LeishMANIAdb
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FHA domain-containing protein

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

Quick info

Protein:
FHA domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania major
UniProt:
Q4QEF3_LEIMA
TriTrypDb:
LmjF.17.0410 , LMJLV39_170009800 * , LMJSD75_170009500 *
Length:
1062

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: 8
NetGPI no yes: 0, no: 8
Cellular components
Term Name Level Count
GO:0030870 Mre11 complex 3 2
GO:0032991 protein-containing complex 1 2
GO:0140513 nuclear protein-containing complex 2 2

Expansion

Sequence features

Q4QEF3
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QEF3

Function

Biological processes
Term Name Level Count
GO:0000075 cell cycle checkpoint signaling 4 2
GO:0000077 DNA damage checkpoint signaling 5 2
GO:0006139 nucleobase-containing compound metabolic process 3 2
GO:0006259 DNA metabolic process 4 2
GO:0006281 DNA repair 5 2
GO:0006302 double-strand break repair 6 2
GO:0006725 cellular aromatic compound metabolic process 3 2
GO:0006807 nitrogen compound metabolic process 2 2
GO:0006950 response to stress 2 2
GO:0006974 DNA damage response 4 2
GO:0007093 mitotic cell cycle checkpoint signaling 4 2
GO:0007095 mitotic G2 DNA damage checkpoint signaling 6 2
GO:0007165 signal transduction 2 2
GO:0007346 regulation of mitotic cell cycle 5 2
GO:0008152 metabolic process 1 2
GO:0009987 cellular process 1 2
GO:0010389 regulation of G2/M transition of mitotic cell cycle 7 2
GO:0010564 regulation of cell cycle process 5 2
GO:0010948 negative regulation of cell cycle process 6 2
GO:0010972 negative regulation of G2/M transition of mitotic cell cycle 8 2
GO:0022402 cell cycle process 2 2
GO:0031570 DNA integrity checkpoint signaling 5 2
GO:0033554 cellular response to stress 3 2
GO:0034641 cellular nitrogen compound metabolic process 3 2
GO:0035556 intracellular signal transduction 3 2
GO:0042770 signal transduction in response to DNA damage 4 2
GO:0043170 macromolecule metabolic process 3 2
GO:0044237 cellular metabolic process 2 2
GO:0044238 primary metabolic process 2 2
GO:0044260 obsolete cellular macromolecule metabolic process 3 2
GO:0044773 mitotic DNA damage checkpoint signaling 6 2
GO:0044774 mitotic DNA integrity checkpoint signaling 5 2
GO:0044818 mitotic G2/M transition checkpoint 5 2
GO:0045786 negative regulation of cell cycle 5 2
GO:0045930 negative regulation of mitotic cell cycle 6 2
GO:0046483 heterocycle metabolic process 3 2
GO:0048519 negative regulation of biological process 3 2
GO:0048523 negative regulation of cellular process 4 2
GO:0050789 regulation of biological process 2 2
GO:0050794 regulation of cellular process 3 2
GO:0050896 response to stimulus 1 2
GO:0051716 cellular response to stimulus 2 2
GO:0051726 regulation of cell cycle 4 2
GO:0065007 biological regulation 1 2
GO:0071704 organic substance metabolic process 2 2
GO:0090304 nucleic acid metabolic process 4 2
GO:1901360 organic cyclic compound metabolic process 3 2
GO:1901987 regulation of cell cycle phase transition 6 2
GO:1901988 negative regulation of cell cycle phase transition 7 2
GO:1901990 regulation of mitotic cell cycle phase transition 6 2
GO:1901991 negative regulation of mitotic cell cycle phase transition 7 2
GO:1902749 regulation of cell cycle G2/M phase transition 7 2
GO:1902750 negative regulation of cell cycle G2/M phase transition 8 2
GO:1903047 mitotic cell cycle process 3 2
Could not find GO molecular_function term for this entry.

