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, unknown function
Species:
Leishmania braziliensis
UniProt:
A4HA64_LEIBR
TriTrypDb:
LbrM.19.1400 , LBRM2903_190019400 * , LBRM2903_190019500 *
Length:
934

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: 6
NetGPI no yes: 0, no: 6
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

A4HA64
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HA64

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 451 455 PF00656 0.410
CLV_C14_Caspase3-7 603 607 PF00656 0.835
CLV_C14_Caspase3-7 617 621 PF00656 0.581
CLV_NRD_NRD_1 166 168 PF00675 0.835
CLV_NRD_NRD_1 459 461 PF00675 0.614
CLV_NRD_NRD_1 492 494 PF00675 0.510
CLV_NRD_NRD_1 50 52 PF00675 0.780
CLV_NRD_NRD_1 95 97 PF00675 0.649
CLV_PCSK_FUR_1 647 651 PF00082 0.558
CLV_PCSK_KEX2_1 166 168 PF00082 0.738
CLV_PCSK_KEX2_1 459 461 PF00082 0.614
CLV_PCSK_KEX2_1 642 644 PF00082 0.731
CLV_PCSK_KEX2_1 646 648 PF00082 0.755
CLV_PCSK_KEX2_1 649 651 PF00082 0.758
CLV_PCSK_KEX2_1 826 828 PF00082 0.598
CLV_PCSK_KEX2_1 95 97 PF00082 0.752
CLV_PCSK_PC1ET2_1 642 644 PF00082 0.731
CLV_PCSK_PC1ET2_1 646 648 PF00082 0.755
CLV_PCSK_PC1ET2_1 649 651 PF00082 0.758
CLV_PCSK_PC1ET2_1 826 828 PF00082 0.523
CLV_PCSK_SKI1_1 138 142 PF00082 0.727
CLV_PCSK_SKI1_1 266 270 PF00082 0.620
CLV_PCSK_SKI1_1 287 291 PF00082 0.812
CLV_PCSK_SKI1_1 299 303 PF00082 0.552
CLV_PCSK_SKI1_1 438 442 PF00082 0.381
CLV_PCSK_SKI1_1 444 448 PF00082 0.533
CLV_PCSK_SKI1_1 466 470 PF00082 0.518
CLV_PCSK_SKI1_1 570 574 PF00082 0.656
CLV_PCSK_SKI1_1 748 752 PF00082 0.579
CLV_PCSK_SKI1_1 888 892 PF00082 0.398
DEG_Nend_UBRbox_3 1 3 PF02207 0.728
DEG_SCF_FBW7_1 116 123 PF00400 0.572
DEG_SPOP_SBC_1 122 126 PF00917 0.578
DEG_SPOP_SBC_1 184 188 PF00917 0.744
DEG_SPOP_SBC_1 191 195 PF00917 0.621
DEG_SPOP_SBC_1 242 246 PF00917 0.651
DEG_SPOP_SBC_1 761 765 PF00917 0.585
DOC_CKS1_1 906 911 PF01111 0.557
DOC_CYCLIN_RxL_1 438 451 PF00134 0.626
DOC_CYCLIN_yCln2_LP_2 226 232 PF00134 0.825
DOC_CYCLIN_yCln2_LP_2 342 348 PF00134 0.705
DOC_MAPK_RevD_3 445 460 PF00069 0.410
DOC_PP1_RVXF_1 102 109 PF00149 0.735
DOC_PP1_RVXF_1 136 142 PF00149 0.725
DOC_PP1_RVXF_1 259 265 PF00149 0.518
DOC_PP4_FxxP_1 171 174 PF00568 0.566
DOC_PP4_FxxP_1 665 668 PF00568 0.669
DOC_PP4_FxxP_1 911 914 PF00568 0.591
