LeishMANIAdb
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Putative leucine-rich repeat protein

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

Quick info

Protein:
Putative leucine-rich repeat protein
Gene product:
leucine-rich repeat protein, putative
Species:
Leishmania major
UniProt:
Q4QHX1_LEIMA
TriTrypDb:
LmjF.09.0530 , LMJLV39_090011100 * , LMJSD75_090010800
Length:
997

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: 7
NetGPI no yes: 0, no: 7
Cellular components
Term Name Level Count
GO:0000151 ubiquitin ligase complex 3 2
GO:0005930 axoneme 2 2
GO:0019005 SCF ubiquitin ligase complex 5 2
GO:0031461 cullin-RING ubiquitin ligase complex 4 2
GO:0032991 protein-containing complex 1 2
GO:0110165 cellular anatomical entity 1 8
GO:0140535 intracellular protein-containing complex 2 2
GO:1902494 catalytic complex 2 2
GO:1990234 transferase complex 3 2
GO:0005929 cilium 4 6
GO:0042995 cell projection 2 6
GO:0043226 organelle 2 6
GO:0043227 membrane-bounded organelle 3 6
GO:0120025 plasma membrane bounded cell projection 3 6

Expansion

Sequence features

Q4QHX1
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QHX1

Function

Biological processes
Term Name Level Count
GO:0006508 proteolysis 4 2
GO:0006511 ubiquitin-dependent protein catabolic process 7 2
GO:0006807 nitrogen compound metabolic process 2 2
GO:0008152 metabolic process 1 2
GO:0009056 catabolic process 2 2
GO:0009057 macromolecule catabolic process 4 2
GO:0009987 cellular process 1 2
GO:0010498 proteasomal protein catabolic process 5 2
GO:0019538 protein metabolic process 3 2
GO:0019941 modification-dependent protein catabolic process 6 2
GO:0030163 protein catabolic process 4 2
GO:0031146 SCF-dependent proteasomal ubiquitin-dependent protein catabolic process 7 2
GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process 6 2
GO:0043170 macromolecule metabolic process 3 2
GO:0043632 modification-dependent macromolecule catabolic process 5 2
GO:0044237 cellular metabolic process 2 2
GO:0044238 primary metabolic process 2 2
GO:0044248 cellular catabolic process 3 2
GO:0044260 obsolete cellular macromolecule metabolic process 3 2
GO:0044265 obsolete cellular macromolecule catabolic process 4 2
GO:0051603 proteolysis involved in protein catabolic process 5 2
GO:0071704 organic substance metabolic process 2 2
GO:1901564 organonitrogen compound metabolic process 3 2
GO:1901565 organonitrogen compound catabolic process 4 2
GO:1901575 organic substance catabolic process 3 2
Could not find GO molecular_function term for this entry.

