LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
Tetratricopeptide repeat - putative
Species:
Leishmania infantum
UniProt:
A4I3Y7_LEIIN
TriTrypDb:
LINF_280032700
Length:
1003

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: 6
NetGPI no yes: 0, no: 6
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

A4I3Y7
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4I3Y7

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0005488 binding 1 5
GO:0043167 ion binding 2 5
GO:0043169 cation binding 3 5
GO:0046872 metal ion binding 4 5

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 190 194 PF00656 0.551
CLV_C14_Caspase3-7 268 272 PF00656 0.663
CLV_NRD_NRD_1 126 128 PF00675 0.491
CLV_NRD_NRD_1 130 132 PF00675 0.480
CLV_NRD_NRD_1 489 491 PF00675 0.497
CLV_NRD_NRD_1 525 527 PF00675 0.396
CLV_NRD_NRD_1 558 560 PF00675 0.517
CLV_NRD_NRD_1 822 824 PF00675 0.413
CLV_NRD_NRD_1 876 878 PF00675 0.652
CLV_NRD_NRD_1 888 890 PF00675 0.716
CLV_NRD_NRD_1 912 914 PF00675 0.669
CLV_PCSK_FUR_1 886 890 PF00082 0.667
CLV_PCSK_KEX2_1 126 128 PF00082 0.491
CLV_PCSK_KEX2_1 130 132 PF00082 0.480
CLV_PCSK_KEX2_1 489 491 PF00082 0.497
CLV_PCSK_KEX2_1 525 527 PF00082 0.394
CLV_PCSK_KEX2_1 558 560 PF00082 0.517
CLV_PCSK_KEX2_1 822 824 PF00082 0.413
CLV_PCSK_KEX2_1 875 877 PF00082 0.645
CLV_PCSK_KEX2_1 886 888 PF00082 0.718
CLV_PCSK_KEX2_1 912 914 PF00082 0.669
CLV_PCSK_PC7_1 126 132 PF00082 0.478
CLV_PCSK_PC7_1 554 560 PF00082 0.573
CLV_PCSK_SKI1_1 152 156 PF00082 0.381
CLV_PCSK_SKI1_1 334 338 PF00082 0.473
CLV_PCSK_SKI1_1 484 488 PF00082 0.419
CLV_PCSK_SKI1_1 525 529 PF00082 0.336
CLV_PCSK_SKI1_1 561 565 PF00082 0.557
CLV_PCSK_SKI1_1 664 668 PF00082 0.366
CLV_PCSK_SKI1_1 682 686 PF00082 0.378
CLV_PCSK_SKI1_1 741 745 PF00082 0.526
CLV_PCSK_SKI1_1 75 79 PF00082 0.371
CLV_PCSK_SKI1_1 809 813 PF00082 0.582
CLV_PCSK_SKI1_1 823 827 PF00082 0.389
CLV_PCSK_SKI1_1 844 848 PF00082 0.375
DEG_APCC_DBOX_1 129 137 PF00400 0.423
DEG_SPOP_SBC_1 282 286 PF00917 0.668
DEG_SPOP_SBC_1 391 395 PF00917 0.556
DEG_SPOP_SBC_1 405 409 PF00917 0.640
DOC_ANK_TNKS_1 188 195 PF00023 0.552
DOC_ANK_TNKS_1 538 545 PF00023 0.461
DOC_ANK_TNKS_1 943 950 PF00023 0.562
DOC_CKS1_1 922 927 PF01111 0.703
DOC_CKS1_1 971 976 PF01111 0.627
DOC_CYCLIN_RxL_1 329 342 PF00134 0.478