DOC_USP7_MATH_1 147 151 PF00917 0.847
DOC_USP7_MATH_1 183 187 PF00917 0.734
DOC_USP7_MATH_1 191 195 PF00917 0.626
DOC_USP7_MATH_1 203 207 PF00917 0.550
DOC_USP7_MATH_1 241 245 PF00917 0.698
DOC_USP7_MATH_1 295 299 PF00917 0.661
DOC_USP7_MATH_1 306 310 PF00917 0.745
DOC_USP7_MATH_1 331 335 PF00917 0.700
DOC_USP7_MATH_1 338 342 PF00917 0.670
DOC_USP7_MATH_1 409 413 PF00917 0.722
DOC_USP7_MATH_1 513 517 PF00917 0.515
DOC_USP7_MATH_1 595 599 PF00917 0.726
DOC_USP7_MATH_1 600 604 PF00917 0.730
DOC_USP7_MATH_1 632 636 PF00917 0.849
DOC_USP7_MATH_1 674 678 PF00917 0.551
DOC_USP7_MATH_1 705 709 PF00917 0.713
DOC_USP7_MATH_1 711 715 PF00917 0.606
DOC_USP7_MATH_1 760 764 PF00917 0.586
DOC_USP7_MATH_1 779 783 PF00917 0.774
DOC_USP7_MATH_1 8 12 PF00917 0.639
DOC_USP7_MATH_1 904 908 PF00917 0.662
DOC_USP7_MATH_1 99 103 PF00917 0.622
DOC_USP7_UBL2_3 642 646 PF12436 0.734
DOC_USP7_UBL2_3 744 748 PF12436 0.584
DOC_WW_Pin1_4 114 119 PF00397 0.533
DOC_WW_Pin1_4 187 192 PF00397 0.829
DOC_WW_Pin1_4 198 203 PF00397 0.571
DOC_WW_Pin1_4 225 230 PF00397 0.720
DOC_WW_Pin1_4 237 242 PF00397 0.690
DOC_WW_Pin1_4 290 295 PF00397 0.766
DOC_WW_Pin1_4 323 328 PF00397 0.642
DOC_WW_Pin1_4 348 353 PF00397 0.746
DOC_WW_Pin1_4 354 359 PF00397 0.742
DOC_WW_Pin1_4 368 373 PF00397 0.549
DOC_WW_Pin1_4 42 47 PF00397 0.771
DOC_WW_Pin1_4 467 472 PF00397 0.689
DOC_WW_Pin1_4 541 546 PF00397 0.777
DOC_WW_Pin1_4 668 673 PF00397 0.576
DOC_WW_Pin1_4 685 690 PF00397 0.766
DOC_WW_Pin1_4 698 703 PF00397 0.556
DOC_WW_Pin1_4 748 753 PF00397 0.744
DOC_WW_Pin1_4 762 767 PF00397 0.748
DOC_WW_Pin1_4 799 804 PF00397 0.693
DOC_WW_Pin1_4 898 903 PF00397 0.597
DOC_WW_Pin1_4 905 910 PF00397 0.665
DOC_WW_Pin1_4 915 920 PF00397 0.790
DOC_WW_Pin1_4 97 102 PF00397 0.759
LIG_14-3-3_CanoR_1 151 157 PF00244 0.710
LIG_14-3-3_CanoR_1 166 172 PF00244 0.704
LIG_14-3-3_CanoR_1 266 275 PF00244 0.532
LIG_14-3-3_CanoR_1 287 294 PF00244 0.707
LIG_14-3-3_CanoR_1 299 306 PF00244 0.546
LIG_14-3-3_CanoR_1 387 391 PF00244 0.767
LIG_14-3-3_CanoR_1 51 56 PF00244 0.656
LIG_14-3-3_CanoR_1 514 521 PF00244 0.401
LIG_14-3-3_CanoR_1 85 93 PF00244 0.702
LIG_14-3-3_CanoR_1 895 899 PF00244 0.605
LIG_14-3-3_CanoR_1 95 101 PF00244 0.737
LIG_Actin_WH2_2 59 76 PF00022 0.577
LIG_AP2alpha_2 161 163 PF02296 0.564
LIG_APCC_ABBA_1 844 849 PF00400 0.737
