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 braziliensis
UniProt:
A4H4J4_LEIBR
TriTrypDb:
LbrM.06.0260 , LBRM2903_060008200 *
Length:
854

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 9
GO:0032991 protein-containing complex 1 9
GO:0140513 nuclear protein-containing complex 2 9
GO:0005737 cytoplasm 2 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A4H4J4
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4H4J4

Function

Biological processes
Term Name Level Count
GO:0000075 cell cycle checkpoint signaling 4 9
GO:0000077 DNA damage checkpoint signaling 5 9
GO:0006139 nucleobase-containing compound metabolic process 3 9
GO:0006259 DNA metabolic process 4 9
GO:0006281 DNA repair 5 9
GO:0006302 double-strand break repair 6 9
GO:0006725 cellular aromatic compound metabolic process 3 9
GO:0006807 nitrogen compound metabolic process 2 9
GO:0006950 response to stress 2 9
GO:0006974 DNA damage response 4 9
GO:0007093 mitotic cell cycle checkpoint signaling 4 9
GO:0007095 mitotic G2 DNA damage checkpoint signaling 6 9
GO:0007165 signal transduction 2 9
GO:0007346 regulation of mitotic cell cycle 5 9
GO:0008152 metabolic process 1 9
GO:0009987 cellular process 1 9
GO:0010389 regulation of G2/M transition of mitotic cell cycle 7 9
GO:0010564 regulation of cell cycle process 5 9
GO:0010948 negative regulation of cell cycle process 6 9
GO:0010972 negative regulation of G2/M transition of mitotic cell cycle 8 9
GO:0022402 cell cycle process 2 9
GO:0031570 DNA integrity checkpoint signaling 5 9
GO:0033554 cellular response to stress 3 9
GO:0034641 cellular nitrogen compound metabolic process 3 9
GO:0035556 intracellular signal transduction 3 9
GO:0042770 signal transduction in response to DNA damage 4 9
GO:0043170 macromolecule metabolic process 3 9
GO:0044237 cellular metabolic process 2 9
GO:0044238 primary metabolic process 2 9
GO:0044260 obsolete cellular macromolecule metabolic process 3 9
GO:0044773 mitotic DNA damage checkpoint signaling 6 9
GO:0044774 mitotic DNA integrity checkpoint signaling 5 9
GO:0044818 mitotic G2/M transition checkpoint 5 9
GO:0045786 negative regulation of cell cycle 5 9
GO:0045930 negative regulation of mitotic cell cycle 6 9
GO:0046483 heterocycle metabolic process 3 9
GO:0048519 negative regulation of biological process 3 9
GO:0048523 negative regulation of cellular process 4 9
GO:0050789 regulation of biological process 2 9
GO:0050794 regulation of cellular process 3 9
GO:0050896 response to stimulus 1 9
GO:0051716 cellular response to stimulus 2 9
GO:0051726 regulation of cell cycle 4 9
GO:0065007 biological regulation 1 9
GO:0071704 organic substance metabolic process 2 9
GO:0090304 nucleic acid metabolic process 4 9
GO:1901360 organic cyclic compound metabolic process 3 9
GO:1901987 regulation of cell cycle phase transition 6 9
