LeishMANIAdb
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ATP-dependent DEAD/H DNA helicase recQ family-like protein

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

Quick info

Protein:
ATP-dependent DEAD/H DNA helicase recQ family-like protein
Gene product:
ATP-dependent DEAD/H DNA helicase recQ family- like protein
Species:
Leishmania braziliensis
UniProt:
A4HIG1_LEIBR
TriTrypDb:
LbrM.30.2240 , LBRM2903_300028800 *
Length:
998

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:0005634 nucleus 5 1
GO:0005694 chromosome 5 1
GO:0005737 cytoplasm 2 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0043228 non-membrane-bounded organelle 3 1
GO:0043229 intracellular organelle 3 1
GO:0043231 intracellular membrane-bounded organelle 4 1
GO:0043232 intracellular non-membrane-bounded organelle 4 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A4HIG1
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HIG1

Function

Biological processes
Term Name Level Count
GO:0000724 double-strand break repair via homologous recombination 7 1
GO:0000725 recombinational repair 6 1
GO:0006139 nucleobase-containing compound metabolic process 3 1
GO:0006259 DNA metabolic process 4 1
GO:0006268 DNA unwinding involved in DNA replication 9 1
GO:0006281 DNA repair 5 1
GO:0006302 double-strand break repair 6 1
GO:0006310 DNA recombination 5 1
GO:0006725 cellular aromatic compound metabolic process 3 1
GO:0006807 nitrogen compound metabolic process 2 1
GO:0006950 response to stress 2 1
GO:0006974 DNA damage response 4 1
GO:0006996 organelle organization 4 1
GO:0008152 metabolic process 1 1
GO:0009987 cellular process 1 1
GO:0016043 cellular component organization 3 1
GO:0032392 DNA geometric change 7 1
GO:0032508 DNA duplex unwinding 8 1
GO:0033554 cellular response to stress 3 1
GO:0034641 cellular nitrogen compound metabolic process 3 1
GO:0043170 macromolecule metabolic process 3 1
GO:0044237 cellular metabolic process 2 1
GO:0044238 primary metabolic process 2 1
GO:0044260 obsolete cellular macromolecule metabolic process 3 1
GO:0046483 heterocycle metabolic process 3 1
GO:0050896 response to stimulus 1 1
GO:0051276 chromosome organization 5 1
GO:0051716 cellular response to stimulus 2 1
GO:0071103 DNA conformation change 6 1
GO:0071704 organic substance metabolic process 2 1
GO:0071840 cellular component organization or biogenesis 2 1
GO:0090304 nucleic acid metabolic process 4 1
GO:1901360 organic cyclic compound metabolic process 3 1
Molecular functions
Term Name Level Count
GO:0000166 nucleotide binding 3 10
