LeishMANIAdb
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DUF4709 domain-containing protein

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

Quick info

Protein:
DUF4709 domain-containing protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania braziliensis
UniProt:
A4HKA9_LEIBR
TriTrypDb:
LbrM.32.1370 , LBRM2903_320019000
Length:
797

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: 9
NetGPI no yes: 0, no: 9
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

A4HKA9
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HKA9

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 161 165 PF00656 0.546
CLV_C14_Caspase3-7 728 732 PF00656 0.670
CLV_NRD_NRD_1 104 106 PF00675 0.430
CLV_NRD_NRD_1 155 157 PF00675 0.600
CLV_NRD_NRD_1 17 19 PF00675 0.604
CLV_NRD_NRD_1 252 254 PF00675 0.338
CLV_NRD_NRD_1 320 322 PF00675 0.406
CLV_NRD_NRD_1 361 363 PF00675 0.642
CLV_NRD_NRD_1 593 595 PF00675 0.445
CLV_NRD_NRD_1 715 717 PF00675 0.470
CLV_NRD_NRD_1 763 765 PF00675 0.607
CLV_NRD_NRD_1 771 773 PF00675 0.673
CLV_PCSK_KEX2_1 104 106 PF00082 0.430
CLV_PCSK_KEX2_1 16 18 PF00082 0.586
CLV_PCSK_KEX2_1 252 254 PF00082 0.338
CLV_PCSK_KEX2_1 269 271 PF00082 0.548
CLV_PCSK_KEX2_1 361 363 PF00082 0.583
CLV_PCSK_KEX2_1 471 473 PF00082 0.650
CLV_PCSK_KEX2_1 593 595 PF00082 0.445
CLV_PCSK_KEX2_1 715 717 PF00082 0.543
CLV_PCSK_KEX2_1 771 773 PF00082 0.671
CLV_PCSK_PC1ET2_1 269 271 PF00082 0.439
CLV_PCSK_PC1ET2_1 471 473 PF00082 0.510
CLV_PCSK_PC1ET2_1 771 773 PF00082 0.653
CLV_PCSK_SKI1_1 143 147 PF00082 0.552
CLV_PCSK_SKI1_1 157 161 PF00082 0.532
CLV_PCSK_SKI1_1 185 189 PF00082 0.534
CLV_PCSK_SKI1_1 253 257 PF00082 0.517
CLV_PCSK_SKI1_1 259 263 PF00082 0.529
CLV_PCSK_SKI1_1 322 326 PF00082 0.398
CLV_PCSK_SKI1_1 346 350 PF00082 0.531
CLV_PCSK_SKI1_1 523 527 PF00082 0.475
CLV_PCSK_SKI1_1 559 563 PF00082 0.497
CLV_PCSK_SKI1_1 679 683 PF00082 0.399
CLV_PCSK_SKI1_1 691 695 PF00082 0.355
CLV_PCSK_SKI1_1 76 80 PF00082 0.500
CLV_PCSK_SKI1_1 781 785 PF00082 0.538
CLV_Separin_Metazoa 358 362 PF03568 0.495
CLV_Separin_Metazoa 413 417 PF03568 0.504
DEG_APCC_DBOX_1 155 163 PF00400 0.615
DEG_APCC_DBOX_1 282 290 PF00400 0.389
DEG_APCC_DBOX_1 345 353 PF00400 0.525
DEG_APCC_DBOX_1 558 566 PF00400 0.384
DEG_SCF_FBW7_1 478 485 PF00400 0.513
DEG_SIAH_1 508 516 PF03145 0.532
