LeishMANIAdb
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EF-hand domain-containing protein

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

Quick info

Protein:
EF-hand domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania braziliensis
UniProt:
A4HCE3_LEIBR
TriTrypDb:
LbrM.22.0820 , LBRM2903_220013700 *
Length:
868

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: 1, no: 5
NetGPI no yes: 0, no: 6
Cellular components
Term Name Level Count
GO:0032991 protein-containing complex 1 1
GO:0034702 monoatomic ion channel complex 4 1
GO:0034703 cation channel complex 5 1
GO:0034704 calcium channel complex 6 1
GO:0098796 membrane protein complex 2 1
GO:0098798 mitochondrial protein-containing complex 2 1
GO:0098800 inner mitochondrial membrane protein complex 3 1
GO:1902495 transmembrane transporter complex 3 1
GO:1990246 uniplex complex 4 1
GO:1990351 transporter complex 2 1

Expansion

Sequence features

A4HCE3
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HCE3

Function

Biological processes
Term Name Level Count
GO:0006810 transport 3 7
GO:0006811 monoatomic ion transport 4 7
GO:0006812 monoatomic cation transport 5 7
GO:0006816 calcium ion transport 7 7
GO:0006851 mitochondrial calcium ion transmembrane transport 4 7
GO:0009987 cellular process 1 7
GO:0030001 metal ion transport 6 7
GO:0034220 monoatomic ion transmembrane transport 3 7
GO:0051179 localization 1 7
GO:0051234 establishment of localization 2 7
GO:0055085 transmembrane transport 2 7
GO:0070588 calcium ion transmembrane transport 6 7
GO:0098655 monoatomic cation transmembrane transport 4 7
GO:0098660 inorganic ion transmembrane transport 4 7
GO:0098662 inorganic cation transmembrane transport 5 7
GO:1990542 mitochondrial transmembrane transport 3 7
GO:0006873 intracellular monoatomic ion homeostasis 4 1
GO:0006874 intracellular calcium ion homeostasis 7 1
GO:0006875 obsolete intracellular metal ion homeostasis 6 1
GO:0019725 cellular homeostasis 2 1
GO:0030003 intracellular monoatomic cation homeostasis 5 1
GO:0036444 calcium import into the mitochondrion 5 1
GO:0042592 homeostatic process 3 1
GO:0048878 chemical homeostasis 4 1
GO:0050801 monoatomic ion homeostasis 5 1
GO:0051560 mitochondrial calcium ion homeostasis 8 1
GO:0055065 obsolete metal ion homeostasis 7 1
GO:0055074 calcium ion homeostasis 8 1
GO:0055080 monoatomic cation homeostasis 6 1
GO:0055082 intracellular chemical homeostasis 3 1
GO:0065007 biological regulation 1 1
GO:0065008 regulation of biological quality 2 1
GO:0072503 obsolete cellular divalent inorganic cation homeostasis 6 1
GO:0072507 obsolete divalent inorganic cation homeostasis 7 1
