407
DOC_WW_Pin1_4 323 328 PF00397 0.360
DOC_WW_Pin1_4 578 583 PF00397 0.472
DOC_WW_Pin1_4 679 684 PF00397 0.489
DOC_WW_Pin1_4 96 101 PF00397 0.535
LIG_14-3-3_CanoR_1 14 22 PF00244 0.688
LIG_14-3-3_CanoR_1 158 166 PF00244 0.477
LIG_14-3-3_CanoR_1 194 198 PF00244 0.534
LIG_14-3-3_CanoR_1 305 309 PF00244 0.420
LIG_14-3-3_CanoR_1 361 366 PF00244 0.379
LIG_14-3-3_CanoR_1 376 380 PF00244 0.320
LIG_14-3-3_CanoR_1 392 401 PF00244 0.361
LIG_14-3-3_CanoR_1 450 458 PF00244 0.360
LIG_14-3-3_CanoR_1 474 481 PF00244 0.438
LIG_14-3-3_CanoR_1 522 532 PF00244 0.348
LIG_14-3-3_CanoR_1 556 565 PF00244 0.378
LIG_14-3-3_CanoR_1 596 605 PF00244 0.492
LIG_14-3-3_CanoR_1 69 77 PF00244 0.452
LIG_14-3-3_CanoR_1 755 759 PF00244 0.525
LIG_14-3-3_CanoR_1 776 784 PF00244 0.423
LIG_14-3-3_CanoR_1 89 98 PF00244 0.547
LIG_14-3-3_CanoR_1 925 929 PF00244 0.484
LIG_Actin_WH2_2 346 363 PF00022 0.474
LIG_Actin_WH2_2 53 71 PF00022 0.249
LIG_Actin_WH2_2 606 624 PF00022 0.326
LIG_APCC_ABBA_1 460 465 PF00400 0.312
LIG_BIR_III_2 601 605 PF00653 0.452
LIG_BIR_III_2 690 694 PF00653 0.439
LIG_BRCT_BRCA1_1 580 584 PF00533 0.386
LIG_FHA_1 132 138 PF00498 0.579
LIG_FHA_1 145 151 PF00498 0.499
LIG_FHA_1 279 285 PF00498 0.357
LIG_FHA_1 299 305 PF00498 0.481
LIG_FHA_1 604 610 PF00498 0.508
LIG_FHA_1 787 793 PF00498 0.352
LIG_FHA_1 861 867 PF00498 0.431
LIG_FHA_1 907 913 PF00498 0.406
LIG_FHA_2 107 113 PF00498 0.499
LIG_FHA_2 117 123 PF00498 0.497
LIG_FHA_2 14 20 PF00498 0.698
LIG_FHA_2 196 202 PF00498 0.401
LIG_FHA_2 242 248 PF00498 0.376
LIG_FHA_2 330 336 PF00498 0.466
LIG_FHA_2 442 448 PF00498 0.438
LIG_FHA_2 638 644 PF00498 0.425
LIG_FHA_2 70 76 PF00498 0.479
LIG_FHA_2 763 769 PF00498 0.473
LIG_FHA_2 99 105 PF00498 0.502
LIG_GBD_Chelix_1 50 58 PF00786 0.383
LIG_LIR_Apic_2 112 118 PF02991 0.479
LIG_LIR_Apic_2 909 913 PF02991 0.392
LIG_LIR_Gen_1 147 153 PF02991 0.450
LIG_LIR_Gen_1 164 174 PF02991 0.455
LIG_LIR_Gen_1 210 221 PF02991 0.411
LIG_LIR_Gen_1 452 462 PF02991 0.346
LIG_LIR_Gen_1 502 513 PF02991 0.375
LIG_LIR_Gen_1 629 636 PF02991 0.390
LIG_LIR_Gen_1 682 693 PF02991 0.449
LIG_LIR_Gen_1 915 924 PF02991 0.506
LIG_LIR_LC3C_4 880 885 PF02991 0.490
LIG_LIR_Nem_3 147 152 PF02991 0.488
LIG_LIR_Nem_3 164 170 PF02991 0.457
LIG_LIR_Nem_3 210 216 PF02991 0.382
LIG_LIR_Nem_3 414 420 PF02991 0.376
LIG_LIR_Nem_3 502 508 PF02991 0.368
LIG_LIR_Nem_3 547 553 PF02991 0.391
LIG_LIR_Nem_3 562 567 PF02991 0.351
LIG_LIR_Nem_3 581 587 PF02991 0.460
LIG_LIR_Nem_3 629 635 PF02991 0.385
LIG_LIR_Nem_3 682 688 PF02991 0.488
LIG_LIR_Nem_3 867 872 PF02991 0.460
LIG_MAD2 776 784 PF02301 0.460
LIG_MYND_1 114 118 PF01753 0.476
LIG_MYND_1 184 188 PF01753 0.489
LIG_NRBOX 53 59 PF00104 0.319
