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:
Repeat of unknown function (DUF1126), putative
Species:
Leishmania major
UniProt:
Q4QI57_LEIMA
TriTrypDb:
LmjF.08.1120 , LMJLV39_080015200 , LMJSD75_080015300 *
Length:
869

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: 28
NetGPI no yes: 0, no: 29
Cellular components
Term Name Level Count
GO:0005819 spindle 5 4
GO:0005930 axoneme 2 4
GO:0043226 organelle 2 4
GO:0043228 non-membrane-bounded organelle 3 4
GO:0043229 intracellular organelle 3 4
GO:0043232 intracellular non-membrane-bounded organelle 4 4
GO:0072686 mitotic spindle 6 4
GO:0110165 cellular anatomical entity 1 4

Expansion

Sequence features

Q4QI57
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QI57

Function

Biological processes
Term Name Level Count
GO:0000226 microtubule cytoskeleton organization 3 4
GO:0000281 mitotic cytokinesis 4 4
GO:0000910 cytokinesis 3 4
GO:0001539 cilium or flagellum-dependent cell motility 3 4
GO:0006996 organelle organization 4 4
GO:0007010 cytoskeleton organization 5 4
GO:0007017 microtubule-based process 2 4
GO:0007051 spindle organization 3 4
GO:0007052 mitotic spindle organization 4 4
GO:0009987 cellular process 1 4
GO:0016043 cellular component organization 3 4
GO:0022402 cell cycle process 2 4
GO:0048870 cell motility 2 4
GO:0060285 cilium-dependent cell motility 4 4
GO:0061640 cytoskeleton-dependent cytokinesis 4 4
GO:0071840 cellular component organization or biogenesis 2 4
GO:1902850 microtubule cytoskeleton organization involved in mitosis 4 4
GO:1903047 mitotic cell cycle process 3 4
Molecular functions
Term Name Level Count
GO:0005488 binding 1 20
GO:0005509 calcium ion binding 5 19
GO:0005515 protein binding 2 4
GO:0008092 cytoskeletal protein binding 3 4
GO:0015631 tubulin binding 4 4
GO:0043014 alpha-tubulin binding 5 4
GO:0043167 ion binding 2 19
GO:0043169 cation binding 3 19
GO:0046872 metal ion binding 4 19

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 163 167 PF00656 0.519
CLV_C14_Caspase3-7 290 294 PF00656 0.414
CLV_C14_Caspase3-7 450 454 PF00656 0.740
CLV_C14_Caspase3-7 599 603 PF00656 0.474
CLV_C14_Caspase3-7 741 745 PF00656 0.550
CLV_MEL_PAP_1 30 36 PF00089 0.576
CLV_NRD_NRD_1 100 102 PF00675 0.578
CLV_NRD_NRD_1 139 141 PF00675 0.268
CLV_NRD_NRD_1 301 303 PF00675 0.263
CLV_NRD_NRD_1 423 425 PF00675 0.714
CLV_NRD_NRD_1 497 499 PF00675 0.255
CLV_NRD_NRD_1 530 532 PF00675 0.295
CLV_NRD_NRD_1 728 730 PF00675 0.520
CLV_NRD_NRD_1 767 769 PF00675 0.514
CLV_NRD_NRD_1 789 791 PF00675 0.385
CLV_NRD_NRD_1 864 866 PF00675 0.682
CLV_PCSK_FUR_1 765 769 PF00082 0.588