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 722 726 PF00656 0.626
CLV_C14_Caspase3-7 781 785 PF00656 0.656
CLV_NRD_NRD_1 131 133 PF00675 0.609
CLV_NRD_NRD_1 523 525 PF00675 0.570
CLV_NRD_NRD_1 875 877 PF00675 0.686
CLV_PCSK_KEX2_1 131 133 PF00082 0.686
CLV_PCSK_KEX2_1 523 525 PF00082 0.570
CLV_PCSK_KEX2_1 586 588 PF00082 0.533
CLV_PCSK_KEX2_1 875 877 PF00082 0.686
CLV_PCSK_KEX2_1 934 936 PF00082 0.746
CLV_PCSK_PC1ET2_1 586 588 PF00082 0.533
CLV_PCSK_PC1ET2_1 934 936 PF00082 0.746
CLV_PCSK_SKI1_1 147 151 PF00082 0.675
CLV_PCSK_SKI1_1 234 238 PF00082 0.480
CLV_PCSK_SKI1_1 496 500 PF00082 0.553
CLV_PCSK_SKI1_1 604 608 PF00082 0.553
CLV_PCSK_SKI1_1 612 616 PF00082 0.428
CLV_PCSK_SKI1_1 699 703 PF00082 0.677
CLV_PCSK_SKI1_1 731 735 PF00082 0.581
CLV_Separin_Metazoa 520 524 PF03568 0.502
DEG_APCC_DBOX_1 461 469 PF00400 0.524
DEG_APCC_DBOX_1 495 503 PF00400 0.592
DEG_APCC_DBOX_1 698 706 PF00400 0.577
DOC_CDC14_PxL_1 289 297 PF14671 0.507
DOC_CKS1_1 35 40 PF01111 0.560
DOC_CYCLIN_RxL_1 320 329 PF00134 0.517
DOC_CYCLIN_RxL_1 447 455 PF00134 0.415
DOC_CYCLIN_RxL_1 735 748 PF00134 0.655
DOC_CYCLIN_yCln2_LP_2 401 404 PF00134 0.522
DOC_CYCLIN_yCln2_LP_2 831 837 PF00134 0.698
DOC_CYCLIN_yCln2_LP_2 870 873 PF00134 0.699
DOC_MAPK_DCC_7 323 332 PF00069 0.516
DOC_MAPK_DCC_7 484 493 PF00069 0.544
DOC_MAPK_gen_1 419 428 PF00069 0.508
DOC_MAPK_gen_1 484 493 PF00069 0.500
DOC_MAPK_HePTP_8 481 493 PF00069 0.538
DOC_MAPK_MEF2A_6 323 332 PF00069 0.516
DOC_MAPK_MEF2A_6 484 493 PF00069 0.544
DOC_PP2B_LxvP_1 325 328 PF13499 0.402
DOC_PP2B_LxvP_1 400 403 PF13499 0.443
DOC_PP2B_LxvP_1 489 492 PF13499 0.466
DOC_PP2B_LxvP_1 502 505 PF13499 0.487
DOC_PP2B_LxvP_1 826 829 PF13499 0.686
DOC_PP2B_LxvP_1 831 834 PF13499 0.658
DOC_PP2B_LxvP_1 870 873 PF13499 0.699
DOC_USP7_MATH_1 142 146 PF00917 0.522
DOC_USP7_MATH_1 156 160 PF00917 0.507
DOC_USP7_MATH_1 2 6 PF00917 0.532
DOC_USP7_MATH_1 210 214 PF00917 0.617
DOC_USP7_MATH_1 227 231 PF00917 0.298
DOC_USP7_MATH_1 279 283 PF00917 0.418
DOC_USP7_MATH_1 360 364 PF00917 0.678
DOC_USP7_MATH_1 365 369 PF00917 0.667
DOC_USP7_MATH_1 480 484 PF00917 0.471
DOC_USP7_MATH_1 688 692 PF00917 0.759
DOC_USP7_MATH_1 713 717 PF00917 0.602
DOC_USP7_MATH_1 762 766 PF00917 0.824
DOC_USP7_MATH_1 854 858 PF00917 0.688
DOC_USP7_MATH_1 929 933 PF00917 0.771
DOC_USP7_MATH_1 943 947 PF00917 0.603
DOC_USP7_MATH_1 975 979 PF00917 0.579
DOC_USP7_MATH_1 988 992 PF00917 0.631
DOC_WW_Pin1_4 236 241 PF00397 0.514
DOC_WW_Pin1_4 34 39 PF00397 0.793
