LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania braziliensis
UniProt:
A4HM64_LEIBR
TriTrypDb:
LbrM.34.0290 , LBRM2903_340007900
Length:
718

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: 7
NetGPI no yes: 0, no: 7
Cellular components
Term Name Level Count
GO:0005654 nucleoplasm 2 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A4HM64
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HM64

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_NRD_NRD_1 333 335 PF00675 0.694
CLV_NRD_NRD_1 387 389 PF00675 0.725
CLV_NRD_NRD_1 6 8 PF00675 0.470
CLV_NRD_NRD_1 678 680 PF00675 0.593
CLV_PCSK_KEX2_1 333 335 PF00082 0.694
CLV_PCSK_KEX2_1 387 389 PF00082 0.672
CLV_PCSK_KEX2_1 394 396 PF00082 0.682
CLV_PCSK_KEX2_1 6 8 PF00082 0.470
CLV_PCSK_KEX2_1 712 714 PF00082 0.670
CLV_PCSK_PC1ET2_1 394 396 PF00082 0.654
CLV_PCSK_PC1ET2_1 712 714 PF00082 0.670
CLV_PCSK_SKI1_1 140 144 PF00082 0.531
CLV_PCSK_SKI1_1 239 243 PF00082 0.525
CLV_PCSK_SKI1_1 424 428 PF00082 0.500
DEG_SCF_FBW7_1 151 158 PF00400 0.510
DEG_SPOP_SBC_1 118 122 PF00917 0.518
DEG_SPOP_SBC_1 361 365 PF00917 0.556
DEG_SPOP_SBC_1 498 502 PF00917 0.733
DOC_ANK_TNKS_1 465 472 PF00023 0.473
DOC_CYCLIN_yClb3_PxF_3 598 606 PF00134 0.479
DOC_CYCLIN_yCln2_LP_2 636 642 PF00134 0.455
DOC_MAPK_MEF2A_6 616 624 PF00069 0.613
DOC_PP2B_LxvP_1 588 591 PF13499 0.694
DOC_PP2B_LxvP_1 620 623 PF13499 0.570
DOC_PP4_FxxP_1 193 196 PF00568 0.608
DOC_USP7_MATH_1 113 117 PF00917 0.447
DOC_USP7_MATH_1 118 122 PF00917 0.562
DOC_USP7_MATH_1 155 159 PF00917 0.691
DOC_USP7_MATH_1 258 262 PF00917 0.479
DOC_USP7_MATH_1 407 411 PF00917 0.726
DOC_USP7_MATH_1 420 424 PF00917 0.520
DOC_USP7_MATH_1 438 442 PF00917 0.670
DOC_USP7_MATH_1 498 502 PF00917 0.741
DOC_USP7_MATH_1 536 540 PF00917 0.613
DOC_WW_Pin1_4 129 134 PF00397 0.633
DOC_WW_Pin1_4 151 156 PF00397 0.736
DOC_WW_Pin1_4 192 197 PF00397 0.543
DOC_WW_Pin1_4 362 367 PF00397 0.765
DOC_WW_Pin1_4 557 562 PF00397 0.784
DOC_WW_Pin1_4 581 586 PF00397 0.633
DOC_WW_Pin1_4 591 596 PF00397 0.711
DOC_WW_Pin1_4 635 640 PF00397 0.662
LIG_14-3-3_CanoR_1 101 109 PF00244 0.525
LIG_14-3-3_CanoR_1 147 151 PF00244 0.744
LIG_14-3-3_CanoR_1 180 187 PF00244 0.499
LIG_14-3-3_CanoR_1 323 330 PF00244 0.632
LIG_14-3-3_CanoR_1 333 337 PF00244 0.648
LIG_14-3-3_CanoR_1 546 554 PF00244 0.627
LIG_14-3-3_CanoR_1 6 11 PF00244 0.522
LIG_14-3-3_CanoR_1 616 620 PF00244 0.696
LIG_14-3-3_CanoR_1 668 674 PF00244 0.583
LIG_Actin_WH2_2 530 548 PF00022 0.661
LIG_Actin_WH2_2 82 100 PF00022 0.588
LIG_BIR_II_1 1 5 PF00653 0.688
LIG_BRCT_BRCA1_1 133 137 PF00533 0.393
LIG_BRCT_BRCA1_1 422 426 PF00533 0.644
LIG_BRCT_BRCA1_1 596 600 PF00533 0.677
LIG_Clathr_ClatBox_1 461 465 PF01394 0.634
LIG_eIF4E_1 599 605 PF01652 0.727
LIG_FHA_1 101 107 PF00498 0.420
LIG_FHA_1 261 267 PF00498 0.517
LIG_FHA_1 279 285 PF00498 0.515
LIG_FHA_1 286 292 PF00498 0.480
