LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania major
UniProt:
E9AER2_LEIMA
TriTrypDb:
LmjF.35.0870 , LMJLV39_350014400 * , LMJSD75_350013900 *
Length:
923

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: 5
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: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 10
NetGPI no yes: 0, no: 10
Cellular components
Term Name Level Count
GO:0005737 cytoplasm 2 2
GO:0005829 cytosol 2 2
GO:0032991 protein-containing complex 1 2
GO:0070209 ASTRA complex 3 2
GO:0110165 cellular anatomical entity 1 2
GO:0140513 nuclear protein-containing complex 2 2

Expansion

Sequence features

E9AER2
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AER2

Function

Biological processes
Term Name Level Count
GO:0000723 telomere maintenance 5 2
GO:0006139 nucleobase-containing compound metabolic process 3 2
GO:0006259 DNA metabolic process 4 2
GO:0006278 RNA-templated DNA biosynthetic process 6 2
GO:0006725 cellular aromatic compound metabolic process 3 2
GO:0006807 nitrogen compound metabolic process 2 2
GO:0006996 organelle organization 4 2
GO:0007004 telomere maintenance via telomerase 7 2
GO:0008152 metabolic process 1 2
GO:0009058 biosynthetic process 2 2
GO:0009059 macromolecule biosynthetic process 4 2
GO:0009987 cellular process 1 2
GO:0010833 telomere maintenance via telomere lengthening 6 2
GO:0016043 cellular component organization 3 2
GO:0018130 heterocycle biosynthetic process 4 2
GO:0019438 aromatic compound biosynthetic process 4 2
GO:0031647 regulation of protein stability 3 2
GO:0032200 telomere organization 6 2
GO:0034641 cellular nitrogen compound metabolic process 3 2
GO:0034654 nucleobase-containing compound biosynthetic process 4 2
GO:0043170 macromolecule metabolic process 3 2
GO:0044237 cellular metabolic process 2 2
GO:0044238 primary metabolic process 2 2
GO:0044249 cellular biosynthetic process 3 2
GO:0044260 obsolete cellular macromolecule metabolic process 3 2
GO:0044271 cellular nitrogen compound biosynthetic process 4 2
GO:0046483 heterocycle metabolic process 3 2
GO:0050821 protein stabilization 4 2
GO:0051276 chromosome organization 5 2
GO:0065007 biological regulation 1 2
GO:0065008 regulation of biological quality 2 2
GO:0071704 organic substance metabolic process 2 2
GO:0071840 cellular component organization or biogenesis 2 2
GO:0071897 DNA biosynthetic process 5 2
GO:0090304 nucleic acid metabolic process 4 2
GO:1901360 organic cyclic compound metabolic process 3 2