GO:0098771 inorganic ion homeostasis 6 1
Molecular functions
Term Name Level Count
GO:0005488 binding 1 7
GO:0005509 calcium ion binding 5 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_Caspase3-7 255 259 PF00656 0.529
CLV_C14_Caspase3-7 331 335 PF00656 0.359
CLV_C14_Caspase3-7 821 825 PF00656 0.621
CLV_NRD_NRD_1 273 275 PF00675 0.474
CLV_NRD_NRD_1 440 442 PF00675 0.720
CLV_NRD_NRD_1 484 486 PF00675 0.611
CLV_NRD_NRD_1 5 7 PF00675 0.625
CLV_NRD_NRD_1 620 622 PF00675 0.520
CLV_PCSK_KEX2_1 173 175 PF00082 0.501
CLV_PCSK_KEX2_1 272 274 PF00082 0.501
CLV_PCSK_KEX2_1 440 442 PF00082 0.720
CLV_PCSK_KEX2_1 5 7 PF00082 0.625
CLV_PCSK_KEX2_1 620 622 PF00082 0.520
CLV_PCSK_KEX2_1 853 855 PF00082 0.683
CLV_PCSK_PC1ET2_1 173 175 PF00082 0.501
CLV_PCSK_PC1ET2_1 853 855 PF00082 0.683
CLV_PCSK_PC7_1 268 274 PF00082 0.453
CLV_PCSK_SKI1_1 143 147 PF00082 0.542
CLV_PCSK_SKI1_1 154 158 PF00082 0.532
CLV_PCSK_SKI1_1 211 215 PF00082 0.454
CLV_PCSK_SKI1_1 463 467 PF00082 0.466
CLV_PCSK_SKI1_1 486 490 PF00082 0.602
CLV_PCSK_SKI1_1 5 9 PF00082 0.691
CLV_PCSK_SKI1_1 620 624 PF00082 0.495
CLV_PCSK_SKI1_1 811 815 PF00082 0.595
CLV_Separin_Metazoa 460 464 PF03568 0.553
CLV_Separin_Metazoa 684 688 PF03568 0.433
DEG_APCC_DBOX_1 594 602 PF00400 0.441
DEG_SCF_FBW7_1 316 322 PF00400 0.525
DEG_SCF_FBW7_1 400 407 PF00400 0.557
DEG_SCF_FBW7_1 527 533 PF00400 0.720
DEG_SPOP_SBC_1 390 394 PF00917 0.575
DEG_SPOP_SBC_1 493 497 PF00917 0.652
DOC_CKS1_1 316 321 PF01111 0.584
DOC_CKS1_1 401 406 PF01111 0.675
DOC_CKS1_1 527 532 PF01111 0.719
DOC_CYCLIN_RxL_1 3 12 PF00134 0.539
DOC_CYCLIN_RxL_1 808 816 PF00134 0.564
DOC_CYCLIN_yCln2_LP_2 461 467 PF00134 0.577
DOC_MAPK_gen_1 272 281 PF00069 0.390
DOC_MAPK_MEF2A_6 662 671 PF00069 0.529
DOC_MAPK_MEF2A_6 795 802 PF00069 0.345
DOC_PP1_RVXF_1 597 604 PF00149 0.439
DOC_PP1_RVXF_1 747 753 PF00149 0.527
DOC_PP2B_LxvP_1 214 217 PF13499 0.480
DOC_PP2B_LxvP_1 24 27 PF13499 0.525
DOC_PP2B_LxvP_1 279 282 PF13499 0.347
DOC_PP4_FxxP_1 849 852 PF00568 0.616
DOC_USP7_MATH_1 127 131 PF00917 0.734
DOC_USP7_MATH_1 16 20 PF00917 0.706
DOC_USP7_MATH_1 264 268 PF00917 0.427
DOC_USP7_MATH_1 362 366 PF00917 0.615
DOC_USP7_MATH_1 377 381 PF00917 0.716
DOC_USP7_MATH_1 382 386 PF00917 0.667
DOC_USP7_MATH_1 404 408 PF00917 0.583
DOC_USP7_MATH_1 420 424 PF00917 0.681
DOC_USP7_MATH_1 425 429 PF00917 0.742
DOC_USP7_MATH_1 493 497 PF00917 0.637
DOC_USP7_MATH_1 530 534 PF00917 0.760
DOC_USP7_MATH_1 547 551 PF00917 0.534
DOC_USP7_MATH_1 553 557 PF00917 0.634
DOC_USP7_MATH_1 561 565 PF00917 0.509
DOC_USP7_MATH_1 736 740 PF00917 0.600
DOC_USP7_MATH_1 809 813 PF00917 0.553
DOC_USP7_MATH_1 9 13 PF00917 0.576
DOC_WW_Pin1_4 123 128 PF00397 0.761
