2ys4
From Proteopedia
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{{STRUCTURE_2ys4| PDB=2ys4 | SCENE= }} | {{STRUCTURE_2ys4| PDB=2ys4 | SCENE= }} | ||
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===Solution structure of the N-terminal PapD-like domain of HYDIN protein from human=== | ===Solution structure of the N-terminal PapD-like domain of HYDIN protein from human=== | ||
| + | ==Disease== | ||
| + | [[http://www.uniprot.org/uniprot/HYDIN_HUMAN HYDIN_HUMAN]] Defects in HYDIN are the cause of primary ciliary dyskinesia 5 (CILD5) [MIM:[http://omim.org/entry/608647 608647]]. An autosomal recessive form of primary dyskinesia, a disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. CILD5 is characterized by early onset of a progressive decline in lung function due to an inability to clear mucus and particles from the airways. Affected individuals have recurrent infections of the sinuses, ears, airways, and lungs. Sperm motility is also decreased. Individuals with CILD5 do not have situs inversus. | ||
==About this Structure== | ==About this Structure== | ||
Revision as of 17:08, 24 March 2013
Solution structure of the N-terminal PapD-like domain of HYDIN protein from human
Disease
[HYDIN_HUMAN] Defects in HYDIN are the cause of primary ciliary dyskinesia 5 (CILD5) [MIM:608647]. An autosomal recessive form of primary dyskinesia, a disorder characterized by abnormalities of motile cilia. Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia; reduced fertility is often observed in male patients due to abnormalities of sperm tails. Half of the patients exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node. Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome. CILD5 is characterized by early onset of a progressive decline in lung function due to an inability to clear mucus and particles from the airways. Affected individuals have recurrent infections of the sinuses, ears, airways, and lungs. Sperm motility is also decreased. Individuals with CILD5 do not have situs inversus.
About this Structure
2ys4 is a 1 chain structure with sequence from Homo sapiens. Full experimental information is available from OCA.
Categories: Homo sapiens | Harada, T. | Kigawa, T. | Koshiba, S. | Li, H. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Tomizawa, T. | Watanabe, S. | Yokoyama, S. | Hydin | National project on protein structural and functional analyse | Nppsfa | Papd-like | Riken structural genomics/proteomics initiative | Rsgi | Structural genomic | Unknown function
