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:
Q4Q8M0_LEIMA
TriTrypDb:
LmjF.28.0500 , LMJLV39_280010500 * , LMJSD75_280010500 *
Length:
712

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: 1, no: 10
NetGPI no yes: 0, no: 11
Could not find GO cellular_component term for this entry.

Expansion

Sequence features

Q4Q8M0
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q8M0

Function

Biological processes
Term Name Level Count
GO:0006457 protein folding 2 12
GO:0009987 cellular process 1 12
Molecular functions
Term Name Level Count
GO:0005488 binding 1 12
GO:0005515 protein binding 2 12
GO:0030544 Hsp70 protein binding 4 12
GO:0031072 heat shock protein binding 3 12
GO:0051879 Hsp90 protein binding 4 12

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_MEL_PAP_1 602 608 PF00089 0.630
CLV_NRD_NRD_1 208 210 PF00675 0.471
CLV_NRD_NRD_1 549 551 PF00675 0.599
CLV_NRD_NRD_1 86 88 PF00675 0.565
CLV_PCSK_FUR_1 332 336 PF00082 0.622
CLV_PCSK_KEX2_1 207 209 PF00082 0.505
CLV_PCSK_KEX2_1 224 226 PF00082 0.453
CLV_PCSK_KEX2_1 334 336 PF00082 0.598
CLV_PCSK_KEX2_1 348 350 PF00082 0.508
CLV_PCSK_KEX2_1 549 551 PF00082 0.592
CLV_PCSK_KEX2_1 85 87 PF00082 0.566
CLV_PCSK_PC1ET2_1 224 226 PF00082 0.610
CLV_PCSK_PC1ET2_1 334 336 PF00082 0.668
CLV_PCSK_PC1ET2_1 348 350 PF00082 0.586
CLV_PCSK_SKI1_1 291 295 PF00082 0.460
CLV_PCSK_SKI1_1 317 321 PF00082 0.548
CLV_PCSK_SKI1_1 414 418 PF00082 0.603
CLV_PCSK_SKI1_1 550 554 PF00082 0.525
CLV_Separin_Metazoa 670 674 PF03568 0.701
DEG_APCC_DBOX_1 134 142 PF00400 0.733
DEG_COP1_1 22 30 PF00400 0.721
DEG_Nend_UBRbox_3 1 3 PF02207 0.664
DOC_ANK_TNKS_1 640 647 PF00023 0.665
DOC_CYCLIN_RxL_1 314 324 PF00134 0.558
DOC_CYCLIN_RxL_1 411 419 PF00134 0.672
DOC_CYCLIN_yCln2_LP_2 151 157 PF00134 0.722
DOC_MAPK_gen_1 332 341 PF00069 0.565
DOC_MAPK_gen_1 458 467 PF00069 0.564
DOC_MAPK_gen_1 586 594 PF00069 0.517
DOC_PP1_RVXF_1 57 64 PF00149 0.664
DOC_PP4_FxxP_1 81 84 PF00568 0.684
DOC_USP7_MATH_1 159 163 PF00917 0.771
DOC_USP7_MATH_1 178 182 PF00917 0.694
DOC_USP7_MATH_1 277 281 PF00917 0.524
DOC_USP7_MATH_1 374 378 PF00917 0.561
DOC_USP7_MATH_1 428 432 PF00917 0.586
DOC_USP7_MATH_1 67 71 PF00917 0.676
DOC_USP7_UBL2_3 334 338 PF12436 0.662
DOC_WW_Pin1_4 490 495 PF00397 0.686
DOC_WW_Pin1_4 615 620 PF00397 0.713
LIG_14-3-3_CanoR_1 110 116 PF00244 0.586
LIG_14-3-3_CanoR_1 117 123 PF00244 0.578
LIG_14-3-3_CanoR_1 129 138 PF00244 0.497
LIG_14-3-3_CanoR_1 186 191 PF00244 0.615
LIG_14-3-3_CanoR_1 194 200 PF00244 0.535
LIG_14-3-3_CanoR_1 207 212 PF00244 0.488
LIG_14-3-3_CanoR_1 247 256 PF00244 0.510
LIG_14-3-3_CanoR_1 479 485 PF00244 0.586
LIG_14-3-3_CanoR_1 521 527 PF00244 0.486
LIG_14-3-3_CanoR_1 565 575 PF00244 0.513
LIG_14-3-3_CanoR_1 605 613 PF00244 0.630
LIG_14-3-3_CanoR_1 689 694 PF00244 0.682
LIG_APCC_ABBA_1 1 6 PF00400 0.551
LIG_APCC_ABBA_1 577 582 PF00400 0.522
LIG_BRCT_BRCA1_1 369 373 PF00533 0.636
