LeishMANIAdb
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Histone acetyltransferase

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

Quick info

Protein:
Histone acetyltransferase
Gene product:
Acetyltransferase (GNAT) family, putative
Species:
Leishmania mexicana
UniProt:
E9ARR5_LEIMU
TriTrypDb:
LmxM.18.1310
Length:
696

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:0016020 membrane 2 7
GO:0110165 cellular anatomical entity 1 7
GO:0000139 Golgi membrane 5 1
GO:0031090 organelle membrane 3 1
GO:0098588 bounding membrane of organelle 4 1

Expansion

Sequence features

E9ARR5
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9ARR5

Function

Biological processes
Term Name Level Count
GO:0007059 chromosome segregation 2 6
GO:0009987 cellular process 1 6
GO:0006473 protein acetylation 6 1
GO:0006474 N-terminal protein amino acid acetylation 5 1
GO:0006475 internal protein amino acid acetylation 7 1
GO:0006807 nitrogen compound metabolic process 2 1
GO:0008152 metabolic process 1 1
GO:0016570 histone modification 5 1
GO:0016573 histone acetylation 6 1
GO:0017196 N-terminal peptidyl-methionine acetylation 6 1
GO:0018193 peptidyl-amino acid modification 5 1
GO:0018205 peptidyl-lysine modification 6 1
GO:0018206 peptidyl-methionine modification 6 1
GO:0018393 internal peptidyl-lysine acetylation 8 1
GO:0018394 peptidyl-lysine acetylation 7 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:0043966 histone H3 acetylation 7 1
GO:0043967 histone H4 acetylation 7 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 7
GO:0004596 peptide alpha-N-acetyltransferase activity 8 7
GO:0008080 N-acetyltransferase activity 6 7
GO:0016407 acetyltransferase activity 5 7
GO:0016410 N-acyltransferase activity 5 7
GO:0016740 transferase activity 2 7
GO:0016746 acyltransferase activity 3 7
GO:0016747 acyltransferase activity, transferring groups other than amino-acyl groups 4 7
GO:0034212 peptide N-acetyltransferase activity 7 7
GO:0004402 histone acetyltransferase activity 4 1
GO:0061733 peptide-lysine-N-acetyltransferase activity 3 1
GO:0140096 catalytic activity, acting on a protein 2 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 223 227 PF00656 0.665
CLV_C14_Caspase3-7 494 498 PF00656 0.536
CLV_C14_Caspase3-7 597 601 PF00656 0.698
CLV_NRD_NRD_1 205 207 PF00675 0.352
CLV_NRD_NRD_1 301 303 PF00675 0.381
CLV_NRD_NRD_1 315 317 PF00675 0.377
CLV_NRD_NRD_1 433 435 PF00675 0.384
CLV_NRD_NRD_1 437 439 PF00675 0.378
CLV_NRD_NRD_1 563 565 PF00675 0.497
CLV_NRD_NRD_1 645 647 PF00675 0.447
CLV_NRD_NRD_1 92 94 PF00675 0.317
CLV_PCSK_FUR_1 561 565 PF00082 0.525
CLV_PCSK_KEX2_1 301 303 PF00082 0.436
CLV_PCSK_KEX2_1 315 317 PF00082 0.333
