LeishMANIAdb
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TPR_REGION domain-containing protein

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

Quick info

Protein:
TPR_REGION domain-containing protein
Gene product:
TPR repeat, putative
Species:
Leishmania braziliensis
UniProt:
A4HEP3_LEIBR
TriTrypDb:
LbrM.26.0390 , LBRM2903_260008800 *
Length:
846

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: 6
NetGPI no yes: 0, no: 6
Cellular components
Term Name Level Count
GO:0000151 ubiquitin ligase complex 3 1
GO:0000152 nuclear ubiquitin ligase complex 3 1
GO:0005680 anaphase-promoting complex 4 1
GO:0005737 cytoplasm 2 1
GO:0031461 cullin-RING ubiquitin ligase complex 4 1
GO:0031974 membrane-enclosed lumen 2 1
GO:0031981 nuclear lumen 5 1
GO:0032838 plasma membrane bounded cell projection cytoplasm 4 1
GO:0032991 protein-containing complex 1 1
GO:0043233 organelle lumen 3 1
GO:0070013 intracellular organelle lumen 4 1
GO:0097014 ciliary plasm 5 1
GO:0099568 cytoplasmic region 3 1
GO:0110165 cellular anatomical entity 1 1
GO:0140513 nuclear protein-containing complex 2 1
GO:0140535 intracellular protein-containing complex 2 1
GO:1902494 catalytic complex 2 1
GO:1990234 transferase complex 3 1

Expansion

Sequence features

A4HEP3
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HEP3

Function

Biological processes
Term Name Level Count
GO:0006508 proteolysis 4 1
GO:0006511 ubiquitin-dependent protein catabolic process 7 1
GO:0006807 nitrogen compound metabolic process 2 1
GO:0007088 regulation of mitotic nuclear division 6 1
GO:0007091 metaphase/anaphase transition of mitotic cell cycle 5 1
GO:0007346 regulation of mitotic cell cycle 5 1
GO:0008152 metabolic process 1 1
GO:0009056 catabolic process 2 1
GO:0009057 macromolecule catabolic process 4 1
GO:0009987 cellular process 1 1
GO:0010498 proteasomal protein catabolic process 5 1
GO:0010564 regulation of cell cycle process 5 1
GO:0010638 positive regulation of organelle organization 6 1
GO:0010965 regulation of mitotic sister chromatid separation 6 1
GO:0016567 protein ubiquitination 7 1
GO:0019538 protein metabolic process 3 1
GO:0019941 modification-dependent protein catabolic process 6 1
GO:0022402 cell cycle process 2 1
GO:0030071 regulation of mitotic metaphase/anaphase transition 7 1
GO:0030163 protein catabolic process 4 1
GO:0031145 anaphase-promoting complex-dependent catabolic process 7 1
GO:0032446 protein modification by small protein conjugation 6 1
GO:0033043 regulation of organelle organization 5 1
GO:0033044 regulation of chromosome organization 6 1
GO:0033045 regulation of sister chromatid segregation 5 1
GO:0036211 protein modification process 4 1
GO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process 6 1
GO:0043170 macromolecule metabolic process 3 1
GO:0043412 macromolecule modification 4 1
GO:0043632 modification-dependent macromolecule catabolic process 5 1
GO:0044237 cellular metabolic process 2 1
GO:0044238 primary metabolic process 2 1
GO:0044248 cellular catabolic process 3 1
GO:0044260 obsolete cellular macromolecule metabolic process 3 1
GO:0044265 obsolete cellular macromolecule catabolic process 4 1
GO:0044770 cell cycle phase transition 3 1
GO:0044772 mitotic cell cycle phase transition 4 1
GO:0044784 metaphase/anaphase transition of cell cycle 4 1
GO:0045787 positive regulation of cell cycle 5 1
GO:0045840 positive regulation of mitotic nuclear division 7 1
GO:0045842 positive regulation of mitotic metaphase/anaphase transition 8 1
GO:0045931 positive regulation of mitotic cell cycle 6 1
GO:0048518 positive regulation of biological process 3 1
GO:0048522 positive regulation of cellular process 4 1
GO:0050789 regulation of biological process 2 1
GO:0050794 regulation of cellular process 3 1
GO:0051128 regulation of cellular component organization 4 1
GO:0051130 positive regulation of cellular component organization 5 1
GO:0051301 cell division 2 1
GO:0051603 proteolysis involved in protein catabolic process 5 1
GO:0051726 regulation of cell cycle 4 1
GO:0051783 regulation of nuclear division 6 1
GO:0051785 positive regulation of nuclear division 7 1
GO:0051983 regulation of chromosome segregation 4 1
GO:0065007 biological regulation 1 1
GO:0070647 protein modification by small protein conjugation or removal 5 1
GO:0071704 organic substance metabolic process 2 1
GO:0090068 positive regulation of cell cycle process 6 1
GO:1901564 organonitrogen compound metabolic process 3 1
GO:1901565 organonitrogen compound catabolic process 4 1
GO:1901575 organic substance catabolic process 3 1
GO:1901970 positive regulation of mitotic sister chromatid separation 7 1
GO:1901987 regulation of cell cycle phase transition 6 1
GO:1901989 positive regulation of cell cycle phase transition 7 1
GO:1901990 regulation of mitotic cell cycle phase transition 6 1
GO:1901992 positive regulation of mitotic cell cycle phase transition 7 1
GO:1902099 regulation of metaphase/anaphase transition of cell cycle 6 1
GO:1902101 positive regulation of metaphase/anaphase transition of cell cycle 7 1
GO:1903047 mitotic cell cycle process 3 1
GO:1905818 regulation of chromosome separation 5 1
GO:1905820 positive regulation of chromosome separation 6 1
Could not find GO molecular_function term for this entry.

