8sgl
From Proteopedia
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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=8sgl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8sgl OCA], [https://pdbe.org/8sgl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8sgl RCSB], [https://www.ebi.ac.uk/pdbsum/8sgl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8sgl ProSAT]</span></td></tr> | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8sgl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8sgl OCA], [https://pdbe.org/8sgl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8sgl RCSB], [https://www.ebi.ac.uk/pdbsum/8sgl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8sgl ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/TCPE_HUMAN TCPE_HUMAN] Hereditary sensory and autonomic neuropathy with spastic paraplegia. The disease is caused by mutations affecting the gene represented in this entry. | ||
== Function == | == Function == | ||
| - | [https://www.uniprot.org/uniprot/ | + | [https://www.uniprot.org/uniprot/TCPE_HUMAN TCPE_HUMAN] Molecular chaperone; assists the folding of proteins upon ATP hydrolysis. As part of the BBS/CCT complex may play a role in the assembly of BBSome, a complex involved in ciliogenesis regulating transports vesicles to the cilia. Known to play a role, in vitro, in the folding of actin and tubulin.<ref>PMID:20080638</ref> |
| + | |||
| + | ==See Also== | ||
| + | *[[Transducin 3D structures|Transducin 3D structures]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
Current revision
CCT G beta 5 complex closed state 15
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