Fatty acids provide highly efficient energy storage, storing much more energy for their weight than carbohydrates like glucose.
Fatty acids are stored as triglycerides in adipose tissue, in which each triglyceride molecule contains three fatty acids and one glycerol. Triglycerides form fatty droplets that exclude water and take up minimal space.
Fatty acids are also more highly reduced than carbohydrates, so they provide more energy during oxidation. The efficiency of energy storage in (...)
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Molecular groups
Articles
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fatty acids
25 October 2004 -
polycomb group proteins
15 September 2003PcG proteins, PcGs, polycomb silencers
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SCA1
2 October 2003See also
spinocerebellar ataxias (SCAs) -
TRNs
6 October 2003TGF-beta-related neurotrophins
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small GTP-ase late endosomal proteins
2 October 2003Members
RAB7
Pathology
small GTP-ase late endosomal protein RAB7 mutations cause Charcot-Marie-Tooth type 2B neuropathy -
lamins
13 July 2003Lamins constitute a family of polypeptides composing the proteinaceous layer apposed to the inner nuclear membrane. In mammals, 3 lamins, A (LMNA), B (LMNB), and C (encoded by LMNA), have been described, with molecular weights ranging from 60,000 to 78,000. Lamins A and C but not lamin B have close sequence homology. Lamins can be classified with the intermediate filament (IF) polypeptides.
Members LMNA lamin-A MIM.150330 LMNB1 lamin-B1 MIM.150340 LMNB2 lamin-B2 MIM.150341 LMNC (...) -
glucan
13 October 2009Definition: A glucan molecule is a polysaccharide of D-glucose monomers linked by glycosidic bonds. Many beta-glucans are medically important.
Types
The α- and β- and numbers clarify the type of O-glycosidic bond.
Alpha glucan
dextran, α-1,6-glucan
glycogen, α-1,4- and α-1,6-glucan
pullulan, α-1,4- and α-1,6-glucan
starch, α-1,4- and α-1,6-glucan
Beta glucan
cellulose, β-1,4-glucan
curdlan, β-1,3-glucan
laminarin, β-1,3- and β-1,6-glucan
chrysolaminarin, β-1,3-glucan (...) -
sarcoglycans
7 October 2003Members
alpha-sarcoglycan
beta-sarcoglycan
gamma-sarcoglycan
epsilon-sarcoglycan (mutations in myoclonus-dystonia)
Pathology (sarcoglycanopathies)
mutations in muscular dystrophy -
COX
6 October 2003cytochrome c oxidase
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postsynpatic proteins
20 October 2003PSDs
SAPs
NMDA-receptor R1
neuroligin