GO:0003676 nucleic acid binding 3 10
GO:0003824 catalytic activity 1 10
GO:0004386 helicase activity 2 10
GO:0005488 binding 1 10
GO:0005524 ATP binding 5 10
GO:0017076 purine nucleotide binding 4 10
GO:0030554 adenyl nucleotide binding 5 10
GO:0032553 ribonucleotide binding 3 10
GO:0032555 purine ribonucleotide binding 4 10
GO:0032559 adenyl ribonucleotide binding 5 10
GO:0035639 purine ribonucleoside triphosphate binding 4 10
GO:0036094 small molecule binding 2 10
GO:0043167 ion binding 2 10
GO:0043168 anion binding 3 10
GO:0097159 organic cyclic compound binding 2 10
GO:0097367 carbohydrate derivative binding 2 10
GO:0140640 catalytic activity, acting on a nucleic acid 2 10
GO:0140657 ATP-dependent activity 1 10
GO:1901265 nucleoside phosphate binding 3 10
GO:1901363 heterocyclic compound binding 2 10
GO:0003678 DNA helicase activity 3 2
GO:0008094 ATP-dependent activity, acting on DNA 2 2
GO:0009378 four-way junction helicase activity 4 1
GO:0043138 3'-5' DNA helicase activity 4 1
GO:0140097 catalytic activity, acting on DNA 3 2
GO:0016787 hydrolase activity 2 2

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 454 458 PF00656 0.388
CLV_C14_Caspase3-7 514 518 PF00656 0.527
CLV_C14_Caspase3-7 681 685 PF00656 0.464
CLV_C14_Caspase3-7 85 89 PF00656 0.359
CLV_NRD_NRD_1 294 296 PF00675 0.304
CLV_NRD_NRD_1 746 748 PF00675 0.641
CLV_PCSK_KEX2_1 13 15 PF00082 0.763
CLV_PCSK_KEX2_1 294 296 PF00082 0.304
CLV_PCSK_KEX2_1 744 746 PF00082 0.624
CLV_PCSK_PC1ET2_1 13 15 PF00082 0.505
CLV_PCSK_PC1ET2_1 744 746 PF00082 0.618
CLV_PCSK_SKI1_1 169 173 PF00082 0.249
CLV_PCSK_SKI1_1 17 21 PF00082 0.788
CLV_PCSK_SKI1_1 294 298 PF00082 0.247
CLV_PCSK_SKI1_1 303 307 PF00082 0.247
CLV_PCSK_SKI1_1 386 390 PF00082 0.414
CLV_PCSK_SKI1_1 540 544 PF00082 0.351
CLV_PCSK_SKI1_1 545 549 PF00082 0.353
CLV_PCSK_SKI1_1 645 649 PF00082 0.478
CLV_PCSK_SKI1_1 700 704 PF00082 0.477
CLV_PCSK_SKI1_1 867 871 PF00082 0.460
CLV_PCSK_SKI1_1 893 897 PF00082 0.541
DEG_APCC_DBOX_1 302 310 PF00400 0.502
DEG_APCC_DBOX_1 354 362 PF00400 0.502
DEG_APCC_DBOX_1 644 652 PF00400 0.462
DEG_MDM2_SWIB_1 977 985 PF02201 0.460
DOC_CDC14_PxL_1 358 366 PF14671 0.502
DOC_CKS1_1 821 826 PF01111 0.356
DOC_CKS1_1 991 996 PF01111 0.527
DOC_CYCLIN_RxL_1 166 173 PF00134 0.409
DOC_CYCLIN_RxL_1 291 299 PF00134 0.458
DOC_CYCLIN_yCln2_LP_2 270 276 PF00134 0.490
DOC_CYCLIN_yCln2_LP_2 333 339 PF00134 0.474
DOC_CYCLIN_yCln2_LP_2 444 450 PF00134 0.348
DOC_CYCLIN_yCln2_LP_2 604 610 PF00134 0.335
DOC_MAPK_DCC_7 269 279 PF00069 0.389
DOC_MAPK_gen_1 744 754 PF00069 0.496