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 114 118 PF00656 0.467
CLV_C14_Caspase3-7 207 211 PF00656 0.427
CLV_C14_Caspase3-7 673 677 PF00656 0.665
CLV_C14_Caspase3-7 711 715 PF00656 0.634
CLV_C14_Caspase3-7 785 789 PF00656 0.548
CLV_C14_Caspase3-7 961 965 PF00656 0.629
CLV_NRD_NRD_1 1016 1018 PF00675 0.739
CLV_NRD_NRD_1 22 24 PF00675 0.417
CLV_NRD_NRD_1 493 495 PF00675 0.640
CLV_NRD_NRD_1 545 547 PF00675 0.575
CLV_NRD_NRD_1 665 667 PF00675 0.581
CLV_NRD_NRD_1 670 672 PF00675 0.646
CLV_NRD_NRD_1 678 680 PF00675 0.622
CLV_NRD_NRD_1 801 803 PF00675 0.714
CLV_NRD_NRD_1 858 860 PF00675 0.792
CLV_NRD_NRD_1 901 903 PF00675 0.685
CLV_NRD_NRD_1 990 992 PF00675 0.706
CLV_PCSK_KEX2_1 1007 1009 PF00082 0.542
CLV_PCSK_KEX2_1 1016 1018 PF00082 0.629
CLV_PCSK_KEX2_1 493 495 PF00082 0.717
CLV_PCSK_KEX2_1 544 546 PF00082 0.584
CLV_PCSK_KEX2_1 665 667 PF00082 0.586
CLV_PCSK_KEX2_1 670 672 PF00082 0.646
CLV_PCSK_KEX2_1 678 680 PF00082 0.622
CLV_PCSK_KEX2_1 801 803 PF00082 0.718
CLV_PCSK_KEX2_1 901 903 PF00082 0.685
CLV_PCSK_KEX2_1 990 992 PF00082 0.756
CLV_PCSK_PC1ET2_1 1007 1009 PF00082 0.679
CLV_PCSK_PC7_1 489 495 PF00082 0.597
CLV_PCSK_PC7_1 666 672 PF00082 0.629
CLV_PCSK_PC7_1 797 803 PF00082 0.692
CLV_PCSK_SKI1_1 301 305 PF00082 0.326
CLV_PCSK_SKI1_1 583 587 PF00082 0.414
CLV_PCSK_SKI1_1 665 669 PF00082 0.569
CLV_PCSK_SKI1_1 678 682 PF00082 0.684
CLV_PCSK_SKI1_1 684 688 PF00082 0.671
DEG_APCC_DBOX_1 876 884 PF00400 0.691
DEG_COP1_1 960 971 PF00400 0.627
DEG_Nend_Nbox_1 1 3 PF02207 0.336
DEG_SPOP_SBC_1 264 268 PF00917 0.581
DEG_SPOP_SBC_1 462 466 PF00917 0.635
DEG_SPOP_SBC_1 789 793 PF00917 0.560
DEG_SPOP_SBC_1 942 946 PF00917 0.635
DOC_MAPK_gen_1 544 550 PF00069 0.547
DOC_MAPK_gen_1 801 807 PF00069 0.548
DOC_MAPK_MEF2A_6 152 160 PF00069 0.328
DOC_PP1_RVXF_1 299 305 PF00149 0.421
DOC_PP2B_LxvP_1 248 251 PF13499 0.417
DOC_PP2B_LxvP_1 876 879 PF13499 0.764
DOC_PP4_FxxP_1 254 257 PF00568 0.388
DOC_PP4_FxxP_1 282 285 PF00568 0.576
DOC_SPAK_OSR1_1 253 257 PF12202 0.454
DOC_USP7_MATH_1 11 15 PF00917 0.438
DOC_USP7_MATH_1 188 192 PF00917 0.450
DOC_USP7_MATH_1 249 253 PF00917 0.584
DOC_USP7_MATH_1 283 287 PF00917 0.545
DOC_USP7_MATH_1 403 407 PF00917 0.328
DOC_USP7_MATH_1 447 451 PF00917 0.766
