蛋白質(zhì)乙?；瘮?shù)據(jù)庫CPLA1.0

For publication of results, please cite the following article: CPLA 1.0: an integrated database of protein lysine acetylation Zexian Liu , Xinjiao Gao, Jun Cao, Haiyan Liu, Yanhong Zhou, Longping Wen, Xiangjiao Yang, Xuebiao Yao, Jian Ren

For publication of results, please cite the following article:

CPLA 1.0: an integrated database of protein lysine acetylation Zexian Liu , Xinjiao Gao, Jun Cao, Haiyan Liu, Yanhong Zhou, Longping Wen, Xiangjiao Yang, Xuebiao Yao, Jian Ren , Yu Xue . Nucleic Acids Research.2010.(Accepted )

There are two types of acetylation processes widely occurred in proteins. The first Nα-terminal acetylation is catalyzed a variety of N-terminal acetyltransferases (NATs), which cotranslationally transfer acetyl moieties from acetyl-coenzyme A (Acetyl-CoA) to the α-amino (Nα) group of protein amino-terminal residues. Although Nα-terminal acetylation is rare in prokaryotes, it was estimated that about 85% of eukaryotic proteins are Nα-terminally modified (Polevoda et al ., 2000 ; Polevoda et al ., 2002 ). The second type is Nε-lysine acetylation, which specifically modifies ε-amino group of protein lysine residues (Yang et al ., 2007 ; Shahbazian et al ., 2007 ; Smith et al ., 2009 ). Although Nε-lysine acetylation is less common, it's one of the most important and ubiquitous post-translational modifications conserved in prokaryotes and eukaryotes. Moreover, the acetylation and deacetylation are dynamically and temporally regulated by histone acetyltransferases (HATs) and histone deacetylases (HDACs), respectively (Yang et al ., 2004 ; Lee et al ., 2007 ).

In 1964, Allfrey et al. firstly observed that lysine acetylation of histones plays an essential role in regulation of gene expression (Allfrey et al ., 1964 ). Later and recent studies in epigenetics solidified this seminal discovery, and proposed acetylation as a key component of the "histone code" (Jenuwein et al ., 2001 ). Beyond histones, a wide range of non-histone proteins can also be lysine acetylated, and involved in a variety of biological processes, such as transcription regulation (Yuan et al ., 2005 ), DNA replication (Terret et al ., 2009 ; Choudhary et al ., 2009 ), cellular signaling (Walkinshaw et al ., 2008 ; Spange et al ., 2009 ), stress response (Brunet et al ., 2004 ) and so on. Aberrance of lysine acetylation and deacetylation is associated with various diseases and cancers (Kim et al ., 2006 ). In particular, acetylation was demonstrated to be implicated in cellular metabolism and aging (Wang et al ., 2010 ; Zhao et al ., 2010 ), while one class of NAD+ dependent HDACs of sirtuins might be potent drug target for promoting longevity (Cohen et al ., 2004 ; Wang et al ., 2010 ).

Since the number of known acetylation sites is rapidly increased, it is an urgent topic to collect the experimental data and provide an integrated resource for the community. Recently, several public databases, such as PhosphoSitePlus , HPRD , SysPTM , and dbPTM , have already contained protein acetylation information. In these databases, both of Nα-terminal and Nε-lysine acetylation data were curated, while lysine acetylation sites are usually only a limited part of total sites. So, thousands of lysine acetylation sites in other species still remain to be collected.

Currently, the CPLA 1.0 database was updated on March 1st, 2010, containing 3,311 unique protein entries with 7,151 lysine acetylation sites. The online service of CPLA 1.0 was implemented in PHP + MySQL + JavaScript. And the local packages of CPLA 1.0 were developed in JAVA 1.5 (J2SE). The database will be updated routinely as new acetylated lysines are reported.

The CPLA 1.0 supports Windows, Unix/Linux and Mac and is freely available for academic researches at: http://cpla.biocuckoo.org/ .

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