GO:1901362 organic cyclic compound biosynthetic process 4 2
GO:1901576 organic substance biosynthetic process 3 2
Molecular functions
Term Name Level Count
GO:0003676 nucleic acid binding 3 2
GO:0003677 DNA binding 4 2
GO:0005488 binding 1 2
GO:0005515 protein binding 2 2
GO:0031072 heat shock protein binding 3 2
GO:0042162 telomeric DNA binding 6 2
GO:0043565 sequence-specific DNA binding 5 2
GO:0051879 Hsp90 protein binding 4 2
GO:0097159 organic cyclic compound binding 2 2
GO:1901363 heterocyclic compound binding 2 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 13 17 PF00656 0.560
CLV_C14_Caspase3-7 406 410 PF00656 0.608
CLV_MEL_PAP_1 457 463 PF00089 0.735
CLV_NRD_NRD_1 170 172 PF00675 0.496
CLV_NRD_NRD_1 179 181 PF00675 0.435
CLV_NRD_NRD_1 220 222 PF00675 0.705
CLV_NRD_NRD_1 708 710 PF00675 0.693
CLV_NRD_NRD_1 722 724 PF00675 0.497
CLV_NRD_NRD_1 819 821 PF00675 0.419
CLV_NRD_NRD_1 843 845 PF00675 0.587
CLV_PCSK_KEX2_1 170 172 PF00082 0.490
CLV_PCSK_KEX2_1 179 181 PF00082 0.435
CLV_PCSK_KEX2_1 220 222 PF00082 0.657
CLV_PCSK_KEX2_1 241 243 PF00082 0.543
CLV_PCSK_KEX2_1 722 724 PF00082 0.594
CLV_PCSK_KEX2_1 843 845 PF00082 0.587
CLV_PCSK_PC1ET2_1 241 243 PF00082 0.543
CLV_PCSK_SKI1_1 114 118 PF00082 0.564
CLV_PCSK_SKI1_1 155 159 PF00082 0.512
CLV_PCSK_SKI1_1 186 190 PF00082 0.480
CLV_PCSK_SKI1_1 19 23 PF00082 0.540
CLV_PCSK_SKI1_1 2 6 PF00082 0.457
CLV_PCSK_SKI1_1 296 300 PF00082 0.433
CLV_PCSK_SKI1_1 8 12 PF00082 0.422
CLV_Separin_Metazoa 829 833 PF03568 0.363
DEG_APCC_DBOX_1 295 303 PF00400 0.399
DEG_APCC_DBOX_1 7 15 PF00400 0.559
DEG_MDM2_SWIB_1 863 871 PF02201 0.473
DEG_Nend_UBRbox_1 1 4 PF02207 0.487
DOC_CKS1_1 21 26 PF01111 0.506
DOC_CKS1_1 257 262 PF01111 0.425
DOC_CKS1_1 772 777 PF01111 0.480
DOC_CYCLIN_RxL_1 180 192 PF00134 0.552
DOC_CYCLIN_RxL_1 853 866 PF00134 0.554
DOC_CYCLIN_yCln2_LP_2 344 350 PF00134 0.476
DOC_CYCLIN_yCln2_LP_2 630 636 PF00134 0.544
DOC_MAPK_DCC_7 832 842 PF00069 0.516
DOC_MAPK_gen_1 170 178 PF00069 0.460
DOC_MAPK_gen_1 42 51 PF00069 0.564
DOC_MAPK_gen_1 448 457 PF00069 0.654
DOC_MAPK_gen_1 620 629 PF00069 0.386
DOC_MAPK_gen_1 709 715 PF00069 0.761
DOC_MAPK_HePTP_8 617 629 PF00069 0.498
DOC_MAPK_MEF2A_6 44 53 PF00069 0.522
DOC_MAPK_MEF2A_6 448 457 PF00069 0.639
DOC_MAPK_MEF2A_6 620 629 PF00069 0.403
DOC_MAPK_RevD_3 164 180 PF00069 0.529
DOC_PP1_RVXF_1 857 864 PF00149 0.550
DOC_PP2B_LxvP_1 630 633 PF13499 0.544
DOC_PP2B_PxIxI_1 710 716 PF00149 0.655
DOC_PP4_FxxP_1 479 482 PF00568 0.727
