LeishMANIAdb
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FSA_C domain-containing protein

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

Quick info

Protein:
FSA_C domain-containing protein
Gene product:
hypothetical protein - conserved
Species:
Leishmania infantum
UniProt:
A4HST0_LEIIN
TriTrypDb:
LINF_060009200
Length:
907

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
Could not find GO cellular_component term for this entry.

Phosphorylation

Amastigote: 252

Expansion

Sequence features

A4HST0
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HST0

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 115 119 PF00656 0.483
CLV_C14_Caspase3-7 611 615 PF00656 0.674
CLV_C14_Caspase3-7 775 779 PF00656 0.551
CLV_NRD_NRD_1 11 13 PF00675 0.487
CLV_NRD_NRD_1 400 402 PF00675 0.694
CLV_NRD_NRD_1 642 644 PF00675 0.634
CLV_NRD_NRD_1 838 840 PF00675 0.580
CLV_PCSK_KEX2_1 11 13 PF00082 0.559
CLV_PCSK_KEX2_1 221 223 PF00082 0.437
CLV_PCSK_KEX2_1 402 404 PF00082 0.694
CLV_PCSK_KEX2_1 838 840 PF00082 0.580
CLV_PCSK_PC1ET2_1 221 223 PF00082 0.508
CLV_PCSK_PC1ET2_1 402 404 PF00082 0.704
CLV_PCSK_PC7_1 834 840 PF00082 0.559
CLV_PCSK_SKI1_1 142 146 PF00082 0.480
CLV_PCSK_SKI1_1 308 312 PF00082 0.476
CLV_PCSK_SKI1_1 356 360 PF00082 0.491
CLV_PCSK_SKI1_1 383 387 PF00082 0.674
CLV_PCSK_SKI1_1 441 445 PF00082 0.461
CLV_PCSK_SKI1_1 839 843 PF00082 0.529
CLV_PCSK_SKI1_1 860 864 PF00082 0.579
CLV_PCSK_SKI1_1 93 97 PF00082 0.470
DEG_APCC_DBOX_1 355 363 PF00400 0.469
DEG_APCC_DBOX_1 520 528 PF00400 0.572
DEG_SCF_TRCP1_1 481 487 PF00400 0.669
DEG_SPOP_SBC_1 699 703 PF00917 0.714
DOC_CKS1_1 227 232 PF01111 0.499
DOC_CKS1_1 690 695 PF01111 0.666
DOC_CYCLIN_RxL_1 139 148 PF00134 0.571
DOC_CYCLIN_RxL_1 353 360 PF00134 0.536
DOC_CYCLIN_RxL_1 62 74 PF00134 0.450
DOC_CYCLIN_yCln2_LP_2 210 216 PF00134 0.589
DOC_CYCLIN_yCln2_LP_2 633 639 PF00134 0.599
DOC_CYCLIN_yCln2_LP_2 69 75 PF00134 0.550
DOC_MAPK_gen_1 221 227 PF00069 0.424
DOC_MAPK_JIP1_4 747 753 PF00069 0.525
DOC_MAPK_MEF2A_6 116 125 PF00069 0.523
DOC_MAPK_MEF2A_6 547 555 PF00069 0.589
DOC_MAPK_MEF2A_6 896 904 PF00069 0.693
DOC_PP1_RVXF_1 365 371 PF00149 0.497
DOC_PP2B_LxvP_1 133 136 PF13499 0.547
DOC_PP2B_LxvP_1 311 314 PF13499 0.621
DOC_PP2B_LxvP_1 69 72 PF13499 0.540
DOC_SPAK_OSR1_1 347 351 PF12202 0.558