DOC_CYCLIN_RxL_1 4 12 PF00134 0.515
DOC_CYCLIN_RxL_1 661 670 PF00134 0.380
DOC_CYCLIN_RxL_1 841 851 PF00134 0.376
DOC_CYCLIN_yCln2_LP_2 161 167 PF00134 0.416
DOC_MAPK_gen_1 126 136 PF00069 0.453
DOC_MAPK_gen_1 475 485 PF00069 0.461
DOC_MAPK_gen_1 525 532 PF00069 0.371
DOC_MAPK_gen_1 72 80 PF00069 0.445
DOC_MAPK_gen_1 822 828 PF00069 0.421
DOC_MAPK_MEF2A_6 478 487 PF00069 0.460
DOC_MAPK_MEF2A_6 525 534 PF00069 0.348
DOC_MAPK_NFAT4_5 525 533 PF00069 0.321
DOC_PP1_RVXF_1 842 849 PF00149 0.375
DOC_PP2B_LxvP_1 161 164 PF13499 0.427
DOC_PP2B_LxvP_1 374 377 PF13499 0.600
DOC_PP4_FxxP_1 774 777 PF00568 0.440
DOC_USP7_MATH_1 119 123 PF00917 0.630
DOC_USP7_MATH_1 276 280 PF00917 0.723
DOC_USP7_MATH_1 282 286 PF00917 0.652
DOC_USP7_MATH_1 375 379 PF00917 0.594
DOC_USP7_MATH_1 391 395 PF00917 0.713
DOC_USP7_MATH_1 405 409 PF00917 0.693
DOC_USP7_MATH_1 585 589 PF00917 0.564
DOC_USP7_MATH_1 842 846 PF00917 0.593
DOC_USP7_MATH_1 894 898 PF00917 0.738
DOC_USP7_MATH_2 219 225 PF00917 0.595
DOC_WW_Pin1_4 111 116 PF00397 0.581
DOC_WW_Pin1_4 269 274 PF00397 0.705
DOC_WW_Pin1_4 366 371 PF00397 0.600
DOC_WW_Pin1_4 426 431 PF00397 0.661
DOC_WW_Pin1_4 448 453 PF00397 0.495
DOC_WW_Pin1_4 502 507 PF00397 0.655
DOC_WW_Pin1_4 618 623 PF00397 0.605
DOC_WW_Pin1_4 761 766 PF00397 0.670
DOC_WW_Pin1_4 784 789 PF00397 0.480
DOC_WW_Pin1_4 906 911 PF00397 0.684
DOC_WW_Pin1_4 914 919 PF00397 0.605
DOC_WW_Pin1_4 921 926 PF00397 0.555
DOC_WW_Pin1_4 970 975 PF00397 0.668
LIG_14-3-3_CanoR_1 174 181 PF00244 0.456
LIG_14-3-3_CanoR_1 334 339 PF00244 0.624
LIG_14-3-3_CanoR_1 668 676 PF00244 0.337
LIG_14-3-3_CanoR_1 682 690 PF00244 0.390
LIG_14-3-3_CanoR_1 892 901 PF00244 0.592
LIG_Actin_WH2_2 545 563 PF00022 0.481
LIG_APCC_ABBA_1 165 170 PF00400 0.525
LIG_APCC_ABBAyCdc20_2 844 850 PF00400 0.374
LIG_BIR_II_1 1 5 PF00653 0.486
LIG_BIR_III_2 449 453 PF00653 0.512
LIG_BIR_III_4 280 284 PF00653 0.713
LIG_BRCT_BRCA1_1 341 345 PF00533 0.445
LIG_BRCT_BRCA1_1 844 848 PF00533 0.389
LIG_CaM_NSCaTE_8 575 582 PF13499 0.471
LIG_EH1_1 641 649 PF00400 0.411
LIG_EH1_1 659 667 PF00400 0.285
LIG_eIF4E_1 661 667 PF01652 0.377
LIG_FHA_1 695 701 PF00498 0.393
LIG_FHA_1 752 758 PF00498 0.465
LIG_FHA_2 140 146 PF00498 0.396
LIG_FHA_2 234 240 PF00498 0.597
LIG_FHA_2 284 290 PF00498 0.656
