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 donovani
UniProt:
A0A3Q8IJT0_LEIDO
TriTrypDb:
LdBPK_181340.1 , LdCL_180018700 , LDHU3_18.1710
Length:
961

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. yes yes: 9
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 11
NetGPI no yes: 0, no: 11
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

A0A3Q8IJT0
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3Q8IJT0

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 288 292 PF00656 0.588
CLV_C14_Caspase3-7 310 314 PF00656 0.617
CLV_NRD_NRD_1 105 107 PF00675 0.647
CLV_NRD_NRD_1 208 210 PF00675 0.510
CLV_NRD_NRD_1 241 243 PF00675 0.685
CLV_NRD_NRD_1 430 432 PF00675 0.527
CLV_NRD_NRD_1 650 652 PF00675 0.636
CLV_NRD_NRD_1 675 677 PF00675 0.596
CLV_NRD_NRD_1 772 774 PF00675 0.594
CLV_NRD_NRD_1 788 790 PF00675 0.424
CLV_NRD_NRD_1 802 804 PF00675 0.524
CLV_NRD_NRD_1 824 826 PF00675 0.633
CLV_NRD_NRD_1 899 901 PF00675 0.742
CLV_PCSK_FUR_1 293 297 PF00082 0.636
CLV_PCSK_KEX2_1 105 107 PF00082 0.663
CLV_PCSK_KEX2_1 208 210 PF00082 0.511
CLV_PCSK_KEX2_1 241 243 PF00082 0.685
CLV_PCSK_KEX2_1 295 297 PF00082 0.638
CLV_PCSK_KEX2_1 650 652 PF00082 0.530
CLV_PCSK_KEX2_1 675 677 PF00082 0.596
CLV_PCSK_KEX2_1 772 774 PF00082 0.569
CLV_PCSK_KEX2_1 788 790 PF00082 0.446
CLV_PCSK_KEX2_1 802 804 PF00082 0.524
CLV_PCSK_KEX2_1 824 826 PF00082 0.608
CLV_PCSK_KEX2_1 899 901 PF00082 0.742
CLV_PCSK_PC1ET2_1 295 297 PF00082 0.638
CLV_PCSK_SKI1_1 105 109 PF00082 0.583
CLV_PCSK_SKI1_1 193 197 PF00082 0.533
CLV_PCSK_SKI1_1 257 261 PF00082 0.586
CLV_PCSK_SKI1_1 5 9 PF00082 0.681
CLV_PCSK_SKI1_1 601 605 PF00082 0.699
CLV_PCSK_SKI1_1 676 680 PF00082 0.566
CLV_PCSK_SKI1_1 751 755 PF00082 0.623
CLV_PCSK_SKI1_1 789 793 PF00082 0.617
CLV_PCSK_SKI1_1 900 904 PF00082 0.654
CLV_Separin_Metazoa 799 803 PF03568 0.575
DEG_APCC_DBOX_1 546 554 PF00400 0.618
DEG_APCC_KENBOX_2 850 854 PF00400 0.759
DEG_SPOP_SBC_1 884 888 PF00917 0.795
DOC_CDC14_PxL_1 774 782 PF14671 0.498
DOC_MAPK_DCC_7 231 240 PF00069 0.637
DOC_MAPK_gen_1 187 196 PF00069 0.603
DOC_MAPK_HePTP_8 228 240 PF00069 0.670
DOC_MAPK_MEF2A_6 231 240 PF00069 0.671
DOC_MIT_MIM_1 204 213 PF04212 0.630
DOC_MIT_MIM_1 768 777 PF04212 0.544
DOC_PP2B_LxvP_1 76 79 PF13499 0.674
DOC_PP4_FxxP_1 8 11 PF00568 0.741
