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 major
UniProt:
Q4Q9F4_LEIMA
TriTrypDb:
LmjF.26.0370 , LMJLV39_260008600 * , LMJSD75_260008500 *
Length:
853

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 2
GO:0000152 nuclear ubiquitin ligase complex 3 2
GO:0005680 anaphase-promoting complex 4 2
GO:0005737 cytoplasm 2 2
GO:0031461 cullin-RING ubiquitin ligase complex 4 2
GO:0031974 membrane-enclosed lumen 2 2
GO:0031981 nuclear lumen 5 2
GO:0032838 plasma membrane bounded cell projection cytoplasm 4 2
GO:0032991 protein-containing complex 1 2
GO:0043233 organelle lumen 3 2
GO:0070013 intracellular organelle lumen 4 2
GO:0097014 ciliary plasm 5 2
GO:0099568 cytoplasmic region 3 2
GO:0110165 cellular anatomical entity 1 2
GO:0140513 nuclear protein-containing complex 2 2
GO:0140535 intracellular protein-containing complex 2 2
GO:1902494 catalytic complex 2 2
GO:1990234 transferase complex 3 2

Expansion

Sequence features

Q4Q9F4
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q9F4

Function

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

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 221 225 PF00656 0.550
CLV_C14_Caspase3-7 507 511 PF00656 0.726
CLV_NRD_NRD_1 240 242 PF00675 0.506
CLV_NRD_NRD_1 363 365 PF00675 0.429
CLV_NRD_NRD_1 557 559 PF00675 0.499
CLV_NRD_NRD_1 80 82 PF00675 0.483
CLV_PCSK_FUR_1 240 244 PF00082 0.534
CLV_PCSK_KEX2_1 240 242 PF00082 0.506
CLV_PCSK_KEX2_1 363 365 PF00082 0.429
CLV_PCSK_KEX2_1 557 559 PF00082 0.472
CLV_PCSK_KEX2_1 80 82 PF00082 0.483
CLV_PCSK_KEX2_1 800 802 PF00082 0.513
CLV_PCSK_PC1ET2_1 242 244 PF00082 0.530
CLV_PCSK_PC1ET2_1 800 802 PF00082 0.513
CLV_PCSK_SKI1_1 107 111 PF00082 0.459
CLV_PCSK_SKI1_1 175 179 PF00082 0.486
CLV_PCSK_SKI1_1 364 368 PF00082 0.482
CLV_PCSK_SKI1_1 792 796 PF00082 0.411
CLV_PCSK_SKI1_1 797 801 PF00082 0.411
DEG_APCC_DBOX_1 363 371 PF00400 0.524
DEG_Nend_UBRbox_1 1 4 PF02207 0.697
DEG_SCF_FBW7_1 301 306 PF00400 0.487
DEG_SPOP_SBC_1 532 536 PF00917 0.727
DOC_CKS1_1 674 679 PF01111 0.529
DOC_CYCLIN_RxL_1 172 184 PF00134 0.589
DOC_CYCLIN_RxL_1 599 608 PF00134 0.556
DOC_CYCLIN_RxL_1 789 798 PF00134 0.411
DOC_CYCLIN_yCln2_LP_2 228 234 PF00134 0.589
DOC_MAPK_gen_1 172 181 PF00069 0.587
DOC_MAPK_gen_1 257 266 PF00069 0.495
DOC_MAPK_gen_1 557 566 PF00069 0.496
DOC_MAPK_HePTP_8 343 355 PF00069 0.578
DOC_MAPK_HePTP_8 554 566 PF00069 0.591
DOC_MAPK_MEF2A_6 268 277 PF00069 0.468