DEG_SPOP_SBC_1 415 419 PF00917 0.624
DOC_ANK_TNKS_1 726 733 PF00023 0.586
DOC_CKS1_1 479 484 PF01111 0.513
DOC_CKS1_1 506 511 PF01111 0.531
DOC_CYCLIN_RxL_1 320 328 PF00134 0.518
DOC_CYCLIN_RxL_1 547 557 PF00134 0.408
DOC_CYCLIN_RxL_1 559 571 PF00134 0.504
DOC_MAPK_gen_1 185 194 PF00069 0.341
DOC_MAPK_gen_1 321 329 PF00069 0.397
DOC_MAPK_gen_1 361 367 PF00069 0.576
DOC_MAPK_MEF2A_6 321 329 PF00069 0.397
DOC_MAPK_NFAT4_5 322 330 PF00069 0.393
DOC_PP1_RVXF_1 232 238 PF00149 0.531
DOC_PP1_RVXF_1 689 695 PF00149 0.457
DOC_PP1_RVXF_1 8 14 PF00149 0.475
DOC_USP7_MATH_1 31 35 PF00917 0.575
DOC_USP7_MATH_1 414 418 PF00917 0.706
DOC_USP7_MATH_1 42 46 PF00917 0.561
DOC_USP7_MATH_1 420 424 PF00917 0.725
DOC_USP7_MATH_1 442 446 PF00917 0.514
DOC_USP7_MATH_1 527 531 PF00917 0.546
DOC_USP7_MATH_1 604 608 PF00917 0.559
DOC_USP7_MATH_1 615 619 PF00917 0.568
DOC_USP7_UBL2_3 185 189 PF12436 0.534
DOC_WW_Pin1_4 478 483 PF00397 0.688
DOC_WW_Pin1_4 505 510 PF00397 0.569
DOC_WW_Pin1_4 569 574 PF00397 0.530
DOC_WW_Pin1_4 720 725 PF00397 0.596
LIG_14-3-3_CanoR_1 104 112 PF00244 0.432
LIG_14-3-3_CanoR_1 234 238 PF00244 0.425
LIG_14-3-3_CanoR_1 252 262 PF00244 0.358
LIG_14-3-3_CanoR_1 299 307 PF00244 0.388
LIG_14-3-3_CanoR_1 362 368 PF00244 0.460
LIG_14-3-3_CanoR_1 416 424 PF00244 0.622
LIG_14-3-3_CanoR_1 472 480 PF00244 0.687
LIG_14-3-3_CanoR_1 484 488 PF00244 0.710
LIG_14-3-3_CanoR_1 646 651 PF00244 0.583
LIG_14-3-3_CanoR_1 669 673 PF00244 0.503
LIG_14-3-3_CanoR_1 8 14 PF00244 0.628
LIG_Actin_WH2_2 330 345 PF00022 0.582
LIG_BRCT_BRCA1_1 113 117 PF00533 0.440
LIG_BRCT_BRCA1_1 280 284 PF00533 0.337
LIG_BRCT_BRCA1_1 636 640 PF00533 0.642
LIG_BRCT_BRCA1_1 99 103 PF00533 0.452
LIG_BRCT_BRCA1_2 636 642 PF00533 0.642
LIG_CaM_IQ_9 135 150 PF13499 0.599
LIG_FHA_1 104 110 PF00498 0.418
LIG_FHA_1 354 360 PF00498 0.613
LIG_FHA_1 501 507 PF00498 0.527
LIG_FHA_1 614 620 PF00498 0.643
LIG_FHA_1 687 693 PF00498 0.546
LIG_FHA_1 720 726 PF00498 0.513
LIG_FHA_1 91 97 PF00498 0.493
LIG_FHA_2 205 211 PF00498 0.480
LIG_FHA_2 304 310 PF00498 0.461
LIG_FHA_2 371 377 PF00498 0.504
LIG_FHA_2 621 627 PF00498 0.675
LIG_FHA_2 782 788 PF00498 0.527
LIG_FHA_2 789 795 PF00498 0.588
LIG_LIR_Gen_1 273 282 PF02991 0.548
LIG_LIR_Gen_1 290 300 PF02991 0.295
LIG_LIR_Gen_1 328 337 PF02991 0.502
LIG_LIR_Gen_1 45 54 PF02991 0.464
