LeishMANIAdb
  • Home
  • Browse
  • Manual
  • FAQ
  • Download

N-acetyltransferase B complex (NatB) non catalytic subunit, putative

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

Quick info

Protein:
N-acetyltransferase B complex (NatB) non catalytic subunit, putative
Gene product:
N-acetyltransferase B complex (NatB) non catalytic subunit, putative
Species:
Leishmania donovani
UniProt:
A0A3S7X316_LEIDO
TriTrypDb:
LdBPK_300540.1 * , LdCL_300010500 , LDHU3_30.0720
Length:
896

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

A0A3S7X316
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3S7X316

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 4
GO:0016740 transferase activity 2 4

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 12 16 PF00656 0.439
CLV_C14_Caspase3-7 638 642 PF00656 0.406
CLV_NRD_NRD_1 323 325 PF00675 0.341
CLV_NRD_NRD_1 354 356 PF00675 0.337
CLV_NRD_NRD_1 396 398 PF00675 0.275
CLV_NRD_NRD_1 485 487 PF00675 0.252
CLV_NRD_NRD_1 679 681 PF00675 0.482
CLV_NRD_NRD_1 710 712 PF00675 0.659
CLV_NRD_NRD_1 833 835 PF00675 0.471
CLV_PCSK_KEX2_1 323 325 PF00082 0.317
CLV_PCSK_KEX2_1 396 398 PF00082 0.263
CLV_PCSK_KEX2_1 485 487 PF00082 0.281
CLV_PCSK_KEX2_1 679 681 PF00082 0.482
CLV_PCSK_KEX2_1 833 835 PF00082 0.534
CLV_PCSK_SKI1_1 208 212 PF00082 0.440
CLV_PCSK_SKI1_1 396 400 PF00082 0.275
CLV_PCSK_SKI1_1 418 422 PF00082 0.364
CLV_PCSK_SKI1_1 508 512 PF00082 0.309
CLV_PCSK_SKI1_1 54 58 PF00082 0.549
CLV_PCSK_SKI1_1 610 614 PF00082 0.276
CLV_PCSK_SKI1_1 66 70 PF00082 0.506
CLV_PCSK_SKI1_1 682 686 PF00082 0.454
DEG_APCC_DBOX_1 507 515 PF00400 0.509
DEG_APCC_DBOX_1 681 689 PF00400 0.452
DEG_APCC_DBOX_1 774 782 PF00400 0.535
DEG_Nend_UBRbox_2 1 3 PF02207 0.555
DEG_SCF_FBW7_1 733 739 PF00400 0.561
DEG_SCF_FBW7_1 847 854 PF00400 0.624
DOC_CKS1_1 366 371 PF01111 0.541
DOC_CKS1_1 733 738 PF01111 0.562
DOC_CYCLIN_RxL_1 679 687 PF00134 0.457
DOC_CYCLIN_yCln2_LP_2 260 266 PF00134 0.536
DOC_MAPK_FxFP_2 795 798 PF00069 0.351
DOC_MAPK_gen_1 355 363 PF00069 0.509
DOC_MAPK_gen_1 54 63 PF00069 0.467
DOC_MAPK_gen_1 610 620 PF00069 0.439
DOC_MAPK_MEF2A_6 613 620 PF00069 0.439
DOC_PP4_FxxP_1 366 369 PF00568 0.529
DOC_PP4_FxxP_1 795 798 PF00568 0.351
DOC_USP7_MATH_1 152 156 PF00917 0.470
DOC_USP7_MATH_1 296 300 PF00917 0.417