DOC_MAPK_MEF2A_6 395 402 PF00069 0.446
DOC_MAPK_NFAT4_5 395 403 PF00069 0.443
DOC_MAPK_RevD_3 280 295 PF00069 0.530
DOC_PP1_RVXF_1 167 173 PF00149 0.458
DOC_PP1_RVXF_1 865 871 PF00149 0.488
DOC_PP2B_LxvP_1 796 799 PF13499 0.560
DOC_PP4_FxxP_1 281 284 PF00568 0.447
DOC_SPAK_OSR1_1 224 228 PF12202 0.490
DOC_USP7_MATH_1 211 215 PF00917 0.522
DOC_USP7_MATH_1 354 358 PF00917 0.514
DOC_USP7_MATH_1 43 47 PF00917 0.503
DOC_USP7_MATH_1 476 480 PF00917 0.740
DOC_USP7_MATH_1 538 542 PF00917 0.389
DOC_USP7_MATH_1 59 63 PF00917 0.471
DOC_USP7_MATH_1 66 70 PF00917 0.483
DOC_USP7_MATH_1 846 850 PF00917 0.532
DOC_USP7_MATH_1 895 899 PF00917 0.667
DOC_USP7_MATH_2 624 630 PF00917 0.427
DOC_WW_Pin1_4 227 232 PF00397 0.456
DOC_WW_Pin1_4 269 274 PF00397 0.476
DOC_WW_Pin1_4 280 285 PF00397 0.476
DOC_WW_Pin1_4 332 337 PF00397 0.544
DOC_WW_Pin1_4 346 351 PF00397 0.404
DOC_WW_Pin1_4 471 476 PF00397 0.695
DOC_WW_Pin1_4 620 625 PF00397 0.453
DOC_WW_Pin1_4 694 699 PF00397 0.544
DOC_WW_Pin1_4 738 743 PF00397 0.728
DOC_WW_Pin1_4 780 785 PF00397 0.519
DOC_WW_Pin1_4 820 825 PF00397 0.460
DOC_WW_Pin1_4 837 842 PF00397 0.449
DOC_WW_Pin1_4 965 970 PF00397 0.473
DOC_WW_Pin1_4 990 995 PF00397 0.518
LIG_14-3-3_CanoR_1 28 35 PF00244 0.637
LIG_14-3-3_CanoR_1 295 304 PF00244 0.500
LIG_14-3-3_CanoR_1 386 394 PF00244 0.411
LIG_14-3-3_CanoR_1 408 413 PF00244 0.480
LIG_14-3-3_CanoR_1 496 500 PF00244 0.537
LIG_14-3-3_CanoR_1 537 547 PF00244 0.494
LIG_14-3-3_CanoR_1 795 799 PF00244 0.442
LIG_14-3-3_CanoR_1 929 935 PF00244 0.491
LIG_14-3-3_CanoR_1 944 949 PF00244 0.551
LIG_BIR_II_1 1 5 PF00653 0.608
LIG_BRCT_BRCA1_1 967 971 PF00533 0.474
LIG_Clathr_ClatBox_1 306 310 PF01394 0.502
LIG_DLG_GKlike_1 408 415 PF00625 0.492
LIG_EH_1 605 609 PF12763 0.364
LIG_eIF4E_1 161 167 PF01652 0.409
LIG_FHA_1 145 151 PF00498 0.447
LIG_FHA_1 185 191 PF00498 0.412
LIG_FHA_1 197 203 PF00498 0.418
LIG_FHA_1 369 375 PF00498 0.549
LIG_FHA_1 42 48 PF00498 0.760
LIG_FHA_1 522 528 PF00498 0.434
LIG_FHA_1 637 643 PF00498 0.496
LIG_FHA_1 771 777 PF00498 0.495
LIG_FHA_1 811 817 PF00498 0.477
LIG_FHA_1 82 88 PF00498 0.285
LIG_FHA_1 974 980 PF00498 0.550
LIG_FHA_2 103 109 PF00498 0.454
LIG_FHA_2 13 19 PF00498 0.751
LIG_FHA_2 500 506 PF00498 0.602
LIG_FHA_2 509 515 PF00498 0.625
LIG_FHA_2 832 838 PF00498 0.429
LIG_FHA_2 892 898 PF00498 0.632
LIG_GBD_Chelix_1 555 563 PF00786 0.302
LIG_LIR_Apic_2 158 164 PF02991 0.447
LIG_LIR_Apic_2 278 284 PF02991 0.447
LIG_LIR_Apic_2 902 906 PF02991 0.577
LIG_LIR_Gen_1 223 233 PF02991 0.470
LIG_LIR_Gen_1 325 333 PF02991 0.447
LIG_LIR_Gen_1 411 418 PF02991 0.552