LIG_PDZ_Class_1 924 929 PF00595 0.318
LIG_PTB_Apo_2 239 246 PF02174 0.446
LIG_PTB_Apo_2 399 406 PF02174 0.361
LIG_PTB_Apo_2 650 657 PF02174 0.405
LIG_PTB_Phospho_1 239 245 PF10480 0.358
LIG_PTB_Phospho_1 399 405 PF10480 0.361
LIG_PTB_Phospho_1 650 656 PF10480 0.444
LIG_RPA_C_Fungi 882 894 PF08784 0.495
LIG_SH2_CRK 213 217 PF00017 0.494
LIG_SH2_CRK 550 554 PF00017 0.388
LIG_SH2_GRB2like 149 152 PF00017 0.536
LIG_SH2_GRB2like 275 278 PF00017 0.423
LIG_SH2_GRB2like 400 403 PF00017 0.564
LIG_SH2_GRB2like 656 659 PF00017 0.530
LIG_SH2_NCK_1 505 509 PF00017 0.446
LIG_SH2_PTP2 149 152 PF00017 0.536
LIG_SH2_PTP2 275 278 PF00017 0.358
LIG_SH2_SRC 149 152 PF00017 0.536
LIG_SH2_SRC 174 177 PF00017 0.550
LIG_SH2_SRC 275 278 PF00017 0.381
LIG_SH2_SRC 505 508 PF00017 0.445
LIG_SH2_SRC 685 688 PF00017 0.590
LIG_SH2_SRC 731 734 PF00017 0.641
LIG_SH2_STAP1 524 528 PF00017 0.498
LIG_SH2_STAP1 544 548 PF00017 0.241
LIG_SH2_STAP1 788 792 PF00017 0.462
LIG_SH2_STAP1 917 921 PF00017 0.340
LIG_SH2_STAT3 788 791 PF00017 0.631
LIG_SH2_STAT5 149 152 PF00017 0.540
LIG_SH2_STAT5 179 182 PF00017 0.652
LIG_SH2_STAT5 21 24 PF00017 0.618
LIG_SH2_STAT5 270 273 PF00017 0.440
LIG_SH2_STAT5 275 278 PF00017 0.415
LIG_SH2_STAT5 405 408 PF00017 0.409
LIG_SH2_STAT5 467 470 PF00017 0.568
LIG_SH2_STAT5 532 535 PF00017 0.396
LIG_SH2_STAT5 587 590 PF00017 0.458
LIG_SH2_STAT5 656 659 PF00017 0.525
LIG_SH2_STAT5 685 688 PF00017 0.578
LIG_SH2_STAT5 788 791 PF00017 0.426
LIG_SH3_3 137 143 PF00018 0.726
LIG_SH3_3 178 184 PF00018 0.613
LIG_SH3_3 433 439 PF00018 0.396
LIG_SH3_3 485 491 PF00018 0.470
LIG_SH3_3 505 511 PF00018 0.560
LIG_SH3_3 815 821 PF00018 0.539
LIG_SH3_3 905 911 PF00018 0.476
LIG_SH3_3 92 98 PF00018 0.647
LIG_SH3_CIN85_PxpxPR_1 514 519 PF14604 0.511
LIG_SUMO_SIM_anti_2 880 886 PF11976 0.545
LIG_SUMO_SIM_par_1 321 326 PF11976 0.443
LIG_SUMO_SIM_par_1 493 499 PF11976 0.422
LIG_SUMO_SIM_par_1 862 868 PF11976 0.539
LIG_SUMO_SIM_par_1 880 886 PF11976 0.358
LIG_TRAF2_1 730 733 PF00917 0.621
LIG_TYR_ITIM 211 216 PF00017 0.583
LIG_TYR_ITIM 548 553 PF00017 0.396
LIG_TYR_ITSM 145 152 PF00017 0.573
LIG_WRC_WIRS_1 212 217 PF05994 0.483
MOD_CDK_SPK_2 578 583 PF00069 0.480
MOD_CDK_SPxK_1 120 126 PF00069 0.623
MOD_CK1_1 10 16 PF00069 0.631
MOD_CK1_1 127 133 PF00069 0.673
MOD_CK1_1 144 150 PF00069 0.583
MOD_CK1_1 24 30 PF00069 0.558
MOD_CK1_1 307 313 PF00069 0.465
MOD_CK1_1 355 361 PF00069 0.512
MOD_CK1_1 441 447 PF00069 0.503
MOD_CK1_1 70 76 PF00069 0.527
MOD_CK1_1 793 799 PF00069 0.407
MOD_CK2_1 106 112 PF00069 0.601
MOD_CK2_1 195 201 PF00069 0.499
MOD_CK2_1 241 247 PF00069 0.433
MOD_CK2_1 441 447 PF00069 0.519
MOD_CK2_1 637 643 PF00069 0.517
MOD_CK2_1 69 75 PF00069 0.563