DOC_USP7_MATH_1 427 431 PF00917 0.537
DOC_USP7_MATH_1 695 699 PF00917 0.512
DOC_USP7_MATH_1 707 711 PF00917 0.559
DOC_USP7_MATH_1 736 740 PF00917 0.626
DOC_USP7_MATH_1 851 855 PF00917 0.623
DOC_USP7_MATH_1 857 861 PF00917 0.567
DOC_USP7_UBL2_3 162 166 PF12436 0.418
DOC_USP7_UBL2_3 317 321 PF12436 0.541
DOC_USP7_UBL2_3 613 617 PF12436 0.509
DOC_USP7_UBL2_3 814 818 PF12436 0.501
DOC_WW_Pin1_4 365 370 PF00397 0.541
DOC_WW_Pin1_4 408 413 PF00397 0.541
DOC_WW_Pin1_4 464 469 PF00397 0.542
DOC_WW_Pin1_4 732 737 PF00397 0.589
DOC_WW_Pin1_4 847 852 PF00397 0.587
LIG_14-3-3_CanoR_1 104 111 PF00244 0.504
LIG_14-3-3_CanoR_1 132 137 PF00244 0.512
LIG_14-3-3_CanoR_1 231 238 PF00244 0.467
LIG_14-3-3_CanoR_1 240 250 PF00244 0.513
LIG_14-3-3_CanoR_1 288 292 PF00244 0.514
LIG_14-3-3_CanoR_1 432 440 PF00244 0.513
LIG_14-3-3_CanoR_1 629 633 PF00244 0.460
LIG_14-3-3_CanoR_1 682 691 PF00244 0.400
LIG_14-3-3_CanoR_1 838 847 PF00244 0.551
LIG_APCC_ABBA_1 253 258 PF00400 0.480
LIG_BRCT_BRCA1_1 685 689 PF00533 0.396
LIG_Clathr_ClatBox_2 542 547 PF01394 0.564
LIG_deltaCOP1_diTrp_1 248 253 PF00928 0.376
LIG_deltaCOP1_diTrp_1 621 627 PF00928 0.580
LIG_eIF4E_1 801 807 PF01652 0.400
LIG_FHA_1 163 169 PF00498 0.417
LIG_FHA_1 366 372 PF00498 0.535
LIG_FHA_1 393 399 PF00498 0.513
LIG_FHA_1 449 455 PF00498 0.461
LIG_FHA_1 489 495 PF00498 0.495
LIG_FHA_1 584 590 PF00498 0.464
LIG_FHA_1 598 604 PF00498 0.480
LIG_FHA_1 641 647 PF00498 0.403
LIG_FHA_1 663 669 PF00498 0.392
LIG_FHA_1 769 775 PF00498 0.432
LIG_FHA_1 867 873 PF00498 0.473
LIG_FHA_2 184 190 PF00498 0.472
LIG_FHA_2 197 203 PF00498 0.470
LIG_FHA_2 215 221 PF00498 0.417
LIG_FHA_2 287 293 PF00498 0.521
LIG_FHA_2 464 470 PF00498 0.509
LIG_FHA_2 606 612 PF00498 0.515
LIG_FHA_2 636 642 PF00498 0.522
LIG_IRF3_LxIS_1 357 364 PF10401 0.564
LIG_LIR_Apic_2 351 357 PF02991 0.532
LIG_LIR_Apic_2 364 369 PF02991 0.475
LIG_LIR_Apic_2 793 798 PF02991 0.344
LIG_LIR_Gen_1 113 121 PF02991 0.275
LIG_LIR_Gen_1 186 192 PF02991 0.382
LIG_LIR_Gen_1 247 256 PF02991 0.374
LIG_LIR_Gen_1 358 367 PF02991 0.514
LIG_LIR_Gen_1 447 457 PF02991 0.475
LIG_LIR_Gen_1 467 477 PF02991 0.541
LIG_LIR_Gen_1 837 847 PF02991 0.585
LIG_LIR_Gen_1 93 100 PF02991 0.440
LIG_LIR_LC3C_4 665 670 PF02991 0.442
LIG_LIR_Nem_3 186 190 PF02991 0.384
