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Details on Person D'Eustachio, Peter, 2020-01-02

Class:Id	InstanceEdit:9672777
_displayName	D'Eustachio, Peter, 2020-01-02
_timestamp	2020-01-02 22:39:13
author	[Person:140934] D'Eustachio, Peter
dateTime	2020-01-02 22:39:08
(authored)	[Reaction:9672770] SLC25A44 transports Leu, Ile and Val from cytosol to mitochondrial matrix [Homo sapiens]
(created)	[Reaction:9672770] SLC25A44 transports Leu, Ile and Val from cytosol to mitochondrial matrix [Homo sapiens] [Person:9672771] Kajimura, Shingo [Person:9672772] Ishikawa, Takamasa [CatalystActivityReference:9672773] branched-chain amino acid transmembrane transporter activity of SLC25A44 [mitochondrial inner membrane] BCAA catabolism in brown fat controls energy homeostasis through SLC25A44 [Person:9672774] Igarashi, Kaori [Person:9672775] Sidossis, Labros [EntityWithAccessionedSequence:9672776] SLC25A44 [mitochondrial inner membrane] [Homo sapiens] [Person:9672778] White, Phillip J [Person:9672779] Murashige, Danielle [Person:9672780] Takahashi, Haruya List all 45 refering instances
(edited)	[Reaction:9672770] SLC25A44 transports Leu, Ile and Val from cytosol to mitochondrial matrix [Homo sapiens]
(modified)	[Reaction:70724] leu, ile, or val + alpha-ketoglutarate <=> a-ketoisocaproate, a-keto-b-methylvalerate, or a-ketoisovalerate + glutamate [BCAT2] [Homo sapiens] [Pathway:70895] Branched-chain amino acid catabolism [Homo sapiens] [Summation:70896] The branched-chain amino acids, leucine, isoleucine, and val... [Reaction:5693148] BCKDK phosphorylates BCKDH [Homo sapiens] [Reaction:5693153] PPM1K dephosphorylates p-BCKDH [Homo sapiens] [PathwayDiagram:6788658] Diagram of Branched-chain amino acid catabolism, Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD, Loss-of-function mutations in DBT cause MSUD2, Loss-of-function mutations in DLD cause MSUD3/DLDD, H139Hfs13* PPM1K causes a mild variant of MSUD, Branched-chain ketoacid dehydrogenase kinase deficiency, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency, 3-methylglutaconic aciduria, Beta-ketothiolase deficiency, Mitochondrial short-chain enoyl-CoA hydratase deficiency 1, and 3-hydroxyisobutyryl-CoA hydrolase deficiency
(revised)	[Reaction:70870] ECHS1 hydrates methacrylyl-CoA [Homo sapiens]
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No pathways have been reviewed or authored by D'Eustachio, Peter, 2020-01-02 (9672777)