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 mexicana
UniProt:
E9AWV4_LEIMU
TriTrypDb:
LmxM.24.1125
Length:
802

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: 5
NetGPI no yes: 0, no: 5
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

E9AWV4
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AWV4

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 179 183 PF00656 0.668
CLV_C14_Caspase3-7 3 7 PF00656 0.864
CLV_C14_Caspase3-7 324 328 PF00656 0.646
CLV_C14_Caspase3-7 691 695 PF00656 0.551
CLV_NRD_NRD_1 191 193 PF00675 0.630
CLV_NRD_NRD_1 219 221 PF00675 0.573
CLV_NRD_NRD_1 293 295 PF00675 0.875
CLV_NRD_NRD_1 305 307 PF00675 0.666
CLV_NRD_NRD_1 312 314 PF00675 0.848
CLV_NRD_NRD_1 425 427 PF00675 0.726
CLV_NRD_NRD_1 67 69 PF00675 0.543
CLV_NRD_NRD_1 713 715 PF00675 0.581
CLV_NRD_NRD_1 785 787 PF00675 0.390
CLV_PCSK_KEX2_1 191 193 PF00082 0.638
CLV_PCSK_KEX2_1 292 294 PF00082 0.883
CLV_PCSK_KEX2_1 311 313 PF00082 0.876
CLV_PCSK_KEX2_1 425 427 PF00082 0.723
CLV_PCSK_KEX2_1 67 69 PF00082 0.547
CLV_PCSK_KEX2_1 727 729 PF00082 0.758
CLV_PCSK_KEX2_1 785 787 PF00082 0.390
CLV_PCSK_PC1ET2_1 311 313 PF00082 0.668
CLV_PCSK_PC1ET2_1 727 729 PF00082 0.758
CLV_PCSK_PC7_1 63 69 PF00082 0.621
CLV_PCSK_PC7_1 781 787 PF00082 0.378
CLV_PCSK_SKI1_1 477 481 PF00082 0.646
CLV_PCSK_SKI1_1 570 574 PF00082 0.708
DEG_APCC_DBOX_1 476 484 PF00400 0.395
DEG_SPOP_SBC_1 328 332 PF00917 0.602
DOC_CKS1_1 369 374 PF01111 0.587
DOC_CKS1_1 99 104 PF01111 0.824
DOC_CYCLIN_yClb3_PxF_3 149 157 PF00134 0.668
DOC_CYCLIN_yCln2_LP_2 787 793 PF00134 0.807
DOC_MAPK_gen_1 292 303 PF00069 0.553
DOC_MAPK_gen_1 389 396 PF00069 0.650
DOC_MAPK_gen_1 473 480 PF00069 0.598
DOC_MAPK_gen_1 785 793 PF00069 0.597
DOC_MAPK_MEF2A_6 786 795 PF00069 0.807
DOC_PP2B_LxvP_1 90 93 PF13499 0.808
DOC_PP4_FxxP_1 668 671 PF00568 0.327
DOC_PP4_MxPP_1 361 364 PF00568 0.473
DOC_USP7_MATH_1 158 162 PF00917 0.876
DOC_USP7_MATH_1 180 184 PF00917 0.877
DOC_USP7_MATH_1 187 191 PF00917 0.790
DOC_USP7_MATH_1 328 332 PF00917 0.578
DOC_USP7_MATH_1 418 422 PF00917 0.603
DOC_USP7_MATH_1 560 564 PF00917 0.431
DOC_USP7_MATH_1 575 579 PF00917 0.521
DOC_USP7_MATH_1 617 621 PF00917 0.525
DOC_USP7_MATH_1 735 739 PF00917 0.561
DOC_USP7_UBL2_3 307 311 PF12436 0.457
DOC_WW_Pin1_4 19 24 PF00397 0.865
DOC_WW_Pin1_4 278 283 PF00397 0.619
DOC_WW_Pin1_4 286 291 PF00397 0.546
DOC_WW_Pin1_4 368 373 PF00397 0.606
