LeishMANIAdb
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Leucine rich repeat family protein

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

Quick info

Protein:
Leucine rich repeat family protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania mexicana
UniProt:
E9AYA1_LEIMU
TriTrypDb:
LmxM.26.1220
Length:
672

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
Cellular components
Term Name Level Count
GO:0005930 axoneme 2 10
GO:0110165 cellular anatomical entity 1 11
GO:0005929 cilium 4 1
GO:0042995 cell projection 2 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0120025 plasma membrane bounded cell projection 3 1

Expansion

Sequence features

E9AYA1
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AYA1

Function

Biological processes
Term Name Level Count
GO:0009987 cellular process 1 10
GO:0016043 cellular component organization 3 10
GO:0022607 cellular component assembly 4 10
GO:0036158 outer dynein arm assembly 7 10
GO:0036159 inner dynein arm assembly 7 10
GO:0043933 protein-containing complex organization 4 10
GO:0065003 protein-containing complex assembly 5 10
GO:0070286 axonemal dynein complex assembly 6 10
GO:0071840 cellular component organization or biogenesis 2 10
Molecular functions
Term Name Level Count
GO:0005488 binding 1 10
GO:0044877 protein-containing complex binding 2 10
GO:0070840 dynein complex binding 3 10

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 171 175 PF00656 0.420
CLV_C14_Caspase3-7 203 207 PF00656 0.449
CLV_C14_Caspase3-7 236 240 PF00656 0.711
CLV_C14_Caspase3-7 526 530 PF00656 0.720
CLV_C14_Caspase3-7 553 557 PF00656 0.782
CLV_NRD_NRD_1 339 341 PF00675 0.720
CLV_NRD_NRD_1 431 433 PF00675 0.402
CLV_NRD_NRD_1 455 457 PF00675 0.413
CLV_NRD_NRD_1 492 494 PF00675 0.514
CLV_NRD_NRD_1 546 548 PF00675 0.701
CLV_NRD_NRD_1 549 551 PF00675 0.708
CLV_PCSK_FUR_1 438 442 PF00082 0.566
CLV_PCSK_FUR_1 547 551 PF00082 0.536
CLV_PCSK_KEX2_1 297 299 PF00082 0.568
CLV_PCSK_KEX2_1 339 341 PF00082 0.720
CLV_PCSK_KEX2_1 433 435 PF00082 0.512
CLV_PCSK_KEX2_1 440 442 PF00082 0.475
CLV_PCSK_KEX2_1 455 457 PF00082 0.294
CLV_PCSK_KEX2_1 486 488 PF00082 0.468
CLV_PCSK_KEX2_1 492 494 PF00082 0.503
CLV_PCSK_KEX2_1 546 548 PF00082 0.660
CLV_PCSK_KEX2_1 549 551 PF00082 0.665
CLV_PCSK_PC1ET2_1 297 299 PF00082 0.584
CLV_PCSK_PC1ET2_1 433 435 PF00082 0.512
CLV_PCSK_PC1ET2_1 440 442 PF00082 0.525
CLV_PCSK_PC1ET2_1 486 488 PF00082 0.567
CLV_PCSK_SKI1_1 173 177 PF00082 0.456
CLV_PCSK_SKI1_1 415 419 PF00082 0.293
CLV_PCSK_SKI1_1 433 437 PF00082 0.462
CLV_PCSK_SKI1_1 440 444 PF00082 0.441
CLV_PCSK_SKI1_1 448 452 PF00082 0.412
CLV_PCSK_SKI1_1 456 460 PF00082 0.351
