LeishMANIAdb
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LisH domain-containing protein

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

Quick info

Protein:
LisH domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania major
UniProt:
Q4Q0N4_LEIMA
TriTrypDb:
LmjF.36.5280 , LMJLV39_360065000 * , LMJSD75_360064700
Length:
1051

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: 9
NetGPI no yes: 0, no: 9
Cellular components
Term Name Level Count
GO:0005768 endosome 7 2
GO:0005802 trans-Golgi network 4 9
GO:0031410 cytoplasmic vesicle 6 2
GO:0031982 vesicle 4 2
GO:0031984 organelle subcompartment 2 9
GO:0043226 organelle 2 2
GO:0043227 membrane-bounded organelle 3 2
GO:0043229 intracellular organelle 3 2
GO:0043231 intracellular membrane-bounded organelle 4 2
GO:0055037 recycling endosome 8 2
GO:0097708 intracellular vesicle 5 2
GO:0098791 Golgi apparatus subcompartment 3 9
GO:0110165 cellular anatomical entity 1 9

Expansion

Sequence features

Q4Q0N4
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q0N4

Function

Biological processes
Term Name Level Count
GO:0006810 transport 3 9
GO:0006869 lipid transport 5 9
GO:0009987 cellular process 1 9
GO:0015850 organic hydroxy compound transport 5 9
GO:0015918 sterol transport 6 9
GO:0030301 cholesterol transport 7 9
GO:0032365 intracellular lipid transport 4 9
GO:0032366 intracellular sterol transport 5 9
GO:0032367 intracellular cholesterol transport 6 9
GO:0046907 intracellular transport 3 9
GO:0051179 localization 1 9
GO:0051234 establishment of localization 2 9
GO:0051641 cellular localization 2 9
GO:0051649 establishment of localization in cell 3 9
GO:0071702 organic substance transport 4 9
Could not find GO molecular_function term for this entry.

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 560 564 PF00656 0.661
CLV_C14_Caspase3-7 675 679 PF00656 0.558
CLV_C14_Caspase3-7 680 684 PF00656 0.554
CLV_NRD_NRD_1 1049 1051 PF00675 0.623
CLV_NRD_NRD_1 133 135 PF00675 0.641
CLV_NRD_NRD_1 149 151 PF00675 0.539
CLV_NRD_NRD_1 177 179 PF00675 0.471
CLV_NRD_NRD_1 256 258 PF00675 0.444
CLV_NRD_NRD_1 27 29 PF00675 0.718
CLV_NRD_NRD_1 272 274 PF00675 0.384
CLV_NRD_NRD_1 298 300 PF00675 0.513
CLV_NRD_NRD_1 435 437 PF00675 0.539
