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Proteintech
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Immunogen sequence: NIDAVHLKA MVDKHKENLA AIMITYPSTN GVFEENISDV CDLIHQHGGQ VYLDGANMNA QVGICRPGDF GSDVSHLNLH KTFCIPHGGG GPGMGPIGVK KHLAPFLPNH PVISLKRNED ACPVGTVSAA PWGSSSILPI SWAYIKMMGG KGLKQATETA ILNANYMAKR LETHYRILFR GARGYVGHEF ILDTRPFKKS ANIEAVDVAK RLQDYGFHAP TMSWPVAGTL MVEPTESEDK AELDRFCDAM ISIRQEIADI EEGRIDPRVN PLKMSPHSLT CVTSSHWDRP YSREVAAFPL PFVKPENKFW PTIARIDDIY GDQHLVCTCP PMEVYESPFS EQKRASS (675-1020 aa encoded by BC111995)
Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Glycine cleavage system P protein; glycine cleavage system protein P; Glycine decarboxylase; glycine decarboxylase P-protein; Glycine dehydrogenase (aminomethyl-transferring); glycine dehydrogenase (decarboxylating); Glycine dehydrogenase (decarboxylating), mitochondrial; glycine dehydrogenase [decarboxylating], mitochondrial; RP11-472F14.1
Gene Aliases: D030049L12Rik; D19Wsu57e; GCE; GCSP; GLDC; HYGN1
UniProt ID: (Human) P23378, (Mouse) Q91W43
Entrez Gene ID: (Human) 2731, (Mouse) 104174
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