locus-tag	class	description
FH779_RS00010	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
FH779_RS00020	ENOG4105DIK	(ABC) transporter
FH779_RS00025	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
FH779_RS00030	ENOG4105DR1	Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration (By similarity)
FH779_RS00050	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
FH779_RS00055	ENOG4107ZIC	Glycerol-3-phosphate cytidylyltransferase
FH779_RS00060	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FH779_RS00070	ENOG4105CQX	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol (By similarity)
FH779_RS00085	ENOG4105F99	Hydroxymethylglutaryl-CoA synthase
FH779_RS00110	ENOG4105DQ4	alcohol dehydrogenase
FH779_RS00135	ENOG4105MK2	5-formyltetrahydrofolate cyclo-ligase
FH779_RS00150	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FH779_RS00180	ENOG4105C7K	acetolactate synthase
FH779_RS00200	ENOG4105UTB	Blue (Type 1) copper domain protein
FH779_RS00205	ENOG4105EIZ	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
FH779_RS00210	ENOG4105CN0	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate (By similarity)
FH779_RS00235	ENOG4108Z1K	This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA (By similarity)
FH779_RS00240	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
FH779_RS00250	ENOG4108K5P	(LipO)protein
FH779_RS00255	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
FH779_RS00275	ENOG4105C5Z	peptidase
FH779_RS00285	ENOG4105FE9	pseudouridine synthase
FH779_RS00300	ENOG4105FE9	pseudouridine synthase
FH779_RS00320	ENOG4105F91	Catalyzes the phosphorylation of NAD to NADP. Utilizes ATP and other nucleoside triphosphates as well as inorganic polyphosphate as a source of phosphorus (By similarity)
FH779_RS00355	ENOG4105CGR	Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) (By similarity)
FH779_RS00365	ENOG4107QRG	dna polymerase iii
FH779_RS00370	ENOG4106N3A	copper homeostasis protein cutc
FH779_RS00380	ENOG4105CWX	Alpha-1,2-mannosidase
FH779_RS00400	ENOG4105M2Z	protein tyrosine serine phosphatase
FH779_RS00420	ENOG4105D5P	Methylmalonyl-coA mutase
FH779_RS00435	ENOG4105CWT	An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism (By similarity)
FH779_RS00445	ENOG4106BRA	Membrane
FH779_RS00450	ENOG4108QSZ	General inhibitor of pancreatic serine proteases inhibits chymotrypsin, trypsin, elastases, factor X, kallikrein as well as a variety of other proteases (By similarity)
FH779_RS00465	ENOG4105C03	ribonuclease
FH779_RS00475	ENOG4105CEN	a g-specific adenine glycosylase
FH779_RS00480	ENOG4108UUM	single-stranded DNA-binding protein
FH779_RS00505	ENOG4105DJT	lAO AO transport system ATPase
FH779_RS00520	ENOG4105CE1	Ferrous iron transport protein b
FH779_RS00530	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
FH779_RS00535	ENOG4105K46	50S ribosomal protein l27
FH779_RS00545	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
FH779_RS00565	ENOG4105CBX	hi0933 family
FH779_RS00580	ENOG4105CZI	D-fructose-1,6-bisphosphate 1-phosphohydrolase class 1
FH779_RS00585	ENOG4105CFH	Aspartokinase
FH779_RS00600	ENOG4105CH7	arginosuccinase
FH779_RS00605	ENOG4107QIJ	Aconitate hydratase 2
FH779_RS00610	ENOG4108I0Z	Aconitate hydratase
FH779_RS00620	ENOG4105KRF	dihydroneopterin aldolase
FH779_RS00625	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
FH779_RS00640	ENOG4105C37	(CBS) domain
FH779_RS00665	ENOG4105RA3	Binds directly to 16S ribosomal RNA (By similarity)
FH779_RS00675	ENOG4108QBX	(LipO)protein
FH779_RS00685	ENOG4105DF5	DNA topoisomerase IV, subunit A
FH779_RS00695	ENOG4105DNX	Dna topoisomerase iv (Subunit b)
FH779_RS00700	ENOG4105CHM	Aminotransferase
FH779_RS00705	ENOG41061HS	cysteine-type endopeptidase activity
FH779_RS00710	ENOG4105C3G	gtp-binding protein
FH779_RS00725	ENOG4105CJ1	ABC, transporter
FH779_RS00735	ENOG4105CHM	Aminotransferase
FH779_RS00745	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FH779_RS00750	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
FH779_RS00760	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
FH779_RS00805	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
FH779_RS00810	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FH779_RS00820	ENOG4105C2V	Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) (By similarity)
FH779_RS00835	ENOG4105D9R	oxidoreductase
FH779_RS00840	ENOG4108S4H	thioesterase Superfamily protein
FH779_RS00845	ENOG4108S4H	thioesterase Superfamily protein
FH779_RS00855	ENOG4105C1P	efflux transporter, rnd family, mfp subunit
FH779_RS00885	ENOG41060VI	Involved in DNA repair and RecF pathway recombination (By similarity)
FH779_RS00895	ENOG4105C28	cystathionine
FH779_RS00915	ENOG4105EV9	Alpha Beta Hydrolase
FH779_RS00920	ENOG4108Z6B	deaminase
FH779_RS00945	ENOG4105CPP	Dehydrogenase, E1 component
FH779_RS00955	ENOG4105F0N	pyrophosphate phospho-hydrolase
FH779_RS00965	ENOG4105IIU	Aminopeptidase
FH779_RS00970	ENOG4105C0F	tryptophanase EC 4.1.99.1
FH779_RS01005	ENOG4105C85	amino acid
FH779_RS01015	ENOG41063V1	Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid (By similarity)
FH779_RS01050	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
FH779_RS01055	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
FH779_RS01060	ENOG4105DK0	Indole-3-glycerol phosphate synthase
FH779_RS01065	ENOG4107RI6	Anthranilate phosphoribosyltransferase
FH779_RS01070	ENOG4105DDQ	anthranilate synthase
FH779_RS01075	ENOG4105CRQ	synthase (Component I)
FH779_RS01080	ENOG4105E39	Enoyl-CoA hydratase
FH779_RS01090	ENOG4105EMU	Dehydrogenase
FH779_RS01140	ENOG4105E9K	Isocitrate dehydrogenase
FH779_RS01150	ENOG4108VVK	transcriptional Regulator, AsnC
FH779_RS01155	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
FH779_RS01160	ENOG4108KB1	transcriptional regulator, arac family
FH779_RS01190	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FH779_RS01205	ENOG4105DHJ	ABC, transporter
FH779_RS01220	ENOG4108UTT	Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin (By similarity)
FH779_RS01235	ENOG4108UGX	Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate (By similarity)
FH779_RS01255	ENOG4105CIM	Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain (By similarity)
FH779_RS01260	ENOG4105E4C	Lytic transglycosylase catalytic
FH779_RS01275	ENOG4108YYH	Nadph-dependent fmn reductase
FH779_RS01280	ENOG4105C0B	DNA polymerase III (alpha subunit)
FH779_RS01285	ENOG4105K63	Thioredoxin
FH779_RS01350	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
FH779_RS01370	ENOG4108URH	decarboxylase
FH779_RS01375	ENOG4108478	ec 3.2.1.18
FH779_RS01380	ENOG4105C9C	Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position (By similarity)
FH779_RS01395	ENOG4105C27	TonB-dependent Receptor Plug
FH779_RS01405	ENOG4107RBJ	symporter
FH779_RS01410	ENOG4107URF	beta-phospho-glucomutase
FH779_RS01420	ENOG4108IUK	alpha amylase, catalytic
FH779_RS01435	ENOG4107T9C	Alpha amylase catalytic region
FH779_RS01440	ENOG4105CG3	alpha amylase, catalytic region
FH779_RS01465	ENOG4105CPP	Dehydrogenase, E1 component
FH779_RS01510	ENOG41076HS	cation diffusion facilitator family transporter
FH779_RS01520	ENOG4105C1G	acyl-Coa dehydrogenase
FH779_RS01525	ENOG41083X6	30S ribosomal protein S21
FH779_RS01530	ENOG4108IYS	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FH779_RS01555	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
FH779_RS01575	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
FH779_RS01580	ENOG4105C64	Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release (By similarity)
FH779_RS01585	ENOG4107VNI	ribosomal protein l10
FH779_RS01590	ENOG4105KBC	Seems to be the binding site for several of the factors involved in protein synthesis and appears to be essential for accurate translation (By similarity)
FH779_RS01595	ENOG4107QIH	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FH779_RS01600	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FH779_RS01610	ENOG4105C7S	Dehydrogenase
FH779_RS01650	ENOG4105C0H	protease
FH779_RS01655	ENOG4105E4Z	Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan (By similarity)
FH779_RS01665	ENOG4105DNP	FAD linked oxidase domain protein
FH779_RS01685	ENOG4108RWI	nicotinamidase
FH779_RS01700	ENOG4105K64	Glycosyl transferase, family 2
FH779_RS01720	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
FH779_RS01730	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FH779_RS01740	ENOG4105EY8	ABC transporter
FH779_RS01760	ENOG4108HWB	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
FH779_RS01800	ENOG4105K64	Glycosyl transferase, family 2
FH779_RS01820	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
FH779_RS01845	ENOG4107QRS	glycosyltransferase group 2 family protein
FH779_RS01850	ENOG4105D5D	udp-galactopyranose mutase
FH779_RS01855	ENOG4105K64	Glycosyl transferase, family 2
FH779_RS01875	ENOG4108ZQD	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
FH779_RS01880	ENOG4105VIE	preprotein translocase, subunit YajC
FH779_RS01890	ENOG4107R6T	Involved in the transcription termination process (By similarity)
FH779_RS01895	ENOG4105BZ1	(ABC) transporter
FH779_RS01910	ENOG4105CMV	Succinyl-CoA synthetase subunit beta
FH779_RS01915	ENOG4105CQU	Part of the ABC transporter complex LolCDE involved in the translocation of mature outer membrane-directed lipoproteins, from the inner membrane to the periplasmic chaperone, LolA. Responsible for the formation of the LolA-lipoprotein complex in an ATP-dependent manner (By similarity)
FH779_RS01940	ENOG4108SHN	Glycosyl transferase, family 2
FH779_RS01945	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
FH779_RS01970	ENOG4105IQ5	FAD linked oxidase domain protein
FH779_RS01990	ENOG4108PQP	glycosyl transferase group 1
FH779_RS01995	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
FH779_RS02000	ENOG4107TAE	Glycosyl transferase (Group 1
FH779_RS02020	ENOG4105ESV	Glycosyl transferase, family 4
FH779_RS02030	ENOG4108QV3	biosynthesis protein
FH779_RS02035	ENOG4105D3Q	Sugar transferase
FH779_RS02040	ENOG4107QX3	carboxylase
FH779_RS02045	ENOG4108ZYK	Acyl carrier protein phosphodiesterase
FH779_RS02055	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
FH779_RS02060	ENOG4105Y3U	Transglycosylase-associated protein
FH779_RS02065	ENOG4106HK8	GPR1 FUN34 yaaH family protein
FH779_RS02070	ENOG4105DHW	Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins
FH779_RS02075	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
FH779_RS02105	ENOG4105CKK	Glycosyl transferase, family 2
FH779_RS02120	ENOG4105CJ3	phosphate transporter
FH779_RS02125	ENOG4107QXV	Phosphate transporter
FH779_RS02140	ENOG4108UKE	Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit (By similarity)
FH779_RS02145	ENOG4108UHY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA (By similarity)
FH779_RS02150	ENOG4105CEJ	Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome (By similarity)
FH779_RS02155	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
FH779_RS02170	ENOG4105EEE	One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit (By similarity)
FH779_RS02175	ENOG4106U5A	One of the primary rRNA binding proteins, this protein initially binds near the 5'-end of the 23S rRNA. It is important during the early stages of 50S assembly. It makes multiple contacts with different domains of the 23S rRNA in the assembled 50S subunit and ribosome (By similarity)
FH779_RS02180	ENOG4105KZR	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
FH779_RS02185	ENOG4105CFD	One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity
FH779_RS02190	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
FH779_RS02195	ENOG4105KAP	The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome (By similarity)
FH779_RS02200	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
FH779_RS02205	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
FH779_RS02210	ENOG4105WNB	50s ribosomal protein l29
FH779_RS02215	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
FH779_RS02220	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
FH779_RS02225	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
FH779_RS02230	ENOG4105CW6	This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits
FH779_RS02235	ENOG4105VBI	Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site (By similarity)
FH779_RS02245	ENOG4108UJY	One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit (By similarity)
FH779_RS02250	ENOG4108R5J	This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center (By similarity)
FH779_RS02255	ENOG4105K4C	This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance (By similarity)
FH779_RS02260	ENOG4108RA9	Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body (By similarity)
FH779_RS02265	ENOG41084HK	50S ribosomal protein L30
FH779_RS02270	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
FH779_RS02275	ENOG4105CGG	The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently (By similarity)
FH779_RS02280	ENOG4105K9U	however, it seems to stimulate more or less all the activities of the other two initiation factors, IF-2 and IF-3 (By similarity)
FH779_RS02285	ENOG410864M	50S ribosomal protein L36
FH779_RS02290	ENOG4108Z04	Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits
FH779_RS02295	ENOG4108UHH	Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome (By similarity)
FH779_RS02300	ENOG4105G6W	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit (By similarity)
FH779_RS02305	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
FH779_RS02310	ENOG4108ZT0	50S ribosomal protein l17
FH779_RS02315	ENOG4105E0K	tonB-dependent siderophore receptor
FH779_RS02350	ENOG4105C6K	Malic enzyme
FH779_RS02365	ENOG4105CFG	Acts as a chaperone (By similarity)
FH779_RS02370	ENOG4108Z7R	Chaperone CsaA
FH779_RS02380	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
FH779_RS02385	ENOG4105KDC	50s ribosomal protein l28
FH779_RS02390	ENOG41083ND	50S ribosomal protein L33
FH779_RS02400	ENOG4105CCP	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC)
FH779_RS02425	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
FH779_RS02450	ENOG4105C9A	Phoh family
FH779_RS02465	ENOG4105C0P	Mg chelatase subunit ChlI
FH779_RS02485	ENOG4107S2Z	UPF0761 membrane protein
FH779_RS02545	ENOG4105EMN	RNA polymerase sigma factor
FH779_RS02560	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
FH779_RS02570	ENOG4105CM2	brancheD-chain amino acid aminotransferase
FH779_RS02585	ENOG4105EEI	dihydropteroate synthase
FH779_RS02600	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
FH779_RS02605	ENOG4105CP7	Triose-phosphate isomerase
FH779_RS02650	ENOG4107T6X	nag kinase
FH779_RS02660	ENOG4105XBY	Regulates arginine biosynthesis genes (By similarity)
FH779_RS02665	ENOG4105CDH	Citrulline--aspartate ligase
FH779_RS02670	ENOG4105C0N	N-acetylglutamate semialdehyde dehydrogenase
FH779_RS02680	ENOG4105C8Y	Acetylornithine aminotransferase
FH779_RS02685	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
FH779_RS02710	ENOG4105CUZ	uba thif-type nad fad binding protein
FH779_RS02715	ENOG4105F8V	Hydrolase, tatD family
FH779_RS02720	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FH779_RS02725	ENOG4105HDK	L-asparaginase
FH779_RS02735	ENOG4109066	lysm domain bon superfamily protein
FH779_RS02740	ENOG4105ER2	Ompa motb domain protein
FH779_RS02745	ENOG4105EEQ	Na H antiporter
FH779_RS02755	ENOG4105C3H	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
FH779_RS02770	ENOG4105CZ8	DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity. The beta chain is required for initiation of replication once it is clamped onto DNA, it slides freely (bidirectional and ATP- independent) along duplex DNA (By similarity)
FH779_RS02780	ENOG41077A9	carbonic anhydrase
FH779_RS02790	ENOG4105EMU	Dehydrogenase
FH779_RS02820	ENOG4105GR3	Histidine kinase
FH779_RS02830	ENOG4105D82	Glutamate dehydrogenase
FH779_RS02845	ENOG4105C5U	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate (By similarity)
FH779_RS02865	ENOG4105DFH	Transport of potassium into the cell (By similarity)
FH779_RS02885	ENOG4105CHU	acetyl-coa acetyltransferase
FH779_RS02890	ENOG4105C1G	acyl-Coa dehydrogenase
FH779_RS02895	ENOG4105NDF	NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form. May also have NAD-dependent lysine demalonylase and desuccinylase activity (By similarity)
FH779_RS02900	ENOG4105IIU	Aminopeptidase
FH779_RS02935	ENOG4105WKZ	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
FH779_RS02985	ENOG4108UKH	Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides (By similarity)
FH779_RS02995	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
FH779_RS03015	ENOG4105IIU	Aminopeptidase
FH779_RS03040	ENOG4105D8C	Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity (By similarity)
FH779_RS03045	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
FH779_RS03050	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FH779_RS03055	ENOG4108K0D	peptidase, M48
FH779_RS03070	ENOG4105KIR	Thiol-disulfide oxidoreductase dcc
FH779_RS03080	ENOG4105ZD5	Uncharacterized protein conserved in bacteria (DUF2314)
FH779_RS03105	ENOG4105CDV	Ompa motb domain protein
FH779_RS03115	ENOG4105DFD	Na H antiporter
FH779_RS03120	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
FH779_RS03150	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
FH779_RS03155	ENOG4105BZ1	(ABC) transporter
FH779_RS03165	ENOG4105C5Q	Transcriptional regulator
FH779_RS03195	ENOG4105RKW	reductase (By
FH779_RS03200	ENOG4105CUB	amino acid
FH779_RS03205	ENOG4105DZR	Type I site-specific deoxyribonuclease
FH779_RS03210	ENOG4105VTR	Integrase
FH779_RS03245	ENOG4105CZN	Potassium uptake protein
FH779_RS03265	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
FH779_RS03290	ENOG4105HMI	Membrane
FH779_RS03295	ENOG4107TPS	domain protein
FH779_RS03320	ENOG4105CA0	peroxidase
FH779_RS03355	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
FH779_RS03360	ENOG4105EUB	pirin domain protein
FH779_RS03365	ENOG4105ECP	epimerase
FH779_RS03370	ENOG4105KVH	Transcriptional regulator
FH779_RS03510	ENOG41090A1	ferritin
FH779_RS03555	ENOG4105CA0	peroxidase
FH779_RS03575	ENOG4108ZVT	methylmalonyl-coA epimerase
FH779_RS03625	ENOG4105FBQ	ATPase associated with various cellular activities aaa_5
FH779_RS03675	ENOG4106R3P	AraC family transcriptional regulator
FH779_RS03705	ENOG4105C1X	Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity (By similarity)
FH779_RS03820	ENOG4107SFQ	iron-sulfur binding
FH779_RS03835	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
FH779_RS03860	ENOG4105C9G	DNA primase is the polymerase that synthesizes small RNA primers for the Okazaki fragments on both template strands at replication forks during chromosomal DNA synthesis (By similarity)
FH779_RS03870	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FH779_RS03875	ENOG4105CH8	Succinyl-CoA ligase ADP-forming subunit alpha
FH779_RS03880	ENOG4108UZ3	Transporter
FH779_RS03885	ENOG4108YXU	transcriptional regulator AsnC family
FH779_RS03905	ENOG4105DJ2	Major Facilitator Superfamily
FH779_RS03910	ENOG4107S4Z	Activates expression of the rhaBAD and rhaT operons (By similarity)
FH779_RS03915	ENOG4108IU3	tonb-dependent siderophore receptor
FH779_RS03930	ENOG4106QJH	hemin transport protein
FH779_RS03940	ENOG4105EHG	Permease protein
FH779_RS03975	ENOG4105E3B	Multicopper oxidase
FH779_RS03995	ENOG4105EHG	Permease protein
FH779_RS04000	ENOG4105E0A	ABC, transporter
FH779_RS04005	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
FH779_RS04010	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FH779_RS04015	ENOG4107ZY3	Histidine kinase
FH779_RS04040	ENOG4107QI1	Mate efflux family protein
FH779_RS04050	ENOG4105E0X	reductase
FH779_RS04055	ENOG4105D49	3-dehydroquinate synthase
FH779_RS04070	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
FH779_RS04075	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
FH779_RS04080	ENOG4108JQ1	Dehydrogenase
FH779_RS04090	ENOG4105DFA	alanine racemase domain protein
FH779_RS04100	ENOG4105KME	endoribonuclease L-psp
FH779_RS04105	ENOG4108ZT1	Transcriptional regulator
FH779_RS04130	ENOG4107S8C	mandelate racemase muconate lactonizing
FH779_RS04160	ENOG4106032	Glutathionylspermidine synthase
FH779_RS04175	ENOG4105CYC	Transferase
FH779_RS04180	ENOG4108XW0	May be a transcriptional activator of genes involved in the multiple antibiotic resistance (Mar) phenotype. It can also activate genes such as sodA, zwf and micF
FH779_RS04190	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
FH779_RS04195	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
FH779_RS04205	ENOG4107RJ9	Cell division protein FtsX
FH779_RS04210	ENOG4105D1X	Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits (By similarity)
