locus-tag	class	description
CLLT_RS00010	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)
CLLT_RS00015	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)
CLLT_RS00020	ENOG4105EKD	Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism (By similarity)
CLLT_RS00030	ENOG4105CSD	Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) (By similarity)
CLLT_RS00050	ENOG4108Z8G	Alkylphosphonate utilization operon protein PhnA
CLLT_RS00060	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
CLLT_RS00065	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
CLLT_RS00070	ENOG4105K5T	PilT protein
CLLT_RS00075	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
CLLT_RS00080	ENOG4108317	Binds directly to 16S ribosomal RNA (By similarity)
CLLT_RS00090	ENOG4105FE9	pseudouridine synthase
CLLT_RS00095	ENOG4105CN5	Metallo-Beta-Lactamase
CLLT_RS00110	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
CLLT_RS00120	ENOG4105EI2	Pseudouridine synthase
CLLT_RS00125	ENOG4107QTF	adenylosuccinate lyase
CLLT_RS00130	ENOG4105BZH	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
CLLT_RS00135	ENOG4105EPD	Oligopeptide transporter, Opt family
CLLT_RS00140	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
CLLT_RS00145	ENOG4105C22	threonyL-tRNA synthetase
CLLT_RS00150	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)
CLLT_RS00160	ENOG4105D29	Helix-turn-helix type 11 domain protein
CLLT_RS00170	ENOG4107R4Q	Functions as an ATPase. May play a role in metal insertion (metal-chelatase) or as a chaperone (By similarity)
CLLT_RS00175	ENOG41084M8	50s ribosomal protein L35
CLLT_RS00180	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)
CLLT_RS00195	ENOG4105DIK	(ABC) transporter
CLLT_RS00210	ENOG4105EKE	dihydroorotase
CLLT_RS00225	ENOG4105DIJ	Phosphoethanolamine transferase
CLLT_RS00230	ENOG4105CGK	Exodeoxyribonuclease III
CLLT_RS00245	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
CLLT_RS00250	ENOG4108RDD	Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine (By similarity)
CLLT_RS00255	ENOG4105CK4	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
CLLT_RS00260	ENOG4105CEE	C4-dicarboxylate transporter
CLLT_RS00265	ENOG4105CXB	phosphoribosylaminoimidazole synthetase
CLLT_RS00275	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)
CLLT_RS00280	ENOG4108UR8	BAX protein
CLLT_RS00295	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
CLLT_RS00300	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)
CLLT_RS00305	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)
CLLT_RS00310	ENOG4105KZZ	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)
CLLT_RS00315	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
CLLT_RS00320	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
CLLT_RS00325	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)
CLLT_RS00330	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
CLLT_RS00335	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
CLLT_RS00340	ENOG41084HJ	50s ribosomal protein l29
CLLT_RS00345	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
CLLT_RS00350	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
CLLT_RS00355	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
CLLT_RS00360	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
CLLT_RS00365	ENOG41082QR	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)
CLLT_RS00370	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)
CLLT_RS00375	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)
CLLT_RS00380	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)
CLLT_RS00385	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)
CLLT_RS00390	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
CLLT_RS00395	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)
CLLT_RS00400	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
CLLT_RS00405	ENOG4107RB3	L-asparaginase
CLLT_RS00410	ENOG4108RAC	Rubrerythrin
CLLT_RS00425	ENOG4105C44	Serine transporter
CLLT_RS00430	ENOG4105EJQ	L-serine dehydratase
CLLT_RS00435	ENOG4105CA1	Removes the N-terminal methionine from nascent proteins (By similarity)
CLLT_RS00440	ENOG4108N3W	hemolysin secretion protein
CLLT_RS00445	ENOG4105CA0	peroxidase
CLLT_RS00455	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)
CLLT_RS00460	ENOG41067V7	50S ribosomal protein L36
CLLT_RS00465	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
CLLT_RS00470	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)
CLLT_RS00475	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)
CLLT_RS00485	ENOG4108ZT0	50S ribosomal protein l17
CLLT_RS00490	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)
CLLT_RS00500	ENOG4105ECC	imidazole-glycerol-phosphate dehydratase
CLLT_RS00525	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)
CLLT_RS00530	ENOG4105K8F	Phosphoribosyl-amp cyclohydrolase
CLLT_RS00535	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS00545	ENOG4105BZE	flagellar hook protein, FlgE
CLLT_RS00555	ENOG4105C2C	drug resistance transporter, Bcr CflA
CLLT_RS00560	ENOG41083MR	nifu domain-containing protein
CLLT_RS00570	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)
CLLT_RS00575	ENOG41084FT	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
CLLT_RS00590	ENOG4105CV1	Transketolase (EC 2.2.1.1)
CLLT_RS00595	ENOG4105CY3	ABC transporter, permease
CLLT_RS00600	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
CLLT_RS00620	ENOG4108Z7T	Destroys radicals which are normally produced within the cells and which are toxic to biological systems (By similarity)
CLLT_RS00640	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)
CLLT_RS00650	ENOG4108STX	response regulator
CLLT_RS00665	ENOG4105CEN	a g-specific adenine glycosylase
CLLT_RS00695	ENOG4107ZYR	domain protein
CLLT_RS00700	ENOG4105CZN	Potassium uptake protein
CLLT_RS00705	ENOG4105DS2	Anaerobic c4-dicarboxylate transporter
CLLT_RS00710	ENOG4108IJ0	Aspartate ammonia-lyase
CLLT_RS00715	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS00720	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS00730	ENOG41068HQ	Protein of unknown function (DUF493)
CLLT_RS00735	ENOG4108YXW	Together with MoaA, is involved in the conversion of 5'- GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
CLLT_RS00755	ENOG4105VIG	Sec-independent protein translocase protein TatC
CLLT_RS00770	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
CLLT_RS00775	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)
CLLT_RS00785	ENOG4105VS8	Flagellar biosynthetic protein fliq
CLLT_RS00800	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
CLLT_RS00810	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)
CLLT_RS00815	ENOG4105C73	Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone (By similarity)
CLLT_RS00860	ENOG4105DD5	Flagellar motor switch protein