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 464 468 PF00656 0.450
CLV_C14_Caspase3-7 655 659 PF00656 0.317
CLV_NRD_NRD_1 554 556 PF00675 0.470
CLV_PCSK_KEX2_1 521 523 PF00082 0.538
CLV_PCSK_KEX2_1 554 556 PF00082 0.470
CLV_PCSK_KEX2_1 797 799 PF00082 0.388
CLV_PCSK_PC1ET2_1 521 523 PF00082 0.538
CLV_PCSK_PC1ET2_1 797 799 PF00082 0.388
CLV_PCSK_SKI1_1 109 113 PF00082 0.471
CLV_PCSK_SKI1_1 180 184 PF00082 0.438
CLV_PCSK_SKI1_1 352 356 PF00082 0.320
CLV_PCSK_SKI1_1 789 793 PF00082 0.312
CLV_PCSK_SKI1_1 794 798 PF00082 0.312
CLV_PCSK_SKI1_1 83 87 PF00082 0.303
DEG_APCC_DBOX_1 351 359 PF00400 0.320
DEG_SCF_SKP2-CKS1_1 300 307 PF00560 0.484
DOC_CYCLIN_RxL_1 174 186 PF00134 0.564
DOC_CYCLIN_RxL_1 596 605 PF00134 0.455
DOC_CYCLIN_RxL_1 786 795 PF00134 0.312
DOC_CYCLIN_yClb1_LxF_4 81 86 PF00134 0.327
DOC_CYCLIN_yCln2_LP_2 230 236 PF00134 0.468
DOC_CYCLIN_yCln2_LP_2 766 772 PF00134 0.231
DOC_MAPK_gen_1 174 183 PF00069 0.469
DOC_MAPK_gen_1 267 277 PF00069 0.362
DOC_MAPK_gen_1 521 527 PF00069 0.528
DOC_MAPK_gen_1 554 563 PF00069 0.484
DOC_MAPK_HePTP_8 345 357 PF00069 0.468
DOC_MAPK_HePTP_8 551 563 PF00069 0.526
DOC_MAPK_MEF2A_6 270 279 PF00069 0.382
DOC_MAPK_MEF2A_6 348 357 PF00069 0.465
DOC_MAPK_MEF2A_6 554 563 PF00069 0.640
DOC_MAPK_NFAT4_5 270 278 PF00069 0.293
DOC_PP1_RVXF_1 597 604 PF00149 0.450
DOC_PP1_RVXF_1 81 87 PF00149 0.319
DOC_PP2B_LxvP_1 525 528 PF13499 0.553
DOC_PP2B_LxvP_1 766 769 PF13499 0.388
DOC_PP2B_LxvP_1 834 837 PF13499 0.432
DOC_USP7_MATH_1 249 253 PF00917 0.300
DOC_USP7_MATH_1 310 314 PF00917 0.304
DOC_USP7_MATH_1 330 334 PF00917 0.461
DOC_USP7_MATH_1 371 375 PF00917 0.482
DOC_USP7_MATH_1 486 490 PF00917 0.640
DOC_USP7_MATH_1 582 586 PF00917 0.551
DOC_USP7_MATH_1 656 660 PF00917 0.389
DOC_USP7_MATH_1 66 70 PF00917 0.465
DOC_USP7_MATH_1 778 782 PF00917 0.306
DOC_USP7_MATH_1 809 813 PF00917 0.508
DOC_USP7_UBL2_3 303 307 PF12436 0.466
DOC_WW_Pin1_4 301 306 PF00397 0.753
DOC_WW_Pin1_4 482 487 PF00397 0.640
DOC_WW_Pin1_4 491 496 PF00397 0.641
DOC_WW_Pin1_4 512 517 PF00397 0.751
DOC_WW_Pin1_4 538 543 PF00397 0.583
DOC_WW_Pin1_4 761 766 PF00397 0.280
LIG_14-3-3_CanoR_1 168 176 PF00244 0.310
LIG_14-3-3_CanoR_1 17 27 PF00244 0.371
LIG_14-3-3_CanoR_1 221 229 PF00244 0.421
LIG_14-3-3_CanoR_1 370 379 PF00244 0.397
LIG_14-3-3_CanoR_1 396 406 PF00244 0.580
LIG_14-3-3_CanoR_1 457 465 PF00244 0.602
LIG_14-3-3_CanoR_1 51 55 PF00244 0.495