DOC_WW_Pin1_4 860 865 PF00397 0.766
DOC_WW_Pin1_4 875 880 PF00397 0.597
DOC_WW_Pin1_4 891 896 PF00397 0.768
DOC_WW_Pin1_4 901 906 PF00397 0.717
LIG_14-3-3_CanoR_1 107 111 PF00244 0.476
LIG_14-3-3_CanoR_1 12 22 PF00244 0.638
LIG_14-3-3_CanoR_1 191 199 PF00244 0.563
LIG_14-3-3_CanoR_1 234 243 PF00244 0.578
LIG_14-3-3_CanoR_1 268 273 PF00244 0.470
LIG_14-3-3_CanoR_1 407 413 PF00244 0.551
LIG_14-3-3_CanoR_1 422 427 PF00244 0.345
LIG_14-3-3_CanoR_1 433 441 PF00244 0.388
LIG_14-3-3_CanoR_1 496 505 PF00244 0.530
LIG_14-3-3_CanoR_1 506 512 PF00244 0.444
LIG_14-3-3_CanoR_1 540 545 PF00244 0.520
LIG_14-3-3_CanoR_1 604 611 PF00244 0.544
LIG_14-3-3_CanoR_1 875 879 PF00244 0.679
LIG_14-3-3_CanoR_1 95 104 PF00244 0.628
LIG_14-3-3_CanoR_1 958 966 PF00244 0.749
LIG_BIR_II_1 1 5 PF00653 0.725
LIG_BIR_III_4 849 853 PF00653 0.667
LIG_BRCT_BRCA1_1 270 274 PF00533 0.481
LIG_BRCT_BRCA1_1 542 546 PF00533 0.450
LIG_BRCT_BRCA1_1 802 806 PF00533 0.726
LIG_BRCT_BRCA1_1 945 949 PF00533 0.677
LIG_FAT_LD_1 468 476 PF03623 0.458
LIG_FHA_1 267 273 PF00498 0.493
LIG_FHA_1 353 359 PF00498 0.633
LIG_FHA_1 373 379 PF00498 0.476
LIG_FHA_1 403 409 PF00498 0.457
LIG_FHA_1 423 429 PF00498 0.294
LIG_FHA_1 498 504 PF00498 0.372
LIG_FHA_1 595 601 PF00498 0.502
LIG_FHA_1 660 666 PF00498 0.533
LIG_FHA_1 823 829 PF00498 0.678
LIG_FHA_1 967 973 PF00498 0.571
LIG_FHA_2 543 549 PF00498 0.562
LIG_FHA_2 603 609 PF00498 0.549
LIG_FHA_2 779 785 PF00498 0.714
LIG_FHA_2 876 882 PF00498 0.689
LIG_GBD_Chelix_1 665 673 PF00786 0.464
LIG_Integrin_isoDGR_2 526 528 PF01839 0.619
LIG_LIR_LC3C_4 329 332 PF02991 0.456
LIG_LIR_Nem_3 275 281 PF02991 0.579
LIG_LIR_Nem_3 554 560 PF02991 0.518
LIG_LIR_Nem_3 946 952 PF02991 0.678
LIG_MAD2 450 458 PF02301 0.408
LIG_NRBOX 231 237 PF00104 0.522
LIG_NRBOX 339 345 PF00104 0.501
LIG_PCNA_yPIPBox_3 183 191 PF02747 0.500
LIG_Pex14_2 270 274 PF04695 0.481
LIG_SH2_CRK 278 282 PF00017 0.442
LIG_SH2_STAT3 130 133 PF00017 0.522
LIG_SH2_STAT3 916 919 PF00017 0.686
LIG_SH2_STAT5 189 192 PF00017 0.432
LIG_SH2_STAT5 195 198 PF00017 0.485
LIG_SH2_STAT5 916 919 PF00017 0.718
LIG_SH3_1 876 882 PF00018 0.706
LIG_SH3_3 193 199 PF00018 0.582
LIG_SH3_3 32 38 PF00018 0.761
LIG_SH3_3 58 64 PF00018 0.593
LIG_SH3_3 658 664 PF00018 0.559
LIG_SH3_3 831 837 PF00018 0.697
LIG_SH3_3 858 864 PF00018 0.660
LIG_SH3_3 876 882 PF00018 0.549
LIG_SUMO_SIM_anti_2 122 129 PF11976 0.648
LIG_SUMO_SIM_anti_2 396 401 PF11976 0.394
LIG_SUMO_SIM_anti_2 466 474 PF11976 0.520
LIG_SUMO_SIM_anti_2 597 602 PF11976 0.506
