locus-tag	class	description
THA_100	ENOG4105C03	ribonuclease
THA_1000	ENOG4105EMN	RNA polymerase sigma factor
THA_1003	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)
THA_1004	ENOG4105BZU	Histidine kinase
THA_1007	ENOG4105CG3	alpha amylase, catalytic region
THA_1008	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
THA_1009	ENOG4105C8Q	Methyl-accepting chemotaxis
THA_101	ENOG4105DBI	uridine monophosphokinase
THA_1010	ENOG4108MVM	Transposase
THA_1014	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
THA_1016	ENOG4105C8Q	Methyl-accepting chemotaxis
THA_1017	ENOG4108JQ7	(ABC) transporter
THA_1019	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
THA_1020	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
THA_1021	ENOG4105DEF	Extracellular solute-binding protein, family 5
THA_1024	ENOG4105JAB	phenazine biosynthesis protein, phzf family
THA_1025	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
THA_1039	ENOG41068B1	Cob-I-yrinic acid a,c-diamide adenosyltransferase
THA_104	ENOG4105KW8	RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs (By similarity)
THA_1040	ENOG4105CIH	Imidazole acetol-phosphate transaminase
THA_1041	ENOG4105DH2	Converts cobyric acid to cobinamide by the addition of aminopropanol on the F carboxylic group (By similarity)
THA_1042	ENOG4105CAA	catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation (By similarity)
THA_1043	ENOG4107Z5K	Joins Ado-cobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin) (By similarity)
THA_1046	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
THA_1049	ENOG4108KHP	Diguanylate cyclase
THA_105	ENOG4105C1N	GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis (By similarity)
THA_1053	ENOG4107R49	K07407 alpha-galactosidase EC 3.2.1.22
THA_1054	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)
THA_1056	ENOG4105X0D	Fimbrial protein
THA_1059	ENOG4105D17	glycoside hydrolase, family 3 domain protein
THA_1061	ENOG4105F0P	binding-protein-dependent transport systems inner membrane Component
THA_1062	ENOG4105DRS	transport system, permease
THA_1064	ENOG4105CE4	GlcNAc 6-P deacetylase
THA_1065	ENOG4105CUP	Catalyzes the synthesis of alpha-ribazole-5'-phosphate from nicotinate mononucleotide (NAMN) and 5,6- dimethylbenzimidazole (DMB) (By similarity)
THA_1067	ENOG41081F0	Precorrin-8x methylmutase
THA_1068	ENOG4105EE8	May catalyze the methylation of C-1 in cobalt-precorrin- 5 and the subsequent extrusion of acetic acid from the resulting intermediate to form cobalt-precorrin-6A (By similarity)
THA_1069	ENOG4108DR9	Cobalt-precorrin-6Y C(5)-methyltransferase
THA_1070	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
THA_1072	ENOG4105CIA	precorrin-4 C(11)-methyltransferase
THA_1073	ENOG4108P62	biosynthesis protein (CbiG)
THA_1074	ENOG4105E4R	Precorrin-3B C17-methyltransferase
THA_1075	ENOG4108JTQ	reductase
THA_1076	ENOG4105C7E	Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) (By similarity)
THA_1077	ENOG4105D6W	Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps (By similarity)
THA_1079	ENOG4105D52	delta-aminolevulinic acid dehydratase
THA_108	ENOG4105CPH	Catalyzes the formation of S-adenosylmethionine from methionine and ATP
THA_1080	ENOG4105CB8	Multifunctional enzyme that catalyzes the SAM-dependent methylation of uroporphyrinogen III at position C-2 and C-7 to form precorrin-2 and then position C-12 or C-18 to form trimethylpyrrocorphin 2. It also catalyzes the conversion of precorrin-2 into siroheme. This reaction consists of the NAD- dependent oxidation of precorrin-2 into sirohydrochlorin and its subsequent ferrochelation into siroheme (By similarity)
THA_1081	ENOG4105CDM	Glutamate-1-semialdehyde aminotransferase
