LeishMANIAdb
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Putative viscerotropic leishmaniasis antigen

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

Quick info

Protein:
Putative viscerotropic leishmaniasis antigen
Gene product:
Protein of unknown function (DUF2946), putative
Species:
Leishmania infantum
UniProt:
A4HSF6_LEIIN
TriTrypDb:
Length:
854

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: 3
NetGPI no yes: 0, no: 3
Cellular components
Term Name Level Count
GO:0016020 membrane 2 4
GO:0110165 cellular anatomical entity 1 4

Expansion

Sequence features

A4HSF6
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HSF6

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_NRD_NRD_1 201 203 PF00675 0.447
CLV_NRD_NRD_1 380 382 PF00675 0.487
CLV_NRD_NRD_1 784 786 PF00675 0.468
CLV_PCSK_FUR_1 782 786 PF00082 0.467
CLV_PCSK_KEX2_1 304 306 PF00082 0.504
CLV_PCSK_KEX2_1 782 784 PF00082 0.468
CLV_PCSK_PC1ET2_1 304 306 PF00082 0.504
CLV_PCSK_PC7_1 779 785 PF00082 0.458
CLV_PCSK_SKI1_1 13 17 PF00082 0.283
CLV_Separin_Metazoa 60 64 PF03568 0.420
DEG_SPOP_SBC_1 295 299 PF00917 0.709
DEG_SPOP_SBC_1 43 47 PF00917 0.405
DOC_CKS1_1 236 241 PF01111 0.784
DOC_MAPK_DCC_7 171 181 PF00069 0.467
DOC_MAPK_gen_1 171 181 PF00069 0.467
DOC_MAPK_MEF2A_6 174 183 PF00069 0.366
DOC_PP1_RVXF_1 109 116 PF00149 0.455
DOC_PP2B_LxvP_1 17 20 PF13499 0.258
DOC_PP2B_PxIxI_1 177 183 PF00149 0.283
DOC_PP4_FxxP_1 269 272 PF00568 0.694
DOC_USP7_MATH_1 223 227 PF00917 0.769
DOC_USP7_MATH_1 349 353 PF00917 0.766
DOC_USP7_MATH_1 43 47 PF00917 0.405
DOC_USP7_MATH_1 66 70 PF00917 0.382
DOC_WW_Pin1_4 219 224 PF00397 0.726
DOC_WW_Pin1_4 235 240 PF00397 0.675
DOC_WW_Pin1_4 282 287 PF00397 0.703
DOC_WW_Pin1_4 771 776 PF00397 0.668
LIG_14-3-3_CanoR_1 131 141 PF00244 0.366
LIG_14-3-3_CanoR_1 240 249 PF00244 0.782
LIG_14-3-3_CanoR_1 25 29 PF00244 0.258
LIG_14-3-3_CanoR_1 329 338 PF00244 0.813
LIG_14-3-3_CanoR_1 74 81 PF00244 0.307
LIG_BIR_II_1 1 5 PF00653 0.695
LIG_BRCT_BRCA1_1 32 36 PF00533 0.316
LIG_BRCT_BRCA1_1 45 49 PF00533 0.355
LIG_eIF4E_1 370 376 PF01652 0.685
LIG_FHA_1 143 149 PF00498 0.403
LIG_FHA_1 158 164 PF00498 0.291
LIG_FHA_1 283 289 PF00498 0.745
LIG_FHA_1 341 347 PF00498 0.785
LIG_FHA_1 358 364 PF00498 0.622
LIG_FHA_1 370 376 PF00498 0.685
LIG_FHA_1 89 95 PF00498 0.330
LIG_FHA_2 331 337 PF00498 0.812
LIG_FHA_2 55 61 PF00498 0.460
LIG_FHA_2 741 747 PF00498 0.550
