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:
N-acetyltransferase B complex (NatB) non catalytic subunit, putative
Species:
Leishmania braziliensis
UniProt:
A4HI03_LEIBR
TriTrypDb:
LbrM.30.0600 , LBRM2903_300011800 *
Length:
899

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: 10
NetGPI no yes: 0, no: 10
Cellular components
Term Name Level Count
GO:0005737 cytoplasm 2 1
GO:0031248 protein acetyltransferase complex 3 1
GO:0031414 N-terminal protein acetyltransferase complex 4 1
GO:0031416 NatB complex 5 1
GO:0032991 protein-containing complex 1 1
GO:0110165 cellular anatomical entity 1 1
GO:0140535 intracellular protein-containing complex 2 1
GO:1902493 acetyltransferase complex 4 1
GO:1902494 catalytic complex 2 1
GO:1990234 transferase complex 3 1

Expansion

Sequence features

A4HI03
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HI03

Function

Biological processes
Term Name Level Count
GO:0006473 protein acetylation 6 1
GO:0006474 N-terminal protein amino acid acetylation 5 1
GO:0006807 nitrogen compound metabolic process 2 1
GO:0008152 metabolic process 1 1
GO:0017196 N-terminal peptidyl-methionine acetylation 6 1
GO:0018193 peptidyl-amino acid modification 5 1
GO:0018206 peptidyl-methionine modification 6 1
GO:0019538 protein metabolic process 3 1
GO:0031365 N-terminal protein amino acid modification 5 1
GO:0036211 protein modification process 4 1
GO:0043170 macromolecule metabolic process 3 1
GO:0043412 macromolecule modification 4 1
GO:0043543 protein acylation 5 1
GO:0044238 primary metabolic process 2 1
GO:0051604 protein maturation 4 1
GO:0071704 organic substance metabolic process 2 1
GO:1901564 organonitrogen compound metabolic process 3 1
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 3
GO:0016740 transferase activity 2 3

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 12 16 PF00656 0.390
CLV_C14_Caspase3-7 638 642 PF00656 0.431
CLV_NRD_NRD_1 323 325 PF00675 0.314
CLV_NRD_NRD_1 396 398 PF00675 0.233
CLV_NRD_NRD_1 485 487 PF00675 0.221
CLV_NRD_NRD_1 65 67 PF00675 0.550
CLV_NRD_NRD_1 679 681 PF00675 0.446
CLV_NRD_NRD_1 710 712 PF00675 0.667
CLV_PCSK_KEX2_1 323 325 PF00082 0.292
CLV_PCSK_KEX2_1 396 398 PF00082 0.233
CLV_PCSK_KEX2_1 485 487 PF00082 0.258
CLV_PCSK_KEX2_1 65 67 PF00082 0.311
CLV_PCSK_KEX2_1 679 681 PF00082 0.446
CLV_PCSK_SKI1_1 208 212 PF00082 0.431
CLV_PCSK_SKI1_1 396 400 PF00082 0.262
CLV_PCSK_SKI1_1 418 422 PF00082 0.274
CLV_PCSK_SKI1_1 66 70 PF00082 0.513
CLV_PCSK_SKI1_1 682 686 PF00082 0.355
