6ocr

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(New page: '''Unreleased structure''' The entry 6ocr is ON HOLD Authors: Zuo, H., Glaaser, I., Zhao, Y., Kurinov, I., Mosyak, L., Wang, H., Liu, J., Park, J., Frangaj, A., Sturchler, E., Zhou, M.,...)
Current revision (14:51, 13 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6ocr is ON HOLD
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==Crystal structure of human KCTD16 T1 domain==
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<StructureSection load='6ocr' size='340' side='right'caption='[[6ocr]], [[Resolution|resolution]] 2.28&Aring;' scene=''>
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Authors: Zuo, H., Glaaser, I., Zhao, Y., Kurinov, I., Mosyak, L., Wang, H., Liu, J., Park, J., Frangaj, A., Sturchler, E., Zhou, M., McDonald, P., Geng, Y., Slesinger, P.A., Fan, Q.R.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6ocr]] is a 15 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=6OCR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6OCR FirstGlance]. <br>
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Description: Crystal structure of human KCTD16 T1 domain
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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]] 2.28&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=6ocr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6ocr OCA], [https://pdbe.org/6ocr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6ocr RCSB], [https://www.ebi.ac.uk/pdbsum/6ocr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6ocr ProSAT]</span></td></tr>
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[[Category: Frangaj, A]]
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</table>
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[[Category: Mcdonald, P]]
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== Function ==
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[[Category: Fan, Q.R]]
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[https://www.uniprot.org/uniprot/KCD16_HUMAN KCD16_HUMAN] Auxiliary subunit of GABA-B receptors that determine the pharmacology and kinetics of the receptor response. Increases agonist potency and markedly alter the G-protein signaling of the receptors by accelerating onset and promoting desensitization (By similarity).
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[[Category: Park, J]]
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__TOC__
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[[Category: Mosyak, L]]
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</StructureSection>
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[[Category: Liu, J]]
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[[Category: Homo sapiens]]
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[[Category: Wang, H]]
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[[Category: Large Structures]]
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[[Category: Zuo, H]]
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[[Category: Fan QR]]
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[[Category: Slesinger, P.A]]
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[[Category: Frangaj A]]
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[[Category: Zhou, M]]
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[[Category: Geng Y]]
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[[Category: Zhao, Y]]
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[[Category: Glaaser I]]
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[[Category: Glaaser, I]]
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[[Category: Kurinov I]]
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[[Category: Kurinov, I]]
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[[Category: Liu J]]
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[[Category: Geng, Y]]
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[[Category: McDonald P]]
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[[Category: Sturchler, E]]
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[[Category: Mosyak L]]
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[[Category: Park J]]
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[[Category: Slesinger PA]]
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[[Category: Sturchler E]]
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[[Category: Wang H]]
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[[Category: Zhao Y]]
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[[Category: Zhou M]]
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[[Category: Zuo H]]

Current revision

Crystal structure of human KCTD16 T1 domain

PDB ID 6ocr

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OCA

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