LIG_LIR_Nem_3 247 253 PF02991 0.377
LIG_LIR_Nem_3 358 363 PF02991 0.509
LIG_LIR_Nem_3 447 452 PF02991 0.464
LIG_LIR_Nem_3 467 473 PF02991 0.541
LIG_LIR_Nem_3 491 495 PF02991 0.466
LIG_LIR_Nem_3 549 554 PF02991 0.479
LIG_LIR_Nem_3 837 843 PF02991 0.582
LIG_LIR_Nem_3 93 97 PF02991 0.410
LIG_NRBOX 802 808 PF00104 0.406
LIG_PCNA_yPIPBox_3 343 356 PF02747 0.564
LIG_Pex14_1 547 551 PF04695 0.564
LIG_PTB_Apo_2 47 54 PF02174 0.476
LIG_PTB_Phospho_1 47 53 PF10480 0.472
LIG_SH2_CRK 120 124 PF00017 0.439
LIG_SH2_CRK 354 358 PF00017 0.541
LIG_SH2_CRK 470 474 PF00017 0.541
LIG_SH2_NCK_1 120 124 PF00017 0.409
LIG_SH2_PTP2 187 190 PF00017 0.359
LIG_SH2_PTP2 449 452 PF00017 0.475
LIG_SH2_SRC 187 190 PF00017 0.369
LIG_SH2_SRC 360 363 PF00017 0.518
LIG_SH2_SRC 742 745 PF00017 0.476
LIG_SH2_SRC 756 759 PF00017 0.492
LIG_SH2_STAP1 197 201 PF00017 0.411
LIG_SH2_STAP1 470 474 PF00017 0.541
LIG_SH2_STAP1 495 499 PF00017 0.492
LIG_SH2_STAP1 729 733 PF00017 0.470
LIG_SH2_STAT3 552 555 PF00017 0.541
LIG_SH2_STAT3 590 593 PF00017 0.564
LIG_SH2_STAT5 114 117 PF00017 0.384
LIG_SH2_STAT5 187 190 PF00017 0.359
LIG_SH2_STAT5 241 244 PF00017 0.429
LIG_SH2_STAT5 327 330 PF00017 0.541
LIG_SH2_STAT5 349 352 PF00017 0.523
LIG_SH2_STAT5 360 363 PF00017 0.438
LIG_SH2_STAT5 449 452 PF00017 0.461
LIG_SH2_STAT5 472 475 PF00017 0.515
LIG_SH2_STAT5 569 572 PF00017 0.538
LIG_SH2_STAT5 742 745 PF00017 0.476
LIG_SH2_STAT5 756 759 PF00017 0.443
LIG_SH2_STAT5 777 780 PF00017 0.524
LIG_SH2_STAT5 801 804 PF00017 0.365
LIG_SH2_STAT5 883 886 PF00017 0.467
LIG_SH3_3 666 672 PF00018 0.431
LIG_SUMO_SIM_anti_2 186 192 PF11976 0.468
LIG_SUMO_SIM_anti_2 330 336 PF11976 0.479
LIG_SUMO_SIM_anti_2 43 49 PF11976 0.394
LIG_SUMO_SIM_anti_2 475 481 PF11976 0.564
LIG_SUMO_SIM_anti_2 665 673 PF11976 0.450
LIG_SUMO_SIM_par_1 665 673 PF11976 0.528
LIG_TRAF2_1 299 302 PF00917 0.510
LIG_TRAF2_1 407 410 PF00917 0.552
LIG_TRAF2_1 553 556 PF00917 0.570
LIG_TYR_ITIM 527 532 PF00017 0.492
LIG_UBA3_1 159 166 PF00899 0.418
LIG_UBA3_1 802 808 PF00899 0.445
LIG_WRC_WIRS_1 363 368 PF05994 0.530
MOD_CK1_1 244 250 PF00069 0.538
MOD_CK1_1 336 342 PF00069 0.541
MOD_CK1_1 785 791 PF00069 0.477
MOD_CK2_1 214 220 PF00069 0.418
MOD_CK2_1 273 279 PF00069 0.576
MOD_CK2_1 296 302 PF00069 0.408
MOD_CK2_1 371 377 PF00069 0.493