CLV_PCSK_SKI1_1 735 739 PF00082 0.304
CLV_PCSK_SKI1_1 828 832 PF00082 0.249
CLV_PCSK_SKI1_1 862 866 PF00082 0.517
DEG_APCC_DBOX_1 681 689 PF00400 0.407
DEG_APCC_DBOX_1 777 785 PF00400 0.405
DEG_Nend_UBRbox_2 1 3 PF02207 0.535
DEG_SCF_FBW7_1 850 857 PF00400 0.500
DOC_CKS1_1 366 371 PF01111 0.514
DOC_CYCLIN_RxL_1 679 687 PF00134 0.502
DOC_MAPK_FxFP_2 798 801 PF00069 0.296
DOC_MAPK_gen_1 393 401 PF00069 0.362
DOC_PP4_FxxP_1 366 369 PF00568 0.514
DOC_PP4_FxxP_1 798 801 PF00568 0.296
DOC_USP7_MATH_1 152 156 PF00917 0.454
DOC_USP7_MATH_1 296 300 PF00917 0.365
DOC_USP7_MATH_1 427 431 PF00917 0.457
DOC_USP7_MATH_1 598 602 PF00917 0.362
DOC_USP7_MATH_1 695 699 PF00917 0.507
DOC_USP7_MATH_1 707 711 PF00917 0.611
DOC_USP7_MATH_1 751 755 PF00917 0.404
DOC_USP7_MATH_1 771 775 PF00917 0.502
DOC_USP7_MATH_1 854 858 PF00917 0.491
DOC_USP7_MATH_1 89 93 PF00917 0.276
DOC_USP7_UBL2_3 162 166 PF12436 0.373
DOC_USP7_UBL2_3 317 321 PF12436 0.514
DOC_USP7_UBL2_3 817 821 PF12436 0.460
DOC_WW_Pin1_4 365 370 PF00397 0.514
DOC_WW_Pin1_4 383 388 PF00397 0.436
DOC_WW_Pin1_4 408 413 PF00397 0.531
DOC_WW_Pin1_4 464 469 PF00397 0.517
DOC_WW_Pin1_4 725 730 PF00397 0.522
DOC_WW_Pin1_4 850 855 PF00397 0.549
LIG_14-3-3_CanoR_1 104 111 PF00244 0.459
LIG_14-3-3_CanoR_1 132 137 PF00244 0.415
LIG_14-3-3_CanoR_1 17 26 PF00244 0.344
LIG_14-3-3_CanoR_1 240 250 PF00244 0.480
LIG_14-3-3_CanoR_1 432 440 PF00244 0.476
LIG_14-3-3_CanoR_1 735 745 PF00244 0.291
LIG_14-3-3_CanoR_1 841 847 PF00244 0.518
LIG_14-3-3_CanoR_1 862 867 PF00244 0.408
LIG_APCC_ABBA_1 253 258 PF00400 0.447
LIG_Clathr_ClatBox_2 542 547 PF01394 0.474
LIG_deltaCOP1_diTrp_1 248 253 PF00928 0.328
LIG_deltaCOP1_diTrp_1 621 627 PF00928 0.514
LIG_FHA_1 163 169 PF00498 0.373
LIG_FHA_1 273 279 PF00498 0.367
LIG_FHA_1 366 372 PF00498 0.515
LIG_FHA_1 393 399 PF00498 0.478
LIG_FHA_1 449 455 PF00498 0.448
LIG_FHA_1 489 495 PF00498 0.455
LIG_FHA_1 56 62 PF00498 0.340
LIG_FHA_1 598 604 PF00498 0.461
LIG_FHA_1 641 647 PF00498 0.433
LIG_FHA_1 663 669 PF00498 0.352
LIG_FHA_1 726 732 PF00498 0.531
LIG_FHA_1 736 742 PF00498 0.376
LIG_FHA_1 870 876 PF00498 0.432
LIG_FHA_2 184 190 PF00498 0.441
LIG_FHA_2 215 221 PF00498 0.404
LIG_FHA_2 287 293 PF00498 0.447
LIG_FHA_2 540 546 PF00498 0.379
LIG_FHA_2 606 612 PF00498 0.479
LIG_FHA_2 616 622 PF00498 0.412
LIG_FHA_2 636 642 PF00498 0.525
LIG_IRF3_LxIS_1 357 364 PF10401 0.474
LIG_LIR_Apic_2 351 357 PF02991 0.551
LIG_LIR_Apic_2 364 369 PF02991 0.454
LIG_LIR_Apic_2 796 801 PF02991 0.307
LIG_LIR_Gen_1 113 121 PF02991 0.297
LIG_LIR_Gen_1 186 192 PF02991 0.340