LIG_14-3-3_CanoR_1 522 528 PF00244 0.586
LIG_14-3-3_CanoR_1 531 537 PF00244 0.601
LIG_14-3-3_CanoR_1 759 766 PF00244 0.264
LIG_14-3-3_CanoR_1 779 784 PF00244 0.330
LIG_14-3-3_CanoR_1 789 794 PF00244 0.302
LIG_Actin_WH2_2 324 342 PF00022 0.338
LIG_Actin_WH2_2 95 111 PF00022 0.297
LIG_BIR_II_1 1 5 PF00653 0.482
LIG_BRCT_BRCA1_1 476 480 PF00533 0.504
LIG_eIF4E_1 596 602 PF01652 0.293
LIG_eIF4E_1 678 684 PF01652 0.363
LIG_FHA_1 225 231 PF00498 0.415
LIG_FHA_1 294 300 PF00498 0.461
LIG_FHA_1 340 346 PF00498 0.571
LIG_FHA_1 397 403 PF00498 0.484
LIG_FHA_1 501 507 PF00498 0.541
LIG_FHA_1 515 521 PF00498 0.503
LIG_FHA_1 565 571 PF00498 0.425
LIG_FHA_1 581 587 PF00498 0.626
LIG_FHA_1 60 66 PF00498 0.389
LIG_FHA_1 659 665 PF00498 0.419
LIG_FHA_1 696 702 PF00498 0.406
LIG_FHA_1 7 13 PF00498 0.513
LIG_FHA_1 765 771 PF00498 0.261
LIG_FHA_2 143 149 PF00498 0.366
LIG_FHA_2 170 176 PF00498 0.356
LIG_FHA_2 212 218 PF00498 0.398
LIG_FHA_2 221 227 PF00498 0.474
LIG_FHA_2 701 707 PF00498 0.349
LIG_FHA_2 790 796 PF00498 0.312
LIG_FHA_2 820 826 PF00498 0.459
LIG_GBD_Chelix_1 686 694 PF00786 0.465
LIG_LIR_Apic_2 825 830 PF02991 0.425
LIG_LIR_Gen_1 148 157 PF02991 0.429
LIG_LIR_Gen_1 423 434 PF02991 0.523
LIG_LIR_Gen_1 753 758 PF02991 0.316
LIG_LIR_Gen_1 828 839 PF02991 0.459
LIG_LIR_Nem_3 148 154 PF02991 0.420
LIG_LIR_Nem_3 347 353 PF02991 0.309
LIG_LIR_Nem_3 423 429 PF02991 0.531
LIG_LIR_Nem_3 677 683 PF02991 0.387
LIG_LIR_Nem_3 753 757 PF02991 0.316
LIG_LIR_Nem_3 781 786 PF02991 0.388
LIG_LIR_Nem_3 828 834 PF02991 0.473
LIG_SH2_CRK 350 354 PF00017 0.443
LIG_SH2_CRK 680 684 PF00017 0.430
LIG_SH2_CRK 741 745 PF00017 0.402
LIG_SH2_CRK 754 758 PF00017 0.242
LIG_SH2_GRB2like 44 47 PF00017 0.327
LIG_SH2_GRB2like 596 599 PF00017 0.298
LIG_SH2_NCK_1 799 803 PF00017 0.312
LIG_SH2_NCK_1 827 831 PF00017 0.474
LIG_SH2_SRC 101 104 PF00017 0.394
LIG_SH2_SRC 246 249 PF00017 0.465
LIG_SH2_SRC 44 47 PF00017 0.454
LIG_SH2_SRC 609 612 PF00017 0.457
LIG_SH2_SRC 678 681 PF00017 0.447
LIG_SH2_SRC 747 750 PF00017 0.388
LIG_SH2_SRC 799 802 PF00017 0.312
LIG_SH2_STAP1 246 250 PF00017 0.498
LIG_SH2_STAP1 426 430 PF00017 0.420
LIG_SH2_STAP1 44 48 PF00017 0.339
LIG_SH2_STAP1 609 613 PF00017 0.453
LIG_SH2_STAP1 747 751 PF00017 0.312
LIG_SH2_STAP1 799 803 PF00017 0.312
LIG_SH2_STAT3 640 643 PF00017 0.458
LIG_SH2_STAT5 101 104 PF00017 0.358
LIG_SH2_STAT5 19 22 PF00017 0.364
