5ht4

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(New page: '''Unreleased structure''' The entry 5ht4 is ON HOLD Authors: Cody, V. Description: 6-substituted pyrrolo[2,3-d]pyrimidine 6-thieno-(4-methoxyphenyl) [[Category: Unreleased Structures]...)
Current revision (10:53, 16 August 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5ht4 is ON HOLD
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==6-substituted pyrrolo[2,3-d]pyrimidine 6-thieno-(4-methoxyphenyl)==
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<StructureSection load='5ht4' size='340' side='right'caption='[[5ht4]], [[Resolution|resolution]] 1.60&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5ht4]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5HT4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5HT4 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.6&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=65J:7-ETHYL-6-[(3-METHOXYPHENYL)SULFANYL]-5-METHYL-7H-PYRROLO[2,3-D]PYRIMIDINE-2,4-DIAMINE'>65J</scene>, <scene name='pdbligand=NDP:NADPH+DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NDP</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5ht4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ht4 OCA], [https://pdbe.org/5ht4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5ht4 RCSB], [https://www.ebi.ac.uk/pdbsum/5ht4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5ht4 ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/DYR_HUMAN DYR_HUMAN] Defects in DHFR are the cause of megaloblastic anemia due to dihydrofolate reductase deficiency (DHFRD) [MIM:[https://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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[https://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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Authors: Cody, V.
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==See Also==
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*[[Dihydrofolate reductase 3D structures|Dihydrofolate reductase 3D structures]]
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Description: 6-substituted pyrrolo[2,3-d]pyrimidine 6-thieno-(4-methoxyphenyl)
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Cody, V]]
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Cody V]]

Current revision

6-substituted pyrrolo[2,3-d]pyrimidine 6-thieno-(4-methoxyphenyl)

PDB ID 5ht4

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