CLLT_RS00870	ENOG4107R33	ppx gppa phosphatase
CLLT_RS00875	ENOG4105K5D	4fe-4S ferredoxin iroN-sulfur binding
CLLT_RS00890	ENOG4105K7Z	Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP (By similarity)
CLLT_RS00895	ENOG4105CA0	peroxidase
CLLT_RS00920	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
CLLT_RS00925	ENOG4105K46	50S ribosomal protein l27
CLLT_RS00930	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
CLLT_RS00935	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)
CLLT_RS00940	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
CLLT_RS00945	ENOG4107QJE	Chromosome Partitioning Protein
CLLT_RS00950	ENOG4105FA0	parb-like partition protein
CLLT_RS00960	ENOG4105YF2	Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) (By similarity)
CLLT_RS00965	ENOG4105PQH	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)
CLLT_RS00970	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
CLLT_RS00975	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)
CLLT_RS00980	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)
CLLT_RS00985	ENOG41082MC	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
CLLT_RS00990	ENOG4105E02	MotA TolQ exbB proton channel
CLLT_RS00995	ENOG4105M8F	Biopolymer transport protein exbD tolR
CLLT_RS01010	ENOG4105KCK	Peptidoglycan-associated lipoprotein
CLLT_RS01025	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
CLLT_RS01030	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)
CLLT_RS01035	ENOG4105CB3	Required for the thiolation of cytidine in position 32 of tRNA, to form 2-thiocytidine (s(2)C32) (By similarity)
CLLT_RS01055	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
CLLT_RS01070	ENOG4108UXA	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
CLLT_RS01075	ENOG4107QTG	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)
CLLT_RS01080	ENOG4105E1Z	Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane
CLLT_RS01095	ENOG4105C7C	involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
CLLT_RS01105	ENOG4105D5I	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate (By similarity)
CLLT_RS01115	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)
CLLT_RS01125	ENOG4105K7D	Required for maturation of 30S ribosomal subunits (By similarity)
CLLT_RS01145	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)
CLLT_RS01150	ENOG4105D07	Signal peptide peptidase, SppA
CLLT_RS01155	ENOG4107SYB	Catalyzes the deamination of 5-methylthioadenosine and S-adenosyl-L-homocysteine into 5-methylthioinosine and S-inosyl-L- homocysteine, respectively. Is also able to deaminate adenosine (By similarity)
CLLT_RS01160	ENOG4108Z38	Catalyzes a trans-dehydration via an enolate intermediate (By similarity)
CLLT_RS01165	ENOG4105DC7	peptidase M24
CLLT_RS01170	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
CLLT_RS01175	ENOG4105FZW	flagellar biosynthesis regulator FlhF
CLLT_RS01180	ENOG4107R21	site-determining protein
CLLT_RS01190	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
CLLT_RS01195	ENOG4105D24	FliM is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
CLLT_RS01200	ENOG4105DD5	Flagellar motor switch protein
CLLT_RS01210	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
CLLT_RS01220	ENOG4108ZAI	phosphatidylglycerophosphatase a
CLLT_RS01225	ENOG4107RIQ	Sulfate adenylate transferase
CLLT_RS01235	ENOG4108UH8	Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) (By similarity)
CLLT_RS01240	ENOG4105D1F	ATP-binding protein
CLLT_RS01245	ENOG4105EJ3	Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA (By similarity)
CLLT_RS01250	ENOG4108RMU	ferritin dps family protein
CLLT_RS01255	ENOG4107QP8	phosphohexose isomerase
CLLT_RS01260	ENOG4105C3Y	UTP-glucose-1-phosphate uridylyltransferase
CLLT_RS01265	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
CLLT_RS01280	ENOG4105C5H	ABC transporter
CLLT_RS01290	ENOG4107QKV	phosphomannomutase
CLLT_RS01305	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
CLLT_RS01330	ENOG4105HMI	Membrane
CLLT_RS01335	ENOG410825D	TRANSCRIPTIONal REGULATOR, LysR family
CLLT_RS01345	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
CLLT_RS01355	ENOG4105CHR	reductase
CLLT_RS01360	ENOG410829W	Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein (By similarity)
CLLT_RS01365	ENOG4105X6C	Flagellar basal body-associated protein FliL
CLLT_RS01375	ENOG4105CH6	catalase
CLLT_RS01380	ENOG4105JXB	ankyrin repeat-containing protein
CLLT_RS01385	ENOG4105CH7	arginosuccinase
CLLT_RS01395	ENOG4105KME	endoribonuclease L-psp
CLLT_RS01400	ENOG4105CEE	C4-dicarboxylate transporter
CLLT_RS01410	ENOG4107RAW	3-carboxy-cis-cis-muconate cycloisomerase
CLLT_RS01415	ENOG4108PGP	mmge prpd family protein
CLLT_RS01420	ENOG4107K9B	ferrous iron transport protein
CLLT_RS01425	ENOG4105CE1	Ferrous iron transport protein b
CLLT_RS01430	ENOG4105ETU	transcriptional activator (TenA
CLLT_RS01435	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
CLLT_RS01440	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
CLLT_RS01445	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)
CLLT_RS01455	ENOG4105ED9	Protein of unknown function (DUF455)
CLLT_RS01470	ENOG4105ECX	polysaccharide export
CLLT_RS01475	ENOG4107V1M	polysaccharide export protein
CLLT_RS01480	ENOG4105C2X	Arabinose 5-phosphate isomerase
CLLT_RS01495	ENOG4107VDP	teichoic acid biosynthesis
CLLT_RS01500	ENOG4107VDP	teichoic acid biosynthesis
CLLT_RS01510	ENOG4108URP	Dtdp-4-dehydrorhamnose 3,5-epimerase
CLLT_RS01515	ENOG4105C30	Nad-dependent epimerase dehydratase
CLLT_RS01530	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
CLLT_RS01545	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
CLLT_RS01550	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
CLLT_RS01560	ENOG4105C6Y	Udp-glucose 6-dehydrogenase
CLLT_RS01575	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
CLLT_RS01580	ENOG4105C11	sulfate adenylyltransferase), subunit 2
CLLT_RS01585	ENOG4105C3T	may be the GTPase, regulating ATP sulfurylase activity (By similarity)
CLLT_RS01595	ENOG4107UCJ	Catalyzes the synthesis of activated sulfate (By similarity)
CLLT_RS01600	ENOG4108RNI	3'(2')5'-bisphosphate nucleotidase
CLLT_RS01610	ENOG4105E12	capsule polysaccharide
CLLT_RS01615	ENOG41084CK	capsule polysaccharide
CLLT_RS01640	ENOG4105CHV	Transcription elongation factor NusA
CLLT_RS01655	ENOG4105KB8	(LipO)protein
CLLT_RS01680	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
CLLT_RS01685	ENOG4108S24	Fumarate reduCtase
CLLT_RS01690	ENOG4105C00	Succinate dehydrogenase (Flavoprotein subunit)
CLLT_RS01695	ENOG4105E33	succinate dehydrogenase
CLLT_RS01715	ENOG4108WHG	pyridoxamine 5'-phosphate
CLLT_RS01720	ENOG4105NF4	modulator of drug activity
CLLT_RS01725	ENOG4105KVH	Transcriptional regulator
CLLT_RS01735	ENOG4105DQ4	alcohol dehydrogenase