LIG_FHA_1 3 9 PF00498 0.489
LIG_FHA_1 349 355 PF00498 0.719
LIG_FHA_1 45 51 PF00498 0.549
LIG_FHA_1 484 490 PF00498 0.617
LIG_FHA_1 507 513 PF00498 0.621
LIG_FHA_1 546 552 PF00498 0.490
LIG_FHA_1 616 622 PF00498 0.571
LIG_FHA_1 631 637 PF00498 0.637
LIG_FHA_2 126 132 PF00498 0.732
LIG_FHA_2 134 140 PF00498 0.562
LIG_FHA_2 207 213 PF00498 0.461
LIG_FHA_2 558 564 PF00498 0.745
LIG_GBD_Chelix_1 354 362 PF00786 0.547
LIG_LIR_Gen_1 261 272 PF02991 0.517
LIG_LIR_Gen_1 288 295 PF02991 0.488
LIG_LIR_Gen_1 509 517 PF02991 0.612
LIG_LIR_Nem_3 261 267 PF02991 0.517
LIG_LIR_Nem_3 288 293 PF02991 0.498
LIG_LIR_Nem_3 35 39 PF02991 0.464
LIG_LIR_Nem_3 423 429 PF02991 0.642
LIG_LIR_Nem_3 509 513 PF02991 0.584
LIG_LIR_Nem_3 597 603 PF02991 0.617
LIG_MAD2 701 709 PF02301 0.593
LIG_MLH1_MIPbox_1 596 600 PF16413 0.748
LIG_SH2_CRK 187 191 PF00017 0.393
LIG_SH2_CRK 457 461 PF00017 0.654
LIG_SH2_CRK 485 489 PF00017 0.671
LIG_SH2_CRK 656 660 PF00017 0.600
LIG_SH2_SRC 217 220 PF00017 0.476
LIG_SH2_STAP1 217 221 PF00017 0.478
LIG_SH2_STAP1 457 461 PF00017 0.654
LIG_SH2_STAP1 656 660 PF00017 0.547
LIG_SH2_STAT5 187 190 PF00017 0.422
LIG_SH2_STAT5 255 258 PF00017 0.499
LIG_SH2_STAT5 264 267 PF00017 0.491
LIG_SH2_STAT5 485 488 PF00017 0.492
LIG_SH2_STAT5 599 602 PF00017 0.624
LIG_SH3_3 112 118 PF00018 0.429
LIG_SH3_3 228 234 PF00018 0.532
LIG_SH3_3 254 260 PF00018 0.339
LIG_SH3_3 363 369 PF00018 0.740
LIG_SH3_3 486 492 PF00018 0.623
LIG_SH3_3 592 598 PF00018 0.742
LIG_SH3_3 655 661 PF00018 0.579
LIG_SUMO_SIM_anti_2 618 623 PF11976 0.683
LIG_TRAF2_1 136 139 PF00917 0.567
LIG_TRAF2_1 162 165 PF00917 0.590
LIG_TRFH_1 603 607 PF08558 0.719
MOD_CK1_1 120 126 PF00069 0.767
MOD_CK1_1 158 164 PF00069 0.595
MOD_CK1_1 2 8 PF00069 0.589
MOD_CK1_1 328 334 PF00069 0.641
MOD_CK1_1 406 412 PF00069 0.636
MOD_CK1_1 530 536 PF00069 0.651
MOD_CK1_1 594 600 PF00069 0.510
MOD_CK1_1 638 644 PF00069 0.554
MOD_CK1_1 9 15 PF00069 0.513
MOD_CK2_1 125 131 PF00069 0.719
MOD_CK2_1 133 139 PF00069 0.623
MOD_CK2_1 206 212 PF00069 0.457
MOD_CK2_1 536 542 PF00069 0.677
MOD_CK2_1 55 61 PF00069 0.433
MOD_GlcNHglycan 169 172 PF01048 0.565
MOD_GlcNHglycan 175 179 PF01048 0.511
MOD_GlcNHglycan 25 28 PF01048 0.482
MOD_GlcNHglycan 303 306 PF01048 0.643
MOD_GlcNHglycan 325 328 PF01048 0.651
MOD_GlcNHglycan 374 377 PF01048 0.731
MOD_GlcNHglycan 405 408 PF01048 0.710
MOD_GlcNHglycan 416 419 PF01048 0.713
MOD_GlcNHglycan 434 437 PF01048 0.679
MOD_GlcNHglycan 440 443 PF01048 0.693
MOD_GlcNHglycan 529 532 PF01048 0.636
MOD_GlcNHglycan 58 61 PF01048 0.524
MOD_GlcNHglycan 611 614 PF01048 0.498
MOD_GlcNHglycan 92 95 PF01048 0.567
MOD_GSK3_1 109 116 PF00069 0.641
MOD_GSK3_1 117 124 PF00069 0.667
MOD_GSK3_1 125 132 PF00069 0.715
MOD_GSK3_1 146 153 PF00069 0.761
MOD_GSK3_1 154 161 PF00069 0.661
MOD_GSK3_1 2 9 PF00069 0.556
MOD_GSK3_1 279 286 PF00069 0.503
