LeishMANIAdb
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Dymeclin

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

Quick info

Protein:
Dymeclin
Gene product:
hypothetical protein, conserved
Species:
Leishmania mexicana
UniProt:
E9B5M0_LEIMU
TriTrypDb:
LmxM.33.4250
Length:
592

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
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

E9B5M0
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9B5M0

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 164 168 PF00656 0.525
CLV_C14_Caspase3-7 504 508 PF00656 0.382
CLV_C14_Caspase3-7 87 91 PF00656 0.727
CLV_NRD_NRD_1 101 103 PF00675 0.568
CLV_NRD_NRD_1 170 172 PF00675 0.553
CLV_NRD_NRD_1 225 227 PF00675 0.688
CLV_NRD_NRD_1 567 569 PF00675 0.756
CLV_PCSK_KEX2_1 101 103 PF00082 0.604
CLV_PCSK_KEX2_1 147 149 PF00082 0.462
CLV_PCSK_KEX2_1 170 172 PF00082 0.553
CLV_PCSK_KEX2_1 225 227 PF00082 0.642
CLV_PCSK_KEX2_1 4 6 PF00082 0.647
CLV_PCSK_KEX2_1 567 569 PF00082 0.756
CLV_PCSK_KEX2_1 61 63 PF00082 0.733
CLV_PCSK_PC1ET2_1 147 149 PF00082 0.462
CLV_PCSK_PC1ET2_1 4 6 PF00082 0.659
CLV_PCSK_PC1ET2_1 61 63 PF00082 0.770
CLV_PCSK_SKI1_1 141 145 PF00082 0.497
CLV_PCSK_SKI1_1 276 280 PF00082 0.409
CLV_PCSK_SKI1_1 367 371 PF00082 0.392
CLV_PCSK_SKI1_1 540 544 PF00082 0.498
DEG_APCC_DBOX_1 275 283 PF00400 0.480
DEG_SPOP_SBC_1 572 576 PF00917 0.586
DEG_SPOP_SBC_1 85 89 PF00917 0.597
DOC_ANK_TNKS_1 240 247 PF00023 0.409
DOC_CDC14_PxL_1 346 354 PF14671 0.532
DOC_CKS1_1 403 408 PF01111 0.619
DOC_CYCLIN_RxL_1 273 280 PF00134 0.435
DOC_CYCLIN_yCln2_LP_2 297 303 PF00134 0.537
DOC_CYCLIN_yCln2_LP_2 348 354 PF00134 0.409
DOC_MAPK_gen_1 170 176 PF00069 0.546
DOC_MAPK_gen_1 4 12 PF00069 0.748
DOC_MAPK_MEF2A_6 276 283 PF00069 0.403
DOC_MAPK_MEF2A_6 295 303 PF00069 0.486
DOC_MAPK_MEF2A_6 357 365 PF00069 0.558
DOC_PP2B_LxvP_1 20 23 PF13499 0.639
DOC_PP2B_LxvP_1 291 294 PF13499 0.521
DOC_PP2B_LxvP_1 297 300 PF13499 0.531
DOC_PP2B_LxvP_1 492 495 PF13499 0.426
DOC_USP7_MATH_1 258 262 PF00917 0.718
DOC_USP7_MATH_1 274 278 PF00917 0.286
DOC_USP7_MATH_1 43 47 PF00917 0.605
DOC_USP7_MATH_1 501 505 PF00917 0.575
DOC_USP7_MATH_1 572 576 PF00917 0.682
DOC_USP7_MATH_1 70 74 PF00917 0.748
DOC_USP7_MATH_1 80 84 PF00917 0.661
DOC_USP7_UBL2_3 422 426 PF12436 0.507
DOC_WW_Pin1_4 208 213 PF00397 0.617
DOC_WW_Pin1_4 23 28 PF00397 0.755
DOC_WW_Pin1_4 285 290 PF00397 0.536
DOC_WW_Pin1_4 336 341 PF00397 0.280
DOC_WW_Pin1_4 402 407 PF00397 0.612
DOC_WW_Pin1_4 73 78 PF00397 0.714
DOC_WW_Pin1_4 81 86 PF00397 0.456
LIG_14-3-3_CanoR_1 216 224 PF00244 0.640
LIG_14-3-3_CanoR_1 295 300 PF00244 0.586
LIG_14-3-3_CanoR_1 357 365 PF00244 0.523
LIG_14-3-3_CanoR_1 401 406 PF00244 0.623
LIG_14-3-3_CanoR_1 458 466 PF00244 0.509
LIG_14-3-3_CanoR_1 502 509 PF00244 0.580
LIG_14-3-3_CanoR_1 552 561 PF00244 0.417
LIG_14-3-3_CanoR_1 56 63 PF00244 0.760
LIG_14-3-3_CanoR_1 64 72 PF00244 0.749
LIG_14-3-3_CanoR_1 75 85 PF00244 0.762