DOC_USP7_MATH_1 222 226 PF00917 0.563
DOC_USP7_MATH_1 360 364 PF00917 0.646
DOC_USP7_MATH_1 432 436 PF00917 0.647
DOC_USP7_MATH_1 480 484 PF00917 0.702
DOC_USP7_MATH_1 511 515 PF00917 0.750
DOC_USP7_MATH_1 559 563 PF00917 0.470
DOC_USP7_MATH_1 823 827 PF00917 0.460
DOC_USP7_MATH_1 857 861 PF00917 0.615
DOC_USP7_MATH_1 895 899 PF00917 0.490
DOC_USP7_UBL2_3 326 330 PF12436 0.541
DOC_WW_Pin1_4 20 25 PF00397 0.656
DOC_WW_Pin1_4 256 261 PF00397 0.413
DOC_WW_Pin1_4 545 550 PF00397 0.609
DOC_WW_Pin1_4 64 69 PF00397 0.437
DOC_WW_Pin1_4 771 776 PF00397 0.486
LIG_14-3-3_CanoR_1 114 119 PF00244 0.602
LIG_14-3-3_CanoR_1 170 178 PF00244 0.550
LIG_14-3-3_CanoR_1 230 235 PF00244 0.512
LIG_14-3-3_CanoR_1 288 295 PF00244 0.484
LIG_14-3-3_CanoR_1 460 465 PF00244 0.654
LIG_14-3-3_CanoR_1 565 574 PF00244 0.503
LIG_Actin_WH2_2 154 172 PF00022 0.538
LIG_ActinCP_TwfCPI_2 479 489 PF01115 0.659
LIG_AP2alpha_1 365 369 PF02296 0.581
LIG_BIR_III_4 569 573 PF00653 0.474
LIG_BRCT_BRCA1_1 232 236 PF00533 0.482
LIG_BRCT_BRCA1_1 320 324 PF00533 0.518
LIG_BRCT_BRCA1_1 328 332 PF00533 0.512
LIG_BRCT_BRCA1_1 567 571 PF00533 0.518
LIG_BRCT_BRCA1_1 579 583 PF00533 0.506
LIG_BRCT_BRCA1_1 859 863 PF00533 0.466
LIG_BRCT_BRCA1_2 320 326 PF00533 0.542
LIG_BRCT_BRCA1_2 567 573 PF00533 0.570
LIG_BRCT_BRCA1_2 859 865 PF00533 0.571
LIG_eIF4E_1 651 657 PF01652 0.518
LIG_EVH1_1 697 701 PF00568 0.630
LIG_FHA_1 130 136 PF00498 0.480
LIG_FHA_1 152 158 PF00498 0.472
LIG_FHA_1 273 279 PF00498 0.461
LIG_FHA_1 340 346 PF00498 0.498
LIG_FHA_1 376 382 PF00498 0.578
LIG_FHA_1 400 406 PF00498 0.439
LIG_FHA_1 588 594 PF00498 0.577
LIG_FHA_1 64 70 PF00498 0.421
LIG_FHA_1 652 658 PF00498 0.542
LIG_FHA_1 700 706 PF00498 0.624
LIG_FHA_1 889 895 PF00498 0.512
LIG_FHA_2 21 27 PF00498 0.692
LIG_FHA_2 311 317 PF00498 0.513
LIG_FHA_2 332 338 PF00498 0.549
LIG_FHA_2 404 410 PF00498 0.633
LIG_FHA_2 519 525 PF00498 0.524
LIG_FHA_2 680 686 PF00498 0.686
LIG_LIR_Gen_1 123 134 PF02991 0.503
LIG_LIR_Gen_1 196 206 PF02991 0.502
LIG_LIR_Gen_1 233 243 PF02991 0.476
LIG_LIR_Gen_1 318 324 PF02991 0.464
LIG_LIR_Gen_1 473 482 PF02991 0.605
LIG_LIR_Gen_1 537 545 PF02991 0.436
LIG_LIR_Gen_1 580 589 PF02991 0.594
LIG_LIR_Gen_1 762 772 PF02991 0.464
LIG_LIR_Gen_1 801 810 PF02991 0.453
LIG_LIR_Gen_1 907 916 PF02991 0.534
LIG_LIR_Nem_3 123 129 PF02991 0.410
LIG_LIR_Nem_3 196 201 PF02991 0.441
LIG_LIR_Nem_3 233 239 PF02991 0.465
LIG_LIR_Nem_3 318 323 PF02991 0.469
LIG_LIR_Nem_3 473 479 PF02991 0.613
