YHR037W
Revision as of 08:20, 23 January 2007 by SGDwikiBot (talk | contribs) (Automated import of articles)
Share your knowledge...Edit this entry!
| Systematic name | YHR037W | |
| Gene name | PUT2 | |
| Aliases | ||
| Feature type | ORF, Verified | |
| Coordinates | Chr VIII:181970..183697 | |
| Don't edit this box! It's automatically regenerated, and edits will be lost when the update script runs. | ||
Description of YHR037W: Delta-1-pyrroline-5-carboxylate dehydrogenase, nuclear-encoded mitochondrial protein involved in utilization of proline as sole nitrogen source; deficiency of the human homolog causes HPII, an autosomal recessive inborn error of metabolism[1][2]
Contents
Community Commentary
About Community Commentary. Please share your knowledge!
References
See Help:References on how to add references
- ↑ Hu CA, et al. (1996) Cloning, characterization, and expression of cDNAs encoding human delta 1-pyrroline-5-carboxylate dehydrogenase. J Biol Chem 271(16):9795-800 SGD PMID 8621661
- ↑ Brandriss MC (1983) Proline utilization in Saccharomyces cerevisiae: analysis of the cloned PUT2 gene. Mol Cell Biol 3(10):1846-56 SGD PMID 6358862
See Help:Categories on how to add the wiki page for this gene to a Category
