LeishMANIAdb
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Uncharacterized protein LmxM_30_0950_1

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

Quick info

Protein:
Uncharacterized protein LmxM_30_0950_1
Gene product:
hypothetical protein
Species:
Leishmania mexicana
UniProt:
E8NHE8_LEIMU
TriTrypDb:
LmxM.30.0950
Length:
621

Annotations

LeishMANIAdb annotations

Although predicted to have a multi-helical architecture, the protein is not hydrophobic enough for a membrane protein.. Unique to kinetoplastids, fast-evolving and duplicated multiple times.

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: 2
Forrest at al. (procyclic) no yes: 2
Silverman et al. no yes: 0
Pissara et al. yes yes: 15
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: 5
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: 18
NetGPI no yes: 0, no: 18
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

E8NHE8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E8NHE8

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 124 128 PF00656 0.848
CLV_C14_Caspase3-7 523 527 PF00656 0.627
CLV_C14_Caspase3-7 81 85 PF00656 0.738
CLV_NRD_NRD_1 305 307 PF00675 0.707
CLV_NRD_NRD_1 514 516 PF00675 0.717
CLV_NRD_NRD_1 540 542 PF00675 0.820
CLV_NRD_NRD_1 577 579 PF00675 0.638
CLV_NRD_NRD_1 63 65 PF00675 0.539
CLV_PCSK_KEX2_1 514 516 PF00082 0.744
CLV_PCSK_KEX2_1 524 526 PF00082 0.783
CLV_PCSK_KEX2_1 539 541 PF00082 0.582
CLV_PCSK_KEX2_1 63 65 PF00082 0.539
CLV_PCSK_PC1ET2_1 524 526 PF00082 0.805
CLV_PCSK_PC1ET2_1 539 541 PF00082 0.582
CLV_PCSK_PC7_1 535 541 PF00082 0.741
CLV_PCSK_SKI1_1 102 106 PF00082 0.608
CLV_PCSK_SKI1_1 21 25 PF00082 0.616
CLV_PCSK_SKI1_1 214 218 PF00082 0.555
CLV_PCSK_SKI1_1 324 328 PF00082 0.665
CLV_PCSK_SKI1_1 525 529 PF00082 0.751
CLV_PCSK_SKI1_1 535 539 PF00082 0.618
CLV_PCSK_SKI1_1 56 60 PF00082 0.625
DEG_APCC_DBOX_1 353 361 PF00400 0.751
DOC_CYCLIN_RxL_1 228 237 PF00134 0.552
DOC_MAPK_MEF2A_6 146 154 PF00069 0.670
DOC_MAPK_MEF2A_6 553 560 PF00069 0.722
DOC_PP1_RVXF_1 368 375 PF00149 0.752
DOC_PP2B_LxvP_1 478 481 PF13499 0.790
DOC_SPAK_OSR1_1 30 34 PF12202 0.609
DOC_USP7_MATH_1 347 351 PF00917 0.741
DOC_USP7_MATH_1 391 395 PF00917 0.659
DOC_USP7_MATH_1 445 449 PF00917 0.648
DOC_USP7_MATH_1 461 465 PF00917 0.575
DOC_USP7_MATH_1 494 498 PF00917 0.598
DOC_USP7_MATH_1 513 517 PF00917 0.709
DOC_USP7_MATH_1 567 571 PF00917 0.553
DOC_USP7_MATH_2 334 340 PF00917 0.760
DOC_USP7_MATH_2 424 430 PF00917 0.692
DOC_WW_Pin1_4 387 392 PF00397 0.694
DOC_WW_Pin1_4 420 425 PF00397 0.751
LIG_14-3-3_CanoR_1 265 270 PF00244 0.702
LIG_14-3-3_CanoR_1 30 39 PF00244 0.654
LIG_14-3-3_CanoR_1 340 349 PF00244 0.493
LIG_14-3-3_CanoR_1 4 9 PF00244 0.809
LIG_14-3-3_CanoR_1 415 421 PF00244 0.693
LIG_14-3-3_CanoR_1 427 431 PF00244 0.582
LIG_14-3-3_CanoR_1 541 549 PF00244 0.689
LIG_Actin_WH2_2 437 455 PF00022 0.712
LIG_AP2alpha_1 50 54 PF02296 0.649
LIG_BIR_III_2 84 88 PF00653 0.705