GO:1901988 negative regulation of cell cycle phase transition 7 9
GO:1901990 regulation of mitotic cell cycle phase transition 6 9
GO:1901991 negative regulation of mitotic cell cycle phase transition 7 9
GO:1902749 regulation of cell cycle G2/M phase transition 7 9
GO:1902750 negative regulation of cell cycle G2/M phase transition 8 9
GO:1903047 mitotic cell cycle process 3 9
GO:0000724 double-strand break repair via homologous recombination 7 1
GO:0000725 recombinational repair 6 1
GO:0006310 DNA recombination 5 1
GO:0006996 organelle organization 4 1
GO:0016043 cellular component organization 3 1
GO:0032392 DNA geometric change 7 1
GO:0032508 DNA duplex unwinding 8 1
GO:0051276 chromosome organization 5 1
GO:0071103 DNA conformation change 6 1
GO:0071840 cellular component organization or biogenesis 2 1
Molecular functions
Term Name Level Count
GO:0003676 nucleic acid binding 3 1
GO:0003677 DNA binding 4 1
GO:0003684 damaged DNA binding 5 1
GO:0005488 binding 1 1
GO:0097159 organic cyclic compound binding 2 1
GO:1901363 heterocyclic compound binding 2 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 507 511 PF00656 0.418
CLV_C14_Caspase3-7 620 624 PF00656 0.658
CLV_C14_Caspase3-7 66 70 PF00656 0.438
CLV_NRD_NRD_1 132 134 PF00675 0.608
CLV_NRD_NRD_1 405 407 PF00675 0.450
CLV_NRD_NRD_1 572 574 PF00675 0.653
CLV_NRD_NRD_1 615 617 PF00675 0.681
CLV_NRD_NRD_1 717 719 PF00675 0.628
CLV_NRD_NRD_1 775 777 PF00675 0.601
CLV_NRD_NRD_1 781 783 PF00675 0.586
CLV_PCSK_KEX2_1 134 136 PF00082 0.715
CLV_PCSK_KEX2_1 405 407 PF00082 0.449
CLV_PCSK_KEX2_1 572 574 PF00082 0.653
CLV_PCSK_KEX2_1 615 617 PF00082 0.610
CLV_PCSK_KEX2_1 717 719 PF00082 0.628
CLV_PCSK_KEX2_1 774 776 PF00082 0.618
CLV_PCSK_KEX2_1 781 783 PF00082 0.582
CLV_PCSK_PC1ET2_1 134 136 PF00082 0.715
CLV_PCSK_SKI1_1 246 250 PF00082 0.402
CLV_PCSK_SKI1_1 406 410 PF00082 0.453
CLV_PCSK_SKI1_1 423 427 PF00082 0.286
CLV_PCSK_SKI1_1 473 477 PF00082 0.373
CLV_PCSK_SKI1_1 630 634 PF00082 0.761
CLV_PCSK_SKI1_1 693 697 PF00082 0.645
CLV_PCSK_SKI1_1 700 704 PF00082 0.628
DEG_APCC_DBOX_1 457 465 PF00400 0.461
DEG_COP1_1 723 732 PF00400 0.618
DEG_Nend_Nbox_1 1 3 PF02207 0.308
DEG_SCF_FBW7_1 249 256 PF00400 0.591
DOC_CDC14_PxL_1 332 340 PF14671 0.279
DOC_CKS1_1 250 255 PF01111 0.502
DOC_CKS1_1 309 314 PF01111 0.510
DOC_CKS1_1 7 12 PF01111 0.292
DOC_CYCLIN_RxL_1 403 413 PF00134 0.418
DOC_CYCLIN_RxL_1 513 521 PF00134 0.315
DOC_CYCLIN_yCln2_LP_2 254 260 PF00134 0.461
DOC_CYCLIN_yCln2_LP_2 328 334 PF00134 0.297
DOC_MAPK_gen_1 21 31 PF00069 0.405
DOC_MAPK_gen_1 470 478 PF00069 0.528
DOC_MAPK_MEF2A_6 145 152 PF00069 0.534
DOC_MAPK_MEF2A_6 182 190 PF00069 0.303
DOC_MAPK_MEF2A_6 321 328 PF00069 0.423
DOC_MAPK_MEF2A_6 39 48 PF00069 0.395
DOC_MAPK_MEF2A_6 717 724 PF00069 0.458
DOC_MAPK_NFAT4_5 145 153 PF00069 0.358
DOC_PP1_RVXF_1 180 186 PF00149 0.365