MOD_GSK3_1 325 332 PF00069 0.611
MOD_GSK3_1 341 348 PF00069 0.686
MOD_GSK3_1 403 410 PF00069 0.675
MOD_GSK3_1 567 574 PF00069 0.671
MOD_GSK3_1 622 629 PF00069 0.581
MOD_GSK3_1 630 637 PF00069 0.502
MOD_GSK3_1 638 645 PF00069 0.479
MOD_N-GLC_1 278 283 PF02516 0.535
MOD_N-GLC_1 403 408 PF02516 0.706
MOD_N-GLC_1 45 50 PF02516 0.557
MOD_NEK2_1 1 6 PF00069 0.602
MOD_NEK2_1 109 114 PF00069 0.622
MOD_NEK2_1 229 234 PF00069 0.346
MOD_NEK2_1 283 288 PF00069 0.503
MOD_NEK2_1 291 296 PF00069 0.532
MOD_NEK2_1 322 327 PF00069 0.481
MOD_NEK2_1 349 354 PF00069 0.684
MOD_NEK2_1 545 550 PF00069 0.676
MOD_NEK2_1 564 569 PF00069 0.711
MOD_NEK2_1 609 614 PF00069 0.646
MOD_NEK2_1 615 620 PF00069 0.621
MOD_PIKK_1 667 673 PF00454 0.524
MOD_PK_1 6 12 PF00069 0.524
MOD_PKA_1 387 393 PF00069 0.803
MOD_PKA_1 6 12 PF00069 0.524
MOD_PKA_2 100 106 PF00069 0.549
MOD_PKA_2 146 152 PF00069 0.686
MOD_PKA_2 179 185 PF00069 0.490
MOD_PKA_2 322 328 PF00069 0.615
MOD_PKA_2 332 338 PF00069 0.649
MOD_PKA_2 349 355 PF00069 0.719
MOD_PKA_2 387 393 PF00069 0.747
MOD_PKA_2 545 551 PF00069 0.639
MOD_PKA_2 6 12 PF00069 0.524
MOD_PKA_2 615 621 PF00069 0.696
MOD_PKA_2 667 673 PF00069 0.582
MOD_Plk_1 138 144 PF00069 0.585
MOD_Plk_1 174 180 PF00069 0.479
MOD_Plk_1 278 284 PF00069 0.408
MOD_Plk_1 45 51 PF00069 0.549
MOD_Plk_2-3 626 632 PF00069 0.737
MOD_Plk_4 138 144 PF00069 0.585
MOD_Plk_4 212 218 PF00069 0.584
MOD_Plk_4 279 285 PF00069 0.543
MOD_Plk_4 615 621 PF00069 0.624
MOD_Plk_4 631 637 PF00069 0.667
MOD_Plk_4 638 644 PF00069 0.587
MOD_ProDKin_1 129 135 PF00069 0.614
MOD_ProDKin_1 151 157 PF00069 0.727
MOD_ProDKin_1 192 198 PF00069 0.543
MOD_ProDKin_1 362 368 PF00069 0.766
MOD_ProDKin_1 557 563 PF00069 0.786
MOD_ProDKin_1 581 587 PF00069 0.635
MOD_ProDKin_1 591 597 PF00069 0.709
MOD_ProDKin_1 635 641 PF00069 0.660
MOD_SUMO_rev_2 132 142 PF00179 0.591
TRG_DiLeu_BaEn_1 139 144 PF01217 0.590
TRG_DiLeu_BaEn_2 137 143 PF01217 0.577
TRG_DiLeu_BaLyEn_6 456 461 PF01217 0.655
TRG_ENDOCYTIC_2 187 190 PF00928 0.397
TRG_ENDOCYTIC_2 264 267 PF00928 0.491
TRG_ENDOCYTIC_2 31 34 PF00928 0.440
TRG_ENDOCYTIC_2 457 460 PF00928 0.661
TRG_ENDOCYTIC_2 656 659 PF00928 0.556
TRG_ER_diArg_1 6 8 PF00400 0.470
TRG_ER_diArg_1 70 73 PF00400 0.639
TRG_NES_CRM1_1 302 314 PF08389 0.418
TRG_NLS_MonoCore_2 711 716 PF00514 0.747
TRG_NLS_MonoExtN_4 709 716 PF00514 0.640
TRG_Pf-PMV_PEXEL_1 701 706 PF00026 0.579

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P5L9 Leptomonas seymouri 63% 98%
A0A3Q8IJ18 Leishmania donovani 82% 100%
A4IAS6 Leishmania infantum 82% 100%
D0A2D1 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 29% 100%
E9AEK2 Leishmania major 82% 100%
E9B5R3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 83% 100%

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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