LIG_SUMO_SIM_par_1 122 129 PF11976 0.630
LIG_SUMO_SIM_par_1 374 379 PF11976 0.508
LIG_SUMO_SIM_par_1 424 429 PF11976 0.385
LIG_SUMO_SIM_par_1 450 455 PF11976 0.520
LIG_SUMO_SIM_par_1 824 830 PF11976 0.681
LIG_TRAF2_1 920 923 PF00917 0.780
LIG_TRAF2_1 994 997 PF00917 0.777
LIG_WRC_WIRS_1 205 210 PF05994 0.416
LIG_WRC_WIRS_1 267 272 PF05994 0.441
MOD_CK1_1 11 17 PF00069 0.661
MOD_CK1_1 282 288 PF00069 0.420
MOD_CK1_1 291 297 PF00069 0.432
MOD_CK1_1 508 514 PF00069 0.558
MOD_CK1_1 547 553 PF00069 0.516
MOD_CK1_1 632 638 PF00069 0.538
MOD_CK1_1 693 699 PF00069 0.596
MOD_CK1_1 714 720 PF00069 0.643
MOD_CK1_1 776 782 PF00069 0.691
MOD_CK1_1 821 827 PF00069 0.737
MOD_CK1_1 904 910 PF00069 0.717
MOD_CK1_1 911 917 PF00069 0.660
MOD_CK1_1 960 966 PF00069 0.797
MOD_CK2_1 14 20 PF00069 0.563
MOD_CK2_1 209 215 PF00069 0.667
MOD_CK2_1 323 329 PF00069 0.419
MOD_CK2_1 542 548 PF00069 0.567
MOD_CK2_1 721 727 PF00069 0.558
MOD_GlcNHglycan 212 215 PF01048 0.663
MOD_GlcNHglycan 255 259 PF01048 0.551
MOD_GlcNHglycan 377 381 PF01048 0.513
MOD_GlcNHglycan 4 7 PF01048 0.534
MOD_GlcNHglycan 427 431 PF01048 0.452
MOD_GlcNHglycan 443 446 PF01048 0.453
MOD_GlcNHglycan 528 531 PF01048 0.665
MOD_GlcNHglycan 695 698 PF01048 0.801
MOD_GlcNHglycan 711 714 PF01048 0.551
MOD_GlcNHglycan 747 750 PF01048 0.653
MOD_GlcNHglycan 788 792 PF01048 0.746
MOD_GlcNHglycan 820 823 PF01048 0.696
MOD_GlcNHglycan 856 859 PF01048 0.639
MOD_GlcNHglycan 945 948 PF01048 0.762
MOD_GlcNHglycan 977 980 PF01048 0.588
MOD_GSK3_1 254 261 PF00069 0.495
MOD_GSK3_1 372 379 PF00069 0.483
MOD_GSK3_1 4 11 PF00069 0.643
MOD_GSK3_1 402 409 PF00069 0.532
MOD_GSK3_1 422 429 PF00069 0.274
MOD_GSK3_1 540 547 PF00069 0.517
MOD_GSK3_1 709 716 PF00069 0.707
MOD_GSK3_1 818 825 PF00069 0.623
MOD_GSK3_1 903 910 PF00069 0.733
MOD_GSK3_1 914 921 PF00069 0.660
MOD_GSK3_1 929 936 PF00069 0.569
MOD_GSK3_1 957 964 PF00069 0.812
MOD_GSK3_1 966 973 PF00069 0.594
MOD_LATS_1 266 272 PF00433 0.499
MOD_LATS_1 574 580 PF00433 0.532
MOD_N-GLC_2 580 582 PF02516 0.366
MOD_NEK2_1 1 6 PF00069 0.697
MOD_NEK2_1 106 111 PF00069 0.563
MOD_NEK2_1 204 209 PF00069 0.426
MOD_NEK2_1 288 293 PF00069 0.447
MOD_NEK2_1 376 381 PF00069 0.406
MOD_NEK2_1 426 431 PF00069 0.359
MOD_NEK2_1 441 446 PF00069 0.510
MOD_NEK2_1 471 476 PF00069 0.410
MOD_NEK2_1 560 565 PF00069 0.458
MOD_NEK2_1 778 783 PF00069 0.811
MOD_NEK2_1 8 13 PF00069 0.645
MOD_NEK2_1 874 879 PF00069 0.617
MOD_NEK2_1 933 938 PF00069 0.806
MOD_NEK2_2 142 147 PF00069 0.496
MOD_NEK2_2 929 934 PF00069 0.726