DOC_USP7_MATH_1 146 150 PF00917 0.614
DOC_USP7_MATH_1 15 19 PF00917 0.731
DOC_USP7_MATH_1 24 28 PF00917 0.671
DOC_USP7_MATH_1 266 270 PF00917 0.598
DOC_USP7_MATH_1 279 283 PF00917 0.618
DOC_USP7_MATH_1 325 329 PF00917 0.575
DOC_USP7_MATH_1 407 411 PF00917 0.530
DOC_USP7_MATH_1 587 591 PF00917 0.682
DOC_USP7_MATH_1 884 888 PF00917 0.740
DOC_USP7_MATH_1 94 98 PF00917 0.690
DOC_USP7_MATH_1 951 955 PF00917 0.706
DOC_USP7_UBL2_3 685 689 PF12436 0.567
DOC_WW_Pin1_4 19 24 PF00397 0.662
DOC_WW_Pin1_4 39 44 PF00397 0.700
DOC_WW_Pin1_4 907 912 PF00397 0.788
DOC_WW_Pin1_4 919 924 PF00397 0.700
DOC_WW_Pin1_4 952 957 PF00397 0.699
LIG_14-3-3_CanoR_1 153 159 PF00244 0.537
LIG_14-3-3_CanoR_1 257 263 PF00244 0.508
LIG_14-3-3_CanoR_1 26 30 PF00244 0.734
LIG_14-3-3_CanoR_1 280 284 PF00244 0.560
LIG_14-3-3_CanoR_1 354 362 PF00244 0.726
LIG_14-3-3_CanoR_1 420 428 PF00244 0.544
LIG_14-3-3_CanoR_1 675 681 PF00244 0.591
LIG_14-3-3_CanoR_1 717 725 PF00244 0.610
LIG_14-3-3_CanoR_1 868 877 PF00244 0.794
LIG_14-3-3_CanoR_1 899 909 PF00244 0.722
LIG_14-3-3_CanoR_1 950 956 PF00244 0.759
LIG_Actin_WH2_2 767 783 PF00022 0.506
LIG_BIR_III_2 14 18 PF00653 0.751
LIG_BRCT_BRCA1_1 953 957 PF00533 0.722
LIG_BRCT_BRCA1_1 99 103 PF00533 0.643
LIG_EVH1_1 76 80 PF00568 0.561
LIG_FAT_LD_1 255 263 PF03623 0.621
LIG_FHA_1 117 123 PF00498 0.648
LIG_FHA_1 235 241 PF00498 0.550
LIG_FHA_1 375 381 PF00498 0.549
LIG_FHA_1 400 406 PF00498 0.573
LIG_FHA_1 431 437 PF00498 0.595
LIG_FHA_1 79 85 PF00498 0.779
LIG_FHA_1 796 802 PF00498 0.509
LIG_FHA_2 154 160 PF00498 0.511
LIG_FHA_2 162 168 PF00498 0.480
LIG_FHA_2 258 264 PF00498 0.564
LIG_FHA_2 286 292 PF00498 0.478
LIG_FHA_2 373 379 PF00498 0.640
LIG_FHA_2 421 427 PF00498 0.611
LIG_FHA_2 454 460 PF00498 0.503
LIG_FHA_2 475 481 PF00498 0.557
LIG_FHA_2 533 539 PF00498 0.636
LIG_FHA_2 590 596 PF00498 0.522
LIG_GBD_Chelix_1 254 262 PF00786 0.591
LIG_HCF-1_HBM_1 365 368 PF13415 0.680
LIG_LIR_Apic_2 6 11 PF02991 0.738
LIG_LIR_Apic_2 65 70 PF02991 0.698
LIG_LIR_Gen_1 332 340 PF02991 0.485
LIG_LIR_Gen_1 674 682 PF02991 0.590
LIG_LIR_Gen_1 734 742 PF02991 0.484
LIG_LIR_Gen_1 826 836 PF02991 0.623
LIG_LIR_Gen_1 854 865 PF02991 0.747
LIG_LIR_Nem_3 305 311 PF02991 0.580
LIG_LIR_Nem_3 332 337 PF02991 0.467
LIG_LIR_Nem_3 525 531 PF02991 0.393