MOD_CK2_1 384 390 PF00069 0.413
MOD_CK2_1 404 410 PF00069 0.535
MOD_CK2_1 550 556 PF00069 0.564
MOD_CK2_1 696 702 PF00069 0.503
MOD_CK2_1 756 762 PF00069 0.504
MOD_CMANNOS 544 547 PF00535 0.341
MOD_CMANNOS 624 627 PF00535 0.469
MOD_GlcNHglycan 205 208 PF01048 0.397
MOD_GlcNHglycan 232 235 PF01048 0.521
MOD_GlcNHglycan 274 278 PF01048 0.615
MOD_GlcNHglycan 600 603 PF01048 0.344
MOD_GlcNHglycan 657 660 PF01048 0.417
MOD_GlcNHglycan 714 717 PF01048 0.677
MOD_GlcNHglycan 721 724 PF01048 0.622
MOD_GlcNHglycan 736 739 PF01048 0.640
MOD_GlcNHglycan 768 771 PF01048 0.531
MOD_GlcNHglycan 786 790 PF01048 0.504
MOD_GlcNHglycan 803 806 PF01048 0.428
MOD_GlcNHglycan 840 843 PF01048 0.526
MOD_GlcNHglycan 853 856 PF01048 0.610
MOD_GSK3_1 179 186 PF00069 0.429
MOD_GSK3_1 287 294 PF00069 0.480
MOD_GSK3_1 333 340 PF00069 0.514
MOD_GSK3_1 361 368 PF00069 0.513
MOD_GSK3_1 404 411 PF00069 0.541
MOD_GSK3_1 428 435 PF00069 0.493
MOD_GSK3_1 464 471 PF00069 0.576
MOD_GSK3_1 728 735 PF00069 0.518
MOD_GSK3_1 773 780 PF00069 0.476
MOD_GSK3_1 834 841 PF00069 0.543
MOD_GSK3_1 843 850 PF00069 0.541
MOD_N-GLC_1 567 572 PF02516 0.341
MOD_N-GLC_1 66 71 PF02516 0.502
MOD_N-GLC_2 83 85 PF02516 0.473
MOD_NEK2_1 110 115 PF00069 0.378
MOD_NEK2_1 161 166 PF00069 0.369
MOD_NEK2_1 203 208 PF00069 0.384
MOD_NEK2_1 214 219 PF00069 0.391
MOD_NEK2_1 333 338 PF00069 0.539
MOD_NEK2_1 361 366 PF00069 0.466
MOD_NEK2_1 434 439 PF00069 0.566
MOD_NEK2_1 567 572 PF00069 0.504
MOD_NEK2_1 664 669 PF00069 0.436
MOD_NEK2_1 684 689 PF00069 0.144
MOD_NEK2_1 728 733 PF00069 0.511
MOD_NEK2_1 843 848 PF00069 0.590
MOD_NEK2_2 251 256 PF00069 0.428
MOD_NEK2_2 883 888 PF00069 0.508
MOD_PIKK_1 241 247 PF00454 0.500
MOD_PIKK_1 605 611 PF00454 0.475
MOD_PKA_1 355 361 PF00069 0.509
MOD_PKA_2 230 236 PF00069 0.475
MOD_PKA_2 287 293 PF00069 0.499
MOD_PKA_2 520 526 PF00069 0.541
MOD_PKA_2 628 634 PF00069 0.554
MOD_PKA_2 678 684 PF00069 0.476
MOD_PKA_2 824 830 PF00069 0.455
MOD_Plk_1 273 279 PF00069 0.570
MOD_Plk_1 291 297 PF00069 0.377
MOD_Plk_1 35 41 PF00069 0.491
MOD_Plk_1 361 367 PF00069 0.468
MOD_Plk_1 468 474 PF00069 0.566
MOD_Plk_1 557 563 PF00069 0.461
MOD_Plk_1 567 573 PF00069 0.461
MOD_Plk_2-3 478 484 PF00069 0.537
MOD_Plk_2-3 550 556 PF00069 0.564
MOD_Plk_4 183 189 PF00069 0.455
MOD_Plk_4 256 262 PF00069 0.511