FH779_RS04215	ENOG4105CJW	magnesium transporter
FH779_RS04225	ENOG4105BZU	Histidine kinase
FH779_RS04230	ENOG4105C7P	2-oxoglutarate dehydrogenase, E1
FH779_RS04235	ENOG4105C7S	Dehydrogenase
FH779_RS04260	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
FH779_RS04265	ENOG4105DEF	Extracellular solute-binding protein, family 5
FH779_RS04270	ENOG4105CBC	glutamate synthase
FH779_RS04285	ENOG4108VKV	Monofunctional biosynthetic peptidoglycan transglycosylase
FH779_RS04300	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FH779_RS04305	ENOG4108UPS	Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis (By similarity)
FH779_RS04335	ENOG4107TT5	NLP P60 protein
FH779_RS04350	ENOG4105H4N	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
FH779_RS04360	ENOG4105C26	Dehydrogenase
FH779_RS04365	ENOG4105CDU	Replicative dna helicase
FH779_RS04370	ENOG4107QM9	Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA (By similarity)
FH779_RS04375	ENOG4105CHU	acetyl-coa acetyltransferase
FH779_RS04405	ENOG4105DBS	Key enzyme in heme biosynthesis. Catalyzes the oxidative decarboxylation of propionic acid side chains of rings A and B of coproporphyrinogen III (By similarity)
FH779_RS04410	ENOG4105E0Y	RtcB Protein
FH779_RS04420	ENOG410756H	nucleotidyltransferase
FH779_RS04440	ENOG41086DT	Membrane protein of unknown function
FH779_RS04445	ENOG4105D9H	Catalyzes the attachment of glycine to tRNA(Gly) (By similarity)
FH779_RS04480	ENOG4108K8S	endonuclease I
FH779_RS04490	ENOG4105BZ5	ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins (By similarity)
FH779_RS04495	ENOG4107XPB	Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ
FH779_RS04505	ENOG4105DR5	peptidase
FH779_RS04525	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
FH779_RS04535	ENOG4107QYD	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
FH779_RS04560	ENOG4105KT7	mgtC SapB transporter
FH779_RS04595	ENOG4107TPS	domain protein
FH779_RS04605	ENOG4108VCT	Sulfite exporter TauE/SafE
FH779_RS04620	ENOG4105CRE	cytochrome C
FH779_RS04630	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
FH779_RS04635	ENOG4105KT5	UmuD protein
FH779_RS04650	ENOG41081WG	50s ribosomal protein l31
FH779_RS04670	ENOG4105C25	Primosomal protein n'
FH779_RS04685	ENOG4105C19	ABC transporter
FH779_RS04695	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FH779_RS04730	ENOG4105CRK	lysyL-tRNA synthetase
FH779_RS04755	ENOG4107QI6	Cysteine desulfurase
FH779_RS04765	ENOG4105CCW	damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage (By similarity)
FH779_RS04770	ENOG4105DXN	mazG family
FH779_RS04780	ENOG4108Z02	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
FH779_RS04785	ENOG4107ZNS	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
FH779_RS04790	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
FH779_RS04795	ENOG4106WTF	Glycosyl transferase, family 2
FH779_RS04800	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
FH779_RS04820	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
FH779_RS04835	ENOG4107S85	alpha-2-macroglobulin domain protein
FH779_RS04840	ENOG4107S1E	Beta-lactamase
FH779_RS04850	ENOG4105C8A	Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP (By similarity)
FH779_RS04890	ENOG4105C31	Tryptophanyl-tRNA synthetase
FH779_RS04895	ENOG4108Z4V	iron-sulfur cluster assembly
FH779_RS04920	ENOG4105C9B	Cysteine desulfurase
FH779_RS04935	ENOG4108UUM	single-stranded DNA-binding protein
FH779_RS04950	ENOG41080C8	DUF218 domain
FH779_RS04955	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
FH779_RS04970	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
FH779_RS04975	ENOG4107ZF2	Phosphatase
FH779_RS04980	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
FH779_RS05010	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
FH779_RS05015	ENOG4107ZXU	DSBA oxidoreductase
FH779_RS05020	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FH779_RS05030	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FH779_RS05040	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FH779_RS05065	ENOG4105K5B	UPF0225 protein
FH779_RS05085	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
FH779_RS05090	ENOG4105EHM	Aminoglycoside phosphotransferase
FH779_RS05100	ENOG4108RCM	Nitroreductase
FH779_RS05110	ENOG4108YYH	Nadph-dependent fmn reductase
FH779_RS05125	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
FH779_RS05130	ENOG4105GR3	Histidine kinase
FH779_RS05150	ENOG4105C3M	thioredoxin reductase
FH779_RS05195	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FH779_RS05205	ENOG4105BZU	Histidine kinase
FH779_RS05270	ENOG4105C27	TonB-dependent Receptor Plug
FH779_RS05295	ENOG4105C4K	Nad synthetase
FH779_RS05305	ENOG4105DWY	Agmatine deiminase
FH779_RS05310	ENOG4105C1G	acyl-Coa dehydrogenase
FH779_RS05315	ENOG4105EXW	epimerase dehydratase
FH779_RS05320	ENOG4105C9K	Endothelin-converting enzyme 1
FH779_RS05345	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
FH779_RS05350	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
FH779_RS05360	ENOG4105CZH	peptidase
FH779_RS05365	ENOG4107XDQ	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
FH779_RS05400	ENOG4108VBV	N-Acetylmuramoyl-L-alanine amidase
FH779_RS05550	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
FH779_RS05555	ENOG4105C4R	Atp-dependent dna helicase
FH779_RS05590	ENOG4105R1U	AraC Family Transcriptional Regulator
FH779_RS05610	ENOG4107R4J	Chloride channel
FH779_RS05630	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FH779_RS05655	ENOG4105C59	p-type ATPase
FH779_RS05660	ENOG4105PGM	cation diffusion facilitator family transporter
FH779_RS05680	ENOG4105D2S	major facilitator superfamily
FH779_RS05710	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FH779_RS05715	ENOG4105DAB	fumarate reductase succinate dehydrogenase flavoprotein domain protein
FH779_RS05735	ENOG41075H3	AraC family transcriptional regulator
FH779_RS05780	ENOG4107QN2	dihydrolipoyl dehydrogenase
FH779_RS05790	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
FH779_RS05795	ENOG4107QN2	dihydrolipoyl dehydrogenase
FH779_RS05800	ENOG4108Z9K	Osmotically inducible protein
FH779_RS05805	ENOG4105ID8	Transcriptional regulator, ARAC family
FH779_RS05810	ENOG4105E6K	4-Hydroxyphenylpyruvate dioxygenase
FH779_RS05825	ENOG4105E3B	Multicopper oxidase
FH779_RS05830	ENOG4105DXI	Major Facilitator superfamily
FH779_RS05890	ENOG4105CKI	cobalamin synthesis protein
FH779_RS05895	ENOG4105DIN	metallophosphoesterase
FH779_RS05905	ENOG4105CK2	sodium dicarboxylate symporter
FH779_RS05920	ENOG4107EEK	Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide (By similarity)
FH779_RS05925	ENOG4105FFM	Resistance to gentamicin, tobramycin, and kanamycin. Tobramycin and kanamycin resistance is due to the ACC activity, specified by N-terminal region, and the gentamicin resistance is due to the APH activity encoded by the C-terminal region of the protein (By similarity)
FH779_RS05940	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
FH779_RS05945	ENOG4105E2N	Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) (By similarity)
FH779_RS05965	ENOG4105K6H	D-cysteine desulfhydrase
FH779_RS05990	ENOG4105F32	YngK protein
FH779_RS06005	ENOG4105CPM	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
FH779_RS06015	ENOG4108VVK	transcriptional Regulator, AsnC
FH779_RS06030	ENOG4105EJQ	L-serine dehydratase
FH779_RS06035	ENOG4105C1J	atp-dependent rna helicase
FH779_RS06040	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
FH779_RS06060	ENOG4105CHM	Aminotransferase
FH779_RS06065	ENOG4107R0I	Cell wall formation (By similarity)
FH779_RS06085	ENOG4105CIN	aminoacyl-histidine dipeptidase
FH779_RS06100	ENOG4105CUB	amino acid
FH779_RS06100	ENOG4105CUB	amino acid
FH779_RS06105	ENOG4105C9M	aspartyl-trna synthetase
FH779_RS06120	ENOG4105CTQ	phosphohexokinase
FH779_RS06140	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
FH779_RS06150	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
FH779_RS06160	ENOG4105E2X	shikimate dehydrogenase
FH779_RS06165	ENOG4105DQR	SNARE associated Golgi
FH779_RS06170	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
FH779_RS06180	ENOG4105VMP	Transcriptional regulator
FH779_RS06200	ENOG4107RSS	Hydrogenase accessory protein HypB
FH779_RS06215	ENOG4105EHG	Permease protein
FH779_RS06220	ENOG4108IPX	Part of the ABC transporter complex HmuTUV involved in hemin import. Responsible for energy coupling to the transport system (By similarity)
FH779_RS06240	ENOG4108YZ9	Urea amidohydrolase subunit gamma
FH779_RS06245	ENOG4105KI2	Urea amidohydrolase subunit beta
FH779_RS06250	ENOG4105CQM	Urea amidohydrolase subunit alpha
FH779_RS06260	ENOG4105HFU	Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly (By similarity)
FH779_RS06265	ENOG4108YH3	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
FH779_RS06270	ENOG4105E8T	Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG (By similarity)
FH779_RS06275	ENOG4108XNJ	Required for maturation of urease via the functional incorporation of the urease nickel metallocenter (By similarity)
FH779_RS06340	ENOG4108VB1	regulatoR
FH779_RS06345	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FH779_RS06395	ENOG4107ZQV	short-chain dehydrogenase reductase
FH779_RS06415	ENOG4105E78	Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring (By similarity)
FH779_RS06420	ENOG4105CZF	Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism (By similarity)
FH779_RS06435	ENOG4107ZXU	DSBA oxidoreductase
FH779_RS06440	ENOG4108RCM	Nitroreductase
FH779_RS06460	ENOG4105VEQ	Cold shock protein
FH779_RS06470	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
FH779_RS06595	ENOG4108HRK	Histidine kinase
FH779_RS06600	ENOG4105DY9	regulatoR
FH779_RS06650	ENOG4105KVH	Transcriptional regulator
FH779_RS06780	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
FH779_RS06805	ENOG4105DFA	alanine racemase domain protein
FH779_RS06840	ENOG4107SCJ	type I restriction enzyme EcoKI subunit R
FH779_RS06845	ENOG4105CVR	type I restriction-modification system
FH779_RS06890	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FH779_RS06965	ENOG4105QNF	Outer membrane lipoprotein
FH779_RS06995	ENOG4105EWK	phytoene
FH779_RS07000	ENOG4105VT2	5-hydroxyisourate hydrolase
FH779_RS07030	ENOG41090A1	ferritin
FH779_RS07130	ENOG4105EMU	Dehydrogenase