LIG_LIR_Gen_1 667 678 PF02991 0.375
LIG_LIR_Gen_1 932 941 PF02991 0.479
LIG_LIR_Nem_3 121 125 PF02991 0.353
LIG_LIR_Nem_3 223 228 PF02991 0.451
LIG_LIR_Nem_3 325 329 PF02991 0.447
LIG_LIR_Nem_3 381 385 PF02991 0.442
LIG_LIR_Nem_3 411 415 PF02991 0.545
LIG_LIR_Nem_3 609 613 PF02991 0.425
LIG_LIR_Nem_3 667 673 PF02991 0.332
LIG_LIR_Nem_3 697 702 PF02991 0.534
LIG_LIR_Nem_3 932 937 PF02991 0.474
LIG_LIR_Nem_3 968 974 PF02991 0.466
LIG_MLH1_MIPbox_1 967 971 PF16413 0.498
LIG_NRBOX 292 298 PF00104 0.444
LIG_NRBOX 460 466 PF00104 0.497
LIG_NRBOX 668 674 PF00104 0.398
LIG_PCNA_PIPBox_1 844 853 PF02747 0.505
LIG_PCNA_yPIPBox_3 395 406 PF02747 0.359
LIG_Pex14_1 318 322 PF04695 0.447
LIG_Pex14_2 322 326 PF04695 0.447
LIG_Pex14_2 977 981 PF04695 0.473
LIG_PTB_Apo_2 964 971 PF02174 0.590
LIG_PTB_Phospho_1 964 970 PF10480 0.590
LIG_SH2_CRK 161 165 PF00017 0.398
LIG_SH2_CRK 710 714 PF00017 0.428
LIG_SH2_CRK 821 825 PF00017 0.448
LIG_SH2_GRB2like 965 968 PF00017 0.577
LIG_SH2_SRC 965 968 PF00017 0.577
LIG_SH2_STAT3 954 957 PF00017 0.626
LIG_SH2_STAT5 117 120 PF00017 0.367
LIG_SH2_STAT5 122 125 PF00017 0.380
LIG_SH2_STAT5 176 179 PF00017 0.502
LIG_SH2_STAT5 328 331 PF00017 0.447
LIG_SH2_STAT5 363 366 PF00017 0.583
LIG_SH2_STAT5 451 454 PF00017 0.367
LIG_SH2_STAT5 585 588 PF00017 0.464
LIG_SH2_STAT5 611 614 PF00017 0.427
LIG_SH2_STAT5 965 968 PF00017 0.461
LIG_SH2_STAT5 970 973 PF00017 0.465
LIG_SH3_3 205 211 PF00018 0.429
LIG_SH3_3 225 231 PF00018 0.513
LIG_SH3_3 270 276 PF00018 0.514
LIG_SH3_3 692 698 PF00018 0.368
LIG_SH3_3 963 969 PF00018 0.471
LIG_SUMO_SIM_par_1 230 238 PF11976 0.490
LIG_SUMO_SIM_par_1 401 407 PF11976 0.284
LIG_SUMO_SIM_par_1 647 653 PF11976 0.388
LIG_SUMO_SIM_par_1 827 834 PF11976 0.415
LIG_TRAF2_1 511 514 PF00917 0.650
LIG_TRAF2_2 66 71 PF00917 0.499
LIG_TYR_ITIM 361 366 PF00017 0.530
LIG_TYR_ITIM 708 713 PF00017 0.448
LIG_UBA3_1 82 91 PF00899 0.445
LIG_WRC_WIRS_1 974 979 PF05994 0.554
MOD_CDC14_SPxK_1 283 286 PF00782 0.459
MOD_CDC14_SPxK_1 697 700 PF00782 0.361
MOD_CDK_SPxK_1 280 286 PF00069 0.459
MOD_CDK_SPxK_1 694 700 PF00069 0.385
MOD_CDK_SPxK_1 738 744 PF00069 0.624
MOD_CDK_SPxK_1 990 996 PF00069 0.418
MOD_CDK_SPxxK_3 738 745 PF00069 0.625
MOD_CK1_1 101 107 PF00069 0.565
MOD_CK1_1 193 199 PF00069 0.509
MOD_CK1_1 27 33 PF00069 0.637
MOD_CK1_1 36 42 PF00069 0.593
MOD_CK1_1 45 51 PF00069 0.650
MOD_CK1_1 474 480 PF00069 0.712
MOD_CK1_1 577 583 PF00069 0.447
MOD_CK1_1 636 642 PF00069 0.490
MOD_CK1_1 650 656 PF00069 0.402
MOD_CK1_1 69 75 PF00069 0.581
MOD_CK1_1 840 846 PF00069 0.409
