LeishMANIAdb
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FYVE-type domain-containing protein

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

Quick info

Protein:
FYVE-type domain-containing protein
Gene product:
3',5'-cyclic nucleotide phosphodiesterase, putative
Species:
Leishmania major
UniProt:
E9AED0_LEIMA
TriTrypDb:
LmjF.29.2680 , LMJLV39_290035100 * , LMJSD75_290035400 *
Length:
1084

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: 6
NetGPI no yes: 0, no: 6
Cellular components
Term Name Level Count
GO:0005737 cytoplasm 2 2
GO:0110165 cellular anatomical entity 1 2

Expansion

Sequence features

E9AED0
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AED0

Function

Biological processes
Term Name Level Count
GO:0007165 signal transduction 2 7
GO:0009987 cellular process 1 7
GO:0050789 regulation of biological process 2 7
GO:0050794 regulation of cellular process 3 7
GO:0065007 biological regulation 1 7
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 7
GO:0004112 cyclic-nucleotide phosphodiesterase activity 6 7
GO:0004114 3',5'-cyclic-nucleotide phosphodiesterase activity 7 7
GO:0005488 binding 1 7
GO:0008081 phosphoric diester hydrolase activity 5 7
GO:0016787 hydrolase activity 2 7
GO:0016788 hydrolase activity, acting on ester bonds 3 7
GO:0042578 phosphoric ester hydrolase activity 4 7
GO:0043167 ion binding 2 7
GO:0043169 cation binding 3 7
GO:0046872 metal ion binding 4 7