DOC_USP7_MATH_1 479 483 PF00917 0.596
DOC_USP7_MATH_1 522 526 PF00917 0.756
DOC_USP7_MATH_1 527 531 PF00917 0.633
DOC_USP7_MATH_1 638 642 PF00917 0.555
DOC_USP7_MATH_1 680 684 PF00917 0.627
DOC_USP7_MATH_1 707 711 PF00917 0.702
DOC_USP7_MATH_1 731 735 PF00917 0.735
DOC_USP7_MATH_1 747 751 PF00917 0.589
DOC_USP7_MATH_1 790 794 PF00917 0.605
DOC_USP7_MATH_1 796 800 PF00917 0.584
DOC_USP7_MATH_1 830 834 PF00917 0.630
DOC_USP7_MATH_1 986 990 PF00917 0.715
DOC_USP7_MATH_2 752 758 PF00917 0.631
DOC_WW_Pin1_4 1011 1016 PF00397 0.701
DOC_WW_Pin1_4 377 382 PF00397 0.512
DOC_WW_Pin1_4 518 523 PF00397 0.762
DOC_WW_Pin1_4 694 699 PF00397 0.626
DOC_WW_Pin1_4 7 12 PF00397 0.500
DOC_WW_Pin1_4 779 784 PF00397 0.688
DOC_WW_Pin1_4 862 867 PF00397 0.719
DOC_WW_Pin1_4 888 893 PF00397 0.696
DOC_WW_Pin1_4 946 951 PF00397 0.613
LIG_14-3-3_CanoR_1 259 264 PF00244 0.428
LIG_14-3-3_CanoR_1 483 490 PF00244 0.716
LIG_14-3-3_CanoR_1 493 499 PF00244 0.666
LIG_14-3-3_CanoR_1 569 574 PF00244 0.350
LIG_14-3-3_CanoR_1 656 663 PF00244 0.505
LIG_14-3-3_CanoR_1 678 686 PF00244 0.642
LIG_14-3-3_CanoR_1 797 805 PF00244 0.709
LIG_14-3-3_CanoR_1 859 868 PF00244 0.699
LIG_14-3-3_CanoR_1 985 992 PF00244 0.757
LIG_14-3-3_CanoR_1 999 1004 PF00244 0.621
LIG_APCC_ABBA_1 451 456 PF00400 0.765
LIG_APCC_ABBAyCdc20_2 294 300 PF00400 0.289
LIG_BRCT_BRCA1_1 412 416 PF00533 0.439
LIG_DLG_GKlike_1 494 502 PF00625 0.512
LIG_DLG_GKlike_1 801 808 PF00625 0.546
LIG_FHA_1 265 271 PF00498 0.523
LIG_FHA_1 407 413 PF00498 0.424
LIG_FHA_1 570 576 PF00498 0.353
LIG_FHA_1 628 634 PF00498 0.444
LIG_FHA_1 662 668 PF00498 0.685
LIG_FHA_1 938 944 PF00498 0.660
LIG_FHA_2 112 118 PF00498 0.452
LIG_FHA_2 181 187 PF00498 0.445
LIG_FHA_2 643 649 PF00498 0.364
LIG_FHA_2 783 789 PF00498 0.542
LIG_FHA_2 919 925 PF00498 0.735
LIG_FHA_2 929 935 PF00498 0.721
LIG_LIR_Apic_2 252 257 PF02991 0.477
LIG_LIR_Apic_2 266 272 PF02991 0.423
LIG_LIR_Apic_2 280 285 PF02991 0.494
LIG_LIR_Gen_1 219 230 PF02991 0.331
LIG_LIR_Gen_1 232 242 PF02991 0.321
LIG_LIR_Gen_1 276 285 PF02991 0.535
LIG_LIR_Gen_1 357 364 PF02991 0.424
LIG_LIR_Gen_1 406 416 PF02991 0.353
LIG_LIR_Gen_1 561 571 PF02991 0.390
LIG_LIR_Nem_3 14 20 PF02991 0.367
LIG_LIR_Nem_3 150 156 PF02991 0.420
LIG_LIR_Nem_3 219 225 PF02991 0.330