DOC_WW_Pin1_4 384 389 PF00397 0.539
DOC_WW_Pin1_4 396 401 PF00397 0.493
DOC_WW_Pin1_4 432 437 PF00397 0.600
DOC_WW_Pin1_4 515 520 PF00397 0.564
DOC_WW_Pin1_4 581 586 PF00397 0.601
DOC_WW_Pin1_4 742 747 PF00397 0.512
DOC_WW_Pin1_4 94 99 PF00397 0.808
LIG_14-3-3_CanoR_1 130 137 PF00244 0.685
LIG_14-3-3_CanoR_1 175 184 PF00244 0.677
LIG_14-3-3_CanoR_1 208 217 PF00244 0.766
LIG_14-3-3_CanoR_1 220 224 PF00244 0.663
LIG_14-3-3_CanoR_1 312 321 PF00244 0.528
LIG_14-3-3_CanoR_1 559 565 PF00244 0.584
LIG_14-3-3_CanoR_1 82 90 PF00244 0.796
LIG_BIR_II_1 1 5 PF00653 0.812
LIG_CtBP_PxDLS_1 500 504 PF00389 0.400
LIG_deltaCOP1_diTrp_1 383 393 PF00928 0.452
LIG_FHA_1 700 706 PF00498 0.492
LIG_FHA_2 385 391 PF00498 0.658
LIG_FHA_2 689 695 PF00498 0.556
LIG_FHA_2 83 89 PF00498 0.745
LIG_HCF-1_HBM_1 514 517 PF13415 0.414
LIG_LIR_Apic_2 276 282 PF02991 0.617
LIG_LIR_Apic_2 665 671 PF02991 0.387
LIG_LIR_Gen_1 390 401 PF02991 0.550
LIG_LIR_Gen_1 598 607 PF02991 0.607
LIG_LIR_Gen_1 87 96 PF02991 0.741
LIG_LIR_Nem_3 245 251 PF02991 0.790
LIG_LIR_Nem_3 390 396 PF02991 0.557
LIG_LIR_Nem_3 399 404 PF02991 0.555
LIG_LIR_Nem_3 506 511 PF02991 0.622
LIG_LIR_Nem_3 598 604 PF02991 0.606
LIG_LIR_Nem_3 750 755 PF02991 0.474
LIG_LIR_Nem_3 87 92 PF02991 0.763
LIG_LYPXL_yS_3 789 792 PF13949 0.809
LIG_MYND_1 23 27 PF01753 0.868
LIG_MYND_1 282 286 PF01753 0.625
LIG_Pex14_1 545 549 PF04695 0.494
LIG_PTAP_UEV_1 28 33 PF05743 0.655
LIG_PTB_Apo_2 600 607 PF02174 0.553
LIG_SH2_CRK 248 252 PF00017 0.802
LIG_SH2_CRK 279 283 PF00017 0.620
LIG_SH2_CRK 601 605 PF00017 0.609
LIG_SH2_CRK 685 689 PF00017 0.583
LIG_SH2_GRB2like 601 604 PF00017 0.555
LIG_SH2_NCK_1 114 118 PF00017 0.664
LIG_SH2_NCK_1 601 605 PF00017 0.553
LIG_SH2_SRC 114 117 PF00017 0.663
LIG_SH2_STAP1 701 705 PF00017 0.494
LIG_SH2_STAT3 703 706 PF00017 0.342
LIG_SH2_STAT5 241 244 PF00017 0.756
LIG_SH2_STAT5 401 404 PF00017 0.510
LIG_SH2_STAT5 487 490 PF00017 0.607
LIG_SH2_STAT5 509 512 PF00017 0.622
LIG_SH2_STAT5 549 552 PF00017 0.507
LIG_SH2_STAT5 646 649 PF00017 0.597
LIG_SH2_STAT5 653 656 PF00017 0.500
LIG_SH2_STAT5 701 704 PF00017 0.541
LIG_SH3_1 359 365 PF00018 0.650
LIG_SH3_1 67 73 PF00018 0.876
LIG_SH3_2 288 293 PF14604 0.537
LIG_SH3_2 372 377 PF14604 0.614
LIG_SH3_2 95 100 PF14604 0.664
LIG_SH3_3 146 152 PF00018 0.662
LIG_SH3_3 248 254 PF00018 0.785
LIG_SH3_3 26 32 PF00018 0.863