LIG_BIR_III_2 736 740 PF00653 0.561
LIG_BRCT_BRCA1_1 167 171 PF00533 0.571
LIG_BRCT_BRCA1_2 167 173 PF00533 0.572
LIG_FHA_1 193 199 PF00498 0.739
LIG_FHA_1 210 216 PF00498 0.695
LIG_FHA_1 380 386 PF00498 0.619
LIG_FHA_1 467 473 PF00498 0.514
LIG_FHA_1 54 60 PF00498 0.677
LIG_FHA_1 829 835 PF00498 0.530
LIG_FHA_2 30 36 PF00498 0.549
LIG_LIR_Apic_2 168 174 PF02991 0.569
LIG_LIR_Apic_2 802 808 PF02991 0.692
LIG_LIR_Apic_2 908 914 PF02991 0.585
LIG_LIR_LC3C_4 516 521 PF02991 0.626
LIG_LIR_Nem_3 714 720 PF02991 0.663
LIG_MYND_1 10 14 PF01753 0.602
LIG_MYND_1 668 672 PF01753 0.805
LIG_MYND_1 910 914 PF01753 0.667
LIG_NRBOX 441 447 PF00104 0.360
LIG_PAM2_1 246 258 PF00658 0.542
LIG_Pex14_1 575 579 PF04695 0.576
LIG_SH2_CRK 652 656 PF00017 0.534
LIG_SH2_CRK 683 687 PF00017 0.739
LIG_SH2_CRK 717 721 PF00017 0.619
LIG_SH2_STAP1 55 59 PF00017 0.607
LIG_SH2_STAP1 579 583 PF00017 0.603
LIG_SH2_STAT3 609 612 PF00017 0.543
LIG_SH2_STAT3 859 862 PF00017 0.578
LIG_SH2_STAT3 864 867 PF00017 0.558
LIG_SH2_STAT5 376 379 PF00017 0.558
LIG_SH2_STAT5 55 58 PF00017 0.727
LIG_SH2_STAT5 706 709 PF00017 0.702
LIG_SH2_STAT5 847 850 PF00017 0.622
LIG_SH2_STAT5 864 867 PF00017 0.558
LIG_SH3_3 11 17 PF00018 0.608
LIG_SH3_3 110 116 PF00018 0.678
LIG_SH3_3 342 348 PF00018 0.711
LIG_SH3_3 378 384 PF00018 0.580
LIG_SH3_3 387 393 PF00018 0.509
LIG_SH3_3 4 10 PF00018 0.691
LIG_SH3_3 625 631 PF00018 0.715
LIG_SH3_3 686 692 PF00018 0.773
LIG_SH3_3 697 703 PF00018 0.798
LIG_SH3_3 749 755 PF00018 0.799
LIG_SH3_3 763 769 PF00018 0.647
LIG_SH3_3 903 909 PF00018 0.767
LIG_SUMO_SIM_par_1 445 451 PF11976 0.532
LIG_SxIP_EBH_1 82 95 PF03271 0.524
LIG_TRAF2_1 483 486 PF00917 0.439
LIG_TRAF2_1 560 563 PF00917 0.535
LIG_TYR_ITIM 715 720 PF00017 0.500
LIG_WW_1 680 683 PF00397 0.589
MOD_CDK_SPxK_1 541 547 PF00069 0.566
MOD_CDK_SPxxK_3 467 474 PF00069 0.509
MOD_CDK_SPxxK_3 97 104 PF00069 0.670
MOD_CK1_1 124 130 PF00069 0.761
MOD_CK1_1 150 156 PF00069 0.643
MOD_CK1_1 186 192 PF00069 0.701
MOD_CK1_1 194 200 PF00069 0.697
MOD_CK1_1 246 252 PF00069 0.704
MOD_CK1_1 279 285 PF00069 0.659
MOD_CK1_1 310 316 PF00069 0.655
MOD_CK1_1 386 392 PF00069 0.570
MOD_CK1_1 412 418 PF00069 0.625
MOD_CK1_1 42 48 PF00069 0.810
MOD_CK1_1 554 560 PF00069 0.695
MOD_CK1_1 685 691 PF00069 0.763
MOD_CK1_1 810 816 PF00069 0.793
