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2QL6

human nicotinamide riboside kinase (NRK1)

2QL6 の概要
エントリーDOI10.2210/pdb2ql6/pdb
関連するPDBエントリー2QG6
分子名称nicotinamide riboside kinase 1, ADENOSINE-5'-DIPHOSPHATE, (1R)-1-[4-(AMINOCARBONYL)-1,3-THIAZOL-2-YL]-1,4-ANHYDRO-D-RIBITOL (3 entities in total)
機能のキーワードnicotinamide riboside kinase, nrk, monophosphate (nmp) kinase, nicotinamide mononucleotide, tiazofurin, adp, signaling protein, transferase
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数16
化学式量合計387713.95
構造登録者
Khan, J.A.,Xiang, S.,Tong, L. (登録日: 2007-07-12, 公開日: 2007-10-02, 最終更新日: 2024-10-30)
主引用文献Khan, J.A.,Xiang, S.,Tong, L.
Crystal structure of human nicotinamide riboside kinase
Structure, 15:1005-1013, 2007
Cited by
PubMed Abstract: Nicotinamide riboside kinase (NRK) has an important role in the biosynthesis of NAD(+) as well as the activation of tiazofurin and other NR analogs for anticancer therapy. NRK belongs to the deoxynucleoside kinase and nucleoside monophosphate (NMP) kinase superfamily, although the degree of sequence conservation is very low. We report here the crystal structures of human NRK1 in a binary complex with the reaction product nicotinamide mononucleotide (NMN) at 1.5 A resolution and in a ternary complex with ADP and tiazofurin at 2.7 A resolution. The active site is located in a groove between the central parallel beta sheet core and the LID and NMP-binding domains. The hydroxyl groups on the ribose of NR are recognized by Asp56 and Arg129, and Asp36 is the general base of the enzyme. Mutation of residues in the active site can abolish the catalytic activity of the enzyme, confirming the structural observations.
PubMed: 17698003
DOI: 10.1016/j.str.2007.06.017
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.7 Å)
構造検証レポート
Validation report summary of 2ql6
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-12-31に公開中

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