LIG_LIR_Gen_1 532 541 PF02991 0.458
LIG_LIR_Gen_1 68 78 PF02991 0.510
LIG_LIR_Nem_3 114 120 PF02991 0.538
LIG_LIR_Nem_3 273 278 PF02991 0.577
LIG_LIR_Nem_3 290 296 PF02991 0.295
LIG_LIR_Nem_3 328 332 PF02991 0.529
LIG_LIR_Nem_3 37 43 PF02991 0.509
LIG_LIR_Nem_3 376 381 PF02991 0.630
LIG_LIR_Nem_3 45 51 PF02991 0.451
LIG_LIR_Nem_3 532 537 PF02991 0.462
LIG_LIR_Nem_3 637 643 PF02991 0.628
LIG_LIR_Nem_3 68 73 PF02991 0.468
LIG_LIR_Nem_3 74 78 PF02991 0.421
LIG_MLH1_MIPbox_1 113 117 PF16413 0.557
LIG_NRBOX 108 114 PF00104 0.455
LIG_PDZ_Class_3 792 797 PF00595 0.610
LIG_Pex14_1 386 390 PF04695 0.586
LIG_Pex14_2 117 121 PF04695 0.457
LIG_SH2_CRK 40 44 PF00017 0.580
LIG_SH2_CRK 70 74 PF00017 0.516
LIG_SH2_GRB2like 48 51 PF00017 0.504
LIG_SH2_NCK_1 275 279 PF00017 0.532
LIG_SH2_NCK_1 70 74 PF00017 0.433
LIG_SH2_SRC 171 174 PF00017 0.523
LIG_SH2_STAP1 48 52 PF00017 0.574
LIG_SH2_STAP1 699 703 PF00017 0.455
LIG_SH2_STAT3 335 338 PF00017 0.383
LIG_SH2_STAT5 326 329 PF00017 0.385
LIG_SH2_STAT5 390 393 PF00017 0.567
LIG_SH3_3 362 368 PF00018 0.497
LIG_SH3_3 503 509 PF00018 0.695
LIG_SUMO_SIM_anti_2 60 66 PF11976 0.459
LIG_SUMO_SIM_par_1 563 568 PF11976 0.505
LIG_SUMO_SIM_par_1 93 100 PF11976 0.483
LIG_TRAF2_1 310 313 PF00917 0.421
LIG_TRAF2_1 317 320 PF00917 0.394
LIG_TRAF2_1 629 632 PF00917 0.574
LIG_TRAF2_1 791 794 PF00917 0.447
LIG_UBA3_1 220 225 PF00899 0.328
LIG_UBA3_1 314 323 PF00899 0.402
LIG_WRC_WIRS_1 326 331 PF05994 0.386
LIG_WRC_WIRS_1 531 536 PF05994 0.525
LIG_WRC_WIRS_1 72 77 PF05994 0.426
LIG_WW_1 488 491 PF00397 0.512
MOD_CDK_SPK_2 569 574 PF00069 0.521
MOD_CDK_SPxK_1 478 484 PF00069 0.514
MOD_CDK_SPxxK_3 720 727 PF00069 0.604
MOD_CK1_1 32 38 PF00069 0.436
MOD_CK1_1 502 508 PF00069 0.674
MOD_CK1_1 517 523 PF00069 0.535
MOD_CK1_1 530 536 PF00069 0.480
MOD_CK1_1 568 574 PF00069 0.518
MOD_CK1_1 60 66 PF00069 0.459
MOD_CK1_1 613 619 PF00069 0.649
MOD_CK1_1 620 626 PF00069 0.628
MOD_CK1_1 635 641 PF00069 0.607
MOD_CK1_1 645 651 PF00069 0.669
MOD_CK1_1 668 674 PF00069 0.475
MOD_CK2_1 147 153 PF00069 0.596
MOD_CK2_1 204 210 PF00069 0.508
MOD_CK2_1 240 246 PF00069 0.514
MOD_CK2_1 303 309 PF00069 0.458
MOD_CK2_1 31 37 PF00069 0.525
MOD_CK2_1 495 501 PF00069 0.610
MOD_CK2_1 620 626 PF00069 0.724
MOD_CK2_1 645 651 PF00069 0.735
MOD_CK2_1 653 659 PF00069 0.769
MOD_CK2_1 781 787 PF00069 0.529