LIG_LIR_Nem_3 228 234 PF02991 0.300
LIG_LIR_Nem_3 276 282 PF02991 0.511
LIG_LIR_Nem_3 300 306 PF02991 0.349
LIG_LIR_Nem_3 357 363 PF02991 0.426
LIG_LIR_Nem_3 37 43 PF02991 0.384
LIG_LIR_Nem_3 406 411 PF02991 0.364
LIG_LIR_Nem_3 561 566 PF02991 0.388
LIG_LIR_Nem_3 870 876 PF02991 0.635
LIG_LYPXL_yS_3 873 876 PF13949 0.644
LIG_Pex14_2 559 563 PF04695 0.452
LIG_PTAP_UEV_1 968 973 PF05743 0.647
LIG_PTB_Apo_2 411 418 PF02174 0.451
LIG_PTB_Phospho_1 411 417 PF10480 0.443
LIG_RPA_C_Fungi 478 490 PF08784 0.593
LIG_SH2_CRK 153 157 PF00017 0.421
LIG_SH2_CRK 18 22 PF00017 0.353
LIG_SH2_CRK 222 226 PF00017 0.310
LIG_SH2_CRK 571 575 PF00017 0.449
LIG_SH2_GRB2like 169 172 PF00017 0.430
LIG_SH2_NCK_1 222 226 PF00017 0.310
LIG_SH2_PTP2 360 363 PF00017 0.326
LIG_SH2_SRC 360 363 PF00017 0.420
LIG_SH2_SRC 417 420 PF00017 0.510
LIG_SH2_STAP1 18 22 PF00017 0.288
LIG_SH2_STAP1 2 6 PF00017 0.484
LIG_SH2_STAP1 571 575 PF00017 0.465
LIG_SH2_STAP1 601 605 PF00017 0.424
LIG_SH2_STAP1 629 633 PF00017 0.432
LIG_SH2_STAT5 142 145 PF00017 0.437
LIG_SH2_STAT5 203 206 PF00017 0.357
LIG_SH2_STAT5 229 232 PF00017 0.324
LIG_SH2_STAT5 26 29 PF00017 0.318
LIG_SH2_STAT5 269 272 PF00017 0.381
LIG_SH2_STAT5 360 363 PF00017 0.326
LIG_SH2_STAT5 562 565 PF00017 0.392
LIG_SH2_STAT5 571 574 PF00017 0.300
LIG_SH2_STAT5 592 595 PF00017 0.483
LIG_SH2_STAT5 629 632 PF00017 0.457
LIG_SH3_2 872 877 PF14604 0.645
LIG_SH3_2 992 997 PF14604 0.559
LIG_SH3_3 182 188 PF00018 0.405
LIG_SH3_3 192 198 PF00018 0.419
LIG_SH3_3 322 328 PF00018 0.443
LIG_SH3_3 784 790 PF00018 0.619
LIG_SH3_3 855 861 PF00018 0.587
LIG_SH3_3 868 874 PF00018 0.626
LIG_SH3_3 891 897 PF00018 0.673
LIG_SH3_3 966 972 PF00018 0.627
LIG_SH3_3 989 995 PF00018 0.710
LIG_SH3_4 848 855 PF00018 0.561
LIG_SUMO_SIM_anti_2 49 55 PF11976 0.334
LIG_TRAF2_1 83 86 PF00917 0.774
LIG_TRAF2_1 913 916 PF00917 0.767
LIG_TRFH_1 279 283 PF08558 0.467
LIG_TYR_ITIM 38 43 PF00017 0.472
LIG_TYR_ITIM 560 565 PF00017 0.392
LIG_TYR_ITIM 871 876 PF00017 0.620
LIG_UBA3_1 407 415 PF00899 0.437
LIG_WRC_WIRS_1 570 575 PF05994 0.301
MOD_CDC14_SPxK_1 10 13 PF00782 0.519
MOD_CDK_SPK_2 1011 1016 PF00069 0.588
MOD_CDK_SPxK_1 1011 1017 PF00069 0.751
MOD_CDK_SPxK_1 7 13 PF00069 0.505
MOD_CK1_1 1011 1017 PF00069 0.772