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 131 135 PF00656 0.461
CLV_MEL_PAP_1 571 577 PF00089 0.338
CLV_NRD_NRD_1 1008 1010 PF00675 0.508
CLV_NRD_NRD_1 187 189 PF00675 0.471
CLV_NRD_NRD_1 231 233 PF00675 0.515
CLV_NRD_NRD_1 69 71 PF00675 0.330
CLV_NRD_NRD_1 778 780 PF00675 0.231
CLV_NRD_NRD_1 894 896 PF00675 0.530
CLV_NRD_NRD_1 971 973 PF00675 0.497
CLV_PCSK_FUR_1 1006 1010 PF00082 0.449
CLV_PCSK_KEX2_1 1006 1008 PF00082 0.519
CLV_PCSK_KEX2_1 187 189 PF00082 0.471
CLV_PCSK_KEX2_1 26 28 PF00082 0.295
CLV_PCSK_KEX2_1 643 645 PF00082 0.295
CLV_PCSK_KEX2_1 971 973 PF00082 0.527
CLV_PCSK_PC1ET2_1 26 28 PF00082 0.295
CLV_PCSK_PC1ET2_1 643 645 PF00082 0.295
CLV_PCSK_SKI1_1 1008 1012 PF00082 0.508
CLV_PCSK_SKI1_1 1066 1070 PF00082 0.499
CLV_PCSK_SKI1_1 187 191 PF00082 0.439
CLV_PCSK_SKI1_1 26 30 PF00082 0.309
CLV_PCSK_SKI1_1 264 268 PF00082 0.546
CLV_PCSK_SKI1_1 379 383 PF00082 0.475
CLV_PCSK_SKI1_1 439 443 PF00082 0.415
CLV_PCSK_SKI1_1 450 454 PF00082 0.397
CLV_PCSK_SKI1_1 488 492 PF00082 0.453
CLV_PCSK_SKI1_1 773 777 PF00082 0.231
CLV_PCSK_SKI1_1 869 873 PF00082 0.629
CLV_PCSK_SKI1_1 899 903 PF00082 0.546
CLV_PCSK_SKI1_1 909 913 PF00082 0.484
CLV_Separin_Metazoa 419 423 PF03568 0.476
CLV_Separin_Metazoa 954 958 PF03568 0.487
DEG_APCC_DBOX_1 455 463 PF00400 0.458
DEG_APCC_DBOX_1 487 495 PF00400 0.457
DEG_APCC_DBOX_1 778 786 PF00400 0.231
DEG_APCC_KENBOX_2 33 37 PF00400 0.295
DEG_SCF_FBW7_2 946 952 PF00400 0.497
DEG_SPOP_SBC_1 100 104 PF00917 0.526
DOC_CDC14_PxL_1 546 554 PF14671 0.406
DOC_CKS1_1 694 699 PF01111 0.348
DOC_CKS1_1 946 951 PF01111 0.502
DOC_CYCLIN_RxL_1 795 806 PF00134 0.309
DOC_MAPK_DCC_7 544 554 PF00069 0.377
DOC_MAPK_gen_1 920 929 PF00069 0.479
DOC_MAPK_HePTP_8 571 583 PF00069 0.382
DOC_MAPK_MEF2A_6 488 495 PF00069 0.502
DOC_MAPK_MEF2A_6 574 583 PF00069 0.381
DOC_MAPK_MEF2A_6 755 763 PF00069 0.348
DOC_PP1_RVXF_1 642 649 PF00149 0.348
DOC_PP4_FxxP_1 823 826 PF00568 0.295
DOC_PP4_FxxP_1 862 865 PF00568 0.426
DOC_USP7_MATH_1 142 146 PF00917 0.548
DOC_USP7_MATH_1 22 26 PF00917 0.251
DOC_USP7_MATH_1 251 255 PF00917 0.455
DOC_USP7_MATH_1 503 507 PF00917 0.730
DOC_USP7_MATH_1 658 662 PF00917 0.348
DOC_USP7_MATH_1 804 808 PF00917 0.348
DOC_USP7_UBL2_3 149 153 PF12436 0.409
DOC_WW_Pin1_4 1058 1063 PF00397 0.598
DOC_WW_Pin1_4 693 698 PF00397 0.503
DOC_WW_Pin1_4 800 805 PF00397 0.472
DOC_WW_Pin1_4 837 842 PF00397 0.295
DOC_WW_Pin1_4 935 940 PF00397 0.532
DOC_WW_Pin1_4 945 950 PF00397 0.537
LIG_14-3-3_CanoR_1 27 31 PF00244 0.295
LIG_14-3-3_CanoR_1 450 459 PF00244 0.402
LIG_14-3-3_CanoR_1 589 593 PF00244 0.414
LIG_14-3-3_CanoR_1 729 734 PF00244 0.348
