6lpf | pdb_00006lpf
From Proteopedia
The crystal structure of human cytoplasmic LRS
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Structural highlights
Disease[SYLC_HUMAN] Acute infantile liver failure-multisystemic involvement syndrome. The disease is caused by mutations affecting the gene represented in this entry. Function[SYLC_HUMAN] Catalyzes the specific attachment of an amino acid to its cognate tRNA in a two step reaction: the amino acid (AA) is first activated by ATP to form AA-AMP and then transferred to the acceptor end of the tRNA. Exhibits a post-transfer editing activity to hydrolyze mischarged tRNAs.[1] References
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This page was last modified 10:09, 27 March 2020.