CLV_PCSK_KEX2_1 346 348 PF00082 0.493
CLV_PCSK_KEX2_1 433 435 PF00082 0.384
CLV_PCSK_KEX2_1 437 439 PF00082 0.378
CLV_PCSK_KEX2_1 522 524 PF00082 0.338
CLV_PCSK_KEX2_1 561 563 PF00082 0.491
CLV_PCSK_KEX2_1 644 646 PF00082 0.445
CLV_PCSK_KEX2_1 92 94 PF00082 0.317
CLV_PCSK_PC1ET2_1 301 303 PF00082 0.436
CLV_PCSK_PC1ET2_1 315 317 PF00082 0.333
CLV_PCSK_PC1ET2_1 346 348 PF00082 0.493
CLV_PCSK_PC1ET2_1 522 524 PF00082 0.338
CLV_PCSK_PC7_1 433 439 PF00082 0.355
CLV_PCSK_SKI1_1 280 284 PF00082 0.291
CLV_PCSK_SKI1_1 321 325 PF00082 0.364
CLV_PCSK_SKI1_1 472 476 PF00082 0.359
CLV_Separin_Metazoa 664 668 PF03568 0.520
DEG_COP1_1 583 593 PF00400 0.627
DEG_SCF_TRCP1_1 572 577 PF00400 0.628
DEG_SPOP_SBC_1 157 161 PF00917 0.678
DEG_SPOP_SBC_1 55 59 PF00917 0.653
DOC_CDC14_PxL_1 381 389 PF14671 0.592
DOC_CKS1_1 590 595 PF01111 0.776
DOC_MAPK_gen_1 301 307 PF00069 0.556
DOC_MAPK_RevD_3 191 207 PF00069 0.520
DOC_MAPK_RevD_3 548 564 PF00069 0.683
DOC_PP1_RVXF_1 657 663 PF00149 0.641
DOC_PP1_RVXF_1 79 85 PF00149 0.533
DOC_PP2B_LxvP_1 550 553 PF13499 0.691
DOC_SPAK_OSR1_1 438 442 PF12202 0.545
DOC_USP7_MATH_1 157 161 PF00917 0.671
DOC_USP7_MATH_1 325 329 PF00917 0.563
DOC_USP7_MATH_1 361 365 PF00917 0.679
DOC_USP7_MATH_1 372 376 PF00917 0.597
DOC_USP7_MATH_1 44 48 PF00917 0.586
DOC_USP7_MATH_1 49 53 PF00917 0.752
DOC_USP7_MATH_1 503 507 PF00917 0.699
DOC_USP7_MATH_1 546 550 PF00917 0.666
DOC_USP7_MATH_1 55 59 PF00917 0.640
DOC_USP7_MATH_1 649 653 PF00917 0.680
DOC_WW_Pin1_4 143 148 PF00397 0.647
DOC_WW_Pin1_4 160 165 PF00397 0.681
DOC_WW_Pin1_4 168 173 PF00397 0.610
DOC_WW_Pin1_4 340 345 PF00397 0.670
DOC_WW_Pin1_4 365 370 PF00397 0.626
DOC_WW_Pin1_4 4 9 PF00397 0.651
DOC_WW_Pin1_4 480 485 PF00397 0.474
DOC_WW_Pin1_4 51 56 PF00397 0.758
DOC_WW_Pin1_4 514 519 PF00397 0.628
DOC_WW_Pin1_4 537 542 PF00397 0.629
DOC_WW_Pin1_4 564 569 PF00397 0.653
DOC_WW_Pin1_4 589 594 PF00397 0.794
DOC_WW_Pin1_4 604 609 PF00397 0.679
DOC_WW_Pin1_4 610 615 PF00397 0.710
DOC_WW_Pin1_4 618 623 PF00397 0.645
LIG_14-3-3_CanoR_1 280 285 PF00244 0.491
LIG_14-3-3_CanoR_1 644 649 PF00244 0.700
LIG_BIR_II_1 1 5 PF00653 0.609
LIG_BIR_III_2 100 104 PF00653 0.511
LIG_BRCT_BRCA1_1 505 509 PF00533 0.613
LIG_deltaCOP1_diTrp_1 134 139 PF00928 0.553
LIG_eIF4E_1 299 305 PF01652 0.565
LIG_EVH1_1 550 554 PF00568 0.665
LIG_FHA_1 214 220 PF00498 0.734
LIG_FHA_1 229 235 PF00498 0.467
LIG_FHA_1 254 260 PF00498 0.487
LIG_FHA_1 268 274 PF00498 0.569
LIG_FHA_2 129 135 PF00498 0.537
LIG_FHA_2 333 339 PF00498 0.681
LIG_FHA_2 404 410 PF00498 0.662
LIG_FHA_2 423 429 PF00498 0.633
LIG_FHA_2 481 487 PF00498 0.482
LIG_FHA_2 515 521 PF00498 0.623
LIG_FHA_2 581 587 PF00498 0.695
LIG_FHA_2 595 601 PF00498 0.639
LIG_LIR_Apic_2 616 622 PF02991 0.643
