3qls
From Proteopedia
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| + | {{STRUCTURE_3qls| PDB=3qls | SCENE= }} | ||
| - | + | ===Candida albicans dihydrofolate reductase complexed with NADPH and 6-methyl-5-[3-methyl-3-(3,4,5-trimethoxyphenyl)but-1-yn-1-yl]pyrimidine-2,4-diamine (UCP115A)=== | |
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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== | ||
| + | [[3qls]] 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=3QLS OCA]. | ||
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| + | ==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 06:42, 20 July 2011
Candida albicans dihydrofolate reductase complexed with NADPH and 6-methyl-5-[3-methyl-3-(3,4,5-trimethoxyphenyl)but-1-yn-1-yl]pyrimidine-2,4-diamine (UCP115A)
Template:ABSTRACT PUBMED 21726415
About this Structure
3qls 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
