LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein, conserved
Species:
Leishmania braziliensis
UniProt:
A4H7Y1_LEIBR
TriTrypDb:
LbrM.15.0110 , LBRM2903_150006100
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: 11
NetGPI no yes: 0, no: 11
Cellular components
Term Name Level Count
GO:0005737 cytoplasm 2 1
GO:0005929 cilium 4 1
GO:0042995 cell projection 2 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0110165 cellular anatomical entity 1 2
GO:0120025 plasma membrane bounded cell projection 3 1
GO:0016020 membrane 2 1

Expansion

Sequence features

A4H7Y1
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4H7Y1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 146 150 PF00656 0.603
CLV_C14_Caspase3-7 283 287 PF00656 0.311
CLV_NRD_NRD_1 108 110 PF00675 0.794
CLV_NRD_NRD_1 234 236 PF00675 0.689
CLV_NRD_NRD_1 260 262 PF00675 0.459
CLV_NRD_NRD_1 387 389 PF00675 0.479
CLV_NRD_NRD_1 690 692 PF00675 0.638
CLV_NRD_NRD_1 717 719 PF00675 0.440
CLV_NRD_NRD_1 758 760 PF00675 0.500
CLV_PCSK_FUR_1 385 389 PF00082 0.552
CLV_PCSK_KEX2_1 108 110 PF00082 0.798
CLV_PCSK_KEX2_1 260 262 PF00082 0.457
CLV_PCSK_KEX2_1 387 389 PF00082 0.453
CLV_PCSK_KEX2_1 690 692 PF00082 0.719
CLV_PCSK_KEX2_1 717 719 PF00082 0.567
CLV_PCSK_KEX2_1 758 760 PF00082 0.500
CLV_PCSK_PC1ET2_1 690 692 PF00082 0.719
CLV_PCSK_SKI1_1 235 239 PF00082 0.738
CLV_PCSK_SKI1_1 273 277 PF00082 0.469
CLV_PCSK_SKI1_1 322 326 PF00082 0.414
CLV_PCSK_SKI1_1 388 392 PF00082 0.457
CLV_PCSK_SKI1_1 608 612 PF00082 0.419
CLV_PCSK_SKI1_1 616 620 PF00082 0.451
DEG_APCC_DBOX_1 615 623 PF00400 0.456
DEG_MDM2_SWIB_1 298 305 PF02201 0.512
DEG_Nend_UBRbox_1 1 4 PF02207 0.735
DEG_SCF_FBW7_1 160 166 PF00400 0.337
DEG_SCF_FBW7_1 555 562 PF00400 0.602
DEG_SCF_TRCP1_1 208 214 PF00400 0.661
DEG_SPOP_SBC_1 227 231 PF00917 0.746
DEG_SPOP_SBC_1 28 32 PF00917 0.509
DEG_SPOP_SBC_1 675 679 PF00917 0.503
DOC_ANK_TNKS_1 13 20 PF00023 0.514
DOC_CKS1_1 115 120 PF01111 0.501
DOC_CKS1_1 160 165 PF01111 0.329
DOC_CKS1_1 380 385 PF01111 0.573
DOC_CYCLIN_RxL_1 613 623 PF00134 0.580
DOC_MAPK_FxFP_2 393 396 PF00069 0.292
DOC_MAPK_gen_1 108 115 PF00069 0.539
DOC_MAPK_gen_1 179 188 PF00069 0.257
DOC_MAPK_HePTP_8 635 647 PF00069 0.554
DOC_MAPK_MEF2A_6 638 647 PF00069 0.531
DOC_PP1_RVXF_1 552 558 PF00149 0.538