CLV_PCSK_KEX2_1 1048 1050 PF00082 0.568
CLV_PCSK_KEX2_1 13 15 PF00082 0.694
CLV_PCSK_KEX2_1 133 135 PF00082 0.645
CLV_PCSK_KEX2_1 211 213 PF00082 0.551
CLV_PCSK_KEX2_1 256 258 PF00082 0.444
CLV_PCSK_KEX2_1 27 29 PF00082 0.679
CLV_PCSK_KEX2_1 272 274 PF00082 0.499
CLV_PCSK_KEX2_1 298 300 PF00082 0.513
CLV_PCSK_KEX2_1 434 436 PF00082 0.587
CLV_PCSK_PC1ET2_1 1048 1050 PF00082 0.531
CLV_PCSK_PC1ET2_1 13 15 PF00082 0.655
CLV_PCSK_PC1ET2_1 211 213 PF00082 0.570
CLV_PCSK_SKI1_1 179 183 PF00082 0.404
CLV_PCSK_SKI1_1 256 260 PF00082 0.371
CLV_PCSK_SKI1_1 654 658 PF00082 0.567
CLV_PCSK_SKI1_1 803 807 PF00082 0.553
CLV_PCSK_SKI1_1 848 852 PF00082 0.600
CLV_PCSK_SKI1_1 865 869 PF00082 0.365
CLV_PCSK_SKI1_1 883 887 PF00082 0.539
CLV_PCSK_SKI1_1 977 981 PF00082 0.480
CLV_Separin_Metazoa 300 304 PF03568 0.508
DEG_APCC_DBOX_1 651 659 PF00400 0.584
DEG_APCC_DBOX_1 780 788 PF00400 0.504
DEG_APCC_DBOX_1 864 872 PF00400 0.442
DEG_APCC_DBOX_1 976 984 PF00400 0.530
DEG_Nend_UBRbox_2 1 3 PF02207 0.753
DEG_SPOP_SBC_1 346 350 PF00917 0.721
DEG_SPOP_SBC_1 39 43 PF00917 0.721
DEG_SPOP_SBC_1 699 703 PF00917 0.557
DOC_CKS1_1 917 922 PF01111 0.521
DOC_CKS1_1 969 974 PF01111 0.455
DOC_CYCLIN_RxL_1 253 262 PF00134 0.484
DOC_CYCLIN_RxL_1 298 311 PF00134 0.521
DOC_CYCLIN_RxL_1 651 660 PF00134 0.529
DOC_CYCLIN_yCln2_LP_2 568 574 PF00134 0.582
DOC_CYCLIN_yCln2_LP_2 807 813 PF00134 0.509
DOC_MAPK_DCC_7 178 188 PF00069 0.312
DOC_MAPK_DCC_7 748 758 PF00069 0.540
DOC_MAPK_gen_1 178 185 PF00069 0.472
DOC_MAPK_gen_1 781 789 PF00069 0.426
DOC_MAPK_gen_1 801 808 PF00069 0.229
DOC_MAPK_gen_1 845 853 PF00069 0.584
DOC_MAPK_MEF2A_6 178 185 PF00069 0.418
DOC_MAPK_MEF2A_6 801 808 PF00069 0.559
DOC_MAPK_MEF2A_6 845 853 PF00069 0.542
DOC_MAPK_NFAT4_5 178 186 PF00069 0.509
DOC_MAPK_RevD_3 421 436 PF00069 0.490
DOC_PP1_RVXF_1 652 658 PF00149 0.466
DOC_PP1_RVXF_1 720 727 PF00149 0.567
DOC_USP7_MATH_1 121 125 PF00917 0.679
DOC_USP7_MATH_1 138 142 PF00917 0.388
DOC_USP7_MATH_1 169 173 PF00917 0.358
DOC_USP7_MATH_1 351 355 PF00917 0.751
DOC_USP7_MATH_1 359 363 PF00917 0.700
DOC_USP7_MATH_1 382 386 PF00917 0.541
DOC_USP7_MATH_1 39 43 PF00917 0.665
DOC_USP7_MATH_1 437 441 PF00917 0.558
DOC_USP7_MATH_1 463 467 PF00917 0.592
DOC_USP7_MATH_1 521 525 PF00917 0.609