LIG_LIR_Nem_3 537 542 PF02991 0.422
LIG_LIR_Nem_3 568 574 PF02991 0.539
LIG_LIR_Nem_3 57 63 PF02991 0.600
LIG_LIR_Nem_3 580 586 PF02991 0.573
LIG_LIR_Nem_3 646 651 PF02991 0.476
LIG_LIR_Nem_3 762 767 PF02991 0.465
LIG_LIR_Nem_3 783 789 PF02991 0.483
LIG_LIR_Nem_3 801 807 PF02991 0.306
LIG_LIR_Nem_3 833 837 PF02991 0.497
LIG_LIR_Nem_3 907 913 PF02991 0.614
LIG_LYPXL_S_1 696 700 PF13949 0.584
LIG_LYPXL_yS_3 697 700 PF13949 0.584
LIG_NRBOX 163 169 PF00104 0.466
LIG_PCNA_yPIPBox_3 230 239 PF02747 0.525
LIG_Pex14_2 194 198 PF04695 0.494
LIG_Pex14_2 320 324 PF04695 0.407
LIG_Pex14_2 365 369 PF04695 0.581
LIG_Pex14_2 751 755 PF04695 0.490
LIG_Pex14_2 804 808 PF04695 0.505
LIG_Pex14_2 863 867 PF04695 0.413
LIG_PTB_Apo_2 267 274 PF02174 0.482
LIG_REV1ctd_RIR_1 476 481 PF16727 0.652
LIG_SH2_CRK 350 354 PF00017 0.481
LIG_SH2_CRK 400 404 PF00017 0.552
LIG_SH2_CRK 539 543 PF00017 0.439
LIG_SH2_CRK 621 625 PF00017 0.493
LIG_SH2_CRK 740 744 PF00017 0.525
LIG_SH2_CRK 858 862 PF00017 0.567
LIG_SH2_CRK 910 914 PF00017 0.544
LIG_SH2_GRB2like 740 743 PF00017 0.619
LIG_SH2_STAP1 274 278 PF00017 0.339
LIG_SH2_STAP1 350 354 PF00017 0.459
LIG_SH2_STAP1 400 404 PF00017 0.552
LIG_SH2_STAP1 437 441 PF00017 0.728
LIG_SH2_STAP1 539 543 PF00017 0.356
LIG_SH2_STAP1 740 744 PF00017 0.515
LIG_SH2_STAP1 910 914 PF00017 0.544
LIG_SH2_STAT5 187 190 PF00017 0.562
LIG_SH2_STAT5 193 196 PF00017 0.446
LIG_SH2_STAT5 274 277 PF00017 0.403
LIG_SH2_STAT5 354 357 PF00017 0.417
LIG_SH2_STAT5 520 523 PF00017 0.658
LIG_SH2_STAT5 773 776 PF00017 0.433
LIG_SH3_1 695 701 PF00018 0.618
LIG_SH3_3 18 24 PF00018 0.666
LIG_SH3_3 280 286 PF00018 0.384
LIG_SH3_3 466 472 PF00018 0.594
LIG_SH3_3 593 599 PF00018 0.447
LIG_SH3_3 626 632 PF00018 0.484
LIG_SH3_3 693 699 PF00018 0.620
LIG_SH3_3 769 775 PF00018 0.446
LIG_SH3_3 97 103 PF00018 0.497
LIG_SUMO_SIM_anti_2 527 534 PF11976 0.474
LIG_SUMO_SIM_anti_2 592 598 PF11976 0.379
LIG_SUMO_SIM_anti_2 626 631 PF11976 0.371
LIG_SUMO_SIM_anti_2 826 833 PF11976 0.443
LIG_SUMO_SIM_anti_2 869 875 PF11976 0.474
LIG_SUMO_SIM_par_1 600 605 PF11976 0.504
LIG_SUMO_SIM_par_1 891 898 PF11976 0.429
LIG_TRAF2_1 472 475 PF00917 0.739
LIG_TRAF2_1 485 488 PF00917 0.540
LIG_TRAF2_1 920 923 PF00917 0.590
LIG_TRFH_1 468 472 PF08558 0.579
LIG_TYR_ITIM 348 353 PF00017 0.374
LIG_TYR_ITIM 619 624 PF00017 0.429
LIG_TYR_ITIM 856 861 PF00017 0.575
LIG_UBA3_1 157 162 PF00899 0.522
LIG_UBA3_1 177 186 PF00899 0.214
LIG_UBA3_1 234 241 PF00899 0.495
LIG_UBA3_1 352 358 PF00899 0.440