DOC_PP1_RVXF_1 433 439 PF00149 0.435
DOC_PP2B_LxvP_1 446 449 PF13499 0.497
DOC_PP2B_PxIxI_1 294 300 PF00149 0.241
DOC_PP4_FxxP_1 158 161 PF00568 0.329
DOC_PP4_FxxP_1 345 348 PF00568 0.481
DOC_PP4_FxxP_1 375 378 PF00568 0.501
DOC_PP4_FxxP_1 628 631 PF00568 0.701
DOC_USP7_MATH_1 273 277 PF00917 0.626
DOC_USP7_MATH_1 353 357 PF00917 0.603
DOC_USP7_MATH_1 358 362 PF00917 0.629
DOC_USP7_MATH_1 370 374 PF00917 0.510
DOC_USP7_MATH_1 391 395 PF00917 0.423
DOC_USP7_MATH_1 449 453 PF00917 0.589
DOC_USP7_MATH_1 679 683 PF00917 0.609
DOC_USP7_MATH_1 813 817 PF00917 0.609
DOC_USP7_UBL2_3 696 700 PF12436 0.579
DOC_WW_Pin1_4 106 111 PF00397 0.461
DOC_WW_Pin1_4 249 254 PF00397 0.618
DOC_WW_Pin1_4 308 313 PF00397 0.395
DOC_WW_Pin1_4 320 325 PF00397 0.411
DOC_WW_Pin1_4 336 341 PF00397 0.270
DOC_WW_Pin1_4 374 379 PF00397 0.630
DOC_WW_Pin1_4 6 11 PF00397 0.436
DOC_WW_Pin1_4 89 94 PF00397 0.771
LIG_14-3-3_CanoR_1 145 151 PF00244 0.521
LIG_14-3-3_CanoR_1 164 168 PF00244 0.401
LIG_14-3-3_CanoR_1 495 501 PF00244 0.437
LIG_14-3-3_CanoR_1 572 580 PF00244 0.631
LIG_14-3-3_CanoR_1 630 635 PF00244 0.548
LIG_14-3-3_CanoR_1 802 807 PF00244 0.481
LIG_Actin_WH2_2 167 184 PF00022 0.451
LIG_APCC_ABBA_1 475 480 PF00400 0.438
LIG_BIR_III_2 575 579 PF00653 0.686
LIG_BIR_III_4 362 366 PF00653 0.498
LIG_BIR_III_4 733 737 PF00653 0.493
LIG_BRCT_BRCA1_1 757 761 PF00533 0.548
LIG_Clathr_ClatBox_1 183 187 PF01394 0.424
LIG_Clathr_ClatBox_1 709 713 PF01394 0.644
LIG_CtBP_PxDLS_1 240 246 PF00389 0.453
LIG_deltaCOP1_diTrp_1 623 628 PF00928 0.647
LIG_EVH1_1 665 669 PF00568 0.644
LIG_FHA_1 147 153 PF00498 0.456
LIG_FHA_1 169 175 PF00498 0.439
LIG_FHA_1 214 220 PF00498 0.480
LIG_FHA_1 288 294 PF00498 0.316
LIG_FHA_1 41 47 PF00498 0.379
LIG_FHA_1 411 417 PF00498 0.399
LIG_FHA_1 479 485 PF00498 0.535
LIG_FHA_1 542 548 PF00498 0.469
LIG_FHA_1 561 567 PF00498 0.496
LIG_FHA_1 653 659 PF00498 0.688
LIG_FHA_1 724 730 PF00498 0.574
LIG_FHA_1 73 79 PF00498 0.416
LIG_FHA_1 758 764 PF00498 0.476
LIG_FHA_2 505 511 PF00498 0.440
LIG_FHA_2 530 536 PF00498 0.529
LIG_LIR_Apic_2 155 161 PF02991 0.383
LIG_LIR_Apic_2 344 348 PF02991 0.562
LIG_LIR_Apic_2 373 378 PF02991 0.503
LIG_LIR_Apic_2 611 617 PF02991 0.527
LIG_LIR_Apic_2 627 631 PF02991 0.686
LIG_LIR_Gen_1 165 174 PF02991 0.542
LIG_LIR_Gen_1 339 350 PF02991 0.311
LIG_LIR_Gen_1 413 422 PF02991 0.437
LIG_LIR_Gen_1 623 632 PF02991 0.672
LIG_LIR_Gen_1 758 768 PF02991 0.579
LIG_LIR_Gen_1 842 853 PF02991 0.654
LIG_LIR_Nem_3 165 170 PF02991 0.446
LIG_LIR_Nem_3 339 345 PF02991 0.395
LIG_LIR_Nem_3 413 417 PF02991 0.385
LIG_LIR_Nem_3 420 425 PF02991 0.419
LIG_LIR_Nem_3 502 508 PF02991 0.404
LIG_LIR_Nem_3 623 628 PF02991 0.676
LIG_LIR_Nem_3 758 764 PF02991 0.579
LIG_LIR_Nem_3 842 848 PF02991 0.669
LIG_LIR_Nem_3 9 15 PF02991 0.430
LIG_MYND_1 336 340 PF01753 0.314
LIG_OCRL_FandH_1 466 478 PF00620 0.394