LIG_14-3-3_CanoR_1 773 778 PF00244 0.386
LIG_14-3-3_CanoR_1 808 813 PF00244 0.348
LIG_14-3-3_CanoR_1 843 849 PF00244 0.389
LIG_14-3-3_CanoR_1 869 874 PF00244 0.576
LIG_14-3-3_CanoR_1 992 1000 PF00244 0.559
LIG_Actin_WH2_2 235 251 PF00022 0.460
LIG_Actin_WH2_2 437 452 PF00022 0.384
LIG_APCC_ABBA_1 583 588 PF00400 0.415
LIG_BIR_II_1 1 5 PF00653 0.533
LIG_BRCT_BRCA1_1 24 28 PF00533 0.251
LIG_BRCT_BRCA1_1 660 664 PF00533 0.348
LIG_BRCT_BRCA1_2 660 666 PF00533 0.309
LIG_CaM_NSCaTE_8 483 490 PF13499 0.503
LIG_deltaCOP1_diTrp_1 553 557 PF00928 0.376
LIG_DLG_GKlike_1 808 816 PF00625 0.348
LIG_FHA_1 1076 1082 PF00498 0.565
LIG_FHA_1 265 271 PF00498 0.543
LIG_FHA_1 318 324 PF00498 0.495
LIG_FHA_1 400 406 PF00498 0.537
LIG_FHA_1 694 700 PF00498 0.457
LIG_FHA_1 707 713 PF00498 0.278
LIG_FHA_1 910 916 PF00498 0.497
LIG_FHA_1 945 951 PF00498 0.713
LIG_FHA_1 978 984 PF00498 0.576
LIG_FHA_2 101 107 PF00498 0.478
LIG_FHA_2 291 297 PF00498 0.409
LIG_FHA_2 356 362 PF00498 0.482
LIG_FHA_2 405 411 PF00498 0.487
LIG_FHA_2 470 476 PF00498 0.421
LIG_FHA_2 526 532 PF00498 0.458
LIG_FHA_2 557 563 PF00498 0.362
LIG_FHA_2 637 643 PF00498 0.295
LIG_FHA_2 88 94 PF00498 0.602
LIG_FHA_2 946 952 PF00498 0.497
LIG_GBD_Chelix_1 989 997 PF00786 0.559
LIG_LIR_Apic_2 522 527 PF02991 0.443
LIG_LIR_Apic_2 735 740 PF02991 0.348
LIG_LIR_Apic_2 821 826 PF02991 0.295
LIG_LIR_Apic_2 859 865 PF02991 0.489
LIG_LIR_Gen_1 219 227 PF02991 0.476
LIG_LIR_Gen_1 25 33 PF02991 0.251
LIG_LIR_Gen_1 556 563 PF02991 0.433
LIG_LIR_Gen_1 689 699 PF02991 0.295
LIG_LIR_Nem_3 219 223 PF02991 0.478
LIG_LIR_Nem_3 25 31 PF02991 0.251
LIG_LIR_Nem_3 532 538 PF02991 0.465
LIG_LIR_Nem_3 556 560 PF02991 0.490
LIG_LIR_Nem_3 670 676 PF02991 0.350
LIG_LIR_Nem_3 689 694 PF02991 0.295
LIG_LIR_Nem_3 713 717 PF02991 0.348
LIG_LYPXL_yS_3 535 538 PF13949 0.411
LIG_MYND_1 632 636 PF01753 0.231
LIG_MYND_3 549 553 PF01753 0.394
LIG_NRBOX 135 141 PF00104 0.431
LIG_OCRL_FandH_1 725 737 PF00620 0.348
LIG_PCNA_yPIPBox_3 127 140 PF02747 0.450
LIG_Pex14_2 819 823 PF04695 0.350
LIG_PTAP_UEV_1 56 61 PF05743 0.309
LIG_Rb_pABgroove_1 822 830 PF01858 0.286
LIG_REV1ctd_RIR_1 28 37 PF16727 0.295
LIG_SH2_CRK 625 629 PF00017 0.286
LIG_SH2_CRK 676 680 PF00017 0.309
LIG_SH2_GRB2like 611 614 PF00017 0.295
LIG_SH2_SRC 473 476 PF00017 0.511
LIG_SH2_STAP1 284 288 PF00017 0.529
LIG_SH2_STAP1 747 751 PF00017 0.348
LIG_SH2_STAT3 330 333 PF00017 0.526
LIG_SH2_STAT5 1038 1041 PF00017 0.622
LIG_SH2_STAT5 673 676 PF00017 0.302
LIG_SH2_STAT5 852 855 PF00017 0.555
LIG_SH3_1 798 804 PF00018 0.348
LIG_SH3_2 57 62 PF14604 0.309
LIG_SH3_3 1044 1050 PF00018 0.591
