Cystathionine: Difference between revisions

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	{{chembox		{{chembox
	\| verifiedrevid = ~~414094014~~		\| verifiedrevid = 443553935
	\| ImageFile_Ref = {{chemboximage\|correct\|??}}		\| ImageFile_Ref = {{chemboximage\|correct\|??}}
	\| ImageFile=Cystathionine.png		\| ImageFile=Cystathionine.png
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	\| ChemSpiderID_Ref = {{chemspidercite\|correct\|chemspider}}		\| ChemSpiderID_Ref = {{chemspidercite\|correct\|chemspider}}
	\| ChemSpiderID = 811		\| ChemSpiderID = 811
			\| ChEBI_Ref = {{ebicite\|correct\|EBI}}
	\| ChEBI = 17755		\| ChEBI = 17755
	\| SMILES = O=C(O)C(N)CSCCC(C(=O)O)N		\| SMILES = O=C(O)C(N)CSCCC(C(=O)O)N
	\| MeSHName=Cystathionine		\| MeSHName=Cystathionine

Revision as of 19:40, 7 August 2011

Cystathionine
Names


IUPAC name 2-amino-4-(2-amino-2-carboxy-ethyl) thio-butanoic acid
Other names L-Cystathionine; S--L-homocysteine
Identifiers
CAS Number	56-88-2
3D model (JSmol)	Interactive image
ChEBI	CHEBI:17755
ChEMBL	ChEMBL209241
ChemSpider	811
ECHA InfoCard	100.000.269
KEGG	C00542
MeSH	Cystathionine
PubChem CID	834
CompTox Dashboard (EPA)	DTXSID20971384
InChI InChI=1S/C7H14N2O4S/c8-4(6(10)11)1-2-14-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)Key: ILRYLPWNYFXEMH-UHFFFAOYSA-N InChI=1/C7H14N2O4S/c8-4(6(10)11)1-2-14-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)Key: ILRYLPWNYFXEMH-UHFFFAOYAH
SMILES O=C(O)C(N)CSCCC(C(=O)O)N
Properties
Chemical formula	C₇H₁₄N₂O₄S
Molar mass	222.263 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references

Chemical compound

Cystathionine is an intermediate in the synthesis of cysteine.

An excess in the urine is called cystathioninuria.

Cysteine metabolism. Cystathionine beta synthase catalyzes the upper reaction and cystathionine gamma-lyase catalyzes the lower reaction.

lysine→	Saccharopine Allysine α-Aminoadipic acid 2-Oxoadipic acid Glutaryl-CoA Glutaconyl-CoA Crotonyl-CoA β-Hydroxybutyryl-CoA
leucine→	β-Hydroxy β-methylbutyric acid β-Hydroxy β-methylbutyryl-CoA Isovaleryl-CoA α-Ketoisocaproic acid β-Ketoisocaproic acid β-Ketoisocaproyl-CoA β-Leucine β-Methylcrotonyl-CoA β-Methylglutaconyl-CoA β-Hydroxy β-methylglutaryl-CoA
tryptophan→alanine→	N′-Formylkynurenine Kynurenine Anthranilic acid 3-Hydroxykynurenine 3-Hydroxyanthranilic acid 2-Amino-3-carboxymuconic semialdehyde 2-Aminomuconic semialdehyde 2-Aminomuconic acid Glutaryl-CoA

histidine→	Urocanic acid Imidazol-4-one-5-propionic acid Formiminoglutamic acid Glutamate-1-semialdehyde
proline→	1-Pyrroline-5-carboxylic acid
arginine→	Agmatine Ornithine Citrulline Cadaverine Putrescine
other	cysteine+glutamate→glutathione: γ-Glutamylcysteine

valine→	α-Ketoisovaleric acid Isobutyryl-CoA Methacrylyl-CoA 3-Hydroxyisobutyryl-CoA 3-Hydroxyisobutyric acid 2-Methyl-3-oxopropanoic acid
isoleucine→	2,3-Dihydroxy-3-methylpentanoic acid 2-Methylbutyryl-CoA Tiglyl-CoA 2-Methylacetoacetyl-CoA
methionine→	generation of homocysteine: S-Adenosyl methionine S-Adenosyl-L-homocysteine Homocysteine conversion to cysteine: Cystathionine α-Ketobutyric acid + Cysteine
threonine→	α-Ketobutyric acid
propionyl-CoA→	Methylmalonyl-CoA

phenylalanine→tyrosine→	4-Hydroxyphenylpyruvic acid Homogentisic acid 4-Maleylacetoacetic acid

Other

Cysteine metabolism	Cysteine sulfinic acid

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