LeishMANIAdb
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Viscerotropic leishmaniasis antigen, putative

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

Quick info

Protein:
Viscerotropic leishmaniasis antigen, putative
Gene product:
viscerotropic leishmaniasis antigen, putative
Species:
Leishmania donovani
UniProt:
A0A3S5H5G8_LEIDO
TriTrypDb:
LdBPK_050240.1 * , LdCL_050007300 , LDHU3_05.0280
Length:
956

Annotations

LeishMANIAdb annotations

A family of very long coiled-coil proteins, likely performing cytoskeletal functions.. Two varieties have evolved, one with an N-terminal FYVE domain (Non-TM) and another with a C-terminal PDZ domain (might be TM)

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: 0
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: 4
NetGPI no yes: 0, no: 4
Cellular components
Term Name Level Count
GO:0016020 membrane 2 5
GO:0110165 cellular anatomical entity 1 5

Expansion

Sequence features

A0A3S5H5G8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3S5H5G8

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_NRD_NRD_1 277 279 PF00675 0.531
CLV_NRD_NRD_1 890 892 PF00675 0.512
CLV_NRD_NRD_1 913 915 PF00675 0.497
CLV_NRD_NRD_1 953 955 PF00675 0.441
CLV_NRD_NRD_1 98 100 PF00675 0.423
CLV_PCSK_KEX2_1 201 203 PF00082 0.475
CLV_PCSK_KEX2_1 890 892 PF00082 0.512
CLV_PCSK_KEX2_1 913 915 PF00082 0.497
CLV_PCSK_KEX2_1 953 955 PF00082 0.441
CLV_PCSK_PC1ET2_1 201 203 PF00082 0.475
CLV_PCSK_SKI1_1 719 723 PF00082 0.331
CLV_PCSK_SKI1_1 841 845 PF00082 0.275
CLV_PCSK_SKI1_1 900 904 PF00082 0.485
DEG_SPOP_SBC_1 192 196 PF00917 0.727
DEG_SPOP_SBC_1 720 724 PF00917 0.555
DOC_CKS1_1 133 138 PF01111 0.674
DOC_MAPK_DCC_7 68 78 PF00069 0.378
DOC_MAPK_DCC_7 808 817 PF00069 0.463
DOC_MAPK_gen_1 68 78 PF00069 0.409
DOC_MAPK_gen_1 736 745 PF00069 0.534
DOC_MAPK_gen_1 806 815 PF00069 0.468
DOC_MAPK_gen_1 860 867 PF00069 0.676
DOC_MAPK_MEF2A_6 71 80 PF00069 0.293
DOC_MAPK_MEF2A_6 744 752 PF00069 0.537
DOC_MAPK_MEF2A_6 780 788 PF00069 0.535
DOC_MAPK_MEF2A_6 808 817 PF00069 0.463
DOC_MAPK_MEF2A_6 860 867 PF00069 0.606
DOC_PP1_RVXF_1 6 13 PF00149 0.400
DOC_PP2B_PxIxI_1 74 80 PF00149 0.231
DOC_PP4_FxxP_1 166 169 PF00568 0.663
DOC_USP7_MATH_1 120 124 PF00917 0.695
DOC_USP7_MATH_1 246 250 PF00917 0.723
DOC_USP7_MATH_1 720 724 PF00917 0.555
DOC_USP7_MATH_1 871 875 PF00917 0.673
DOC_USP7_MATH_1 912 916 PF00917 0.679
DOC_USP7_MATH_1 923 927 PF00917 0.684
DOC_WW_Pin1_4 116 121 PF00397 0.699
DOC_WW_Pin1_4 132 137 PF00397 0.740
DOC_WW_Pin1_4 179 184 PF00397 0.681
DOC_WW_Pin1_4 867 872 PF00397 0.656
DOC_WW_Pin1_4 875 880 PF00397 0.662
DOC_WW_Pin1_4 885 890 PF00397 0.623
DOC_WW_Pin1_4 944 949 PF00397 0.703
LIG_14-3-3_CanoR_1 137 146 PF00244 0.677
LIG_14-3-3_CanoR_1 226 235 PF00244 0.720
LIG_14-3-3_CanoR_1 28 38 PF00244 0.419
LIG_14-3-3_CanoR_1 719 729 PF00244 0.527
LIG_14-3-3_CanoR_1 896 904 PF00244 0.648
LIG_14-3-3_CanoR_1 913 923 PF00244 0.666
LIG_14-3-3_CanoR_1 924 930 PF00244 0.669