LIG_SH3_3 285 291 PF00018 0.574
LIG_SH3_3 298 304 PF00018 0.674
LIG_SH3_3 357 363 PF00018 0.651
LIG_SH3_3 366 372 PF00018 0.566
LIG_SH3_3 579 585 PF00018 0.604
LIG_SH3_3 67 73 PF00018 0.876
LIG_SH3_3 790 796 PF00018 0.808
LIG_SH3_3 90 96 PF00018 0.799
LIG_SH3_4 307 314 PF00018 0.463
LIG_SH3_CIN85_PxpxPR_1 372 377 PF14604 0.558
LIG_SUMO_SIM_anti_2 322 327 PF11976 0.537
LIG_SUMO_SIM_par_1 789 794 PF11976 0.754
LIG_TYR_ITIM 787 792 PF00017 0.770
LIG_WW_3 289 293 PF00397 0.674
LIG_WW_3 374 378 PF00397 0.743
LIG_WW_3 97 101 PF00397 0.571
MOD_CDC14_SPxK_1 289 292 PF00782 0.789
MOD_CDC14_SPxK_1 97 100 PF00782 0.570
MOD_CDK_SPK_2 278 283 PF00069 0.786
MOD_CDK_SPK_2 384 389 PF00069 0.768
MOD_CDK_SPxK_1 286 292 PF00069 0.789
MOD_CDK_SPxK_1 94 100 PF00069 0.571
MOD_CDK_SPxxK_3 286 293 PF00069 0.790
MOD_CDK_SPxxK_3 384 391 PF00069 0.766
MOD_CK1_1 150 156 PF00069 0.825
MOD_CK1_1 219 225 PF00069 0.620
MOD_CK1_1 315 321 PF00069 0.694
MOD_CK1_1 330 336 PF00069 0.745
MOD_CK1_1 340 346 PF00069 0.715
MOD_CK1_1 384 390 PF00069 0.553
MOD_CK1_1 432 438 PF00069 0.767
MOD_CK1_1 584 590 PF00069 0.672
MOD_CK1_1 602 608 PF00069 0.481
MOD_CK1_1 619 625 PF00069 0.704
MOD_CK1_1 648 654 PF00069 0.647
MOD_CK1_1 745 751 PF00069 0.679
MOD_CK2_1 311 317 PF00069 0.688
MOD_CK2_1 33 39 PF00069 0.864
MOD_CK2_1 384 390 PF00069 0.845
MOD_CK2_1 735 741 PF00069 0.641
MOD_DYRK1A_RPxSP_1 94 98 PF00069 0.568
MOD_GlcNHglycan 107 110 PF01048 0.779
MOD_GlcNHglycan 160 163 PF01048 0.692
MOD_GlcNHglycan 168 171 PF01048 0.685
MOD_GlcNHglycan 178 181 PF01048 0.765
MOD_GlcNHglycan 210 213 PF01048 0.756
MOD_GlcNHglycan 431 434 PF01048 0.622
MOD_GlcNHglycan 522 526 PF01048 0.562
MOD_GlcNHglycan 619 622 PF01048 0.670
MOD_GlcNHglycan 721 724 PF01048 0.751
MOD_GSK3_1 176 183 PF00069 0.760
MOD_GSK3_1 19 26 PF00069 0.760
MOD_GSK3_1 243 250 PF00069 0.585
MOD_GSK3_1 263 270 PF00069 0.199
MOD_GSK3_1 274 281 PF00069 0.782
MOD_GSK3_1 282 289 PF00069 0.693
MOD_GSK3_1 311 318 PF00069 0.705
MOD_GSK3_1 396 403 PF00069 0.730
MOD_GSK3_1 533 540 PF00069 0.770
MOD_GSK3_1 615 622 PF00069 0.772
MOD_GSK3_1 626 633 PF00069 0.507
MOD_GSK3_1 706 713 PF00069 0.709
MOD_GSK3_1 78 85 PF00069 0.617
MOD_GSK3_1 94 101 PF00069 0.864
MOD_LATS_1 309 315 PF00433 0.784
MOD_N-GLC_1 4 9 PF02516 0.776
MOD_N-GLC_1 602 607 PF02516 0.483
MOD_N-GLC_1 77 82 PF02516 0.764
MOD_NEK2_1 136 141 PF00069 0.700
MOD_NEK2_1 242 247 PF00069 0.556