FH779_RS07170	ENOG4105WKZ	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
FH779_RS07200	ENOG4105D6J	arsenicaL-resistance protein
FH779_RS07220	ENOG4105VEQ	Cold shock protein
FH779_RS07240	ENOG4108RCM	Nitroreductase
FH779_RS07250	ENOG4108ZHJ	Organic hydroperoxide resistance protein
FH779_RS07255	ENOG4105K56	Transcriptional regulator
FH779_RS07260	ENOG4105E0X	reductase
FH779_RS07265	ENOG4108KBJ	Inner membrane protein YkgB
FH779_RS07290	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FH779_RS07320	ENOG4108F3G	Type I restriction-modification system, R subunit
FH779_RS07340	ENOG4107SUZ	Sodium/hydrogen exchanger family
FH779_RS07355	ENOG4108Z9Z	response to DNA damage stimulus
FH779_RS07370	ENOG4105CYX	Short-chain dehydrogenase reductase Sdr
FH779_RS07380	ENOG4105EUH	cytochrome C oxidase, cbb3-type, subunit i
FH779_RS07385	ENOG41067HZ	cytochrome C, class I
FH779_RS07415	ENOG4105EMU	Dehydrogenase
FH779_RS07435	ENOG4108DIG	cyanophycin synthetase
FH779_RS07460	ENOG41090A1	ferritin
FH779_RS07475	ENOG4105MHH	HipA N-terminal domain protein
FH779_RS07510	ENOG41090HT	Inherit from COG: transposase
FH779_RS07515	ENOG4105C0D	helicase
FH779_RS07525	ENOG4105KT5	UmuD protein
FH779_RS07530	ENOG4105CQ3	Poorly processive error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by polIV. Exhibits no 3-5 exonuclease (proofreading) activity. May be involved in translesional synthesis in conjunction with the beta clamp from polIII (By similarity)
FH779_RS07535	ENOG4105CII	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision (By similarity)
FH779_RS07540	ENOG4108RAV	Conserved protein
FH779_RS07570	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
FH779_RS07605	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
FH779_RS07635	ENOG4108WBT	adenosyltransferase
FH779_RS07650	ENOG4105C3D	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA (By similarity)
FH779_RS07655	ENOG41067S4	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system (By similarity)
FH779_RS07670	ENOG4105CZH	peptidase
FH779_RS07675	ENOG4108BDP	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
FH779_RS07700	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
FH779_RS07720	ENOG4107TDE	lipolytic protein G-D-S-L family
FH779_RS07740	ENOG4107TDE	lipolytic protein G-D-S-L family
FH779_RS07745	ENOG4105E4I	Glycoside hydrolase family 28
FH779_RS07750	ENOG4105F5H	Glycosyl Hydrolase Family 88
FH779_RS07790	ENOG4105ETE	Transcriptional regulator (LacI family
FH779_RS07795	ENOG4105CTX	dehydratase
FH779_RS07800	ENOG4107QZW	Altronate oxidoreductase
FH779_RS07805	ENOG4105DPW	Major facilitator superfamily MFS_1
FH779_RS07810	ENOG4108UHU	Aldolase
FH779_RS07820	ENOG4105D2H	Uronic isomerase
FH779_RS07915	ENOG4107QN2	dihydrolipoyl dehydrogenase
FH779_RS07940	ENOG4105D37	Low-affinity potassium transport system. Interacts with Trk system potassium uptake protein TrkA (By similarity)
FH779_RS07945	ENOG4105C1A	potassium transporter peripheral membrane
FH779_RS07950	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
FH779_RS08010	ENOG4105K89	arsenate reductase
FH779_RS08045	ENOG4105QNF	Outer membrane lipoprotein
FH779_RS08050	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
FH779_RS08060	ENOG4105D42	Cleaves the N-terminal amino acid of tripeptides (By similarity)
FH779_RS08075	ENOG4105DHU	Bile acid
FH779_RS08135	ENOG4105E6K	4-Hydroxyphenylpyruvate dioxygenase
FH779_RS08140	ENOG4106CKV	Pap2 superfamily protein
FH779_RS08150	ENOG4105C7S	Dehydrogenase
FH779_RS08155	ENOG4105CPP	Dehydrogenase, E1 component
FH779_RS08160	ENOG4105DZS	Phenylacetate-CoA ligase
FH779_RS08170	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
FH779_RS08175	ENOG4105CRS	phenylacetate-CoA oxygenase PaaG subunit
FH779_RS08180	ENOG4105N76	Phenylacetate-CoA oxygenase, subunit
FH779_RS08185	ENOG4105D9S	phenylacetate-CoA oxygenase PaaI subunit
FH779_RS08190	ENOG4108ZA2	phenylacetate-CoA oxygenase PaaJ subunit
FH779_RS08195	ENOG4108UKI	Enoyl-CoA hydratase
FH779_RS08200	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
FH779_RS08210	ENOG4105CHU	acetyl-coa acetyltransferase
FH779_RS08220	ENOG4105DXM	phenylacetic acid degradation protein
FH779_RS08245	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FH779_RS08260	ENOG4105HMI	Membrane
FH779_RS08265	ENOG4105DUM	transcriptional regulator, lysR family
FH779_RS08280	ENOG4108Z9K	Osmotically inducible protein
FH779_RS08310	ENOG4105CZ9	Domain of unknown function (DU1801)
FH779_RS08330	ENOG4105G6Z	alkaline phosphatase
FH779_RS08345	ENOG4108IQE	Amp-dependent synthetase and ligase
FH779_RS08350	ENOG4108IQE	Amp-dependent synthetase and ligase
FH779_RS08360	ENOG4108IQE	Amp-dependent synthetase and ligase
FH779_RS08370	ENOG4105C1J	atp-dependent rna helicase
FH779_RS08385	ENOG4105KRQ	Addiction module toxin, Txe YoeB family
FH779_RS08390	ENOG4106A4F	Removes the N-terminal methionine from nascent proteins (By similarity)
FH779_RS08405	ENOG4105C8E	extradiol ring-cleavage dioxygenase class IIi protein subunit b
FH779_RS08410	ENOG4108YYC	ycei family
FH779_RS08415	ENOG4105BZG	amino acid carrier protein
FH779_RS08425	ENOG4105I3K	Ferric uptake regulator, Fur family
FH779_RS08430	ENOG4105EZR	dyp-type peroxidase family protein
FH779_RS08445	ENOG4105C8Y	Acetylornithine aminotransferase
FH779_RS08460	ENOG4105C2C	drug resistance transporter, Bcr CflA
FH779_RS08475	ENOG4105SYT	Methylenetetrahydrofolate reductase
FH779_RS08480	ENOG4105C3R	Methionine synthase
FH779_RS08485	ENOG4105C3R	Methionine synthase
FH779_RS08490	ENOG4105D6E	homoserine dehydrogenase
FH779_RS08500	ENOG4105D05	Receptor
FH779_RS08520	ENOG4105CA4	amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner (By similarity)
FH779_RS08545	ENOG4107YXA	Transcriptional regulator, BadM Rrf2 family
FH779_RS08550	ENOG4107THF	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
FH779_RS08580	ENOG4108RYK	Nad-dependent epimerase dehydratase
FH779_RS08600	ENOG4105CJJ	Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress (By similarity)
FH779_RS08620	ENOG4108YYS	metal-dependent hydrolase (By similarity)
FH779_RS08665	ENOG4107USA	Thioredoxin
FH779_RS08685	ENOG4105CH6	catalase
FH779_RS08695	ENOG4105C56	H( )-stimulated, divalent metal cation uptake system (By similarity)
FH779_RS08705	ENOG4105CWR	In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance (By similarity)
FH779_RS08725	ENOG4107TUM	Amidinotransferase
FH779_RS08755	ENOG4105NQG	DoxX
FH779_RS08760	ENOG4108Z02	Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions (By similarity)
FH779_RS08765	ENOG41074FZ	May increase the rate of spontaneous hydrolysis of aminoacrylate to malonic semialdehyde. Required to remove a toxic intermediate produce in the pyrimidine nitrogen degradation (By similarity)
FH779_RS08775	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
FH779_RS08780	ENOG4105D52	delta-aminolevulinic acid dehydratase
FH779_RS08790	ENOG4105CB9	Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY
FH779_RS08795	ENOG4105EJF	Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage (By similarity)
FH779_RS08815	ENOG4105CA0	peroxidase
FH779_RS08830	ENOG4107RBB	ABC transporter, permease
FH779_RS08840	ENOG4105D6C	Part of the ABC transporter complex MacAB involved in macrolide export. Transmembrane domains (TMD) form a pore in the inner membrane and the ATP-binding domain (NBD) is responsible for energy generation (By similarity)
FH779_RS08850	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FH779_RS08860	ENOG4105C59	p-type ATPase
FH779_RS08875	ENOG4105C9Q	fumarate hydratase class II
FH779_RS08920	ENOG4105KHC	sulfurtransferase
FH779_RS08940	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
FH779_RS08950	ENOG4105FBJ	fumarylacetoacetate (faa) hydrolase
FH779_RS08965	ENOG4105MN5	HAD-superfamily hydrolase subfamily IA variant 3
FH779_RS08975	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
FH779_RS08980	ENOG41090A1	ferritin
FH779_RS09005	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
FH779_RS09010	ENOG4108I5U	Uridine phosphorylase
FH779_RS09045	ENOG4105DKX	Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) (By similarity)
FH779_RS09050	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
FH779_RS09065	ENOG4105KPY	Small multidrug resistance protein
FH779_RS09090	ENOG4105C77	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 (By similarity)
FH779_RS09110	ENOG4105HB7	Glyoxalase Bleomycin resistance protein (Dioxygenase
FH779_RS09130	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
FH779_RS09185	ENOG4108VAC	response regulator
FH779_RS09195	ENOG4105C27	TonB-dependent Receptor Plug
FH779_RS09205	ENOG4108HRK	Histidine kinase
FH779_RS09225	ENOG4107R8N	Glycosyl transferase, family 2
FH779_RS09240	ENOG4105D3G	Pseudouridine synthase
FH779_RS09250	ENOG4105ENJ	RND efflux system, outer membrane lipoprotein
FH779_RS09280	ENOG4105BZ5	ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins (By similarity)
FH779_RS09295	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
FH779_RS09300	ENOG4107QJE	Chromosome Partitioning Protein
FH779_RS09305	ENOG4105FA0	parb-like partition protein
FH779_RS09315	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
FH779_RS09355	ENOG4105EQ6	Hydrolyzes dipeptides containing N-terminal aspartate residues. May play a role in allowing the cell to use peptide aspartate to spare carbon otherwise required for the synthesis of the aspartate family of amino acids (By similarity)
FH779_RS09370	ENOG4108IUX	(ABC) transporter
FH779_RS09385	ENOG4105VEQ	Cold shock protein
FH779_RS09390	ENOG4105CSA	Coproporphyrinogen iii oxidase
FH779_RS09400	ENOG4105C8Y	Acetylornithine aminotransferase
FH779_RS09405	ENOG4105D0M	Protease HtpX homolog
FH779_RS09420	ENOG4108S7T	Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) (By similarity)
FH779_RS09425	ENOG4108UJU	UPF0301 protein
FH779_RS09455	ENOG4105DY9	regulatoR
FH779_RS09490	ENOG4105CEY	Amp-dependent synthetase and ligase
FH779_RS09500	ENOG4105CHH	sulfate transporter
FH779_RS09560	ENOG4105EW6	flavin reductase domain protein, FMN-binding
FH779_RS09610	ENOG410874W	AraC family transcriptional regulator
FH779_RS09615	ENOG4108KBJ	Inner membrane protein YkgB
FH779_RS09625	ENOG4105EUB	pirin domain protein
FH779_RS09635	ENOG4105DF9	Lipoate-protein, ligase
FH779_RS09640	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FH779_RS09690	ENOG4105C59	p-type ATPase
