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:
E9AYK5_LEIMU
TriTrypDb:
LmxM.26.2250
Length:
823

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: 10
NetGPI no yes: 0, no: 10
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

E9AYK5
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AYK5

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 279 283 PF00656 0.476
CLV_NRD_NRD_1 29 31 PF00675 0.506
CLV_NRD_NRD_1 345 347 PF00675 0.720
CLV_NRD_NRD_1 350 352 PF00675 0.714
CLV_NRD_NRD_1 503 505 PF00675 0.599
CLV_NRD_NRD_1 661 663 PF00675 0.690
CLV_NRD_NRD_1 71 73 PF00675 0.605
CLV_NRD_NRD_1 95 97 PF00675 0.524
CLV_PCSK_FUR_1 628 632 PF00082 0.643
CLV_PCSK_KEX2_1 29 31 PF00082 0.506
CLV_PCSK_KEX2_1 344 346 PF00082 0.666
CLV_PCSK_KEX2_1 350 352 PF00082 0.593
CLV_PCSK_KEX2_1 487 489 PF00082 0.528
CLV_PCSK_KEX2_1 502 504 PF00082 0.599
CLV_PCSK_KEX2_1 630 632 PF00082 0.620
CLV_PCSK_KEX2_1 661 663 PF00082 0.709
CLV_PCSK_KEX2_1 97 99 PF00082 0.496
CLV_PCSK_PC1ET2_1 487 489 PF00082 0.528
CLV_PCSK_PC1ET2_1 630 632 PF00082 0.650
CLV_PCSK_PC1ET2_1 97 99 PF00082 0.448
CLV_PCSK_PC7_1 346 352 PF00082 0.474
CLV_PCSK_PC7_1 483 489 PF00082 0.524
CLV_PCSK_SKI1_1 30 34 PF00082 0.569
CLV_PCSK_SKI1_1 449 453 PF00082 0.762
CLV_PCSK_SKI1_1 463 467 PF00082 0.589
CLV_PCSK_SKI1_1 528 532 PF00082 0.668
CLV_PCSK_SKI1_1 569 573 PF00082 0.583
CLV_PCSK_SKI1_1 631 635 PF00082 0.626
CLV_PCSK_SKI1_1 784 788 PF00082 0.549
DEG_COP1_1 684 692 PF00400 0.615
DEG_SCF_FBW7_1 677 684 PF00400 0.498
DEG_SPOP_SBC_1 16 20 PF00917 0.657
DOC_CDC14_PxL_1 686 694 PF14671 0.560
DOC_CKS1_1 678 683 PF01111 0.501
DOC_CYCLIN_yCln2_LP_2 138 144 PF00134 0.694
DOC_CYCLIN_yCln2_LP_2 551 557 PF00134 0.569
DOC_MAPK_gen_1 449 458 PF00069 0.612
DOC_MAPK_gen_1 487 495 PF00069 0.553
DOC_MAPK_gen_1 70 78 PF00069 0.487
DOC_PP1_RVXF_1 536 543 PF00149 0.423
DOC_PP2B_LxvP_1 138 141 PF13499 0.582
DOC_PP4_FxxP_1 475 478 PF00568 0.677
DOC_PP4_FxxP_1 678 681 PF00568 0.440
DOC_USP7_MATH_1 133 137 PF00917 0.614
DOC_USP7_MATH_1 263 267 PF00917 0.608
DOC_USP7_MATH_1 276 280 PF00917 0.691
DOC_USP7_MATH_1 325 329 PF00917 0.540
DOC_USP7_MATH_1 506 510 PF00917 0.718
DOC_USP7_MATH_1 577 581 PF00917 0.722
DOC_USP7_MATH_1 589 593 PF00917 0.456
DOC_USP7_UBL2_3 784 788 PF12436 0.567
DOC_WW_Pin1_4 288 293 PF00397 0.759
DOC_WW_Pin1_4 458 463 PF00397 0.701