MOD_CK1_1 840 846 PF00069 0.585
MOD_CK1_1 97 103 PF00069 0.769
MOD_CK2_1 274 280 PF00069 0.528
MOD_CK2_1 323 329 PF00069 0.573
MOD_CK2_1 557 563 PF00069 0.529
MOD_CMANNOS 575 578 PF00535 0.571
MOD_GlcNHglycan 126 129 PF01048 0.809
MOD_GlcNHglycan 152 155 PF01048 0.752
MOD_GlcNHglycan 245 248 PF01048 0.779
MOD_GlcNHglycan 256 259 PF01048 0.544
MOD_GlcNHglycan 276 279 PF01048 0.636
MOD_GlcNHglycan 3 6 PF01048 0.566
MOD_GlcNHglycan 309 312 PF01048 0.683
MOD_GlcNHglycan 403 407 PF01048 0.637
MOD_GlcNHglycan 41 44 PF01048 0.722
MOD_GlcNHglycan 410 414 PF01048 0.616
MOD_GlcNHglycan 415 418 PF01048 0.545
MOD_GlcNHglycan 581 584 PF01048 0.677
MOD_GlcNHglycan 602 605 PF01048 0.830
MOD_GlcNHglycan 656 659 PF01048 0.551
MOD_GlcNHglycan 707 710 PF01048 0.626
MOD_GlcNHglycan 726 729 PF01048 0.758
MOD_GlcNHglycan 745 748 PF01048 0.569
MOD_GlcNHglycan 809 812 PF01048 0.699
MOD_GlcNHglycan 902 905 PF01048 0.751
MOD_GlcNHglycan 915 918 PF01048 0.540
MOD_GlcNHglycan 923 926 PF01048 0.755
MOD_GlcNHglycan 97 100 PF01048 0.738
MOD_GSK3_1 116 123 PF00069 0.699
MOD_GSK3_1 124 131 PF00069 0.625
MOD_GSK3_1 172 179 PF00069 0.737
MOD_GSK3_1 183 190 PF00069 0.662
MOD_GSK3_1 194 201 PF00069 0.736
MOD_GSK3_1 237 244 PF00069 0.735
MOD_GSK3_1 246 253 PF00069 0.770
MOD_GSK3_1 285 292 PF00069 0.633
MOD_GSK3_1 29 36 PF00069 0.587
MOD_GSK3_1 295 302 PF00069 0.650
MOD_GSK3_1 306 313 PF00069 0.751
MOD_GSK3_1 379 386 PF00069 0.638
MOD_GSK3_1 398 405 PF00069 0.655
MOD_GSK3_1 409 416 PF00069 0.727
MOD_GSK3_1 508 515 PF00069 0.399
MOD_GSK3_1 551 558 PF00069 0.693
MOD_GSK3_1 591 598 PF00069 0.695
MOD_GSK3_1 619 626 PF00069 0.693
MOD_GSK3_1 769 776 PF00069 0.610
MOD_GSK3_1 786 793 PF00069 0.582
MOD_GSK3_1 894 901 PF00069 0.651
MOD_GSK3_1 95 102 PF00069 0.629
MOD_NEK2_1 1 6 PF00069 0.611
MOD_NEK2_1 289 294 PF00069 0.688
MOD_NEK2_1 317 322 PF00069 0.577
MOD_NEK2_1 431 436 PF00069 0.362
MOD_NEK2_2 203 208 PF00069 0.757
MOD_NEK2_2 842 847 PF00069 0.479
MOD_PIKK_1 231 237 PF00454 0.703
MOD_PIKK_1 279 285 PF00454 0.523
MOD_PIKK_1 340 346 PF00454 0.605
MOD_PIKK_1 505 511 PF00454 0.519
MOD_PIKK_1 551 557 PF00454 0.774
MOD_PIKK_1 858 864 PF00454 0.540
MOD_PKA_1 51 57 PF00069 0.651
MOD_PKA_1 641 647 PF00069 0.682
MOD_PKA_1 95 101 PF00069 0.568
MOD_PKA_2 150 156 PF00069 0.674