LIG_FHA_2 378 384 PF00498 0.794
LIG_FHA_2 499 505 PF00498 0.612
LIG_FHA_2 569 575 PF00498 0.430
LIG_FHA_2 906 912 PF00498 0.681
LIG_FHA_2 922 928 PF00498 0.556
LIG_Integrin_RGD_1 608 610 PF01839 0.584
LIG_LIR_Apic_2 771 777 PF02991 0.457
LIG_LIR_Gen_1 48 57 PF02991 0.367
LIG_LIR_Gen_1 935 945 PF02991 0.579
LIG_LIR_Nem_3 48 53 PF02991 0.380
LIG_LIR_Nem_3 935 940 PF02991 0.621
LIG_LIR_Nem_3 992 998 PF02991 0.437
LIG_LYPXL_S_1 80 84 PF13949 0.376
LIG_LYPXL_yS_3 81 84 PF13949 0.368
LIG_PCNA_APIM_2 129 135 PF02747 0.401
LIG_PCNA_yPIPBox_3 741 753 PF02747 0.494
LIG_Pex14_2 704 708 PF04695 0.374
LIG_REV1ctd_RIR_1 640 650 PF16727 0.360
LIG_RPA_C_Fungi 485 497 PF08784 0.416
LIG_SH2_CRK 535 539 PF00017 0.365
LIG_SH2_CRK 88 92 PF00017 0.375
LIG_SH2_NCK_1 88 92 PF00017 0.421
LIG_SH2_PTP2 810 813 PF00017 0.389
LIG_SH2_STAT5 132 135 PF00017 0.430
LIG_SH2_STAT5 149 152 PF00017 0.375
LIG_SH2_STAT5 168 171 PF00017 0.459
LIG_SH2_STAT5 313 316 PF00017 0.634
LIG_SH2_STAT5 463 466 PF00017 0.388
LIG_SH2_STAT5 661 664 PF00017 0.406
LIG_SH2_STAT5 810 813 PF00017 0.444
LIG_SH2_STAT5 816 819 PF00017 0.400
LIG_SH3_2 115 120 PF14604 0.574
LIG_SH3_3 112 118 PF00018 0.560
LIG_SH3_3 161 167 PF00018 0.416
LIG_SH3_3 203 209 PF00018 0.634
LIG_SH3_3 304 310 PF00018 0.563
LIG_SH3_3 350 356 PF00018 0.527
LIG_SH3_3 364 370 PF00018 0.607
LIG_SH3_3 79 85 PF00018 0.389
LIG_SH3_3 913 919 PF00018 0.724
LIG_SH3_3 968 974 PF00018 0.783
LIG_SH3_5 309 313 PF00018 0.611
LIG_SUMO_SIM_anti_2 198 205 PF11976 0.641
LIG_SUMO_SIM_anti_2 383 388 PF11976 0.563
LIG_SUMO_SIM_par_1 372 380 PF11976 0.572
LIG_TRAF2_1 121 124 PF00917 0.531
LIG_TRAF2_1 257 260 PF00917 0.580
LIG_TRAF2_1 46 49 PF00917 0.417
LIG_TRAF2_2 444 449 PF00917 0.550
LIG_WW_3 117 121 PF00397 0.578
LIG_WW_3 969 973 PF00397 0.634
MOD_CDC14_SPxK_1 909 912 PF00782 0.656
MOD_CDK_SPK_2 111 116 PF00069 0.577
MOD_CDK_SPK_2 784 789 PF00069 0.473
MOD_CDK_SPxK_1 906 912 PF00069 0.660
MOD_CDK_SPxxK_3 761 768 PF00069 0.560
MOD_CDK_SPxxK_3 784 791 PF00069 0.517
MOD_CDK_SPxxK_3 906 913 PF00069 0.662
MOD_CK1_1 285 291 PF00069 0.725
MOD_CK1_1 293 299 PF00069 0.749
MOD_CK1_1 300 306 PF00069 0.736
MOD_CK1_1 42 48 PF00069 0.488
MOD_CK1_1 500 506 PF00069 0.558
MOD_CK1_1 586 592 PF00069 0.518
MOD_CK1_1 917 923 PF00069 0.668
