locus-tag	class	description
BA172_RS00015	COG0139	Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP
BA172_RS00020	COG2166	iron-sulfur cluster assembly
BA172_RS00025	COG0316	Belongs to the HesB IscA family
BA172_RS00025	COG0694	Involved in iron-sulfur cluster biogenesis. Binds a 4Fe- 4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe S proteins. Could also act as a scaffold chaperone for damaged Fe S proteins
BA172_RS00040	COG1185	polyribonucleotide nucleotidyltransferase activity
BA172_RS00045	COG0184	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome
BA172_RS00060	COG0109	protoheme IX farnesyltransferase activity
BA172_RS00065	COG3125	oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor
BA172_RS00070	COG1845	cytochrome c oxidase, subunit III
BA172_RS00080	COG1622	oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor
BA172_RS00090	COG0828	Belongs to the bacterial ribosomal protein bS21 family
BA172_RS00095	COG0533	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction
BA172_RS00100	COG0305	Participates in initiation and elongation during chromosome replication
BA172_RS00105	COG0359	binds to the 23S rRNA
BA172_RS00110	COG0238	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
BA172_RS00145	COG0008	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)
BA172_RS00180	COG0267	Belongs to the bacterial ribosomal protein bL33 family
BA172_RS00185	COG0227	Belongs to the bacterial ribosomal protein bL28 family
BA172_RS00195	COG0742	ribosomal rna small subunit methyltransferase
BA172_RS00200	COG1190	Belongs to the class-II aminoacyl-tRNA synthetase family
BA172_RS00205	COG1186	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA
BA172_RS00210	COG0060	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)
BA172_RS00215	COG0268	Binds directly to 16S ribosomal RNA
BA172_RS00220	COG0536	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. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control
BA172_RS00225	COG0211	Belongs to the bacterial ribosomal protein bL27 family
BA172_RS00230	COG0261	This protein binds to 23S rRNA in the presence of protein L20
BA172_RS00235	COG0203	ribosomal protein L17
BA172_RS00240	COG0202	RNA polymerase activity
BA172_RS00245	COG0522	One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit
BA172_RS00250	COG0100	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
BA172_RS00255	COG0099	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
BA172_RS00260	COG0257	Belongs to the bacterial ribosomal protein bL36 family
BA172_RS00270	COG0200	Binds to the 23S rRNA
BA172_RS00275	COG0098	Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body
BA172_RS00285	COG0097	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
BA172_RS00290	COG0096	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
BA172_RS00295	COG0199	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
BA172_RS00300	COG0094	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
BA172_RS00305	COG0198	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit
BA172_RS00310	COG0093	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome
BA172_RS00315	COG0186	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA
BA172_RS00320	COG0255	Belongs to the universal ribosomal protein uL29 family
BA172_RS00325	COG0197	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs
BA172_RS00330	COG0092	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation
BA172_RS00335	COG0091	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
BA172_RS00340	COG0185	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA
BA172_RS00345	COG0090	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
BA172_RS00350	COG0089	rRNA binding
BA172_RS00355	COG0088	Forms part of the polypeptide exit tunnel
BA172_RS00365	COG0051	transcription antitermination factor activity, RNA binding
BA172_RS00370	COG0050	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis
BA172_RS00375	COG0480	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
BA172_RS00380	COG0049	tRNA binding
BA172_RS00385	COG0048	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
BA172_RS00390	COG0086	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates
BA172_RS00395	COG0085	RNA polymerase activity
BA172_RS00405	COG0244	Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors
BA172_RS00415	COG0080	Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors
BA172_RS00445	COG1023	phosphogluconate dehydrogenase (decarboxylating) activity
BA172_RS00455	COG0842	Transport permease protein