LIG_BRCT_BRCA1_1 267 271 PF00533 0.686
LIG_BRCT_BRCA1_1 585 589 PF00533 0.528
LIG_CSL_BTD_1 388 391 PF09270 0.679
LIG_EH1_1 608 616 PF00400 0.595
LIG_eIF4E_1 283 289 PF01652 0.422
LIG_FHA_1 143 149 PF00498 0.705
LIG_FHA_1 180 186 PF00498 0.616
LIG_FHA_1 201 207 PF00498 0.603
LIG_FHA_1 264 270 PF00498 0.707
LIG_FHA_1 437 443 PF00498 0.570
LIG_FHA_1 482 488 PF00498 0.576
LIG_FHA_1 53 59 PF00498 0.659
LIG_FHA_1 592 598 PF00498 0.520
LIG_FHA_2 101 107 PF00498 0.605
LIG_FHA_2 30 36 PF00498 0.655
LIG_FHA_2 469 475 PF00498 0.784
LIG_LIR_Gen_1 174 183 PF02991 0.633
LIG_LIR_Gen_1 226 235 PF02991 0.737
LIG_LIR_Gen_1 298 304 PF02991 0.636
LIG_LIR_Gen_1 605 615 PF02991 0.645
LIG_LIR_Nem_3 149 154 PF02991 0.647
LIG_LIR_Nem_3 163 168 PF02991 0.420
LIG_LIR_Nem_3 17 23 PF02991 0.666
LIG_LIR_Nem_3 174 178 PF02991 0.465
LIG_LIR_Nem_3 226 230 PF02991 0.730
LIG_LIR_Nem_3 298 302 PF02991 0.626
LIG_LIR_Nem_3 464 469 PF02991 0.720
LIG_Pex14_2 50 54 PF04695 0.649
LIG_SH2_CRK 165 169 PF00017 0.622
LIG_SH2_CRK 20 24 PF00017 0.668
LIG_SH2_CRK 227 231 PF00017 0.709
LIG_SH2_CRK 283 287 PF00017 0.603
LIG_SH2_CRK 291 295 PF00017 0.522
LIG_SH2_CRK 299 303 PF00017 0.471
LIG_SH2_GRB2like 542 545 PF00017 0.663
LIG_SH2_STAP1 469 473 PF00017 0.736
LIG_SH2_STAT3 37 40 PF00017 0.660
LIG_SH2_STAT5 175 178 PF00017 0.646
LIG_SH2_STAT5 195 198 PF00017 0.310
LIG_SH2_STAT5 283 286 PF00017 0.626
LIG_SH2_STAT5 291 294 PF00017 0.500
LIG_SH2_STAT5 337 340 PF00017 0.748
LIG_SH2_STAT5 37 40 PF00017 0.660
LIG_SH2_STAT5 432 435 PF00017 0.729
LIG_SH2_STAT5 542 545 PF00017 0.663
LIG_SH3_3 147 153 PF00018 0.621
LIG_SH3_3 385 391 PF00018 0.727
LIG_SH3_3 439 445 PF00018 0.723
LIG_SH3_3 493 499 PF00018 0.833
LIG_SH3_3 563 569 PF00018 0.374
LIG_SH3_3 86 92 PF00018 0.794
LIG_SUMO_SIM_anti_2 438 445 PF11976 0.722
LIG_SUMO_SIM_par_1 325 332 PF11976 0.469
LIG_TRAF2_1 25 28 PF00917 0.604
LIG_TYR_ITIM 18 23 PF00017 0.657
LIG_TYR_ITIM 225 230 PF00017 0.700
LIG_TYR_ITIM 289 294 PF00017 0.453
LIG_UBA3_1 206 214 PF00899 0.621
LIG_UBA3_1 342 348 PF00899 0.708
LIG_UBA3_1 572 579 PF00899 0.527
LIG_UBA3_1 610 617 PF00899 0.627
LIG_WRC_WIRS_1 371 376 PF05994 0.737
MOD_CDK_SPxxK_3 420 427 PF00069 0.757
MOD_CK1_1 250 256 PF00069 0.646
MOD_CK1_1 300 306 PF00069 0.676
MOD_CK1_1 364 370 PF00069 0.676
MOD_CK1_1 373 379 PF00069 0.573
MOD_CK1_1 414 420 PF00069 0.717
MOD_CK1_1 516 522 PF00069 0.791
MOD_CK2_1 100 106 PF00069 0.607
MOD_CK2_1 29 35 PF00069 0.650
MOD_CK2_1 420 426 PF00069 0.631
MOD_CK2_1 468 474 PF00069 0.743
MOD_GlcNHglycan 118 121 PF01048 0.820
MOD_GlcNHglycan 127 130 PF01048 0.803
MOD_GlcNHglycan 241 245 PF01048 0.685
MOD_GlcNHglycan 384 387 PF01048 0.785
MOD_GlcNHglycan 393 396 PF01048 0.512
MOD_GlcNHglycan 492 495 PF01048 0.804
MOD_GlcNHglycan 517 521 PF01048 0.838
MOD_GlcNHglycan 580 583 PF01048 0.673
MOD_GlcNHglycan 585 588 PF01048 0.610
MOD_GSK3_1 196 203 PF00069 0.606
MOD_GSK3_1 259 266 PF00069 0.705
MOD_GSK3_1 356 363 PF00069 0.805