CLLT_RS01740	ENOG4108F3G	Type I restriction-modification system, R subunit
CLLT_RS01750	ENOG4107UNZ	domain protein
CLLT_RS01760	ENOG4107R3N	Filamentation induced by cAMP protein fic
CLLT_RS01770	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
CLLT_RS01775	ENOG4108ZEX	molybdopterin converting factor, subunit 2
CLLT_RS01810	ENOG4108J2R	molybdopterin oxidoreductase
CLLT_RS01815	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
CLLT_RS01820	ENOG4105QAX	Iron-sulfur
CLLT_RS01825	ENOG4105F4R	Transcriptional regulator mode
CLLT_RS01830	ENOG4105VFE	sira family
CLLT_RS01840	ENOG4105C26	Dehydrogenase
CLLT_RS01845	ENOG4105CK7	Sodium proline symporter
CLLT_RS01855	ENOG41066VF	YeeE YedE family protein
CLLT_RS01865	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
CLLT_RS01885	ENOG4105C1M	carbamoyl-phosphate synthetase glutamine chain
CLLT_RS01940	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
CLLT_RS01945	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)
CLLT_RS01950	ENOG4108UJD	30S ribosomal protein S9
CLLT_RS01955	ENOG4108WHA	ompa motb domain protein
CLLT_RS01960	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
CLLT_RS01975	ENOG4105GVR	general secretion pathway protein D
CLLT_RS01985	ENOG4107QHF	type ii secretion system protein e
CLLT_RS01990	ENOG4105D7Q	type ii secretion system
CLLT_RS02020	ENOG4105YKR	
CLLT_RS02025	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
CLLT_RS02050	ENOG4105CG2	Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 (By similarity)
CLLT_RS02070	ENOG4105MHQ	Low-potential electron donor to a number of redox enzymes (By similarity)
CLLT_RS02095	ENOG4105E3S	small subunit
CLLT_RS02105	ENOG4105BZA	Phosphoglycerate kinase
CLLT_RS02110	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
CLLT_RS02145	ENOG4105C9Q	fumarate hydratase class II
CLLT_RS02150	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
CLLT_RS02160	ENOG4105DVY	radical SAM domain protein
CLLT_RS02165	ENOG4105C7N	Xanthine uracil vitamin C permease
CLLT_RS02175	ENOG4107QY8	reductase
CLLT_RS02195	ENOG4105YIC	Major outer membrane protein
CLLT_RS02200	ENOG410802Z	Protein of unknown function (DUF328)
CLLT_RS02225	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
CLLT_RS02245	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
CLLT_RS02250	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
CLLT_RS02255	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)
CLLT_RS02260	ENOG4108VZM	50s ribosomal protein L10
CLLT_RS02265	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)
CLLT_RS02270	ENOG4108IIJ	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
CLLT_RS02275	ENOG4105D27	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
CLLT_RS02280	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)
CLLT_RS02285	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)
CLLT_RS02290	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)
CLLT_RS02295	ENOG4105C37	(CBS) domain
CLLT_RS02300	ENOG4108DQG	in Escherichia coli SbmA is involved in uptake of microcin J25
CLLT_RS02305	ENOG4105CK7	Sodium proline symporter
CLLT_RS02315	ENOG4105E0C	molybdate abc transporter
CLLT_RS02350	ENOG41067XB	TonB family
CLLT_RS02355	ENOG4105M15	transport protein ExbD
CLLT_RS02360	ENOG4105M8K	biopolymer transport protein
CLLT_RS02365	ENOG4105D05	Receptor
CLLT_RS02370	ENOG4107QMP	dna polymerase iii subunits gamma and tau
CLLT_RS02375	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)
CLLT_RS02380	ENOG4105C59	p-type ATPase
CLLT_RS02395	ENOG4108ZI0	d,d-heptose 1,7-bisphosphate phosphatase
CLLT_RS02400	ENOG4105CUI	Catalyzes the interconversion between ADP-D-glycero- beta-D-manno-heptose and ADP-L-glycero-beta-D-manno-heptose via an epimerization at carbon 6 of the heptose (By similarity)
CLLT_RS02405	ENOG4105DW0	Catalyzes the ADP transfer to D-glycero-D-manno-heptose 1-phosphate, yielding ADP-D,D-heptose (By similarity)
CLLT_RS02410	ENOG4105F55	Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate (By similarity)
CLLT_RS02420	ENOG4107RSR	Malate quinone oxidoreductase
CLLT_RS02435	ENOG4108TX7	
CLLT_RS02445	ENOG410855J	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
CLLT_RS02465	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)
CLLT_RS02480	ENOG4105E2X	shikimate dehydrogenase
CLLT_RS02485	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)
CLLT_RS02500	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)
CLLT_RS02520	ENOG4105DN9	Na H antiporter
CLLT_RS02525	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
CLLT_RS02530	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)
CLLT_RS02550	ENOG4105E7H	involved in the assembly of LPS in the outer leaflet of the outer membrane. Determines N-hexane tolerance and is involved in outer membrane permeability. Essential for envelope biogenesis (By similarity)
CLLT_RS02560	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
CLLT_RS02630	ENOG4107QUV	Domain protein
CLLT_RS02640	ENOG4105ZGC	lipoprotein carrier protein
CLLT_RS02645	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
CLLT_RS02655	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
CLLT_RS02665	ENOG4105CFZ	Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III (By similarity)
CLLT_RS02670	ENOG41082XB	radical SAM domain protein
CLLT_RS02690	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)
CLLT_RS02700	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
CLLT_RS02705	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
CLLT_RS02715	ENOG4105C2W	permease
CLLT_RS02725	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)
CLLT_RS02730	ENOG4105M7K	Involved in the transcription termination process (By similarity)
CLLT_RS02735	ENOG4106EG9	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
CLLT_RS02745	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS02750	ENOG4105DC1	bifunctional purine biosynthesis protein purh
CLLT_RS02755	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)
CLLT_RS02760	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
CLLT_RS02775	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
CLLT_RS02790	ENOG4105VG0	50S ribosomal protein l34
CLLT_RS02810	ENOG4107YD3	Thioesterase
CLLT_RS02830	ENOG4108MR7	Arylsulfotransferase
CLLT_RS02835	ENOG4105DS2	Anaerobic c4-dicarboxylate transporter
CLLT_RS02840	ENOG4105CIN	aminoacyl-histidine dipeptidase
CLLT_RS02845	ENOG4105KK6	nuclease
CLLT_RS02860	ENOG4105PFA	Catalyzes the conversion of 5-hydroxyuridine (ho5U) to 5-methoxyuridine (mo5U) at position 34 in tRNA (By similarity)
CLLT_RS02875	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)
CLLT_RS02880	ENOG4105D0M	Protease HtpX homolog
CLLT_RS02890	ENOG4105C5H	ABC transporter
CLLT_RS02895	ENOG4107RN3	metallophosphoesterase
CLLT_RS02900	ENOG4105DJ4	phosphatidylserine decarboxylase