DOC_WW_Pin1_4 27 32 PF00397 0.728
DOC_WW_Pin1_4 315 320 PF00397 0.574
DOC_WW_Pin1_4 375 380 PF00397 0.799
DOC_WW_Pin1_4 384 389 PF00397 0.673
DOC_WW_Pin1_4 396 401 PF00397 0.629
DOC_WW_Pin1_4 406 411 PF00397 0.745
DOC_WW_Pin1_4 526 531 PF00397 0.758
DOC_WW_Pin1_4 824 829 PF00397 0.491
LIG_14-3-3_CanoR_1 143 152 PF00244 0.618
LIG_14-3-3_CanoR_1 272 278 PF00244 0.566
LIG_14-3-3_CanoR_1 565 572 PF00244 0.574
LIG_14-3-3_CanoR_1 713 723 PF00244 0.665
LIG_14-3-3_CanoR_1 749 753 PF00244 0.525
LIG_14-3-3_CanoR_1 795 801 PF00244 0.550
LIG_Actin_WH2_2 584 601 PF00022 0.440
LIG_Actin_WH2_2 671 689 PF00022 0.617
LIG_Actin_WH2_2 700 715 PF00022 0.552
LIG_BIR_III_2 676 680 PF00653 0.611
LIG_BIR_III_2 726 730 PF00653 0.533
LIG_BRCT_BRCA1_1 245 249 PF00533 0.819
LIG_CSL_BTD_1 527 530 PF09270 0.619
LIG_deltaCOP1_diTrp_1 340 343 PF00928 0.562
LIG_deltaCOP1_diTrp_1 509 516 PF00928 0.453
LIG_FHA_1 197 203 PF00498 0.482
LIG_FHA_1 347 353 PF00498 0.561
LIG_FHA_1 434 440 PF00498 0.599
LIG_FHA_1 496 502 PF00498 0.515
LIG_FHA_1 543 549 PF00498 0.721
LIG_FHA_1 609 615 PF00498 0.584
LIG_FHA_1 698 704 PF00498 0.542
LIG_FHA_1 76 82 PF00498 0.682
LIG_FHA_1 94 100 PF00498 0.384
LIG_FHA_2 116 122 PF00498 0.697
LIG_FHA_2 144 150 PF00498 0.685
LIG_FHA_2 155 161 PF00498 0.759
LIG_FHA_2 253 259 PF00498 0.567
LIG_FHA_2 479 485 PF00498 0.718
LIG_FHA_2 715 721 PF00498 0.427
LIG_Integrin_isoDGR_2 335 337 PF01839 0.331
LIG_LIR_Apic_2 398 404 PF02991 0.569
LIG_LIR_Gen_1 20 31 PF02991 0.734
LIG_LIR_Gen_1 308 316 PF02991 0.445
LIG_LIR_Gen_1 340 351 PF02991 0.458
LIG_LIR_Gen_1 542 551 PF02991 0.508
LIG_LIR_Gen_1 583 591 PF02991 0.287
LIG_LIR_Gen_1 653 661 PF02991 0.353
LIG_LIR_Gen_1 789 798 PF02991 0.565
LIG_LIR_Gen_1 830 837 PF02991 0.496
LIG_LIR_Nem_3 187 192 PF02991 0.504
LIG_LIR_Nem_3 20 26 PF02991 0.664
LIG_LIR_Nem_3 308 312 PF02991 0.441
LIG_LIR_Nem_3 324 330 PF02991 0.346
LIG_LIR_Nem_3 340 346 PF02991 0.542
LIG_LIR_Nem_3 525 531 PF02991 0.663
LIG_LIR_Nem_3 542 546 PF02991 0.467
LIG_LIR_Nem_3 583 587 PF02991 0.448
LIG_LIR_Nem_3 650 654 PF02991 0.491
LIG_LIR_Nem_3 789 793 PF02991 0.457
LIG_LIR_Nem_3 812 817 PF02991 0.595
LIG_LIR_Nem_3 830 834 PF02991 0.356
LIG_NRBOX 519 525 PF00104 0.455
LIG_Pex14_2 289 293 PF04695 0.432
LIG_Pex14_2 309 313 PF04695 0.244
LIG_SH2_CRK 401 405 PF00017 0.572
LIG_SH2_CRK 543 547 PF00017 0.505
LIG_SH2_CRK 654 658 PF00017 0.389
LIG_SH2_CRK 85 89 PF00017 0.431
LIG_SH2_STAP1 275 279 PF00017 0.365
LIG_SH2_STAP1 306 310 PF00017 0.432
LIG_SH2_STAP1 360 364 PF00017 0.413
LIG_SH2_STAP1 483 487 PF00017 0.604
LIG_SH2_STAP1 531 535 PF00017 0.507
LIG_SH2_STAP1 584 588 PF00017 0.291
LIG_SH2_STAT3 862 865 PF00017 0.495