DOC_MAPK_MEF2A_6 346 355 PF00069 0.572
DOC_MAPK_MEF2A_6 396 404 PF00069 0.617
DOC_MAPK_MEF2A_6 557 566 PF00069 0.598
DOC_PP1_RVXF_1 447 454 PF00149 0.529
DOC_PP1_RVXF_1 600 607 PF00149 0.552
DOC_PP2B_LxvP_1 769 772 PF13499 0.513
DOC_PP2B_LxvP_1 837 840 PF13499 0.529
DOC_USP7_MATH_1 328 332 PF00917 0.518
DOC_USP7_MATH_1 369 373 PF00917 0.466
DOC_USP7_MATH_1 383 387 PF00917 0.658
DOC_USP7_MATH_1 498 502 PF00917 0.755
DOC_USP7_MATH_1 575 579 PF00917 0.638
DOC_USP7_MATH_1 64 68 PF00917 0.590
DOC_USP7_MATH_1 659 663 PF00917 0.411
DOC_USP7_MATH_1 765 769 PF00917 0.319
DOC_USP7_MATH_1 781 785 PF00917 0.397
DOC_USP7_MATH_1 812 816 PF00917 0.624
DOC_USP7_MATH_2 494 500 PF00917 0.625
DOC_WW_Pin1_4 299 304 PF00397 0.765
DOC_WW_Pin1_4 489 494 PF00397 0.690
DOC_WW_Pin1_4 501 506 PF00397 0.537
DOC_WW_Pin1_4 673 678 PF00397 0.488
LIG_14-3-3_CanoR_1 2 11 PF00244 0.629
LIG_14-3-3_CanoR_1 219 227 PF00244 0.486
LIG_14-3-3_CanoR_1 368 377 PF00244 0.444
LIG_14-3-3_CanoR_1 396 404 PF00244 0.653
LIG_14-3-3_CanoR_1 455 463 PF00244 0.582
LIG_14-3-3_CanoR_1 476 485 PF00244 0.778
LIG_14-3-3_CanoR_1 49 53 PF00244 0.568
LIG_14-3-3_CanoR_1 624 633 PF00244 0.562
LIG_14-3-3_CanoR_1 648 654 PF00244 0.436
LIG_14-3-3_CanoR_1 692 700 PF00244 0.497
LIG_14-3-3_CanoR_1 792 797 PF00244 0.402
LIG_14-3-3_CanoR_1 80 86 PF00244 0.501
LIG_14-3-3_CanoR_1 98 106 PF00244 0.256
LIG_BIR_III_2 224 228 PF00653 0.441
LIG_eIF4E_1 681 687 PF01652 0.456
LIG_FHA_1 206 212 PF00498 0.494
LIG_FHA_1 338 344 PF00498 0.637
LIG_FHA_1 371 377 PF00498 0.520
LIG_FHA_1 5 11 PF00498 0.633
LIG_FHA_1 568 574 PF00498 0.500
LIG_FHA_1 58 64 PF00498 0.494
LIG_FHA_1 584 590 PF00498 0.680
LIG_FHA_1 662 668 PF00498 0.411
LIG_FHA_1 699 705 PF00498 0.470
LIG_FHA_1 98 104 PF00498 0.280
LIG_FHA_2 219 225 PF00498 0.584
LIG_FHA_2 287 293 PF00498 0.661
LIG_FHA_2 502 508 PF00498 0.778
LIG_FHA_2 793 799 PF00498 0.411
LIG_FHA_2 823 829 PF00498 0.519
LIG_GBD_Chelix_1 689 697 PF00786 0.586
LIG_LIR_Apic_2 828 833 PF02991 0.482
LIG_LIR_Gen_1 146 155 PF02991 0.524
LIG_LIR_Gen_1 421 432 PF02991 0.613
LIG_LIR_Gen_1 756 765 PF02991 0.416
LIG_LIR_Gen_1 784 794 PF02991 0.436
LIG_LIR_Gen_1 831 840 PF02991 0.540
LIG_LIR_Nem_3 146 152 PF02991 0.454
LIG_LIR_Nem_3 421 427 PF02991 0.529
LIG_LIR_Nem_3 450 456 PF02991 0.553
LIG_LIR_Nem_3 756 760 PF02991 0.416
LIG_LIR_Nem_3 784 789 PF02991 0.513
LIG_LIR_Nem_3 831 837 PF02991 0.547
LIG_PDZ_Class_3 848 853 PF00595 0.614
LIG_REV1ctd_RIR_1 451 459 PF16727 0.499