MOD_CK1_1 929 935 PF00069 0.574
MOD_CK1_1 997 1003 PF00069 0.452
MOD_CK2_1 118 124 PF00069 0.556
MOD_CK2_1 197 203 PF00069 0.566
MOD_CK2_1 233 239 PF00069 0.632
MOD_CK2_1 377 383 PF00069 0.738
MOD_CK2_1 392 398 PF00069 0.520
MOD_CK2_1 42 48 PF00069 0.425
MOD_CK2_1 498 504 PF00069 0.614
MOD_CK2_1 568 574 PF00069 0.433
MOD_CK2_1 866 872 PF00069 0.457
MOD_CK2_1 905 911 PF00069 0.681
MOD_Cter_Amidation 873 876 PF01082 0.614
MOD_GlcNHglycan 181 184 PF01048 0.492
MOD_GlcNHglycan 232 236 PF01048 0.666
MOD_GlcNHglycan 289 293 PF01048 0.680
MOD_GlcNHglycan 395 398 PF01048 0.649
MOD_GlcNHglycan 414 417 PF01048 0.652
MOD_GlcNHglycan 435 438 PF01048 0.486
MOD_GlcNHglycan 44 47 PF01048 0.535
MOD_GlcNHglycan 464 467 PF01048 0.379
MOD_GlcNHglycan 535 538 PF01048 0.352
MOD_GlcNHglycan 580 583 PF01048 0.483
MOD_GlcNHglycan 585 588 PF01048 0.563
MOD_GlcNHglycan 594 597 PF01048 0.700
MOD_GlcNHglycan 896 899 PF01048 0.658
MOD_GlcNHglycan 932 935 PF01048 0.653
MOD_GlcNHglycan 937 940 PF01048 0.532
MOD_GlcNHglycan 961 964 PF01048 0.760
MOD_GlcNHglycan 984 988 PF01048 0.570
MOD_GSK3_1 179 186 PF00069 0.504
MOD_GSK3_1 281 288 PF00069 0.670
MOD_GSK3_1 293 300 PF00069 0.768
MOD_GSK3_1 313 320 PF00069 0.695
MOD_GSK3_1 406 413 PF00069 0.561
MOD_GSK3_1 450 457 PF00069 0.447
MOD_GSK3_1 498 505 PF00069 0.655
MOD_GSK3_1 533 540 PF00069 0.439
MOD_GSK3_1 583 590 PF00069 0.576
MOD_GSK3_1 614 621 PF00069 0.644
MOD_GSK3_1 917 924 PF00069 0.657
MOD_GSK3_1 926 933 PF00069 0.589
MOD_GSK3_1 959 966 PF00069 0.683
MOD_GSK3_1 979 986 PF00069 0.732
MOD_N-GLC_1 296 301 PF02516 0.694
MOD_N-GLC_2 56 58 PF02516 0.348
MOD_NEK2_1 202 207 PF00069 0.601
MOD_NEK2_1 233 238 PF00069 0.605
MOD_NEK2_1 406 411 PF00069 0.643
MOD_NEK2_1 433 438 PF00069 0.492
MOD_NEK2_1 583 588 PF00069 0.612
MOD_NEK2_1 737 742 PF00069 0.537
MOD_NEK2_1 848 853 PF00069 0.471
MOD_NEK2_1 905 910 PF00069 0.581
MOD_NEK2_1 926 931 PF00069 0.566
MOD_NEK2_1 994 999 PF00069 0.427
MOD_NEK2_2 2 7 PF00069 0.520
MOD_NEK2_2 677 682 PF00069 0.491
MOD_PIKK_1 313 319 PF00454 0.605
MOD_PIKK_1 377 383 PF00454 0.669
MOD_PIKK_1 848 854 PF00454 0.446
MOD_PK_1 912 918 PF00069 0.670
MOD_PKA_1 888 894 PF00069 0.624
MOD_PKA_1 912 918 PF00069 0.670
MOD_PKA_2 119 125 PF00069 0.552
MOD_PKA_2 221 227 PF00069 0.579