FH779_RS09730	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FH779_RS09770	ENOG4105CVR	type I restriction-modification system
FH779_RS09800	ENOG4105DZR	Type I site-specific deoxyribonuclease
FH779_RS09855	ENOG4105H3G	oxidoreductase
FH779_RS09875	ENOG4108NEV	two component transcriptional regulator, LytTR family
FH779_RS09880	ENOG4105C2F	Histidine kinase
FH779_RS09905	ENOG4105D6N	CoA-transferase, subunit a
FH779_RS09915	ENOG4105CWX	Alpha-1,2-mannosidase
FH779_RS09920	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
FH779_RS09955	ENOG4108D32	Methyltransferase
FH779_RS09975	ENOG4105DR9	pseudouridine synthase
FH779_RS10010	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
FH779_RS10020	ENOG4105EE5	Membrane protein terC
FH779_RS10025	ENOG4108HCJ	Hydrolase
FH779_RS10040	ENOG4105EUB	pirin domain protein
FH779_RS10055	ENOG4105E6M	Sulphatase-modifying factor protein
FH779_RS10060	ENOG4107EES	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide the precursor of murein (By similarity)
FH779_RS10070	ENOG4108K8S	endonuclease I
FH779_RS10075	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
FH779_RS10080	ENOG41061TZ	Short-chain dehydrogenase reductase Sdr
FH779_RS10110	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FH779_RS10115	ENOG4105CAE	Modifies the free amino group of the aminoacyl moiety of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by (I) promoting its recognition by IF2 and (II) impairing its binding to EFTu-GTP (By similarity)
FH779_RS10120	ENOG4105K70	DNA-binding protein
FH779_RS10125	ENOG4105CSH	Transporter
FH779_RS10140	ENOG4105DA0	Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) (By similarity)
FH779_RS10145	ENOG4108Z66	YbaK ebsC protein
FH779_RS10180	ENOG4105CT7	inner membrane cred family protein
FH779_RS10205	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FH779_RS10215	ENOG4105CPC	Aldo Keto reductase
FH779_RS10220	ENOG4105C2F	Histidine kinase
FH779_RS10225	ENOG4108NEV	two component transcriptional regulator, LytTR family
FH779_RS10230	ENOG4105F27	Major Facilitator
FH779_RS10235	ENOG4108YZK	glyoxalase bleomycin resistance protein dioxygenase
FH779_RS10240	ENOG4105CCY	NADH flavin oxidoreductase, NADH oxidase
FH779_RS10245	ENOG4105CEP	NADH dehydrogenase
FH779_RS10260	ENOG4105EGD	dinuclear metal center protein, YbgI family
FH779_RS10265	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FH779_RS10305	ENOG4105SFS	phosphoesterase RecJ domain protein
FH779_RS10315	ENOG4107XH4	PPIases accelerate the folding of proteins (By similarity)
FH779_RS10345	ENOG4105EQY	Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif (By similarity)
FH779_RS10370	ENOG4105D5P	Methylmalonyl-coA mutase
FH779_RS10380	ENOG4105D5S	Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine (By similarity)
FH779_RS10385	ENOG4108URH	decarboxylase
FH779_RS10390	ENOG4105C98	muts2 protein
FH779_RS10405	ENOG4105D3R	alkyl hydroperoxide reductase
FH779_RS10410	ENOG41080RH	Thioredoxin
FH779_RS10435	ENOG410667J	hydrolase
FH779_RS10445	ENOG4105C26	Dehydrogenase
FH779_RS10450	ENOG4105C1G	acyl-Coa dehydrogenase
FH779_RS10465	ENOG4105CI2	imidazolone-5-propionate hydrolase
FH779_RS10470	ENOG4105CKW	Inner membrane protein yedI
FH779_RS10480	ENOG4105MDH	Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity (By similarity)
FH779_RS10485	ENOG4105IU0	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
FH779_RS10500	ENOG4105DEU	major facilitator superfamily
FH779_RS10520	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FH779_RS10525	ENOG4105C5S	asparaginyl-tRNA synthetase
FH779_RS10540	ENOG4108VCV	Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another (By similarity)
FH779_RS10545	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
FH779_RS10550	ENOG4105F8V	Hydrolase, tatD family
FH779_RS10570	ENOG4105DEN	Luciferase family
FH779_RS10630	ENOG4105C75	arginyL-tRNA synthetase
FH779_RS10635	ENOG4105C1J	atp-dependent rna helicase
FH779_RS10645	ENOG4105EW9	transcriptional regulator AsnC family
FH779_RS10650	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
FH779_RS10665	ENOG4105CHR	reductase
FH779_RS10670	ENOG4105C4A	Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) (By similarity)
FH779_RS10675	ENOG4108UB4	uncharacterized protein ygjQ
FH779_RS10685	ENOG4105DRH	Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase (By similarity)
FH779_RS10690	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FH779_RS10695	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FH779_RS10700	ENOG4105D7M	Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FH779_RS10705	ENOG4105DCI	Phosphohydrolase
FH779_RS10710	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FH779_RS10715	ENOG4105K8N	protein family UPF0079, ATPase
FH779_RS10720	ENOG4105DCF	alanine dehydrogenase
FH779_RS10745	ENOG4107RF4	Phosphodiesterase
FH779_RS10755	ENOG4105CB1	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (By similarity)
FH779_RS10760	ENOG4105CHD	Transfers the gamma-phosphate of ATP to the 4'-position of a tetraacyldisaccharide 1-phosphate intermediate (termed DS-1- P) to form tetraacyldisaccharide 1,4'-bis-phosphate (lipid IVA) (By similarity)
FH779_RS10790	ENOG4108IQE	Amp-dependent synthetase and ligase
FH779_RS10800	ENOG4107QI1	Mate efflux family protein
FH779_RS10820	ENOG4105C29	acyl-CoA thioesterase
FH779_RS10900	ENOG4105D1Q	UPF0246 protein
FH779_RS10905	ENOG4107RTD	sua5 ycio yrdc ywlc family protein
FH779_RS10935	ENOG4105CJX	Molecular chaperone. Has ATPase activity (By similarity)
FH779_RS10940	ENOG4105E33	succinate dehydrogenase
FH779_RS10955	ENOG4105EMN	RNA polymerase sigma factor
FH779_RS11000	ENOG4105DBI	uridine monophosphokinase
FH779_RS11010	ENOG4105CMN	Methylmalonyl-coA mutase
FH779_RS11025	ENOG4105BZ1	(ABC) transporter
FH779_RS11040	ENOG4107KET	secretion protein, HlyD family
FH779_RS11050	ENOG4105C5H	ABC transporter
FH779_RS11065	ENOG4107QP3	malate synthase g
FH779_RS11095	ENOG4107S4Z	Activates expression of the rhaBAD and rhaT operons (By similarity)
FH779_RS11130	ENOG4105DWV	Homoserine O-trans-acetylase
FH779_RS11155	ENOG4105RK9	auxin efflux carrier
FH779_RS11170	ENOG4105CCZ	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids (By similarity)
FH779_RS11180	ENOG4105JPG	D-isomer specific 2-hydroxyacid dehydrogenase
FH779_RS11185	ENOG4105DGW	oligopeptidase A
FH779_RS11190	ENOG4105BZU	Histidine kinase
FH779_RS11200	ENOG4105FF5	Membrane
FH779_RS11270	ENOG4105E4T	pyridine nucleotide-disulfide oxidoreductase
FH779_RS11290	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FH779_RS11325	ENOG4105IPI	Membrane
FH779_RS11330	ENOG4105D44	asparaginase
FH779_RS11345	ENOG4105CYC	Transferase
FH779_RS11350	ENOG41083MR	nifu domain-containing protein
FH779_RS11355	ENOG4108Z0R	Transferase
FH779_RS11360	ENOG4108V06	Glutathione peroxidase
FH779_RS11365	ENOG4105FJR	Lmbe family
FH779_RS11415	ENOG4105CI6	Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving
FH779_RS11425	ENOG4105EA8	2-Nitropropane dioxygenase
FH779_RS11435	ENOG4105C5X	domain protein
FH779_RS11445	ENOG4107QXG	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FH779_RS11460	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
FH779_RS11465	ENOG4107P26	
FH779_RS11480	ENOG4105C5H	ABC transporter
FH779_RS11490	ENOG4107W2A	UPF0173 metal-dependent hydrolase
FH779_RS11495	ENOG4105EIS	1,4-dihydroxy-2-naphthoate octaprenyltransferase
FH779_RS11525	ENOG4105XJB	lipolytic protein G-D-S-L family
FH779_RS11540	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FH779_RS11550	ENOG4105E4F	Isochorismate synthase
FH779_RS11555	ENOG4105KA0	thioesterase Superfamily protein
FH779_RS11570	ENOG4105K7K	Transcriptional regulator
FH779_RS11585	ENOG4107Y70	Heat shock protein
FH779_RS11610	ENOG4107QN2	dihydrolipoyl dehydrogenase
FH779_RS11620	ENOG4107QJZ	Glycosyl transferase, family 2
FH779_RS11630	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
FH779_RS11655	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FH779_RS11685	ENOG4105CJ1	ABC, transporter
FH779_RS11705	ENOG4108YXN	Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs (By similarity)
FH779_RS11725	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FH779_RS11735	ENOG4105CHR	reductase
FH779_RS11745	ENOG4105C84	Histidine ammonia-lyase
FH779_RS11750	ENOG4105P52	geranylgeranyl reductase
FH779_RS11760	ENOG4108YY1	This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site (By similarity)
FH779_RS11765	ENOG4105CSR	polyphosphate kinase 2
FH779_RS11770	ENOG4105CSR	polyphosphate kinase 2
FH779_RS11775	ENOG4105CSR	polyphosphate kinase 2
FH779_RS11790	ENOG4108KF3	Electron transport protein SCO1 SenC
FH779_RS11795	ENOG4105NF4	modulator of drug activity
FH779_RS11805	ENOG4105CMU	LysR family (Transcriptional regulator
FH779_RS11815	ENOG4105ENE	Histidine kinase
FH779_RS11830	ENOG410635A	Membrane
FH779_RS11845	ENOG4107EER	Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component (By similarity)
FH779_RS11860	ENOG4105C11	sulfate adenylyltransferase), subunit 2
FH779_RS11865	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
FH779_RS11890	ENOG4105C6P	ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner (By similarity)
FH779_RS11905	ENOG4105CPK	Glycosyl transferase (Group 1
FH779_RS11910	ENOG4107QK9	Beta-lactamase
FH779_RS11915	ENOG4105D17	glycoside hydrolase, family 3 domain protein
FH779_RS11920	ENOG4105DU1	integral membrane protein, terc
FH779_RS11935	ENOG4105EBA	Specifically methylates the adenine in position 1618 of 23S rRNA (By similarity)
FH779_RS11950	ENOG41065RQ	ADP-ribosylation crystallin J1
FH779_RS11955	ENOG4105VYA	Uncharacterized conserved protein (DUF2132)
FH779_RS11965	ENOG4105C12	Phosphoribosylglycinamide synthetase
FH779_RS11980	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
FH779_RS11985	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
FH779_RS11990	ENOG4107QUV	Domain protein
FH779_RS12030	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
FH779_RS12045	ENOG4107QIK	phosphoribosylformylglycinamidine synthase
FH779_RS12055	ENOG4105E0M	Sulfatase
FH779_RS12060	ENOG4105CBD	Diacylglycerol kinase
FH779_RS12065	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FH779_RS12070	ENOG4105GR3	Histidine kinase
FH779_RS12080	ENOG4105C5H	ABC transporter
FH779_RS12085	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FH779_RS12100	ENOG4105D9K	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions (By similarity)