LIG_SH2_CRK 348 352 PF00017 0.531
LIG_SH2_CRK 683 687 PF00017 0.549
LIG_SH2_CRK 744 748 PF00017 0.478
LIG_SH2_CRK 757 761 PF00017 0.322
LIG_SH2_NCK_1 802 806 PF00017 0.411
LIG_SH2_NCK_1 830 834 PF00017 0.525
LIG_SH2_SRC 244 247 PF00017 0.591
LIG_SH2_SRC 42 45 PF00017 0.588
LIG_SH2_SRC 612 615 PF00017 0.580
LIG_SH2_SRC 681 684 PF00017 0.567
LIG_SH2_SRC 750 753 PF00017 0.513
LIG_SH2_SRC 802 805 PF00017 0.411
LIG_SH2_STAP1 244 248 PF00017 0.587
LIG_SH2_STAP1 612 616 PF00017 0.577
LIG_SH2_STAP1 750 754 PF00017 0.411
LIG_SH2_STAP1 802 806 PF00017 0.411
LIG_SH2_STAP1 99 103 PF00017 0.436
LIG_SH2_STAT3 643 646 PF00017 0.513
LIG_SH2_STAT5 204 207 PF00017 0.589
LIG_SH2_STAT5 42 45 PF00017 0.510
LIG_SH2_STAT5 528 531 PF00017 0.604
LIG_SH2_STAT5 644 647 PF00017 0.411
LIG_SH2_STAT5 99 102 PF00017 0.358
LIG_SH3_3 487 493 PF00018 0.731
LIG_SH3_3 846 852 PF00018 0.721
LIG_SUMO_SIM_anti_2 235 240 PF11976 0.572
LIG_SUMO_SIM_anti_2 406 411 PF11976 0.467
LIG_SUMO_SIM_par_1 408 413 PF11976 0.443
LIG_TRAF2_1 143 146 PF00917 0.487
LIG_TRAF2_1 294 297 PF00917 0.629
LIG_TRAF2_1 840 843 PF00917 0.564
LIG_TRAF2_1 848 851 PF00917 0.629
LIG_TYR_ITIM 832 837 PF00017 0.546
MOD_CDK_SPK_2 501 506 PF00069 0.656
MOD_CDK_SPxK_1 299 305 PF00069 0.754
MOD_CK1_1 288 294 PF00069 0.488
MOD_CK1_1 331 337 PF00069 0.552
MOD_CK1_1 395 401 PF00069 0.667
MOD_CK1_1 501 507 PF00069 0.719
MOD_CK1_1 515 521 PF00069 0.754
MOD_CK1_1 567 573 PF00069 0.581
MOD_CK1_1 815 821 PF00069 0.654
MOD_CK2_1 286 292 PF00069 0.537
MOD_CK2_1 456 462 PF00069 0.575
MOD_CK2_1 476 482 PF00069 0.781
MOD_CK2_1 501 507 PF00069 0.796
MOD_CK2_1 515 521 PF00069 0.672
MOD_CK2_1 624 630 PF00069 0.673
MOD_CK2_1 792 798 PF00069 0.411
MOD_GlcNHglycan 107 110 PF01048 0.362
MOD_GlcNHglycan 326 329 PF01048 0.595
MOD_GlcNHglycan 385 388 PF01048 0.735
MOD_GlcNHglycan 517 521 PF01048 0.779
MOD_GlcNHglycan 60 63 PF01048 0.487
MOD_GlcNHglycan 783 786 PF01048 0.439
MOD_GlcNHglycan 816 820 PF01048 0.568
MOD_GSK3_1 164 171 PF00069 0.468
MOD_GSK3_1 299 306 PF00069 0.644
MOD_GSK3_1 324 331 PF00069 0.514
MOD_GSK3_1 337 344 PF00069 0.501
MOD_GSK3_1 47 54 PF00069 0.447
MOD_GSK3_1 496 503 PF00069 0.730
MOD_GSK3_1 512 519 PF00069 0.726
MOD_GSK3_1 526 533 PF00069 0.698
MOD_GSK3_1 573 580 PF00069 0.562
MOD_GSK3_1 581 588 PF00069 0.693
MOD_GSK3_1 620 627 PF00069 0.544
MOD_GSK3_1 669 676 PF00069 0.504
MOD_GSK3_1 777 784 PF00069 0.418
MOD_GSK3_1 97 104 PF00069 0.494