DOC_USP7_MATH_1 134 138 PF00917 0.464
DOC_USP7_MATH_1 36 40 PF00917 0.589
DOC_USP7_MATH_1 512 516 PF00917 0.548
DOC_USP7_MATH_1 642 646 PF00917 0.640
DOC_USP7_MATH_1 699 703 PF00917 0.788
DOC_USP7_MATH_1 75 79 PF00917 0.599
DOC_USP7_MATH_1 786 790 PF00917 0.780
DOC_WW_Pin1_4 226 231 PF00397 0.470
DOC_WW_Pin1_4 378 383 PF00397 0.588
DOC_WW_Pin1_4 484 489 PF00397 0.782
DOC_WW_Pin1_4 490 495 PF00397 0.785
DOC_WW_Pin1_4 558 563 PF00397 0.548
DOC_WW_Pin1_4 603 608 PF00397 0.641
DOC_WW_Pin1_4 677 682 PF00397 0.687
DOC_WW_Pin1_4 689 694 PF00397 0.576
LIG_14-3-3_CanoR_1 403 410 PF00244 0.779
LIG_14-3-3_CanoR_1 441 450 PF00244 0.525
LIG_14-3-3_CanoR_1 506 516 PF00244 0.525
LIG_14-3-3_CanoR_1 568 572 PF00244 0.534
LIG_14-3-3_CanoR_1 600 606 PF00244 0.560
LIG_14-3-3_CanoR_1 704 709 PF00244 0.667
LIG_14-3-3_CanoR_1 734 743 PF00244 0.709
LIG_14-3-3_CanoR_1 762 767 PF00244 0.493
LIG_14-3-3_CanoR_1 773 777 PF00244 0.692
LIG_14-3-3_CanoR_1 896 904 PF00244 0.704
LIG_APCC_ABBA_1 61 66 PF00400 0.511
LIG_APCC_ABBAyCdc20_2 93 99 PF00400 0.472
LIG_BRCT_BRCA1_1 15 19 PF00533 0.570
LIG_BRCT_BRCA1_1 512 516 PF00533 0.599
LIG_BRCT_BRCA1_1 57 61 PF00533 0.420
LIG_BRCT_BRCA1_1 836 840 PF00533 0.524
LIG_Clathr_ClatBox_1 261 265 PF01394 0.620
LIG_Clathr_ClatBox_1 290 294 PF01394 0.359
LIG_deltaCOP1_diTrp_1 15 23 PF00928 0.554
LIG_FHA_1 130 136 PF00498 0.578
LIG_FHA_1 139 145 PF00498 0.540
LIG_FHA_1 19 25 PF00498 0.546
LIG_FHA_1 227 233 PF00498 0.399
LIG_FHA_1 26 32 PF00498 0.615
LIG_FHA_1 271 277 PF00498 0.638
LIG_FHA_1 315 321 PF00498 0.651
LIG_FHA_1 372 378 PF00498 0.581
LIG_FHA_1 455 461 PF00498 0.511
LIG_FHA_1 661 667 PF00498 0.588
LIG_FHA_1 713 719 PF00498 0.510
LIG_FHA_1 772 778 PF00498 0.633
LIG_FHA_1 814 820 PF00498 0.582
LIG_FHA_2 431 437 PF00498 0.656
LIG_FHA_2 467 473 PF00498 0.569
LIG_FHA_2 611 617 PF00498 0.740
LIG_FHA_2 773 779 PF00498 0.750
LIG_FHA_2 798 804 PF00498 0.807
LIG_FHA_2 864 870 PF00498 0.589
LIG_Integrin_isoDGR_2 365 367 PF01839 0.475
LIG_IRF3_LxIS_1 897 903 PF10401 0.696
LIG_LIR_Apic_2 2 6 PF02991 0.535
LIG_LIR_Gen_1 452 460 PF02991 0.463
LIG_LIR_Gen_1 468 478 PF02991 0.427
LIG_LIR_Gen_1 570 580 PF02991 0.528
LIG_LIR_Gen_1 818 826 PF02991 0.442
LIG_LIR_Gen_1 894 905 PF02991 0.587
LIG_LIR_LC3C_4 714 719 PF02991 0.552
LIG_LIR_Nem_3 277 282 PF02991 0.491
LIG_LIR_Nem_3 433 438 PF02991 0.541
