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 donovani
UniProt:
A0A3S7WV24_LEIDO
TriTrypDb:
LdCL_180018200 , LDHU3_18.1640
Length:
706

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

A0A3S7WV24
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3S7WV24

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_Caspase3-7 224 228 PF00656 0.708
CLV_C14_Caspase3-7 339 343 PF00656 0.688
CLV_C14_Caspase3-7 541 545 PF00656 0.645
CLV_C14_Caspase3-7 607 611 PF00656 0.712
CLV_NRD_NRD_1 25 27 PF00675 0.380
CLV_NRD_NRD_1 302 304 PF00675 0.365
CLV_NRD_NRD_1 316 318 PF00675 0.390
CLV_NRD_NRD_1 415 417 PF00675 0.479
CLV_NRD_NRD_1 435 437 PF00675 0.337
CLV_NRD_NRD_1 439 441 PF00675 0.384
CLV_NRD_NRD_1 570 572 PF00675 0.497
CLV_NRD_NRD_1 655 657 PF00675 0.464
CLV_NRD_NRD_1 93 95 PF00675 0.331
CLV_PCSK_FUR_1 568 572 PF00082 0.535
CLV_PCSK_KEX2_1 25 27 PF00082 0.367
CLV_PCSK_KEX2_1 302 304 PF00082 0.421
CLV_PCSK_KEX2_1 316 318 PF00082 0.324
CLV_PCSK_KEX2_1 415 417 PF00082 0.473
CLV_PCSK_KEX2_1 435 437 PF00082 0.337
CLV_PCSK_KEX2_1 439 441 PF00082 0.384
CLV_PCSK_KEX2_1 568 570 PF00082 0.489
CLV_PCSK_KEX2_1 654 656 PF00082 0.466
CLV_PCSK_KEX2_1 93 95 PF00082 0.331
CLV_PCSK_PC1ET2_1 302 304 PF00082 0.421
CLV_PCSK_PC1ET2_1 316 318 PF00082 0.314
CLV_PCSK_PC7_1 435 441 PF00082 0.353
CLV_PCSK_SKI1_1 281 285 PF00082 0.406
CLV_PCSK_SKI1_1 322 326 PF00082 0.394
CLV_PCSK_SKI1_1 474 478 PF00082 0.335
DEG_SPOP_SBC_1 158 162 PF00917 0.697
DEG_SPOP_SBC_1 41 45 PF00917 0.661
DEG_SPOP_SBC_1 56 60 PF00917 0.688
DEG_SPOP_SBC_1 73 77 PF00917 0.609
DOC_CDC14_PxL_1 383 391 PF14671 0.609
DOC_CKS1_1 602 607 PF01111 0.835
DOC_MAPK_gen_1 302 308 PF00069 0.584
DOC_MAPK_RevD_3 555 571 PF00069 0.681
DOC_PP1_RVXF_1 675 682 PF00149 0.576
DOC_PP1_RVXF_1 80 86 PF00149 0.565
DOC_PP2B_LxvP_1 356 359 PF13499 0.638
DOC_PP2B_LxvP_1 557 560 PF13499 0.692
DOC_SPAK_OSR1_1 440 444 PF12202 0.562
DOC_USP7_MATH_1 158 162 PF00917 0.685
DOC_USP7_MATH_1 209 213 PF00917 0.622
DOC_USP7_MATH_1 359 363 PF00917 0.682
DOC_USP7_MATH_1 365 369 PF00917 0.690
DOC_USP7_MATH_1 374 378 PF00917 0.607
DOC_USP7_MATH_1 50 54 PF00917 0.805
DOC_USP7_MATH_1 505 509 PF00917 0.728
DOC_USP7_MATH_1 56 60 PF00917 0.668
DOC_USP7_MATH_1 560 564 PF00917 0.741
