6jec

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m (Protected "6jec" [edit=sysop:move=sysop])
Current revision (09:06, 9 April 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6jec is ON HOLD
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==Structure of a triple-helix region of human collagen type II==
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<StructureSection load='6jec' size='340' side='right'caption='[[6jec]], [[Resolution|resolution]] 2.05&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6jec]] is a 3 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=6JEC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6JEC 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]] 2.049&#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=ACE:ACETYL+GROUP'>ACE</scene>, <scene name='pdbligand=HYP:4-HYDROXYPROLINE'>HYP</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=6jec FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6jec OCA], [https://pdbe.org/6jec PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6jec RCSB], [https://www.ebi.ac.uk/pdbsum/6jec PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6jec ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/CO1A2_HUMAN CO1A2_HUMAN] Osteogenesis imperfecta type 4;Osteogenesis imperfecta type 1;Ehlers-Danlos syndrome type 7B;Ehlers-Danlos/osteogenesis imperfecta syndrome;Osteogenesis imperfecta type 2;Ehlers-Danlos syndrome, cardiac valvular type;High bone mass osteogenesis imperfecta;Osteogenesis imperfecta type 3. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. A chromosomal aberration involving COL1A2 may be a cause of lipoblastomas, which are benign tumors resulting from transformation of adipocytes, usually diagnosed in children. Translocation t(7;8)(p22;q13) with PLAG1.
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== Function ==
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[https://www.uniprot.org/uniprot/CO1A2_HUMAN CO1A2_HUMAN] Type I collagen is a member of group I collagen (fibrillar forming collagen).
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Authors: Yang, X., Zhu, Y., Ye, S., Zhang, R.
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==See Also==
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*[[Collagen 3D structures|Collagen 3D structures]]
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Description: Structure of a triple-helix region of human collagen type II
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__TOC__
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[[Category: Unreleased Structures]]
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</StructureSection>
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[[Category: Yang, X]]
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[[Category: Homo sapiens]]
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[[Category: Zhu, Y]]
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[[Category: Large Structures]]
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[[Category: Zhang, R]]
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[[Category: Yang X]]
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[[Category: Ye, S]]
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[[Category: Ye S]]
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[[Category: Zhang R]]
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[[Category: Zhu Y]]

Current revision

Structure of a triple-helix region of human collagen type II

PDB ID 6jec

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