MOD_CK2_1 727 733 PF00069 0.474
MOD_CK2_1 762 768 PF00069 0.637
MOD_CK2_1 799 805 PF00069 0.617
MOD_Cter_Amidation 43 46 PF01082 0.670
MOD_GlcNHglycan 109 112 PF01048 0.622
MOD_GlcNHglycan 137 140 PF01048 0.632
MOD_GlcNHglycan 23 26 PF01048 0.593
MOD_GlcNHglycan 476 479 PF01048 0.563
MOD_GlcNHglycan 485 488 PF01048 0.635
MOD_GlcNHglycan 558 561 PF01048 0.401
MOD_GlcNHglycan 664 667 PF01048 0.557
MOD_GlcNHglycan 69 72 PF01048 0.626
MOD_GlcNHglycan 75 80 PF01048 0.620
MOD_GlcNHglycan 778 781 PF01048 0.508
MOD_GlcNHglycan 795 798 PF01048 0.555
MOD_GlcNHglycan 848 851 PF01048 0.624
MOD_GlcNHglycan 876 879 PF01048 0.415
MOD_GlcNHglycan 91 94 PF01048 0.724
MOD_GSK3_1 10 17 PF00069 0.620
MOD_GSK3_1 114 121 PF00069 0.665
MOD_GSK3_1 127 134 PF00069 0.659
MOD_GSK3_1 20 27 PF00069 0.587
MOD_GSK3_1 232 239 PF00069 0.379
MOD_GSK3_1 254 261 PF00069 0.485
MOD_GSK3_1 420 427 PF00069 0.459
MOD_GSK3_1 786 793 PF00069 0.439
MOD_GSK3_1 89 96 PF00069 0.709
MOD_LATS_1 359 365 PF00433 0.409
MOD_LATS_1 521 527 PF00433 0.409
MOD_LATS_1 554 560 PF00433 0.318
MOD_N-GLC_1 216 221 PF02516 0.525
MOD_N-GLC_1 241 246 PF02516 0.532
MOD_N-GLC_1 392 397 PF02516 0.409
MOD_N-GLC_1 637 642 PF02516 0.474
MOD_NEK2_1 240 245 PF00069 0.405
MOD_NEK2_1 258 263 PF00069 0.480
MOD_NEK2_1 284 289 PF00069 0.499
MOD_NEK2_1 304 309 PF00069 0.390
MOD_NEK2_1 360 365 PF00069 0.478
MOD_NEK2_1 539 544 PF00069 0.511
MOD_NEK2_1 591 596 PF00069 0.570
MOD_NEK2_1 738 743 PF00069 0.443
MOD_NEK2_1 906 911 PF00069 0.459
MOD_NEK2_2 549 554 PF00069 0.380
MOD_NEK2_2 762 767 PF00069 0.540
MOD_PIKK_1 124 130 PF00454 0.599
MOD_PIKK_1 152 158 PF00454 0.576
MOD_PIKK_1 603 609 PF00454 0.507
MOD_PK_1 799 805 PF00069 0.705
MOD_PKA_2 10 16 PF00069 0.659
MOD_PKA_2 157 163 PF00069 0.562
MOD_PKA_2 193 199 PF00069 0.649
MOD_PKA_2 298 304 PF00069 0.428
MOD_PKA_2 355 361 PF00069 0.426
MOD_PKA_2 375 381 PF00069 0.393
MOD_PKA_2 449 455 PF00069 0.392
MOD_PKA_2 754 760 PF00069 0.600
MOD_PKA_2 93 99 PF00069 0.704
MOD_PKB_1 390 398 PF00069 0.456
MOD_PKB_1 67 75 PF00069 0.518
MOD_Plk_1 240 246 PF00069 0.466
MOD_Plk_1 392 398 PF00069 0.456
MOD_Plk_1 636 642 PF00069 0.474
MOD_Plk_2-3 241 247 PF00069 0.431
MOD_Plk_2-3 298 304 PF00069 0.560
MOD_Plk_2-3 637 643 PF00069 0.340
MOD_Plk_2-3 790 796 PF00069 0.634
MOD_Plk_4 211 217 PF00069 0.477
MOD_Plk_4 241 247 PF00069 0.460
MOD_Plk_4 254 260 PF00069 0.493
MOD_Plk_4 284 290 PF00069 0.361
MOD_Plk_4 329 335 PF00069 0.496
MOD_Plk_4 420 426 PF00069 0.458
MOD_ProDKin_1 114 120 PF00069 0.643
MOD_ProDKin_1 127 133 PF00069 0.664
MOD_ProDKin_1 141 147 PF00069 0.602
MOD_ProDKin_1 195 201 PF00069 0.581
MOD_ProDKin_1 260 266 PF00069 0.467
MOD_ProDKin_1 323 329 PF00069 0.408