LIG_SH2_STAT5 206 209 PF00017 0.476
LIG_SH2_STAT5 218 221 PF00017 0.352
LIG_SH2_STAT5 320 323 PF00017 0.368
LIG_SH2_STAT5 426 429 PF00017 0.472
LIG_SH2_STAT5 641 644 PF00017 0.375
LIG_SH2_STAT5 831 834 PF00017 0.394
LIG_SH3_2 492 497 PF14604 0.565
LIG_SH3_3 489 495 PF00018 0.778
LIG_SH3_5 674 678 PF00018 0.303
LIG_SUMO_SIM_anti_2 237 244 PF11976 0.460
LIG_SUMO_SIM_anti_2 408 413 PF11976 0.402
LIG_SUMO_SIM_par_1 410 415 PF11976 0.379
LIG_SUMO_SIM_par_1 503 509 PF11976 0.541
LIG_SUMO_SIM_par_1 611 618 PF11976 0.300
LIG_SUMO_SIM_par_1 767 775 PF11976 0.340
LIG_TRAF2_1 145 148 PF00917 0.394
LIG_TRAF2_1 391 394 PF00917 0.529
LIG_TYR_ITIM 829 834 PF00017 0.472
MOD_CDC14_SPxK_1 494 497 PF00782 0.563
MOD_CDK_SPxK_1 301 307 PF00069 0.637
MOD_CDK_SPxK_1 491 497 PF00069 0.565
MOD_CK1_1 169 175 PF00069 0.297
MOD_CK1_1 2 8 PF00069 0.495
MOD_CK1_1 211 217 PF00069 0.305
MOD_CK1_1 388 394 PF00069 0.661
MOD_CK1_1 397 403 PF00069 0.588
MOD_CK1_1 485 491 PF00069 0.724
MOD_CK1_1 500 506 PF00069 0.718
MOD_CK1_1 512 518 PF00069 0.556
MOD_CK1_1 564 570 PF00069 0.489
MOD_CK1_1 581 587 PF00069 0.491
MOD_CK1_1 695 701 PF00069 0.304
MOD_CK1_1 764 770 PF00069 0.238
MOD_CK1_1 812 818 PF00069 0.567
MOD_CK1_1 820 826 PF00069 0.513
MOD_CK2_1 142 148 PF00069 0.330
MOD_CK2_1 169 175 PF00069 0.297
MOD_CK2_1 211 217 PF00069 0.310
MOD_CK2_1 249 255 PF00069 0.363
MOD_CK2_1 388 394 PF00069 0.639
MOD_CK2_1 458 464 PF00069 0.548
MOD_CK2_1 478 484 PF00069 0.461
MOD_CK2_1 512 518 PF00069 0.585
MOD_CK2_1 538 544 PF00069 0.412
MOD_CK2_1 621 627 PF00069 0.547
MOD_CK2_1 656 662 PF00069 0.396
MOD_CK2_1 700 706 PF00069 0.334
MOD_CK2_1 789 795 PF00069 0.312
MOD_GlcNHglycan 109 112 PF01048 0.383
MOD_GlcNHglycan 328 331 PF01048 0.490
MOD_GlcNHglycan 373 376 PF01048 0.352
MOD_GlcNHglycan 388 391 PF01048 0.704
MOD_GlcNHglycan 480 483 PF01048 0.527
MOD_GlcNHglycan 488 491 PF01048 0.641
MOD_GlcNHglycan 499 502 PF01048 0.558
MOD_GlcNHglycan 511 514 PF01048 0.703
MOD_GlcNHglycan 580 583 PF01048 0.476
MOD_GlcNHglycan 62 65 PF01048 0.422
MOD_GlcNHglycan 694 697 PF01048 0.306
MOD_GlcNHglycan 714 717 PF01048 0.433
MOD_GlcNHglycan 761 764 PF01048 0.241
MOD_GlcNHglycan 813 817 PF01048 0.467
MOD_GlcNHglycan 843 846 PF01048 0.503
MOD_GSK3_1 103 110 PF00069 0.436
MOD_GSK3_1 166 173 PF00069 0.368
MOD_GSK3_1 2 9 PF00069 0.476
MOD_GSK3_1 207 214 PF00069 0.370
MOD_GSK3_1 220 227 PF00069 0.450