LIG_SH2_STAT5 23 26 PF00017 0.632
LIG_SH2_STAT5 593 596 PF00017 0.440
LIG_SH2_STAT5 862 865 PF00017 0.495
LIG_SH3_3 28 34 PF00018 0.598
LIG_SH3_3 524 530 PF00018 0.704
LIG_SH3_3 646 652 PF00018 0.362
LIG_SH3_3 676 682 PF00018 0.505
LIG_SUMO_SIM_anti_2 799 804 PF11976 0.455
LIG_SUMO_SIM_par_1 201 207 PF11976 0.471
LIG_SUMO_SIM_par_1 212 219 PF11976 0.497
LIG_SUMO_SIM_par_1 348 353 PF11976 0.564
LIG_SUMO_SIM_par_1 6 12 PF11976 0.501
LIG_SUMO_SIM_par_1 796 801 PF11976 0.455
LIG_TRAF2_1 145 148 PF00917 0.542
LIG_TRAF2_1 718 721 PF00917 0.538
LIG_WRC_WIRS_1 312 317 PF05994 0.449
LIG_WRC_WIRS_1 584 589 PF05994 0.322
MOD_CDK_SPK_2 400 405 PF00069 0.564
MOD_CK1_1 116 122 PF00069 0.713
MOD_CK1_1 130 136 PF00069 0.659
MOD_CK1_1 163 169 PF00069 0.675
MOD_CK1_1 231 237 PF00069 0.578
MOD_CK1_1 378 384 PF00069 0.699
MOD_CK1_1 423 429 PF00069 0.583
MOD_CK1_1 496 502 PF00069 0.594
MOD_CK1_1 522 528 PF00069 0.515
MOD_CK1_1 554 560 PF00069 0.617
MOD_CK1_1 564 570 PF00069 0.560
MOD_CK1_1 583 589 PF00069 0.514
MOD_CK1_1 644 650 PF00069 0.403
MOD_CK2_1 115 121 PF00069 0.674
MOD_CK2_1 143 149 PF00069 0.660
MOD_CK2_1 154 160 PF00069 0.766
MOD_CK2_1 256 262 PF00069 0.451
MOD_CK2_1 714 720 PF00069 0.422
MOD_CK2_1 736 742 PF00069 0.553
MOD_CK2_1 758 764 PF00069 0.667
MOD_CK2_1 804 810 PF00069 0.503
MOD_CK2_1 824 830 PF00069 0.260
MOD_CMANNOS 513 516 PF00535 0.698
MOD_GlcNHglycan 11 14 PF01048 0.653
MOD_GlcNHglycan 115 118 PF01048 0.593
MOD_GlcNHglycan 163 166 PF01048 0.673
MOD_GlcNHglycan 230 233 PF01048 0.771
MOD_GlcNHglycan 236 239 PF01048 0.716
MOD_GlcNHglycan 364 367 PF01048 0.725
MOD_GlcNHglycan 380 383 PF01048 0.568
MOD_GlcNHglycan 384 387 PF01048 0.702
MOD_GlcNHglycan 425 428 PF01048 0.783
MOD_GlcNHglycan 45 48 PF01048 0.622
MOD_GlcNHglycan 498 501 PF01048 0.584
MOD_GlcNHglycan 509 512 PF01048 0.611
MOD_GlcNHglycan 55 58 PF01048 0.625
MOD_GlcNHglycan 553 556 PF01048 0.564
MOD_GlcNHglycan 643 646 PF01048 0.472
MOD_GlcNHglycan 68 71 PF01048 0.494
MOD_GlcNHglycan 709 712 PF01048 0.420
MOD_GlcNHglycan 760 763 PF01048 0.592
MOD_GSK3_1 112 119 PF00069 0.691
MOD_GSK3_1 123 130 PF00069 0.714
MOD_GSK3_1 156 163 PF00069 0.705
MOD_GSK3_1 228 235 PF00069 0.779
MOD_GSK3_1 249 256 PF00069 0.748
MOD_GSK3_1 264 271 PF00069 0.507
MOD_GSK3_1 311 318 PF00069 0.397
MOD_GSK3_1 377 384 PF00069 0.795
MOD_GSK3_1 388 395 PF00069 0.656
MOD_GSK3_1 396 403 PF00069 0.525
MOD_GSK3_1 425 432 PF00069 0.704
MOD_GSK3_1 451 458 PF00069 0.624
MOD_GSK3_1 492 499 PF00069 0.508
MOD_GSK3_1 522 529 PF00069 0.734
MOD_GSK3_1 547 554 PF00069 0.695
MOD_GSK3_1 608 615 PF00069 0.590
MOD_GSK3_1 730 737 PF00069 0.765
MOD_GSK3_1 820 827 PF00069 0.512