CLV_PCSK_KEX2_1 172 174 PF00082 0.274
CLV_PCSK_KEX2_1 301 303 PF00082 0.303
CLV_PCSK_KEX2_1 423 425 PF00082 0.692
CLV_PCSK_KEX2_1 497 499 PF00082 0.255
CLV_PCSK_KEX2_1 529 531 PF00082 0.296
CLV_PCSK_KEX2_1 728 730 PF00082 0.539
CLV_PCSK_KEX2_1 767 769 PF00082 0.517
CLV_PCSK_KEX2_1 789 791 PF00082 0.421
CLV_PCSK_KEX2_1 840 842 PF00082 0.454
CLV_PCSK_KEX2_1 864 866 PF00082 0.751
CLV_PCSK_PC1ET2_1 172 174 PF00082 0.268
CLV_PCSK_PC1ET2_1 529 531 PF00082 0.301
CLV_PCSK_PC1ET2_1 840 842 PF00082 0.337
CLV_PCSK_SKI1_1 110 114 PF00082 0.381
CLV_PCSK_SKI1_1 175 179 PF00082 0.274
CLV_PCSK_SKI1_1 220 224 PF00082 0.403
CLV_PCSK_SKI1_1 385 389 PF00082 0.257
CLV_PCSK_SKI1_1 397 401 PF00082 0.351
CLV_PCSK_SKI1_1 424 428 PF00082 0.678
CLV_PCSK_SKI1_1 434 438 PF00082 0.645
CLV_PCSK_SKI1_1 447 451 PF00082 0.735
CLV_PCSK_SKI1_1 483 487 PF00082 0.308
CLV_PCSK_SKI1_1 497 501 PF00082 0.287
CLV_PCSK_SKI1_1 532 536 PF00082 0.326
CLV_PCSK_SKI1_1 728 732 PF00082 0.490
CLV_PCSK_SKI1_1 737 741 PF00082 0.424
DEG_APCC_DBOX_1 219 227 PF00400 0.384
DEG_SPOP_SBC_1 858 862 PF00917 0.508
DEG_SPOP_SBC_1 88 92 PF00917 0.397
DOC_ANK_TNKS_1 291 298 PF00023 0.527
DOC_CKS1_1 782 787 PF01111 0.416
DOC_CYCLIN_RxL_1 431 440 PF00134 0.497
DOC_CYCLIN_yCln2_LP_2 29 32 PF00134 0.563
DOC_CYCLIN_yCln2_LP_2 408 414 PF00134 0.540
DOC_CYCLIN_yCln2_LP_2 486 492 PF00134 0.570
DOC_MAPK_DCC_7 779 788 PF00069 0.394
DOC_MAPK_FxFP_2 811 814 PF00069 0.371
DOC_MAPK_gen_1 140 146 PF00069 0.488
DOC_MAPK_gen_1 301 309 PF00069 0.448
DOC_MAPK_gen_1 529 536 PF00069 0.414
DOC_MAPK_gen_1 644 652 PF00069 0.400
DOC_MAPK_MEF2A_6 301 309 PF00069 0.513
DOC_MAPK_MEF2A_6 370 378 PF00069 0.490
DOC_PP1_RVXF_1 115 122 PF00149 0.411
DOC_PP1_RVXF_1 279 286 PF00149 0.445
DOC_PP2B_LxvP_1 29 32 PF13499 0.555
DOC_PP2B_LxvP_1 408 411 PF13499 0.535
DOC_PP4_FxxP_1 125 128 PF00568 0.539
DOC_PP4_FxxP_1 71 74 PF00568 0.730
DOC_PP4_FxxP_1 774 777 PF00568 0.641
DOC_PP4_FxxP_1 811 814 PF00568 0.348
DOC_SPAK_OSR1_1 498 502 PF12202 0.486
DOC_USP7_MATH_1 12 16 PF00917 0.705
DOC_USP7_MATH_1 432 436 PF00917 0.735
DOC_USP7_MATH_1 462 466 PF00917 0.497
DOC_USP7_MATH_1 730 734 PF00917 0.580
DOC_USP7_MATH_1 858 862 PF00917 0.736
DOC_USP7_MATH_1 88 92 PF00917 0.588
DOC_USP7_UBL2_3 535 539 PF12436 0.498
DOC_WW_Pin1_4 319 324 PF00397 0.469
DOC_WW_Pin1_4 781 786 PF00397 0.384
DOC_WW_Pin1_4 796 801 PF00397 0.428
DOC_WW_Pin1_4 90 95 PF00397 0.425
LIG_14-3-3_CanoR_1 110 115 PF00244 0.304
LIG_14-3-3_CanoR_1 204 213 PF00244 0.443
LIG_14-3-3_CanoR_1 220 230 PF00244 0.264
LIG_14-3-3_CanoR_1 319 323 PF00244 0.513
LIG_14-3-3_CanoR_1 403 409 PF00244 0.554
LIG_14-3-3_CanoR_1 423 427 PF00244 0.566
