HUGO ID Detailed Result 7422


HUGO ID 7422
Symbol MT-CO3
Name mitochondrially encoded cytochrome c oxidase III
#Occurrence 30
#Paper 1

 


PMID Match String Actual String Score Flanking text Edited by Edit
16647138COX3COX30.6Three forms of COX enzymes designated as COX-1 COX-2 and COX-3 occur in mammalian tissues 
16647138COX3COX-34.6Three forms of COX enzymes designated as COX-1 COX-2 and COX-3 occur in mammalian tissues 
16647138COX3COX-34.6COX-3 is a new acetaminophen-sensitive isoform of the COX family 
16647138COX3COX-34.6Although different pharmacological properties have been described for COX-3 compared with COX-1 or COX-2 enzymes many investigators consider it 
16647138COX3COX-34.6Thus COX-3 is a product of the COX-1 gene but retains intron 
16647138COX3COX-34.6COX-3 is a glycoprotein 
16647138COX3COX-34.6Comparison of canine COX-3 activity with murine COX-1 and COX-2 demonstrates that analgesic/antipyretic analgesic 
16647138COX3COX-34.6drugs such as acetaminophen phenacetin antipyrine and dipyrone selectively inhibit COX-3 and some nonsteroidal anti-inflammatory drugs potently inhibit COX-3 
16647138COX3COX-34.6selectively inhibit COX-3 and some nonsteroidal anti-inflammatory drugs potently inhibit COX-3 
16647138COX3COX-34.6Thus inhibition of COX-3 could represent a primary central mechanism by which these drugs 
16647138COX3COX-34.6COX-3 mRNA expression is highest in choroid plexus and spinal cord 
16647138COX3COX-34.6COX-3 mRNA levels are also higher in major brain arteries and 
16647138COX3COX-34.6The expression pattern of COX-3 mRNA in the rat CNS primarily relates to the vascular 
16647138COX3COX-34.6The expression studies of COX-3 mRNA in primary cultures of neurons astrocytes endothelial cells pericytes 
16647138COX3COX-34.6pericytes and choroidal epithelial cells indicate that the mRNA of COX-3 is present in all of these cell types except neurons 
16647138COX3COX-34.6Cerebral endothelial cells showed the highest COX-3 expression ( Kis et al. 2003 
16647138COX3COX-34.6COX-3 mRNA was cloned and sequenced from rat cerebral endothelial cells 
16647138COX3COX-34.6the 98-base-pair intron 1 of COX-1 gene remains unprocessed in COX-3 inducing a frameshift mutation and a 127-amino-acid open reading frame 
16647138COX3COX-34.6Rat COX-3 is a cytosolic glycoprotein 
16647138COX3COX-34.6Amino acid analysis also shows that COX-3 protein has a very basic character with a p I 
16647138COX3COX-34.6In addition to the abundance of basic amino acids the COX-3 protein is also very rich in proline (11.81%) 11.81% 
16647138COX3COX-34.6To determine the function of COX-3 COS-7 cells were transfected with COX-3 
16647138COX3COX-34.6determine the function of COX-3 COS-7 cells were transfected with COX-3 
16647138COX3COX-34.6by acetaminophen ( Snipes et al. 2005 suggesting that this COX-3 variant may not be involved in the generation of prostaglandins 
16647138COX3COX-34.6This is in contrast to the canine COX-3 which has COX activity 
16647138COX3COX-34.6Thus there are differences between rat and dog COX-3 proteins 
16647138COX3COX-34.6Collectively these studies suggest that dogs possess a COX-3 splice variant with cyclooxygenase activity whereas rats have a COX-3 
16647138COX3COX-34.6COX-3 splice variant with cyclooxygenase activity whereas rats have a COX-3 splice variant that lacks cyclooxygenase activity 
16647138COX3COX-34.6settled only when information on expression properties and roles of COX-3 variants in various mammalian species becomes available ( Table 1 
16647138COX3COX-34.6developing diffuse pain (writhing) writhing with COX-isozyme-deficient mice indicate that COX-3 plays an important role in chronic pain and inflammation in