DOC_PP2B_LxvP_1 511 514 PF13499 0.463
DOC_PP4_FxxP_1 164 167 PF00568 0.355
DOC_PP4_FxxP_1 393 396 PF00568 0.483
DOC_PP4_FxxP_1 734 737 PF00568 0.625
DOC_USP7_MATH_1 143 147 PF00917 0.567
DOC_USP7_MATH_1 227 231 PF00917 0.757
DOC_USP7_MATH_1 547 551 PF00917 0.485
DOC_USP7_MATH_1 580 584 PF00917 0.533
DOC_USP7_MATH_1 596 600 PF00917 0.368
DOC_USP7_MATH_1 675 679 PF00917 0.553
DOC_USP7_MATH_1 693 697 PF00917 0.621
DOC_USP7_UBL2_3 686 690 PF12436 0.719
DOC_USP7_UBL2_3 96 100 PF12436 0.524
DOC_WW_Pin1_4 100 105 PF00397 0.720
DOC_WW_Pin1_4 114 119 PF00397 0.711
DOC_WW_Pin1_4 159 164 PF00397 0.329
DOC_WW_Pin1_4 379 384 PF00397 0.526
DOC_WW_Pin1_4 426 431 PF00397 0.454
DOC_WW_Pin1_4 450 455 PF00397 0.435
DOC_WW_Pin1_4 543 548 PF00397 0.502
DOC_WW_Pin1_4 555 560 PF00397 0.465
DOC_WW_Pin1_4 568 573 PF00397 0.407
DOC_WW_Pin1_4 576 581 PF00397 0.427
DOC_WW_Pin1_4 583 588 PF00397 0.418
DOC_WW_Pin1_4 733 738 PF00397 0.632
DOC_WW_Pin1_4 8 13 PF00397 0.572
LIG_14-3-3_CanoR_1 170 178 PF00244 0.484
LIG_14-3-3_CanoR_1 228 233 PF00244 0.701
LIG_14-3-3_CanoR_1 273 280 PF00244 0.439
LIG_14-3-3_CanoR_1 589 593 PF00244 0.553
LIG_14-3-3_CanoR_1 674 681 PF00244 0.659
LIG_14-3-3_CanoR_1 701 709 PF00244 0.439
LIG_Actin_WH2_2 277 292 PF00022 0.481
LIG_Actin_WH2_2 313 328 PF00022 0.591
LIG_Actin_WH2_2 333 351 PF00022 0.649
LIG_BRCT_BRCA1_1 627 631 PF00533 0.406
LIG_CtBP_PxDLS_1 482 486 PF00389 0.523
LIG_deltaCOP1_diTrp_1 299 302 PF00928 0.440
LIG_deltaCOP1_diTrp_1 494 497 PF00928 0.590
LIG_FHA_1 191 197 PF00498 0.464
LIG_FHA_1 221 227 PF00498 0.649
LIG_FHA_1 23 29 PF00498 0.510
LIG_FHA_1 395 401 PF00498 0.538
LIG_FHA_1 486 492 PF00498 0.577
LIG_FHA_1 506 512 PF00498 0.422
LIG_FHA_1 589 595 PF00498 0.463
LIG_FHA_1 613 619 PF00498 0.549
LIG_FHA_1 762 768 PF00498 0.545
LIG_FHA_2 101 107 PF00498 0.553
LIG_FHA_2 153 159 PF00498 0.380
LIG_FHA_2 240 246 PF00498 0.718
LIG_FHA_2 478 484 PF00498 0.460
LIG_FHA_2 502 508 PF00498 0.524
LIG_FHA_2 701 707 PF00498 0.443
LIG_LIR_Apic_2 162 167 PF02991 0.358
LIG_LIR_Gen_1 151 161 PF02991 0.579
LIG_LIR_Gen_1 269 278 PF02991 0.542
LIG_LIR_Gen_1 299 307 PF02991 0.427
LIG_LIR_Gen_1 453 463 PF02991 0.428
LIG_LIR_Gen_1 531 540 PF02991 0.563
LIG_LIR_Gen_1 591 596 PF02991 0.407
LIG_LIR_Gen_1 620 629 PF02991 0.456
LIG_LIR_Gen_1 706 716 PF02991 0.620
