Search Results

Overview

Uniprot IDQ9H7Z6
Protein NameHistone acetyltransferase KAT8
Gene NameKAT8
OrganismHomo sapiens

Kla Sites from experimental identification

Position Flanking peptide
121 TVKDAVQKNSEKYLS
145 ITRNQKRKHDEINHV

Function

Histone acetyltransferase that catalyzes histone H4 acetylation at 'Lys-5'- and 'Lys-8' (H4K5ac and H4K8ac) or 'Lys-16' (H4K16ac), depending on the context (PubMed:12397079, PubMed:16227571, PubMed:16543150, PubMed:20018852, PubMed:21217699, PubMed:22020126, PubMed:22547026, PubMed:31794431, PubMed:33837287). Catalytic component of the MSL histone acetyltransferase complex, a multiprotein complex that mediates the majority of histone H4 acetylation at 'Lys-16' (H4K16ac), an epigenetic mark that prevents chromatin compaction (PubMed:12397079, PubMed:16227571, PubMed:16543150, PubMed:21217699, PubMed:22020126, PubMed:22547026, PubMed:33657400, PubMed:33837287). H4K16ac constitutes the only acetylation mark intergenerationally transmitted and regulates key biological processes, such as oogenesis, embryonic stem cell pluripotency, hematopoiesis or glucose metabolism (By similarity). The MSL complex is required for chromosome stability and genome integrity by maintaining homeostatic levels of H4K16ac (PubMed:33837287). The MSL complex is also involved in gene dosage by promoting up-regulation of genes expressed by the X chromosome (By similarity). X up-regulation is required to compensate for autosomal biallelic expression (By similarity). The MSL complex also participates in gene dosage compensation by promoting expression of Tsix non-coding RNA (By similarity). As part of the NSL histone acetyltransferase complex, catalyzes histone H4 acetylation at 'Lys-5'- and 'Lys-8' (H4K5ac and H4K8ac) at transcription start sites and promotes transcription initiation (PubMed:20018852, PubMed:22547026, PubMed:33657400). The NSL complex also acts as a regulator of gene expression in mitochondria: KAT8 associates with mitochondrial DNA and controls expression of respiratory genes in an acetyltransferase-dependent mechanism (PubMed:27768893). Also functions as an acetyltransferase for non-histone targets, such as ALKBH5, COX17, IRF3, KDM1A/LSD1, LMNA, PAX7 or TP53/p53 (PubMed:17189187, PubMed:19854137, PubMed:37369679). Acts as an inhibitor of antiviral immunity by acetylating IRF3, preventing IRF3 recruitment to promoters (By similarity). Acts as a regulator of asymmetric division in muscle stem cells by mediating acetylation of PAX7 (By similarity). As part of the NSL complex, acetylates TP53/p53 at 'Lys-120' (PubMed:17189187, PubMed:19854137). Acts as a regulator of epithelial-to-mesenchymal transition as part of the NSL complex by mediating acetylation of KDM1A/LSD1 (PubMed:27292636). The NSL complex is required for nuclear architecture maintenance by mediating acetylation of LMNA (By similarity). Promotes mitochondrial integrity by catalyzing acetylation of COX17 (By similarity). In addition to protein acetyltransferase activity, able to mediate protein propionylation (PubMed:29321206)

Protein Sequence

10 MAAQGAAAAV 20 AAGTSGVAGE 30 GEPGPGENAA 40 AEGTAPSPGR 50 VSPPTPARGE 60 PEVTVEIGET 70 YLCRRPDSTW 80 HSAEVIQSRV 90 NDQEGREEFY 100 VHYVGFNRRL 110 DEWVDKNRLA 120 LTKTVKDAVQ 130 KNSEKYLSEL 140 AEQPERKITR 150 NQKRKHDEIN 160 HVQKTYAEMD 170 PTTAALEKEH 180 EAITKVKYVD 190 KIHIGNYEID 200 AWYFSPFPED 210 YGKQPKLWLC 220 EYCLKYMKYE 230 KSYRFHLGQC 240 QWRQPPGKEI 250 YRKSNISVYE 260 VDGKDHKIYC 270 QNLCLLAKLF 280 LDHKTLYFDV 290 EPFVFYILTE 300 VDRQGAHIVG 310 YFSKEKESPD 320 GNNVACILTL 330 PPYQRRGYGK 340 FLIAFSYELS 350 KLESTVGSPE 360 KPLSDLGKLS 370 YRSYWSWVLL 380 EILRDFRGTL 390 SIKDLSQMTS 400 ITQNDIISTL 410 QSLNMVKYWK 420 GQHVICVTPK 430 LVEEHLKSAQ 440 YKKPPITVDS 450 VCLKWAPPKH KQVKLSKK

Gene Ontology

Classification GO ID Description
Cellular Component GO:0005694 chromosome
Cellular Component GO:0000123 histone acetyltransferase complex
Cellular Component GO:0000776 kinetochore
Cellular Component GO:0005739 mitochondrion
Cellular Component GO:0071339 MLL1 complex
Cellular Component GO:0072487 MSL complex
Cellular Component GO:0044545 NSL complex
Cellular Component GO:0035267 NuA4 histone acetyltransferase complex
Cellular Component GO:0016363 nuclear matrix
Cellular Component GO:0005654 nucleoplasm
Cellular Component GO:0005634 nucleus
Molecular Function GO:0019899 enzyme binding
Molecular Function GO:0010485 histone H4 acetyltransferase activity
Molecular Function GO:0046972 histone H4K16 acetyltransferase activity
Molecular Function GO:0043995 histone H4K5 acetyltransferase activity
Molecular Function GO:0043996 histone H4K8 acetyltransferase activity
Molecular Function GO:1990841 promoter-specific chromatin binding
Molecular Function GO:0061920 protein propionyltransferase activity
Molecular Function GO:0061733 protein-lysine-acetyltransferase activity
Molecular Function GO:0061629 RNA polymerase II-specific DNA-binding transcription factor binding
Molecular Function GO:0003713 transcription coactivator activity
Molecular Function GO:0008270 zinc ion binding
Biological Process GO:0009048 dosage compensation by inactivation of X chromosome
Biological Process GO:0030099 myeloid cell differentiation
Biological Process GO:0045892 negative regulation of DNA-templated transcription
Biological Process GO:0010719 negative regulation of epithelial to mesenchymal transition
Biological Process GO:0032480 negative regulation of type I interferon production
Biological Process GO:0022008 neurogenesis
Biological Process GO:0048477 oogenesis
Biological Process GO:0045893 positive regulation of DNA-templated transcription
Biological Process GO:1902726 positive regulation of skeletal muscle satellite cell differentiation
Biological Process GO:0060261 positive regulation of transcription initiation by RNA polymerase II
Biological Process GO:0035166 post-embryonic hemopoiesis
Biological Process GO:0010506 regulation of autophagy
Biological Process GO:1903108 regulation of mitochondrial transcription
Biological Process GO:0050684 regulation of mRNA processing
Biological Process GO:0045815 transcription initiation-coupled chromatin remodeling

Reference

[1] Yang Z, Yan C, Ma J, Peng P, Ren X et al.. Lactylome analysis suggests lactylation-dependent mechanisms of metabolic adaptation in hepatocellular carcinoma.. Nat Metab 5(1):61-79. 2023 Jan. PMID: 36593272.