DOC_WW_Pin1_4 543 548 PF00397 0.677
DOC_WW_Pin1_4 677 682 PF00397 0.545
DOC_WW_Pin1_4 736 741 PF00397 0.700
LIG_14-3-3_CanoR_1 171 177 PF00244 0.610
LIG_14-3-3_CanoR_1 361 365 PF00244 0.571
LIG_14-3-3_CanoR_1 442 451 PF00244 0.732
LIG_14-3-3_CanoR_1 483 487 PF00244 0.525
LIG_14-3-3_CanoR_1 528 533 PF00244 0.663
LIG_14-3-3_CanoR_1 569 574 PF00244 0.623
LIG_14-3-3_CanoR_1 661 670 PF00244 0.580
LIG_14-3-3_CanoR_1 796 805 PF00244 0.606
LIG_BIR_II_1 1 5 PF00653 0.690
LIG_BRCT_BRCA1_1 135 139 PF00533 0.635
LIG_BRCT_BRCA1_1 453 457 PF00533 0.588
LIG_Clathr_ClatBox_1 492 496 PF01394 0.625
LIG_eIF4E_1 183 189 PF01652 0.559
LIG_FHA_1 17 23 PF00498 0.617
LIG_FHA_1 183 189 PF00498 0.619
LIG_FHA_1 202 208 PF00498 0.574
LIG_FHA_1 395 401 PF00498 0.567
LIG_FHA_1 700 706 PF00498 0.693
LIG_FHA_1 711 717 PF00498 0.518
LIG_FHA_1 737 743 PF00498 0.725
LIG_FHA_1 767 773 PF00498 0.669
LIG_FHA_1 8 14 PF00498 0.628
LIG_FHA_2 19 25 PF00498 0.592
LIG_FHA_2 361 367 PF00498 0.626
LIG_FHA_2 416 422 PF00498 0.669
LIG_FHA_2 534 540 PF00498 0.634
LIG_FHA_2 612 618 PF00498 0.658
LIG_LIR_Apic_2 473 478 PF02991 0.678
LIG_LIR_Apic_2 769 774 PF02991 0.672
LIG_LIR_Gen_1 170 181 PF02991 0.624
LIG_LIR_Gen_1 190 201 PF02991 0.373
LIG_LIR_Gen_1 799 810 PF02991 0.563
LIG_LIR_Nem_3 170 176 PF02991 0.610
LIG_LIR_Nem_3 190 196 PF02991 0.375
LIG_LIR_Nem_3 197 202 PF02991 0.474
LIG_LIR_Nem_3 473 479 PF02991 0.523
LIG_LIR_Nem_3 621 625 PF02991 0.640
LIG_LIR_Nem_3 799 805 PF02991 0.618
LIG_LIR_Nem_3 816 822 PF02991 0.564
LIG_LYPXL_yS_3 479 482 PF13949 0.659
LIG_MAD2 368 376 PF02301 0.711
LIG_PTB_Apo_2 49 56 PF02174 0.556
LIG_SH2_NCK_1 193 197 PF00017 0.635
LIG_SH2_NCK_1 362 366 PF00017 0.624
LIG_SH2_PTP2 173 176 PF00017 0.598
LIG_SH2_PTP2 373 376 PF00017 0.672
LIG_SH2_STAP1 815 819 PF00017 0.615
LIG_SH2_STAT5 173 176 PF00017 0.598
LIG_SH2_STAT5 260 263 PF00017 0.527
LIG_SH2_STAT5 362 365 PF00017 0.591
LIG_SH2_STAT5 373 376 PF00017 0.598
LIG_SH2_STAT5 4 7 PF00017 0.633
LIG_SH2_STAT5 417 420 PF00017 0.708
LIG_SH2_STAT5 729 732 PF00017 0.719
LIG_SH2_STAT5 771 774 PF00017 0.686
LIG_SH2_STAT5 802 805 PF00017 0.676
LIG_SH2_STAT5 815 818 PF00017 0.585
LIG_SH3_1 373 379 PF00018 0.672
LIG_SH3_3 138 144 PF00018 0.694
LIG_SH3_3 215 221 PF00018 0.676
LIG_SH3_3 289 295 PF00018 0.782
LIG_SH3_3 361 367 PF00018 0.681
LIG_SH3_3 373 379 PF00018 0.728
LIG_SH3_3 667 673 PF00018 0.562
LIG_SH3_3 804 810 PF00018 0.511
LIG_SUMO_SIM_par_1 553 559 PF11976 0.686
LIG_TRAF2_1 747 750 PF00917 0.469
LIG_TYR_ITIM 360 365 PF00017 0.631
LIG_TYR_ITIM 817 822 PF00017 0.584
LIG_UBA3_1 27 36 PF00899 0.620
LIG_WRC_WIRS_1 196 201 PF05994 0.515
LIG_WW_3 573 577 PF00397 0.568
MOD_CDK_SPK_2 291 296 PF00069 0.766
MOD_CDK_SPK_2 458 463 PF00069 0.710
MOD_CDK_SPxK_1 543 549 PF00069 0.510
MOD_CK1_1 120 126 PF00069 0.694
MOD_CK1_1 18 24 PF00069 0.712
MOD_CK1_1 266 272 PF00069 0.577
MOD_CK1_1 291 297 PF00069 0.732
MOD_CK1_1 34 40 PF00069 0.550
MOD_CK1_1 432 438 PF00069 0.598
MOD_CK1_1 580 586 PF00069 0.526
MOD_CK1_1 592 598 PF00069 0.442
MOD_CK1_1 63 69 PF00069 0.636
MOD_CK1_1 699 705 PF00069 0.692
MOD_CK2_1 265 271 PF00069 0.466
MOD_CK2_1 360 366 PF00069 0.570
MOD_CK2_1 415 421 PF00069 0.636
MOD_CK2_1 511 517 PF00069 0.661
MOD_CK2_1 611 617 PF00069 0.652
MOD_Cter_Amidation 348 351 PF01082 0.475
MOD_Cter_Amidation 94 97 PF01082 0.416
MOD_GlcNHglycan 107 110 PF01048 0.740
MOD_GlcNHglycan 122 125 PF01048 0.747
MOD_GlcNHglycan 217 221 PF01048 0.562
MOD_GlcNHglycan 278 281 PF01048 0.589
MOD_GlcNHglycan 327 330 PF01048 0.790
MOD_GlcNHglycan 33 36 PF01048 0.573
MOD_GlcNHglycan 405 408 PF01048 0.757
MOD_GlcNHglycan 508 511 PF01048 0.624
MOD_GlcNHglycan 61 65 PF01048 0.602
MOD_GlcNHglycan 640 643 PF01048 0.626
MOD_GlcNHglycan 664 667 PF01048 0.677
MOD_GlcNHglycan 698 701 PF01048 0.638
MOD_GSK3_1 105 112 PF00069 0.566
MOD_GSK3_1 114 121 PF00069 0.574
MOD_GSK3_1 129 136 PF00069 0.586
MOD_GSK3_1 142 149 PF00069 0.494
MOD_GSK3_1 179 186 PF00069 0.575
MOD_GSK3_1 263 270 PF00069 0.642
MOD_GSK3_1 298 305 PF00069 0.630
MOD_GSK3_1 308 315 PF00069 0.615
MOD_GSK3_1 34 41 PF00069 0.627
MOD_GSK3_1 394 401 PF00069 0.530
MOD_GSK3_1 411 418 PF00069 0.494
MOD_GSK3_1 429 436 PF00069 0.634
MOD_GSK3_1 452 459 PF00069 0.637
MOD_GSK3_1 528 535 PF00069 0.677
MOD_GSK3_1 577 584 PF00069 0.782
MOD_GSK3_1 589 596 PF00069 0.561
MOD_GSK3_1 656 663 PF00069 0.711
MOD_GSK3_1 677 684 PF00069 0.619
MOD_GSK3_1 688 695 PF00069 0.655
MOD_GSK3_1 696 703 PF00069 0.611
MOD_GSK3_1 706 713 PF00069 0.527
MOD_GSK3_1 738 745 PF00069 0.791
MOD_N-GLC_1 183 188 PF02516 0.563
MOD_N-GLC_1 48 53 PF02516 0.588
MOD_N-GLC_1 543 548 PF02516 0.532
MOD_N-GLC_1 681 686 PF02516 0.610
