PPGR - Gene Detail

Gene ID	gene-IMY05_018G0000300 View in Genome Browser
Position	CM029816.1:18228-19814 (+) 1586bp
Gene Type	gene
Gene Description (Protein Product)	Sarcosine oxidase
Organism	Salix suchowensis
Also AS	AT2G24580

upstream:

Database	EntryID	E-Value	Start	end	InterPro ID	Description

Protein-protein interaction (PPI)

gene-IMY05_C4538000600 The glycine cleavage system catalyzes the degradation of glycine

gene-IMY05_C1039000200 Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family

gene-IMY05_019G0033300 low-specificity L-threonine aldolase 1

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Orthologous ID	Species Number	All hits in PereRegDB	Hits of this species	Orthologous Detail

GO Term	Description	GO Category
GO:0003674	molecular_function	MF
GO:0003824	catalytic activity	MF
GO:0008115	sarcosine oxidase activity	MF
GO:0008150	biological_process	BP
GO:0008152	metabolic process	BP
GO:0016491	oxidoreductase activity	MF
GO:0016645	oxidoreductase activity, acting on the CH-NH group of donors	MF
GO:0016647	oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor	MF
GO:0055114	obsolete oxidation-reduction process	BP

KEGG Term	Name	Description
map04146	Peroxisome	Peroxisomes are essential organelles that play a key role in redox signalling and lipid homeostasis. They contribute to many crucial metabolic processes such as fatty acid oxidation, biosynthesis of ether lipids and free radical detoxification. The biogenesis of peroxisomes starts with the early peroxins PEX3, PEX16 and PEX19 and proceeds via several steps. The import of membrane proteins into peroxisomes needs PEX19 for recognition, targeting and insertion via docking at PEX3. Matrix proteins in the cytosol are recognized by peroxisomal targeting signals (PTS) and transported to the docking complex at the peroxisomal membrane. Peroxisomes' deficiencies lead to severe and often fatal inherited peroxisomal disorders (PD). PDs are usually classified in two groups. The first group is disorders of peroxisome biogenesis which include Zellweger syndrome, and the second group is single peroxisomal enzyme deficiencies.
map01100	Metabolic pathways	-
map00310	Lysine degradation	-
map00260	Glycine, serine and threonine metabolism	Serine is derived from 3-phospho-D-glycerate, an intermediate of glycolysis [MD:M00020], and glycine is derived from serine. Threonine is an essential amino acid, which animals cannot synthesize. In bacteria and plants, threonine is derived from aspartate [MD:M00018].