MOD_CK1_1 891 897 PF00069 0.609
MOD_CK2_1 43 49 PF00069 0.542
MOD_CK2_1 499 505 PF00069 0.815
MOD_CK2_1 508 514 PF00069 0.762
MOD_CK2_1 577 583 PF00069 0.447
MOD_CK2_1 620 626 PF00069 0.386
MOD_CK2_1 684 690 PF00069 0.510
MOD_CK2_1 69 75 PF00069 0.671
MOD_CK2_1 831 837 PF00069 0.566
MOD_CK2_1 891 897 PF00069 0.552
MOD_CK2_1 929 935 PF00069 0.456
MOD_DYRK1A_RPxSP_1 694 698 PF00069 0.339
MOD_GlcNHglycan 101 104 PF01048 0.610
MOD_GlcNHglycan 187 190 PF01048 0.247
MOD_GlcNHglycan 315 318 PF01048 0.302
MOD_GlcNHglycan 418 421 PF01048 0.631
MOD_GlcNHglycan 427 431 PF01048 0.394
MOD_GlcNHglycan 461 464 PF01048 0.501
MOD_GlcNHglycan 476 479 PF01048 0.590
MOD_GlcNHglycan 540 543 PF01048 0.312
MOD_GlcNHglycan 576 579 PF01048 0.290
MOD_GlcNHglycan 61 64 PF01048 0.726
MOD_GlcNHglycan 635 638 PF01048 0.506
MOD_GlcNHglycan 654 657 PF01048 0.578
MOD_GlcNHglycan 68 71 PF01048 0.760
MOD_GlcNHglycan 729 732 PF01048 0.693
MOD_GlcNHglycan 824 827 PF01048 0.511
MOD_GSK3_1 364 371 PF00069 0.463
MOD_GSK3_1 41 48 PF00069 0.635
MOD_GSK3_1 459 466 PF00069 0.442
MOD_GSK3_1 495 502 PF00069 0.702
MOD_GSK3_1 54 61 PF00069 0.694
MOD_GSK3_1 574 581 PF00069 0.447
MOD_GSK3_1 622 629 PF00069 0.462
MOD_GSK3_1 633 640 PF00069 0.360
MOD_GSK3_1 690 697 PF00069 0.523
MOD_GSK3_1 794 801 PF00069 0.640
MOD_GSK3_1 8 15 PF00069 0.575
MOD_GSK3_1 810 817 PF00069 0.527
MOD_GSK3_1 833 840 PF00069 0.558
MOD_GSK3_1 89 96 PF00069 0.413
MOD_GSK3_1 891 898 PF00069 0.553
MOD_GSK3_1 973 980 PF00069 0.562
MOD_GSK3_1 98 105 PF00069 0.544
MOD_N-GLC_1 732 737 PF02516 0.756
MOD_NEK2_1 118 123 PF00069 0.448
MOD_NEK2_1 24 29 PF00069 0.688
MOD_NEK2_1 252 257 PF00069 0.517
MOD_NEK2_1 287 292 PF00069 0.530
MOD_NEK2_1 296 301 PF00069 0.441
MOD_NEK2_1 327 332 PF00069 0.547
MOD_NEK2_1 364 369 PF00069 0.478
MOD_NEK2_1 464 469 PF00069 0.421
MOD_NEK2_1 52 57 PF00069 0.668
MOD_NEK2_1 555 560 PF00069 0.409
MOD_NEK2_1 58 63 PF00069 0.487
MOD_NEK2_1 617 622 PF00069 0.460
MOD_NEK2_1 635 640 PF00069 0.460
MOD_NEK2_1 647 652 PF00069 0.395
MOD_NEK2_1 671 676 PF00069 0.498
MOD_NEK2_1 727 732 PF00069 0.713
MOD_NEK2_1 8 13 PF00069 0.711
MOD_NEK2_1 810 815 PF00069 0.549
MOD_NEK2_1 831 836 PF00069 0.331
MOD_NEK2_1 93 98 PF00069 0.454
MOD_NEK2_1 960 965 PF00069 0.485
MOD_NEK2_1 977 982 PF00069 0.442
MOD_PIKK_1 102 108 PF00454 0.519
MOD_PIKK_1 296 302 PF00454 0.477
MOD_PIKK_1 540 546 PF00454 0.449
MOD_PIKK_1 8 14 PF00454 0.734
MOD_PIKK_1 840 846 PF00454 0.335
MOD_PKA_1 13 19 PF00069 0.762
MOD_PKA_1 745 751 PF00069 0.715
MOD_PKA_2 13 19 PF00069 0.616
MOD_PKA_2 174 180 PF00069 0.502
