LeishMANIAdb
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Dymeclin

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

Quick info

Protein:
Dymeclin
Gene product:
Dyggve-Melchior-Clausen syndrome protein, putative
Species:
Leishmania major
UniProt:
E9AC29_LEIMA
TriTrypDb:
LmjF.01.0380 , LMJLV39_010009000 * , LMJSD75_010009100 *
Length:
818

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: 11
NetGPI no yes: 0, no: 11
Cellular components
Term Name Level Count
GO:0005794 Golgi apparatus 5 2
GO:0043226 organelle 2 2
GO:0043227 membrane-bounded organelle 3 2
GO:0043229 intracellular organelle 3 2
GO:0043231 intracellular membrane-bounded organelle 4 2
GO:0110165 cellular anatomical entity 1 3
GO:0016020 membrane 2 1

Expansion

Sequence features

E9AC29
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AC29

Function

Biological processes
Term Name Level Count
GO:0006996 organelle organization 4 2
GO:0007030 Golgi organization 5 2
GO:0009987 cellular process 1 2
GO:0016043 cellular component organization 3 2
GO:0071840 cellular component organization or biogenesis 2 2
Could not find GO molecular_function term for this entry.

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 723 727 PF00656 0.553
CLV_NRD_NRD_1 5 7 PF00675 0.420
CLV_NRD_NRD_1 617 619 PF00675 0.319
CLV_NRD_NRD_1 686 688 PF00675 0.277
CLV_NRD_NRD_1 724 726 PF00675 0.257
CLV_NRD_NRD_1 80 82 PF00675 0.358
CLV_PCSK_KEX2_1 617 619 PF00082 0.319
CLV_PCSK_KEX2_1 686 688 PF00082 0.275
CLV_PCSK_KEX2_1 724 726 PF00082 0.257
CLV_PCSK_KEX2_1 80 82 PF00082 0.358
CLV_PCSK_PC7_1 613 619 PF00082 0.318
CLV_PCSK_SKI1_1 105 109 PF00082 0.322
CLV_PCSK_SKI1_1 148 152 PF00082 0.291
CLV_PCSK_SKI1_1 172 176 PF00082 0.339
CLV_PCSK_SKI1_1 314 318 PF00082 0.291
CLV_PCSK_SKI1_1 413 417 PF00082 0.457
CLV_PCSK_SKI1_1 434 438 PF00082 0.476
CLV_PCSK_SKI1_1 476 480 PF00082 0.356
CLV_PCSK_SKI1_1 602 606 PF00082 0.379
CLV_PCSK_SKI1_1 652 656 PF00082 0.306
CLV_PCSK_SKI1_1 69 73 PF00082 0.262
CLV_Separin_Metazoa 169 173 PF03568 0.527
CLV_Separin_Metazoa 77 81 PF03568 0.474
DEG_APCC_DBOX_1 601 609 PF00400 0.440
DEG_SPOP_SBC_1 268 272 PF00917 0.440
DEG_SPOP_SBC_1 563 567 PF00917 0.530
DEG_SPOP_SBC_1 579 583 PF00917 0.388
DOC_CYCLIN_RxL_1 167 179 PF00134 0.539
DOC_CYCLIN_RxL_1 473 483 PF00134 0.422
DOC_CYCLIN_RxL_1 66 76 PF00134 0.484
DOC_MAPK_FxFP_2 442 445 PF00069 0.262
DOC_MAPK_gen_1 67 74 PF00069 0.481
DOC_MAPK_MEF2A_6 440 449 PF00069 0.339
DOC_PP1_RVXF_1 432 438 PF00149 0.291
DOC_PP1_RVXF_1 65 71 PF00149 0.454
DOC_PP2B_LxvP_1 266 269 PF13499 0.491
DOC_PP4_FxxP_1 442 445 PF00568 0.248
DOC_PP4_FxxP_1 785 788 PF00568 0.437