MOD_Plk_4 362 368 PF00069 0.457
MOD_Plk_4 371 377 PF00069 0.441
MOD_Plk_4 468 474 PF00069 0.564
MOD_Plk_4 478 484 PF00069 0.492
MOD_Plk_4 488 494 PF00069 0.328
MOD_Plk_4 557 563 PF00069 0.461
MOD_Plk_4 585 591 PF00069 0.541
MOD_Plk_4 635 641 PF00069 0.509
MOD_Plk_4 647 653 PF00069 0.476
MOD_Plk_4 664 670 PF00069 0.450
MOD_Plk_4 684 690 PF00069 0.144
MOD_Plk_4 777 783 PF00069 0.474
MOD_ProDKin_1 365 371 PF00069 0.541
MOD_ProDKin_1 408 414 PF00069 0.541
MOD_ProDKin_1 464 470 PF00069 0.542
MOD_ProDKin_1 732 738 PF00069 0.592
MOD_ProDKin_1 847 853 PF00069 0.580
MOD_SUMO_for_1 870 873 PF00179 0.526
MOD_SUMO_for_1 887 890 PF00179 0.239
MOD_SUMO_rev_2 309 319 PF00179 0.531
MOD_SUMO_rev_2 605 615 PF00179 0.509
TRG_DiLeu_BaEn_1 475 480 PF01217 0.542
TRG_DiLeu_BaEn_4 301 307 PF01217 0.528
TRG_DiLeu_BaLyEn_6 528 533 PF01217 0.513
TRG_ENDOCYTIC_2 114 117 PF00928 0.179
TRG_ENDOCYTIC_2 120 123 PF00928 0.369
TRG_ENDOCYTIC_2 187 190 PF00928 0.359
TRG_ENDOCYTIC_2 360 363 PF00928 0.541
TRG_ENDOCYTIC_2 449 452 PF00928 0.475
TRG_ENDOCYTIC_2 470 473 PF00928 0.558
TRG_ENDOCYTIC_2 529 532 PF00928 0.461
TRG_ENDOCYTIC_2 551 554 PF00928 0.464
TRG_ENDOCYTIC_2 94 97 PF00928 0.391
TRG_ER_diArg_1 396 398 PF00400 0.471
TRG_ER_diArg_1 485 487 PF00400 0.513
TRG_ER_diArg_1 678 680 PF00400 0.489
TRG_ER_diArg_1 833 835 PF00400 0.333
TRG_NLS_MonoExtN_4 709 715 PF00514 0.598
TRG_Pf-PMV_PEXEL_1 104 108 PF00026 0.470
TRG_Pf-PMV_PEXEL_1 17 21 PF00026 0.563
TRG_Pf-PMV_PEXEL_1 240 245 PF00026 0.520
TRG_Pf-PMV_PEXEL_1 308 312 PF00026 0.341
TRG_Pf-PMV_PEXEL_1 418 423 PF00026 0.354
TRG_Pf-PMV_PEXEL_1 432 436 PF00026 0.243

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I184 Leptomonas seymouri 67% 98%
A0A1X0P396 Trypanosomatidae 43% 100%
A0A3S5IR93 Trypanosoma rangeli 43% 100%
A4HI03 Leishmania braziliensis 85% 100%
A4I580 Leishmania infantum 100% 100%
C9ZQK9 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 44% 100%
E9B0H7 Leishmania mexicana (strain MHOM/GT/2001/U1103) 95% 100%
Q17DK2 Aedes aegypti 21% 95%
Q294E0 Drosophila pseudoobscura pseudoobscura 21% 93%
Q4Q7Q4 Leishmania major 96% 100%
Q7PYI4 Anopheles gambiae 22% 91%
Q9VDQ7 Drosophila melanogaster 21% 95%
V5BGT7 Trypanosoma cruzi 47% 100%

Download

Download
LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS