Data Retrieval and Storage

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Our first challenge was finding a way to expand the database for EvoGEM. Last year, EvoGEM only had a small database of BioBrick parts, all of which were added manually. Since the iGEM registry consisted of hundreds of parts, manually adding parts was not practical. In addition, more parts were needed to make more sophisticated tests with EvoGEM. Also, we wanted to have some way of comparing the retrieved parts. We needed to answer the following questions about each part:

• If it is an enzyme, what reactions does it catalyze?
• If it is a molecule, what is its molecular structure, and what are the synonyms for the molecule name?

The answers to these questions would allow EvoGEM to better distinguish between different compounds. How do we accomplish this, though? By creating a Perl script!

Perl is a programming language that is powerful in text processing facilities. Since it effectively uses string matching, it is an ideal language for searching text and manipulating text files, which is exactly what we needed for retrieving and expanding EvoGEM's local database.

If a protein makes up one of the parts retrieved from the iGEM database, the registry provides its amino acid sequence, which can be used to infer all other required information. Namely, the program sends this amino acid sequence to UniProt. UniProt is a large database of proteins and enzymes. This database can be queried by a Blast algorithm, which is a very powerful programming tool. When inputting the DNA or amino acid sequence, UniProt gives results that are closest to the initial search. Besides giving the name of the protein searched, UniProt will give the reagents from the reaction that the protein catalyzes. All this information is useful for EvoGEM and is stored in a local database. Visit [http://www.uniprot.com Uniprot] to see this database.

The reagents from the reaction that the protein catalyzes are put through ChemSpider. This large database is much like UniProt except that it is for chemistry. Searching and querying in ChemSpider is simple because molecules can be queried using synonyms. After a molecule is queried, ChemSpider produces information about the molecule such as its SMILES, which is a simplified molecular input line entry specification. As useful as this information can be, we needed something that is machine-readable and that could be used for comparisons of metabolic pathways. What is this machine readable format? It is known as the IUPAC International Chemical Identifier (InChI). This InChi is a unique "fingerprint" of the molecule that is not ambiguous like SMILES and is supplied only by IUPAC. An example of an InChi would look like this:

1/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-8,10-11H,1H2/t2-,5+/m0/s1

To see this database, visit: [http://www.chemspider.com ChemSpider]

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