MOD_CK1_1 129 135 PF00069 0.333
MOD_CK1_1 394 400 PF00069 0.544
MOD_CK1_1 406 412 PF00069 0.375
MOD_CK1_1 488 494 PF00069 0.686
MOD_CK1_1 674 680 PF00069 0.649
MOD_CK1_1 682 688 PF00069 0.610
MOD_CK1_1 7 13 PF00069 0.505
MOD_CK1_1 782 788 PF00069 0.762
MOD_CK1_1 791 797 PF00069 0.737
MOD_CK1_1 803 809 PF00069 0.722
MOD_CK1_1 89 95 PF00069 0.545
MOD_CK1_1 927 933 PF00069 0.585
MOD_CK2_1 249 255 PF00069 0.505
MOD_CK2_1 341 347 PF00069 0.533
MOD_CK2_1 371 377 PF00069 0.460
MOD_CK2_1 625 631 PF00069 0.563
MOD_CK2_1 642 648 PF00069 0.350
MOD_CK2_1 733 739 PF00069 0.590
MOD_CK2_1 910 916 PF00069 0.701
MOD_CK2_1 918 924 PF00069 0.744
MOD_CK2_1 928 934 PF00069 0.714
MOD_CK2_1 946 952 PF00069 0.554
MOD_Cter_Amidation 542 545 PF01082 0.592
MOD_GlcNHglycan 1003 1006 PF01048 0.669
MOD_GlcNHglycan 1010 1013 PF01048 0.621
MOD_GlcNHglycan 1038 1042 PF01048 0.806
MOD_GlcNHglycan 128 131 PF01048 0.638
MOD_GlcNHglycan 13 16 PF01048 0.443
MOD_GlcNHglycan 161 165 PF01048 0.424
MOD_GlcNHglycan 308 312 PF01048 0.349
MOD_GlcNHglycan 373 376 PF01048 0.488
MOD_GlcNHglycan 393 396 PF01048 0.259
MOD_GlcNHglycan 444 448 PF01048 0.810
MOD_GlcNHglycan 465 468 PF01048 0.634
MOD_GlcNHglycan 471 474 PF01048 0.660
MOD_GlcNHglycan 475 478 PF01048 0.686
MOD_GlcNHglycan 485 488 PF01048 0.610
MOD_GlcNHglycan 522 525 PF01048 0.682
MOD_GlcNHglycan 538 541 PF01048 0.572
MOD_GlcNHglycan 658 661 PF01048 0.540
MOD_GlcNHglycan 735 738 PF01048 0.812
MOD_GlcNHglycan 775 778 PF01048 0.756
MOD_GlcNHglycan 794 797 PF01048 0.695
MOD_GlcNHglycan 812 815 PF01048 0.651
MOD_GlcNHglycan 88 91 PF01048 0.748
MOD_GlcNHglycan 898 901 PF01048 0.700
MOD_GlcNHglycan 904 907 PF01048 0.669
MOD_GlcNHglycan 969 972 PF01048 0.664
MOD_GlcNHglycan 979 982 PF01048 0.719
MOD_GlcNHglycan 992 995 PF01048 0.715
MOD_GSK3_1 107 114 PF00069 0.448
MOD_GSK3_1 122 129 PF00069 0.498
MOD_GSK3_1 216 223 PF00069 0.537
MOD_GSK3_1 258 265 PF00069 0.553
MOD_GSK3_1 273 280 PF00069 0.379
MOD_GSK3_1 283 290 PF00069 0.427
MOD_GSK3_1 390 397 PF00069 0.540
MOD_GSK3_1 406 413 PF00069 0.265
MOD_GSK3_1 433 440 PF00069 0.625
MOD_GSK3_1 443 450 PF00069 0.785
MOD_GSK3_1 469 476 PF00069 0.745
MOD_GSK3_1 479 486 PF00069 0.599
MOD_GSK3_1 502 509 PF00069 0.543
MOD_GSK3_1 518 525 PF00069 0.713
