2P8C
Crystal structure of N-succinyl Arg/Lys racemase from Bacillus cereus ATCC 14579 complexed with N-succinyl Arg.
2P8C の概要
エントリーDOI | 10.2210/pdb2p8c/pdb |
関連するPDBエントリー | 2P88 2P8B |
分子名称 | Mandelate racemase/muconate lactonizing enzyme family protein, MAGNESIUM ION, N~2~-(3-CARBOXYPROPANOYL)-L-ARGININE, ... (4 entities in total) |
機能のキーワード | enolase superfamily, prediction of function, n-succinyl amino acid racemase, lyase |
由来する生物種 | Bacillus cereus ATCC 14579 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 41297.69 |
構造登録者 | Fedorov, A.A.,Song, L.,Fedorov, E.V.,Gerlt, J.A.,Almo, S.C. (登録日: 2007-03-22, 公開日: 2007-07-03, 最終更新日: 2023-08-30) |
主引用文献 | Song, L.,Kalyanaraman, C.,Fedorov, A.A.,Fedorov, E.V.,Glasner, M.E.,Brown, S.,Imker, H.J.,Babbitt, P.C.,Almo, S.C.,Jacobson, M.P.,Gerlt, J.A. Prediction and assignment of function for a divergent N-succinyl amino acid racemase. Nat.Chem.Biol., 3:486-491, 2007 Cited by PubMed Abstract: The protein databases contain many proteins with unknown function. A computational approach for predicting ligand specificity that requires only the sequence of the unknown protein would be valuable for directing experiment-based assignment of function. We focused on a family of unknown proteins in the mechanistically diverse enolase superfamily and used two approaches to assign function: (i) enzymatic assays using libraries of potential substrates, and (ii) in silico docking of the same libraries using a homology model based on the most similar (35% sequence identity) characterized protein. The results matched closely; an experimentally determined structure confirmed the predicted structure of the substrate-liganded complex. We assigned the N-succinyl arginine/lysine racemase function to the family, correcting the annotation (L-Ala-D/L-Glu epimerase) based on the function of the most similar characterized homolog. These studies establish that ligand docking to a homology model can facilitate functional assignment of unknown proteins by restricting the identities of the possible substrates that must be experimentally tested. PubMed: 17603539DOI: 10.1038/nchembio.2007.11 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2 Å) |
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