Target intelligence / Profile preview

N-alpha-acetyltransferase 40, NatD catalytic subunit (NAA40)

Target
NAA40
Molecular classification
Enzyme, Histone acetyltransferase, Protein N-terminal acetyltransferase, Chromatin modification factor
01

Overview

N-alpha-acetyltransferase 40 (NAA40, also called NatD catalytic subunit) is a protein acetyltransferase enzyme that specifically catalyzes N-terminal acetylation of histones H4 and H2A, thus regulating chromatin structure and gene expression[1][3][6]. Unlike other N-terminal acetyltransferases, NAA40 shows high substrate specificity, targeting the Ser-Gly-Arg-Gly N-terminus of H4 and H2A. NAA40 is localized primarily in the nucleoplasm and cytosol and is involved in chromatin remodeling, developmental regulation, and the suppression of apoptosis. Genetic and functional studies in human and model organisms indicate key roles in developmental transitions and potential contributions to diseases such as cancer and rare congenital anomalies[1][2][5][6].

Other names
PATT1hNatDNatDNAT11FLJ13848N-acetyltransferase 11N-alpha-acetyltransferase Dprotein acetyltransferase 1EC 2.3.1.257N(alpha)-acetyltransferase 40 (NatD) catalytic subunit homologN-alpha acetyl transferase 40NAA40_HUMANNatD catalytic subunit
02

Mechanism of action

Inhibitors would potentially block N-terminal acetylation of target histones, altering chromatin states and gene expression

03

Biological functions

Histone acetylation (specifically histones H4 and H2A)Chromatin remodelingRegulation of gene expressionNegative regulation of apoptosisPotential role in hepatic lipid metabolismDevelopmental regulation (in model organisms)
04

Disease associations

Cancer (implicated via regulation of apoptosis and cell proliferation)Potentially involved in rare developmental syndromes (e.g., microphthalmia syndromic 1, pulmonary subvalvular stenosis)
05

Safety considerations

Potential challenges related to global chromatin disturbance and essential developmental/mechanistic roles (inhibition may cause broad effects on gene regulation and cell viability)

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