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Escherichia coli K-12 substr. MG1655 Compound: L-leucine

Abbrev Name: leu

Synonyms: (2S)-α-2-amino-4-methylvaleric acid, L, leu, leucine, 2-amino-4-methylvaleric acid, (2S)-α-leucine, L-leu

Superclasses: an amino acid or its derivative an amino acid a neutral amino acid
an amino acid or its derivative an amino acid a non-polar amino acid
an amino acid or its derivative an amino acid an alpha amino acid a branched-chain amino acid
an amino acid or its derivative an amino acid an alpha amino acid a standard alpha amino acid
an amino acid or its derivative an amino acid an L-amino acid

Component of: Lrp-Leucine DNA-binding transcriptional dual regulator (extended summary available)

Chemical Formula: C6H13NO2

Molecular Weight: 131.17 Daltons

Monoisotopic Molecular Weight: 131.0946286667 Daltons

SMILES: CC(C)CC([N+])C([O-])=O

InChI: InChI=1S/C6H13NO2/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t5-/m0/s1

InChIKey: InChIKey=ROHFNLRQFUQHCH-YFKPBYRVSA-N

Unification Links: CAS:61-90-5 , ChEBI:57427 , HMDB:HMDB00687 , IAF1260:33942 , KEGG:C00123 , MetaboLights:MTBLC57427 , NCI:46709 , PubChem:7045798

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -84.2

Reactions known to consume the compound:

tRNA charging :
tRNAleu + L-leucine + ATP + H+ → L-leucyl-tRNAleu + AMP + diphosphate

Reactions known to produce the compound:

Not in pathways:
L-alanyl-L-leucine + H2O → L-alanine + L-leucine


a peptide + H2O → a standard α amino acid + a peptide
a protein + H2O → a peptide + a standard α amino acid
a protein + H2O → a peptide + a standard α amino acid
a protein + H2O → a standard α amino acid + a peptide
amino acids(n) + H2O → a standard α amino acid + amino acids(n-1)
β-aspartyl dipeptide + H2O → L-aspartate + a standard α amino acid
a dipetide with L-aspartate at the N-terminal + H2O → L-aspartate + a standard α amino acid
a tripeptide + H2O → a dipeptide + a standard α amino acid
a dipeptide with proline at the C-terminal + H2O → L-proline + a standard α amino acid
a dipeptide + H2O → 2 a standard α amino acid


a polypeptide + H2O → a polypeptide + an L-amino acid

Reactions known to both consume and produce the compound:

leucine biosynthesis :
L-leucine + 2-oxoglutarate ↔ 4-methyl-2-oxopentanoate + L-glutamate

In Reactions of unknown directionality:

Not in pathways:
Lrp + L-leucine = Lrp-leu


L-methionine + a 2-oxo carboxylate = 2-oxo-4-methylthiobutanoate + a standard α amino acid


a 5-L-glutamyl-[peptide][periplasmic space] + an amino acid[periplasmic space] = a 5-L-glutamyl-amino acid[periplasmic space] + a peptide[periplasmic space]

In Transport reactions:
ATP + L-leucine[periplasmic space] + H2O → ADP + L-leucine[cytosol] + phosphate + H+ ,
Na+[periplasmic space] + L-leucine[periplasmic space] → Na+[cytosol] + L-leucine[cytosol] ,
L-leucine[cytosol] + H+[periplasmic space]L-leucine[periplasmic space] + H+[cytosol] ,
an L-amino acid[cytosol]an L-amino acid[periplasmic space]

Enzymes inhibited by L-leucine, sorted by the type of inhibition, are:

Inhibitor (Mechanism unknown) of: threonine deaminase [Vonder72] , aspartate kinase [Huang93] , acetolactate synthase [Gollop83] , acetohydroxybutanoate synthase , acetohydroxybutanoate synthase [Gollop83] , phenylalanine aminotransferase [Powell78a] , leucine aminotransferase [Powell78a] , acetolactate synthase , tyrosine aminotransferase [Powell78a] , 2-isopropylmalate synthase [Stieglitz74]

In Growth Media: Neidhardt EZ rich defined medium , Davis and Mingioli medium A , PMA nitrogen source test + leu , PMA carbon source test + leu , M56 medium

Transcription Units regulated by related protein Lrp-Leucine DNA-binding transcriptional dual regulator (23 total):


References

Gollop83: Gollop N, Chipman DM, Barak Z (1983). "Inhibition of acetohydroxy acid synthase by leucine." Biochim Biophys Acta 1983;748(1);34-9. PMID: 6351926

Huang93: Huang KJ, Hseu TH (1993). "Effects of lysine-sensitive aspartokinase III on lysine biosynthesis in Escherichia coli K-12." Proc Natl Sci Counc Repub China B 17(3);91-7. PMID: 8290655

Powell78a: Powell JT, Morrison JF (1978). "Role of the Escherichia coli aromatic amino acid aminotransferase in leucine biosynthesis." J Bacteriol 136(1);1-4. PMID: 361681

Stieglitz74: Stieglitz BI, Calvo JM (1974). "Distribution of the isopropylmalate pathway to leucine among diverse bacteria." J Bacteriol 118(3);935-41. PMID: 4829932

Vonder72: Vonder Haar RA, Umbarger HE (1972). "Isoleucine and valine metabolism in Escherichia coli. XIX. Inhibition of isoleucine biosynthesis by glycyl-leucine." J Bacteriol 112(1);142-7. PMID: 4562390


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Please cite the following article in publications resulting from the use of EcoCyc: Nucleic Acids Research 41:D605-12 2013
Page generated by SRI International Pathway Tools version 18.5 on Sat Dec 20, 2014, BIOCYC13A.