DOC_USP7_MATH_1 559 563 PF00917 0.708
DOC_USP7_MATH_1 601 605 PF00917 0.697
DOC_USP7_MATH_1 699 703 PF00917 0.633
DOC_USP7_MATH_1 705 709 PF00917 0.616
DOC_USP7_MATH_1 757 761 PF00917 0.567
DOC_USP7_MATH_1 918 922 PF00917 0.703
DOC_USP7_UBL2_3 1044 1048 PF12436 0.622
DOC_WW_Pin1_4 229 234 PF00397 0.418
DOC_WW_Pin1_4 271 276 PF00397 0.493
DOC_WW_Pin1_4 361 366 PF00397 0.608
DOC_WW_Pin1_4 48 53 PF00397 0.764
DOC_WW_Pin1_4 497 502 PF00397 0.590
DOC_WW_Pin1_4 555 560 PF00397 0.809
DOC_WW_Pin1_4 636 641 PF00397 0.801
DOC_WW_Pin1_4 68 73 PF00397 0.622
DOC_WW_Pin1_4 709 714 PF00397 0.662
DOC_WW_Pin1_4 751 756 PF00397 0.621
DOC_WW_Pin1_4 774 779 PF00397 0.535
DOC_WW_Pin1_4 916 921 PF00397 0.673
DOC_WW_Pin1_4 968 973 PF00397 0.477
DOC_WW_Pin1_4 993 998 PF00397 0.618
LIG_14-3-3_CanoR_1 218 222 PF00244 0.315
LIG_14-3-3_CanoR_1 278 282 PF00244 0.507
LIG_14-3-3_CanoR_1 303 308 PF00244 0.446
LIG_14-3-3_CanoR_1 332 336 PF00244 0.758
LIG_14-3-3_CanoR_1 690 700 PF00244 0.722
LIG_14-3-3_CanoR_1 781 789 PF00244 0.501
LIG_14-3-3_CanoR_1 905 911 PF00244 0.665
LIG_Actin_WH2_2 174 189 PF00022 0.520
LIG_Actin_WH2_2 394 410 PF00022 0.531
LIG_Actin_WH2_2 475 493 PF00022 0.446
LIG_BIR_III_4 855 859 PF00653 0.559
LIG_BRCT_BRCA1_1 719 723 PF00533 0.594
LIG_Clathr_ClatBox_1 258 262 PF01394 0.473
LIG_deltaCOP1_diTrp_1 23 30 PF00928 0.693
LIG_EH1_1 372 380 PF00400 0.525
LIG_eIF4E_1 888 894 PF01652 0.471
LIG_FHA_1 341 347 PF00498 0.730
LIG_FHA_1 361 367 PF00498 0.612
LIG_FHA_1 412 418 PF00498 0.417
LIG_FHA_1 427 433 PF00498 0.477
LIG_FHA_1 692 698 PF00498 0.659
LIG_FHA_1 783 789 PF00498 0.494
LIG_FHA_1 791 797 PF00498 0.534
LIG_FHA_1 862 868 PF00498 0.545
LIG_FHA_1 951 957 PF00498 0.470
LIG_FHA_1 969 975 PF00498 0.370
LIG_FHA_2 101 107 PF00498 0.656
LIG_FHA_2 1036 1042 PF00498 0.720
LIG_FHA_2 351 357 PF00498 0.797
LIG_FHA_2 420 426 PF00498 0.575
LIG_FHA_2 45 51 PF00498 0.735
LIG_FHA_2 550 556 PF00498 0.697
LIG_FHA_2 644 650 PF00498 0.749
LIG_FHA_2 684 690 PF00498 0.815
LIG_FHA_2 71 77 PF00498 0.753
LIG_GBD_Chelix_1 159 167 PF00786 0.411
LIG_GBD_Chelix_1 533 541 PF00786 0.598
LIG_LIR_Apic_2 208 213 PF02991 0.448
LIG_LIR_Gen_1 1001 1010 PF02991 0.484
LIG_LIR_Gen_1 224 233 PF02991 0.501
LIG_LIR_Gen_1 244 254 PF02991 0.233
