3qlr
From Proteopedia
(Difference between revisions)
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+ | The line below this paragraph, containing "STRUCTURE_3qlr", creates the "Structure Box" on the page. | ||
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+ | {{STRUCTURE_3qlr| PDB=3qlr | SCENE= }} | ||
- | + | ===Candida albicans dihydrofolate reductase complexed with NADPH and 6-methyl-5-[(3R)-3-(3,4,5-trimethoxyphenyl)pent-1-yn-1-yl]pyrimidine-2,4-diamine (UCP112A)=== | |
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+ | The line below this paragraph, {{ABSTRACT_PUBMED_21726415}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 21726415 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_21726415}} | ||
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+ | ==About this Structure== | ||
+ | [[3qlr]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Candida_albicans Candida albicans]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3QLR OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:021726415</ref><references group="xtra"/> | ||
+ | [[Category: Candida albicans]] | ||
+ | [[Category: Anderson, A C.]] | ||
+ | [[Category: Bendel, S D.]] | ||
+ | [[Category: Paulsen, J L.]] | ||
+ | [[Category: Antifungal agent]] | ||
+ | [[Category: Candida albican]] | ||
+ | [[Category: Drug design]] | ||
+ | [[Category: Enzyme inhibitor]] | ||
+ | [[Category: Fungal protein]] | ||
+ | [[Category: Model]] | ||
+ | [[Category: Molecular structure]] | ||
+ | [[Category: Oxidoreductase-oxidoreductase inhibitor complex]] | ||
+ | [[Category: Structure-activity relationship]] | ||
+ | [[Category: Tetrahydrofolate dehydrogenase]] |
Revision as of 06:45, 20 July 2011
Candida albicans dihydrofolate reductase complexed with NADPH and 6-methyl-5-[(3R)-3-(3,4,5-trimethoxyphenyl)pent-1-yn-1-yl]pyrimidine-2,4-diamine (UCP112A)
Template:ABSTRACT PUBMED 21726415
About this Structure
3qlr is a 2 chain structure with sequence from Candida albicans. Full crystallographic information is available from OCA.
Reference
- Paulsen JL, Bendel SD, Anderson AC. Crystal structures of Candida albicans dihydrofolate reductase bound to propargyl-linked antifolates reveal the flexibility of active site loop residues critical for ligand potency and selectivity. Chem Biol Drug Des. 2011 Jul 5. doi: 10.1111/j.1747-0285.2011.01169.x. PMID:21726415 doi:10.1111/j.1747-0285.2011.01169.x
Categories: Candida albicans | Anderson, A C. | Bendel, S D. | Paulsen, J L. | Antifungal agent | Candida albican | Drug design | Enzyme inhibitor | Fungal protein | Model | Molecular structure | Oxidoreductase-oxidoreductase inhibitor complex | Structure-activity relationship | Tetrahydrofolate dehydrogenase