MOD_N-GLC_2 411 413 PF02516 0.470
MOD_NEK2_1 105 110 PF00069 0.602
MOD_NEK2_1 161 166 PF00069 0.510
MOD_NEK2_1 195 200 PF00069 0.508
MOD_NEK2_1 31 36 PF00069 0.576
MOD_NEK2_1 415 420 PF00069 0.625
MOD_NEK2_1 424 429 PF00069 0.655
MOD_NEK2_1 482 487 PF00069 0.498
MOD_NEK2_1 532 537 PF00069 0.650
MOD_NEK2_1 561 566 PF00069 0.699
MOD_NEK2_1 692 697 PF00069 0.713
MOD_NEK2_1 91 96 PF00069 0.644
MOD_PIKK_1 133 139 PF00454 0.630
MOD_PIKK_1 258 264 PF00454 0.720
MOD_PIKK_1 415 421 PF00454 0.636
MOD_PIKK_1 611 617 PF00454 0.644
MOD_PIKK_1 656 662 PF00454 0.569
MOD_PKA_2 258 264 PF00069 0.567
MOD_PKA_2 318 324 PF00069 0.673
MOD_PKA_2 360 366 PF00069 0.558
MOD_PKA_2 482 488 PF00069 0.523
MOD_PKA_2 561 567 PF00069 0.698
MOD_PKA_2 660 666 PF00069 0.617
MOD_PKA_2 710 716 PF00069 0.598
MOD_PKA_2 91 97 PF00069 0.692
MOD_Plk_1 133 139 PF00069 0.630
MOD_Plk_1 183 189 PF00069 0.559
MOD_Plk_1 593 599 PF00069 0.554
MOD_Plk_1 719 725 PF00069 0.628
MOD_Plk_4 172 178 PF00069 0.513
MOD_Plk_4 360 366 PF00069 0.627
MOD_Plk_4 452 458 PF00069 0.631
MOD_Plk_4 511 517 PF00069 0.668
MOD_Plk_4 605 611 PF00069 0.646
MOD_ProDKin_1 288 294 PF00069 0.759
MOD_ProDKin_1 458 464 PF00069 0.702
MOD_ProDKin_1 543 549 PF00069 0.678
MOD_ProDKin_1 677 683 PF00069 0.546
MOD_ProDKin_1 736 742 PF00069 0.702
TRG_DiLeu_BaLyEn_6 184 189 PF01217 0.559
TRG_DiLeu_BaLyEn_6 27 32 PF01217 0.381
TRG_DiLeu_BaLyEn_6 343 348 PF01217 0.615
TRG_ENDOCYTIC_2 173 176 PF00928 0.467
TRG_ENDOCYTIC_2 193 196 PF00928 0.369
TRG_ENDOCYTIC_2 362 365 PF00928 0.571
TRG_ENDOCYTIC_2 479 482 PF00928 0.527
TRG_ENDOCYTIC_2 802 805 PF00928 0.624
TRG_ENDOCYTIC_2 819 822 PF00928 0.584
TRG_ER_diArg_1 256 259 PF00400 0.559
TRG_ER_diArg_1 28 30 PF00400 0.505
TRG_ER_diArg_1 343 346 PF00400 0.661
TRG_ER_diArg_1 502 504 PF00400 0.678
TRG_Pf-PMV_PEXEL_1 187 191 PF00026 0.576
TRG_Pf-PMV_PEXEL_1 549 553 PF00026 0.568

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P3Z2 Leptomonas seymouri 55% 99%
A0A1X0P794 Trypanosomatidae 32% 100%
A0A3Q8IG16 Leishmania donovani 90% 100%
A0A3R7KYT8 Trypanosoma rangeli 35% 100%
A4HF69 Leishmania braziliensis 77% 98%
A4I2F2 Leishmania infantum 90% 100%
C9ZX52 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 32% 100%
Q4Q8W7 Leishmania major 89% 100%
V5AUK1 Trypanosoma cruzi 35% 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