LIG_14-3-3_CanoR_1 497 502 PF00244 0.465
LIG_14-3-3_CanoR_1 67 72 PF00244 0.694
LIG_14-3-3_CanoR_1 710 715 PF00244 0.687
LIG_14-3-3_CanoR_1 755 761 PF00244 0.400
LIG_14-3-3_CanoR_1 8 12 PF00244 0.701
LIG_APCC_ABBA_1 305 310 PF00400 0.510
LIG_BIR_II_1 1 5 PF00653 0.655
LIG_BIR_III_4 456 460 PF00653 0.529
LIG_BIR_III_4 609 613 PF00653 0.584
LIG_BIR_III_4 697 701 PF00653 0.413
LIG_BRCT_BRCA1_1 192 196 PF00533 0.565
LIG_BRCT_BRCA1_1 253 257 PF00533 0.572
LIG_BRCT_BRCA1_1 271 275 PF00533 0.552
LIG_BRCT_BRCA1_1 414 418 PF00533 0.546
LIG_BRCT_BRCA1_1 506 510 PF00533 0.442
LIG_FHA_1 150 156 PF00498 0.453
LIG_FHA_1 377 383 PF00498 0.461
LIG_FHA_1 431 437 PF00498 0.634
LIG_FHA_1 828 834 PF00498 0.544
LIG_FHA_2 111 117 PF00498 0.490
LIG_FHA_2 448 454 PF00498 0.641
LIG_FHA_2 557 563 PF00498 0.468
LIG_FHA_2 593 599 PF00498 0.598
LIG_FHA_2 686 692 PF00498 0.376
LIG_FHA_2 773 779 PF00498 0.580
LIG_FHA_2 799 805 PF00498 0.399
LIG_GBD_Chelix_1 620 628 PF00786 0.459
LIG_LIR_Apic_2 69 74 PF02991 0.508
LIG_LIR_Apic_2 773 777 PF02991 0.559
LIG_LIR_Apic_2 810 814 PF02991 0.439
LIG_LIR_Gen_1 189 199 PF02991 0.447
LIG_LIR_Gen_1 638 645 PF02991 0.493
LIG_LIR_Gen_1 684 693 PF02991 0.451
LIG_LIR_Nem_3 145 149 PF02991 0.557
LIG_LIR_Nem_3 189 194 PF02991 0.427
LIG_LIR_Nem_3 208 213 PF02991 0.469
LIG_LIR_Nem_3 243 248 PF02991 0.457
LIG_LIR_Nem_3 254 260 PF02991 0.485
LIG_LIR_Nem_3 366 372 PF02991 0.545
LIG_LIR_Nem_3 479 485 PF02991 0.561
LIG_LIR_Nem_3 507 513 PF02991 0.482
LIG_LIR_Nem_3 638 642 PF02991 0.387
LIG_LIR_Nem_3 684 690 PF02991 0.478
LIG_LIR_Nem_3 810 816 PF02991 0.472
LIG_MLH1_MIPbox_1 414 418 PF16413 0.546
LIG_MYND_1 27 31 PF01753 0.656
LIG_Pex14_2 121 125 PF04695 0.462
LIG_Pex14_2 218 222 PF04695 0.481
LIG_REV1ctd_RIR_1 397 407 PF16727 0.346
LIG_SH2_GRB2like 504 507 PF00017 0.592
LIG_SH2_NCK_1 513 517 PF00017 0.533
LIG_SH2_PTP2 191 194 PF00017 0.545
LIG_SH2_SRC 627 630 PF00017 0.512
LIG_SH2_STAP1 395 399 PF00017 0.516
LIG_SH2_STAP1 513 517 PF00017 0.494
LIG_SH2_STAP1 589 593 PF00017 0.376
LIG_SH2_STAP1 831 835 PF00017 0.483
LIG_SH2_STAT5 191 194 PF00017 0.502
LIG_SH2_STAT5 21 24 PF00017 0.613
LIG_SH2_STAT5 330 333 PF00017 0.510
LIG_SH2_STAT5 395 398 PF00017 0.531
LIG_SH2_STAT5 417 420 PF00017 0.597
LIG_SH2_STAT5 504 507 PF00017 0.452
LIG_SH2_STAT5 558 561 PF00017 0.463
LIG_SH2_STAT5 627 630 PF00017 0.458
LIG_SH2_STAT5 686 689 PF00017 0.400
LIG_SH2_STAT5 807 810 PF00017 0.440
LIG_SH2_STAT5 821 824 PF00017 0.506
LIG_SH2_STAT5 843 846 PF00017 0.343
LIG_SH3_1 543 549 PF00018 0.524
LIG_SH3_3 174 180 PF00018 0.529
LIG_SH3_3 227 233 PF00018 0.380
LIG_SH3_3 442 448 PF00018 0.680