MOD_LATS_1 141 147 PF00433 0.542
MOD_N-GLC_1 130 135 PF02516 0.586
MOD_NEK2_1 298 303 PF00069 0.396
MOD_NEK2_1 346 351 PF00069 0.513
MOD_NEK2_1 641 646 PF00069 0.680
MOD_NEK2_1 8 13 PF00069 0.751
MOD_NEK2_1 837 842 PF00069 0.409
MOD_NEK2_2 516 521 PF00069 0.430
MOD_NEK2_2 809 814 PF00069 0.502
MOD_OFUCOSY 534 539 PF10250 0.759
MOD_PIKK_1 164 170 PF00454 0.711
MOD_PIKK_1 697 703 PF00454 0.639
MOD_PIKK_1 736 742 PF00454 0.806
MOD_PKA_1 273 279 PF00069 0.439
MOD_PKA_2 112 118 PF00069 0.591
MOD_PKA_2 273 279 PF00069 0.439
MOD_PKA_2 404 410 PF00069 0.546
MOD_PKA_2 43 49 PF00069 0.725
MOD_PKA_2 564 570 PF00069 0.585
MOD_PKA_2 661 667 PF00069 0.478
MOD_PKA_2 707 713 PF00069 0.667
MOD_PKA_2 748 754 PF00069 0.524
MOD_PKA_2 783 789 PF00069 0.481
MOD_Plk_1 541 547 PF00069 0.505
MOD_Plk_1 574 580 PF00069 0.594
MOD_Plk_1 601 607 PF00069 0.303
MOD_Plk_1 809 815 PF00069 0.557
MOD_Plk_2-3 451 457 PF00069 0.430
MOD_Plk_4 256 262 PF00069 0.658
MOD_Plk_4 273 279 PF00069 0.524
MOD_Plk_4 346 352 PF00069 0.455
MOD_Plk_4 519 525 PF00069 0.569
MOD_Plk_4 574 580 PF00069 0.559
MOD_Plk_4 583 589 PF00069 0.441
MOD_Plk_4 77 83 PF00069 0.676
MOD_Plk_4 798 804 PF00069 0.364
MOD_Plk_4 837 843 PF00069 0.415
MOD_ProDKin_1 123 129 PF00069 0.760
MOD_ProDKin_1 27 33 PF00069 0.726
MOD_ProDKin_1 315 321 PF00069 0.578
MOD_ProDKin_1 375 381 PF00069 0.801
MOD_ProDKin_1 384 390 PF00069 0.672
MOD_ProDKin_1 396 402 PF00069 0.628
MOD_ProDKin_1 406 412 PF00069 0.745
MOD_ProDKin_1 526 532 PF00069 0.756
MOD_ProDKin_1 824 830 PF00069 0.489
MOD_SUMO_rev_2 480 488 PF00179 0.596
MOD_SUMO_rev_2 761 768 PF00179 0.731
TRG_DiLeu_BaEn_1 148 153 PF01217 0.569
TRG_DiLeu_BaEn_1 342 347 PF01217 0.453
TRG_DiLeu_BaLyEn_6 618 623 PF01217 0.586
TRG_ENDOCYTIC_2 23 26 PF00928 0.786
TRG_ENDOCYTIC_2 275 278 PF00928 0.361
TRG_ENDOCYTIC_2 306 309 PF00928 0.432
TRG_ENDOCYTIC_2 543 546 PF00928 0.511
TRG_ENDOCYTIC_2 584 587 PF00928 0.442
TRG_ENDOCYTIC_2 654 657 PF00928 0.476
TRG_ENDOCYTIC_2 85 88 PF00928 0.433
TRG_ER_diArg_1 272 274 PF00400 0.501
TRG_ER_diArg_1 4 6 PF00400 0.532
TRG_ER_diArg_1 439 441 PF00400 0.579
TRG_ER_diArg_1 620 622 PF00400 0.515
TRG_NES_CRM1_1 321 334 PF08389 0.498
TRG_Pf-PMV_PEXEL_1 621 626 PF00026 0.615
TRG_Pf-PMV_PEXEL_1 639 643 PF00026 0.431
TRG_Pf-PMV_PEXEL_1 766 770 PF00026 0.502
TRG_Pf-PMV_PEXEL_1 811 816 PF00026 0.504
TRG_Pf-PMV_PEXEL_1 97 101 PF00026 0.686

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6M5 Leptomonas seymouri 35% 100%
A0A3S7WX62 Leishmania donovani 63% 98%
A4HZW6 Leishmania infantum 63% 98%
E9AVS4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 62% 100%
Q4QBQ5 Leishmania major 62% 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