LIG_LIR_Gen_1 247 256 PF02991 0.324
LIG_LIR_Gen_1 358 367 PF02991 0.504
LIG_LIR_Gen_1 447 457 PF02991 0.433
LIG_LIR_Gen_1 467 477 PF02991 0.514
LIG_LIR_Gen_1 840 850 PF02991 0.576
LIG_LIR_Gen_1 92 100 PF02991 0.369
LIG_LIR_LC3C_4 43 47 PF02991 0.225
LIG_LIR_Nem_3 186 190 PF02991 0.343
LIG_LIR_Nem_3 247 253 PF02991 0.330
LIG_LIR_Nem_3 358 363 PF02991 0.504
LIG_LIR_Nem_3 447 452 PF02991 0.451
LIG_LIR_Nem_3 467 473 PF02991 0.514
LIG_LIR_Nem_3 491 495 PF02991 0.424
LIG_LIR_Nem_3 549 554 PF02991 0.443
LIG_LIR_Nem_3 840 846 PF02991 0.575
LIG_LIR_Nem_3 92 97 PF02991 0.355
LIG_NRBOX 805 811 PF00104 0.360
LIG_PCNA_yPIPBox_3 343 356 PF02747 0.474
LIG_Pex14_1 547 551 PF04695 0.474
LIG_SH2_CRK 120 124 PF00017 0.408
LIG_SH2_CRK 354 358 PF00017 0.514
LIG_SH2_CRK 470 474 PF00017 0.514
LIG_SH2_NCK_1 120 124 PF00017 0.350
LIG_SH2_NCK_1 354 358 PF00017 0.362
LIG_SH2_PTP2 187 190 PF00017 0.307
LIG_SH2_PTP2 449 452 PF00017 0.433
LIG_SH2_SRC 187 190 PF00017 0.317
LIG_SH2_SRC 360 363 PF00017 0.497
LIG_SH2_SRC 745 748 PF00017 0.431
LIG_SH2_SRC 759 762 PF00017 0.207
LIG_SH2_STAP1 197 201 PF00017 0.361
LIG_SH2_STAP1 470 474 PF00017 0.514
LIG_SH2_STAP1 495 499 PF00017 0.451
LIG_SH2_STAP1 838 842 PF00017 0.399
LIG_SH2_STAT3 552 555 PF00017 0.514
LIG_SH2_STAT3 590 593 PF00017 0.474
LIG_SH2_STAT5 114 117 PF00017 0.362
LIG_SH2_STAT5 187 190 PF00017 0.307
LIG_SH2_STAT5 327 330 PF00017 0.533
LIG_SH2_STAT5 349 352 PF00017 0.489
LIG_SH2_STAT5 360 363 PF00017 0.400
LIG_SH2_STAT5 449 452 PF00017 0.423
LIG_SH2_STAT5 472 475 PF00017 0.516
LIG_SH2_STAT5 569 572 PF00017 0.514
LIG_SH2_STAT5 745 748 PF00017 0.431
LIG_SH2_STAT5 759 762 PF00017 0.207
LIG_SH2_STAT5 780 783 PF00017 0.502
LIG_SH2_STAT5 886 889 PF00017 0.460
LIG_SH3_3 277 283 PF00018 0.411
LIG_SH3_3 666 672 PF00018 0.384
LIG_SUMO_SIM_anti_2 186 192 PF11976 0.435
LIG_SUMO_SIM_anti_2 275 282 PF11976 0.377
LIG_SUMO_SIM_anti_2 330 336 PF11976 0.451
LIG_SUMO_SIM_anti_2 43 50 PF11976 0.338
LIG_SUMO_SIM_anti_2 475 481 PF11976 0.474
LIG_SUMO_SIM_par_1 665 673 PF11976 0.415
LIG_TRAF2_1 299 302 PF00917 0.510
LIG_TRAF2_1 553 556 PF00917 0.562
LIG_TYR_ITIM 527 532 PF00017 0.451
LIG_UBA3_1 159 166 PF00899 0.372
LIG_UBA3_1 809 817 PF00899 0.455
LIG_WRC_WIRS_1 363 368 PF05994 0.514
MOD_CDK_SPK_2 383 388 PF00069 0.362
MOD_CDK_SPK_2 730 735 PF00069 0.274
MOD_CK1_1 244 250 PF00069 0.561
MOD_CK1_1 273 279 PF00069 0.584
MOD_CK1_1 336 342 PF00069 0.514
MOD_CK1_1 355 361 PF00069 0.553
MOD_CK1_1 379 385 PF00069 0.450
MOD_CK1_1 407 413 PF00069 0.393
MOD_CK1_1 667 673 PF00069 0.260