DOC_USP7_MATH_1 133 137 PF00917 0.439
DOC_USP7_MATH_1 158 162 PF00917 0.518
DOC_USP7_MATH_1 16 20 PF00917 0.605
DOC_USP7_MATH_1 25 29 PF00917 0.425
DOC_USP7_MATH_1 484 488 PF00917 0.513
DOC_USP7_MATH_1 57 61 PF00917 0.587
DOC_USP7_MATH_1 670 674 PF00917 0.539
DOC_WW_Pin1_4 129 134 PF00397 0.539
DOC_WW_Pin1_4 200 205 PF00397 0.539
DOC_WW_Pin1_4 226 231 PF00397 0.483
DOC_WW_Pin1_4 343 348 PF00397 0.480
DOC_WW_Pin1_4 468 473 PF00397 0.539
DOC_WW_Pin1_4 674 679 PF00397 0.504
DOC_WW_Pin1_4 90 95 PF00397 0.539
LIG_14-3-3_CanoR_1 172 178 PF00244 0.575
LIG_14-3-3_CanoR_1 222 232 PF00244 0.478
LIG_14-3-3_CanoR_1 256 265 PF00244 0.493
LIG_14-3-3_CanoR_1 314 323 PF00244 0.522
LIG_14-3-3_CanoR_1 358 367 PF00244 0.587
LIG_14-3-3_CanoR_1 413 419 PF00244 0.319
LIG_14-3-3_CanoR_1 440 445 PF00244 0.309
LIG_14-3-3_CanoR_1 550 556 PF00244 0.508
LIG_Actin_WH2_2 533 548 PF00022 0.477
LIG_Actin_WH2_2 586 604 PF00022 0.539
LIG_Actin_WH2_2 92 107 PF00022 0.504
LIG_APCC_ABBA_1 193 198 PF00400 0.444
LIG_BRCT_BRCA1_1 442 446 PF00533 0.248
LIG_BRCT_BRCA1_1 781 785 PF00533 0.437
LIG_BRCT_BRCA1_1 9 13 PF00533 0.585
LIG_FHA_1 12 18 PF00498 0.590
LIG_FHA_1 140 146 PF00498 0.537
LIG_FHA_1 190 196 PF00498 0.483
LIG_FHA_1 315 321 PF00498 0.558
LIG_FHA_1 405 411 PF00498 0.352
LIG_FHA_1 451 457 PF00498 0.297
LIG_FHA_1 469 475 PF00498 0.539
LIG_FHA_1 540 546 PF00498 0.519
LIG_FHA_1 63 69 PF00498 0.455
LIG_FHA_1 649 655 PF00498 0.537
LIG_FHA_1 91 97 PF00498 0.463
LIG_FHA_2 164 170 PF00498 0.457
LIG_FHA_2 564 570 PF00498 0.547
LIG_FHA_2 580 586 PF00498 0.566
LIG_GBD_Chelix_1 393 401 PF00786 0.457
LIG_LIR_Apic_2 219 223 PF02991 0.405
LIG_LIR_Apic_2 782 788 PF02991 0.437
LIG_LIR_Gen_1 194 204 PF02991 0.448
LIG_LIR_Gen_1 240 248 PF02991 0.541
LIG_LIR_Gen_1 307 316 PF02991 0.539
LIG_LIR_Gen_1 349 357 PF02991 0.509
LIG_LIR_Gen_1 443 454 PF02991 0.331
LIG_LIR_Gen_1 775 783 PF02991 0.464
LIG_LIR_Nem_3 194 199 PF02991 0.452
LIG_LIR_Nem_3 240 244 PF02991 0.481
LIG_LIR_Nem_3 307 312 PF02991 0.539
LIG_LIR_Nem_3 349 353 PF02991 0.509
LIG_LIR_Nem_3 362 367 PF02991 0.387
LIG_LIR_Nem_3 443 449 PF02991 0.289
LIG_LIR_Nem_3 775 779 PF02991 0.453
LIG_LIR_Nem_3 782 786 PF02991 0.429
LIG_LYPXL_yS_3 444 447 PF13949 0.308
LIG_MLH1_MIPbox_1 9 13 PF16413 0.585
LIG_NRBOX 170 176 PF00104 0.539
LIG_NRBOX 209 215 PF00104 0.510
LIG_NRBOX 366 372 PF00104 0.364
LIG_NRBOX 396 402 PF00104 0.257
LIG_PCNA_yPIPBox_3 502 515 PF02747 0.248
LIG_Pex14_2 241 245 PF04695 0.546
LIG_Pex14_2 442 446 PF04695 0.248
LIG_Pex14_2 785 789 PF04695 0.437
LIG_SH2_NCK_1 647 651 PF00017 0.457
LIG_SH2_PTP2 372 375 PF00017 0.334
LIG_SH2_SRC 647 650 PF00017 0.388