FH779_RS12110	ENOG4108R80	One of the components of the high-affinity ATP-driven potassium transport (or KDP) system, which catalyzes the hydrolysis of ATP coupled with the exchange of hydrogen and potassium ions. The C subunit may be involved in assembly of the KDP complex (By similarity)
FH779_RS12120	ENOG4105C08	Histidine kinase
FH779_RS12125	ENOG4105BZU	Histidine kinase
FH779_RS12195	ENOG4105C3H	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
FH779_RS12250	ENOG4105DGM	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
FH779_RS12280	ENOG4105CDY	transcriptional regulatory protein
FH779_RS12285	ENOG4105DGW	oligopeptidase A
FH779_RS12300	ENOG4105DFU	Cell wall formation (By similarity)
FH779_RS12310	ENOG4105KPY	Small multidrug resistance protein
FH779_RS12320	ENOG4105DUF	Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively (By similarity)
FH779_RS12385	ENOG4105EYW	Ion transport protein
FH779_RS12390	ENOG4107U9T	Pfam:Ribonuclease_BN
FH779_RS12395	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
FH779_RS12405	ENOG4108V82	Pyrophosphatase that hydrolyzes non-canonical purine nucleotides such as XTP and ITP dITP to their respective monophosphate derivatives. Might exclude non-canonical purines from DNA precursor pool, thus preventing their incorporation into DNA and avoiding chromosomal lesions (By similarity)
FH779_RS12410	ENOG4105IES	Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA (By similarity)
FH779_RS12415	ENOG4105EYH	Exonuclease
FH779_RS12455	ENOG4108IUZ	ABC transporter
FH779_RS12470	ENOG4105EHZ	conserved protein UCP016719
FH779_RS12520	ENOG4105CI3	gtp-binding protein typa
FH779_RS12535	ENOG4108HRK	Histidine kinase
FH779_RS12540	ENOG4105DY9	regulatoR
FH779_RS12575	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
FH779_RS12580	ENOG4105VEJ	Heat shock protein
FH779_RS12590	ENOG4107RH7	Nicotinate phosphoribosyltransferase
FH779_RS12600	ENOG4107RAQ	aminopeptidase
FH779_RS12605	ENOG41080B9	Binds together with S18 to 16S ribosomal RNA (By similarity)
FH779_RS12610	ENOG4105VH8	Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit (By similarity)
FH779_RS12615	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
FH779_RS12625	ENOG4105C2F	Histidine kinase
FH779_RS12630	ENOG4108NEV	two component transcriptional regulator, LytTR family
FH779_RS12635	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
FH779_RS12650	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
FH779_RS12660	ENOG4105C1G	acyl-Coa dehydrogenase
FH779_RS12665	ENOG4105ERH	Fumarylacetoacetate hydrolase
FH779_RS12670	ENOG4108UM5	This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly (By similarity)
FH779_RS12675	ENOG4108UJD	30S ribosomal protein S9
FH779_RS12680	ENOG4105CE9	30S ribosomal protein S2
FH779_RS12685	ENOG4105CU7	Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome (By similarity)
FH779_RS12695	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
FH779_RS12710	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
FH779_RS12725	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
FH779_RS12730	ENOG4108MCI	Transcriptional regulator, ARAC family
FH779_RS12760	ENOG4105EH2	Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) (By similarity)
FH779_RS12770	ENOG4105CKJ	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing (By similarity)
FH779_RS12775	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
FH779_RS12795	ENOG4105CI2	imidazolone-5-propionate hydrolase
FH779_RS12810	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
FH779_RS12825	ENOG4107SN7	NLP P60 protein
FH779_RS12835	ENOG4108IQF	Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA (By similarity)
FH779_RS12845	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
FH779_RS12875	ENOG4108V0P	LemA family
FH779_RS12885	ENOG4105DF6	Fe-S oxidoreductase
FH779_RS12895	ENOG4105DF6	Fe-S oxidoreductase
FH779_RS12905	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
FH779_RS12915	ENOG4105KME	endoribonuclease L-psp
FH779_RS12925	ENOG4105CEZ	Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) (By similarity)
FH779_RS12935	ENOG4105WXV	50S ribosomal protein L32
FH779_RS12940	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
FH779_RS12945	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
FH779_RS12950	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
FH779_RS12960	ENOG4105CHN	ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP (By similarity)
FH779_RS12975	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FH779_RS12980	ENOG4105CNI	cell division protein FtsW
FH779_RS13000	ENOG4105DFF	Rod shape-determining protein mreb
FH779_RS13010	ENOG4105EEI	dihydropteroate synthase
FH779_RS13020	ENOG4105CII	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision (By similarity)
FH779_RS13025	ENOG4105D7A	ATP-binding protein
FH779_RS13040	ENOG4105EBW	Rhomboid-type serine protease that catalyzes intramembrane proteolysis (By similarity)
FH779_RS13045	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
FH779_RS13050	ENOG4105CK7	Sodium proline symporter
FH779_RS13055	ENOG4105C7Z	Conserved Protein
FH779_RS13060	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
FH779_RS13065	ENOG4105DWP	Membrane
FH779_RS13085	ENOG4105E1F	short-chain dehydrogenase reductase
FH779_RS13130	ENOG4107T7F	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
FH779_RS13140	ENOG4105C07	amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) (By similarity)
FH779_RS13175	ENOG4105CP4	Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth (By similarity)
FH779_RS13195	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
FH779_RS13205	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
FH779_RS13210	ENOG4105CPF	Cell wall formation (By similarity)
FH779_RS13215	ENOG4105D9P	serine threonine protein kinase
FH779_RS13220	ENOG4105C34	Pseudouridine synthase
FH779_RS13225	ENOG4105C1J	atp-dependent rna helicase
FH779_RS13245	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
FH779_RS13260	ENOG4105CII	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision (By similarity)
FH779_RS13265	ENOG4107R2I	The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. The AddA nuclease domain is required for chi fragment generation
FH779_RS13300	ENOG4105CMR	udp-glucose 4-epimerase
FH779_RS13320	ENOG4105C0G	Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives (By similarity)
FH779_RS13335	ENOG4105CEV	competence damage-inducible protein
FH779_RS13350	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FH779_RS13360	ENOG4108ZEY	Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its highly electrophilic allylic isomer, dimethylallyl diphosphate (DMAPP) (By similarity)
FH779_RS13365	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
FH779_RS13370	ENOG4105KEM	Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation (By similarity)
FH779_RS13375	ENOG4105C3H	Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins (By similarity)
FH779_RS13385	ENOG4105KNE	Phosphatidate cytidylyltransferase
FH779_RS13390	ENOG41071I4	Phosphatidylserine decarboxylase proenzyme
FH779_RS13405	ENOG4105F3K	May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO (By similarity)
FH779_RS13410	ENOG4107RJ1	sodium solute
FH779_RS13415	ENOG4105II7	pyrroline-5-carboxylate reductase
FH779_RS13425	ENOG4105C2V	Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) (By similarity)
FH779_RS13440	ENOG4105C2V	Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) (By similarity)
FH779_RS13455	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FH779_RS13490	ENOG41080WS	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
FH779_RS13495	ENOG4105C9R	An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate (By similarity). It may play a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control
FH779_RS13505	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
FH779_RS13520	ENOG4105D4P	Coproporphyrinogen iii oxidase
FH779_RS13525	ENOG4105CXR	Phospho-2-dehydro-3-deoxyoctonate aldolase
FH779_RS13550	ENOG4105CAK	Cell division ATP-binding protein ftsE
FH779_RS13555	ENOG4105VG0	50S ribosomal protein l34
FH779_RS13560	ENOG4105C24	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FH779_RS13570	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
FH779_RS13575	ENOG4105CN1	protease
FH779_RS13580	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
FH779_RS13595	ENOG4105FQP	Beta-lactamase
FH779_RS13600	ENOG4105FE8	tRNA (Guanosine-2'-O-)-methyltransferase
FH779_RS13610	ENOG4105D2N	Aldolase
FH779_RS13615	ENOG4108IDZ	Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA (By similarity)
FH779_RS13645	ENOG4107QJZ	Glycosyl transferase, family 2
FH779_RS13655	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FH779_RS13660	ENOG4105BZU	Histidine kinase
FH779_RS13670	ENOG4105BZU	Histidine kinase
FH779_RS13680	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
FH779_RS13685	ENOG4108UHF	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
FH779_RS13745	ENOG4105DZ0	fad dependent oxidoreductase
FH779_RS13755	ENOG4105WMR	Protein CrcB homolog
FH779_RS13795	ENOG4105C0R	drug resistance transporter emrb qaca subfamily
FH779_RS13815	ENOG4108ZGB	N-(5'-phosphoribosyl)anthranilate isomerase
FH779_RS13820	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
FH779_RS13840	ENOG4105C4P	Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template (By similarity)
FH779_RS13865	ENOG4105C5H	ABC transporter
FH779_RS13910	ENOG4105E6M	Sulphatase-modifying factor protein
FH779_RS13930	ENOG4105CIW	Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine (By similarity)
FH779_RS13935	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
FH779_RS13965	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
FH779_RS13970	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
FH779_RS13980	ENOG4105MQS	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FH779_RS13985	ENOG4105CQI	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate (By similarity)
FH779_RS13990	ENOG4105CYQ	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) (By similarity)
FH779_RS14000	ENOG4105DWT	malate dehydrogenase (quinone)
FH779_RS14010	ENOG4105KTH	gatB Yqey
FH779_RS14015	ENOG4105CDK	Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity (By similarity)
