As part of our ongoing collaborative efforts in Structural Genomics we have identified a number of yeast gene products with no known structural homologue. One of the identified proteins, Pyridoxamine 5?-phosphate oxidase, was expressed in E. coli, purified to homogeneity and crystallized. The initial characterization of very small crystals (~10 microns maximum dimension) at X9B showed that diffraction extends to at least 3.0E and is consistent with the hexagonal space group P3121 (or enantiomorph) (a=b=74.8, c=157.7E). The solution of this structure will particularly interesting as it promises to provide a non-conventional fold for a flavin containing protein, and is likely to represent a completely novel fold. Furthermore, this structure will be of great interest to the field of basic metabolic chemistry as this enzyme is responsible for the biosynthesis of vitamin b6 and pyridoxal-5?-phosphate.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001633-17
Application #
6205786
Study Section
Project Start
1999-09-01
Project End
2000-08-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
17
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
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