DEG_COP1_1 659 671 PF00400 0.606
DEG_ODPH_VHL_1 72 85 PF01847 0.486
DEG_SPOP_SBC_1 555 559 PF00917 0.658
DOC_CDC14_PxL_1 408 416 PF14671 0.435
DOC_CYCLIN_RxL_1 410 420 PF00134 0.270
DOC_CYCLIN_RxL_1 434 447 PF00134 0.497
DOC_CYCLIN_yCln2_LP_2 105 111 PF00134 0.587
DOC_MAPK_gen_1 201 210 PF00069 0.524
DOC_MAPK_gen_1 339 346 PF00069 0.709
DOC_MAPK_gen_1 410 419 PF00069 0.410
DOC_MAPK_gen_1 438 445 PF00069 0.491
DOC_PP1_RVXF_1 82 88 PF00149 0.393
DOC_PP2B_LxvP_1 105 108 PF13499 0.401
DOC_USP7_MATH_1 129 133 PF00917 0.551
DOC_USP7_MATH_1 175 179 PF00917 0.506
DOC_USP7_MATH_1 246 250 PF00917 0.774
DOC_USP7_MATH_1 25 29 PF00917 0.735
DOC_USP7_MATH_1 359 363 PF00917 0.466
DOC_USP7_MATH_1 555 559 PF00917 0.720
DOC_USP7_MATH_1 591 595 PF00917 0.752
DOC_USP7_MATH_1 600 604 PF00917 0.702
DOC_USP7_MATH_1 650 654 PF00917 0.791
DOC_WW_Pin1_4 148 153 PF00397 0.742
DOC_WW_Pin1_4 239 244 PF00397 0.690
DOC_WW_Pin1_4 249 254 PF00397 0.698
DOC_WW_Pin1_4 289 294 PF00397 0.501
DOC_WW_Pin1_4 318 323 PF00397 0.587
DOC_WW_Pin1_4 52 57 PF00397 0.387
LIG_14-3-3_CanoR_1 306 316 PF00244 0.479
LIG_14-3-3_CanoR_1 339 344 PF00244 0.804
LIG_14-3-3_CanoR_1 357 366 PF00244 0.284
LIG_14-3-3_CanoR_1 372 377 PF00244 0.390
LIG_14-3-3_CanoR_1 455 463 PF00244 0.575
LIG_14-3-3_CanoR_1 497 507 PF00244 0.582
LIG_14-3-3_CanoR_1 549 555 PF00244 0.774
LIG_14-3-3_CanoR_1 624 629 PF00244 0.836
LIG_14-3-3_CanoR_1 640 648 PF00244 0.642
LIG_Actin_WH2_2 404 420 PF00022 0.408
LIG_AP2alpha_2 112 114 PF02296 0.664
LIG_APCC_ABBA_1 137 142 PF00400 0.459
LIG_APCC_ABBA_1 77 82 PF00400 0.460
LIG_APCC_ABBAyCdc20_2 440 446 PF00400 0.491
LIG_BIR_II_1 1 5 PF00653 0.704
LIG_BRCT_BRCA1_1 210 214 PF00533 0.457
LIG_BRCT_BRCA1_2 210 216 PF00533 0.376
LIG_Clathr_ClatBox_1 405 409 PF01394 0.402
LIG_Clathr_ClatBox_1 442 446 PF01394 0.402
LIG_eIF4E_1 187 193 PF01652 0.546
LIG_FHA_1 308 314 PF00498 0.521
LIG_FHA_1 38 44 PF00498 0.443
LIG_FHA_1 59 65 PF00498 0.257
LIG_FHA_1 7 13 PF00498 0.754
LIG_FHA_2 558 564 PF00498 0.696
LIG_FHA_2 566 572 PF00498 0.691
LIG_FHA_2 73 79 PF00498 0.548
LIG_LIR_Gen_1 174 183 PF02991 0.396
LIG_LIR_Gen_1 200 210 PF02991 0.434
LIG_LIR_Gen_1 312 322 PF02991 0.446
LIG_LIR_Gen_1 78 88 PF02991 0.400
LIG_LIR_Nem_3 174 179 PF02991 0.407
LIG_LIR_Nem_3 200 205 PF02991 0.449
LIG_LIR_Nem_3 312 317 PF02991 0.435
LIG_LIR_Nem_3 489 494 PF02991 0.550
LIG_LIR_Nem_3 75 80 PF02991 0.423
LIG_LYPXL_S_1 179 183 PF13949 0.383
LIG_LYPXL_yS_3 180 183 PF13949 0.381
LIG_PDZ_Class_3 667 672 PF00595 0.488
LIG_PTB_Apo_2 187 194 PF02174 0.521
LIG_PTB_Apo_2 63 70 PF02174 0.496
LIG_PTB_Phospho_1 63 69 PF10480 0.566
LIG_REV1ctd_RIR_1 212 219 PF16727 0.381