MOD_PKA_2 165 171 PF00069 0.559
MOD_PKA_2 386 392 PF00069 0.767
MOD_PKA_2 431 437 PF00069 0.363
MOD_PKA_2 513 519 PF00069 0.627
MOD_PKA_2 718 724 PF00069 0.566
MOD_PKA_2 779 785 PF00069 0.671
MOD_PKA_2 84 90 PF00069 0.579
MOD_PKA_2 894 900 PF00069 0.602
MOD_PKA_2 94 100 PF00069 0.679
MOD_Plk_1 279 285 PF00069 0.791
MOD_Plk_1 402 408 PF00069 0.550
MOD_Plk_1 605 611 PF00069 0.557
MOD_Plk_4 109 115 PF00069 0.739
MOD_Plk_4 222 228 PF00069 0.724
MOD_Plk_4 250 256 PF00069 0.708
MOD_Plk_4 271 277 PF00069 0.622
MOD_Plk_4 33 39 PF00069 0.555
MOD_Plk_4 391 397 PF00069 0.640
MOD_Plk_4 711 717 PF00069 0.630
MOD_Plk_4 842 848 PF00069 0.506
MOD_ProDKin_1 114 120 PF00069 0.533
MOD_ProDKin_1 187 193 PF00069 0.830
MOD_ProDKin_1 198 204 PF00069 0.572
MOD_ProDKin_1 225 231 PF00069 0.721
MOD_ProDKin_1 237 243 PF00069 0.689
MOD_ProDKin_1 290 296 PF00069 0.767
MOD_ProDKin_1 323 329 PF00069 0.644
MOD_ProDKin_1 348 354 PF00069 0.748
MOD_ProDKin_1 368 374 PF00069 0.551
MOD_ProDKin_1 42 48 PF00069 0.769
MOD_ProDKin_1 467 473 PF00069 0.688
MOD_ProDKin_1 541 547 PF00069 0.783
MOD_ProDKin_1 668 674 PF00069 0.576
MOD_ProDKin_1 685 691 PF00069 0.767
MOD_ProDKin_1 698 704 PF00069 0.552
MOD_ProDKin_1 748 754 PF00069 0.742
MOD_ProDKin_1 762 768 PF00069 0.749
MOD_ProDKin_1 799 805 PF00069 0.693
MOD_ProDKin_1 898 904 PF00069 0.600
MOD_ProDKin_1 905 911 PF00069 0.668
MOD_ProDKin_1 915 921 PF00069 0.790
MOD_ProDKin_1 97 103 PF00069 0.758
MOD_SUMO_rev_2 635 644 PF00179 0.574
TRG_DiLeu_BaLyEn_6 258 263 PF01217 0.522
TRG_DiLeu_BaLyEn_6 441 446 PF01217 0.356
TRG_DiLeu_BaLyEn_6 468 473 PF01217 0.517
TRG_ENDOCYTIC_2 683 686 PF00928 0.740
TRG_ENDOCYTIC_2 717 720 PF00928 0.620
TRG_ER_diArg_1 136 139 PF00400 0.826
TRG_ER_diArg_1 166 169 PF00400 0.745
TRG_ER_diArg_1 459 462 PF00400 0.514
TRG_Pf-PMV_PEXEL_1 315 319 PF00026 0.539
TRG_Pf-PMV_PEXEL_1 497 501 PF00026 0.473
TRG_Pf-PMV_PEXEL_1 64 69 PF00026 0.571
TRG_Pf-PMV_PEXEL_1 875 879 PF00026 0.567

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I094 Leptomonas seymouri 34% 86%
A0A3S5H766 Leishmania donovani 62% 99%
A4HYD5 Leishmania infantum 63% 94%
E9AS68 Leishmania mexicana (strain MHOM/GT/2001/U1103) 61% 94%
Q4QD98 Leishmania major 61% 97%

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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