LIG_14-3-3_CanoR_1 86 92 PF00244 0.716
LIG_Actin_WH2_2 341 359 PF00022 0.542
LIG_BIR_II_1 1 5 PF00653 0.695
LIG_CaM_IQ_9 306 321 PF13499 0.486
LIG_EH1_1 196 204 PF00400 0.356
LIG_FHA_1 151 157 PF00498 0.544
LIG_FHA_1 194 200 PF00498 0.462
LIG_FHA_1 333 339 PF00498 0.541
LIG_FHA_1 356 362 PF00498 0.539
LIG_FHA_1 371 377 PF00498 0.394
LIG_FHA_1 381 387 PF00498 0.412
LIG_FHA_1 415 421 PF00498 0.225
LIG_FHA_1 460 466 PF00498 0.570
LIG_FHA_1 489 495 PF00498 0.540
LIG_FHA_1 50 56 PF00498 0.628
LIG_FHA_2 164 170 PF00498 0.595
LIG_FHA_2 331 337 PF00498 0.439
LIG_FHA_2 403 409 PF00498 0.603
LIG_FHA_2 48 54 PF00498 0.739
LIG_FHA_2 568 574 PF00498 0.794
LIG_FHA_2 578 584 PF00498 0.727
LIG_FHA_2 85 91 PF00498 0.743
LIG_GBD_Chelix_1 12 20 PF00786 0.689
LIG_GBD_Chelix_1 172 180 PF00786 0.544
LIG_GBD_Chelix_1 194 202 PF00786 0.514
LIG_GBD_Chelix_1 521 529 PF00786 0.403
LIG_LIR_Gen_1 121 131 PF02991 0.410
LIG_LIR_Gen_1 468 478 PF02991 0.404
LIG_LIR_Gen_1 527 535 PF02991 0.409
LIG_LIR_Nem_3 121 127 PF02991 0.355
LIG_LIR_Nem_3 468 474 PF02991 0.420
LIG_LIR_Nem_3 527 531 PF02991 0.395
LIG_NRBOX 129 135 PF00104 0.467
LIG_NRBOX 274 280 PF00104 0.374
LIG_NRBOX 311 317 PF00104 0.571
LIG_PCNA_PIPBox_1 191 200 PF02747 0.525
LIG_PCNA_yPIPBox_3 191 200 PF02747 0.506
LIG_SH2_CRK 471 475 PF00017 0.358
LIG_SH2_STAP1 471 475 PF00017 0.358
LIG_SH3_3 21 27 PF00018 0.767
LIG_SH3_3 358 364 PF00018 0.564
LIG_SH3_3 400 406 PF00018 0.466
LIG_SH3_3 79 85 PF00018 0.722
LIG_SUMO_SIM_anti_2 129 135 PF11976 0.253
LIG_SUMO_SIM_anti_2 277 283 PF11976 0.491
LIG_SUMO_SIM_anti_2 327 333 PF11976 0.378
LIG_SUMO_SIM_anti_2 8 15 PF11976 0.749
LIG_SUMO_SIM_anti_2 95 101 PF11976 0.646
LIG_SUMO_SIM_par_1 129 135 PF11976 0.348
LIG_SUMO_SIM_par_1 327 333 PF11976 0.438
LIG_TRAF2_1 334 337 PF00917 0.601
LIG_TRAF2_1 542 545 PF00917 0.296
LIG_WRC_WIRS_1 194 199 PF05994 0.467
MOD_CDK_SPK_2 81 86 PF00069 0.742
MOD_CK1_1 123 129 PF00069 0.469
MOD_CK1_1 217 223 PF00069 0.605
MOD_CK1_1 237 243 PF00069 0.721
MOD_CK1_1 261 267 PF00069 0.578
MOD_CK1_1 269 275 PF00069 0.396
MOD_CK1_1 277 283 PF00069 0.354
MOD_CK1_1 425 431 PF00069 0.637
MOD_CK1_1 442 448 PF00069 0.480
MOD_CK1_1 534 540 PF00069 0.512
MOD_CK1_1 66 72 PF00069 0.681
MOD_CK1_1 73 79 PF00069 0.665
MOD_CK1_1 81 87 PF00069 0.455
MOD_CK2_1 12 18 PF00069 0.653
MOD_CK2_1 123 129 PF00069 0.538
MOD_CK2_1 324 330 PF00069 0.358
MOD_CK2_1 356 362 PF00069 0.497
MOD_CK2_1 402 408 PF00069 0.631
MOD_CK2_1 457 463 PF00069 0.549
MOD_CK2_1 567 573 PF00069 0.724
MOD_GlcNHglycan 236 239 PF01048 0.749
MOD_GlcNHglycan 358 361 PF01048 0.519
MOD_GlcNHglycan 380 383 PF01048 0.384
MOD_GlcNHglycan 436 439 PF01048 0.494
MOD_GlcNHglycan 467 470 PF01048 0.418
MOD_GlcNHglycan 533 536 PF01048 0.471
MOD_GlcNHglycan 562 565 PF01048 0.476
MOD_GlcNHglycan 67 71 PF01048 0.551
MOD_GlcNHglycan 78 81 PF01048 0.697
MOD_GSK3_1 119 126 PF00069 0.460
MOD_GSK3_1 233 240 PF00069 0.668
MOD_GSK3_1 314 321 PF00069 0.495