MOD_GSK3_1 625 632 PF00069 0.469
MOD_GSK3_1 638 645 PF00069 0.376
MOD_GSK3_1 666 673 PF00069 0.727
MOD_GSK3_1 674 681 PF00069 0.703
MOD_GSK3_1 7 14 PF00069 0.499
MOD_GSK3_1 788 795 PF00069 0.700
MOD_GSK3_1 796 803 PF00069 0.617
MOD_GSK3_1 806 813 PF00069 0.518
MOD_GSK3_1 862 869 PF00069 0.770
MOD_GSK3_1 924 931 PF00069 0.613
MOD_GSK3_1 933 940 PF00069 0.622
MOD_GSK3_1 942 949 PF00069 0.658
MOD_GSK3_1 963 970 PF00069 0.645
MOD_GSK3_1 977 984 PF00069 0.634
MOD_GSK3_1 986 993 PF00069 0.664
MOD_GSK3_1 999 1006 PF00069 0.579
MOD_LATS_1 1035 1041 PF00433 0.650
MOD_N-GLC_1 1008 1013 PF02516 0.671
MOD_N-GLC_1 208 213 PF02516 0.401
MOD_N-GLC_1 290 295 PF02516 0.502
MOD_N-GLC_1 364 369 PF02516 0.437
MOD_N-GLC_1 731 736 PF02516 0.628
MOD_N-GLC_1 838 843 PF02516 0.703
MOD_N-GLC_1 957 962 PF02516 0.647
MOD_N-GLC_1 999 1004 PF02516 0.781
MOD_N-GLC_2 623 625 PF02516 0.443
MOD_NEK2_1 122 127 PF00069 0.431
MOD_NEK2_1 160 165 PF00069 0.347
MOD_NEK2_1 180 185 PF00069 0.305
MOD_NEK2_1 208 213 PF00069 0.430
MOD_NEK2_1 341 346 PF00069 0.479
MOD_NEK2_1 371 376 PF00069 0.475
MOD_NEK2_1 4 9 PF00069 0.482
MOD_NEK2_1 506 511 PF00069 0.498
MOD_NEK2_1 536 541 PF00069 0.690
MOD_NEK2_1 773 778 PF00069 0.582
MOD_NEK2_1 808 813 PF00069 0.808
MOD_NEK2_1 943 948 PF00069 0.718
MOD_NEK2_2 403 408 PF00069 0.340
MOD_NEK2_2 629 634 PF00069 0.437
MOD_PIKK_1 1048 1054 PF00454 0.661
MOD_PIKK_1 341 347 PF00454 0.487
MOD_PIKK_1 506 512 PF00454 0.486
MOD_PIKK_1 747 753 PF00454 0.778
MOD_PIKK_1 838 844 PF00454 0.610
MOD_PIKK_1 910 916 PF00454 0.686
MOD_PIKK_1 944 950 PF00454 0.828
MOD_PIKK_1 963 969 PF00454 0.546
MOD_PK_1 1055 1061 PF00069 0.543
MOD_PK_1 819 825 PF00069 0.616
MOD_PK_1 999 1005 PF00069 0.564
MOD_PKA_1 493 499 PF00069 0.614
MOD_PKA_1 670 676 PF00069 0.667
MOD_PKA_1 678 684 PF00069 0.605
MOD_PKA_1 801 807 PF00069 0.678
MOD_PKA_1 990 996 PF00069 0.681
MOD_PKA_2 107 113 PF00069 0.443
MOD_PKA_2 258 264 PF00069 0.524
MOD_PKA_2 488 494 PF00069 0.702
MOD_PKA_2 595 601 PF00069 0.404
MOD_PKA_2 670 676 PF00069 0.718
MOD_PKA_2 678 684 PF00069 0.666
MOD_PKA_2 796 802 PF00069 0.710
MOD_PKA_2 977 983 PF00069 0.777
MOD_PKA_2 984 990 PF00069 0.795
MOD_PKB_1 483 491 PF00069 0.643
MOD_PKB_1 567 575 PF00069 0.310
MOD_Plk_1 1037 1043 PF00069 0.652