LIG_LIR_Gen_1 109 119 PF02991 0.508
LIG_LIR_Gen_1 375 385 PF02991 0.647
LIG_LIR_Gen_1 483 493 PF02991 0.547
LIG_LIR_Gen_1 76 86 PF02991 0.451
LIG_LIR_Nem_3 109 114 PF02991 0.477
LIG_LIR_Nem_3 295 299 PF02991 0.538
LIG_LIR_Nem_3 375 380 PF02991 0.680
LIG_LIR_Nem_3 483 488 PF02991 0.545
LIG_LIR_Nem_3 673 679 PF02991 0.318
LIG_LIR_Nem_3 76 82 PF02991 0.464
LIG_MYND_1 548 552 PF01753 0.626
LIG_NRBOX 303 309 PF00104 0.591
LIG_PCNA_yPIPBox_3 437 449 PF02747 0.529
LIG_RPA_C_Fungi 240 252 PF08784 0.334
LIG_RPA_C_Fungi 461 473 PF08784 0.371
LIG_SH2_CRK 485 489 PF00017 0.425
LIG_SH2_CRK 687 691 PF00017 0.334
LIG_SH2_STAP1 106 110 PF00017 0.380
LIG_SH2_STAP1 111 115 PF00017 0.318
LIG_SH2_STAP1 292 296 PF00017 0.445
LIG_SH2_STAP1 485 489 PF00017 0.400
LIG_SH2_STAT3 284 287 PF00017 0.334
LIG_SH2_STAT5 106 109 PF00017 0.371
LIG_SH2_STAT5 258 261 PF00017 0.288
LIG_SH2_STAT5 284 287 PF00017 0.298
LIG_SH2_STAT5 296 299 PF00017 0.447
LIG_SH2_STAT5 383 386 PF00017 0.487
LIG_SH2_STAT5 492 495 PF00017 0.441
LIG_SH3_3 169 175 PF00018 0.518
LIG_SH3_3 261 267 PF00018 0.324
LIG_SH3_3 29 35 PF00018 0.432
LIG_SH3_3 545 551 PF00018 0.684
LIG_SH3_3 587 593 PF00018 0.612
LIG_SUMO_SIM_par_1 122 128 PF11976 0.275
LIG_TRAF2_1 131 134 PF00917 0.334
LIG_TRAF2_1 186 189 PF00917 0.453
LIG_TRAF2_1 406 409 PF00917 0.414
LIG_TRAF2_1 425 428 PF00917 0.494
LIG_TRAF2_1 533 536 PF00917 0.608
LIG_TYR_ITIM 685 690 PF00017 0.334
LIG_WRC_WIRS_1 259 264 PF05994 0.290
MOD_CDC14_SPxK_1 343 346 PF00782 0.515
MOD_CDC14_SPxK_1 567 570 PF00782 0.556
MOD_CDK_SPK_2 143 148 PF00069 0.553
MOD_CDK_SPxK_1 340 346 PF00069 0.516
MOD_CDK_SPxK_1 564 570 PF00069 0.560
MOD_CDK_SPxK_1 604 610 PF00069 0.616
MOD_CDK_SPxxK_3 340 347 PF00069 0.517
MOD_CK1_1 156 162 PF00069 0.598
MOD_CK1_1 16 22 PF00069 0.537
MOD_CK1_1 163 169 PF00069 0.571
MOD_CK1_1 178 184 PF00069 0.571
MOD_CK1_1 2 8 PF00069 0.535
MOD_CK1_1 222 228 PF00069 0.562
MOD_CK1_1 253 259 PF00069 0.334
MOD_CK1_1 364 370 PF00069 0.592
MOD_CK1_1 54 60 PF00069 0.549
MOD_CK1_1 555 561 PF00069 0.629
MOD_CK1_1 573 579 PF00069 0.597
MOD_CK1_1 613 619 PF00069 0.576
MOD_CK1_1 621 627 PF00069 0.490
MOD_CK2_1 106 112 PF00069 0.401
MOD_CK2_1 128 134 PF00069 0.396
MOD_CK2_1 386 392 PF00069 0.424
MOD_CK2_1 403 409 PF00069 0.468
MOD_CK2_1 422 428 PF00069 0.524
MOD_CK2_1 514 520 PF00069 0.557
MOD_CK2_1 60 66 PF00069 0.593
MOD_CK2_1 649 655 PF00069 0.576
MOD_GlcNHglycan 155 158 PF01048 0.605
MOD_GlcNHglycan 165 168 PF01048 0.579
MOD_GlcNHglycan 226 229 PF01048 0.470
MOD_GlcNHglycan 327 330 PF01048 0.554
MOD_GlcNHglycan 359 362 PF01048 0.646
MOD_GlcNHglycan 46 49 PF01048 0.459
MOD_GlcNHglycan 493 496 PF01048 0.348
MOD_GlcNHglycan 505 508 PF01048 0.600
MOD_GlcNHglycan 571 575 PF01048 0.583