LIG_LIR_Apic_2 266 272 PF02991 0.692
LIG_LIR_Apic_2 777 781 PF02991 0.647
LIG_LIR_Gen_1 147 158 PF02991 0.427
LIG_LIR_Gen_1 46 56 PF02991 0.438
LIG_LIR_Nem_3 147 153 PF02991 0.433
LIG_LIR_Nem_3 80 84 PF02991 0.328
LIG_Pex14_2 86 90 PF04695 0.305
LIG_SH2_NCK_1 150 154 PF00017 0.455
LIG_SH2_STAP1 54 58 PF00017 0.421
LIG_SH2_STAT5 143 146 PF00017 0.340
LIG_SH2_STAT5 200 203 PF00017 0.451
LIG_SH2_STAT5 71 74 PF00017 0.466
LIG_SH3_3 119 125 PF00018 0.434
LIG_SH3_3 233 239 PF00018 0.770
LIG_SH3_3 313 319 PF00018 0.801
LIG_SH3_3 351 357 PF00018 0.754
LIG_SH3_3 790 796 PF00018 0.630
LIG_SH3_CIN85_PxpxPR_1 401 406 PF14604 0.653
LIG_SH3_CIN85_PxpxPR_1 764 769 PF14604 0.675
LIG_SUMO_SIM_par_1 27 33 PF11976 0.316
LIG_TRAF2_1 417 420 PF00917 0.659
LIG_TRAF2_1 450 453 PF00917 0.639
LIG_TRAF2_1 483 486 PF00917 0.657
LIG_TRAF2_1 516 519 PF00917 0.670
LIG_TRAF2_1 549 552 PF00917 0.657
LIG_TRAF2_1 582 585 PF00917 0.733
LIG_TRAF2_1 615 618 PF00917 0.654
LIG_TRAF2_1 648 651 PF00917 0.666
LIG_TRAF2_1 681 684 PF00917 0.647
LIG_TRAF2_1 714 717 PF00917 0.645
LIG_TRAF2_1 747 750 PF00917 0.639
LIG_TRAF2_1 813 816 PF00917 0.641
LIG_TRAF2_2 276 281 PF00917 0.702
LIG_TYR_ITIM 148 153 PF00017 0.436
LIG_WW_3 60 64 PF00397 0.420
MOD_CDK_SPK_2 235 240 PF00069 0.785
MOD_CDK_SPK_2 771 776 PF00069 0.668
MOD_CDK_SPxxK_3 282 289 PF00069 0.706
MOD_CK1_1 135 141 PF00069 0.445
MOD_CK1_1 241 247 PF00069 0.776
MOD_CK1_1 290 296 PF00069 0.706
MOD_CK1_1 359 365 PF00069 0.717
MOD_CK1_1 371 377 PF00069 0.717
MOD_CK1_1 69 75 PF00069 0.387
MOD_CK1_1 77 83 PF00069 0.316
MOD_CK1_1 774 780 PF00069 0.654
MOD_CK2_1 54 60 PF00069 0.462
MOD_CK2_1 740 746 PF00069 0.551
MOD_GlcNHglycan 118 121 PF01048 0.627
MOD_GlcNHglycan 134 137 PF01048 0.641
MOD_GlcNHglycan 293 296 PF01048 0.569
MOD_GlcNHglycan 32 35 PF01048 0.302
MOD_GlcNHglycan 351 354 PF01048 0.500
MOD_GlcNHglycan 390 393 PF01048 0.509
MOD_GSK3_1 153 160 PF00069 0.426
MOD_GSK3_1 219 226 PF00069 0.785
MOD_GSK3_1 234 241 PF00069 0.674
MOD_GSK3_1 253 260 PF00069 0.822
MOD_GSK3_1 287 294 PF00069 0.709
MOD_GSK3_1 336 343 PF00069 0.754
MOD_GSK3_1 69 76 PF00069 0.366
MOD_GSK3_1 787 794 PF00069 0.648
MOD_N-GLC_1 113 118 PF02516 0.691
MOD_N-GLC_1 132 137 PF02516 0.631
MOD_N-GLC_1 153 158 PF02516 0.628
MOD_N-GLC_1 388 393 PF02516 0.553
MOD_N-GLC_2 157 159 PF02516 0.608
MOD_NEK2_1 1 6 PF00069 0.695
MOD_NEK2_1 132 137 PF00069 0.436