LIG_LIR_Nem_3 452 456 PF02991 0.383
LIG_LIR_Nem_3 468 474 PF02991 0.390
LIG_LIR_Nem_3 570 576 PF02991 0.529
LIG_LIR_Nem_3 58 64 PF02991 0.412
LIG_LIR_Nem_3 765 769 PF02991 0.410
LIG_LIR_Nem_3 818 823 PF02991 0.437
LIG_LIR_Nem_3 866 871 PF02991 0.456
LIG_LIR_Nem_3 894 900 PF02991 0.623
LIG_LYPXL_yS_3 214 217 PF13949 0.449
LIG_NRBOX 256 262 PF00104 0.606
LIG_NRBOX 306 312 PF00104 0.494
LIG_PCNA_yPIPBox_3 247 261 PF02747 0.581
LIG_Pex14_2 19 23 PF04695 0.566
LIG_Pex14_2 470 474 PF04695 0.462
LIG_PTB_Apo_2 861 868 PF02174 0.433
LIG_PTB_Phospho_1 861 867 PF10480 0.436
LIG_SH2_CRK 3 7 PF00017 0.624
LIG_SH2_CRK 760 764 PF00017 0.403
LIG_SH2_NCK_1 340 344 PF00017 0.521
LIG_SH2_STAP1 155 159 PF00017 0.459
LIG_SH2_STAP1 767 771 PF00017 0.470
LIG_SH2_STAT3 546 549 PF00017 0.630
LIG_SH2_STAT5 3 6 PF00017 0.709
LIG_SH2_STAT5 752 755 PF00017 0.445
LIG_SH3_3 210 216 PF00018 0.456
LIG_SH3_3 224 230 PF00018 0.208
LIG_SH3_3 556 562 PF00018 0.564
LIG_SUMO_SIM_anti_2 34 40 PF11976 0.470
LIG_SUMO_SIM_anti_2 376 381 PF11976 0.528
LIG_SUMO_SIM_anti_2 523 529 PF11976 0.535
LIG_SUMO_SIM_anti_2 566 573 PF11976 0.585
LIG_SUMO_SIM_anti_2 662 669 PF11976 0.574
LIG_SUMO_SIM_anti_2 714 720 PF11976 0.518
LIG_SUMO_SIM_par_1 130 137 PF11976 0.470
LIG_SUMO_SIM_par_1 662 669 PF11976 0.574
LIG_TRAF2_1 414 417 PF00917 0.687
LIG_TRFH_1 603 607 PF08558 0.589
LIG_TYR_ITSM 864 871 PF00017 0.535
LIG_WRPW_2 279 282 PF00400 0.471
LIG_WRPW_2 61 64 PF00400 0.548
LIG_WW_1 271 274 PF00397 0.660
LIG_WW_3 5 9 PF00397 0.607
MOD_CDK_SPK_2 378 383 PF00069 0.452
MOD_CK1_1 108 114 PF00069 0.529
MOD_CK1_1 378 384 PF00069 0.599
MOD_CK1_1 442 448 PF00069 0.524
MOD_CK1_1 473 479 PF00069 0.588
MOD_CK1_1 484 490 PF00069 0.725
MOD_CK1_1 493 499 PF00069 0.448
MOD_CK1_1 510 516 PF00069 0.305
MOD_CK1_1 557 563 PF00069 0.576
MOD_CK1_1 564 570 PF00069 0.499
MOD_CK1_1 606 612 PF00069 0.618
MOD_CK1_1 703 709 PF00069 0.683
MOD_CK1_1 711 717 PF00069 0.464
MOD_CK1_1 737 743 PF00069 0.748
MOD_CK1_1 825 831 PF00069 0.477
MOD_CK1_1 895 901 PF00069 0.725
MOD_CK2_1 108 114 PF00069 0.416
MOD_CK2_1 249 255 PF00069 0.704
MOD_CK2_1 354 360 PF00069 0.571
MOD_CK2_1 411 417 PF00069 0.758
MOD_CK2_1 430 436 PF00069 0.655
MOD_CK2_1 46 52 PF00069 0.504
MOD_CK2_1 466 472 PF00069 0.461
MOD_CK2_1 610 616 PF00069 0.739
MOD_CK2_1 642 648 PF00069 0.645