CLLT_RS02905	ENOG4105VM1	flagellar
CLLT_RS02930	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
CLLT_RS02945	ENOG4105C3F	Signal peptidase i
CLLT_RS02955	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)
CLLT_RS02970	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
CLLT_RS02990	ENOG4105CNI	cell division protein FtsW
CLLT_RS03230	ENOG4106050	phage regulatory protein, rha family
CLLT_RS03305	ENOG4105CDA	abc transporter atp-binding protein
CLLT_RS03310	ENOG4105E5Q	amino acid AbC transporter
CLLT_RS03330	ENOG4105DR5	peptidase
CLLT_RS03340	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
CLLT_RS03360	ENOG4105CNI	cell division protein FtsW
CLLT_RS03365	ENOG4105C34	Pseudouridine synthase
CLLT_RS03375	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
CLLT_RS03380	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
CLLT_RS03395	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
CLLT_RS03400	ENOG410692R	Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits (By similarity)
CLLT_RS03405	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)
CLLT_RS03410	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)
CLLT_RS03420	ENOG4105C5C	n-acetylmuramoyl-l-alanine amidase
CLLT_RS03435	ENOG4105DZP	Membrane-associated zinc metalloprotease
CLLT_RS03445	ENOG4105CAN	Short-chain dehydrogenase reductase Sdr
CLLT_RS03450	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
CLLT_RS03460	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
CLLT_RS03465	ENOG4105BZ1	(ABC) transporter
CLLT_RS03470	ENOG4105C8N	cysteinyl-tRNA synthetase
CLLT_RS03475	ENOG4105CJR	Integral membrane protein (MviN
CLLT_RS03485	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)
CLLT_RS03490	ENOG4105CPF	Cell wall formation (By similarity)
CLLT_RS03510	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
CLLT_RS03515	ENOG4105C6K	Malic enzyme
CLLT_RS03520	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
CLLT_RS03525	ENOG4105D01	(LipO)protein
CLLT_RS03535	ENOG4108UMI	ABC transporter, permease
CLLT_RS03540	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
CLLT_RS03555	ENOG4105F0N	pyrophosphate phospho-hydrolase
CLLT_RS03560	ENOG4105CC8	Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism (By similarity)
CLLT_RS03570	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)
CLLT_RS03575	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
CLLT_RS03585	ENOG4105F8V	Hydrolase, tatD family
CLLT_RS03590	ENOG4105E9H	Lytic Murein transglycosylase
CLLT_RS03595	ENOG4105K6T	rare lipoprotein A
CLLT_RS03615	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
CLLT_RS03630	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)
CLLT_RS03635	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)
CLLT_RS03645	ENOG4108PJD	permease
CLLT_RS03650	ENOG41085FC	arsR family transcriptional regulator
CLLT_RS03655	ENOG4105D4P	Coproporphyrinogen iii oxidase
CLLT_RS03665	ENOG4105CFH	Aspartokinase
CLLT_RS03680	ENOG4105EEI	dihydropteroate synthase
CLLT_RS03685	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)
CLLT_RS03690	ENOG4105DX0	Hemolysin A
CLLT_RS03700	ENOG4105DA6	Catalyzes the conversion of 5-methoxyuridine (mo5U) to uridine-5-oxyacetic acid (cmo5U) at position 34 in tRNA. May also participate in the methylation of uridine-5-oxyacetic acid (cmo5U) to uridine-5-oxyacetic acid methyl ester (mcmo5U) (By similarity)
CLLT_RS03705	ENOG4105C3G	gtp-binding protein
CLLT_RS03710	ENOG4105BZ6	Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides (By similarity)
CLLT_RS03720	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
CLLT_RS03730	ENOG4108YZG	isomerase
CLLT_RS03735	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
CLLT_RS03740	ENOG4105BZU	Histidine kinase
CLLT_RS03750	ENOG4105DKF	Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) (By similarity)
CLLT_RS03760	ENOG4105CB5	ATP-dependent DNA helicase recG
CLLT_RS03765	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
CLLT_RS03770	ENOG4105E5Q	amino acid AbC transporter
CLLT_RS03775	ENOG4105DRP	amino acid AbC transporter
CLLT_RS03785	ENOG4105CT1	(ABC) transporter
CLLT_RS03790	ENOG4105CSH	Transporter
CLLT_RS03800	ENOG4105D49	3-dehydroquinate synthase
CLLT_RS03810	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)
CLLT_RS03815	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)
CLLT_RS03820	ENOG4108RIR	Molybdenum cofactor biosynthesis protein
CLLT_RS03840	ENOG4105WMR	Protein CrcB homolog
CLLT_RS03845	ENOG4105E9Q	Acyl-transferase
CLLT_RS03855	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
CLLT_RS03870	ENOG4105CN1	protease
CLLT_RS03875	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
CLLT_RS03880	ENOG4105E3S	small subunit
CLLT_RS03885	ENOG4105DPX	Hydrogenase, large subunit
CLLT_RS03890	ENOG4105X7T	Ni Fe-hydrogenase, b-type cytochrome subunit
CLLT_RS03895	ENOG4108USZ	hydrogenase
CLLT_RS03940	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)
CLLT_RS03955	ENOG4108YYC	ycei family
CLLT_RS03960	ENOG4105FD2	Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) (By similarity)
CLLT_RS04000	ENOG4108EU4	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)
CLLT_RS04005	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
CLLT_RS04010	ENOG4105CVM	Molybdenum cofactor synthesis domain protein
CLLT_RS04035	ENOG4108UMA	3-octaprenyl-4-hydroxybenzoate carboxy-lyase
CLLT_RS04040	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
CLLT_RS04045	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
CLLT_RS04050	ENOG4105CUT	histidyl-tRNA synthetase
CLLT_RS04055	ENOG4105DP5	Catalyzes the biosynthesis of agmatine from arginine (By similarity)
CLLT_RS04070	ENOG4105DFA	alanine racemase domain protein
CLLT_RS04075	ENOG4105DTW	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
CLLT_RS04080	ENOG4108IUZ	ABC transporter
CLLT_RS04085	ENOG4105K8N	protein family UPF0079, ATPase
CLLT_RS04090	ENOG41082I2	s4 domain protein
CLLT_RS04095	ENOG4105CDH	Citrulline--aspartate ligase
CLLT_RS04100	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
CLLT_RS04105	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
CLLT_RS04115	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)
CLLT_RS04145	ENOG4107TPX	flagellar hook-associated
CLLT_RS04155	ENOG4105D3H	Catalyzes the decarboxylation of 3-octaprenyl-4-hydroxy benzoate to 2-octaprenylphenol (By similarity)
CLLT_RS04160	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
CLLT_RS04170	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)
CLLT_RS04175	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
CLLT_RS04180	ENOG4105EAH	synthase
CLLT_RS04195	ENOG4108VXP	Specifically catalyzes the dephosphorylation of 2- phosphoglycolate. Is involved in the dissimilation of the intracellular 2-phosphoglycolate formed during the DNA repair of 3'-phosphoglycolate ends, a major class of DNA lesions induced by oxidative stress (By similarity)