BA172_RS00460	COG1131	(ABC) transporter
BA172_RS00475	COG0361	One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex
BA172_RS00480	COG0482	sulfurtransferase activity
BA172_RS00485	COG0520	Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine
BA172_RS00490	COG0719	Fe-S assembly protein
BA172_RS00500	COG0719	Fe-S assembly protein
BA172_RS00505	COG3705	Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine
BA172_RS00515	COG0129	dihydroxy-acid dehydratase activity
BA172_RS00520	COG0466	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
BA172_RS00525	COG0124	histidyl-tRNA synthetase
BA172_RS00540	COG0172	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)
BA172_RS00550	COG0135	phosphoribosylanthranilate isomerase activity
BA172_RS00555	COG0101	tRNA pseudouridine synthase activity
BA172_RS00560	COG0136	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate
BA172_RS00565	COG0473	3-isopropylmalate dehydrogenase activity
BA172_RS00570	COG0066	3-isopropylmalate dehydratase activity
BA172_RS00575	COG0078	Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline
BA172_RS00580	COG0355	proton-transporting ATP synthase activity, rotational mechanism
BA172_RS00590	COG0224	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
BA172_RS00595	COG0056	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit
BA172_RS00615	COG0356	it plays a direct role in the translocation of protons across the membrane
BA172_RS00630	COG0752	glycyl-tRNA synthetase alpha subunit
BA172_RS00645	COG0187	DNA topoisomerase II activity
BA172_RS00650	COG0230	Belongs to the bacterial ribosomal protein bL34 family
BA172_RS00660	COG0838	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
BA172_RS00665	COG0377	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
BA172_RS00670	COG0852	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
BA172_RS00670	COG0649	NAD binding
BA172_RS00675	COG1905	PFAM NADH dehydrogenase (ubiquinone) 24 kDa subunit
BA172_RS00690	COG1005	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
BA172_RS00695	COG1143	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
BA172_RS00700	COG0839	Belongs to the complex I subunit 6 family
BA172_RS00705	COG0713	ATP synthesis coupled electron transport
BA172_RS00715	COG1008	NDH-1 shuttles electrons from NAD(P)H, 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 plastoquinone. 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
BA172_RS00725	COG0484	heat shock protein binding
BA172_RS00730	COG0443	Heat shock 70 kDa protein
BA172_RS00735	COG0576	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
BA172_RS00740	COG0691	Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene
BA172_RS00760	COG0335	large ribosomal subunit rRNA binding
BA172_RS00765	COG0806	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes
BA172_RS00770	COG0228	four-way junction DNA binding
BA172_RS00775	COG0059	Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate
BA172_RS00780	COG0440	acetolactate synthase activity
BA172_RS00785	COG0028	Belongs to the TPP enzyme family
BA172_RS00825	COG0131	Imidazoleglycerol-phosphate dehydratase
BA172_RS00830	COG0118	IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR
BA172_RS00835	COG0106	1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase
BA172_RS00840	COG0107	imidazoleglycerol-phosphate synthase activity
BA172_RS00845	COG0079	Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily
BA172_RS00865	COG0249	that it carries out the mismatch recognition step. This protein has a weak ATPase activity
BA172_RS00885	COG0102	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
BA172_RS00890	COG0040	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
BA172_RS00900	COG0154	amidase activity
BA172_RS00905	COG0064	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)
BA172_RS00915	COG1562	ergosterol biosynthetic process
BA172_RS00925	COG0216	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA
BA172_RS00930	COG0462	Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P)
BA172_RS00935	COG1825	This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance
BA172_RS00950	COG0134	indole-3-glycerol-phosphate synthase activity
BA172_RS00955	COG0547	Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA)
BA172_RS00960	COG0512	Glutamine amidotransferase of anthranilate synthase
BA172_RS00980	COG0489	protein tyrosine kinase activity
BA172_RS00995	COG0278	Belongs to the glutaredoxin family. Monothiol subfamily
BA172_RS01000	COG0137	argininosuccinate synthase activity