LIG_LIR_Nem_3 674 680 PF02991 0.594
LIG_LIR_Nem_3 734 739 PF02991 0.482
LIG_LIR_Nem_3 826 832 PF02991 0.574
LIG_LIR_Nem_3 854 860 PF02991 0.743
LIG_REV1ctd_RIR_1 274 284 PF16727 0.592
LIG_RPA_C_Fungi 275 287 PF08784 0.506
LIG_SH2_CRK 147 151 PF00017 0.600
LIG_SH2_CRK 677 681 PF00017 0.598
LIG_SH2_CRK 736 740 PF00017 0.567
LIG_SH2_SRC 67 70 PF00017 0.763
LIG_SH2_STAP1 154 158 PF00017 0.553
LIG_SH2_STAP1 482 486 PF00017 0.487
LIG_SH2_STAT3 531 534 PF00017 0.420
LIG_SH2_STAT5 147 150 PF00017 0.599
LIG_SH2_STAT5 368 371 PF00017 0.610
LIG_SH2_STAT5 95 98 PF00017 0.677
LIG_SH3_3 74 80 PF00018 0.626
LIG_SH3_3 887 893 PF00018 0.780
LIG_SH3_3 953 959 PF00018 0.643
LIG_SH3_CIN85_PxpxPR_1 894 899 PF14604 0.721
LIG_Sin3_3 464 471 PF02671 0.557
LIG_SUMO_SIM_par_1 321 329 PF11976 0.530
LIG_TRAF2_1 170 173 PF00917 0.646
LIG_TRAF2_1 268 271 PF00917 0.560
LIG_TRAF2_1 362 365 PF00917 0.694
LIG_TRAF2_1 671 674 PF00917 0.571
LIG_TRAF2_1 794 797 PF00917 0.521
LIG_TRAF2_2 11 16 PF00917 0.684
LIG_UBA3_1 323 331 PF00899 0.444
LIG_WRPW_1 957 961 PF00400 0.713
LIG_WRPW_2 957 960 PF00400 0.708
MOD_CDC14_SPxK_1 42 45 PF00782 0.732
MOD_CDC14_SPxK_1 955 958 PF00782 0.708
MOD_CDK_SPxK_1 39 45 PF00069 0.740
MOD_CDK_SPxK_1 952 958 PF00069 0.719
MOD_CDK_SPxxK_3 19 26 PF00069 0.691
MOD_CK1_1 163 169 PF00069 0.582
MOD_CK1_1 261 267 PF00069 0.601
MOD_CK1_1 269 275 PF00069 0.582
MOD_CK1_1 282 288 PF00069 0.380
MOD_CK1_1 33 39 PF00069 0.665
MOD_CK1_1 430 436 PF00069 0.607
MOD_CK1_1 582 588 PF00069 0.727
MOD_CK1_1 910 916 PF00069 0.758
MOD_CK1_1 931 937 PF00069 0.757
MOD_CK1_1 952 958 PF00069 0.727
MOD_CK1_1 97 103 PF00069 0.593
MOD_CK2_1 153 159 PF00069 0.494
MOD_CK2_1 167 173 PF00069 0.458
MOD_CK2_1 257 263 PF00069 0.570
MOD_CK2_1 265 271 PF00069 0.611
MOD_CK2_1 372 378 PF00069 0.642
MOD_CK2_1 420 426 PF00069 0.578
MOD_CK2_1 445 451 PF00069 0.508
MOD_CK2_1 453 459 PF00069 0.533
MOD_CK2_1 532 538 PF00069 0.544
MOD_CK2_1 589 595 PF00069 0.617
MOD_CK2_1 668 674 PF00069 0.561
MOD_CK2_1 846 852 PF00069 0.729
MOD_GlcNHglycan 284 287 PF01048 0.489
MOD_GlcNHglycan 32 35 PF01048 0.678
MOD_GlcNHglycan 433 436 PF01048 0.600
MOD_GlcNHglycan 589 592 PF01048 0.708
MOD_GlcNHglycan 637 640 PF01048 0.679
MOD_GlcNHglycan 835 839 PF01048 0.633
MOD_GlcNHglycan 848 851 PF01048 0.599
MOD_GlcNHglycan 852 856 PF01048 0.541