FH779_RS14020	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
FH779_RS14030	ENOG4105DFU	Cell wall formation (By similarity)
FH779_RS14035	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
FH779_RS14040	ENOG4105CNI	cell division protein FtsW
FH779_RS14045	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
FH779_RS14050	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
FH779_RS14055	ENOG4107EEN	Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan (By similarity)
FH779_RS14060	ENOG4105CJN	penicillin-binding protein
FH779_RS14070	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
FH779_RS14075	ENOG4107YM1	mraZ protein
FH779_RS14085	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
FH779_RS14095	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
FH779_RS14100	ENOG4105D1H	recombination factor protein RarA
FH779_RS14115	ENOG4105VAS	Could be involved in insertion of integral membrane proteins into the membrane (By similarity)
FH779_RS14120	ENOG4107QZC	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
FH779_RS14130	ENOG4107RNH	Outer membrane receptor FepA
FH779_RS14175	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FH779_RS14195	ENOG4105KRQ	Addiction module toxin, Txe YoeB family
FH779_RS14210	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FH779_RS14230	ENOG4105KRQ	Addiction module toxin, Txe YoeB family
FH779_RS14250	ENOG4105C90	Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS (By similarity)
FH779_RS14270	ENOG4105CGK	Exodeoxyribonuclease III
FH779_RS14295	ENOG41068WN	
FH779_RS14305	ENOG4105C13	Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC-XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids (By similarity)
FH779_RS14310	ENOG4105CN1	protease
FH779_RS14315	ENOG4105D1W	Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate (By similarity)
FH779_RS14335	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
FH779_RS14345	ENOG4106H78	methyltransferase
FH779_RS14360	ENOG4108V1T	peptidylprolyl cis-trans isomerase
FH779_RS14370	ENOG4105C6E	dna polymerase iii
FH779_RS14375	ENOG4105ID8	Transcriptional regulator, ARAC family
FH779_RS14385	ENOG4105DZC	cytosine deaminase
FH779_RS14390	ENOG4107SNB	ankyrin repeat protein YahD
FH779_RS14395	ENOG4105DZC	cytosine deaminase
FH779_RS14405	ENOG4105CNU	cell division protein FtsK
FH779_RS14415	ENOG4108M8S	permease YjgP YjgQ family protein
FH779_RS14420	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
FH779_RS14430	ENOG4105FDR	Membrane
FH779_RS14440	ENOG4105CAV	thus facilitating recognition of the initiation point. It is needed to translate mRNA with a short Shine-Dalgarno (SD) purine-rich sequence (By similarity)
FH779_RS14455	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
FH779_RS14460	ENOG4105C5H	ABC transporter
FH779_RS14470	ENOG4108NEV	two component transcriptional regulator, LytTR family
FH779_RS14485	ENOG4105C7D	DNA gyrase negatively supercoils closed circular double- stranded DNA in an ATP-dependent manner and also catalyzes the interconversion of other topological isomers of double-stranded DNA rings, including catenanes and knotted rings (By similarity)
FH779_RS14490	ENOG4105D28	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
FH779_RS14515	ENOG4105C2N	RNA methyltransferase TrmH family group 3
FH779_RS14535	ENOG4108YYV	Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis (By similarity)
FH779_RS14540	ENOG4105EAA	nucleoside
FH779_RS14550	ENOG4105C10	Electron transfer flavoprotein
FH779_RS14560	ENOG4105DCX	Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. Together with TatB, TatC is part of a receptor directly interacting with Tat signal peptides (By similarity)
FH779_RS14565	ENOG4105C2X	Arabinose 5-phosphate isomerase
FH779_RS14570	ENOG4105C9U	ATP-dependent DNA helicase RecQ
FH779_RS14575	ENOG4105CJI	Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate (By similarity)
FH779_RS14590	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
FH779_RS14610	ENOG4105C2M	dna polymerase I
FH779_RS14615	ENOG4108ZIT	Ferredoxin, 2FE-2S
FH779_RS14630	ENOG4105CAY	ferredoxin--nadp reductase
FH779_RS14635	ENOG4105KVH	Transcriptional regulator
FH779_RS14655	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
FH779_RS14660	ENOG4105DYT	3-hydroxyacyl-CoA dehydrogenase
FH779_RS14670	ENOG4105E26	Catalyzes the methyl esterification of L-isoaspartyl residues in peptides and proteins that result from spontaneous decomposition of normal L-aspartyl and L-asparaginyl residues. It plays a role in the repair and or degradation of damaged proteins (By similarity)
FH779_RS14680	ENOG4105GR3	Histidine kinase
FH779_RS14685	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FH779_RS14690	ENOG4105C5W	Aldolase
FH779_RS14700	ENOG4105C28	cystathionine
FH779_RS14715	ENOG4105C1J	atp-dependent rna helicase
FH779_RS14720	ENOG4108IJ0	Aspartate ammonia-lyase
FH779_RS14745	ENOG41087YS	Phage shock protein A
FH779_RS14765	ENOG4105CKJ	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing (By similarity)
FH779_RS14775	ENOG4108S2Y	peptide Chain Release factor
FH779_RS14810	ENOG4105C4S	Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner (By similarity)
FH779_RS14825	ENOG4105C5I	Dehydrogenase
FH779_RS14855	ENOG410902V	Modulates RecA activity (By similarity)
FH779_RS14865	ENOG4105DJV	ribulose-phosphate 3-epimerase
FH779_RS14880	ENOG4105CJW	magnesium transporter
FH779_RS14885	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
FH779_RS14890	ENOG41088SP	formiminoglutamate hydrolase
FH779_RS14895	ENOG4105EN6	Membrane
FH779_RS14900	ENOG4105EN6	Membrane
FH779_RS14955	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
FH779_RS14960	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
FH779_RS14970	ENOG4105D3C	The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters (By similarity)
FH779_RS14975	ENOG4106HB6	Alpha beta hydrolase
FH779_RS14985	ENOG4105C65	Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism (By similarity)
FH779_RS14990	ENOG4105J80	Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex (By similarity)
FH779_RS14995	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
FH779_RS15000	ENOG4107Z4P	F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation (By similarity)
FH779_RS15005	ENOG4107Z65	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
FH779_RS15010	ENOG4105VHG	atp synthase
FH779_RS15015	ENOG4105EE4	it plays a direct role in the translocation of protons across the membrane (By similarity)
FH779_RS15030	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
FH779_RS15065	ENOG4105C8N	cysteinyl-tRNA synthetase
FH779_RS15070	ENOG4105EUJ	GTP cyclohydrolase i
FH779_RS15075	ENOG4105C84	Histidine ammonia-lyase
FH779_RS15090	ENOG4105CGP	Urocanate hydratase
FH779_RS15095	ENOG4105EUB	pirin domain protein
FH779_RS15100	ENOG410830R	acetyltransferase
FH779_RS15110	ENOG4105CFB	Gamma-glutamyltranspeptidase (EC 2.3.2.2)
FH779_RS15115	ENOG4105CHI	Involved in the active translocation of vitamin B12 (cyanocobalamin) across the outer membrane to the periplasmic space. It derives its energy for transport by interacting with the trans-periplasmic membrane protein TonB (By similarity)
FH779_RS15120	ENOG4107QHU	One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex (By similarity)
FH779_RS15125	ENOG4105CHV	Transcription elongation factor NusA
FH779_RS15130	ENOG41090IP	Required for maturation of 30S ribosomal subunits (By similarity)
FH779_RS15140	ENOG4105CUY	Mechanosensitive ion channel
FH779_RS15145	ENOG4105CSZ	Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate (By similarity)
FH779_RS15150	ENOG4105EV9	Alpha Beta Hydrolase
FH779_RS15160	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FH779_RS15185	ENOG41072GX	Peptidase M22 Glycoprotease
FH779_RS15190	ENOG4105CAJ	Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain (By similarity)
FH779_RS15210	ENOG4107RA1	nh(3)-dependent nad( ) synthetase
FH779_RS15225	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
FH779_RS15235	ENOG4105KA4	The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB (By similarity)
FH779_RS15245	ENOG4105FQP	Beta-lactamase
FH779_RS15250	ENOG4105FQP	Beta-lactamase
FH779_RS15255	ENOG4108K2B	transcriptional regulator
FH779_RS15270	ENOG4105C58	cytochrome c oxidase accessory protein ccog
FH779_RS15275	ENOG4105D6P	C-type cytochrome. Part of the cbb3-type cytochrome c oxidase complex (By similarity)
FH779_RS15310	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
FH779_RS15320	ENOG4105E21	Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity (By similarity)
FH779_RS15325	ENOG4105CEK	Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine (By similarity)
FH779_RS15330	ENOG4105CIH	Imidazole acetol-phosphate transaminase
FH779_RS15335	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
FH779_RS15350	ENOG4105CJV	Phosphoribosylformimino-5-aminoimidazole carboxamide ribotide isomerase
FH779_RS15360	ENOG4105C0S	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit (By similarity)
FH779_RS15365	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
FH779_RS15385	ENOG41082IR	Excinuclease ABC C subunit domain protein
FH779_RS15390	ENOG4105CJ2	(LipO)protein
FH779_RS15435	ENOG4105KVH	Transcriptional regulator
FH779_RS15455	ENOG4105K5M	30s ribosomal protein S16
FH779_RS15460	ENOG4107YAY	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
FH779_RS15465	ENOG4105CX6	glutaminyL-tRNA synthetase
FH779_RS15475	ENOG4105W5Q	DNA repair protein (RadC
FH779_RS15560	ENOG4105CUT	histidyl-tRNA synthetase
FH779_RS15565	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
FH779_RS15585	ENOG4105C27	TonB-dependent Receptor Plug
FH779_RS15615	ENOG4105F6H	The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate (By similarity)
FH779_RS15620	ENOG4105E2D	ec 3.2.1.52
FH779_RS15630	ENOG4107P5I	polyketide synthase
FH779_RS15635	ENOG4105D7N	magnesium and cobalt transport protein CorA
FH779_RS15640	ENOG4105DA0	Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) (By similarity)
FH779_RS15655	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
FH779_RS15660	ENOG41074B2	UPF0747 protein
FH779_RS15690	ENOG4108Z03	MAF-like protein
FH779_RS15695	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
FH779_RS15705	ENOG4108HYK	gCN5-related N-acetyltransferase
FH779_RS15710	ENOG4105VRT	cytoplasmic protein