LIG_LIR_Nem_3 116 122 PF02991 0.727
LIG_LIR_Nem_3 151 156 PF02991 0.545
LIG_LIR_Nem_3 299 305 PF02991 0.426
LIG_LIR_Nem_3 389 395 PF02991 0.415
LIG_LIR_Nem_3 429 435 PF02991 0.399
LIG_LIR_Nem_3 453 459 PF02991 0.405
LIG_LIR_Nem_3 531 536 PF02991 0.612
LIG_LIR_Nem_3 542 548 PF02991 0.399
LIG_LIR_Nem_3 60 65 PF02991 0.620
LIG_LIR_Nem_3 620 624 PF02991 0.414
LIG_LIR_Nem_3 644 649 PF02991 0.411
LIG_LIR_Nem_3 706 712 PF02991 0.566
LIG_LIR_Nem_3 720 725 PF02991 0.379
LIG_MYND_1 426 430 PF01753 0.530
LIG_Pex14_2 298 302 PF04695 0.488
LIG_PTAP_UEV_1 326 331 PF05743 0.449
LIG_SH2_CRK 533 537 PF00017 0.609
LIG_SH2_NCK_1 119 123 PF00017 0.727
LIG_SH2_PTP2 519 522 PF00017 0.475
LIG_SH2_SRC 65 68 PF00017 0.464
LIG_SH2_STAP1 43 47 PF00017 0.604
LIG_SH2_STAP1 533 537 PF00017 0.615
LIG_SH2_STAP1 551 555 PF00017 0.503
LIG_SH2_STAP1 62 66 PF00017 0.649
LIG_SH2_STAT3 435 438 PF00017 0.537
LIG_SH2_STAT5 312 315 PF00017 0.379
LIG_SH2_STAT5 456 459 PF00017 0.394
LIG_SH2_STAT5 519 522 PF00017 0.411
LIG_SH2_STAT5 569 572 PF00017 0.540
LIG_SH2_STAT5 65 68 PF00017 0.582
LIG_SH2_STAT5 725 728 PF00017 0.508
LIG_SH2_STAT5 733 736 PF00017 0.482
LIG_SH2_STAT5 785 788 PF00017 0.562
LIG_SH3_1 377 383 PF00018 0.337
LIG_SH3_2 380 385 PF14604 0.573
LIG_SH3_2 405 410 PF14604 0.607
LIG_SH3_3 112 118 PF00018 0.706
LIG_SH3_3 193 199 PF00018 0.517
LIG_SH3_3 243 249 PF00018 0.594
LIG_SH3_3 321 327 PF00018 0.442
LIG_SH3_3 359 365 PF00018 0.523
LIG_SH3_3 377 383 PF00018 0.567
LIG_SH3_3 402 408 PF00018 0.563
LIG_SH3_3 52 58 PF00018 0.477
LIG_SH3_3 560 566 PF00018 0.486
LIG_SH3_4 96 103 PF00018 0.534
LIG_Sin3_3 409 416 PF02671 0.628
LIG_Sin3_3 88 95 PF02671 0.521
LIG_SUMO_SIM_anti_2 29 37 PF11976 0.697
LIG_SUMO_SIM_par_1 303 308 PF11976 0.542
LIG_SUMO_SIM_par_1 312 317 PF11976 0.227
LIG_TRAF2_1 104 107 PF00917 0.554
LIG_TRAF2_1 293 296 PF00917 0.519
LIG_TRAF2_1 367 370 PF00917 0.721
LIG_TYR_ITSM 115 122 PF00017 0.742
LIG_Vh1_VBS_1 595 613 PF01044 0.495
LIG_WRC_WIRS_1 456 461 PF05994 0.516
LIG_WRC_WIRS_1 618 623 PF05994 0.438
MOD_CDC14_SPxK_1 586 589 PF00782 0.312
MOD_CDK_SPxK_1 379 385 PF00069 0.577
MOD_CDK_SPxK_1 583 589 PF00069 0.302
MOD_CDK_SPxK_1 8 14 PF00069 0.507
MOD_CDK_SPxxK_3 163 170 PF00069 0.376
MOD_CK1_1 148 154 PF00069 0.626
MOD_CK1_1 190 196 PF00069 0.572
MOD_CK1_1 213 219 PF00069 0.697