MOD_GlcNHglycan 651 654 PF01048 0.552
MOD_GSK3_1 102 109 PF00069 0.339
MOD_GSK3_1 139 146 PF00069 0.503
MOD_GSK3_1 149 156 PF00069 0.573
MOD_GSK3_1 158 165 PF00069 0.577
MOD_GSK3_1 215 222 PF00069 0.624
MOD_GSK3_1 224 231 PF00069 0.507
MOD_GSK3_1 357 364 PF00069 0.576
MOD_GSK3_1 39 46 PF00069 0.741
MOD_GSK3_1 50 57 PF00069 0.530
MOD_GSK3_1 503 510 PF00069 0.625
MOD_GSK3_1 570 577 PF00069 0.610
MOD_GSK3_1 9 16 PF00069 0.532
MOD_N-GLC_1 457 462 PF02516 0.279
MOD_NEK2_1 324 329 PF00069 0.623
MOD_NEK2_1 457 462 PF00069 0.520
MOD_NEK2_1 509 514 PF00069 0.641
MOD_NEK2_1 56 61 PF00069 0.567
MOD_PIKK_1 125 131 PF00454 0.343
MOD_PIKK_1 149 155 PF00454 0.602
MOD_PIKK_1 175 181 PF00454 0.481
MOD_PIKK_1 283 289 PF00454 0.334
MOD_PIKK_1 361 367 PF00454 0.645
MOD_PKA_1 644 650 PF00069 0.602
MOD_PKA_2 139 145 PF00069 0.486
MOD_PKA_2 213 219 PF00069 0.453
MOD_PKA_2 644 650 PF00069 0.684
MOD_Plk_2-3 386 392 PF00069 0.424
MOD_Plk_2-3 422 428 PF00069 0.507
MOD_Plk_4 106 112 PF00069 0.401
MOD_Plk_4 228 234 PF00069 0.360
MOD_Plk_4 372 378 PF00069 0.572
MOD_Plk_4 379 385 PF00069 0.381
MOD_Plk_4 386 392 PF00069 0.440
MOD_Plk_4 615 621 PF00069 0.542
MOD_ProDKin_1 143 149 PF00069 0.560
MOD_ProDKin_1 160 166 PF00069 0.601
MOD_ProDKin_1 168 174 PF00069 0.488
MOD_ProDKin_1 340 346 PF00069 0.588
MOD_ProDKin_1 365 371 PF00069 0.521
MOD_ProDKin_1 4 10 PF00069 0.557
MOD_ProDKin_1 480 486 PF00069 0.308
MOD_ProDKin_1 51 57 PF00069 0.709
MOD_ProDKin_1 514 520 PF00069 0.519
MOD_ProDKin_1 537 543 PF00069 0.530
MOD_ProDKin_1 564 570 PF00069 0.560
MOD_ProDKin_1 589 595 PF00069 0.756
MOD_ProDKin_1 604 610 PF00069 0.597
MOD_ProDKin_1 618 624 PF00069 0.541
MOD_SUMO_rev_2 210 219 PF00179 0.424
MOD_SUMO_rev_2 516 524 PF00179 0.422
MOD_SUMO_rev_2 642 652 PF00179 0.558
TRG_DiLeu_BaEn_2 434 440 PF01217 0.458
TRG_ENDOCYTIC_2 111 114 PF00928 0.338
TRG_ENDOCYTIC_2 477 480 PF00928 0.383
TRG_ENDOCYTIC_2 485 488 PF00928 0.490
TRG_ENDOCYTIC_2 687 690 PF00928 0.334
TRG_ER_diArg_1 397 400 PF00400 0.448
TRG_ER_diArg_1 432 434 PF00400 0.451
TRG_ER_diArg_1 437 439 PF00400 0.351
TRG_ER_diArg_1 560 563 PF00400 0.613
TRG_ER_diArg_1 643 646 PF00400 0.581
TRG_ER_diArg_1 80 83 PF00400 0.407
TRG_ER_diArg_1 91 93 PF00400 0.321
TRG_NLS_Bipartite_1 301 319 PF00514 0.423
TRG_NLS_MonoCore_2 313 318 PF00514 0.458
TRG_NLS_MonoExtN_4 314 319 PF00514 0.429
TRG_Pf-PMV_PEXEL_1 195 199 PF00026 0.407
TRG_Pf-PMV_PEXEL_1 92 96 PF00026 0.381

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P4M7 Leptomonas seymouri 44% 84%
A0A3S7WV24 Leishmania donovani 86% 99%
A4H9N7 Leishmania braziliensis 66% 98%
A4HY02 Leishmania infantum 86% 86%
Q4QDQ8 Leishmania major 85% 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