MOD_GlcNHglycan 874 877 PF01048 0.702
MOD_GlcNHglycan 887 890 PF01048 0.802
MOD_GlcNHglycan 905 908 PF01048 0.734
MOD_GlcNHglycan 930 933 PF01048 0.720
MOD_GlcNHglycan 951 954 PF01048 0.686
MOD_GSK3_1 148 155 PF00069 0.553
MOD_GSK3_1 15 22 PF00069 0.741
MOD_GSK3_1 159 166 PF00069 0.510
MOD_GSK3_1 257 264 PF00069 0.549
MOD_GSK3_1 265 272 PF00069 0.534
MOD_GSK3_1 278 285 PF00069 0.393
MOD_GSK3_1 35 42 PF00069 0.779
MOD_GSK3_1 353 360 PF00069 0.672
MOD_GSK3_1 426 433 PF00069 0.623
MOD_GSK3_1 635 642 PF00069 0.692
MOD_GSK3_1 78 85 PF00069 0.734
MOD_GSK3_1 863 870 PF00069 0.669
MOD_GSK3_1 903 910 PF00069 0.794
MOD_GSK3_1 919 926 PF00069 0.776
MOD_N-GLC_1 407 412 PF02516 0.399
MOD_N-GLC_1 928 933 PF02516 0.774
MOD_NEK2_1 126 131 PF00069 0.509
MOD_NEK2_1 133 138 PF00069 0.533
MOD_NEK2_1 213 218 PF00069 0.623
MOD_NEK2_1 247 252 PF00069 0.595
MOD_NEK2_1 353 358 PF00069 0.696
MOD_NEK2_1 386 391 PF00069 0.589
MOD_NEK2_1 453 458 PF00069 0.572
MOD_NEK2_1 471 476 PF00069 0.542
MOD_NEK2_1 507 512 PF00069 0.537
MOD_NEK2_1 55 60 PF00069 0.752
MOD_NEK2_1 84 89 PF00069 0.761
MOD_NEK2_1 860 865 PF00069 0.745
MOD_PIKK_1 269 275 PF00454 0.669
MOD_PIKK_1 33 39 PF00454 0.774
MOD_PIKK_1 353 359 PF00454 0.700
MOD_PIKK_1 386 392 PF00454 0.531
MOD_PIKK_1 420 426 PF00454 0.591
MOD_PIKK_1 445 451 PF00454 0.546
MOD_PIKK_1 471 477 PF00454 0.595
MOD_PIKK_1 55 61 PF00454 0.708
MOD_PIKK_1 669 675 PF00454 0.455
MOD_PIKK_1 716 722 PF00454 0.617
MOD_PIKK_1 78 84 PF00454 0.718
MOD_PIKK_1 900 906 PF00454 0.786
MOD_PKA_1 431 437 PF00069 0.581
MOD_PKA_2 116 122 PF00069 0.541
MOD_PKA_2 152 158 PF00069 0.572
MOD_PKA_2 25 31 PF00069 0.812
MOD_PKA_2 279 285 PF00069 0.583
MOD_PKA_2 316 322 PF00069 0.626
MOD_PKA_2 353 359 PF00069 0.725
MOD_PKA_2 430 436 PF00069 0.540
MOD_PKA_2 579 585 PF00069 0.699
MOD_PKA_2 587 593 PF00069 0.734
MOD_PKA_2 716 722 PF00069 0.539
MOD_PKA_2 860 866 PF00069 0.745
MOD_PKA_2 867 873 PF00069 0.760
MOD_PKA_2 949 955 PF00069 0.769
MOD_Plk_1 229 235 PF00069 0.574
MOD_Plk_1 24 30 PF00069 0.774
MOD_Plk_1 601 607 PF00069 0.641
MOD_Plk_1 97 103 PF00069 0.654
MOD_Plk_2-3 167 173 PF00069 0.572
MOD_Plk_2-3 589 595 PF00069 0.520
MOD_Plk_4 15 21 PF00069 0.728
MOD_Plk_4 279 285 PF00069 0.505
MOD_Plk_4 335 341 PF00069 0.594
MOD_Plk_4 388 394 PF00069 0.595
