Burns RO, Umbarger HE, Gross SR (1963). “The biosynthesis of leucine. III. The conversion of α-hydroxy-β-carboxyisocaproate to α-ketoisocaproate.”. 《Biochemistry》 2 (5): 1053–8. doi:10.1021/bi00905a024. PMID14087358.
Calvo JM, Stevens CM, Kalyanpur MG, Umbarger HE (December 1964). “The Absolute Configuration of α-carboxyisocaproic Acid (3-Isopropylmalic Acid), an Intermediate in Leucine Biosynthesis”. 《Biochemistry》 3 (12): 2024–7. doi:10.1021/bi00900a043. PMID14269331.
Németh A, Svingor A, Pócsik M, Dobó J, Magyar C, Szilágyi A, Gál P, Závodszky P (February 2000). “Mirror image mutations reveal the significance of an intersubunit ion cluster in the stability of 3-isopropylmalate dehydrogenase”. 《FEBS Lett.》 468 (1): 48–52. doi:10.1016/S0014-5793(00)01190-X. PMID10683439. S2CID44544921.
nih.gov
ncbi.nlm.nih.gov
Burns RO, Umbarger HE, Gross SR (1963). “The biosynthesis of leucine. III. The conversion of α-hydroxy-β-carboxyisocaproate to α-ketoisocaproate.”. 《Biochemistry》 2 (5): 1053–8. doi:10.1021/bi00905a024. PMID14087358.
Calvo JM, Stevens CM, Kalyanpur MG, Umbarger HE (December 1964). “The Absolute Configuration of α-carboxyisocaproic Acid (3-Isopropylmalic Acid), an Intermediate in Leucine Biosynthesis”. 《Biochemistry》 3 (12): 2024–7. doi:10.1021/bi00900a043. PMID14269331.
Parsons SJ, Burns RO (February 1969). “Purification and Properties of β-Isopropylmalate Dehydrogenase”. 《J. Biol. Chem.》 244 (3): 996–1003. PMID4889950.
Németh A, Svingor A, Pócsik M, Dobó J, Magyar C, Szilágyi A, Gál P, Závodszky P (February 2000). “Mirror image mutations reveal the significance of an intersubunit ion cluster in the stability of 3-isopropylmalate dehydrogenase”. 《FEBS Lett.》 468 (1): 48–52. doi:10.1016/S0014-5793(00)01190-X. PMID10683439. S2CID44544921.
semanticscholar.org
api.semanticscholar.org
Németh A, Svingor A, Pócsik M, Dobó J, Magyar C, Szilágyi A, Gál P, Závodszky P (February 2000). “Mirror image mutations reveal the significance of an intersubunit ion cluster in the stability of 3-isopropylmalate dehydrogenase”. 《FEBS Lett.》 468 (1): 48–52. doi:10.1016/S0014-5793(00)01190-X. PMID10683439. S2CID44544921.