CLLT_RS04210	ENOG4105KNI	merR family transcriptional Regulator
CLLT_RS04215	ENOG4105DVC	DnaJ domain protein
CLLT_RS04220	ENOG4105C0H	protease
CLLT_RS04235	ENOG4105C4R	Atp-dependent dna helicase
CLLT_RS04240	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
CLLT_RS04245	ENOG4107RU9	Transcriptional regulator, Crp Fnr family
CLLT_RS04255	ENOG4107QXP	Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine (By similarity)
CLLT_RS04260	ENOG4105WMM	Probably plays a role in a hydrogenase nickel cofactor insertion step (By similarity)
CLLT_RS04265	ENOG4105C45	hydrogenase expression formation protein (HypE)
CLLT_RS04270	ENOG4105CQS	hydrogenase expression formation protein HypD
CLLT_RS04275	ENOG4105WRB	Hydrogenase assembly chaperone hypC hupF
CLLT_RS04290	ENOG4108P97	
CLLT_RS04300	ENOG4105UQX	Mate efflux family protein
CLLT_RS04315	ENOG4105E2Z	phosphate ABC transporter (Permease
CLLT_RS04340	ENOG41090A1	ferritin
CLLT_RS04350	ENOG4105V2T	cytochrome C
CLLT_RS04365	ENOG4105CRE	cytochrome C
CLLT_RS04375	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)
CLLT_RS04380	ENOG4108ZP8	Acetolactate synthase small subunit
CLLT_RS04385	ENOG4105C7K	acetolactate synthase
CLLT_RS04395	ENOG4105DQU	oxidoreductase, subunit beta
CLLT_RS04400	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
CLLT_RS04410	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
CLLT_RS04425	ENOG4105CNU	cell division protein FtsK
CLLT_RS04430	ENOG4105DTJ	flagellar hook-associated protein
CLLT_RS04480	ENOG4105DHM	ATPase which is responsible for recognizing, binding, unfolding and translocation of pupylated proteins into the bacterial 20S proteasome core particle. May be essential for opening the gate of the 20S proteasome via an interaction with its C-terminus, thereby allowing substrate entry and access to the site of proteolysis. Thus, the C-termini of the proteasomal ATPase may function like a 'key in a lock' to induce gate opening and therefore regulate proteolysis (By similarity)
CLLT_RS04490	ENOG4105C0B	DNA polymerase III (alpha subunit)
CLLT_RS04500	ENOG4107S0N	DJ-1 family
CLLT_RS04510	ENOG41076HS	cation diffusion facilitator family transporter
CLLT_RS04515	ENOG4105DWY	Agmatine deiminase
CLLT_RS04530	ENOG4105C4K	Nad synthetase
CLLT_RS04540	ENOG4107QID	Threonine synthase
CLLT_RS04545	ENOG4105CET	Activates KDO (a required 8-carbon sugar) for incorporation into bacterial lipopolysaccharide in Gram-negative bacteria (By similarity)
CLLT_RS04550	ENOG4107R0W	ABC transporter
CLLT_RS04555	ENOG4105E5Q	amino acid AbC transporter
CLLT_RS04570	ENOG4105CEP	NADH dehydrogenase
CLLT_RS04575	ENOG4105C8J	)-transporter
CLLT_RS04600	ENOG4105EIN	peptidylprolyl cis-trans isomerase
CLLT_RS04605	ENOG4105CSM	endonuclease III
CLLT_RS04610	ENOG4105D6U	Sodium Glutamate Symporter
CLLT_RS04620	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)
CLLT_RS04625	ENOG4105DJY	efflux transporter, rnd family, mfp subunit
CLLT_RS04630	ENOG4108RCM	Nitroreductase
CLLT_RS04635	ENOG4105CEY	Amp-dependent synthetase and ligase
CLLT_RS04640	ENOG4105CAY	ferredoxin--nadp reductase
CLLT_RS04645	ENOG4105D8J	Specifically methylates the guanine in position 1207 of 16S rRNA in the 30S particle (By similarity)
CLLT_RS04660	ENOG4105DK0	Indole-3-glycerol phosphate synthase
CLLT_RS04670	ENOG4105CR7	Catalyzes the transfer of selenium from selenophosphate for conversion of 2-thiouridine to 2-selenouridine at the wobble position in tRNA (By similarity)
CLLT_RS04685	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)
CLLT_RS04705	ENOG4105CFG	Acts as a chaperone (By similarity)
CLLT_RS04710	ENOG4105K90	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
CLLT_RS04715	ENOG4108122	heat-inducible transcription repressor
CLLT_RS04730	ENOG4108KA0	Inherit from COG: Phosphoesterase, DHHA1
CLLT_RS04735	ENOG4105D7B	Flagellar biosynthesis protein flha
CLLT_RS04745	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
CLLT_RS04750	ENOG4105CYJ	ribosomal RNA small subunit methyltransferase B
CLLT_RS04755	ENOG4105GSH	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
CLLT_RS04760	ENOG4105C79	DNA protecting protein DprA
CLLT_RS04770	ENOG4105C6M	Alpha-keto-beta-hydroxylacyl reductoisomerase
CLLT_RS04775	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
CLLT_RS04785	ENOG4108ZDX	Binds together with S18 to 16S ribosomal RNA (By similarity)
CLLT_RS04790	ENOG4108UUM	single-stranded DNA-binding protein
CLLT_RS04795	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)
CLLT_RS04800	ENOG4105EZI	multiple antibiotic resistance (MarC)-related protein
CLLT_RS04820	ENOG4105II7	pyrroline-5-carboxylate reductase
CLLT_RS04825	ENOG410821Z	Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum (By similarity)
CLLT_RS04835	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)
CLLT_RS04840	ENOG4107SDU	Methyl-accepting chemotaxis
CLLT_RS04855	ENOG4105C7B	Threonine dehydratase
CLLT_RS04865	ENOG4105CZM	Major Facilitator
CLLT_RS04875	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
CLLT_RS04880	ENOG4107S6Z	Na H antiporter
CLLT_RS04885	ENOG4105EMU	Dehydrogenase
CLLT_RS04900	ENOG4105EMK	carboxylate amino acid amine transporter
CLLT_RS04915	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
CLLT_RS04935	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)
CLLT_RS04940	ENOG4105CN7	Flagellar biosynthetic protein FliP
CLLT_RS04950	ENOG4105CRQ	synthase (Component I)
CLLT_RS04980	ENOG4105KUZ	arsenate reductase
CLLT_RS04985	ENOG4105C7V	phospho-2-dehydro-3-deoxyheptonate aldolase
CLLT_RS04995	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)
CLLT_RS05000	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
CLLT_RS05010	ENOG4105VB6	UPF0109 protein
CLLT_RS05015	ENOG4105K5M	30s ribosomal protein S16
CLLT_RS05020	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
CLLT_RS05025	ENOG4105EI2	Pseudouridine synthase
CLLT_RS05030	ENOG4105D8A	3-Deoxy-D-manno-octulosonic-acid transferase
CLLT_RS05040	ENOG4105EGD	dinuclear metal center protein, YbgI family
CLLT_RS05045	ENOG4108HMW	glycyl-tRNA synthetase, alpha subunit
CLLT_RS05055	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
CLLT_RS05060	ENOG4105CFP	Peptidase U32
CLLT_RS05070	ENOG4105C5F	glutamine synthetase
CLLT_RS05075	ENOG4105CIY	formyltetrahydrofolate deformylase
CLLT_RS05095	ENOG4105DJ2	Major Facilitator Superfamily
CLLT_RS05115	ENOG4108ZMS	Electron transfer subunit of the periplasmic nitrate reductase complex NapAB (By similarity)
CLLT_RS05120	ENOG4105GXZ	Ferredoxin-type protein NapH
CLLT_RS05125	ENOG4108BGM	Quinol dehydrogenase periplasmic component
CLLT_RS05130	ENOG4107QIW	Catalytic subunit of the periplasmic nitrate reductase (NAP). Only expressed at high levels during aerobic growth. NapAB complex receives electrons from the membrane-anchored tetraheme protein NapC, thus allowing electron flow between membrane and periplasm. Essential function for nitrate assimilation and may have a role in anaerobic metabolism (By similarity)
CLLT_RS05135	ENOG4105CGA	flagellar basal-body rod protein FlgG
CLLT_RS05140	ENOG4105KTQ	flagellar basal-body rod protein
CLLT_RS05145	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
CLLT_RS05150	ENOG4105CUU	Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) (By similarity)
CLLT_RS05160	ENOG4105EAU	Plays a role in nitrite reduction (By similarity)
CLLT_RS05175	ENOG4105DJV	ribulose-phosphate 3-epimerase
CLLT_RS05180	ENOG4105VB9	50S ribosomal protein l28
CLLT_RS05195	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS05205	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
CLLT_RS05210	ENOG4105K5Y	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
CLLT_RS05230	ENOG4108JA2	transcriptioN-repair coupling factor
CLLT_RS05240	ENOG4105DR5	peptidase
CLLT_RS05245	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
CLLT_RS05260	ENOG4105C8T	Leucyl-tRNA synthetase
CLLT_RS05270	ENOG4107RAB	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)
CLLT_RS05275	ENOG4107QN8	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)
CLLT_RS05280	ENOG4105VIE	preprotein translocase, subunit YajC
CLLT_RS05285	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
CLLT_RS05290	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
CLLT_RS05295	ENOG4107QV7	Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) (By similarity)
CLLT_RS05300	ENOG4105CXT	aspartate transcarbamylase
CLLT_RS05305	ENOG4105DPN	Oligoendopeptidase f
CLLT_RS05315	ENOG4105C4R	Atp-dependent dna helicase
CLLT_RS05335	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
CLLT_RS05350	ENOG4105C2Z	ATP-dependent CLP protease ATP-binding subunit
CLLT_RS05355	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)
CLLT_RS05360	ENOG4105Q75	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
CLLT_RS05365	ENOG4108ZC9	flagellar basal-body rod protein flgc
CLLT_RS05370	ENOG41084DA	flagellar hook-basal body complex protein fliE
CLLT_RS05375	ENOG4105CJN	penicillin-binding protein
CLLT_RS05380	ENOG4105CFX	Catalyzes the ferrous insertion into protoporphyrin IX (By similarity)
CLLT_RS05385	ENOG4105DRI	Involved in the oxidation of myo-inositol (MI) to 2- keto-myo-inositol (2KMI or 2-inosose) (By similarity)
CLLT_RS05390	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
CLLT_RS05400	ENOG4107YJQ	MAF-like protein
CLLT_RS05410	ENOG4105CCD	The exact function is not known. Can catalyze the reduction of a variety of substrates like dimethyl sulfoxide, trimethylamine N-oxide, phenylmethyl sulfoxide and L-methionine sulfoxide. Cannot reduce cyclic N-oxides. Shows no activity as sulfite oxidase (By similarity)
CLLT_RS05435	ENOG4108ZBZ	Catalyzes the excretion of spermidine (By similarity)
CLLT_RS05440	ENOG41090TI	Catalyzes the excretion of spermidine (By similarity)
CLLT_RS05445	ENOG4105CDY	transcriptional regulatory protein
CLLT_RS05450	ENOG4108ZCU	PPIases accelerate the folding of proteins
CLLT_RS05460	ENOG4107T5V	SNARE associated Golgi
CLLT_RS05470	ENOG4107XM3	UPF0442 protein
CLLT_RS05475	ENOG4105C75	arginyL-tRNA synthetase
CLLT_RS05480	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)
CLLT_RS05485	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
CLLT_RS05495	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
CLLT_RS05500	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)
CLLT_RS05505	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)
CLLT_RS05510	ENOG4105CE9	30S ribosomal protein S2
CLLT_RS05520	ENOG4105DJ5	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
CLLT_RS05525	ENOG4108R5F	Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis (By similarity)
CLLT_RS05540	ENOG4105DBW	Multi-copper polyphenol oxidoreductase laccase
CLLT_RS05575	ENOG4105YIC	Major outer membrane protein
CLLT_RS05590	ENOG4105CP9	extracellular ligand-binding receptor
CLLT_RS05595	ENOG4105C32	Amino acid ABC transporter (Permease)
CLLT_RS05600	ENOG4105CF8	branched-chain amino acid ABC transporter, permease
CLLT_RS05605	ENOG4105C0Z	ABC transporter
CLLT_RS05610	ENOG4108IV0	ABC, transporter
CLLT_RS05615	ENOG4105CRE	cytochrome C
CLLT_RS05625	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)
CLLT_RS05645	ENOG410820E	Thiamine monophosphate
CLLT_RS05650	ENOG4105C4U	4-methyl-5-beta-hydroxyethylthiazole kinase
CLLT_RS05655	ENOG4105DWF	phosphomethylpyrimidine kinase
CLLT_RS05660	ENOG4105KJF	protein tyrosine phosphatase
CLLT_RS05675	ENOG4107T1C	Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate (By similarity)
CLLT_RS05680	ENOG4105D52	delta-aminolevulinic acid dehydratase
CLLT_RS05685	ENOG4105T1H	UPF0763 protein
CLLT_RS05690	ENOG4105D4P	Coproporphyrinogen iii oxidase
CLLT_RS05695	ENOG4105DF6	Fe-S oxidoreductase
CLLT_RS05705	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
CLLT_RS05730	ENOG4105D60	lipoprotein releasing system transmembrane protein
CLLT_RS05745	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)
CLLT_RS05760	ENOG4105C8P	)-transporter
CLLT_RS05765	ENOG4108UV6	Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) (By similarity)
CLLT_RS05770	ENOG4105D41	biosynthesis protein thiH
CLLT_RS05795	ENOG4105C9Y	Catalyzes the hydrolysis of N-succinyl-L,L- diaminopimelic acid (SDAP), forming succinate and LL-2,6- diaminoheptanedioate (DAP), an intermediate involved in the bacterial biosynthesis of lysine and meso-diaminopimelic acid, an essential component of bacterial cell walls (By similarity)
CLLT_RS05805	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)
CLLT_RS05810	ENOG4105C98	muts2 protein
CLLT_RS05835	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)
CLLT_RS05840	ENOG4105C3P	Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) (By similarity)
CLLT_RS05845	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)
CLLT_RS05850	ENOG4105CEV	competence damage-inducible protein
CLLT_RS05865	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)
CLLT_RS05890	ENOG4107SJW	iron permease, FTR1
CLLT_RS05910	ENOG4108JMC	lipopolysaccharide core biosynthesis protein
CLLT_RS05925	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
CLLT_RS05940	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
CLLT_RS05945	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)
CLLT_RS05955	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
CLLT_RS05960	ENOG4105C25	Primosomal protein n'
CLLT_RS05985	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)
CLLT_RS05990	ENOG4108JQ1	Dehydrogenase
CLLT_RS06000	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)
