1u68

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==About this Structure==
==About this Structure==
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1U68 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=1rr5 1rr5]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U68 OCA].
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1U68 is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=1rr5 1rr5]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U68 OCA].
==Reference==
==Reference==
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Discovery of potent inhibitors of dihydroneopterin aldolase using CrystaLEAD high-throughput X-ray crystallographic screening and structure-directed lead optimization., Sanders WJ, Nienaber VL, Lerner CG, McCall JO, Merrick SM, Swanson SJ, Harlan JE, Stoll VS, Stamper GF, Betz SF, Condroski KR, Meadows RP, Severin JM, Walter KA, Magdalinos P, Jakob CG, Wagner R, Beutel BA, J Med Chem. 2004 Mar 25;47(7):1709-18. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15027862 15027862]
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<ref group="xtra">PMID:15027862</ref><references group="xtra"/>
[[Category: Dihydroneopterin aldolase]]
[[Category: Dihydroneopterin aldolase]]
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[[Category: Single protein]]
 
[[Category: Staphylococcus aureus]]
[[Category: Staphylococcus aureus]]
[[Category: Betz, S F.]]
[[Category: Betz, S F.]]
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[[Category: Dhna]]
[[Category: Dhna]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 14:47:03 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 08:29:41 2009''

Revision as of 06:29, 18 February 2009

Image:1u68.png

Template:STRUCTURE 1u68

DHNA 7,8 DIHYDRONEOPTERIN COMPLEX

Template:ABSTRACT PUBMED 15027862

About this Structure

1U68 is a 1 chain structure of sequence from Staphylococcus aureus. This structure supersedes the now removed PDB entry 1rr5. Full crystallographic information is available from OCA.

Reference

  • Sanders WJ, Nienaber VL, Lerner CG, McCall JO, Merrick SM, Swanson SJ, Harlan JE, Stoll VS, Stamper GF, Betz SF, Condroski KR, Meadows RP, Severin JM, Walter KA, Magdalinos P, Jakob CG, Wagner R, Beutel BA. Discovery of potent inhibitors of dihydroneopterin aldolase using CrystaLEAD high-throughput X-ray crystallographic screening and structure-directed lead optimization. J Med Chem. 2004 Mar 25;47(7):1709-18. PMID:15027862 doi:http://dx.doi.org/10.1021/jm030497y

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