locus-tag	class	description
THITE_152278	COG1063	alcohol dehydrogenase
THITE_2011436	COG0484	heat shock protein binding
THITE_2012986	COG2227	3-demethylubiquinone-9 3-O-methyltransferase activity
THITE_2038450	COG0300	oxidoreductase activity
THITE_2039441	COG0167	dihydroorotate dehydrogenase activity
THITE_2039507	COG0277	FAD linked oxidase domain protein
THITE_2039513	COG2815	serine threonine protein kinase
THITE_2039513	COG0515	serine threonine protein kinase
THITE_2043847	COG1024	Enoyl-CoA hydratase
THITE_2043847	COG1250	3-hydroxyacyl-CoA dehydrogenase
THITE_2044835	COG0009	L-threonylcarbamoyladenylate synthase
THITE_2045416	COG3119	arylsulfatase activity
THITE_2046723	COG1902	pentaerythritol trinitrate reductase activity
THITE_2086862	COG2226	methyltransferase
THITE_2088123	COG1001	Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family
THITE_2126245	COG0666	response to abiotic stimulus
THITE_2141268	COG2814	Major facilitator Superfamily
THITE_2141925	COG0272	DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA
THITE_2141944	COG0330	HflC and HflK could
THITE_2142693	COG2755	lipolytic protein G-D-S-L family
THITE_2143714	COG1028	Short-chain dehydrogenase reductase Sdr
THITE_34477	COG0314	molybdopterin synthase activity
THITE_34894	COG0007	Multifunctional enzyme that catalyzes the SAM-dependent methylations of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 via precorrin-1. Then it catalyzes the NAD- dependent ring dehydrogenation of precorrin-2 to yield sirohydrochlorin. Finally, it catalyzes the ferrochelation of sirohydrochlorin to yield siroheme
THITE_34894	COG1648	precorrin-2 dehydrogenase activity
THITE_37833	COG2021	Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine
THITE_48906	COG0503	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis