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Author: Badtke, MP
Author: Tavis, JE
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Methods Article

Combining genetic and biochemical approaches to identify functional molecular contact points

Matthew P. Badtke1, Feng Cao1 and John E. Tavis2*

1 Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine. St. Louis, MO 63104. USA.
2 Department of Molecular Microbiology and Immunology and Saint Louis University Liver Center, Saint Louis University School of Medicine. St. Louis, MO 63104. USA.

* To whom correspondence should be addressed: John E. Tavis, Saint Louis University School of Medicine, Department of Molecular Microbiology and Immunology. 1402 S. Grand Blvd., St. Louis, MO 63104. USA. Phone: 615-322-8644. Fax: 615-322-8397. Email: tavisje@slu.edu

Biol. Proced. Online 2006;8:77-86. doi:10.1251/bpo121
Submitted: May 02, 2006; Accepted: July 19, 2006; Published: August 10, 2006.

Indexing terms: Hepatitis B Virus, Duck; Protein Interaction Mapping.


Figure 3 Enlarged

Fig. 3:

Sequence homology aligment of multiple hepadnaviruses. P sequences from eight hepadnaviruses were aligned. Sequences with a >80% homology are shaded green. The T3 motif is indicated. DHBV, Duck hepatitis B virus, SHBV, Stork hepatitis B virus, HHBV, Heron hepatitis B virus, RGHBV, Ross’ goose hepatitis B virus, WHV, Woodchuck hepatitis virus, GSHV, Ground squirrel hepatitis virus, WMHBV, Wooly monkey hepatitis B virus, HBV, Hepatitis B virus. Modified from a figure originally published in (9).

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