MOD_CK2_1 662 668 PF00069 0.606
MOD_CK2_1 786 792 PF00069 0.736
MOD_CK2_1 797 803 PF00069 0.680
MOD_CK2_1 825 831 PF00069 0.477
MOD_CK2_1 863 869 PF00069 0.583
MOD_GlcNHglycan 107 110 PF01048 0.546
MOD_GlcNHglycan 147 150 PF01048 0.506
MOD_GlcNHglycan 327 330 PF01048 0.629
MOD_GlcNHglycan 412 416 PF01048 0.816
MOD_GlcNHglycan 441 444 PF01048 0.474
MOD_GlcNHglycan 475 478 PF01048 0.630
MOD_GlcNHglycan 480 484 PF01048 0.663
MOD_GlcNHglycan 509 512 PF01048 0.627
MOD_GlcNHglycan 530 533 PF01048 0.605
MOD_GlcNHglycan 556 559 PF01048 0.559
MOD_GlcNHglycan 610 613 PF01048 0.629
MOD_GlcNHglycan 644 647 PF01048 0.642
MOD_GlcNHglycan 73 76 PF01048 0.648
MOD_GlcNHglycan 824 827 PF01048 0.486
MOD_GSK3_1 134 141 PF00069 0.575
MOD_GSK3_1 270 277 PF00069 0.591
MOD_GSK3_1 37 44 PF00069 0.588
MOD_GSK3_1 371 378 PF00069 0.579
MOD_GSK3_1 454 461 PF00069 0.584
MOD_GSK3_1 466 473 PF00069 0.464
MOD_GSK3_1 486 493 PF00069 0.614
MOD_GSK3_1 506 513 PF00069 0.638
MOD_GSK3_1 554 561 PF00069 0.567
MOD_GSK3_1 563 570 PF00069 0.506
MOD_GSK3_1 606 613 PF00069 0.717
MOD_GSK3_1 699 706 PF00069 0.733
MOD_GSK3_1 708 715 PF00069 0.623
MOD_GSK3_1 71 78 PF00069 0.543
MOD_GSK3_1 733 740 PF00069 0.641
MOD_GSK3_1 888 895 PF00069 0.752
MOD_LATS_1 245 251 PF00433 0.714
MOD_N-GLC_1 282 287 PF02516 0.471
MOD_N-GLC_1 422 427 PF02516 0.736
MOD_N-GLC_1 430 435 PF02516 0.687
MOD_N-GLC_1 863 868 PF02516 0.595
MOD_NEK2_1 105 110 PF00069 0.285
MOD_NEK2_1 127 132 PF00069 0.583
MOD_NEK2_1 145 150 PF00069 0.350
MOD_NEK2_1 157 162 PF00069 0.286
MOD_NEK2_1 199 204 PF00069 0.554
MOD_NEK2_1 232 237 PF00069 0.438
MOD_NEK2_1 324 329 PF00069 0.677
MOD_NEK2_1 439 444 PF00069 0.429
MOD_NEK2_1 526 531 PF00069 0.504
MOD_NEK2_1 56 61 PF00069 0.423
MOD_NEK2_1 585 590 PF00069 0.444
MOD_NEK2_1 88 93 PF00069 0.428
MOD_NEK2_1 900 905 PF00069 0.583
MOD_NEK2_2 535 540 PF00069 0.506
MOD_PIKK_1 134 140 PF00454 0.532
MOD_PIKK_1 249 255 PF00454 0.690
MOD_PIKK_1 37 43 PF00454 0.484
MOD_PIKK_1 735 741 PF00454 0.763
MOD_PIKK_1 844 850 PF00454 0.583
MOD_PIKK_1 874 880 PF00454 0.586
MOD_PKA_2 567 573 PF00069 0.534
MOD_PKA_2 642 648 PF00069 0.606
MOD_PKA_2 703 709 PF00069 0.676
MOD_PKA_2 733 739 PF00069 0.677
MOD_PKA_2 772 778 PF00069 0.652
MOD_PKA_2 895 901 PF00069 0.729
MOD_PKB_1 401 409 PF00069 0.743
MOD_PKB_1 858 866 PF00069 0.587