MOD_Plk_1 123 129 PF00069 0.438
MOD_Plk_1 160 166 PF00069 0.351
MOD_Plk_1 307 313 PF00069 0.275
MOD_Plk_1 34 40 PF00069 0.361
MOD_Plk_1 403 409 PF00069 0.344
MOD_Plk_1 443 449 PF00069 0.531
MOD_Plk_1 654 660 PF00069 0.508
MOD_Plk_1 963 969 PF00069 0.694
MOD_Plk_1 999 1005 PF00069 0.682
MOD_Plk_2-3 41 47 PF00069 0.379
MOD_Plk_2-3 595 601 PF00069 0.496
MOD_Plk_4 1055 1061 PF00069 0.556
MOD_Plk_4 16 22 PF00069 0.405
MOD_Plk_4 180 186 PF00069 0.398
MOD_Plk_4 220 226 PF00069 0.319
MOD_Plk_4 265 271 PF00069 0.652
MOD_Plk_4 403 409 PF00069 0.388
MOD_Plk_4 48 54 PF00069 0.348
MOD_Plk_4 569 575 PF00069 0.348
MOD_Plk_4 803 809 PF00069 0.544
MOD_Plk_4 890 896 PF00069 0.636
MOD_ProDKin_1 1011 1017 PF00069 0.704
MOD_ProDKin_1 377 383 PF00069 0.502
MOD_ProDKin_1 518 524 PF00069 0.764
MOD_ProDKin_1 694 700 PF00069 0.629
MOD_ProDKin_1 7 13 PF00069 0.505
MOD_ProDKin_1 779 785 PF00069 0.692
MOD_ProDKin_1 862 868 PF00069 0.719
MOD_ProDKin_1 888 894 PF00069 0.697
MOD_ProDKin_1 946 952 PF00069 0.617
MOD_SUMO_rev_2 577 581 PF00179 0.442
MOD_SUMO_rev_2 600 607 PF00179 0.384
TRG_DiLeu_BaEn_1 101 106 PF01217 0.397
TRG_DiLeu_BaEn_2 381 387 PF01217 0.467
TRG_DiLeu_BaEn_2 554 560 PF01217 0.487
TRG_DiLeu_BaEn_4 418 424 PF01217 0.538
TRG_ENDOCYTIC_2 153 156 PF00928 0.423
TRG_ENDOCYTIC_2 17 20 PF00928 0.338
TRG_ENDOCYTIC_2 222 225 PF00928 0.301
TRG_ENDOCYTIC_2 360 363 PF00928 0.326
TRG_ENDOCYTIC_2 40 43 PF00928 0.479
TRG_ENDOCYTIC_2 562 565 PF00928 0.380
TRG_ENDOCYTIC_2 571 574 PF00928 0.438
TRG_ENDOCYTIC_2 873 876 PF00928 0.655
TRG_ER_diArg_1 1015 1017 PF00400 0.719
TRG_ER_diArg_1 511 514 PF00400 0.543
TRG_ER_diArg_1 544 546 PF00400 0.666
TRG_ER_diArg_1 566 569 PF00400 0.357
TRG_ER_diArg_1 665 667 PF00400 0.562
TRG_ER_diArg_1 895 898 PF00400 0.699
TRG_ER_diArg_1 990 992 PF00400 0.738
TRG_NES_CRM1_1 179 193 PF08389 0.369
TRG_NES_CRM1_1 564 578 PF08389 0.387

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I2V4 Leptomonas seymouri 48% 97%
A0A3S5H703 Leishmania donovani 87% 100%
A0A3S5IS81 Trypanosoma rangeli 32% 100%
A4H8Y4 Leishmania braziliensis 56% 92%
A4HXB4 Leishmania infantum 84% 100%
E9AR10 Leishmania mexicana (strain MHOM/GT/2001/U1103) 81% 99%
V5D6I4 Trypanosoma cruzi 30% 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