MI6: Metal Ion-Binding Site Prediction and Docking Server

Yu Feng Lin, Chih Wen Cheng, Chung-Shiuan Shih, Jenn-Kang Hwang, Chin Sheng Yu, Chih Hao Lu

Research output: Contribution to journalArticlepeer-review

44 Scopus citations


The structure of a protein determines its biological function(s) and its interactions with other factors; the binding regions tend to be conserved in sequence and structure, and the interacting residues involved are usually in close 3D space. The Protein Data Bank currently contains more than 110 000 protein structures, approximately one-third of which contain metal ions. Identifying and characterizing metal ion-binding sites is thus essential for investigating a protein's function(s) and interactions. However, experimental approaches are time-consuming and costly. The web server reported here was built to predict metal ion-binding residues and to generate the predicted metal ion-bound 3D structure. Binding templates have been constructed for regions that bind 12 types of metal ion-binding residues have been used to construct binding templates. The templates include residues within 3.5 angstrom of the metal ion, and the fragment transformation method was used for structural comparison between query proteins and templates without any data training. Through the adjustment of scoring functions, which are based on the similarity of structure and binding residues. Twelve kinds of metal ions (Ca2+, Cu2+, Fe3+, Mn2+, Zn2+, Cd2+, Fe2+, Ni2+, Hg2+, Co2+, and Cu+) binding residues prediction are supported. MIB also provides the metal ions docking after prediction. The MIB server is available at http://bioinfo.cmu.edu.tw/MIB/.
Original languageEnglish
Pages (from-to)2287-2291
Number of pages5
JournalJournal of Chemical Information and Modeling
Issue number12
StatePublished - Dec 2016



Fingerprint Dive into the research topics of 'MI6: Metal Ion-Binding Site Prediction and Docking Server'. Together they form a unique fingerprint.

Cite this