MOD_ProDKin_1 578 584 PF00069 0.562
MOD_ProDKin_1 679 685 PF00069 0.587
MOD_ProDKin_1 96 102 PF00069 0.651
MOD_SUMO_rev_2 886 895 PF00179 0.683
TRG_DiLeu_BaEn_1 182 187 PF01217 0.591
TRG_DiLeu_BaEn_1 903 908 PF01217 0.479
TRG_DiLeu_BaEn_4 182 188 PF01217 0.574
TRG_ENDOCYTIC_2 149 152 PF00928 0.582
TRG_ENDOCYTIC_2 213 216 PF00928 0.512
TRG_ENDOCYTIC_2 275 278 PF00928 0.471
TRG_ENDOCYTIC_2 505 508 PF00928 0.438
TRG_ENDOCYTIC_2 550 553 PF00928 0.411
TRG_ENDOCYTIC_2 569 572 PF00928 0.414
TRG_ENDOCYTIC_2 656 659 PF00928 0.530
TRG_ENDOCYTIC_2 685 688 PF00928 0.598
TRG_ENDOCYTIC_2 917 920 PF00928 0.451
TRG_ER_diArg_1 319 322 PF00400 0.443
TRG_ER_diArg_1 353 356 PF00400 0.288
TRG_ER_diArg_1 37 40 PF00400 0.676
TRG_ER_diArg_1 389 392 PF00400 0.444
TRG_ER_diArg_1 46 49 PF00400 0.607
TRG_ER_diArg_1 518 520 PF00400 0.553
TRG_ER_diArg_1 522 524 PF00400 0.467
TRG_ER_diArg_1 593 596 PF00400 0.592
TRG_ER_diArg_1 66 69 PF00400 0.496
TRG_ER_diArg_1 713 715 PF00400 0.371
TRG_ER_diArg_1 8 11 PF00400 0.616
TRG_ER_diArg_1 831 834 PF00400 0.576
TRG_NLS_MonoExtC_3 44 49 PF00514 0.631
TRG_Pf-PMV_PEXEL_1 714 719 PF00026 0.426

Homologs

Protein Taxonomy Sequence identity Coverage
A0A1X0NYY7 Trypanosomatidae 42% 100%
A0A3Q8IAD3 Leishmania donovani 54% 95%
A0A3Q8IAF8 Leishmania donovani 71% 97%
A0A3Q8IAK8 Leishmania donovani 75% 95%
A0A3Q8IJ32 Leishmania donovani 90% 100%
A0A3S5H6Y1 Leishmania donovani 73% 98%
A0A3S7WTZ8 Leishmania donovani 62% 90%
A0A3S7WU13 Leishmania donovani 87% 99%
A0A422NAR5 Trypanosoma rangeli 44% 100%
A4H8M5 Leishmania braziliensis 63% 100%
A4H8M7 Leishmania braziliensis 75% 100%
A4H8N1 Leishmania braziliensis 53% 100%
A4HWZ5 Leishmania infantum 87% 99%
A4HWZ6 Leishmania infantum 71% 100%
A4HWZ8 Leishmania infantum 73% 100%
A4HX00 Leishmania infantum 62% 90%
A4HX01 Leishmania infantum 54% 100%
A4HX05 Leishmania infantum 70% 96%
E8NHI9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 99%
E9AGP0 Leishmania infantum 81% 100%
E9AQQ9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 96% 100%
E9AQR0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 78% 100%
E9AQR2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 72% 98%
E9AQR3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 65% 91%
E9AQR4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 55% 95%
Q4QER2 Leishmania major 54% 100%
Q4QER3 Leishmania major 62% 91%
Q4QER4 Leishmania major 79% 100%
Q4QER5 Leishmania major 87% 99%
Q4QER6 Leishmania major 87% 99%
Q4QER7 Leishmania major 80% 99%
Q4QER8 Leishmania major 70% 100%
Q4QER9 Leishmania major 71% 100%
Q4QES0 Leishmania major 86% 99%
V5ANJ8 Trypanosoma cruzi 44% 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