MOD_PIKK_1 234 240 PF00454 0.571
MOD_PIKK_1 317 323 PF00454 0.520
MOD_PIKK_1 505 511 PF00454 0.541
MOD_PIKK_1 560 566 PF00454 0.567
MOD_PIKK_1 612 618 PF00454 0.470
MOD_PIKK_1 918 924 PF00454 0.706
MOD_PK_1 268 274 PF00069 0.494
MOD_PK_1 540 546 PF00069 0.517
MOD_PKA_2 106 112 PF00069 0.522
MOD_PKA_2 11 17 PF00069 0.675
MOD_PKA_2 190 196 PF00069 0.556
MOD_PKA_2 346 352 PF00069 0.524
MOD_PKA_2 406 412 PF00069 0.550
MOD_PKA_2 432 438 PF00069 0.536
MOD_PKA_2 505 511 PF00069 0.560
MOD_PKA_2 539 545 PF00069 0.458
MOD_PKA_2 762 768 PF00069 0.738
MOD_PKA_2 874 880 PF00069 0.680
MOD_PKA_2 957 963 PF00069 0.730
MOD_Plk_1 254 260 PF00069 0.480
MOD_Plk_1 323 329 PF00069 0.503
MOD_Plk_1 547 553 PF00069 0.416
MOD_Plk_1 635 641 PF00069 0.523
MOD_Plk_1 988 994 PF00069 0.639
MOD_Plk_4 204 210 PF00069 0.440
MOD_Plk_4 227 233 PF00069 0.526
MOD_Plk_4 279 285 PF00069 0.368
MOD_Plk_4 4 10 PF00069 0.618
MOD_Plk_4 408 414 PF00069 0.529
MOD_Plk_4 498 504 PF00069 0.563
MOD_Plk_4 547 553 PF00069 0.470
MOD_Plk_4 568 574 PF00069 0.544
MOD_Plk_4 715 721 PF00069 0.562
MOD_Plk_4 773 779 PF00069 0.692
MOD_ProDKin_1 236 242 PF00069 0.524
MOD_ProDKin_1 34 40 PF00069 0.791
MOD_ProDKin_1 860 866 PF00069 0.766
MOD_ProDKin_1 875 881 PF00069 0.598
MOD_ProDKin_1 891 897 PF00069 0.765
MOD_ProDKin_1 901 907 PF00069 0.716
MOD_SUMO_for_1 70 73 PF00179 0.545
TRG_DiLeu_BaEn_1 122 127 PF01217 0.643
TRG_DiLeu_BaEn_4 122 128 PF01217 0.648
TRG_DiLeu_BaEn_4 73 79 PF01217 0.479
TRG_DiLeu_BaLyEn_6 231 236 PF01217 0.520
TRG_DiLeu_BaLyEn_6 339 344 PF01217 0.427
TRG_ENDOCYTIC_2 278 281 PF00928 0.566
TRG_ER_diArg_1 130 132 PF00400 0.612
TRG_ER_diArg_1 344 347 PF00400 0.398
TRG_ER_diArg_1 522 524 PF00400 0.563
TRG_ER_diArg_1 874 876 PF00400 0.693
TRG_ER_diArg_1 9 12 PF00400 0.529
TRG_NES_CRM1_1 647 659 PF08389 0.524
TRG_Pf-PMV_PEXEL_1 234 238 PF00026 0.434
TRG_Pf-PMV_PEXEL_1 450 455 PF00026 0.520
TRG_Pf-PMV_PEXEL_1 604 608 PF00026 0.553
TRG_Pf-PMV_PEXEL_1 612 616 PF00026 0.428
TRG_Pf-PMV_PEXEL_1 640 644 PF00026 0.432
TRG_Pf-PMV_PEXEL_1 740 745 PF00026 0.640
TRG_Pf-PMV_PEXEL_1 80 84 PF00026 0.523
TRG_Pf-PMV_PEXEL_1 935 939 PF00026 0.737

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3S7WQP1 Leishmania donovani 92% 100%
A0A422NV64 Trypanosoma rangeli 28% 92%
A4H5N0 Leishmania braziliensis 70% 100%
A4HTW7 Leishmania infantum 92% 100%
D0A9D1 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 29% 95%
E9AMQ4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 88% 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