3j1u
From Proteopedia
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| - | [[Image:3j1u.jpg|left|200px]] | ||
| - | + | ==Low affinity dynein microtubule binding domain - tubulin complex== | |
| + | <SX load='3j1u' size='340' side='right' viewer='molstar' caption='[[3j1u]], [[Resolution|resolution]] 9.70Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[3j1u]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Bos_taurus Bos taurus] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3J1U OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3J1U FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 9.7Å</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=3j1u FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3j1u OCA], [https://pdbe.org/3j1u PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3j1u RCSB], [https://www.ebi.ac.uk/pdbsum/3j1u PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3j1u ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/DYHC1_MOUSE DYHC1_MOUSE] Defects in Dync1h1 are the cause of the 'Legs at odd angles' (LOA) phenotype, an autosomal dominant trait where affected animals display unusual twisting of the body and clenching of the hindlimbs when suspended by the tail. Heterozygotes suffer age-related progressive loss of muscle tone and locomotor ability without major reduction in life-span while homozygotes show a more severe phenotype with an inability to move or feed, and die within 24 hours of birth. LOA mutants display defects in migration of facial motor neuron cell bodies and impaired retrograde transport in spinal cord motor neurons. Defects in Dync1h1 are the cause of the Cramping 1 (Cra1) phenotype, an autosomal dominant trait where affected animals display unusual twisting of the body and clenching of the hindlimbs when suspended by the tail. Heterozygotes suffer age-related progressive loss of muscle tone and locomotor ability without major reduction in life-span while homozygotes show a more severe phenotype with an inability to move or feed, and die within 24 hours of birth. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/DYHC1_MOUSE DYHC1_MOUSE] Cytoplasmic dynein 1 acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. Dynein has ATPase activity; the force-producing power stroke is thought to occur on release of ADP. | ||
| - | == | + | ==See Also== |
| - | + | *[[Dynein 3D structures|Dynein 3D structures]] | |
| - | + | *[[Tubulin 3D Structures|Tubulin 3D Structures]] | |
| - | + | __TOC__ | |
| - | [[ | + | </SX> |
[[Category: Bos taurus]] | [[Category: Bos taurus]] | ||
| + | [[Category: Large Structures]] | ||
[[Category: Mus musculus]] | [[Category: Mus musculus]] | ||
| - | [[Category: Hernandez-Lopez | + | [[Category: Hernandez-Lopez R]] |
| - | [[Category: Huang | + | [[Category: Huang J]] |
| - | [[Category: Leschziner | + | [[Category: Leschziner AE]] |
| - | [[Category: Reck-Peterson | + | [[Category: Reck-Peterson SL]] |
| - | [[Category: Redwine | + | [[Category: Redwine WB]] |
| - | [[Category: Zou | + | [[Category: Zou S]] |
| - | + | ||
Current revision
Low affinity dynein microtubule binding domain - tubulin complex
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