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5hve

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Current revision (18:05, 1 February 2017) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5hve is ON HOLD until Paper Publication
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==5-methyl-6-(3'-trifluromethoxyphenylthio)[2,3-d]pyrimidine 2,4-diamine==
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<StructureSection load='5hve' size='340' side='right' caption='[[5hve]], [[Resolution|resolution]] 1.46&Aring;' scene=''>
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Authors: Cody, V.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5hve]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HVE OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5HVE FirstGlance]. <br>
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Description: 5-methyl-6-(3'-trifluromethoxyphenylthio)[2,3-d]pyrimidine 2,4-diamine
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=65Q:5-METHYL-6-{[3-(TRIFLUOROMETHOXY)PHENYL]SULFANYL}THIENO[2,3-D]PYRIMIDINE-2,4-DIAMINE'>65Q</scene>, <scene name='pdbligand=NDP:NADPH+DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NDP</scene></td></tr>
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[[Category: Unreleased Structures]]
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Dihydrofolate_reductase Dihydrofolate reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.5.1.3 1.5.1.3] </span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5hve FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5hve OCA], [http://pdbe.org/5hve PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5hve RCSB], [http://www.ebi.ac.uk/pdbsum/5hve PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5hve ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[[http://www.uniprot.org/uniprot/DYR_HUMAN DYR_HUMAN]] Defects in DHFR are the cause of megaloblastic anemia due to dihydrofolate reductase deficiency (DHFRD) [MIM:[http://omim.org/entry/613839 613839]]. DHFRD is an inborn error of metabolism, characterized by megaloblastic anemia and/or pancytopenia, severe cerebral folate deficiency, and cerebral tetrahydrobiopterin deficiency. Clinical features include variable neurologic symptoms, ranging from severe developmental delay and generalized seizures in infancy, to childhood absence epilepsy with learning difficulties, to lack of symptoms.<ref>PMID:21310276</ref> <ref>PMID:21310277</ref>
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== Function ==
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[[http://www.uniprot.org/uniprot/DYR_HUMAN DYR_HUMAN]] Key enzyme in folate metabolism. Contributes to the de novo mitochondrial thymidylate biosynthesis pathway. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis. Binds its own mRNA and that of DHFRL1.<ref>PMID:21876188</ref> <ref>PMID:12096917</ref>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Dihydrofolate reductase]]
[[Category: Cody, V]]
[[Category: Cody, V]]
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[[Category: Dihydrofolate reductase inhibitor complex with nadph]]
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[[Category: Oxidoreductase-oxidoreductase inhibitor complex]]

Current revision

5-methyl-6-(3'-trifluromethoxyphenylthio)[2,3-d]pyrimidine 2,4-diamine

5hve, resolution 1.46Å

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