LIG_LIR_Gen_1 372 382 PF02991 0.478
LIG_LIR_Gen_1 524 534 PF02991 0.494
LIG_LIR_Gen_1 660 670 PF02991 0.605
LIG_LIR_Nem_3 1001 1006 PF02991 0.478
LIG_LIR_Nem_3 224 228 PF02991 0.483
LIG_LIR_Nem_3 244 249 PF02991 0.222
LIG_LIR_Nem_3 372 377 PF02991 0.482
LIG_LIR_Nem_3 400 406 PF02991 0.463
LIG_LIR_Nem_3 414 419 PF02991 0.331
LIG_LIR_Nem_3 524 529 PF02991 0.510
LIG_LIR_Nem_3 660 665 PF02991 0.582
LIG_LIR_Nem_3 809 815 PF02991 0.382
LIG_LIR_Nem_3 90 95 PF02991 0.669
LIG_LIR_Nem_3 973 979 PF02991 0.540
LIG_LYPXL_S_1 402 406 PF13949 0.506
LIG_LYPXL_S_1 887 891 PF13949 0.429
LIG_LYPXL_yS_3 888 891 PF13949 0.429
LIG_MYND_1 630 634 PF01753 0.734
LIG_NRBOX 481 487 PF00104 0.507
LIG_NRBOX 537 543 PF00104 0.606
LIG_PCNA_yPIPBox_3 388 402 PF02747 0.543
LIG_Pex14_2 657 661 PF04695 0.515
LIG_SH2_CRK 210 214 PF00017 0.480
LIG_SH2_CRK 246 250 PF00017 0.483
LIG_SH2_CRK 535 539 PF00017 0.505
LIG_SH2_CRK 976 980 PF00017 0.460
LIG_SH2_NCK_1 246 250 PF00017 0.452
LIG_SH2_SRC 526 529 PF00017 0.389
LIG_SH2_STAP1 526 530 PF00017 0.512
LIG_SH2_STAT5 246 249 PF00017 0.558
LIG_SH2_STAT5 597 600 PF00017 0.695
LIG_SH2_STAT5 978 981 PF00017 0.373
LIG_SH3_3 362 368 PF00018 0.431
LIG_SH3_3 398 404 PF00018 0.457
LIG_SH3_3 495 501 PF00018 0.569
LIG_SH3_3 526 532 PF00018 0.503
LIG_SH3_3 624 630 PF00018 0.811
LIG_SH3_3 631 637 PF00018 0.801
LIG_SH3_3 667 673 PF00018 0.716
LIG_SH3_3 772 778 PF00018 0.549
LIG_SH3_3 807 813 PF00018 0.509
LIG_SH3_3 876 882 PF00018 0.497
LIG_SH3_3 914 920 PF00018 0.520
LIG_SH3_3 966 972 PF00018 0.474
LIG_SUMO_SIM_par_1 257 262 PF11976 0.376
LIG_SUMO_SIM_par_1 417 422 PF11976 0.454
LIG_SUMO_SIM_par_1 828 834 PF11976 0.570
LIG_SUMO_SIM_par_1 98 106 PF11976 0.676
LIG_TRAF2_1 137 140 PF00917 0.500
LIG_TRAF2_1 17 20 PF00917 0.651
LIG_TRAF2_1 821 824 PF00917 0.495
LIG_TRAF2_1 9 12 PF00917 0.763
LIG_TYR_ITIM 533 538 PF00017 0.591
LIG_TYR_ITIM 886 891 PF00017 0.464
LIG_TYR_ITIM 974 979 PF00017 0.571
LIG_UBA3_1 205 211 PF00899 0.529
LIG_UBA3_1 537 544 PF00899 0.617
LIG_WRC_WIRS_1 658 663 PF05994 0.587
MOD_CDC14_SPxK_1 232 235 PF00782 0.494
MOD_CDC14_SPxK_1 51 54 PF00782 0.715
MOD_CDK_SPxK_1 229 235 PF00069 0.483
MOD_CDK_SPxK_1 48 54 PF00069 0.715
MOD_CDK_SPxxK_3 271 278 PF00069 0.489
