5EXV
Crystal structure of heme binding protein HutX from Vibrio cholerae
5EXV の概要
| エントリーDOI | 10.2210/pdb5exv/pdb |
| 分子名称 | Hemin-degrading HemS.ChuX domain protein (1 entity in total) |
| 機能のキーワード | heme oxygenase, heme-binding protein |
| 由来する生物種 | Vibrio cholerae |
| タンパク質・核酸の鎖数 | 6 |
| 化学式量合計 | 127447.13 |
| 構造登録者 | |
| 主引用文献 | Sekine, Y.,Tanzawa, T.,Tanaka, Y.,Ishimori, K.,Uchida, T. Cytoplasmic Heme-Binding Protein (HutX) from Vibrio cholerae Is an Intracellular Heme Transport Protein for the Heme-Degrading Enzyme, HutZ Biochemistry, 55:884-893, 2016 Cited by PubMed Abstract: HutZ is a cytoplasmic heme-binding protein from Vibrio cholerae. Although we have previously identified HutZ as a heme-degrading enzyme [Uchida, T., et al. (2012) Chem. Commun. 48, 6741-6743], the heme transport protein for HutZ remained unknown. To identify the heme transport protein for HutZ, we focused on the heme utilization operon, hutWXZ. To this end, we constructed an expression system for HutX in Escherichia coli and purified it to homogeneity. An absorption spectral analysis demonstrated that HutX binds heme with a 1:1 stoichiometry and a dissociation constant of 7.4 nM. The crystal structure of HutX displays a fold similar to that of the homologous protein, ChuX, from E. coli O157:H7. A structural comparison of HutX and ChuX, and resonance Raman spectra of heme-HutX, suggest that the axial ligand of the ferric heme is Tyr90. The heme bound to HutX is transferred to HutZ with biphasic dissociation kinetics of 8.3 × 10(-2) and 1.5 × 10(-2) s(-1), values distinctly larger than those for transfer from HutX to apomyoglobin. Surface plasmon resonance experiments confirmed that HutX interacts with HutZ with a dissociation constant of ∼400 μM. These results suggest that heme is transferred from HutX to HutZ via a specific protein-protein interaction. Therefore, we can conclude that HutX is a cytoplasmic heme transport protein for HutZ. PubMed: 26807477DOI: 10.1021/acs.biochem.5b01273 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.901 Å) |
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