LIG_SH3_3 534 540 PF00018 0.552
LIG_SH3_3 543 549 PF00018 0.496
LIG_SH3_3 647 653 PF00018 0.559
LIG_SH3_3 779 785 PF00018 0.534
LIG_SH3_3 811 817 PF00018 0.396
LIG_SH3_CIN85_PxpxPR_1 538 543 PF14604 0.545
LIG_SUMO_SIM_anti_2 688 694 PF11976 0.539
LIG_SUMO_SIM_par_1 150 157 PF11976 0.456
LIG_SUMO_SIM_par_1 410 416 PF11976 0.557
LIG_SUMO_SIM_par_1 613 618 PF11976 0.515
LIG_SUMO_SIM_par_1 647 654 PF11976 0.419
LIG_TRAF2_1 187 190 PF00917 0.486
LIG_WRC_WIRS_1 143 148 PF05994 0.423
LIG_WRC_WIRS_1 636 641 PF05994 0.443
LIG_WRC_WIRS_1 771 776 PF05994 0.435
LIG_WW_3 30 34 PF00397 0.578
MOD_CDC14_SPxK_1 93 96 PF00782 0.430
MOD_CDK_SPxK_1 90 96 PF00069 0.426
MOD_CK1_1 322 328 PF00069 0.407
MOD_CK1_1 440 446 PF00069 0.630
MOD_CK1_1 713 719 PF00069 0.614
MOD_CK2_1 262 268 PF00069 0.455
MOD_CK2_1 318 324 PF00069 0.331
MOD_CK2_1 592 598 PF00069 0.565
MOD_CK2_1 648 654 PF00069 0.406
MOD_CK2_1 798 804 PF00069 0.443
MOD_Cter_Amidation 765 768 PF01082 0.540
MOD_GlcNHglycan 162 165 PF01048 0.301
MOD_GlcNHglycan 253 256 PF01048 0.568
MOD_GlcNHglycan 263 267 PF01048 0.548
MOD_GlcNHglycan 338 341 PF01048 0.379
MOD_GlcNHglycan 514 517 PF01048 0.317
MOD_GlcNHglycan 715 718 PF01048 0.632
MOD_GSK3_1 258 265 PF00069 0.567
MOD_GSK3_1 318 325 PF00069 0.335
MOD_GSK3_1 422 429 PF00069 0.604
MOD_GSK3_1 619 626 PF00069 0.485
MOD_GSK3_1 627 634 PF00069 0.421
MOD_GSK3_1 63 70 PF00069 0.689
MOD_GSK3_1 681 688 PF00069 0.519
MOD_GSK3_1 794 801 PF00069 0.521
MOD_GSK3_1 860 867 PF00069 0.779
MOD_LATS_1 629 635 PF00433 0.545
MOD_N-GLC_1 12 17 PF02516 0.609
MOD_N-GLC_1 205 210 PF02516 0.239
MOD_N-GLC_1 67 72 PF02516 0.621
MOD_N-GLC_1 826 831 PF02516 0.527
MOD_NEK2_1 329 334 PF00069 0.316
MOD_NEK2_1 383 388 PF00069 0.449
MOD_NEK2_1 437 442 PF00069 0.566
MOD_NEK2_1 499 504 PF00069 0.274
MOD_NEK2_1 556 561 PF00069 0.200
MOD_NEK2_1 57 62 PF00069 0.688
MOD_NEK2_1 7 12 PF00069 0.654
MOD_NEK2_1 756 761 PF00069 0.385
MOD_NEK2_1 78 83 PF00069 0.595
MOD_NEK2_1 89 94 PF00069 0.547
MOD_NEK2_2 404 409 PF00069 0.357
MOD_NEK2_2 476 481 PF00069 0.423
MOD_PIKK_1 258 264 PF00454 0.517
MOD_PIKK_1 504 510 PF00454 0.487
MOD_PIKK_1 819 825 PF00454 0.589
MOD_PK_1 338 344 PF00069 0.374
MOD_PKA_1 497 503 PF00069 0.340
MOD_PKA_2 291 297 PF00069 0.408
MOD_PKA_2 318 324 PF00069 0.326
MOD_PKA_2 422 428 PF00069 0.625
MOD_PKA_2 497 503 PF00069 0.368
MOD_PKA_2 57 63 PF00069 0.693
MOD_PKA_2 66 72 PF00069 0.723
MOD_PKA_2 681 687 PF00069 0.573
MOD_PKA_2 7 13 PF00069 0.711
MOD_PKA_2 778 784 PF00069 0.499
MOD_Plk_1 149 155 PF00069 0.304
MOD_Plk_1 269 275 PF00069 0.513
MOD_Plk_1 310 316 PF00069 0.297
MOD_Plk_1 346 352 PF00069 0.361
MOD_Plk_1 412 418 PF00069 0.464