LIG_BRCT_BRCA1_1 563 567 PF00533 0.558
LIG_FHA_1 217 223 PF00498 0.515
LIG_FHA_1 284 290 PF00498 0.467
LIG_FHA_1 367 373 PF00498 0.557
LIG_FHA_1 404 410 PF00498 0.653
LIG_FHA_1 411 417 PF00498 0.617
LIG_FHA_1 501 507 PF00498 0.556
LIG_FHA_1 574 580 PF00498 0.465
LIG_FHA_1 645 651 PF00498 0.677
LIG_FHA_1 96 102 PF00498 0.540
LIG_FHA_2 168 174 PF00498 0.743
LIG_FHA_2 612 618 PF00498 0.708
LIG_FHA_2 665 671 PF00498 0.702
LIG_FHA_2 678 684 PF00498 0.680
LIG_Integrin_isoDGR_2 384 386 PF01839 0.615
LIG_LIR_Apic_2 78 84 PF02991 0.674
LIG_LIR_Gen_1 106 116 PF02991 0.521
LIG_LIR_Gen_1 128 138 PF02991 0.727
LIG_LIR_Gen_1 558 567 PF02991 0.430
LIG_LIR_Gen_1 60 67 PF02991 0.679
LIG_LIR_Gen_1 94 105 PF02991 0.536
LIG_LIR_Nem_3 106 111 PF02991 0.533
LIG_LIR_Nem_3 128 134 PF02991 0.727
LIG_LIR_Nem_3 210 214 PF02991 0.545
LIG_LIR_Nem_3 377 383 PF02991 0.615
LIG_LIR_Nem_3 558 563 PF02991 0.415
LIG_LIR_Nem_3 576 580 PF02991 0.359
LIG_LIR_Nem_3 597 602 PF02991 0.542
LIG_LIR_Nem_3 60 66 PF02991 0.620
LIG_LIR_Nem_3 70 76 PF02991 0.509
LIG_LIR_Nem_3 94 100 PF02991 0.545
LIG_RPA_C_Fungi 247 259 PF08784 0.541
LIG_SH2_CRK 131 135 PF00017 0.725
LIG_SH2_CRK 380 384 PF00017 0.603
LIG_SH2_CRK 560 564 PF00017 0.444
LIG_SH2_CRK 97 101 PF00017 0.509
LIG_SH2_GRB2like 233 236 PF00017 0.541
LIG_SH2_SRC 343 346 PF00017 0.635
LIG_SH2_STAP1 303 307 PF00017 0.419
LIG_SH2_STAP1 343 347 PF00017 0.641
LIG_SH2_STAP1 97 101 PF00017 0.509
LIG_SH2_STAT5 256 259 PF00017 0.499
LIG_SH2_STAT5 283 286 PF00017 0.400
LIG_SH2_STAT5 437 440 PF00017 0.456
LIG_SH2_STAT5 97 100 PF00017 0.511
LIG_SH3_3 25 31 PF00018 0.650
LIG_SH3_3 39 45 PF00018 0.477
LIG_SH3_3 668 674 PF00018 0.713
LIG_SUMO_SIM_anti_2 607 614 PF11976 0.617
LIG_TRAF2_1 10 13 PF00917 0.742
LIG_TRAF2_1 237 240 PF00917 0.545
LIG_TRAF2_1 242 245 PF00917 0.579
LIG_TRAF2_1 528 531 PF00917 0.607
LIG_TRAF2_1 697 700 PF00917 0.683
LIG_WRC_WIRS_1 678 683 PF05994 0.701
MOD_CK1_1 133 139 PF00069 0.701
MOD_CK1_1 189 195 PF00069 0.659
MOD_CK1_1 198 204 PF00069 0.542
MOD_CK1_1 250 256 PF00069 0.420
MOD_CK1_1 431 437 PF00069 0.504
MOD_CK1_1 480 486 PF00069 0.669
MOD_CK1_1 561 567 PF00069 0.552
MOD_CK1_1 569 575 PF00069 0.447
MOD_CK1_1 659 665 PF00069 0.691
MOD_CK2_1 136 142 PF00069 0.760
MOD_CK2_1 480 486 PF00069 0.625
MOD_CK2_1 650 656 PF00069 0.601
MOD_CK2_1 664 670 PF00069 0.651
MOD_CK2_1 677 683 PF00069 0.697
MOD_CK2_1 68 74 PF00069 0.695
MOD_Cter_Amidation 222 225 PF01082 0.606
MOD_GlcNHglycan 135 138 PF01048 0.735
MOD_GlcNHglycan 161 164 PF01048 0.700
MOD_GlcNHglycan 180 183 PF01048 0.722
MOD_GlcNHglycan 194 197 PF01048 0.697
MOD_GlcNHglycan 201 204 PF01048 0.617
MOD_GlcNHglycan 312 315 PF01048 0.615
MOD_GlcNHglycan 376 379 PF01048 0.555
MOD_GlcNHglycan 433 436 PF01048 0.495
MOD_GlcNHglycan 479 482 PF01048 0.569
MOD_GlcNHglycan 683 686 PF01048 0.601
MOD_GSK3_1 125 132 PF00069 0.727
MOD_GSK3_1 167 174 PF00069 0.662