CLLT_RS06005	ENOG4105C48	Converts 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate into isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP) (By similarity)
CLLT_RS06020	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
CLLT_RS06025	ENOG4105K59	histidine triad (HIT) protein
CLLT_RS06030	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
CLLT_RS06035	ENOG4107QSA	Oxaloacetate decarboxylase
CLLT_RS06040	ENOG4105C8J	)-transporter
CLLT_RS06045	ENOG4105C8J	)-transporter
CLLT_RS06050	ENOG4105C8J	)-transporter
CLLT_RS06055	ENOG41084IH	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)
CLLT_RS06070	ENOG4107SDU	Methyl-accepting chemotaxis
CLLT_RS06080	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
CLLT_RS06085	ENOG4105CHT	Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) (By similarity)
CLLT_RS06095	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
CLLT_RS06105	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)
CLLT_RS06110	ENOG4105KJP	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
CLLT_RS06135	ENOG4107S2Z	UPF0761 membrane protein
CLLT_RS06150	ENOG4105DR5	peptidase
CLLT_RS06155	ENOG4105CJW	magnesium transporter
CLLT_RS06160	ENOG4108V1J	Has antioxidant activity. Could remove peroxides or H(2)O(2) (By similarity)
CLLT_RS06165	ENOG4105CDU	Replicative dna helicase
CLLT_RS06170	ENOG4105C6T	cysteine synthase
CLLT_RS06175	ENOG410841J	DNA-binding protein Hu
CLLT_RS06190	ENOG4105CK0	Membrane bOund o-acyl transferase mboat family protein
CLLT_RS06205	ENOG4105F0R	Cytidylyltransferase
CLLT_RS06210	ENOG4105EJZ	Glucose-1-phosphate cytidylyltransferase
CLLT_RS06215	ENOG4107SE4	UDP-N-acetylglucosamine 2-epimerase
CLLT_RS06220	ENOG4105D2T	synthase
CLLT_RS06235	ENOG4108IAJ	Nad-dependent epimerase dehydratase
CLLT_RS06260	ENOG4105CG5	Glycosyl transferase (Group 1
CLLT_RS06265	ENOG4106WTF	Glycosyl transferase, family 2
CLLT_RS06275	ENOG4105DKP	glycosyl transferase, family 9
CLLT_RS06285	ENOG4105CMR	udp-glucose 4-epimerase
CLLT_RS06290	ENOG4105BZ1	(ABC) transporter
CLLT_RS06295	ENOG4105CG5	Glycosyl transferase (Group 1
CLLT_RS06300	ENOG4105CG5	Glycosyl transferase (Group 1
CLLT_RS06305	ENOG4107ZAZ	Oligosaccharyl transferase, STT3 subunit
CLLT_RS06310	ENOG4105CGN	Glycosyl transferase (Group 1
CLLT_RS06315	ENOG4105D3Q	Sugar transferase
CLLT_RS06320	ENOG4105MME	Sugar o-acyltransferase, sialic acid o-acetyltransferase neud family
CLLT_RS06325	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
CLLT_RS06330	ENOG4105C5E	polysaccharide biosynthesis protein
CLLT_RS06335	ENOG4108VYJ	response regulator receiver protein
CLLT_RS06340	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
CLLT_RS06345	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)
CLLT_RS06355	ENOG4106PT6	cdpdiacylglycerol-serine O-phosphatidyltransferase
CLLT_RS06370	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)
CLLT_RS06385	ENOG4105NAU	thioesterase Superfamily protein
CLLT_RS06390	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
CLLT_RS06405	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)
CLLT_RS06410	ENOG4105F4G	Membrane
CLLT_RS06415	ENOG4107RDB	Major Facilitator
CLLT_RS06440	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
CLLT_RS06450	ENOG4108IJ6	ABC transporter
CLLT_RS06460	ENOG4105C1Y	Converts seryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec) required for selenoprotein biosynthesis (By similarity)
CLLT_RS06465	ENOG4105EM7	Selenocysteine-specific translation elongation factor
CLLT_RS06480	ENOG4105D82	Glutamate dehydrogenase
CLLT_RS06485	ENOG4108XUR	Pfam:DUF178
CLLT_RS06490	ENOG4105C6K	Malic enzyme
CLLT_RS06495	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)
CLLT_RS06505	ENOG4105CER	acetyl-CoA carboxylase biotin carboxylase
CLLT_RS06510	ENOG4105KM4	Acetyl-CoA carboxylase, biotin carboxyl carrier protein
CLLT_RS06515	ENOG4105DHP	deoxycytidine triphosphate deaminase
CLLT_RS06520	ENOG4105C5E	polysaccharide biosynthesis protein
CLLT_RS06525	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
CLLT_RS06530	ENOG4105EQQ	protein containing aminopeptidase domain
CLLT_RS06565	ENOG4107QV8	Conserved hypothetical protein 698
CLLT_RS06585	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
CLLT_RS06600	ENOG4108P1X	synthase
CLLT_RS06610	ENOG4105CHR	reductase
CLLT_RS06615	ENOG4105F0R	Cytidylyltransferase
CLLT_RS06620	ENOG4107DKY	pseudaminic acid biosynthesis-associated protein PseG
CLLT_RS06625	ENOG4105VDT	-acetyltransferase
CLLT_RS06635	ENOG4107RFD	Non-specific O-methyltransferase that catalyzes the 2 O- methylation steps in the ubiquinone biosynthetic pathway (By similarity)
CLLT_RS06645	ENOG4105HF0	Membrane
CLLT_RS06650	ENOG4105D00	flagellar biosynthetic protein flhB
CLLT_RS06655	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS06660	ENOG4105D3R	alkyl hydroperoxide reductase
CLLT_RS06670	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)
CLLT_RS06680	ENOG4105YQ2	50s ribosomal protein l32
CLLT_RS06685	ENOG4105C6B	Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA (By similarity)
CLLT_RS06695	ENOG4108SEK	ompa motb domain protein
CLLT_RS06700	ENOG4105E14	MotA TolQ exbB proton channel
CLLT_RS06705	ENOG4105C2M	dna polymerase I
CLLT_RS06720	ENOG4105W39	Membrane
CLLT_RS06725	ENOG4105CG0	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
CLLT_RS06735	ENOG41080I0	Required for disulfide bond formation in some periplasmic proteins. Acts by oxidizing the DsbA protein (By similarity)
CLLT_RS06740	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)
CLLT_RS06745	ENOG4105D22	carbon starvation protein
CLLT_RS06755	ENOG4107QM1	Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine (By similarity)
CLLT_RS06760	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
CLLT_RS06765	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)
CLLT_RS06780	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)
CLLT_RS06790	ENOG4105CS3	FliG is one of three proteins (FliG, FliN, FliM) that forms the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation (By similarity)
CLLT_RS06795	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
CLLT_RS06800	ENOG4105CIH	Imidazole acetol-phosphate transaminase
CLLT_RS06805	ENOG4105CQC	Prephenate dehydratase
CLLT_RS06815	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
CLLT_RS06825	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
CLLT_RS06830	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)
CLLT_RS06835	ENOG4107V25	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
CLLT_RS06865	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)
CLLT_RS06870	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)
CLLT_RS06880	ENOG4108TMH	cytolethal distending toxin
CLLT_RS06885	ENOG4106BMH	cytolethal distending toxin
CLLT_RS06900	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)