MOD_CK1_1 739 745 PF00069 0.430
MOD_CK1_1 788 794 PF00069 0.459
MOD_CK2_1 17 23 PF00069 0.452
MOD_CK2_1 214 220 PF00069 0.404
MOD_CK2_1 273 279 PF00069 0.555
MOD_CK2_1 296 302 PF00069 0.364
MOD_CK2_1 550 556 PF00069 0.474
MOD_CK2_1 615 621 PF00069 0.372
MOD_CK2_1 759 765 PF00069 0.489
MOD_CK2_1 89 95 PF00069 0.224
MOD_CMANNOS 544 547 PF00535 0.314
MOD_CMANNOS 624 627 PF00535 0.314
MOD_GlcNHglycan 232 235 PF01048 0.439
MOD_GlcNHglycan 272 275 PF01048 0.540
MOD_GlcNHglycan 381 384 PF01048 0.207
MOD_GlcNHglycan 49 52 PF01048 0.534
MOD_GlcNHglycan 600 603 PF01048 0.374
MOD_GlcNHglycan 630 633 PF01048 0.302
MOD_GlcNHglycan 697 700 PF01048 0.452
MOD_GlcNHglycan 719 722 PF01048 0.756
MOD_GlcNHglycan 773 776 PF01048 0.527
MOD_GlcNHglycan 789 793 PF01048 0.477
MOD_GlcNHglycan 806 809 PF01048 0.469
MOD_GlcNHglycan 856 859 PF01048 0.417
MOD_GSK3_1 179 186 PF00069 0.392
MOD_GSK3_1 214 221 PF00069 0.483
MOD_GSK3_1 244 251 PF00069 0.425
MOD_GSK3_1 287 294 PF00069 0.417
MOD_GSK3_1 333 340 PF00069 0.493
MOD_GSK3_1 361 368 PF00069 0.503
MOD_GSK3_1 379 386 PF00069 0.424
MOD_GSK3_1 404 411 PF00069 0.528
MOD_GSK3_1 428 435 PF00069 0.456
MOD_GSK3_1 464 471 PF00069 0.474
MOD_GSK3_1 713 720 PF00069 0.633
MOD_GSK3_1 721 728 PF00069 0.552
MOD_GSK3_1 735 742 PF00069 0.535
MOD_GSK3_1 767 774 PF00069 0.505
MOD_GSK3_1 776 783 PF00069 0.450
MOD_GSK3_1 837 844 PF00069 0.506
MOD_GSK3_1 846 853 PF00069 0.501
MOD_N-GLC_1 248 253 PF02516 0.301
MOD_N-GLC_1 567 572 PF02516 0.314
MOD_N-GLC_1 612 617 PF02516 0.162
MOD_N-GLC_1 66 71 PF02516 0.454
MOD_N-GLC_1 771 776 PF02516 0.287
MOD_N-GLC_1 862 867 PF02516 0.300
MOD_N-GLC_2 83 85 PF02516 0.440
MOD_NEK2_1 110 115 PF00069 0.353
MOD_NEK2_1 161 166 PF00069 0.323
MOD_NEK2_1 214 219 PF00069 0.361
MOD_NEK2_1 313 318 PF00069 0.439
MOD_NEK2_1 333 338 PF00069 0.514
MOD_NEK2_1 361 366 PF00069 0.451
MOD_NEK2_1 434 439 PF00069 0.568
MOD_NEK2_1 55 60 PF00069 0.397
MOD_NEK2_1 567 572 PF00069 0.465
MOD_NEK2_1 630 635 PF00069 0.558
MOD_NEK2_1 664 669 PF00069 0.432
MOD_NEK2_1 684 689 PF00069 0.320
MOD_NEK2_1 736 741 PF00069 0.526
MOD_NEK2_1 842 847 PF00069 0.543
MOD_NEK2_2 886 891 PF00069 0.387
MOD_PIKK_1 17 23 PF00454 0.370
MOD_PIKK_1 241 247 PF00454 0.410
MOD_PIKK_1 605 611 PF00454 0.436
MOD_PKA_2 287 293 PF00069 0.440
MOD_PKA_2 379 385 PF00069 0.366
MOD_PKA_2 520 526 PF00069 0.514
MOD_PKA_2 628 634 PF00069 0.530
MOD_PKA_2 678 684 PF00069 0.436
MOD_Plk_1 248 254 PF00069 0.243
MOD_Plk_1 291 297 PF00069 0.313
MOD_Plk_1 3 9 PF00069 0.320
MOD_Plk_1 35 41 PF00069 0.447