FH779_RS15720	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
FH779_RS15725	ENOG4107ZT5	Thiol disulfide interchange protein
FH779_RS15730	ENOG4105D7Z	glutathione synthase
FH779_RS15755	ENOG4107RNH	Outer membrane receptor FepA
FH779_RS15765	ENOG4105CRQ	synthase (Component I)
FH779_RS15785	ENOG4107TCE	N-acetyltransferase
FH779_RS15795	ENOG4105D1F	ATP-binding protein
FH779_RS15800	ENOG41083MR	nifu domain-containing protein
FH779_RS15810	ENOG4108R4Z	Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine (By similarity)
FH779_RS15845	ENOG4105DQR	SNARE associated Golgi
FH779_RS15850	ENOG4105DQR	SNARE associated Golgi
FH779_RS15855	ENOG41080R2	UPF0102 protein
FH779_RS15860	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
FH779_RS15865	ENOG4105EBE	Peptidase U61, LD-carboxypeptidase A
FH779_RS15890	ENOG4108IYU	L-aspartate oxidase
FH779_RS15895	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
FH779_RS15905	ENOG4108DJF	Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) (By similarity)
FH779_RS15915	ENOG4107UGT	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
FH779_RS15935	ENOG4105D64	Mechanosensitive ion channel
FH779_RS15940	ENOG4105UYK	outer membrane protein a
FH779_RS15945	ENOG4105C6U	Exchanges the guanine residue with 7-aminomethyl-7- deazaguanine in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). After this exchange, a cyclopentendiol moiety is attached to the 7-aminomethyl group of 7-deazaguanine, resulting in the hypermodified nucleoside queuosine (Q) (7-(((4,5-cis- dihydroxy-2-cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) (By similarity)
FH779_RS15960	ENOG4105C22	threonyL-tRNA synthetase
FH779_RS15965	ENOG4108UUX	IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins (By similarity)
FH779_RS15970	ENOG4105VJV	50s ribosomal protein L35
FH779_RS15975	ENOG4108YZX	Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit (By similarity)
FH779_RS15985	ENOG4105CZ7	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
FH779_RS16020	ENOG4105CSV	Glutaminase
FH779_RS16025	ENOG4105CAT	Cytidine monophosphate kinase
FH779_RS16040	ENOG4105CUY	Mechanosensitive ion channel
FH779_RS16045	ENOG4105DUN	Mediates zinc uptake. May also transport other divalent cations (By similarity)
FH779_RS16070	ENOG4108H5C	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate (By similarity)
FH779_RS16085	ENOG4105C68	Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage (By similarity)
FH779_RS16090	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
FH779_RS16100	ENOG4105CSM	endonuclease III
FH779_RS16140	ENOG4105CY8	phosphoribosylaminoimidazole carboxylase atpase subunit
FH779_RS16145	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
FH779_RS16160	ENOG4107UUG	Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins (By similarity)
FH779_RS16180	ENOG4105BZ1	(ABC) transporter
FH779_RS16190	ENOG4105D7W	serine acetyltransferase
FH779_RS16200	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
FH779_RS16210	ENOG4105D0V	Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
FH779_RS16220	ENOG4105EMN	RNA polymerase sigma factor
FH779_RS16235	ENOG4105EGY	DNA internalization-related competence protein ComEC Rec2
FH779_RS16245	ENOG4105DUX	Transporter
FH779_RS16250	ENOG4105DUX	Transporter
FH779_RS16255	ENOG4105C5Z	peptidase
FH779_RS16300	ENOG4105CGM	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
FH779_RS16315	ENOG4105CNR	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FH779_RS16320	ENOG4105C8S	subunit m
FH779_RS16325	ENOG4105D65	subunit l
FH779_RS16330	ENOG4108373	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FH779_RS16335	ENOG4105DF2	NADH dehydrogenase subunit j
FH779_RS16340	ENOG4105P3U	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FH779_RS16345	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
FH779_RS16355	ENOG4107QIZ	NADH dehydrogenase
FH779_RS16360	ENOG4105GKE	subunit e
FH779_RS16365	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FH779_RS16370	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FH779_RS16375	ENOG4105ES3	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
FH779_RS16380	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
FH779_RS16385	ENOG4108JA2	transcriptioN-repair coupling factor
FH779_RS16390	ENOG4105C01	Dihydroxy-acid dehydratase
FH779_RS16395	ENOG4105C7K	acetolactate synthase
FH779_RS16405	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
FH779_RS16410	ENOG4105C7B	Threonine dehydratase
FH779_RS16420	ENOG4107RDY	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
FH779_RS16425	ENOG4105CFH	Aspartokinase
FH779_RS16455	ENOG4105CCA	Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle (By similarity)
FH779_RS16460	ENOG4105NHU	Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group (By similarity)
FH779_RS16485	ENOG4105KW6	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance (By similarity)
FH779_RS16490	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
FH779_RS16515	ENOG4108RWN	rrna methyltransferase
FH779_RS16520	ENOG4105CFP	Peptidase U32
FH779_RS16540	ENOG4105W5Q	DNA repair protein (RadC
FH779_RS16595	ENOG4105C26	Dehydrogenase
FH779_RS16605	ENOG4105C20	Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) (By similarity)
FH779_RS16610	ENOG4105C8F	Beta-lactamase domain protein
FH779_RS16615	ENOG4105MA4	psp1 domain protein
FH779_RS16620	ENOG410647Z	gliding motility-associated lipoprotein GldH
FH779_RS16625	ENOG4108JQC	penicillin-binding protein 1A
FH779_RS16635	ENOG41080VW	acetyltransferase
FH779_RS16640	ENOG4105CKH	Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation (By similarity)
FH779_RS16655	ENOG4105VG1	fes assembly suf system protein
FH779_RS16670	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
FH779_RS16675	ENOG4105BZU	Histidine kinase
FH779_RS16685	ENOG4105C8T	Leucyl-tRNA synthetase
FH779_RS16690	ENOG4108Z12	YiaAB two helix domain-containing protein
FH779_RS16705	ENOG4105DSS	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation (By similarity)
FH779_RS16710	ENOG4108XM1	transcriptional regulator AsnC family
FH779_RS16770	ENOG4105DWV	Homoserine O-trans-acetylase
FH779_RS16785	ENOG4105C4J	Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits (By similarity)
FH779_RS16790	ENOG4105DTN	riboflavin biosynthesis protein ribF
FH779_RS16810	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
FH779_RS16815	ENOG4108Y6J	UPF0403 protein
FH779_RS16820	ENOG4105WG6	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
FH779_RS16830	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
FH779_RS16835	ENOG4105DY9	regulatoR
FH779_RS16845	ENOG4105C2F	Histidine kinase
FH779_RS16870	ENOG4107QVM	von Willebrand factor, type A
FH779_RS16890	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
FH779_RS16915	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
FH779_RS16920	ENOG4105C2J	ABC transporter
FH779_RS16925	ENOG4105BZA	Phosphoglycerate kinase
FH779_RS16930	ENOG4108YZG	isomerase
FH779_RS16935	ENOG4105CU9	asparagine synthetase A
FH779_RS16945	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
FH779_RS16975	ENOG4105CKD	glutathione-regulated potassium-efflux system protein
FH779_RS16980	ENOG4105P9C	Participates in cysteine desulfuration mediated by SufS. Cysteine desulfuration mobilizes sulfur from L-cysteine to yield L-alanine and constitutes an essential step in sulfur metabolism for biosynthesis of a variety of sulfur-containing biomolecules. Functions as a sulfur acceptor for SufS, by mediating the direct transfer of the sulfur atom from the S-sulfanylcysteine of SufS, an intermediate product of cysteine desulfuration process (By similarity)
FH779_RS16985	ENOG4105CBD	Diacylglycerol kinase
FH779_RS16990	ENOG4108JQ1	Dehydrogenase
FH779_RS16995	ENOG4105DDZ	Methyltransferase required for the conversion of demethylmenaquinone (DMKH2) to menaquinone (MKH2) and the conversion of 2-polyprenyl-6-methoxy-1,4-benzoquinol (DDMQH2) to 2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinol (DMQH2) (By similarity)
FH779_RS17000	ENOG4105C2I	pirin domain protein
FH779_RS17010	ENOG4108ZG0	Ompa motb domain protein
FH779_RS17025	ENOG4107RE5	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
FH779_RS17030	ENOG41080AX	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
FH779_RS17035	ENOG4105D78	K07001 NTE family protein
FH779_RS17045	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
FH779_RS17050	ENOG4107T8J	thymidine kinase
FH779_RS17090	ENOG4105BZU	Histidine kinase
FH779_RS17105	ENOG4105D3Q	Sugar transferase
FH779_RS17130	ENOG4108TJN	glycosyl transferase group 1
FH779_RS17170	ENOG4107ZIF	6-carboxy-5,6,7,8-tetrahydropterin synthase
FH779_RS17175	ENOG4105MJ2	Competence protein
FH779_RS17200	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
FH779_RS17225	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
FH779_RS17230	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
FH779_RS17235	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
FH779_RS17245	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
FH779_RS17250	ENOG4108R6K	riboflavin synthase, subunit alpha
FH779_RS17260	ENOG4107S47	Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC) (By similarity)
FH779_RS17265	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
FH779_RS17270	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
FH779_RS17275	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
FH779_RS17280	ENOG4108ZBM	Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Also processes some mRNAs, and tRNAs when they are encoded in the rRNA operon (By similarity)
FH779_RS17295	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
FH779_RS17300	ENOG4107ZIC	Glycerol-3-phosphate cytidylyltransferase
FH779_RS17310	ENOG4107QQG	Dehydrogenase
FH779_RS17315	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
FH779_RS17320	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
FH779_RS17325	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
FH779_RS17330	ENOG4108IAJ	Nad-dependent epimerase dehydratase
FH779_RS17340	ENOG4107QQG	Dehydrogenase
FH779_RS17370	ENOG4107UU3	sucrose-phosphate synthase (EC 2.4.1.14)
FH779_RS17395	ENOG4105CAQ	asparagine synthetase
FH779_RS17405	ENOG4105D3Q	Sugar transferase
FH779_RS17410	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
FH779_RS17530	ENOG4105D6J	arsenicaL-resistance protein