MOD_CK2_1 788 794 PF00069 0.585
MOD_Cter_Amidation 14 17 PF01082 0.659
MOD_Cter_Amidation 267 270 PF01082 0.558
MOD_GlcNHglycan 149 152 PF01048 0.534
MOD_GlcNHglycan 315 318 PF01048 0.370
MOD_GlcNHglycan 368 371 PF01048 0.566
MOD_GlcNHglycan 418 421 PF01048 0.517
MOD_GlcNHglycan 424 427 PF01048 0.531
MOD_GlcNHglycan 458 461 PF01048 0.575
MOD_GlcNHglycan 475 478 PF01048 0.554
MOD_GlcNHglycan 485 488 PF01048 0.703
MOD_GlcNHglycan 567 570 PF01048 0.582
MOD_GlcNHglycan 612 615 PF01048 0.725
MOD_GlcNHglycan 87 90 PF01048 0.415
MOD_GSK3_1 233 240 PF00069 0.449
MOD_GSK3_1 25 32 PF00069 0.478
MOD_GSK3_1 274 281 PF00069 0.482
MOD_GSK3_1 303 310 PF00069 0.472
MOD_GSK3_1 366 373 PF00069 0.550
MOD_GSK3_1 416 423 PF00069 0.666
MOD_GSK3_1 478 485 PF00069 0.671
MOD_GSK3_1 487 494 PF00069 0.527
MOD_GSK3_1 495 502 PF00069 0.576
MOD_GSK3_1 513 520 PF00069 0.558
MOD_GSK3_1 563 570 PF00069 0.516
MOD_GSK3_1 613 620 PF00069 0.715
MOD_GSK3_1 632 639 PF00069 0.546
MOD_GSK3_1 642 649 PF00069 0.613
MOD_GSK3_1 726 733 PF00069 0.745
MOD_GSK3_1 81 88 PF00069 0.530
MOD_N-GLC_1 354 359 PF02516 0.473
MOD_N-GLC_1 370 375 PF02516 0.501
MOD_N-GLC_1 626 631 PF02516 0.628
MOD_N-GLC_1 632 637 PF02516 0.558
MOD_N-GLC_1 659 664 PF02516 0.604
MOD_NEK2_1 162 167 PF00069 0.442
MOD_NEK2_1 179 184 PF00069 0.539
MOD_NEK2_1 226 231 PF00069 0.376
MOD_NEK2_1 248 253 PF00069 0.457
MOD_NEK2_1 263 268 PF00069 0.449
MOD_NEK2_1 288 293 PF00069 0.424
MOD_NEK2_1 325 330 PF00069 0.415
MOD_NEK2_1 435 440 PF00069 0.534
MOD_NEK2_1 565 570 PF00069 0.561
MOD_NEK2_1 57 62 PF00069 0.515
MOD_NEK2_1 636 641 PF00069 0.632
MOD_NEK2_1 725 730 PF00069 0.534
MOD_NEK2_1 96 101 PF00069 0.456
MOD_NEK2_2 233 238 PF00069 0.477
MOD_NEK2_2 9 14 PF00069 0.474
MOD_PIKK_1 263 269 PF00454 0.575
MOD_PIKK_1 347 353 PF00454 0.407
MOD_PIKK_1 380 386 PF00454 0.492
MOD_PIKK_1 435 441 PF00454 0.687
MOD_PIKK_1 454 460 PF00454 0.460
MOD_PIKK_1 788 794 PF00454 0.444
MOD_PK_1 188 194 PF00069 0.343
MOD_PKA_1 188 194 PF00069 0.538
MOD_PKA_1 471 477 PF00069 0.659
MOD_PKA_2 103 109 PF00069 0.441
MOD_PKA_2 233 239 PF00069 0.449
MOD_PKA_2 248 254 PF00069 0.397
MOD_PKA_2 298 304 PF00069 0.387
MOD_PKA_2 415 421 PF00069 0.622
MOD_PKA_2 471 477 PF00069 0.767
MOD_PKA_2 483 489 PF00069 0.607
MOD_PKA_2 645 651 PF00069 0.596
MOD_PKA_2 668 674 PF00069 0.660