MOD_NEK2_1 337 342 PF00069 0.609
MOD_NEK2_1 394 399 PF00069 0.524
MOD_NEK2_1 507 512 PF00069 0.790
MOD_NEK2_1 521 526 PF00069 0.561
MOD_NEK2_1 533 538 PF00069 0.644
MOD_NEK2_1 624 629 PF00069 0.505
MOD_NEK2_1 645 650 PF00069 0.517
MOD_NEK2_1 755 760 PF00069 0.448
MOD_NEK2_2 180 185 PF00069 0.790
MOD_NEK2_2 274 279 PF00069 0.783
MOD_OFUCOSY 630 635 PF10250 0.669
MOD_OFUCOSY 704 710 PF10250 0.603
MOD_PIKK_1 173 179 PF00454 0.790
MOD_PIKK_1 337 343 PF00454 0.864
MOD_PIKK_1 537 543 PF00454 0.767
MOD_PKA_1 311 317 PF00069 0.785
MOD_PKA_2 129 135 PF00069 0.578
MOD_PKA_2 150 156 PF00069 0.767
MOD_PKA_2 219 225 PF00069 0.687
MOD_PKA_2 267 273 PF00069 0.365
MOD_PKA_2 295 301 PF00069 0.702
MOD_PKA_2 311 317 PF00069 0.703
MOD_PKA_2 558 564 PF00069 0.737
MOD_Plk_1 243 249 PF00069 0.580
MOD_Plk_1 274 280 PF00069 0.804
MOD_Plk_1 602 608 PF00069 0.483
MOD_Plk_1 664 670 PF00069 0.466
MOD_Plk_4 243 249 PF00069 0.580
MOD_Plk_4 274 280 PF00069 0.782
MOD_Plk_4 584 590 PF00069 0.672
MOD_Plk_4 602 608 PF00069 0.469
MOD_Plk_4 716 722 PF00069 0.456
MOD_ProDKin_1 19 25 PF00069 0.854
MOD_ProDKin_1 278 284 PF00069 0.789
MOD_ProDKin_1 286 292 PF00069 0.688
MOD_ProDKin_1 368 374 PF00069 0.766
MOD_ProDKin_1 384 390 PF00069 0.673
MOD_ProDKin_1 396 402 PF00069 0.610
MOD_ProDKin_1 432 438 PF00069 0.758
MOD_ProDKin_1 515 521 PF00069 0.711
MOD_ProDKin_1 581 587 PF00069 0.761
MOD_ProDKin_1 742 748 PF00069 0.634
MOD_ProDKin_1 94 100 PF00069 0.774
TRG_DiLeu_BaEn_1 474 479 PF01217 0.754
TRG_DiLeu_BaLyEn_6 675 680 PF01217 0.520
TRG_DiLeu_LyEn_5 474 479 PF01217 0.462
TRG_ENDOCYTIC_2 114 117 PF00928 0.568
TRG_ENDOCYTIC_2 248 251 PF00928 0.761
TRG_ENDOCYTIC_2 401 404 PF00928 0.634
TRG_ENDOCYTIC_2 508 511 PF00928 0.796
TRG_ENDOCYTIC_2 601 604 PF00928 0.775
TRG_ENDOCYTIC_2 685 688 PF00928 0.735
TRG_ENDOCYTIC_2 789 792 PF00928 0.773
TRG_ER_diArg_1 191 194 PF00400 0.852
TRG_ER_diArg_1 291 294 PF00400 0.869
TRG_ER_diArg_1 424 426 PF00400 0.665
TRG_ER_diArg_1 475 478 PF00400 0.588
TRG_ER_diArg_1 483 486 PF00400 0.674
TRG_ER_diArg_1 67 69 PF00400 0.686
TRG_ER_diArg_1 784 786 PF00400 0.456
TRG_Pf-PMV_PEXEL_1 678 683 PF00026 0.698

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8ICW0 Leishmania donovani 84% 100%
A4HDG9 Leishmania braziliensis 61% 100%
A4I0V0 Leishmania infantum 84% 100%
Q4QAM0 Leishmania major 84% 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