MOD_Plk_1 653 659 PF00069 0.530
MOD_Plk_1 67 73 PF00069 0.660
MOD_Plk_4 133 139 PF00069 0.386
MOD_Plk_4 149 155 PF00069 0.151
MOD_Plk_4 413 419 PF00069 0.586
MOD_Plk_4 432 438 PF00069 0.672
MOD_Plk_4 499 505 PF00069 0.268
MOD_Plk_4 584 590 PF00069 0.479
MOD_Plk_4 635 641 PF00069 0.531
MOD_Plk_4 778 784 PF00069 0.481
MOD_Plk_4 846 852 PF00069 0.611
MOD_ProDKin_1 319 325 PF00069 0.316
MOD_ProDKin_1 781 787 PF00069 0.381
MOD_ProDKin_1 796 802 PF00069 0.428
MOD_ProDKin_1 90 96 PF00069 0.426
MOD_SUMO_rev_2 561 569 PF00179 0.420
MOD_SUMO_rev_2 716 726 PF00179 0.561
MOD_SUMO_rev_2 733 741 PF00179 0.495
TRG_DiLeu_BaEn_1 804 809 PF01217 0.309
TRG_DiLeu_BaEn_2 303 309 PF01217 0.314
TRG_DiLeu_BaEn_4 189 195 PF01217 0.423
TRG_ENDOCYTIC_2 122 125 PF00928 0.330
TRG_ENDOCYTIC_2 191 194 PF00928 0.417
TRG_ENDOCYTIC_2 286 289 PF00928 0.369
TRG_ENDOCYTIC_2 369 372 PF00928 0.423
TRG_ENDOCYTIC_2 842 845 PF00928 0.442
TRG_ER_diArg_1 180 183 PF00400 0.306
TRG_ER_diArg_1 300 302 PF00400 0.418
TRG_ER_diArg_1 497 499 PF00400 0.303
TRG_ER_diArg_1 764 767 PF00400 0.542
TRG_ER_diArg_1 788 790 PF00400 0.362
TRG_NLS_MonoCore_2 528 533 PF00514 0.423
TRG_Pf-PMV_PEXEL_1 274 278 PF00026 0.457
TRG_Pf-PMV_PEXEL_1 734 738 PF00026 0.443
TRG_Pf-PMV_PEXEL_1 790 794 PF00026 0.362

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P5H4 Leptomonas seymouri 70% 100%
A0A0N1HZ98 Leptomonas seymouri 22% 100%
A0A0N1I3M2 Leptomonas seymouri 22% 100%
A0A0N1PBW1 Leptomonas seymouri 25% 100%
A0A0S4IJW8 Bodo saltans 35% 100%
A0A1X0NEV8 Trypanosomatidae 46% 100%
A0A1X0NLI2 Trypanosomatidae 24% 100%
A0A3Q8IDH4 Leishmania donovani 23% 100%
A0A3Q8IPU3 Leishmania donovani 24% 100%
A0A3R7KM50 Trypanosoma rangeli 47% 100%
A0A3R7L048 Trypanosoma rangeli 24% 100%
A0A3S5H688 Leishmania donovani 96% 100%
A0A422NK00 Trypanosoma rangeli 27% 100%
A4HE78 Leishmania braziliensis 23% 100%
A4HFK9 Leishmania braziliensis 23% 100%
A4HTP5 Leishmania infantum 95% 100%
A4I1J2 Leishmania infantum 23% 100%
C9ZJX4 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 22% 100%
C9ZPE7 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 44% 100%
D0A5T5 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 23% 100%
E9AD64 Leishmania major 23% 100%
E9AHF6 Leishmania infantum 23% 100%
E9AI34 Leishmania braziliensis 87% 100%
E9AMI2 Leishmania mexicana (strain MHOM/GT/2001/U1103) 94% 100%
E9AXM7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 24% 100%
E9AYY9 Leishmania mexicana (strain MHOM/GT/2001/U1103) 22% 100%
Q4Q9U5 Leishmania major 24% 100%
V5ASV2 Trypanosoma cruzi 24% 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