MOD_NEK2_1 242 247 PF00069 0.697
MOD_NEK2_1 288 293 PF00069 0.711
MOD_NEK2_1 29 34 PF00069 0.397
MOD_NEK2_1 35 40 PF00069 0.306
MOD_NEK2_1 368 373 PF00069 0.736
MOD_NEK2_1 388 393 PF00069 0.790
MOD_NEK2_1 44 49 PF00069 0.350
MOD_NEK2_1 88 93 PF00069 0.308
MOD_PIKK_1 795 801 PF00454 0.578
MOD_PK_1 118 124 PF00069 0.430
MOD_PKA_2 24 30 PF00069 0.258
MOD_PKA_2 288 294 PF00069 0.710
MOD_PKA_2 328 334 PF00069 0.750
MOD_PKA_2 349 355 PF00069 0.715
MOD_PKA_2 69 75 PF00069 0.381
MOD_PKA_2 791 797 PF00069 0.616
MOD_Plk_1 280 286 PF00069 0.703
MOD_Plk_1 430 436 PF00069 0.743
MOD_Plk_1 463 469 PF00069 0.608
MOD_Plk_1 496 502 PF00069 0.630
MOD_Plk_1 529 535 PF00069 0.632
MOD_Plk_1 562 568 PF00069 0.652
MOD_Plk_1 595 601 PF00069 0.646
MOD_Plk_1 628 634 PF00069 0.627
MOD_Plk_1 66 72 PF00069 0.405
MOD_Plk_1 661 667 PF00069 0.625
MOD_Plk_1 694 700 PF00069 0.610
MOD_Plk_1 727 733 PF00069 0.611
MOD_Plk_1 826 832 PF00069 0.613
MOD_Plk_4 24 30 PF00069 0.316
MOD_Plk_4 362 368 PF00069 0.686
MOD_Plk_4 371 377 PF00069 0.649
MOD_Plk_4 45 51 PF00069 0.385
MOD_ProDKin_1 219 225 PF00069 0.728
MOD_ProDKin_1 235 241 PF00069 0.675
MOD_ProDKin_1 282 288 PF00069 0.704
MOD_ProDKin_1 771 777 PF00069 0.665
MOD_SUMO_for_1 303 306 PF00179 0.703
MOD_SUMO_rev_2 251 256 PF00179 0.685
TRG_DiLeu_BaEn_4 419 425 PF01217 0.620
TRG_DiLeu_BaEn_4 452 458 PF01217 0.648
TRG_DiLeu_BaEn_4 485 491 PF01217 0.666
TRG_DiLeu_BaEn_4 518 524 PF01217 0.677
TRG_DiLeu_BaEn_4 551 557 PF01217 0.626
TRG_DiLeu_BaEn_4 584 590 PF01217 0.734
TRG_DiLeu_BaEn_4 617 623 PF01217 0.622
TRG_DiLeu_BaEn_4 650 656 PF01217 0.632
TRG_DiLeu_BaEn_4 683 689 PF01217 0.611
TRG_DiLeu_BaEn_4 716 722 PF01217 0.613
TRG_DiLeu_BaEn_4 749 755 PF01217 0.655
TRG_ENDOCYTIC_2 150 153 PF00928 0.459
TRG_ER_diArg_1 405 408 PF00400 0.623
TRG_ER_diArg_1 68 71 PF00400 0.373
TRG_ER_diArg_1 768 771 PF00400 0.676
TRG_ER_diArg_1 781 784 PF00400 0.631
TRG_ER_diArg_1 839 842 PF00400 0.564
TRG_NLS_Bipartite_1 381 403 PF00514 0.706
TRG_NLS_MonoCore_2 398 403 PF00514 0.674
TRG_NLS_MonoExtC_3 397 402 PF00514 0.679
TRG_NLS_MonoExtN_4 324 330 PF00514 0.732
TRG_NLS_MonoExtN_4 397 403 PF00514 0.713
TRG_Pf-PMV_PEXEL_1 202 206 PF00026 0.443

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3S5H5G8 Leishmania donovani 92% 89%
Q4QJH9 Leishmania major 66% 69%

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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