MOD_PKA_2 27 33 PF00069 0.492
MOD_PKA_2 322 328 PF00069 0.447
MOD_PKA_2 354 360 PF00069 0.535
MOD_PKA_2 495 501 PF00069 0.536
MOD_PKA_2 745 751 PF00069 0.715
MOD_PKA_2 794 800 PF00069 0.436
MOD_PKB_1 927 935 PF00069 0.464
MOD_Plk_1 732 738 PF00069 0.771
MOD_Plk_1 977 983 PF00069 0.514
MOD_Plk_2-3 74 80 PF00069 0.342
MOD_Plk_4 137 143 PF00069 0.490
MOD_Plk_4 322 328 PF00069 0.449
MOD_Plk_4 617 623 PF00069 0.399
MOD_Plk_4 664 670 PF00069 0.358
MOD_Plk_4 914 920 PF00069 0.518
MOD_Plk_4 960 966 PF00069 0.521
MOD_Plk_4 977 983 PF00069 0.459
MOD_ProDKin_1 227 233 PF00069 0.456
MOD_ProDKin_1 269 275 PF00069 0.476
MOD_ProDKin_1 280 286 PF00069 0.476
MOD_ProDKin_1 332 338 PF00069 0.544
MOD_ProDKin_1 346 352 PF00069 0.404
MOD_ProDKin_1 471 477 PF00069 0.699
MOD_ProDKin_1 620 626 PF00069 0.450
MOD_ProDKin_1 694 700 PF00069 0.550
MOD_ProDKin_1 738 744 PF00069 0.729
MOD_ProDKin_1 780 786 PF00069 0.513
MOD_ProDKin_1 820 826 PF00069 0.447
MOD_ProDKin_1 837 843 PF00069 0.446
MOD_ProDKin_1 965 971 PF00069 0.473
MOD_ProDKin_1 990 996 PF00069 0.529
MOD_SUMO_for_1 268 271 PF00179 0.389
TRG_DiLeu_BaEn_2 665 671 PF01217 0.332
TRG_DiLeu_BaLyEn_6 166 171 PF01217 0.490
TRG_DiLeu_BaLyEn_6 228 233 PF01217 0.447
TRG_DiLeu_BaLyEn_6 292 297 PF01217 0.502
TRG_DiLeu_BaLyEn_6 333 338 PF01217 0.530
TRG_DiLeu_BaLyEn_6 599 604 PF01217 0.335
TRG_ENDOCYTIC_2 122 125 PF00928 0.303
TRG_ENDOCYTIC_2 363 366 PF00928 0.538
TRG_ENDOCYTIC_2 605 608 PF00928 0.404
TRG_ENDOCYTIC_2 710 713 PF00928 0.418
TRG_ENDOCYTIC_2 934 937 PF00928 0.512
TRG_ER_diArg_1 293 295 PF00400 0.538
TRG_ER_diArg_1 613 616 PF00400 0.392
TRG_ER_diArg_1 736 739 PF00400 0.735
TRG_ER_diArg_1 745 747 PF00400 0.700
TRG_ER_diArg_1 856 859 PF00400 0.419
TRG_ER_diArg_1 927 930 PF00400 0.450
TRG_ER_diArg_1 943 946 PF00400 0.482
TRG_NES_CRM1_1 553 566 PF08389 0.447
TRG_NLS_MonoCore_2 743 748 PF00514 0.691
TRG_NLS_MonoExtN_4 742 748 PF00514 0.721
TRG_Pf-PMV_PEXEL_1 169 173 PF00026 0.265
TRG_Pf-PMV_PEXEL_1 17 21 PF00026 0.507
TRG_Pf-PMV_PEXEL_1 294 298 PF00026 0.325
TRG_Pf-PMV_PEXEL_1 431 435 PF00026 0.350
TRG_Pf-PMV_PEXEL_1 946 950 PF00026 0.653

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1IMF3 Leptomonas seymouri 59% 91%
A0A1X0P1S1 Trypanosomatidae 43% 100%
A0A3R7L9G4 Trypanosoma rangeli 44% 100%
A0A3S7X3I6 Leishmania donovani 79% 100%
A4I5Q7 Leishmania infantum 78% 100%
C9ZR26 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 42% 100%
E9B102 Leishmania mexicana (strain MHOM/GT/2001/U1103) 80% 100%
Q4Q764 Leishmania major 77% 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