DOC_USP7_MATH_1 609 613 PF00917 0.669
DOC_USP7_MATH_1 659 663 PF00917 0.711
DOC_WW_Pin1_4 1 6 PF00397 0.754
DOC_WW_Pin1_4 144 149 PF00397 0.663
DOC_WW_Pin1_4 161 166 PF00397 0.711
DOC_WW_Pin1_4 501 506 PF00397 0.630
DOC_WW_Pin1_4 52 57 PF00397 0.786
DOC_WW_Pin1_4 571 576 PF00397 0.653
DOC_WW_Pin1_4 598 603 PF00397 0.787
DOC_WW_Pin1_4 614 619 PF00397 0.679
DOC_WW_Pin1_4 628 633 PF00397 0.576
LIG_14-3-3_CanoR_1 281 286 PF00244 0.512
LIG_14-3-3_CanoR_1 345 350 PF00244 0.675
LIG_14-3-3_CanoR_1 594 600 PF00244 0.713
LIG_14-3-3_CanoR_1 654 659 PF00244 0.677
LIG_BIR_III_2 101 105 PF00653 0.527
LIG_BRCT_BRCA1_1 375 379 PF00533 0.659
LIG_CaM_IQ_9 126 141 PF13499 0.528
LIG_deltaCOP1_diTrp_1 135 140 PF00928 0.581
LIG_eIF4E_1 300 306 PF01652 0.552
LIG_FHA_1 215 221 PF00498 0.676
LIG_FHA_1 230 236 PF00498 0.468
LIG_FHA_1 255 261 PF00498 0.468
LIG_FHA_1 269 275 PF00498 0.468
LIG_FHA_1 30 36 PF00498 0.668
LIG_FHA_1 47 53 PF00498 0.677
LIG_FHA_2 130 136 PF00498 0.562
LIG_FHA_2 334 340 PF00498 0.703
LIG_FHA_2 406 412 PF00498 0.671
LIG_FHA_2 425 431 PF00498 0.495
LIG_FHA_2 539 545 PF00498 0.646
LIG_FHA_2 588 594 PF00498 0.701
LIG_FHA_2 605 611 PF00498 0.627
LIG_LIR_Apic_2 626 632 PF02991 0.637
LIG_LIR_Gen_1 110 120 PF02991 0.522
LIG_LIR_Gen_1 376 387 PF02991 0.627
LIG_LIR_Nem_3 110 115 PF02991 0.488
LIG_LIR_Nem_3 22 27 PF02991 0.600
LIG_LIR_Nem_3 296 300 PF02991 0.541
LIG_LIR_Nem_3 376 382 PF02991 0.674
LIG_LIR_Nem_3 634 638 PF02991 0.595
LIG_LYPXL_yS_3 635 638 PF13949 0.599
LIG_NRBOX 304 310 PF00104 0.588
LIG_PCNA_yPIPBox_3 439 451 PF02747 0.541
LIG_Rb_LxCxE_1 665 678 PF01857 0.571
LIG_RPA_C_Fungi 241 253 PF08784 0.363
LIG_RPA_C_Fungi 463 475 PF08784 0.393
LIG_SH2_CRK 487 491 PF00017 0.364
LIG_SH2_CRK 697 701 PF00017 0.363
LIG_SH2_SRC 349 352 PF00017 0.543
LIG_SH2_STAP1 107 111 PF00017 0.400
LIG_SH2_STAP1 112 116 PF00017 0.339
LIG_SH2_STAP1 293 297 PF00017 0.404
LIG_SH2_STAP1 487 491 PF00017 0.352
LIG_SH2_STAT3 285 288 PF00017 0.363
LIG_SH2_STAT5 107 110 PF00017 0.398
LIG_SH2_STAT5 259 262 PF00017 0.302
LIG_SH2_STAT5 285 288 PF00017 0.302
LIG_SH2_STAT5 297 300 PF00017 0.433
LIG_SH2_STAT5 385 388 PF00017 0.500
LIG_SH2_STAT5 494 497 PF00017 0.428
LIG_SH3_3 169 175 PF00018 0.633
LIG_SH3_3 262 268 PF00018 0.352