LIG_14-3-3_CterR_2 953 956 PF00244 0.688
LIG_BIR_II_1 1 5 PF00653 0.380
LIG_eIF4E_1 267 273 PF01652 0.632
LIG_FHA_1 180 186 PF00498 0.651
LIG_FHA_1 238 244 PF00498 0.745
LIG_FHA_1 255 261 PF00498 0.655
LIG_FHA_1 267 273 PF00498 0.668
LIG_FHA_1 40 46 PF00498 0.358
LIG_FHA_1 55 61 PF00498 0.331
LIG_FHA_1 760 766 PF00498 0.479
LIG_FHA_1 876 882 PF00498 0.659
LIG_FHA_2 228 234 PF00498 0.758
LIG_FHA_2 929 935 PF00498 0.680
LIG_LIR_Apic_2 163 169 PF02991 0.657
LIG_LIR_Gen_1 44 55 PF02991 0.385
LIG_LIR_Nem_3 44 50 PF02991 0.382
LIG_SH2_CRK 946 950 PF00017 0.701
LIG_SH2_NCK_1 47 51 PF00017 0.407
LIG_SH2_NCK_1 946 950 PF00017 0.701
LIG_SH2_SRC 792 795 PF00017 0.496
LIG_SH2_STAP1 825 829 PF00017 0.547
LIG_SH2_STAT5 40 43 PF00017 0.388
LIG_SH2_STAT5 792 795 PF00017 0.496
LIG_SH2_STAT5 908 911 PF00017 0.683
LIG_SH2_STAT5 946 949 PF00017 0.699
LIG_SH2_STAT5 97 100 PF00017 0.404
LIG_SH3_3 130 136 PF00018 0.679
LIG_SH3_3 16 22 PF00018 0.394
LIG_SH3_3 210 216 PF00018 0.724
LIG_SH3_3 248 254 PF00018 0.663
LIG_SH3_3 876 882 PF00018 0.669
LIG_SUMO_SIM_par_1 761 766 PF11976 0.550
LIG_SUMO_SIM_par_1 813 819 PF11976 0.504
LIG_TRAF2_1 314 317 PF00917 0.712
LIG_TRAF2_1 347 350 PF00917 0.609
LIG_TRAF2_1 380 383 PF00917 0.603
LIG_TRAF2_1 413 416 PF00917 0.633
LIG_TRAF2_1 446 449 PF00917 0.632
LIG_TRAF2_1 479 482 PF00917 0.647
LIG_TRAF2_1 512 515 PF00917 0.629
LIG_TRAF2_1 545 548 PF00917 0.623
LIG_TRAF2_1 578 581 PF00917 0.623
LIG_TRAF2_1 611 614 PF00917 0.616
LIG_TRAF2_1 644 647 PF00917 0.599
LIG_TRAF2_1 677 680 PF00917 0.581
LIG_TRAF2_1 710 713 PF00917 0.567
LIG_TRAF2_1 931 934 PF00917 0.680
LIG_TRAF2_2 173 178 PF00917 0.754
LIG_TYR_ITIM 45 50 PF00017 0.385
MOD_CDK_SPK_2 132 137 PF00069 0.675
MOD_CDK_SPK_2 885 890 PF00069 0.662
MOD_CDK_SPxK_1 885 891 PF00069 0.665
MOD_CDK_SPxxK_3 179 186 PF00069 0.683
MOD_CK1_1 138 144 PF00069 0.798
MOD_CK1_1 187 193 PF00069 0.760
MOD_CK1_1 256 262 PF00069 0.667
MOD_CK1_1 268 274 PF00069 0.724
MOD_CK1_1 32 38 PF00069 0.440
MOD_CK1_1 872 878 PF00069 0.672
MOD_CK1_1 898 904 PF00069 0.687
MOD_CK1_1 907 913 PF00069 0.643
MOD_CK1_1 915 921 PF00069 0.626
MOD_CK1_1 928 934 PF00069 0.641
MOD_CK2_1 721 727 PF00069 0.512
MOD_CK2_1 750 756 PF00069 0.551
MOD_CK2_1 915 921 PF00069 0.706
MOD_CK2_1 928 934 PF00069 0.652
MOD_Cter_Amidation 858 861 PF01082 0.471
MOD_GlcNHglycan 15 18 PF01048 0.599
MOD_GlcNHglycan 190 193 PF01048 0.501
MOD_GlcNHglycan 248 251 PF01048 0.540
MOD_GlcNHglycan 287 290 PF01048 0.517
MOD_GlcNHglycan 31 34 PF01048 0.516
MOD_GlcNHglycan 874 877 PF01048 0.447
MOD_GlcNHglycan 897 900 PF01048 0.493
MOD_GlcNHglycan 937 941 PF01048 0.429
MOD_GSK3_1 116 123 PF00069 0.699
MOD_GSK3_1 131 138 PF00069 0.728
MOD_GSK3_1 150 157 PF00069 0.648
MOD_GSK3_1 184 191 PF00069 0.784
MOD_GSK3_1 233 240 PF00069 0.734
MOD_GSK3_1 50 57 PF00069 0.362
MOD_GSK3_1 867 874 PF00069 0.665
MOD_GSK3_1 890 897 PF00069 0.658
MOD_GSK3_1 903 910 PF00069 0.619
MOD_GSK3_1 924 931 PF00069 0.678
MOD_LATS_1 850 856 PF00433 0.583