MOD_N-GLC_1 501 506 PF02516 0.726
MOD_N-GLC_2 91 93 PF02516 0.474
MOD_NEK2_1 1 6 PF00069 0.629
MOD_NEK2_1 205 210 PF00069 0.560
MOD_NEK2_1 232 237 PF00069 0.445
MOD_NEK2_1 285 290 PF00069 0.525
MOD_NEK2_1 31 36 PF00069 0.424
MOD_NEK2_1 314 319 PF00069 0.425
MOD_NEK2_1 370 375 PF00069 0.500
MOD_NEK2_1 377 382 PF00069 0.524
MOD_NEK2_1 410 415 PF00069 0.451
MOD_NEK2_1 48 53 PF00069 0.555
MOD_NEK2_1 564 569 PF00069 0.545
MOD_NEK2_1 820 825 PF00069 0.566
MOD_PIKK_1 437 443 PF00454 0.588
MOD_PIKK_1 496 502 PF00454 0.799
MOD_PIKK_1 573 579 PF00454 0.584
MOD_PIKK_1 661 667 PF00454 0.280
MOD_PK_1 341 347 PF00069 0.533
MOD_PK_1 512 518 PF00069 0.656
MOD_PKA_2 1 7 PF00069 0.644
MOD_PKA_2 218 224 PF00069 0.451
MOD_PKA_2 377 383 PF00069 0.648
MOD_PKA_2 395 401 PF00069 0.637
MOD_PKA_2 437 443 PF00069 0.613
MOD_PKA_2 48 54 PF00069 0.569
MOD_PKA_2 530 536 PF00069 0.736
MOD_PKA_2 691 697 PF00069 0.506
MOD_PKA_2 97 103 PF00069 0.376
MOD_Plk_1 341 347 PF00069 0.533
MOD_Plk_1 64 70 PF00069 0.483
MOD_Plk_1 842 848 PF00069 0.593
MOD_Plk_4 191 197 PF00069 0.478
MOD_Plk_4 206 212 PF00069 0.500
MOD_Plk_4 38 44 PF00069 0.489
MOD_Plk_4 81 87 PF00069 0.457
MOD_ProDKin_1 299 305 PF00069 0.754
MOD_ProDKin_1 489 495 PF00069 0.692
MOD_ProDKin_1 501 507 PF00069 0.537
MOD_ProDKin_1 673 679 PF00069 0.479
MOD_SUMO_for_1 523 526 PF00179 0.771
MOD_SUMO_rev_2 167 177 PF00179 0.481
TRG_DiLeu_BaEn_1 206 211 PF01217 0.521
TRG_DiLeu_BaEn_4 720 726 PF01217 0.690
TRG_DiLeu_LyEn_5 720 725 PF01217 0.573
TRG_ENDOCYTIC_2 348 351 PF00928 0.531
TRG_ENDOCYTIC_2 424 427 PF00928 0.468
TRG_ENDOCYTIC_2 683 686 PF00928 0.551
TRG_ENDOCYTIC_2 744 747 PF00928 0.411
TRG_ENDOCYTIC_2 757 760 PF00928 0.411
TRG_ENDOCYTIC_2 834 837 PF00928 0.546
TRG_ER_diArg_1 169 172 PF00400 0.519
TRG_ER_diArg_1 239 241 PF00400 0.487
TRG_ER_diArg_1 556 558 PF00400 0.488
TRG_ER_diArg_1 591 594 PF00400 0.511
TRG_ER_diArg_1 79 81 PF00400 0.511
TRG_NES_CRM1_1 408 421 PF08389 0.524
TRG_NLS_MonoExtC_3 240 246 PF00514 0.535
TRG_NLS_MonoExtN_4 172 179 PF00514 0.492
TRG_NLS_MonoExtN_4 240 245 PF00514 0.536
TRG_Pf-PMV_PEXEL_1 8 12 PF00026 0.513

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P507 Leptomonas seymouri 51% 100%
A0A3Q8IDI5 Leishmania donovani 93% 100%
A4HEP3 Leishmania braziliensis 73% 100%
A4I1X3 Leishmania infantum 93% 100%
E9AY19 Leishmania mexicana (strain MHOM/GT/2001/U1103) 90% 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