TY - JOUR
T1 - Functional insights from structural genomics
AU - Forouhar, Farhad
AU - Kuzin, Alexandre
AU - Seetharaman, Jayaraman
AU - Lee, Insun
AU - Zhou, Weihong
AU - Abashidze, Mariam
AU - Chen, Yang
AU - Yong, Wei
AU - Janjua, Haleema
AU - Fang, Yingyi
AU - Wang, Dongyan
AU - Cunningham, Kellie
AU - Xiao, Rong
AU - Acton, Thomas B.
AU - Pichersky, Eran
AU - Klessig, Daniel F.
AU - Porter, Carl W.
AU - Montelione, Gaetano T.
AU - Tong, Liang
N1 - Funding Information:
Acknowledgements We thank Randy Abramowitz and John Schwanof at the NSLS for setting up the beamlines; G. DeTitta of Hauptman Woodward Research Institute for crystallization screening. This research was supported by grants from the Protein Structure Initiative of the National Institutes of Health (P50 GM62413 and U54 GM074958).
PY - 2007/9
Y1 - 2007/9
N2 - Structural genomics efforts have produced structural information, either directly or by modeling, for thousands of proteins over the past few years. While many of these proteins have known functions, a large percentage of them have not been characterized at the functional level. The structural information has provided valuable functional insights on some of these proteins, through careful structural analyses, serendipity, and structure-guided functional screening. Some of the success stories based on structures solved at the Northeast Structural Genomics Consortium (NESG) are reported here. These include a novel methyl salicylate esterase with important role in plant innate immunity, a novel RNA methyltransferase (H. influenzae yggJ (HI0303)), a novel spermidine/spermine N-acetyltransferase (B. subtilis PaiA), a novel methyltransferase or AdoMet binding protein (A. fulgidus AF_0241), an ATP:cob(I)alamin adenosyltransferase (B. subtilis YvqK), a novel carboxysome pore (E. coli EutN), a proline racemase homolog with a disrupted active site (B. melitensis BME11586), an FMN-dependent enzyme (S. pneumoniae SP_1951), and a 12-stranded β-barrel with a novel fold (V. parahaemolyticus VPA1032).
AB - Structural genomics efforts have produced structural information, either directly or by modeling, for thousands of proteins over the past few years. While many of these proteins have known functions, a large percentage of them have not been characterized at the functional level. The structural information has provided valuable functional insights on some of these proteins, through careful structural analyses, serendipity, and structure-guided functional screening. Some of the success stories based on structures solved at the Northeast Structural Genomics Consortium (NESG) are reported here. These include a novel methyl salicylate esterase with important role in plant innate immunity, a novel RNA methyltransferase (H. influenzae yggJ (HI0303)), a novel spermidine/spermine N-acetyltransferase (B. subtilis PaiA), a novel methyltransferase or AdoMet binding protein (A. fulgidus AF_0241), an ATP:cob(I)alamin adenosyltransferase (B. subtilis YvqK), a novel carboxysome pore (E. coli EutN), a proline racemase homolog with a disrupted active site (B. melitensis BME11586), an FMN-dependent enzyme (S. pneumoniae SP_1951), and a 12-stranded β-barrel with a novel fold (V. parahaemolyticus VPA1032).
KW - Acetyltransferase
KW - Methyltransferase
KW - Spermine
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U2 - 10.1007/s10969-007-9018-3
DO - 10.1007/s10969-007-9018-3
M3 - Article
C2 - 17588214
AN - SCOPUS:37249075428
SN - 1345-711X
VL - 8
SP - 37
EP - 44
JO - Journal of Structural and Functional Genomics
JF - Journal of Structural and Functional Genomics
IS - 2-3
ER -