LIG_Pex14_1 2 6 PF04695 0.313
LIG_Pex14_1 341 345 PF04695 0.441
LIG_REV1ctd_RIR_1 465 474 PF16727 0.469
LIG_SH2_CRK 282 286 PF00017 0.423
LIG_SH2_CRK 505 509 PF00017 0.360
LIG_SH2_CRK 614 618 PF00017 0.500
LIG_SH2_CRK 663 667 PF00017 0.645
LIG_SH2_NCK_1 121 125 PF00017 0.546
LIG_SH2_NCK_1 282 286 PF00017 0.452
LIG_SH2_NCK_1 663 667 PF00017 0.645
LIG_SH2_SRC 121 124 PF00017 0.575
LIG_SH2_SRC 334 337 PF00017 0.406
LIG_SH2_SRC 428 431 PF00017 0.355
LIG_SH2_STAT5 334 337 PF00017 0.435
LIG_SH2_STAT5 398 401 PF00017 0.408
LIG_SH2_STAT5 428 431 PF00017 0.379
LIG_SH3_1 321 327 PF00018 0.417
LIG_SH3_1 334 340 PF00018 0.376
LIG_SH3_1 663 669 PF00018 0.646
LIG_SH3_3 321 327 PF00018 0.386
LIG_SH3_3 334 340 PF00018 0.332
LIG_SH3_3 345 351 PF00018 0.426
LIG_SH3_3 480 486 PF00018 0.487
LIG_SH3_3 575 581 PF00018 0.682
LIG_SH3_3 591 597 PF00018 0.685
LIG_SH3_3 663 669 PF00018 0.556
LIG_SH3_3 791 797 PF00018 0.559
LIG_SH3_4 696 703 PF00018 0.468
LIG_SUMO_SIM_anti_2 187 194 PF11976 0.309
LIG_SUMO_SIM_anti_2 296 301 PF11976 0.235
LIG_SUMO_SIM_par_1 63 72 PF11976 0.390
LIG_SUMO_SIM_par_1 707 713 PF11976 0.556
LIG_SUMO_SIM_par_1 821 830 PF11976 0.654
LIG_TRAF2_1 532 535 PF00917 0.503
LIG_TRAF2_1 557 560 PF00917 0.603
LIG_TRFH_1 663 667 PF08558 0.645
LIG_TYR_ITIM 503 508 PF00017 0.330
LIG_TYR_ITIM 603 608 PF00017 0.500
MOD_CK1_1 108 114 PF00069 0.610
MOD_CK1_1 239 245 PF00069 0.541
MOD_CK1_1 373 379 PF00069 0.574
MOD_CK1_1 380 386 PF00069 0.579
MOD_CK1_1 410 416 PF00069 0.405
MOD_CK1_1 452 458 PF00069 0.635
MOD_CK1_1 499 505 PF00069 0.510
MOD_CK1_1 550 556 PF00069 0.561
MOD_CK1_1 590 596 PF00069 0.516
MOD_CK1_1 642 648 PF00069 0.557
MOD_CK1_1 723 729 PF00069 0.616
MOD_CK1_1 748 754 PF00069 0.481
MOD_CK1_1 816 822 PF00069 0.619
MOD_CK2_1 222 228 PF00069 0.648
MOD_CK2_1 349 355 PF00069 0.631
MOD_CK2_1 358 364 PF00069 0.747
MOD_CK2_1 454 460 PF00069 0.369
MOD_CK2_1 529 535 PF00069 0.541
MOD_Cter_Amidation 22 25 PF01082 0.280
MOD_Cter_Amidation 570 573 PF01082 0.659
MOD_GlcNHglycan 102 105 PF01048 0.496
MOD_GlcNHglycan 137 140 PF01048 0.692
MOD_GlcNHglycan 141 144 PF01048 0.726
MOD_GlcNHglycan 224 227 PF01048 0.607
MOD_GlcNHglycan 231 234 PF01048 0.660
MOD_GlcNHglycan 238 241 PF01048 0.620
MOD_GlcNHglycan 275 278 PF01048 0.563
MOD_GlcNHglycan 351 354 PF01048 0.703
MOD_GlcNHglycan 368 371 PF01048 0.587
MOD_GlcNHglycan 409 412 PF01048 0.425
MOD_GlcNHglycan 446 449 PF01048 0.530
MOD_GlcNHglycan 520 523 PF01048 0.577
MOD_GlcNHglycan 590 593 PF01048 0.614
MOD_GlcNHglycan 680 684 PF01048 0.563
MOD_GlcNHglycan 757 760 PF01048 0.639
MOD_GlcNHglycan 789 792 PF01048 0.619
MOD_GlcNHglycan 815 818 PF01048 0.563
MOD_GlcNHglycan 94 97 PF01048 0.536
MOD_GSK3_1 135 142 PF00069 0.692
MOD_GSK3_1 146 153 PF00069 0.519
MOD_GSK3_1 218 225 PF00069 0.635
MOD_GSK3_1 249 256 PF00069 0.695
MOD_GSK3_1 269 276 PF00069 0.422