MOD_N-GLC_1 10 15 PF02516 0.644
MOD_N-GLC_1 285 290 PF02516 0.470
MOD_N-GLC_1 29 34 PF02516 0.504
MOD_N-GLC_1 50 55 PF02516 0.595
MOD_N-GLC_2 54 56 PF02516 0.551
MOD_NEK2_1 139 144 PF00069 0.701
MOD_NEK2_1 185 190 PF00069 0.646
MOD_NEK2_1 265 270 PF00069 0.681
MOD_NEK2_1 285 290 PF00069 0.674
MOD_NEK2_1 29 34 PF00069 0.416
MOD_NEK2_1 895 900 PF00069 0.668
MOD_NEK2_1 903 908 PF00069 0.617
MOD_PIKK_1 853 859 PF00454 0.571
MOD_PK_1 15 21 PF00069 0.392
MOD_PKA_1 890 896 PF00069 0.705
MOD_PKA_2 185 191 PF00069 0.704
MOD_PKA_2 225 231 PF00069 0.797
MOD_PKA_2 246 252 PF00069 0.742
MOD_PKA_2 890 896 PF00069 0.691
MOD_PKA_2 912 918 PF00069 0.680
MOD_PKA_2 923 929 PF00069 0.684
MOD_Plk_1 177 183 PF00069 0.680
MOD_Plk_1 327 333 PF00069 0.586
MOD_Plk_1 360 366 PF00069 0.601
MOD_Plk_1 393 399 PF00069 0.610
MOD_Plk_1 426 432 PF00069 0.618
MOD_Plk_1 459 465 PF00069 0.620
MOD_Plk_1 492 498 PF00069 0.626
MOD_Plk_1 525 531 PF00069 0.612
MOD_Plk_1 558 564 PF00069 0.606
MOD_Plk_1 591 597 PF00069 0.599
MOD_Plk_1 624 630 PF00069 0.581
MOD_Plk_1 657 663 PF00069 0.553
MOD_Plk_1 690 696 PF00069 0.556
MOD_Plk_1 853 859 PF00069 0.540
MOD_Plk_1 936 942 PF00069 0.628
MOD_Plk_4 259 265 PF00069 0.645
MOD_Plk_4 268 274 PF00069 0.609
MOD_Plk_4 750 756 PF00069 0.473
MOD_Plk_4 759 765 PF00069 0.482
MOD_Plk_4 904 910 PF00069 0.645
MOD_ProDKin_1 116 122 PF00069 0.701
MOD_ProDKin_1 132 138 PF00069 0.740
MOD_ProDKin_1 179 185 PF00069 0.681
MOD_ProDKin_1 867 873 PF00069 0.656
MOD_ProDKin_1 875 881 PF00069 0.665
MOD_ProDKin_1 885 891 PF00069 0.626
MOD_ProDKin_1 944 950 PF00069 0.704
MOD_SUMO_for_1 200 203 PF00179 0.640
MOD_SUMO_rev_2 148 153 PF00179 0.647
MOD_SUMO_rev_2 709 718 PF00179 0.546
TRG_DiLeu_BaEn_1 317 322 PF01217 0.570
TRG_DiLeu_BaEn_1 449 454 PF01217 0.602
TRG_DiLeu_BaEn_1 515 520 PF01217 0.599
TRG_DiLeu_BaEn_1 548 553 PF01217 0.592
TRG_DiLeu_BaEn_1 581 586 PF01217 0.589
TRG_DiLeu_BaEn_1 614 619 PF01217 0.578
TRG_DiLeu_BaEn_1 759 764 PF01217 0.573
TRG_DiLeu_BaEn_4 349 355 PF01217 0.615
TRG_DiLeu_BaEn_4 382 388 PF01217 0.610
TRG_DiLeu_BaEn_4 415 421 PF01217 0.643
TRG_DiLeu_BaEn_4 481 487 PF01217 0.660
TRG_DiLeu_BaEn_4 646 652 PF01217 0.603
TRG_DiLeu_BaEn_4 679 685 PF01217 0.571
TRG_DiLeu_BaLyEn_6 879 884 PF01217 0.670
TRG_ENDOCYTIC_2 47 50 PF00928 0.408
TRG_ENDOCYTIC_2 908 911 PF00928 0.605
TRG_ER_diArg_1 741 744 PF00400 0.602
TRG_ER_diArg_1 889 891 PF00400 0.704
TRG_ER_diArg_1 952 954 PF00400 0.683
TRG_NES_CRM1_1 783 794 PF08389 0.536
TRG_NLS_Bipartite_1 278 299 PF00514 0.631
TRG_NLS_MonoExtN_4 221 227 PF00514 0.664
TRG_NLS_MonoExtN_4 294 299 PF00514 0.620
TRG_Pf-PMV_PEXEL_1 914 919 PF00026 0.423
TRG_Pf-PMV_PEXEL_1 99 103 PF00026 0.347

Homologs

Protein Taxonomy Sequence identity Coverage
A4HSF6 Leishmania infantum 92% 100%
E9AKC8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 72% 85%
Q4QJH9 Leishmania major 68% 77%

Download

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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