MOD_CDK_SPxxK_3 774 781 PF00069 0.576
MOD_CDK_SPxxK_3 993 1000 PF00069 0.604
MOD_CK1_1 194 200 PF00069 0.533
MOD_CK1_1 3 9 PF00069 0.560
MOD_CK1_1 341 347 PF00069 0.753
MOD_CK1_1 440 446 PF00069 0.639
MOD_CK1_1 466 472 PF00069 0.634
MOD_CK1_1 513 519 PF00069 0.739
MOD_CK1_1 549 555 PF00069 0.739
MOD_CK1_1 562 568 PF00069 0.619
MOD_CK1_1 620 626 PF00069 0.814
MOD_CK1_1 729 735 PF00069 0.526
MOD_CK1_1 765 771 PF00069 0.601
MOD_CK1_1 861 867 PF00069 0.461
MOD_CK1_1 922 928 PF00069 0.687
MOD_CK1_1 993 999 PF00069 0.505
MOD_CK2_1 100 106 PF00069 0.654
MOD_CK2_1 14 20 PF00069 0.659
MOD_CK2_1 350 356 PF00069 0.720
MOD_CK2_1 419 425 PF00069 0.464
MOD_CK2_1 549 555 PF00069 0.684
MOD_CK2_1 683 689 PF00069 0.812
MOD_CK2_1 70 76 PF00069 0.688
MOD_CK2_1 81 87 PF00069 0.643
MOD_GlcNHglycan 1028 1031 PF01048 0.724
MOD_GlcNHglycan 194 197 PF01048 0.541
MOD_GlcNHglycan 291 297 PF01048 0.550
MOD_GlcNHglycan 325 328 PF01048 0.783
MOD_GlcNHglycan 442 445 PF01048 0.642
MOD_GlcNHglycan 468 471 PF01048 0.551
MOD_GlcNHglycan 519 522 PF01048 0.639
MOD_GlcNHglycan 523 526 PF01048 0.551
MOD_GlcNHglycan 552 555 PF01048 0.730
MOD_GlcNHglycan 559 562 PF01048 0.701
MOD_GlcNHglycan 6 9 PF01048 0.718
MOD_GlcNHglycan 603 606 PF01048 0.731
MOD_GlcNHglycan 674 677 PF01048 0.631
MOD_GlcNHglycan 678 682 PF01048 0.685
MOD_GlcNHglycan 73 76 PF01048 0.731
MOD_GlcNHglycan 739 742 PF01048 0.523
MOD_GlcNHglycan 764 767 PF01048 0.528
MOD_GlcNHglycan 827 830 PF01048 0.553
MOD_GlcNHglycan 89 92 PF01048 0.651
MOD_GlcNHglycan 911 914 PF01048 0.667
MOD_GlcNHglycan 926 929 PF01048 0.683
MOD_GlcNHglycan 992 995 PF01048 0.567
MOD_GSK3_1 1017 1024 PF00069 0.641
MOD_GSK3_1 229 236 PF00069 0.408
MOD_GSK3_1 310 317 PF00069 0.667
MOD_GSK3_1 338 345 PF00069 0.693
MOD_GSK3_1 346 353 PF00069 0.730
MOD_GSK3_1 360 367 PF00069 0.554
MOD_GSK3_1 380 387 PF00069 0.417
MOD_GSK3_1 40 47 PF00069 0.657
MOD_GSK3_1 474 481 PF00069 0.471
MOD_GSK3_1 513 520 PF00069 0.716
MOD_GSK3_1 536 543 PF00069 0.627
MOD_GSK3_1 546 553 PF00069 0.661
MOD_GSK3_1 555 562 PF00069 0.611
MOD_GSK3_1 616 623 PF00069 0.783
MOD_GSK3_1 64 71 PF00069 0.705
MOD_GSK3_1 668 675 PF00069 0.578
MOD_GSK3_1 701 708 PF00069 0.792
MOD_GSK3_1 729 736 PF00069 0.506
MOD_GSK3_1 825 832 PF00069 0.553
MOD_GSK3_1 854 861 PF00069 0.526
