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dc.contributor.authorChang, Chin-Yuanen_US
dc.contributor.authorHsieh, Yin-Chengen_US
dc.contributor.authorWang, Ting-Yien_US
dc.contributor.authorChen, Chun-Jungen_US
dc.contributor.authorWu, Tung-Kungen_US
dc.date.accessioned2014-12-08T15:09:49Z-
dc.date.available2014-12-08T15:09:49Z-
dc.date.issued2009-03-01en_US
dc.identifier.issn1744-3091en_US
dc.identifier.urihttp://dx.doi.org/10.1107/S174430910900092Xen_US
dc.identifier.urihttp://hdl.handle.net/11536/7524-
dc.description.abstractThe aminoacylhistidine dipeptidase (PepD) protein encoded by Vibrio alginolyticus pepD was successfully overexpressed and characterized and the putative active-site residues responsible for metal binding and catalysis were identified. The purified enzyme contained two zinc ions per monomer. The recombinant dipeptidase enzyme, which was identified as a homodimer in solution, exhibited broad substrate specificity for Xaa-His dipeptides, with highest activity towards the His-His dipeptide. The purified protein was crystallized using the hanging-drop vapour-diffusion method. Preliminary crystallographic analysis showed that the crystal belonged to space group P6(1) or P6(5), with unit-cell parameters a = b = 80.42, c = 303.11 angstrom. The crystal contained two molecules per asymmetric unit and the predicted solvent content was 53.4%.en_US
dc.language.isoen_USen_US
dc.titlePurification, crystallization and preliminary X-ray analysis of an aminoacylhistidine dipeptidase (PepD) from Vibrio alginolyticusen_US
dc.typeArticleen_US
dc.identifier.doi10.1107/S174430910900092Xen_US
dc.identifier.journalACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY AND CRYSTALLIZATION COMMUNICATIONSen_US
dc.citation.volume65en_US
dc.citation.issueen_US
dc.citation.spage216en_US
dc.citation.epage218en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000263773200006-
dc.citation.woscount2-
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