MOD_CK1_1 220 226 PF00069 0.656
MOD_CK1_1 29 35 PF00069 0.705
MOD_CK1_1 332 338 PF00069 0.687
MOD_CK1_1 441 447 PF00069 0.520
MOD_CK1_1 455 461 PF00069 0.443
MOD_CK1_1 464 470 PF00069 0.548
MOD_CK1_1 503 509 PF00069 0.588
MOD_CK1_1 583 589 PF00069 0.302
MOD_CK1_1 620 626 PF00069 0.500
MOD_CK1_1 679 685 PF00069 0.632
MOD_CK2_1 100 106 PF00069 0.551
MOD_CK2_1 152 158 PF00069 0.364
MOD_CK2_1 239 245 PF00069 0.695
MOD_CK2_1 363 369 PF00069 0.592
MOD_CK2_1 38 44 PF00069 0.647
MOD_CK2_1 462 468 PF00069 0.560
MOD_CK2_1 477 483 PF00069 0.358
MOD_CK2_1 700 706 PF00069 0.674
MOD_GlcNHglycan 207 211 PF01048 0.718
MOD_GlcNHglycan 315 319 PF01048 0.420
MOD_GlcNHglycan 327 330 PF01048 0.540
MOD_GlcNHglycan 337 340 PF01048 0.718
MOD_GlcNHglycan 4 7 PF01048 0.627
MOD_GlcNHglycan 445 448 PF01048 0.514
MOD_GlcNHglycan 533 536 PF01048 0.625
MOD_GlcNHglycan 627 630 PF01048 0.491
MOD_GlcNHglycan 694 698 PF01048 0.716
MOD_GlcNHglycan 764 767 PF01048 0.426
MOD_GSK3_1 148 155 PF00069 0.496
MOD_GSK3_1 159 166 PF00069 0.406
MOD_GSK3_1 190 197 PF00069 0.568
MOD_GSK3_1 206 213 PF00069 0.516
MOD_GSK3_1 216 223 PF00069 0.689
MOD_GSK3_1 22 29 PF00069 0.775
MOD_GSK3_1 274 281 PF00069 0.444
MOD_GSK3_1 314 321 PF00069 0.535
MOD_GSK3_1 325 332 PF00069 0.590
MOD_GSK3_1 395 402 PF00069 0.485
MOD_GSK3_1 501 508 PF00069 0.487
MOD_GSK3_1 531 538 PF00069 0.541
MOD_GSK3_1 543 550 PF00069 0.411
MOD_GSK3_1 555 562 PF00069 0.616
MOD_GSK3_1 576 583 PF00069 0.510
MOD_GSK3_1 608 615 PF00069 0.393
MOD_GSK3_1 675 682 PF00069 0.681
MOD_GSK3_1 96 103 PF00069 0.637
MOD_LATS_1 498 504 PF00433 0.518
MOD_LATS_1 94 100 PF00433 0.525
MOD_N-GLC_1 372 377 PF02516 0.610
MOD_NEK2_1 1 6 PF00069 0.642
MOD_NEK2_1 194 199 PF00069 0.631
MOD_NEK2_1 226 231 PF00069 0.533
MOD_NEK2_1 274 279 PF00069 0.540
MOD_NEK2_1 298 303 PF00069 0.545
MOD_NEK2_1 399 404 PF00069 0.412
MOD_NEK2_1 412 417 PF00069 0.495
MOD_NEK2_1 485 490 PF00069 0.577
MOD_NEK2_1 509 514 PF00069 0.498
MOD_NEK2_2 372 377 PF00069 0.671
MOD_NEK2_2 38 43 PF00069 0.668
MOD_NEK2_2 474 479 PF00069 0.447
MOD_OFUCOSY 593 598 PF10250 0.547
MOD_PIKK_1 171 177 PF00454 0.449
MOD_PIKK_1 213 219 PF00454 0.549
MOD_PIKK_1 228 234 PF00454 0.517
MOD_PIKK_1 483 489 PF00454 0.596
MOD_PIKK_1 580 586 PF00454 0.490
MOD_PIKK_1 657 663 PF00454 0.699
MOD_PIKK_1 710 716 PF00454 0.624