MOD_Plk_1 274 280 PF00069 0.634
MOD_Plk_1 282 288 PF00069 0.500
MOD_Plk_1 375 381 PF00069 0.562
MOD_Plk_1 422 428 PF00069 0.685
MOD_Plk_1 451 457 PF00069 0.469
MOD_Plk_1 465 471 PF00069 0.449
MOD_Plk_1 711 717 PF00069 0.565
MOD_Plk_1 863 869 PF00069 0.541
MOD_Plk_1 892 898 PF00069 0.718
MOD_Plk_2-3 466 472 PF00069 0.491
MOD_Plk_2-3 662 668 PF00069 0.606
MOD_Plk_2-3 888 894 PF00069 0.690
MOD_Plk_4 375 381 PF00069 0.519
MOD_Plk_4 466 472 PF00069 0.429
MOD_Plk_4 512 518 PF00069 0.607
MOD_Plk_4 567 573 PF00069 0.519
MOD_Plk_4 585 591 PF00069 0.309
MOD_Plk_4 662 668 PF00069 0.601
MOD_Plk_4 712 718 PF00069 0.487
MOD_Plk_4 762 768 PF00069 0.449
MOD_Plk_4 772 778 PF00069 0.645
MOD_Plk_4 815 821 PF00069 0.523
MOD_ProDKin_1 226 232 PF00069 0.473
MOD_ProDKin_1 378 384 PF00069 0.599
MOD_ProDKin_1 484 490 PF00069 0.783
MOD_ProDKin_1 558 564 PF00069 0.549
MOD_ProDKin_1 603 609 PF00069 0.657
MOD_ProDKin_1 677 683 PF00069 0.677
MOD_ProDKin_1 689 695 PF00069 0.588
MOD_SUMO_for_1 149 152 PF00179 0.417
MOD_SUMO_for_1 19 22 PF00179 0.596
MOD_SUMO_for_1 262 265 PF00179 0.668
TRG_DiLeu_BaEn_1 52 57 PF01217 0.501
TRG_DiLeu_BaEn_1 616 621 PF01217 0.608
TRG_DiLeu_BaEn_1 831 836 PF01217 0.454
TRG_DiLeu_BaLyEn_6 166 171 PF01217 0.599
TRG_DiLeu_BaLyEn_6 445 450 PF01217 0.479
TRG_DiLeu_LyEn_5 831 836 PF01217 0.454
TRG_ENDOCYTIC_2 214 217 PF00928 0.449
TRG_ENDOCYTIC_2 760 763 PF00928 0.404
TRG_ENDOCYTIC_2 868 871 PF00928 0.450
TRG_ER_diArg_1 10 12 PF00400 0.576
TRG_ER_diArg_1 123 126 PF00400 0.475
TRG_ER_diArg_1 367 370 PF00400 0.596
TRG_ER_diArg_1 400 403 PF00400 0.729
TRG_ER_diArg_1 838 840 PF00400 0.580
TRG_ER_diArg_1 857 860 PF00400 0.553
TRG_NLS_MonoExtC_3 400 405 PF00514 0.727
TRG_NLS_MonoExtN_4 401 406 PF00514 0.760
TRG_Pf-PMV_PEXEL_1 11 15 PF00026 0.478
TRG_Pf-PMV_PEXEL_1 356 360 PF00026 0.479
TRG_Pf-PMV_PEXEL_1 448 452 PF00026 0.496

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6G5 Leptomonas seymouri 43% 100%
A0A1X0NMA5 Trypanosomatidae 31% 100%
A0A3S5H5Q0 Leishmania donovani 99% 100%
A0A422NGV5 Trypanosoma rangeli 32% 100%
A4H4K4 Leishmania braziliensis 81% 100%
C9ZTD6 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 31% 100%
E9AKR7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 90% 100%
Q4QJ40 Leishmania major 93% 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