CLLT_RS06905	ENOG4108S6J	ABC transporter, periplasmic molybdate-binding protein
CLLT_RS06910	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
CLLT_RS06920	ENOG4108HWY	Beta-lactamase
CLLT_RS06930	ENOG410825B	Type 11 methyltransferase
CLLT_RS06935	ENOG4105HSA	Protein of unknown function (DUF452)
CLLT_RS06940	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)
CLLT_RS06945	ENOG4108JPX	Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor (By similarity)
CLLT_RS06950	ENOG4107S77	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)
CLLT_RS06955	ENOG41080TC	multidrug resistance protein
CLLT_RS06965	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS06970	ENOG4105D44	asparaginase
CLLT_RS06980	ENOG4105CU6	carbamoyl-phosphate synthetase ammonia chain
CLLT_RS06995	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)
CLLT_RS07000	ENOG4105DAF	Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell (By similarity)
CLLT_RS07005	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)
CLLT_RS07010	ENOG4105WPN	DNA integration recombination invertion protein
CLLT_RS07015	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
CLLT_RS07020	ENOG4108F90	4-oxalocrotonate tautomerase
CLLT_RS07025	ENOG4105CM2	brancheD-chain amino acid aminotransferase
CLLT_RS07030	ENOG4105EPW	hflc protein
CLLT_RS07050	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
CLLT_RS07060	ENOG4105C3M	thioredoxin reductase
CLLT_RS07065	ENOG4105K63	Thioredoxin
CLLT_RS07070	ENOG41082UM	UPF0102 protein
CLLT_RS07075	ENOG4105D6E	homoserine dehydrogenase
CLLT_RS07080	ENOG4105CHM	Aminotransferase
CLLT_RS07105	ENOG41082DI	50s ribosomal protein l31
CLLT_RS07110	ENOG4107YV6	Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit (By similarity)
CLLT_RS07130	ENOG4107XWN	Catalyzes the conversion of 6-carboxy-5,6,7,8- tetrahydropterin (CPH4) to 7-carboxy-7-deazaguanine (CDG) (By similarity)
CLLT_RS07135	ENOG4105CM1	Catalyzes, together with MoaC, the conversion of 5'-GTP to cyclic pyranopterin monophosphate (cPMP or molybdopterin precursor Z) (By similarity)
CLLT_RS07155	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)
CLLT_RS07165	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)
CLLT_RS07175	ENOG4105D65	subunit l
CLLT_RS07180	ENOG4105M5H	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)
CLLT_RS07185	ENOG4107UFS	subunit j
CLLT_RS07190	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)
CLLT_RS07195	ENOG4108IB6	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)
CLLT_RS07220	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
CLLT_RS07225	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)
CLLT_RS07230	ENOG4105KWU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
CLLT_RS07240	ENOG4108JEI	Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system (By similarity)
CLLT_RS07245	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
CLLT_RS07260	ENOG4105C94	Transporter
CLLT_RS07270	ENOG4107QR9	Iron-sulfur cluster binding protein
CLLT_RS07275	ENOG4105CHG	glycolate oxidase (iron-sulfur subunit)
CLLT_RS07280	ENOG4105DAA	L-lactate
CLLT_RS07295	ENOG4105XEZ	This methylase recognizes the double-stranded sequence TCGA, causes specific methylation on A-4 on both strands and protects the DNA from cleavage by the
CLLT_RS07350	ENOG4105EE5	Membrane protein terC
CLLT_RS07355	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
CLLT_RS07360	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)
CLLT_RS07375	ENOG4105C0P	Mg chelatase subunit ChlI
CLLT_RS07380	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)
CLLT_RS07390	ENOG4105CCQ	Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins (By similarity)
CLLT_RS07395	ENOG4105DEA	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation
CLLT_RS07400	ENOG4105EUJ	GTP cyclohydrolase i
CLLT_RS07405	ENOG4108JIR	Flagellum-specific ATP synthase
CLLT_RS07430	ENOG4107XTC	May be involved in the formation or repair of Fe-S clusters present in iron-sulfur proteins
CLLT_RS07435	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
CLLT_RS07440	ENOG4105DRC	Na( ) H( ) antiporter that extrudes sodium in exchange for external protons (By similarity)
CLLT_RS07450	ENOG4105EN6	Membrane
CLLT_RS07460	ENOG4105D10	5-enolpyruvylshikimate-3-phosphate phospholyase
CLLT_RS07480	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)
CLLT_RS07490	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS07495	ENOG4108JQB	penicillin-binding protein 1C
CLLT_RS07500	ENOG4107S52	alpha-2-macroglobulin domain protein
CLLT_RS07515	ENOG4105D64	Mechanosensitive ion channel
CLLT_RS07520	ENOG4107B2H	carbonic anhydrase
CLLT_RS07525	ENOG4105HFZ	Membrane
CLLT_RS07530	ENOG4105NU9	Preprotein translocase subunit SecG
CLLT_RS07535	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)
CLLT_RS07540	ENOG4107VCP	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)
CLLT_RS07550	ENOG4105E05	Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides (By similarity)
CLLT_RS07565	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)
CLLT_RS07580	ENOG4105CI3	gtp-binding protein typa
CLLT_RS07595	ENOG410822I	Flagellar hook capping protein
CLLT_RS07600	ENOG4105BZE	flagellar hook protein, FlgE
CLLT_RS07620	ENOG4105MZU	cell filamentation protein
CLLT_RS07645	ENOG4105IBP	Cyclic peptide transporter
CLLT_RS07670	ENOG4108VAU	general secretion pathway protein G
CLLT_RS07685	ENOG4105CEA	Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) (By similarity)
CLLT_RS07690	ENOG4105KNE	Phosphatidate cytidylyltransferase
CLLT_RS07715	ENOG4105C01	Dihydroxy-acid dehydratase
CLLT_RS07740	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS07745	ENOG4105C8Q	Methyl-accepting chemotaxis
CLLT_RS07755	ENOG4105DHM	ATPase which is responsible for recognizing, binding, unfolding and translocation of pupylated proteins into the bacterial 20S proteasome core particle. May be essential for opening the gate of the 20S proteasome via an interaction with its C-terminus, thereby allowing substrate entry and access to the site of proteolysis. Thus, the C-termini of the proteasomal ATPase may function like a 'key in a lock' to induce gate opening and therefore regulate proteolysis (By similarity)
CLLT_RS07765	ENOG4108VPT	UPF0234 protein
CLLT_RS07770	ENOG4105C5I	Dehydrogenase
CLLT_RS07775	ENOG4106032	Glutathionylspermidine synthase
CLLT_RS07780	ENOG4108UHV	Lipoprotein
CLLT_RS07785	ENOG4105CCF	Lysine exporter protein (Lyse ygga)
CLLT_RS07790	ENOG41082DJ	30S ribosomal protein S21
CLLT_RS07825	ENOG4105CSA	Coproporphyrinogen iii oxidase
CLLT_RS07830	ENOG4108YXA	Membrane
CLLT_RS07840	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
CLLT_RS07850	ENOG4105D1H	recombination factor protein RarA
CLLT_RS07870	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)