Document Detail


Molecular cloning, sequence, function and structural basis of human heart 150 kDa oxygen-regulated protein, an ER chaperone.
MedLine Citation:
PMID:  17131193     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Apoptosis of heart tissues followed by hypoxia and ischemia leads finally to cardiac insufficiency. The full-length coding sequence of 3301 bp including cDNA(s) of the ER chaperone ORP150, which was specifically induced by hypoxia stress, was cloned from human cardiac infarct. Phylogenetic analyses reveal that human heart ORP150 shares a highly conserved N-terminal ATPase domain among its related family members. Moreover, hydropathic profiling reveals that their ca. 70 N-terminal residues and unique C-terminal halves exhibit similar hydropathy profiles among members. These findings suggest that ORP150 is structurally and functionally well conserved in distant species.
Authors:
Satoru Takeuchi
Related Documents :
12476883 - Advances in airway management.
3518093 - Accidental severe hypothermia.
5440513 - Atrial parasystole.
Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  The protein journal     Volume:  25     ISSN:  1572-3887     ISO Abbreviation:  Protein J.     Publication Date:  2006 Dec 
Date Detail:
Created Date:  2006-12-07     Completed Date:  2007-04-23     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101212092     Medline TA:  Protein J     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  517-28     Citation Subset:  IM    
Affiliation:
Department of Protein Research, Hibergenome (formerly ProstaColon), 85 NE, Takamatsu, Kahoku, Ishikawa, 929-1215, Japan. prostacolon@yahoo.co.jp
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adenosine Triphosphatases / chemistry
Base Sequence
Brain / metabolism
Cloning, Molecular
Endoplasmic Reticulum / metabolism*
Humans
Molecular Chaperones / chemistry*,  genetics
Molecular Sequence Data
Myocardial Infarction / metabolism
Myocardium / chemistry*,  metabolism
Phylogeny
Protein Conformation
Protein Structure, Secondary
Protein Structure, Tertiary
Proteins / chemistry*,  genetics,  isolation & purification
Chemical
Reg. No./Substance:
0/Molecular Chaperones; 0/Proteins; 0/oxygen-regulated proteins; EC 3.6.1.-/Adenosine Triphosphatases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Spirituality, coping, and HIV risk and prevention in a sample of severely mentally ill Puerto Rican ...
Next Document:  Pair-wise interactions of polymerization inhibitory contact site mutations of hemoglobin-S.