MOD_GSK3_1 301 308 PF00069 0.633
MOD_GSK3_1 326 333 PF00069 0.471
MOD_GSK3_1 339 346 PF00069 0.379
MOD_GSK3_1 382 389 PF00069 0.548
MOD_GSK3_1 474 481 PF00069 0.527
MOD_GSK3_1 482 489 PF00069 0.603
MOD_GSK3_1 534 541 PF00069 0.688
MOD_GSK3_1 574 581 PF00069 0.522
MOD_GSK3_1 695 702 PF00069 0.318
MOD_GSK3_1 708 715 PF00069 0.419
MOD_LATS_1 129 135 PF00433 0.299
MOD_N-GLC_2 93 95 PF02516 0.405
MOD_NEK2_1 142 147 PF00069 0.343
MOD_NEK2_1 207 212 PF00069 0.462
MOD_NEK2_1 234 239 PF00069 0.391
MOD_NEK2_1 287 292 PF00069 0.495
MOD_NEK2_1 293 298 PF00069 0.515
MOD_NEK2_1 379 384 PF00069 0.588
MOD_NEK2_1 412 417 PF00069 0.562
MOD_NEK2_1 458 463 PF00069 0.413
MOD_NEK2_1 50 55 PF00069 0.547
MOD_NEK2_1 561 566 PF00069 0.506
MOD_NEK2_1 758 763 PF00069 0.310
MOD_NEK2_1 817 822 PF00069 0.490
MOD_NEK2_1 841 846 PF00069 0.544
MOD_NEK2_2 471 476 PF00069 0.525
MOD_PIKK_1 458 464 PF00454 0.391
MOD_PIKK_1 534 540 PF00454 0.490
MOD_PK_1 131 137 PF00069 0.319
MOD_PKA_2 220 226 PF00069 0.437
MOD_PKA_2 339 345 PF00069 0.360
MOD_PKA_2 379 385 PF00069 0.582
MOD_PKA_2 50 56 PF00069 0.493
MOD_PKA_2 574 580 PF00069 0.482
MOD_PKA_2 758 764 PF00069 0.231
MOD_PKA_2 778 784 PF00069 0.231
MOD_PKB_1 476 484 PF00069 0.530
MOD_Plk_1 66 72 PF00069 0.384
MOD_Plk_4 288 294 PF00069 0.429
MOD_Plk_4 772 778 PF00069 0.249
MOD_ProDKin_1 301 307 PF00069 0.745
MOD_ProDKin_1 482 488 PF00069 0.644
MOD_ProDKin_1 491 497 PF00069 0.642
MOD_ProDKin_1 512 518 PF00069 0.752
MOD_ProDKin_1 538 544 PF00069 0.575
MOD_ProDKin_1 761 767 PF00069 0.280
MOD_SUMO_rev_2 169 179 PF00179 0.382
TRG_DiLeu_BaLyEn_6 349 354 PF01217 0.307
TRG_ENDOCYTIC_2 350 353 PF00928 0.445
TRG_ENDOCYTIC_2 426 429 PF00928 0.457
TRG_ENDOCYTIC_2 680 683 PF00928 0.432
TRG_ENDOCYTIC_2 741 744 PF00928 0.312
TRG_ENDOCYTIC_2 754 757 PF00928 0.312
TRG_ENDOCYTIC_2 831 834 PF00928 0.475
TRG_ER_diArg_1 475 478 PF00400 0.534
TRG_ER_diArg_1 553 555 PF00400 0.459
TRG_NES_CRM1_1 410 423 PF08389 0.452
TRG_NLS_MonoExtN_4 174 181 PF00514 0.399
TRG_Pf-PMV_PEXEL_1 10 14 PF00026 0.410
TRG_Pf-PMV_PEXEL_1 440 444 PF00026 0.397

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P507 Leptomonas seymouri 47% 100%
A0A3Q8IDI5 Leishmania donovani 74% 99%
A4I1X3 Leishmania infantum 74% 99%
E9AY19 Leishmania mexicana (strain MHOM/GT/2001/U1103) 73% 99%
Q4Q9F4 Leishmania major 73% 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