MOD_PKA_2 300 306 PF00069 0.752
MOD_PKA_2 339 345 PF00069 0.453
MOD_PKA_2 667 673 PF00069 0.339
MOD_PKA_2 888 894 PF00069 0.669
MOD_PKA_2 912 918 PF00069 0.670
MOD_PKB_1 886 894 PF00069 0.642
MOD_Plk_1 197 203 PF00069 0.563
MOD_Plk_1 357 363 PF00069 0.729
MOD_Plk_1 694 700 PF00069 0.396
MOD_Plk_2-3 417 423 PF00069 0.605
MOD_Plk_4 197 203 PF00069 0.631
MOD_Plk_4 290 296 PF00069 0.778
MOD_Plk_4 334 340 PF00069 0.417
MOD_Plk_4 866 872 PF00069 0.478
MOD_Plk_4 997 1003 PF00069 0.467
MOD_ProDKin_1 111 117 PF00069 0.583
MOD_ProDKin_1 269 275 PF00069 0.706
MOD_ProDKin_1 366 372 PF00069 0.602
MOD_ProDKin_1 426 432 PF00069 0.648
MOD_ProDKin_1 448 454 PF00069 0.483
MOD_ProDKin_1 502 508 PF00069 0.654
MOD_ProDKin_1 618 624 PF00069 0.604
MOD_ProDKin_1 761 767 PF00069 0.660
MOD_ProDKin_1 784 790 PF00069 0.488
MOD_ProDKin_1 906 912 PF00069 0.685
MOD_ProDKin_1 914 920 PF00069 0.606
MOD_ProDKin_1 921 927 PF00069 0.554
MOD_ProDKin_1 970 976 PF00069 0.668
TRG_DiLeu_BaLyEn_6 208 213 PF01217 0.676
TRG_DiLeu_BaLyEn_6 643 648 PF01217 0.537
TRG_DiLeu_BaLyEn_6 661 666 PF01217 0.270
TRG_DiLeu_BaLyEn_6 862 867 PF01217 0.478
TRG_DiLeu_BaLyEn_6 95 100 PF01217 0.456
TRG_DiLeu_BaLyEn_6 975 980 PF01217 0.627
TRG_DiLeu_LyEn_5 428 433 PF01217 0.479
TRG_ENDOCYTIC_2 535 538 PF00928 0.352
TRG_ENDOCYTIC_2 81 84 PF00928 0.387
TRG_ENDOCYTIC_2 88 91 PF00928 0.385
TRG_ER_diArg_1 125 127 PF00400 0.520
TRG_ER_diArg_1 129 131 PF00400 0.470
TRG_ER_diArg_1 319 322 PF00400 0.571
TRG_ER_diArg_1 489 491 PF00400 0.548
TRG_ER_diArg_1 525 527 PF00400 0.394
TRG_ER_diArg_1 538 541 PF00400 0.434
TRG_ER_diArg_1 558 561 PF00400 0.521
TRG_ER_diArg_1 788 791 PF00400 0.514
TRG_ER_diArg_1 821 823 PF00400 0.408
TRG_ER_diArg_1 863 866 PF00400 0.443
TRG_ER_diArg_1 875 877 PF00400 0.647
TRG_ER_diArg_1 885 888 PF00400 0.707
TRG_Pf-PMV_PEXEL_1 7 12 PF00026 0.468
TRG_Pf-PMV_PEXEL_1 729 733 PF00026 0.392
TRG_Pf-PMV_PEXEL_1 98 102 PF00026 0.480
TRG_Pf-PMV_PEXEL_1 988 992 PF00026 0.672

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I1B1 Leptomonas seymouri 54% 100%
A0A3Q8IE47 Leishmania donovani 100% 100%
A4HGV7 Leishmania braziliensis 76% 100%
E9B077 Leishmania mexicana (strain MHOM/GT/2001/U1103) 90% 100%
Q4Q808 Leishmania major 91% 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