LIG_SH3_3 30 36 PF00018 0.482
LIG_SH3_3 352 358 PF00018 0.590
LIG_SH3_3 569 575 PF00018 0.544
LIG_SH3_3 599 605 PF00018 0.600
LIG_TRAF2_1 187 190 PF00917 0.492
LIG_TRAF2_1 199 202 PF00917 0.356
LIG_TRAF2_1 408 411 PF00917 0.427
LIG_TRAF2_1 427 430 PF00917 0.608
LIG_TRAF2_1 535 538 PF00917 0.729
LIG_TYR_ITIM 695 700 PF00017 0.363
LIG_WRC_WIRS_1 260 265 PF05994 0.302
MOD_CDC14_SPxK_1 574 577 PF00782 0.562
MOD_CDK_SPK_2 144 149 PF00069 0.575
MOD_CDK_SPK_2 628 633 PF00069 0.516
MOD_CDK_SPxK_1 571 577 PF00069 0.562
MOD_CDK_SPxK_1 614 620 PF00069 0.621
MOD_CK1_1 157 163 PF00069 0.658
MOD_CK1_1 164 170 PF00069 0.627
MOD_CK1_1 17 23 PF00069 0.646
MOD_CK1_1 179 185 PF00069 0.695
MOD_CK1_1 223 229 PF00069 0.570
MOD_CK1_1 254 260 PF00069 0.363
MOD_CK1_1 366 372 PF00069 0.604
MOD_CK1_1 501 507 PF00069 0.617
MOD_CK1_1 55 61 PF00069 0.628
MOD_CK1_1 562 568 PF00069 0.622
MOD_CK1_1 598 604 PF00069 0.634
MOD_CK1_1 623 629 PF00069 0.579
MOD_CK1_1 631 637 PF00069 0.487
MOD_CK2_1 107 113 PF00069 0.436
MOD_CK2_1 129 135 PF00069 0.430
MOD_CK2_1 388 394 PF00069 0.445
MOD_CK2_1 405 411 PF00069 0.520
MOD_CK2_1 424 430 PF00069 0.466
MOD_CK2_1 61 67 PF00069 0.797
MOD_CK2_1 659 665 PF00069 0.602
MOD_DYRK1A_RPxSP_1 571 575 PF00069 0.538
MOD_GlcNHglycan 156 159 PF01048 0.640
MOD_GlcNHglycan 166 169 PF01048 0.631
MOD_GlcNHglycan 227 230 PF01048 0.486
MOD_GlcNHglycan 328 331 PF01048 0.595
MOD_GlcNHglycan 361 364 PF01048 0.649
MOD_GlcNHglycan 499 503 PF01048 0.562
MOD_GlcNHglycan 507 510 PF01048 0.615
MOD_GlcNHglycan 520 523 PF01048 0.597
MOD_GlcNHglycan 597 600 PF01048 0.613
MOD_GlcNHglycan 610 614 PF01048 0.641
MOD_GlcNHglycan 63 66 PF01048 0.720
MOD_GlcNHglycan 661 664 PF01048 0.587
MOD_GSK3_1 1 8 PF00069 0.618
MOD_GSK3_1 10 17 PF00069 0.562
MOD_GSK3_1 140 147 PF00069 0.654
MOD_GSK3_1 150 157 PF00069 0.714
MOD_GSK3_1 159 166 PF00069 0.662
MOD_GSK3_1 210 217 PF00069 0.507
MOD_GSK3_1 225 232 PF00069 0.476
MOD_GSK3_1 341 348 PF00069 0.652
MOD_GSK3_1 359 366 PF00069 0.697
MOD_GSK3_1 37 44 PF00069 0.701
MOD_GSK3_1 46 53 PF00069 0.635
MOD_GSK3_1 501 508 PF00069 0.668
MOD_GSK3_1 510 517 PF00069 0.575
MOD_GSK3_1 57 64 PF00069 0.564
MOD_GSK3_1 73 80 PF00069 0.493
MOD_N-GLC_1 105 110 PF02516 0.317