MOD_GSK3_1 918 925 PF00069 0.731
MOD_N-GLC_1 1017 1022 PF02516 0.693
MOD_N-GLC_1 683 688 PF02516 0.575
MOD_NEK2_1 1 6 PF00069 0.605
MOD_NEK2_1 1022 1027 PF00069 0.640
MOD_NEK2_1 191 196 PF00069 0.466
MOD_NEK2_1 205 210 PF00069 0.321
MOD_NEK2_1 330 335 PF00069 0.706
MOD_NEK2_1 419 424 PF00069 0.429
MOD_NEK2_1 426 431 PF00069 0.481
MOD_NEK2_1 474 479 PF00069 0.564
MOD_NEK2_1 575 580 PF00069 0.482
MOD_NEK2_1 641 646 PF00069 0.724
MOD_NEK2_1 657 662 PF00069 0.486
MOD_NEK2_1 700 705 PF00069 0.655
MOD_NEK2_1 81 86 PF00069 0.685
MOD_NEK2_1 831 836 PF00069 0.565
MOD_NEK2_1 923 928 PF00069 0.748
MOD_PIKK_1 366 372 PF00454 0.562
MOD_PIKK_1 393 399 PF00454 0.522
MOD_PIKK_1 40 46 PF00454 0.668
MOD_PIKK_1 411 417 PF00454 0.288
MOD_PIKK_1 426 432 PF00454 0.524
MOD_PIKK_1 513 519 PF00454 0.622
MOD_PIKK_1 643 649 PF00454 0.682
MOD_PIKK_1 904 910 PF00454 0.649
MOD_PKA_2 217 223 PF00069 0.558
MOD_PKA_2 277 283 PF00069 0.440
MOD_PKA_2 331 337 PF00069 0.711
MOD_PKA_2 782 788 PF00069 0.431
MOD_PKA_2 81 87 PF00069 0.687
MOD_PKA_2 861 867 PF00069 0.464
MOD_PKA_2 904 910 PF00069 0.607
MOD_Plk_1 1017 1023 PF00069 0.626
MOD_Plk_1 292 298 PF00069 0.537
MOD_Plk_1 341 347 PF00069 0.761
MOD_Plk_1 426 432 PF00069 0.542
MOD_Plk_1 437 443 PF00069 0.681
MOD_Plk_1 717 723 PF00069 0.411
MOD_Plk_1 950 956 PF00069 0.542
MOD_Plk_4 100 106 PF00069 0.635
MOD_Plk_4 1035 1041 PF00069 0.684
MOD_Plk_4 205 211 PF00069 0.415
MOD_Plk_4 217 223 PF00069 0.406
MOD_Plk_4 244 250 PF00069 0.486
MOD_Plk_4 303 309 PF00069 0.502
MOD_Plk_4 369 375 PF00069 0.533
MOD_Plk_4 419 425 PF00069 0.449
MOD_Plk_4 478 484 PF00069 0.396
MOD_Plk_4 578 584 PF00069 0.507
MOD_Plk_4 81 87 PF00069 0.643
MOD_Plk_4 889 895 PF00069 0.474
MOD_Plk_4 919 925 PF00069 0.635
MOD_Plk_4 950 956 PF00069 0.441
MOD_Plk_4 960 966 PF00069 0.394
MOD_Plk_4 970 976 PF00069 0.253
MOD_ProDKin_1 229 235 PF00069 0.423
MOD_ProDKin_1 271 277 PF00069 0.489
MOD_ProDKin_1 361 367 PF00069 0.598
MOD_ProDKin_1 48 54 PF00069 0.767
MOD_ProDKin_1 497 503 PF00069 0.597
MOD_ProDKin_1 555 561 PF00069 0.805
MOD_ProDKin_1 636 642 PF00069 0.800
MOD_ProDKin_1 68 74 PF00069 0.618
MOD_ProDKin_1 709 715 PF00069 0.652
MOD_ProDKin_1 751 757 PF00069 0.619
MOD_ProDKin_1 774 780 PF00069 0.532
