From Wikipedia, the free encyclopedia
3-isopropylmalate dehydratase
Identifiers
EC no. 4.2.1.33
CAS no. 37290-72-5
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Gene Ontology AmiGO / QuickGO
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PMC articles
PubMed articles
NCBI proteins

3-Isopropylmalate dehydratase ( EC 4.2.1.33) is an aconitase homologue, [1] [2] [3] which catalyses the isomerisation of 2-isopropylmalate to 3-isopropylmalate, via dehydration, in the biosynthesis of leucine.

References

  1. ^ Gross SR, Burns RO, Umbarger HE (1963). "The biosynthesis of leucine. II. The enzymic isomerization of beta-carboxy-beta-hydroxyisocaproate and alpha-hydroxy-beta-carboxyisocaproate". Biochemistry. 2 (5): 1046–52. doi: 10.1021/bi00905a023. PMID  14087357.
  2. ^ Calvo JM, Stevens CM, Kalyanpur MG, Umbarger HE (December 1964). "The absolute configuration of alpha-hydroxy-beta-carboxyisocaproic acid (3-isopropylmalic acid), an intermediate in leucine biosynthesis". Biochemistry. 3 (12): 2024–7. doi: 10.1021/bi00900a043. PMID  14269331.
  3. ^ Cole FE, Kalyanpur MG, Stevens CM (August 1973). "Absolute configuration of alpha isopropylmalate and the mechanism of its conversion to beta isopropylmalate in the biosynthesis of leucine". Biochemistry. 12 (17): 3346–50. doi: 10.1021/bi00741a031. PMID  4270046.

External links


From Wikipedia, the free encyclopedia
3-isopropylmalate dehydratase
Identifiers
EC no. 4.2.1.33
CAS no. 37290-72-5
Databases
IntEnz IntEnz view
BRENDA BRENDA entry
ExPASy NiceZyme view
KEGG KEGG entry
MetaCyc metabolic pathway
PRIAM profile
PDB structures RCSB PDB PDBe PDBsum
Gene Ontology AmiGO / QuickGO
Search
PMC articles
PubMed articles
NCBI proteins

3-Isopropylmalate dehydratase ( EC 4.2.1.33) is an aconitase homologue, [1] [2] [3] which catalyses the isomerisation of 2-isopropylmalate to 3-isopropylmalate, via dehydration, in the biosynthesis of leucine.

References

  1. ^ Gross SR, Burns RO, Umbarger HE (1963). "The biosynthesis of leucine. II. The enzymic isomerization of beta-carboxy-beta-hydroxyisocaproate and alpha-hydroxy-beta-carboxyisocaproate". Biochemistry. 2 (5): 1046–52. doi: 10.1021/bi00905a023. PMID  14087357.
  2. ^ Calvo JM, Stevens CM, Kalyanpur MG, Umbarger HE (December 1964). "The absolute configuration of alpha-hydroxy-beta-carboxyisocaproic acid (3-isopropylmalic acid), an intermediate in leucine biosynthesis". Biochemistry. 3 (12): 2024–7. doi: 10.1021/bi00900a043. PMID  14269331.
  3. ^ Cole FE, Kalyanpur MG, Stevens CM (August 1973). "Absolute configuration of alpha isopropylmalate and the mechanism of its conversion to beta isopropylmalate in the biosynthesis of leucine". Biochemistry. 12 (17): 3346–50. doi: 10.1021/bi00741a031. PMID  4270046.

External links



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