MOD_Plk_1 361 367 PF00069 0.420
MOD_Plk_1 468 474 PF00069 0.555
MOD_Plk_1 557 563 PF00069 0.420
MOD_Plk_1 567 573 PF00069 0.420
MOD_Plk_1 612 618 PF00069 0.414
MOD_Plk_1 862 868 PF00069 0.526
MOD_Plk_2-3 478 484 PF00069 0.457
MOD_Plk_2-3 550 556 PF00069 0.474
MOD_Plk_4 183 189 PF00069 0.414
MOD_Plk_4 256 262 PF00069 0.481
MOD_Plk_4 273 279 PF00069 0.621
MOD_Plk_4 337 343 PF00069 0.362
MOD_Plk_4 35 41 PF00069 0.368
MOD_Plk_4 362 368 PF00069 0.440
MOD_Plk_4 468 474 PF00069 0.474
MOD_Plk_4 478 484 PF00069 0.451
MOD_Plk_4 488 494 PF00069 0.328
MOD_Plk_4 557 563 PF00069 0.420
MOD_Plk_4 585 591 PF00069 0.514
MOD_Plk_4 635 641 PF00069 0.517
MOD_Plk_4 647 653 PF00069 0.422
MOD_Plk_4 664 670 PF00069 0.385
MOD_Plk_4 684 690 PF00069 0.358
MOD_Plk_4 751 757 PF00069 0.307
MOD_Plk_4 780 786 PF00069 0.416
MOD_ProDKin_1 365 371 PF00069 0.514
MOD_ProDKin_1 383 389 PF00069 0.436
MOD_ProDKin_1 408 414 PF00069 0.531
MOD_ProDKin_1 464 470 PF00069 0.517
MOD_ProDKin_1 725 731 PF00069 0.508
MOD_ProDKin_1 850 856 PF00069 0.543
MOD_SUMO_for_1 873 876 PF00179 0.396
TRG_DiLeu_BaEn_1 475 480 PF01217 0.517
TRG_DiLeu_BaEn_4 301 307 PF01217 0.526
TRG_DiLeu_BaLyEn_6 528 533 PF01217 0.499
TRG_ENDOCYTIC_2 114 117 PF00928 0.294
TRG_ENDOCYTIC_2 120 123 PF00928 0.347
TRG_ENDOCYTIC_2 187 190 PF00928 0.307
TRG_ENDOCYTIC_2 360 363 PF00928 0.514
TRG_ENDOCYTIC_2 449 452 PF00928 0.462
TRG_ENDOCYTIC_2 470 473 PF00928 0.541
TRG_ENDOCYTIC_2 529 532 PF00928 0.420
TRG_ENDOCYTIC_2 551 554 PF00928 0.437
TRG_ENDOCYTIC_2 94 97 PF00928 0.331
TRG_ER_diArg_1 396 398 PF00400 0.434
TRG_ER_diArg_1 485 487 PF00400 0.514
TRG_ER_diArg_1 678 680 PF00400 0.453
TRG_NLS_MonoExtN_4 709 715 PF00514 0.565
TRG_Pf-PMV_PEXEL_1 104 108 PF00026 0.444
TRG_Pf-PMV_PEXEL_1 17 21 PF00026 0.441
TRG_Pf-PMV_PEXEL_1 240 245 PF00026 0.410
TRG_Pf-PMV_PEXEL_1 308 312 PF00026 0.324
TRG_Pf-PMV_PEXEL_1 418 423 PF00026 0.355
TRG_Pf-PMV_PEXEL_1 432 436 PF00026 0.173
TRG_Pf-PMV_PEXEL_1 828 832 PF00026 0.249
TRG_Pf-PMV_PEXEL_1 98 103 PF00026 0.514

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I184 Leptomonas seymouri 67% 99%
A0A1X0P396 Trypanosomatidae 43% 100%
A0A3S5IR93 Trypanosoma rangeli 43% 100%
A0A3S7X316 Leishmania donovani 85% 100%
A4I580 Leishmania infantum 85% 100%
C9ZQK9 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 44% 100%
E9B0H7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 84% 100%
Q4Q7Q4 Leishmania major 85% 100%
Q7PYI4 Anopheles gambiae 22% 91%
V5BGT7 Trypanosoma cruzi 46% 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