MOD_ProDKin_1 19 25 PF00069 0.665
MOD_ProDKin_1 39 45 PF00069 0.699
MOD_ProDKin_1 907 913 PF00069 0.787
MOD_ProDKin_1 919 925 PF00069 0.701
MOD_ProDKin_1 952 958 PF00069 0.698
MOD_SUMO_for_1 122 125 PF00179 0.622
MOD_SUMO_for_1 794 797 PF00179 0.580
MOD_SUMO_rev_2 163 171 PF00179 0.587
MOD_SUMO_rev_2 214 224 PF00179 0.636
MOD_SUMO_rev_2 328 333 PF00179 0.530
MOD_SUMO_rev_2 349 353 PF00179 0.677
MOD_SUMO_rev_2 465 474 PF00179 0.594
MOD_SUMO_rev_2 696 701 PF00179 0.539
MOD_SUMO_rev_2 748 753 PF00179 0.564
MOD_SUMO_rev_2 813 821 PF00179 0.540
TRG_DiLeu_BaEn_1 400 405 PF01217 0.595
TRG_DiLeu_BaEn_1 734 739 PF01217 0.544
TRG_DiLeu_BaEn_1 796 801 PF01217 0.613
TRG_DiLeu_BaEn_2 317 323 PF01217 0.601
TRG_DiLeu_BaEn_4 559 565 PF01217 0.641
TRG_DiLeu_BaEn_4 608 614 PF01217 0.665
TRG_DiLeu_BaEn_4 696 702 PF01217 0.512
TRG_DiLeu_BaEn_4 748 754 PF01217 0.589
TRG_DiLeu_BaEn_4 796 802 PF01217 0.528
TRG_DiLeu_BaLyEn_6 103 108 PF01217 0.649
TRG_DiLeu_BaLyEn_6 254 259 PF01217 0.619
TRG_ENDOCYTIC_2 147 150 PF00928 0.599
TRG_ENDOCYTIC_2 617 620 PF00928 0.472
TRG_ENDOCYTIC_2 677 680 PF00928 0.601
TRG_ENDOCYTIC_2 736 739 PF00928 0.462
TRG_ENDOCYTIC_2 857 860 PF00928 0.745
TRG_ER_diArg_1 105 107 PF00400 0.647
TRG_ER_diArg_1 208 210 PF00400 0.515
TRG_ER_diArg_1 240 242 PF00400 0.595
TRG_ER_diArg_1 675 677 PF00400 0.428
TRG_ER_diArg_1 701 704 PF00400 0.484
TRG_ER_diArg_1 772 775 PF00400 0.616
TRG_ER_diArg_1 801 803 PF00400 0.610
TRG_ER_diArg_1 898 900 PF00400 0.722
TRG_Pf-PMV_PEXEL_1 105 109 PF00026 0.557
TRG_Pf-PMV_PEXEL_1 169 173 PF00026 0.490
TRG_Pf-PMV_PEXEL_1 208 212 PF00026 0.526
TRG_Pf-PMV_PEXEL_1 413 417 PF00026 0.505
TRG_Pf-PMV_PEXEL_1 487 492 PF00026 0.514
TRG_Pf-PMV_PEXEL_1 691 695 PF00026 0.620
TRG_Pf-PMV_PEXEL_1 772 776 PF00026 0.581

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1IKJ3 Leptomonas seymouri 62% 98%
A0A0S4JNT6 Bodo saltans 30% 100%
A0A1X0P823 Trypanosomatidae 37% 100%
A0A422NIX4 Trypanosoma rangeli 35% 100%
A4H9N9 Leishmania braziliensis 81% 100%
A4HY07 Leishmania infantum 100% 100%
D0A592 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 32% 100%
E9ARS0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 93% 100%
Q4QDQ3 Leishmania major 93% 100%
V5BJ58 Trypanosoma cruzi 34% 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