June 24, 2019
I’m an essential amino acid that you don’t run across too often.
What molecule am I?
Image of Selenocysteine 3D Image of Selenocysteine

Selenocysteine is often called the 21st essential (protein-forming) amino acid. It is found in countless species of all domains of life. Much research has been reported on the biochemistry of selenocysteine in the North American plant Astragalus bisulcatus.

Scientists long believed that fungi were an exception to the broad prevalence of selenocysteine in life forms. But recently, Vadim N. Gladyshev, Marco Mariotti, and co-workers at Harvard Medical School (Boston) found selenocysteine-containing proteins in three fungus phyla. A few fungal genes that contain selenoproteins behave similarly to those in other organisms; but the mechanisms and purposes of other fungal “selenogenes” are as yet unknown.

Selenium’s wealth of natural and synthetic isotopes makes radiolabeled selenocysteine (Sec) a valuable tool in analytical chemistry and biochemistry. Specifically, 73Se-Sec is used in positron emission tomography (PET); 75Se-Sec in protein X-ray crystallography; and 77Se-Sec in high-resolution nuclear magnetic resonance (NMR) spectroscopy.

Selenocysteine hazard information

GHS classification*: skin corrosion/irritation, category 2
H315—Causes skin irritationChemical Safety Warning
GHS classification: serious eye damage/eye irritation, category 2A
H319—Causes serious eye irritationChemical Safety Warning
GHS classification: specific target organ toxicity, single exposure; respiratory tract irritation, category 3
H335—May cause respiratory irritationChemical Safety Warning

*Globally Harmonized System of Classification and Labeling of Chemicals. Explanation of pictograms.

Selenocysteine fast facts

CAS Reg. No.10236-58-5
Empirical formulaC3H7NO2Se
Molar mass168.05 g/mol
AppearanceWhite to light yellow crystals or powder
Melting point143–146 ºC
Water solubility≈400 g/L

MOTW update

Loratadine was the Molecule of the Week for July 10, 2006. It is a venerable nonsedating antihistamine that is widely used to combat environmental allergens. Recently, Heather B. Miller, Meghan S. Blackledge, and colleagues at High Point University (NC) discovered that loratadine causes some otherwise antibiotic-resistant bacteria (e.g., Staphylococcus epidermidis and S. aureus) to become susceptible to β-lactam antibiotics and vancomycin (the September 5, 2016 MOTW). 

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Learn more about this molecule from CAS, the most authoritative and comprehensive source for chemical information.

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