LIG_SH2_CRK 102 106 PF00017 0.627
LIG_SH2_CRK 385 389 PF00017 0.408
LIG_SH2_CRK 53 57 PF00017 0.437
LIG_SH2_CRK 69 73 PF00017 0.425
LIG_SH2_GRB2like 511 514 PF00017 0.611
LIG_SH2_NCK_1 69 73 PF00017 0.570
LIG_SH2_SRC 511 514 PF00017 0.689
LIG_SH2_STAP1 140 144 PF00017 0.633
LIG_SH2_STAP1 225 229 PF00017 0.576
LIG_SH2_STAP1 69 73 PF00017 0.570
LIG_SH2_STAT5 102 105 PF00017 0.581
LIG_SH2_STAT5 140 143 PF00017 0.633
LIG_SH2_STAT5 187 190 PF00017 0.473
LIG_SH2_STAT5 511 514 PF00017 0.656
LIG_SH2_STAT5 63 66 PF00017 0.417
LIG_SH2_STAT5 80 83 PF00017 0.388
LIG_SH3_3 287 293 PF00018 0.649
LIG_SH3_3 346 352 PF00018 0.746
LIG_SH3_5 507 511 PF00018 0.691
LIG_SUMO_SIM_anti_2 284 292 PF11976 0.676
LIG_SUMO_SIM_anti_2 377 384 PF11976 0.365
LIG_SUMO_SIM_anti_2 387 392 PF11976 0.475
LIG_SUMO_SIM_anti_2 402 409 PF11976 0.242
LIG_SUMO_SIM_par_1 389 394 PF11976 0.335
LIG_SUMO_SIM_par_1 402 409 PF11976 0.384
LIG_TRAF2_1 475 478 PF00917 0.610
LIG_TYR_ITIM 383 388 PF00017 0.435
LIG_UBA3_1 407 415 PF00899 0.343
LIG_WRC_WIRS_1 373 378 PF05994 0.436
LIG_WW_3 618 622 PF00397 0.706
MOD_CK1_1 151 157 PF00069 0.745
MOD_CK1_1 23 29 PF00069 0.683
MOD_CK1_1 242 248 PF00069 0.707
MOD_CK1_1 249 255 PF00069 0.777
MOD_CK1_1 362 368 PF00069 0.377
MOD_CK1_1 540 546 PF00069 0.766
MOD_CK1_1 557 563 PF00069 0.738
MOD_CK2_1 197 203 PF00069 0.552
MOD_CK2_1 396 402 PF00069 0.262
MOD_CK2_1 499 505 PF00069 0.507
MOD_CK2_1 557 563 PF00069 0.721
MOD_CK2_1 610 616 PF00069 0.805
MOD_CK2_1 72 78 PF00069 0.461
MOD_Cter_Amidation 547 550 PF01082 0.562
MOD_GlcNHglycan 210 213 PF01048 0.468
MOD_GlcNHglycan 226 229 PF01048 0.390
MOD_GlcNHglycan 244 247 PF01048 0.700
MOD_GlcNHglycan 248 251 PF01048 0.760
MOD_GlcNHglycan 27 30 PF01048 0.681
MOD_GlcNHglycan 419 422 PF01048 0.392
MOD_GlcNHglycan 521 524 PF01048 0.553
MOD_GlcNHglycan 580 584 PF01048 0.787
MOD_GlcNHglycan 601 605 PF01048 0.774
MOD_GSK3_1 1 8 PF00069 0.708
MOD_GSK3_1 11 18 PF00069 0.696
MOD_GSK3_1 175 182 PF00069 0.453
MOD_GSK3_1 20 27 PF00069 0.626
MOD_GSK3_1 238 245 PF00069 0.775
MOD_GSK3_1 249 256 PF00069 0.704
MOD_GSK3_1 274 281 PF00069 0.719
MOD_GSK3_1 285 292 PF00069 0.554
MOD_GSK3_1 358 365 PF00069 0.416
MOD_GSK3_1 550 557 PF00069 0.706
MOD_GSK3_1 561 568 PF00069 0.622
MOD_GSK3_1 575 582 PF00069 0.699
MOD_GSK3_1 589 596 PF00069 0.730
MOD_LATS_1 337 343 PF00433 0.613
MOD_LATS_1 498 504 PF00433 0.429
MOD_N-GLC_1 20 25 PF02516 0.779
MOD_N-GLC_1 208 213 PF02516 0.393
MOD_N-GLC_1 31 36 PF02516 0.633
MOD_N-GLC_1 58 63 PF02516 0.266
MOD_NEK2_1 1 6 PF00069 0.679
MOD_NEK2_1 192 197 PF00069 0.544
MOD_NEK2_1 24 29 PF00069 0.693
MOD_NEK2_1 255 260 PF00069 0.644
MOD_NEK2_1 391 396 PF00069 0.319