MOD_GSK3_1 387 394 PF00069 0.687
MOD_GSK3_1 426 433 PF00069 0.689
MOD_GSK3_1 490 497 PF00069 0.582
MOD_GSK3_1 547 554 PF00069 0.769
MOD_N-GLC_1 411 416 PF02516 0.717
MOD_N-GLC_1 591 596 PF02516 0.519
MOD_N-GLC_2 290 292 PF02516 0.559
MOD_NEK2_1 105 110 PF00069 0.693
MOD_NEK2_1 198 203 PF00069 0.618
MOD_NEK2_1 269 274 PF00069 0.643
MOD_NEK2_1 295 300 PF00069 0.653
MOD_NEK2_1 341 346 PF00069 0.504
MOD_NEK2_1 360 365 PF00069 0.751
MOD_NEK2_1 382 387 PF00069 0.769
MOD_NEK2_1 452 457 PF00069 0.696
MOD_NEK2_1 50 55 PF00069 0.648
MOD_NEK2_1 572 577 PF00069 0.599
MOD_NEK2_2 445 450 PF00069 0.643
MOD_NMyristoyl 1 7 PF02799 0.848
MOD_PIKK_1 200 206 PF00454 0.601
MOD_PIKK_1 365 371 PF00454 0.764
MOD_PIKK_1 389 395 PF00454 0.549
MOD_PIKK_1 414 420 PF00454 0.717
MOD_PK_1 4 10 PF00069 0.873
MOD_PKA_1 578 584 PF00069 0.673
MOD_PKA_2 29 35 PF00069 0.650
MOD_PKA_2 3 9 PF00069 0.810
MOD_PKA_2 414 420 PF00069 0.700
MOD_PKA_2 426 432 PF00069 0.584
MOD_PKA_2 490 496 PF00069 0.800
MOD_PKA_2 513 519 PF00069 0.738
MOD_Plk_1 551 557 PF00069 0.747
MOD_Plk_4 100 106 PF00069 0.708
MOD_Plk_4 171 177 PF00069 0.621
MOD_Plk_4 265 271 PF00069 0.700
MOD_Plk_4 445 451 PF00069 0.639
MOD_Plk_4 567 573 PF00069 0.591
MOD_Plk_4 610 616 PF00069 0.638
MOD_ProDKin_1 387 393 PF00069 0.692
MOD_ProDKin_1 420 426 PF00069 0.757
TRG_DiLeu_BaEn_2 584 590 PF01217 0.556
TRG_DiLeu_BaLyEn_6 163 168 PF01217 0.629
TRG_DiLeu_BaLyEn_6 337 342 PF01217 0.696
TRG_DiLeu_BaLyEn_6 395 400 PF01217 0.686
TRG_DiLeu_BaLyEn_6 532 537 PF01217 0.709
TRG_ENDOCYTIC_2 164 167 PF00928 0.598
TRG_ENDOCYTIC_2 175 178 PF00928 0.470
TRG_ENDOCYTIC_2 195 198 PF00928 0.303
TRG_ENDOCYTIC_2 20 23 PF00928 0.661
TRG_ENDOCYTIC_2 227 230 PF00928 0.716
TRG_ENDOCYTIC_2 282 285 PF00928 0.625
TRG_ENDOCYTIC_2 291 294 PF00928 0.485
TRG_ENDOCYTIC_2 299 302 PF00928 0.427
TRG_ENDOCYTIC_2 469 472 PF00928 0.726
TRG_ER_diArg_1 513 515 PF00400 0.616
TRG_ER_diArg_1 540 542 PF00400 0.667
TRG_NES_CRM1_1 317 331 PF08389 0.515
TRG_NLS_Bipartite_1 524 543 PF00514 0.786
TRG_NLS_MonoCore_2 537 542 PF00514 0.762
TRG_NLS_MonoExtN_4 535 542 PF00514 0.759
TRG_Pf-PMV_PEXEL_1 166 170 PF00026 0.620

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IFG5 Leishmania donovani 88% 100%
A0A3Q8ISI8 Leishmania donovani 87% 100%
A0A3S7X4A3 Leishmania donovani 88% 100%
A4HJ70 Leishmania braziliensis 61% 99%
A4HJ71 Leishmania braziliensis 64% 99%
A4HJ73 Leishmania braziliensis 64% 100%
A4HJW7 Leishmania braziliensis 59% 100%
A4I6I2 Leishmania infantum 88% 94%
A4I6L8 Leishmania infantum 89% 100%
E8NHD1 Leishmania infantum 88% 100%
E8NHD2 Leishmania infantum 85% 100%
E8NHE7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 95% 100%
E9B1P3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 95% 100%
Q4Q6G7 Leishmania major 86% 100%
Q4Q6G8 Leishmania major 87% 100%
Q4Q6H0 Leishmania major 86% 100%
Q9BHE5 Leishmania major 87% 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