LIG_SH3_3 2 8 PF00018 0.488
LIG_SH3_3 54 60 PF00018 0.279
LIG_SH3_3 798 804 PF00018 0.295
LIG_SH3_3 943 949 PF00018 0.525
LIG_SUMO_SIM_anti_2 134 141 PF11976 0.424
LIG_SUMO_SIM_anti_2 926 931 PF11976 0.487
LIG_SUMO_SIM_par_1 287 293 PF11976 0.400
LIG_TRAF2_1 114 117 PF00917 0.465
LIG_TRAF2_1 241 244 PF00917 0.507
LIG_TRAF2_1 293 296 PF00917 0.437
LIG_TRAF2_1 416 419 PF00917 0.472
LIG_TRAF2_1 472 475 PF00917 0.515
LIG_TRAF2_1 855 858 PF00917 0.615
LIG_TRAF2_1 982 985 PF00917 0.522
LIG_TYR_ITIM 533 538 PF00017 0.445
LIG_TYR_ITIM 674 679 PF00017 0.402
LIG_UBA3_1 136 143 PF00899 0.431
LIG_UBA3_1 634 643 PF00899 0.295
MOD_CDC14_SPxK_1 840 843 PF00782 0.348
MOD_CDK_SPK_2 935 940 PF00069 0.497
MOD_CDK_SPxK_1 837 843 PF00069 0.348
MOD_CK1_1 1061 1067 PF00069 0.662
MOD_CK1_1 110 116 PF00069 0.470
MOD_CK1_1 160 166 PF00069 0.464
MOD_CK1_1 399 405 PF00069 0.415
MOD_CK1_1 47 53 PF00069 0.459
MOD_CK1_1 506 512 PF00069 0.617
MOD_CK1_1 803 809 PF00069 0.348
MOD_CK1_1 837 843 PF00069 0.328
MOD_CK1_1 876 882 PF00069 0.521
MOD_CK1_1 945 951 PF00069 0.571
MOD_CK1_1 991 997 PF00069 0.506
MOD_CK2_1 100 106 PF00069 0.503
MOD_CK2_1 1069 1075 PF00069 0.572
MOD_CK2_1 110 116 PF00069 0.487
MOD_CK2_1 238 244 PF00069 0.635
MOD_CK2_1 269 275 PF00069 0.551
MOD_CK2_1 290 296 PF00069 0.434
MOD_CK2_1 355 361 PF00069 0.481
MOD_CK2_1 404 410 PF00069 0.489
MOD_CK2_1 469 475 PF00069 0.493
MOD_CK2_1 525 531 PF00069 0.463
MOD_CK2_1 556 562 PF00069 0.419
MOD_CK2_1 636 642 PF00069 0.295
MOD_CK2_1 729 735 PF00069 0.348
MOD_CK2_1 75 81 PF00069 0.462
MOD_CK2_1 879 885 PF00069 0.685
MOD_CMANNOS 480 483 PF00535 0.499
MOD_GlcNHglycan 1071 1074 PF01048 0.509
MOD_GlcNHglycan 1078 1081 PF01048 0.505
MOD_GlcNHglycan 112 115 PF01048 0.460
MOD_GlcNHglycan 159 162 PF01048 0.525
MOD_GlcNHglycan 16 19 PF01048 0.295
MOD_GlcNHglycan 166 169 PF01048 0.513
MOD_GlcNHglycan 197 200 PF01048 0.440
MOD_GlcNHglycan 366 369 PF01048 0.506
MOD_GlcNHglycan 49 52 PF01048 0.295
MOD_GlcNHglycan 505 508 PF01048 0.655
MOD_GlcNHglycan 808 811 PF01048 0.299
MOD_GSK3_1 1033 1040 PF00069 0.643
MOD_GSK3_1 160 167 PF00069 0.455
MOD_GSK3_1 22 29 PF00069 0.303
MOD_GSK3_1 243 250 PF00069 0.476
MOD_GSK3_1 252 259 PF00069 0.444
MOD_GSK3_1 290 297 PF00069 0.584
MOD_GSK3_1 396 403 PF00069 0.504
MOD_GSK3_1 43 50 PF00069 0.397
MOD_GSK3_1 502 509 PF00069 0.723
MOD_GSK3_1 51 58 PF00069 0.295
MOD_GSK3_1 665 672 PF00069 0.280
MOD_GSK3_1 800 807 PF00069 0.348
MOD_GSK3_1 869 876 PF00069 0.796
MOD_N-GLC_1 132 137 PF02516 0.441
MOD_NEK2_1 154 159 PF00069 0.461
MOD_NEK2_1 252 257 PF00069 0.495
MOD_NEK2_1 363 368 PF00069 0.509
MOD_NEK2_1 43 48 PF00069 0.295
