NCBI Description of OPLAH
|The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD).|
Community Annotation of OPLAH Add / Edit OPLAH: Annotations
No community annotations yet for OPLAH.
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