MOD_NEK2_1 417 422 PF00069 0.389
MOD_NEK2_1 424 429 PF00069 0.411
MOD_NEK2_1 610 615 PF00069 0.809
MOD_NEK2_2 175 180 PF00069 0.514
MOD_NEK2_2 359 364 PF00069 0.482
MOD_NEK2_2 58 63 PF00069 0.266
MOD_PIKK_1 100 106 PF00454 0.572
MOD_PIKK_1 610 616 PF00454 0.809
MOD_PIKK_1 626 632 PF00454 0.833
MOD_PK_1 339 345 PF00069 0.504
MOD_PKA_1 339 345 PF00069 0.718
MOD_PKA_1 549 555 PF00069 0.626
MOD_PKA_2 307 313 PF00069 0.484
MOD_PKA_2 339 345 PF00069 0.796
MOD_PKA_2 499 505 PF00069 0.507
MOD_PKA_2 540 546 PF00069 0.753
MOD_PKA_2 549 555 PF00069 0.701
MOD_PKA_2 575 581 PF00069 0.749
MOD_PKA_2 6 12 PF00069 0.679
MOD_PKA_2 623 629 PF00069 0.540
MOD_PKB_1 432 440 PF00069 0.519
MOD_PKB_1 547 555 PF00069 0.529
MOD_PKB_1 638 646 PF00069 0.619
MOD_Plk_1 158 164 PF00069 0.698
MOD_Plk_1 197 203 PF00069 0.497
MOD_Plk_1 20 26 PF00069 0.752
MOD_Plk_1 285 291 PF00069 0.647
MOD_Plk_1 58 64 PF00069 0.261
MOD_Plk_2-3 565 571 PF00069 0.604
MOD_Plk_4 129 135 PF00069 0.586
MOD_Plk_4 175 181 PF00069 0.414
MOD_Plk_4 285 291 PF00069 0.647
MOD_Plk_4 339 345 PF00069 0.504
MOD_Plk_4 58 64 PF00069 0.362
MOD_Plk_4 91 97 PF00069 0.483
MOD_ProDKin_1 148 154 PF00069 0.741
MOD_ProDKin_1 239 245 PF00069 0.694
MOD_ProDKin_1 249 255 PF00069 0.698
MOD_ProDKin_1 289 295 PF00069 0.492
MOD_ProDKin_1 318 324 PF00069 0.598
MOD_ProDKin_1 52 58 PF00069 0.389
MOD_SUMO_rev_2 112 121 PF00179 0.504
MOD_SUMO_rev_2 478 488 PF00179 0.554
MOD_SUMO_rev_2 613 620 PF00179 0.732
MOD_SUMO_rev_2 78 86 PF00179 0.410
TRG_DiLeu_BaEn_1 402 407 PF01217 0.400
TRG_DiLeu_BaLyEn_6 250 255 PF01217 0.583
TRG_DiLeu_BaLyEn_6 438 443 PF01217 0.552
TRG_DiLeu_BaLyEn_6 490 495 PF01217 0.596
TRG_ENDOCYTIC_2 102 105 PF00928 0.614
TRG_ENDOCYTIC_2 180 183 PF00928 0.381
TRG_ENDOCYTIC_2 385 388 PF00928 0.408
TRG_ENDOCYTIC_2 69 72 PF00928 0.492
TRG_ENDOCYTIC_2 80 83 PF00928 0.331
TRG_ER_diArg_1 339 341 PF00400 0.711
TRG_ER_diArg_1 431 434 PF00400 0.512
TRG_ER_diArg_1 455 457 PF00400 0.413
TRG_ER_diArg_1 491 493 PF00400 0.513
TRG_ER_diArg_1 546 549 PF00400 0.720
TRG_ER_diArg_1 638 641 PF00400 0.517
TRG_NLS_MonoExtN_4 429 436 PF00514 0.523
TRG_Pf-PMV_PEXEL_1 441 446 PF00026 0.554

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P4C5 Leptomonas seymouri 52% 100%
A0A0S4JQS0 Bodo saltans 37% 100%
A0A3Q8IFU8 Leishmania donovani 87% 100%
A0A422N6Q2 Trypanosoma rangeli 40% 100%
A4HEX7 Leishmania braziliensis 72% 98%
A4I251 Leishmania infantum 87% 100%
C9ZRV3 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 39% 100%
Q4Q972 Leishmania major 89% 100%
V5DQX0 Trypanosoma cruzi 38% 91%

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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