MOD_NEK2_1 466 471 PF00069 0.545
MOD_NEK2_1 598 603 PF00069 0.373
MOD_NEK2_1 627 632 PF00069 0.374
MOD_NEK2_1 669 674 PF00069 0.276
MOD_NEK2_1 699 704 PF00069 0.295
MOD_NEK2_1 856 861 PF00069 0.444
MOD_NEK2_2 51 56 PF00069 0.270
MOD_PIKK_1 404 410 PF00454 0.528
MOD_PIKK_1 75 81 PF00454 0.504
MOD_PIKK_1 869 875 PF00454 0.581
MOD_PIKK_1 87 93 PF00454 0.499
MOD_PKA_1 26 32 PF00069 0.295
MOD_PKA_2 26 32 PF00069 0.295
MOD_PKA_2 588 594 PF00069 0.411
MOD_PKA_2 75 81 PF00069 0.457
MOD_PKA_2 985 991 PF00069 0.556
MOD_Plk_1 132 138 PF00069 0.444
MOD_Plk_1 294 300 PF00069 0.533
MOD_Plk_1 587 593 PF00069 0.306
MOD_Plk_1 669 675 PF00069 0.289
MOD_Plk_2-3 132 138 PF00069 0.459
MOD_Plk_2-3 181 187 PF00069 0.408
MOD_Plk_2-3 219 225 PF00069 0.478
MOD_Plk_2-3 355 361 PF00069 0.481
MOD_Plk_2-3 556 562 PF00069 0.419
MOD_Plk_2-3 743 749 PF00069 0.348
MOD_Plk_4 132 138 PF00069 0.444
MOD_Plk_4 51 57 PF00069 0.286
MOD_Plk_4 525 531 PF00069 0.485
MOD_Plk_4 669 675 PF00069 0.276
MOD_Plk_4 722 728 PF00069 0.295
MOD_Plk_4 729 735 PF00069 0.295
MOD_Plk_4 757 763 PF00069 0.308
MOD_ProDKin_1 1058 1064 PF00069 0.594
MOD_ProDKin_1 693 699 PF00069 0.503
MOD_ProDKin_1 800 806 PF00069 0.472
MOD_ProDKin_1 837 843 PF00069 0.295
MOD_ProDKin_1 935 941 PF00069 0.535
MOD_ProDKin_1 945 951 PF00069 0.529
MOD_SUMO_for_1 1068 1071 PF00179 0.590
MOD_SUMO_for_1 178 181 PF00179 0.484
MOD_SUMO_for_1 216 219 PF00179 0.518
MOD_SUMO_for_1 227 230 PF00179 0.425
MOD_SUMO_for_1 393 396 PF00179 0.521
MOD_SUMO_rev_2 104 113 PF00179 0.526
MOD_SUMO_rev_2 174 184 PF00179 0.466
MOD_SUMO_rev_2 219 227 PF00179 0.398
MOD_SUMO_rev_2 738 746 PF00179 0.348
TRG_DiLeu_BaEn_1 132 137 PF01217 0.432
TRG_DiLeu_BaEn_1 436 441 PF01217 0.488
TRG_DiLeu_BaEn_1 568 573 PF01217 0.440
TRG_DiLeu_BaEn_1 713 718 PF01217 0.348
TRG_DiLeu_BaEn_4 243 249 PF01217 0.458
TRG_DiLeu_BaEn_4 307 313 PF01217 0.452
TRG_ENDOCYTIC_2 535 538 PF00928 0.465
TRG_ENDOCYTIC_2 625 628 PF00928 0.295
TRG_ENDOCYTIC_2 676 679 PF00928 0.441
TRG_ER_diArg_1 1006 1009 PF00400 0.530
TRG_ER_diArg_1 187 189 PF00400 0.471
TRG_ER_diArg_1 971 973 PF00400 0.527
TRG_NES_CRM1_1 816 829 PF08389 0.286
TRG_Pf-PMV_PEXEL_1 127 131 PF00026 0.488
TRG_Pf-PMV_PEXEL_1 187 191 PF00026 0.622
TRG_Pf-PMV_PEXEL_1 739 743 PF00026 0.295
TRG_Pf-PMV_PEXEL_1 920 924 PF00026 0.499

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I536 Leptomonas seymouri 42% 90%
A0A3S7X2S6 Leishmania donovani 90% 100%
A4HHS5 Leishmania braziliensis 73% 100%
A4I4X6 Leishmania infantum 90% 100%
E9ALF6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 87% 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