MOD_ProDKin_1 916 922 PF00069 0.672
MOD_ProDKin_1 968 974 PF00069 0.468
MOD_ProDKin_1 993 999 PF00069 0.607
MOD_SUMO_for_1 1043 1046 PF00179 0.649
TRG_DiLeu_BaEn_1 244 249 PF01217 0.511
TRG_DiLeu_BaEn_1 651 656 PF01217 0.594
TRG_DiLeu_BaEn_1 951 956 PF01217 0.485
TRG_DiLeu_BaEn_3 718 724 PF01217 0.398
TRG_DiLeu_BaEn_4 11 17 PF01217 0.528
TRG_DiLeu_BaLyEn_6 181 186 PF01217 0.497
TRG_DiLeu_BaLyEn_6 254 259 PF01217 0.469
TRG_DiLeu_BaLyEn_6 266 271 PF01217 0.424
TRG_DiLeu_BaLyEn_6 415 420 PF01217 0.466
TRG_DiLeu_BaLyEn_6 581 586 PF01217 0.564
TRG_DiLeu_BaLyEn_6 810 815 PF01217 0.462
TRG_DiLeu_LyEn_5 651 656 PF01217 0.439
TRG_ENDOCYTIC_2 1010 1013 PF00928 0.431
TRG_ENDOCYTIC_2 246 249 PF00928 0.466
TRG_ENDOCYTIC_2 403 406 PF00928 0.510
TRG_ENDOCYTIC_2 526 529 PF00928 0.478
TRG_ENDOCYTIC_2 535 538 PF00928 0.435
TRG_ENDOCYTIC_2 872 875 PF00928 0.560
TRG_ENDOCYTIC_2 888 891 PF00928 0.282
TRG_ENDOCYTIC_2 92 95 PF00928 0.673
TRG_ENDOCYTIC_2 976 979 PF00928 0.583
TRG_ER_diArg_1 1049 1051 PF00400 0.587
TRG_ER_diArg_1 128 131 PF00400 0.667
TRG_ER_diArg_1 133 135 PF00400 0.433
TRG_ER_diArg_1 145 148 PF00400 0.567
TRG_ER_diArg_1 256 258 PF00400 0.444
TRG_ER_diArg_1 271 273 PF00400 0.491
TRG_ER_diArg_1 297 299 PF00400 0.504
TRG_ER_diArg_1 433 436 PF00400 0.453
TRG_ER_diArg_1 54 57 PF00400 0.723
TRG_ER_diArg_1 652 655 PF00400 0.491
TRG_ER_diArg_1 780 783 PF00400 0.445
TRG_ER_diArg_1 999 1002 PF00400 0.532
TRG_Pf-PMV_PEXEL_1 1002 1007 PF00026 0.534
TRG_Pf-PMV_PEXEL_1 14 18 PF00026 0.707
TRG_Pf-PMV_PEXEL_1 150 155 PF00026 0.574
TRG_Pf-PMV_PEXEL_1 235 239 PF00026 0.525
TRG_Pf-PMV_PEXEL_1 257 262 PF00026 0.475
TRG_Pf-PMV_PEXEL_1 287 291 PF00026 0.458
TRG_Pf-PMV_PEXEL_1 865 869 PF00026 0.550
TRG_Pf-PMV_PEXEL_1 93 98 PF00026 0.634
TRG_Pf-PMV_PEXEL_1 943 947 PF00026 0.642

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I1A2 Leptomonas seymouri 53% 100%
A0A3Q8IHU6 Leishmania donovani 89% 100%
A0A3S5IRG6 Trypanosoma rangeli 28% 100%
A4HQ42 Leishmania braziliensis 74% 100%
A4IDU9 Leishmania infantum 90% 100%
D0A8S2 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 26% 100%
E9ATW2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 88% 100%
V5DND2 Trypanosoma cruzi 27% 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