MOD_PK_1 349 355 PF00069 0.518
MOD_PKA_2 169 175 PF00069 0.491
MOD_PKA_2 227 233 PF00069 0.699
MOD_PKA_2 325 331 PF00069 0.631
MOD_PKA_2 588 594 PF00069 0.552
MOD_PKA_2 700 706 PF00069 0.700
MOD_Plk_1 151 157 PF00069 0.560
MOD_Plk_1 298 304 PF00069 0.508
MOD_Plk_1 332 338 PF00069 0.503
MOD_Plk_1 751 757 PF00069 0.659
MOD_Plk_2-3 152 158 PF00069 0.502
MOD_Plk_2-3 239 245 PF00069 0.497
MOD_Plk_4 239 245 PF00069 0.617
MOD_Plk_4 31 37 PF00069 0.666
MOD_Plk_4 38 44 PF00069 0.558
MOD_Plk_4 395 401 PF00069 0.498
MOD_Plk_4 452 458 PF00069 0.539
MOD_Plk_4 617 623 PF00069 0.500
MOD_Plk_4 738 744 PF00069 0.576
MOD_ProDKin_1 100 106 PF00069 0.721
MOD_ProDKin_1 114 120 PF00069 0.711
MOD_ProDKin_1 159 165 PF00069 0.333
MOD_ProDKin_1 379 385 PF00069 0.530
MOD_ProDKin_1 426 432 PF00069 0.454
MOD_ProDKin_1 450 456 PF00069 0.432
MOD_ProDKin_1 543 549 PF00069 0.497
MOD_ProDKin_1 555 561 PF00069 0.474
MOD_ProDKin_1 568 574 PF00069 0.404
MOD_ProDKin_1 576 582 PF00069 0.432
MOD_ProDKin_1 583 589 PF00069 0.424
MOD_ProDKin_1 733 739 PF00069 0.635
MOD_ProDKin_1 8 14 PF00069 0.574
MOD_SUMO_for_1 749 752 PF00179 0.608
MOD_SUMO_rev_2 72 80 PF00179 0.599
TRG_DiLeu_BaEn_2 616 622 PF01217 0.383
TRG_DiLeu_BaEn_2 729 735 PF01217 0.560
TRG_DiLeu_BaLyEn_6 374 379 PF01217 0.481
TRG_DiLeu_BaLyEn_6 573 578 PF01217 0.564
TRG_ENDOCYTIC_2 119 122 PF00928 0.721
TRG_ENDOCYTIC_2 185 188 PF00928 0.360
TRG_ENDOCYTIC_2 271 274 PF00928 0.423
TRG_ENDOCYTIC_2 456 459 PF00928 0.394
TRG_ENDOCYTIC_2 518 521 PF00928 0.385
TRG_ENDOCYTIC_2 533 536 PF00928 0.522
TRG_ER_diArg_1 385 388 PF00400 0.493
TRG_ER_diArg_1 716 718 PF00400 0.431
TRG_ER_diArg_1 757 759 PF00400 0.502
TRG_Pf-PMV_PEXEL_1 479 483 PF00026 0.477

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1PCR8 Leptomonas seymouri 48% 98%
A0A0S4KHH2 Bodo saltans 29% 92%
A0A1X0NTL8 Trypanosomatidae 38% 100%
A0A3Q8IA12 Leishmania donovani 74% 100%
A0A422NS84 Trypanosoma rangeli 35% 100%
A4HWA8 Leishmania infantum 74% 100%
C9ZNU4 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 33% 100%
E9AQ08 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 100%
Q4QFH3 Leishmania major 72% 100%
V5AWK1 Trypanosoma cruzi 34% 96%

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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