BA172_RS01005	COG0234	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter
BA172_RS01010	COG0459	protein refolding
BA172_RS01015	COG0481	GTPase activity
BA172_RS01025	COG0525	valine-tRNA ligase activity
BA172_RS01030	COG0450	alkyl hydroperoxide reductase
BA172_RS01035	COG1145	4fe-4S ferredoxin, iron-sulfur binding domain protein
BA172_RS01040	COG0159	tryptophan synthase activity
BA172_RS01045	COG0133	tryptophan synthase activity
BA172_RS01050	COG0319	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA
BA172_RS01055	COG0495	leucyl-tRNA aminoacylation
BA172_RS01060	COG0013	Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain
BA172_RS01065	COG0527	aspartate kinase activity
BA172_RS01080	COG0320	Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives
BA172_RS01095	COG0173	Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn)
BA172_RS01100	COG2239	Acts as a magnesium transporter
BA172_RS01105	COG1502	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol
BA172_RS01110	COG1219	ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP
BA172_RS01120	COG0740	serine-type endopeptidase activity
BA172_RS01155	COG0008	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)
BA172_RS01165	COG0242	peptide deformylase activity
BA172_RS01170	COG0837	glucose binding
BA172_RS01175	COG0364	Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone
BA172_RS01185	COG2814	Major facilitator Superfamily
BA172_RS01190	COG2814	Major facilitator Superfamily
BA172_RS01195	COG0685	methylenetetrahydrofolate reductase (NAD(P)H) activity
BA172_RS01200	COG1301	dicarboxylic acid transport
BA172_RS01205	COG0757	Catalyzes a trans-dehydration via an enolate intermediate
BA172_RS01210	COG0442	prolyl-tRNA aminoacylation
BA172_RS01215	COG1121	(ABC) transporter
BA172_RS01230	COG0290	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
BA172_RS01235	COG0291	Belongs to the bacterial ribosomal protein bL35 family
BA172_RS01240	COG0292	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
BA172_RS01245	COG0016	Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily
BA172_RS01250	COG0072	phenylalanine-tRNA ligase activity
BA172_RS01255	COG0858	One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA
BA172_RS01265	COG0532	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
BA172_RS01265	COG0532	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
BA172_RS01270	COG0195	Participates in both transcription termination and antitermination
BA172_RS01285	COG0465	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
BA172_RS01310	COG0289	4-hydroxy-tetrahydrodipicolinate reductase
BA172_RS01315	COG0289	4-hydroxy-tetrahydrodipicolinate reductase
BA172_RS01320	COG0762	integral membrane protein
BA172_RS01325	COG0162	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)
BA172_RS01325	COG0162	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)
BA172_RS01335	COG0624	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
BA172_RS01345	COG0024	Methionine aminopeptidase
BA172_RS01350	COG0052	Belongs to the universal ribosomal protein uS2 family
BA172_RS01360	COG0587	DNA-directed DNA polymerase activity
BA172_RS01365	COG0037	tRNA processing
BA172_RS01375	COG0722	Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP)
BA172_RS01380	COG0620	Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation
BA172_RS01385	COG0140	phosphoribosyl-ATP diphosphatase activity
BA172_RS01390	COG1220	this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis
BA172_RS01395	COG5405	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery
BA172_RS01400	COG0254	rRNA binding
BA172_RS01405	COG0703	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate
BA172_RS01410	COG0337	Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ)
BA172_RS01420	COG1530	ribonuclease E activity
BA172_RS01425	COG0564	pseudouridine synthase activity
BA172_RS01430	COG0333	Belongs to the bacterial ribosomal protein bL32 family
BA172_RS01435	COG0236	Carrier of the growing fatty acid chain in fatty acid biosynthesis
BA172_RS01440	COG0119	Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate)
BA172_RS01445	COG1278	Cold shock
BA172_RS01450	COG0082	Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system
BA172_RS01455	COG0065	Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate
BA172_RS01465	COG0653	protein targeting
BA172_RS01480	COG0128	3-phosphoshikimate 1-carboxyvinyltransferase activity
BA172_RS01490	COG0329	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA)
BA172_RS01500	COG0508	dehydrogenase complex catalyzes the overall conversion of