MOD_GSK3_1 33 40 PF00069 0.798
MOD_GSK3_1 332 339 PF00069 0.491
MOD_GSK3_1 378 385 PF00069 0.446
MOD_GSK3_1 393 400 PF00069 0.469
MOD_GSK3_1 43 50 PF00069 0.595
MOD_GSK3_1 453 460 PF00069 0.554
MOD_GSK3_1 501 508 PF00069 0.594
MOD_GSK3_1 530 537 PF00069 0.491
MOD_GSK3_1 567 574 PF00069 0.780
MOD_GSK3_1 62 69 PF00069 0.687
MOD_GSK3_1 71 78 PF00069 0.631
MOD_GSK3_1 80 87 PF00069 0.695
MOD_LATS_1 35 41 PF00433 0.502
MOD_N-GLC_1 285 290 PF02516 0.538
MOD_N-GLC_1 370 375 PF02516 0.371
MOD_N-GLC_1 43 48 PF02516 0.683
MOD_NEK2_1 176 181 PF00069 0.544
MOD_NEK2_1 198 203 PF00069 0.497
MOD_NEK2_1 214 219 PF00069 0.478
MOD_NEK2_1 356 361 PF00069 0.504
MOD_NEK2_1 380 385 PF00069 0.471
MOD_NEK2_1 397 402 PF00069 0.458
MOD_NEK2_1 414 419 PF00069 0.289
MOD_NEK2_1 453 458 PF00069 0.495
MOD_NEK2_1 465 470 PF00069 0.419
MOD_NEK2_1 47 52 PF00069 0.566
MOD_NEK2_1 530 535 PF00069 0.427
MOD_NEK2_2 488 493 PF00069 0.628
MOD_PIKK_1 318 324 PF00454 0.467
MOD_PIKK_1 387 393 PF00454 0.462
MOD_PK_1 295 301 PF00069 0.499
MOD_PKA_1 567 573 PF00069 0.580
MOD_PKA_2 215 221 PF00069 0.657
MOD_PKA_2 318 324 PF00069 0.520
MOD_PKA_2 356 362 PF00069 0.486
MOD_PKA_2 457 463 PF00069 0.567
MOD_PKA_2 501 507 PF00069 0.530
MOD_PKA_2 55 61 PF00069 0.710
MOD_PKA_2 566 572 PF00069 0.761
MOD_PKA_2 63 69 PF00069 0.776
MOD_PKA_2 85 91 PF00069 0.724
MOD_PKB_1 399 407 PF00069 0.658
MOD_Plk_1 119 125 PF00069 0.420
MOD_Plk_1 43 49 PF00069 0.678
MOD_Plk_2-3 129 135 PF00069 0.253
MOD_Plk_4 129 135 PF00069 0.339
MOD_Plk_4 151 157 PF00069 0.533
MOD_Plk_4 176 182 PF00069 0.502
MOD_Plk_4 193 199 PF00069 0.398
MOD_Plk_4 277 283 PF00069 0.465
MOD_Plk_4 324 330 PF00069 0.344
MOD_Plk_4 442 448 PF00069 0.491
MOD_Plk_4 476 482 PF00069 0.439
MOD_ProDKin_1 208 214 PF00069 0.619
MOD_ProDKin_1 23 29 PF00069 0.758
MOD_ProDKin_1 285 291 PF00069 0.536
MOD_ProDKin_1 336 342 PF00069 0.279
MOD_ProDKin_1 402 408 PF00069 0.605
MOD_ProDKin_1 73 79 PF00069 0.717
MOD_ProDKin_1 81 87 PF00069 0.455
MOD_SUMO_for_1 421 424 PF00179 0.383
MOD_SUMO_rev_2 260 269 PF00179 0.629
MOD_SUMO_rev_2 541 549 PF00179 0.579
TRG_DiLeu_BaEn_1 129 134 PF01217 0.462
TRG_DiLeu_BaEn_1 341 346 PF01217 0.340
TRG_DiLeu_BaEn_1 545 550 PF01217 0.519
TRG_DiLeu_BaEn_1 582 587 PF01217 0.643
TRG_DiLeu_BaLyEn_6 297 302 PF01217 0.542
TRG_DiLeu_LyEn_5 341 346 PF01217 0.374
TRG_ENDOCYTIC_2 470 473 PF00928 0.350
TRG_ER_diArg_1 100 102 PF00400 0.616
TRG_ER_diArg_1 170 172 PF00400 0.553
TRG_ER_diArg_1 224 226 PF00400 0.535

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P709 Leptomonas seymouri 41% 99%
A0A0S4KM98 Bodo saltans 24% 80%
A0A1X0PAI7 Trypanosomatidae 30% 100%
A0A3R7M5G0 Trypanosoma rangeli 31% 100%
A0A3S7X8L9 Leishmania donovani 85% 100%
A4HBE8 Leishmania braziliensis 72% 100%
A4IAJ6 Leishmania infantum 85% 100%
C9ZLP4 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 31% 100%
Q4Q2B6 Leishmania major 84% 100%
V5BRD9 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