LIG_SH2_STAP1 482 486 PF00017 0.539
LIG_SH2_STAP1 624 628 PF00017 0.439
LIG_SH2_STAT3 532 535 PF00017 0.462
LIG_SH2_STAT3 597 600 PF00017 0.491
LIG_SH2_STAT5 12 15 PF00017 0.501
LIG_SH2_STAT5 264 267 PF00017 0.539
LIG_SH2_STAT5 338 341 PF00017 0.456
LIG_SH2_STAT5 372 375 PF00017 0.289
LIG_SH2_STAT5 532 535 PF00017 0.484
LIG_SH2_STAT5 597 600 PF00017 0.491
LIG_SH2_STAT5 628 631 PF00017 0.534
LIG_SH3_3 152 158 PF00018 0.462
LIG_SH3_3 249 255 PF00018 0.457
LIG_SH3_3 292 298 PF00018 0.491
LIG_SH3_3 511 517 PF00018 0.289
LIG_SH3_3 80 86 PF00018 0.491
LIG_SH3_3 811 817 PF00018 0.689
LIG_SUMO_SIM_anti_2 166 172 PF11976 0.472
LIG_SUMO_SIM_anti_2 208 214 PF11976 0.457
LIG_SUMO_SIM_anti_2 451 459 PF11976 0.290
LIG_SUMO_SIM_anti_2 680 686 PF11976 0.463
LIG_SUMO_SIM_anti_2 769 775 PF11976 0.539
LIG_SUMO_SIM_par_1 264 272 PF11976 0.527
LIG_SUMO_SIM_par_1 399 404 PF11976 0.318
LIG_SUMO_SIM_par_1 451 459 PF11976 0.310
LIG_SUMO_SIM_par_1 492 497 PF11976 0.370
LIG_TRAF2_1 677 680 PF00917 0.507
LIG_TRAF2_1 775 778 PF00917 0.539
LIG_TYR_ITIM 370 375 PF00017 0.289
LIG_TYR_ITIM 622 627 PF00017 0.448
LIG_UBA3_1 103 112 PF00899 0.578
LIG_UBA3_1 319 328 PF00899 0.448
LIG_UBA3_1 400 406 PF00899 0.240
LIG_UBA3_1 654 663 PF00899 0.527
MOD_CK1_1 346 352 PF00069 0.469
MOD_CK1_1 746 752 PF00069 0.537
MOD_CK2_1 163 169 PF00069 0.537
MOD_CK2_1 304 310 PF00069 0.462
MOD_CK2_1 563 569 PF00069 0.467
MOD_CK2_1 579 585 PF00069 0.553
MOD_CK2_1 674 680 PF00069 0.510
MOD_CK2_1 748 754 PF00069 0.556
MOD_CK2_1 772 778 PF00069 0.506
MOD_GlcNHglycan 114 117 PF01048 0.322
MOD_GlcNHglycan 135 138 PF01048 0.282
MOD_GlcNHglycan 160 163 PF01048 0.320
MOD_GlcNHglycan 179 182 PF01048 0.155
MOD_GlcNHglycan 276 279 PF01048 0.329
MOD_GlcNHglycan 286 289 PF01048 0.317
MOD_GlcNHglycan 329 332 PF01048 0.278
MOD_GlcNHglycan 354 357 PF01048 0.334
MOD_GlcNHglycan 483 487 PF01048 0.291
MOD_GlcNHglycan 551 554 PF01048 0.272
MOD_GlcNHglycan 701 704 PF01048 0.347
MOD_GlcNHglycan 708 712 PF01048 0.383
MOD_GlcNHglycan 748 751 PF01048 0.313
MOD_GlcNHglycan 795 798 PF01048 0.409
MOD_GSK3_1 108 115 PF00069 0.499
MOD_GSK3_1 129 136 PF00069 0.436
MOD_GSK3_1 173 180 PF00069 0.482
MOD_GSK3_1 246 253 PF00069 0.519
MOD_GSK3_1 339 346 PF00069 0.517
MOD_GSK3_1 404 411 PF00069 0.263
MOD_GSK3_1 574 581 PF00069 0.568
MOD_GSK3_1 670 677 PF00069 0.434
MOD_GSK3_1 693 700 PF00069 0.507
MOD_GSK3_1 7 14 PF00069 0.567
MOD_GSK3_1 739 746 PF00069 0.548
MOD_GSK3_1 748 755 PF00069 0.556
MOD_N-GLC_1 404 409 PF02516 0.535
MOD_N-GLC_2 304 306 PF02516 0.257
MOD_NEK2_1 108 113 PF00069 0.520
MOD_NEK2_1 153 158 PF00069 0.472
MOD_NEK2_1 173 178 PF00069 0.426
MOD_NEK2_1 199 204 PF00069 0.481