LIG_WRC_WIRS_1 512 517 PF05994 0.600
MOD_CDK_SPxxK_3 20 27 PF00069 0.503
MOD_CK1_1 215 221 PF00069 0.668
MOD_CK1_1 251 257 PF00069 0.553
MOD_CK1_1 339 345 PF00069 0.317
MOD_CK1_1 418 424 PF00069 0.567
MOD_CK1_1 442 448 PF00069 0.650
MOD_CK1_1 530 536 PF00069 0.541
MOD_CK1_1 587 593 PF00069 0.591
MOD_CK1_1 676 682 PF00069 0.692
MOD_CK1_1 781 787 PF00069 0.479
MOD_CK2_1 310 316 PF00069 0.475
MOD_CK2_1 460 466 PF00069 0.740
MOD_CK2_1 482 488 PF00069 0.650
MOD_CK2_1 518 524 PF00069 0.522
MOD_CK2_1 531 537 PF00069 0.410
MOD_CK2_1 679 685 PF00069 0.686
MOD_CK2_1 823 829 PF00069 0.484
MOD_CK2_1 866 872 PF00069 0.535
MOD_CK2_1 98 104 PF00069 0.446
MOD_CMANNOS 228 231 PF00535 0.414
MOD_Cter_Amidation 707 710 PF01082 0.724
MOD_GlcNHglycan 250 253 PF01048 0.531
MOD_GlcNHglycan 320 323 PF01048 0.540
MOD_GlcNHglycan 334 337 PF01048 0.498
MOD_GlcNHglycan 406 409 PF01048 0.556
MOD_GlcNHglycan 441 444 PF01048 0.677
MOD_GlcNHglycan 561 564 PF01048 0.426
MOD_GlcNHglycan 639 642 PF01048 0.416
MOD_GlcNHglycan 675 678 PF01048 0.720
MOD_GlcNHglycan 706 709 PF01048 0.766
MOD_GlcNHglycan 81 85 PF01048 0.646
MOD_GlcNHglycan 868 871 PF01048 0.546
MOD_GSK3_1 332 339 PF00069 0.516
MOD_GSK3_1 399 406 PF00069 0.406
MOD_GSK3_1 415 422 PF00069 0.560
MOD_GSK3_1 527 534 PF00069 0.474
MOD_GSK3_1 64 71 PF00069 0.496
MOD_GSK3_1 673 680 PF00069 0.637
MOD_GSK3_1 699 706 PF00069 0.643
MOD_GSK3_1 709 716 PF00069 0.632
MOD_GSK3_1 76 83 PF00069 0.510
MOD_GSK3_1 857 864 PF00069 0.495
MOD_N-GLC_1 114 119 PF02516 0.596
MOD_N-GLC_1 418 423 PF02516 0.566
MOD_N-GLC_1 732 737 PF02516 0.721
MOD_NEK2_1 119 124 PF00069 0.486
MOD_NEK2_1 129 134 PF00069 0.358
MOD_NEK2_1 136 141 PF00069 0.344
MOD_NEK2_1 14 19 PF00069 0.600
MOD_NEK2_1 206 211 PF00069 0.487
MOD_NEK2_1 381 386 PF00069 0.594
MOD_NEK2_1 403 408 PF00069 0.543
MOD_NEK2_1 415 420 PF00069 0.399
MOD_NEK2_1 459 464 PF00069 0.722
MOD_NEK2_1 665 670 PF00069 0.523
MOD_NEK2_1 861 866 PF00069 0.463
MOD_NEK2_1 98 103 PF00069 0.397
MOD_NEK2_2 212 217 PF00069 0.671
MOD_NEK2_2 399 404 PF00069 0.429
MOD_NEK2_2 895 900 PF00069 0.509
MOD_PIKK_1 215 221 PF00454 0.716
MOD_PIKK_1 432 438 PF00454 0.669
MOD_PIKK_1 442 448 PF00454 0.600
MOD_PIKK_1 665 671 PF00454 0.473
MOD_PK_1 709 715 PF00069 0.729
MOD_PKA_1 709 715 PF00069 0.761
MOD_PKA_2 14 20 PF00069 0.580
MOD_PKA_2 287 293 PF00069 0.496
MOD_PKA_2 459 465 PF00069 0.613
MOD_PKA_2 480 486 PF00069 0.729
MOD_PKA_2 587 593 PF00069 0.547
MOD_PKB_1 575 583 PF00069 0.557
MOD_PKB_1 736 744 PF00069 0.548
