2hqh
From Proteopedia
(Difference between revisions)
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|PDB= 2hqh |SIZE=350|CAPTION= <scene name='initialview01'>2hqh</scene>, resolution 1.8Å | |PDB= 2hqh |SIZE=350|CAPTION= <scene name='initialview01'>2hqh</scene>, resolution 1.8Å | ||
|SITE= | |SITE= | ||
- | |LIGAND= <scene name='pdbligand=ZN:ZINC ION'>ZN</scene> | + | |LIGAND= <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene> |
|ACTIVITY= | |ACTIVITY= | ||
|GENE= DCTN1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), RSN, CYLN1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |GENE= DCTN1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), RSN, CYLN1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | ||
+ | |DOMAIN= | ||
+ | |RELATEDENTRY=[[1txq|1TXQ]] | ||
+ | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2hqh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2hqh OCA], [http://www.ebi.ac.uk/pdbsum/2hqh PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2hqh RCSB]</span> | ||
}} | }} | ||
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==Disease== | ==Disease== | ||
- | Known | + | Known disease associated with this structure: Neuropathy, distal hereditary motor, type VIIB OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601143 601143]], Amyotrophic lateral sclerosis, susceptibility to OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601143 601143]] |
==About this Structure== | ==About this Structure== | ||
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[[Category: Hayashi, I.]] | [[Category: Hayashi, I.]] | ||
[[Category: Ikura, M.]] | [[Category: Ikura, M.]] | ||
- | [[Category: ZN]] | ||
[[Category: beta/beta structure]] | [[Category: beta/beta structure]] | ||
[[Category: protein binding]] | [[Category: protein binding]] | ||
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[[Category: zinc finger motif]] | [[Category: zinc finger motif]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:33:57 2008'' |
Revision as of 00:33, 31 March 2008
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, resolution 1.8Å | |||||||
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Ligands: | |||||||
Gene: | DCTN1 (Homo sapiens), RSN, CYLN1 (Homo sapiens) | ||||||
Related: | 1TXQ
| ||||||
Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Crystal structure of p150Glued and CLIP-170
Disease
Known disease associated with this structure: Neuropathy, distal hereditary motor, type VIIB OMIM:[601143], Amyotrophic lateral sclerosis, susceptibility to OMIM:[601143]
About this Structure
2HQH is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Mar 31 03:33:57 2008