MOD_NEK2_1 213 218 PF00069 0.430
MOD_NEK2_1 248 253 PF00069 0.490
MOD_NEK2_1 302 307 PF00069 0.539
MOD_NEK2_1 381 386 PF00069 0.250
MOD_NEK2_1 392 397 PF00069 0.226
MOD_NEK2_1 401 406 PF00069 0.145
MOD_NEK2_1 414 419 PF00069 0.234
MOD_NEK2_1 449 454 PF00069 0.276
MOD_NEK2_1 540 545 PF00069 0.491
MOD_NEK2_1 555 560 PF00069 0.466
MOD_NEK2_1 748 753 PF00069 0.388
MOD_PIKK_1 456 462 PF00454 0.284
MOD_PIKK_1 693 699 PF00454 0.559
MOD_PKA_2 108 114 PF00069 0.529
MOD_PKA_2 408 414 PF00069 0.356
MOD_PKA_2 549 555 PF00069 0.500
MOD_PKA_2 807 813 PF00069 0.619
MOD_Plk_1 189 195 PF00069 0.524
MOD_Plk_1 737 743 PF00069 0.457
MOD_Plk_1 753 759 PF00069 0.367
MOD_Plk_2-3 718 724 PF00069 0.403
MOD_Plk_2-3 766 772 PF00069 0.539
MOD_Plk_4 213 219 PF00069 0.509
MOD_Plk_4 237 243 PF00069 0.534
MOD_Plk_4 269 275 PF00069 0.388
MOD_Plk_4 365 371 PF00069 0.253
MOD_Plk_4 381 387 PF00069 0.214
MOD_Plk_4 450 456 PF00069 0.300
MOD_Plk_4 743 749 PF00069 0.491
MOD_Plk_4 790 796 PF00069 0.492
MOD_ProDKin_1 129 135 PF00069 0.539
MOD_ProDKin_1 200 206 PF00069 0.539
MOD_ProDKin_1 226 232 PF00069 0.483
MOD_ProDKin_1 343 349 PF00069 0.480
MOD_ProDKin_1 468 474 PF00069 0.539
MOD_ProDKin_1 674 680 PF00069 0.504
MOD_ProDKin_1 90 96 PF00069 0.539
TRG_DiLeu_BaEn_1 169 174 PF01217 0.432
TRG_DiLeu_BaEn_1 388 393 PF01217 0.348
TRG_DiLeu_BaLyEn_6 201 206 PF01217 0.553
TRG_DiLeu_BaLyEn_6 463 468 PF01217 0.491
TRG_DiLeu_LyEn_5 169 174 PF01217 0.527
TRG_ENDOCYTIC_2 372 375 PF00928 0.274
TRG_ENDOCYTIC_2 444 447 PF00928 0.308
TRG_ENDOCYTIC_2 624 627 PF00928 0.439
TRG_ENDOCYTIC_2 776 779 PF00928 0.469
TRG_ENDOCYTIC_2 783 786 PF00928 0.430
TRG_ER_diArg_1 629 632 PF00400 0.446
TRG_ER_diArg_1 67 70 PF00400 0.449
TRG_ER_diArg_1 685 687 PF00400 0.478
TRG_ER_diArg_1 79 81 PF00400 0.492
TRG_ER_FFAT_2 8 18 PF00635 0.544
TRG_NES_CRM1_1 366 377 PF08389 0.388
TRG_NES_CRM1_1 592 606 PF08389 0.491
TRG_Pf-PMV_PEXEL_1 434 438 PF00026 0.491
TRG_Pf-PMV_PEXEL_1 476 480 PF00026 0.222
TRG_Pf-PMV_PEXEL_1 502 506 PF00026 0.480
TRG_Pf-PMV_PEXEL_1 602 606 PF00026 0.288
TRG_Pf-PMV_PEXEL_1 632 636 PF00026 0.240

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6M9 Leptomonas seymouri 55% 97%
A0A0S4JPV7 Bodo saltans 25% 100%
A0A1X0P2R5 Trypanosomatidae 32% 100%
A0A3S5H4V0 Leishmania donovani 91% 100%
A0A422NY99 Trypanosoma rangeli 33% 100%
A4H364 Leishmania braziliensis 73% 99%
A4HRG1 Leishmania infantum 91% 100%
C9ZXI6 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 29% 100%
E9AJC6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 85% 99%
V5AX12 Trypanosoma cruzi 32% 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