MOD_Plk_1 114 120 PF00069 0.574
MOD_Plk_1 222 228 PF00069 0.529
MOD_Plk_1 336 342 PF00069 0.461
MOD_Plk_2-3 685 691 PF00069 0.576
MOD_Plk_4 114 120 PF00069 0.555
MOD_Plk_4 129 135 PF00069 0.340
MOD_Plk_4 156 162 PF00069 0.399
MOD_Plk_4 223 229 PF00069 0.497
MOD_Plk_4 230 236 PF00069 0.412
MOD_Plk_4 399 405 PF00069 0.413
MOD_Plk_4 460 466 PF00069 0.732
MOD_Plk_4 527 533 PF00069 0.519
MOD_Plk_4 589 595 PF00069 0.463
MOD_Plk_4 597 603 PF00069 0.445
MOD_Plk_4 709 715 PF00069 0.661
MOD_Plk_4 781 787 PF00069 0.394
MOD_Plk_4 82 88 PF00069 0.570
MOD_Plk_4 823 829 PF00069 0.416
MOD_Plk_4 863 869 PF00069 0.443
MOD_Plk_4 908 914 PF00069 0.574
MOD_ProDKin_1 20 26 PF00069 0.653
MOD_ProDKin_1 256 262 PF00069 0.416
MOD_ProDKin_1 545 551 PF00069 0.603
MOD_ProDKin_1 64 70 PF00069 0.433
MOD_ProDKin_1 771 777 PF00069 0.482
MOD_SUMO_for_1 428 431 PF00179 0.515
MOD_SUMO_rev_2 148 157 PF00179 0.557
MOD_SUMO_rev_2 240 248 PF00179 0.530
MOD_SUMO_rev_2 483 491 PF00179 0.749
MOD_SUMO_rev_2 712 721 PF00179 0.669
TRG_DiLeu_BaEn_1 589 594 PF01217 0.403
TRG_DiLeu_BaEn_1 612 617 PF01217 0.480
TRG_DiLeu_BaEn_2 327 333 PF01217 0.556
TRG_DiLeu_BaLyEn_6 340 345 PF01217 0.476
TRG_DiLeu_BaLyEn_6 410 415 PF01217 0.629
TRG_ENDOCYTIC_2 350 353 PF00928 0.381
TRG_ENDOCYTIC_2 400 403 PF00928 0.554
TRG_ENDOCYTIC_2 476 479 PF00928 0.732
TRG_ENDOCYTIC_2 539 542 PF00928 0.416
TRG_ENDOCYTIC_2 621 624 PF00928 0.406
TRG_ENDOCYTIC_2 697 700 PF00928 0.568
TRG_ENDOCYTIC_2 740 743 PF00928 0.547
TRG_ENDOCYTIC_2 858 861 PF00928 0.571
TRG_ENDOCYTIC_2 910 913 PF00928 0.545
TRG_ER_diArg_1 169 171 PF00400 0.443
TRG_ER_diArg_1 178 180 PF00400 0.437
TRG_ER_diArg_1 574 577 PF00400 0.587
TRG_ER_diArg_1 722 724 PF00400 0.594
TRG_ER_diArg_1 734 737 PF00400 0.585
TRG_ER_diArg_1 842 844 PF00400 0.535
TRG_NES_CRM1_1 34 47 PF08389 0.462
TRG_NES_CRM1_1 494 509 PF08389 0.692
TRG_Pf-PMV_PEXEL_1 565 569 PF00026 0.553
TRG_Pf-PMV_PEXEL_1 900 905 PF00026 0.520

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P438 Leptomonas seymouri 53% 100%
A0A1X0NJ45 Trypanosomatidae 31% 95%
A0A3Q8ILW9 Leishmania donovani 92% 100%
A0A3R7MMH0 Trypanosoma rangeli 32% 95%
A4HMB8 Leishmania braziliensis 77% 100%
A4IAY4 Leishmania infantum 92% 100%
C9ZNI1 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 31% 96%
E9B5W7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 92% 100%
V5BAN0 Trypanosoma cruzi 30% 94%

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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