MOD_GSK3_1 289 296 PF00069 0.307
MOD_GSK3_1 33 40 PF00069 0.471
MOD_GSK3_1 349 356 PF00069 0.580
MOD_GSK3_1 366 373 PF00069 0.632
MOD_GSK3_1 374 381 PF00069 0.545
MOD_GSK3_1 449 456 PF00069 0.554
MOD_GSK3_1 541 548 PF00069 0.522
MOD_GSK3_1 63 70 PF00069 0.426
MOD_GSK3_1 744 751 PF00069 0.563
MOD_GSK3_1 827 834 PF00069 0.693
MOD_GSK3_1 92 99 PF00069 0.745
MOD_N-GLC_1 478 483 PF02516 0.454
MOD_N-GLC_1 802 807 PF02516 0.481
MOD_NEK2_1 186 191 PF00069 0.525
MOD_NEK2_1 241 246 PF00069 0.526
MOD_NEK2_1 287 292 PF00069 0.397
MOD_NEK2_1 417 422 PF00069 0.411
MOD_NEK2_1 42 47 PF00069 0.413
MOD_NEK2_1 429 434 PF00069 0.435
MOD_NEK2_1 450 455 PF00069 0.589
MOD_NEK2_1 48 53 PF00069 0.503
MOD_NEK2_1 546 551 PF00069 0.446
MOD_NEK2_1 67 72 PF00069 0.383
MOD_NEK2_1 720 725 PF00069 0.623
MOD_NEK2_1 744 749 PF00069 0.539
MOD_NEK2_2 511 516 PF00069 0.406
MOD_PIKK_1 218 224 PF00454 0.620
MOD_PIKK_1 226 232 PF00454 0.565
MOD_PIKK_1 241 247 PF00454 0.508
MOD_PIKK_1 560 566 PF00454 0.738
MOD_PKA_1 775 781 PF00069 0.630
MOD_PKA_2 163 169 PF00069 0.450
MOD_PKA_2 571 577 PF00069 0.605
MOD_PKA_2 775 781 PF00069 0.630
MOD_PKB_1 133 141 PF00069 0.682
MOD_PKB_1 800 808 PF00069 0.477
MOD_Plk_1 186 192 PF00069 0.409
MOD_Plk_1 33 39 PF00069 0.378
MOD_Plk_1 609 615 PF00069 0.768
MOD_Plk_1 68 74 PF00069 0.453
MOD_Plk_1 802 808 PF00069 0.479
MOD_Plk_2-3 504 510 PF00069 0.374
MOD_Plk_4 186 192 PF00069 0.301
MOD_Plk_4 410 416 PF00069 0.350
MOD_Plk_4 504 510 PF00069 0.428
MOD_Plk_4 547 553 PF00069 0.407
MOD_Plk_4 590 596 PF00069 0.516
MOD_Plk_4 609 615 PF00069 0.461
MOD_Plk_4 720 726 PF00069 0.633
MOD_Plk_4 73 79 PF00069 0.325
MOD_ProDKin_1 106 112 PF00069 0.456
MOD_ProDKin_1 249 255 PF00069 0.619
MOD_ProDKin_1 308 314 PF00069 0.393
MOD_ProDKin_1 320 326 PF00069 0.414
MOD_ProDKin_1 336 342 PF00069 0.266
MOD_ProDKin_1 374 380 PF00069 0.630
MOD_ProDKin_1 6 12 PF00069 0.430
MOD_ProDKin_1 89 95 PF00069 0.773
TRG_DiLeu_BaEn_1 504 509 PF01217 0.364
TRG_DiLeu_LyEn_5 480 485 PF01217 0.523
TRG_ENDOCYTIC_2 282 285 PF00928 0.456
TRG_ENDOCYTIC_2 422 425 PF00928 0.406
TRG_ENDOCYTIC_2 505 508 PF00928 0.378
TRG_ENDOCYTIC_2 605 608 PF00928 0.502
TRG_ENDOCYTIC_2 668 671 PF00928 0.550
TRG_ER_diArg_1 614 616 PF00400 0.681
TRG_ER_diArg_1 774 776 PF00400 0.606
TRG_ER_diArg_1 810 813 PF00400 0.555
TRG_NES_CRM1_1 460 472 PF08389 0.297
TRG_NLS_MonoExtC_3 132 137 PF00514 0.614
TRG_NLS_MonoExtN_4 133 138 PF00514 0.612
TRG_Pf-PMV_PEXEL_1 419 424 PF00026 0.279

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6V8 Leptomonas seymouri 46% 95%
A0A0S4JDA4 Bodo saltans 28% 100%
A0A3S5H5P2 Leishmania donovani 73% 100%
A4HSR9 Leishmania infantum 73% 100%
E9AKQ6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
Q4QJ51 Leishmania major 73% 98%
V5B5S6 Trypanosoma cruzi 29% 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