MOD_GSK3_1 195 202 PF00069 0.674
MOD_GSK3_1 517 524 PF00069 0.446
MOD_GSK3_1 555 562 PF00069 0.495
MOD_GSK3_1 565 572 PF00069 0.494
MOD_GSK3_1 611 618 PF00069 0.638
MOD_GSK3_1 656 663 PF00069 0.619
MOD_GSK3_1 677 684 PF00069 0.664
MOD_GSK3_1 91 98 PF00069 0.606
MOD_N-GLC_1 167 172 PF02516 0.748
MOD_N-GLC_1 431 436 PF02516 0.560
MOD_N-GLC_1 664 669 PF02516 0.704
MOD_N-GLC_2 664 666 PF02516 0.700
MOD_NEK2_1 302 307 PF00069 0.516
MOD_NEK2_1 33 38 PF00069 0.703
MOD_NEK2_1 416 421 PF00069 0.627
MOD_NEK2_1 475 480 PF00069 0.498
MOD_NEK2_1 522 527 PF00069 0.602
MOD_NEK2_1 555 560 PF00069 0.468
MOD_NEK2_1 660 665 PF00069 0.599
MOD_NEK2_1 677 682 PF00069 0.718
MOD_NEK2_2 130 135 PF00069 0.728
MOD_NEK2_2 343 348 PF00069 0.587
MOD_PIKK_1 453 459 PF00454 0.491
MOD_PK_1 588 594 PF00069 0.573
MOD_PKA_1 207 213 PF00069 0.563
MOD_PKA_1 216 222 PF00069 0.555
MOD_PKA_2 207 213 PF00069 0.563
MOD_PKA_2 248 254 PF00069 0.526
MOD_PKA_2 277 283 PF00069 0.511
MOD_PKA_2 604 610 PF00069 0.593
MOD_PKA_2 91 97 PF00069 0.574
MOD_Plk_1 167 173 PF00069 0.683
MOD_Plk_1 343 349 PF00069 0.629
MOD_Plk_1 431 437 PF00069 0.494
MOD_Plk_1 625 631 PF00069 0.602
MOD_Plk_1 68 74 PF00069 0.704
MOD_Plk_1 95 101 PF00069 0.517
MOD_Plk_4 111 117 PF00069 0.531
MOD_Plk_4 167 173 PF00069 0.701
MOD_Plk_4 522 528 PF00069 0.564
MOD_Plk_4 588 594 PF00069 0.550
MOD_Plk_4 656 662 PF00069 0.624
MOD_Plk_4 95 101 PF00069 0.517
MOD_ProDKin_1 490 496 PF00069 0.684
MOD_ProDKin_1 615 621 PF00069 0.711
MOD_SUMO_for_1 697 700 PF00179 0.656
MOD_SUMO_rev_2 121 125 PF00179 0.616
TRG_DiLeu_BaEn_1 12 17 PF01217 0.672
TRG_DiLeu_BaEn_1 551 556 PF01217 0.521
TRG_DiLeu_BaEn_1 656 661 PF01217 0.610
TRG_DiLeu_BaLyEn_6 467 472 PF01217 0.539
TRG_ENDOCYTIC_2 131 134 PF00928 0.723
TRG_ENDOCYTIC_2 336 339 PF00928 0.618
TRG_ENDOCYTIC_2 380 383 PF00928 0.597
TRG_ENDOCYTIC_2 536 539 PF00928 0.523
TRG_ENDOCYTIC_2 560 563 PF00928 0.383
TRG_ENDOCYTIC_2 97 100 PF00928 0.511
TRG_ER_diArg_1 207 209 PF00400 0.514
TRG_ER_diArg_1 458 461 PF00400 0.505
TRG_ER_diArg_1 688 691 PF00400 0.660
TRG_ER_diArg_1 84 87 PF00400 0.689
TRG_NLS_MonoExtC_3 333 338 PF00514 0.693
TRG_NLS_MonoExtN_4 332 338 PF00514 0.692
TRG_Pf-PMV_PEXEL_1 236 240 PF00026 0.551
TRG_Pf-PMV_PEXEL_1 264 268 PF00026 0.556
TRG_Pf-PMV_PEXEL_1 317 321 PF00026 0.583
TRG_Pf-PMV_PEXEL_1 470 474 PF00026 0.516

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I228 Leptomonas seymouri 71% 100%
A0A0S4JB35 Bodo saltans 28% 96%
A0A1X0NZW8 Trypanosomatidae 31% 92%
A0A3Q8IAV8 Leishmania donovani 96% 100%
A0A3R7KXE4 Trypanosoma rangeli 32% 100%
A4HG90 Leishmania braziliensis 86% 100%
A4I3C4 Leishmania infantum 96% 100%
D0A822 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 31% 97%
E9AZL1 Leishmania mexicana (strain MHOM/GT/2001/U1103) 94% 100%
V5DH70 Trypanosoma cruzi 30% 95%

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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