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AASS Polyclonal Antibody, 100ul Miscellaneous This protein is thought to

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AASS Polyclonal Antibody, 100ul Miscellaneous This protein is thought toAASS encodes a bifunctional enzyme (aminoadipate semialdehyde synthase) that catalyzes the first two steps in the mammalian lysine degradation pathway. The N terminal and the C terminal portions of this enzyme contain lysine ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha aminoadipic semialdehyde. Mutations in AASS are associated with familial hyperlysinemia.

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Description

This protein is thought to be part of a family of integral Golgi membrane proteins

but not glycoproteins undergoing productive folding

TNK2 encodes a tyrosine kinase that binds Cdc42Hs in its GTP-bound form and inhibits both the intrinsic and GTPase-activating protein (GAP)-stimulated GTPase activity of Cdc42Hs

Mutations in RPS19 cause Diamond-Blackfan anemia (DBA)

This gene encodes the cytosolic isozyme

AASS Polyclonal Antibody, 100ul Miscellaneous This protein is thought toAASS encodes a bifunctional enzyme (aminoadipate semialdehyde synthase) that catalyzes the first two steps in the mammalian lysine degradation pathway. The N terminal and the C terminal portions of this enzyme contain lysine ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha aminoadipic semialdehyde. Mutations in AASS are associated with familial hyperlysinemia.

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