| Literature DB >> 14983064 |
Qi Zheng1, Wan-Ming Yang, Wen-Hao Yu, Bin Cai, Xin-Chen Teng, Yi Xie, Hong-Zhe Sun, Ming-Jie Zhang, Zhong-Xian Huang.
Abstract
MT3 shows apparently different properties and function from MT1 even though they have 70% sequence homology. Possibly the two inserts, Thr5 and a negatively charged hexapeptide at position-55 in MT3, play important roles. A series of MT3 variants around the EAAEAE hexapeptide have been prepared by site-directed mutagenesis and their properties and reactivity towards pH, EDTA and DTNB have been studied. Our detailed studies revealed that the EAAEAE insert is essential to the property of MT3. It is the hexapeptide insert, to some extent, making the MT3 alpha-domain looser and lower stability of the metal-thiolate cluster, which could be accessed more easily.Entities:
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Year: 2003 PMID: 14983064 DOI: 10.1093/protein/gzg127
Source DB: PubMed Journal: Protein Eng ISSN: 0269-2139