MOD_PKA_2 708 714 PF00069 0.638
MOD_PKA_2 726 732 PF00069 0.802
MOD_PKA_2 9 15 PF00069 0.586
MOD_Plk_1 25 31 PF00069 0.485
MOD_Plk_1 289 295 PF00069 0.309
MOD_Plk_1 370 376 PF00069 0.567
MOD_Plk_1 632 638 PF00069 0.590
MOD_Plk_1 709 715 PF00069 0.569
MOD_Plk_2-3 71 77 PF00069 0.429
MOD_Plk_4 25 31 PF00069 0.594
MOD_Plk_4 303 309 PF00069 0.541
MOD_Plk_4 530 536 PF00069 0.457
MOD_Plk_4 60 66 PF00069 0.411
MOD_Plk_4 735 741 PF00069 0.651
MOD_ProDKin_1 478 484 PF00069 0.688
MOD_ProDKin_1 505 511 PF00069 0.570
MOD_ProDKin_1 569 575 PF00069 0.531
MOD_ProDKin_1 720 726 PF00069 0.601
MOD_SUMO_rev_2 150 159 PF00179 0.561
MOD_SUMO_rev_2 210 216 PF00179 0.531
MOD_SUMO_rev_2 316 324 PF00179 0.353
MOD_SUMO_rev_2 793 797 PF00179 0.471
TRG_DiLeu_BaEn_1 108 113 PF01217 0.497
TRG_DiLeu_BaEn_2 556 562 PF01217 0.446
TRG_DiLeu_BaLyEn_6 133 138 PF01217 0.551
TRG_DiLeu_BaLyEn_6 250 255 PF01217 0.324
TRG_DiLeu_LyEn_5 108 113 PF01217 0.483
TRG_ENDOCYTIC_2 217 220 PF00928 0.436
TRG_ENDOCYTIC_2 275 278 PF00928 0.600
TRG_ENDOCYTIC_2 326 329 PF00928 0.371
TRG_ENDOCYTIC_2 40 43 PF00928 0.543
TRG_ENDOCYTIC_2 48 51 PF00928 0.474
TRG_ENDOCYTIC_2 70 73 PF00928 0.511
TRG_ER_diArg_1 103 105 PF00400 0.447
TRG_ER_diArg_1 16 18 PF00400 0.621
TRG_ER_diArg_1 252 254 PF00400 0.338
TRG_ER_diArg_1 360 362 PF00400 0.643
TRG_ER_diArg_1 715 717 PF00400 0.484
TRG_ER_diArg_1 8 11 PF00400 0.634
TRG_NES_CRM1_1 108 123 PF08389 0.501
TRG_NES_CRM1_1 53 68 PF08389 0.469
TRG_NES_CRM1_1 544 557 PF08389 0.550
TRG_NLS_MonoExtN_4 768 775 PF00514 0.519
TRG_Pf-PMV_PEXEL_1 136 141 PF00026 0.480
TRG_Pf-PMV_PEXEL_1 143 147 PF00026 0.486
TRG_Pf-PMV_PEXEL_1 157 161 PF00026 0.406
TRG_Pf-PMV_PEXEL_1 17 21 PF00026 0.467
TRG_Pf-PMV_PEXEL_1 252 257 PF00026 0.398
TRG_Pf-PMV_PEXEL_1 550 555 PF00026 0.435
TRG_Pf-PMV_PEXEL_1 715 719 PF00026 0.460
TRG_Pf-PMV_PEXEL_1 778 782 PF00026 0.655

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1ICL4 Leptomonas seymouri 60% 100%
A0A1X0NVY2 Trypanosomatidae 39% 100%
A0A3S5ISI8 Trypanosoma rangeli 39% 100%
A0A3S7X5E6 Leishmania donovani 77% 100%
A4I7T9 Leishmania infantum 77% 100%
D0A9Z9 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 36% 100%
E9B2P7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 75% 100%
Q4Q5G0 Leishmania major 76% 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