MOD_NEK2_1 325 330 PF00069 0.658
MOD_NEK2_1 459 464 PF00069 0.539
MOD_NEK2_1 511 516 PF00069 0.675
MOD_NEK2_1 57 62 PF00069 0.613
MOD_NEK2_2 216 221 PF00069 0.506
MOD_NEK2_2 374 379 PF00069 0.588
MOD_PIKK_1 126 132 PF00454 0.470
MOD_PIKK_1 150 156 PF00454 0.633
MOD_PIKK_1 284 290 PF00454 0.363
MOD_PIKK_1 363 369 PF00454 0.686
MOD_PKA_1 654 660 PF00069 0.642
MOD_PKA_2 140 146 PF00069 0.514
MOD_PKA_2 220 226 PF00069 0.519
MOD_PKA_2 654 660 PF00069 0.683
MOD_Plk_1 179 185 PF00069 0.435
MOD_Plk_2-3 388 394 PF00069 0.442
MOD_Plk_2-3 424 430 PF00069 0.466
MOD_Plk_4 107 113 PF00069 0.475
MOD_Plk_4 193 199 PF00069 0.393
MOD_Plk_4 229 235 PF00069 0.465
MOD_Plk_4 281 287 PF00069 0.374
MOD_Plk_4 374 380 PF00069 0.579
MOD_Plk_4 381 387 PF00069 0.477
MOD_Plk_4 388 394 PF00069 0.464
MOD_Plk_4 460 466 PF00069 0.344
MOD_Plk_4 625 631 PF00069 0.504
MOD_ProDKin_1 1 7 PF00069 0.703
MOD_ProDKin_1 144 150 PF00069 0.582
MOD_ProDKin_1 161 167 PF00069 0.643
MOD_ProDKin_1 501 507 PF00069 0.532
MOD_ProDKin_1 52 58 PF00069 0.747
MOD_ProDKin_1 571 577 PF00069 0.562
MOD_ProDKin_1 598 604 PF00069 0.749
MOD_ProDKin_1 614 620 PF00069 0.597
MOD_ProDKin_1 628 634 PF00069 0.446
MOD_SUMO_rev_2 652 662 PF00179 0.590
TRG_DiLeu_BaEn_2 436 442 PF01217 0.468
TRG_ENDOCYTIC_2 112 115 PF00928 0.359
TRG_ENDOCYTIC_2 479 482 PF00928 0.389
TRG_ENDOCYTIC_2 487 490 PF00928 0.352
TRG_ENDOCYTIC_2 635 638 PF00928 0.485
TRG_ENDOCYTIC_2 697 700 PF00928 0.363
TRG_ER_diArg_1 24 26 PF00400 0.488
TRG_ER_diArg_1 399 402 PF00400 0.513
TRG_ER_diArg_1 415 417 PF00400 0.635
TRG_ER_diArg_1 434 436 PF00400 0.384
TRG_ER_diArg_1 439 441 PF00400 0.465
TRG_ER_diArg_1 567 570 PF00400 0.613
TRG_ER_diArg_1 653 656 PF00400 0.573
TRG_ER_diArg_1 81 84 PF00400 0.440
TRG_ER_diArg_1 92 94 PF00400 0.336
TRG_NLS_Bipartite_1 302 320 PF00514 0.408
TRG_NLS_MonoCore_2 314 319 PF00514 0.456
TRG_NLS_MonoExtN_4 315 320 PF00514 0.430
TRG_Pf-PMV_PEXEL_1 93 97 PF00026 0.409

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P4M7 Leptomonas seymouri 45% 85%
A4H9N7 Leishmania braziliensis 70% 100%
A4HY02 Leishmania infantum 100% 100%
E9ARR5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 86% 99%
Q4QDQ8 Leishmania major 89% 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