THA_1082	ENOG4105CFT	Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import (By similarity)
THA_1088	ENOG4108UMW	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
THA_109	ENOG410857I	Binds directly to 16S ribosomal RNA (By similarity)
THA_1090	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
THA_1091	ENOG4108V0P	LemA family
THA_1093	ENOG4108RCM	Nitroreductase
THA_1096	ENOG4105SYT	Methylenetetrahydrofolate reductase
THA_1099	ENOG4105CFH	Aspartokinase
THA_11	ENOG4107RSD	Multi-copper polyphenol oxidoreductase laccase
THA_1105	ENOG4105DBV	ornithine carbamoyltransferase
THA_1106	ENOG4105CEU	Arginine dihydrolase
THA_1107	ENOG4108MVM	Transposase
THA_1110	ENOG4105C8Q	Methyl-accepting chemotaxis
THA_1113	ENOG4107V9E	glucose-1-phosphate thymidylyltransferase
THA_1114	ENOG410667J	hydrolase
THA_1116	ENOG4105CUT	histidyl-tRNA synthetase
THA_1118	ENOG4107S6Z	Na H antiporter
THA_112	ENOG4108MVM	Transposase
THA_1121	ENOG4105CJ1	ABC, transporter
THA_1124	ENOG4105I08	Pseudouridine synthase
THA_1125	ENOG4105EEI	dihydropteroate synthase
THA_1127	ENOG4105C5R	Aminotransferase
THA_1128	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)
THA_1133	ENOG4108IJ6	ABC transporter
THA_1136	ENOG4108SA1	esterase
THA_114	ENOG4106K5Q	Modifies the topological state of DNA by introducing positive supercoils in an ATP-dependent process. It cleaves transiently a single DNA strand and remains covalently bound to the 5' DNA end through a tyrosine residue. May be involved in rewinding the DNA strands in the regions of the chromosome that have opened up to allow transcription or replication (By similarity)
THA_1141	ENOG4107Z0G	Domain of unknown function DUF20
THA_1142	ENOG4105HDK	L-asparaginase
THA_1147	ENOG4105CDB	Required for chromosome condensation and partitioning (By similarity)
THA_1148	ENOG4105DFU	Cell wall formation (By similarity)
THA_1149	ENOG4105DVQ	Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) (By similarity)
THA_115	ENOG4105EHU	Circadian clock protein KaiC
THA_1150	ENOG4105C5I	Dehydrogenase
THA_1161	ENOG4105Z5Q	
THA_1163	ENOG4105KIJ	D-ornithine aminomutase S component
THA_1164	ENOG4105EQ5	D-Lysine 5,6-aminomutase alpha subunit
THA_1165	ENOG4105F8V	Hydrolase, tatD family
THA_1166	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)
THA_1171	ENOG4105DC6	This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex (By similarity)
THA_1173	ENOG4105CIM	Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain (By similarity)
THA_1175	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)
THA_1176	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)
THA_1178	ENOG4105CSA	Coproporphyrinogen iii oxidase
THA_1179	ENOG4105CNI	cell division protein FtsW
THA_118	ENOG4105BZU	Histidine kinase
THA_1181	ENOG4105C7R	Atpase associated with various cellular activities aaa_3
THA_1184	ENOG4105DPN	Oligoendopeptidase f
THA_1186	ENOG4105DI7	Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs (By similarity)
THA_1188	ENOG4105DX0	Hemolysin A
THA_119	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
THA_1190	ENOG4105CBS	Chea signal transduction histidine kinase
THA_1191	ENOG4105YVF	chew protein
THA_1192	ENOG4107YTP	response regulator receiver protein
THA_1194	ENOG4105CN7	Flagellar biosynthetic protein FliP
THA_1195	ENOG4105VS8	Flagellar biosynthetic protein fliq
THA_1196	ENOG4108ZMD	Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis (By similarity)
THA_1197	ENOG4105CE9	30S ribosomal protein S2
THA_1198	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)
THA_1199	ENOG4107N8V	50s ribosomal protein L35
THA_120	ENOG4108UTW	Plays a role in the regulation of phosphate uptake
THA_1200	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)
THA_1204	ENOG4105CA9	Pyruvate kinase
THA_1207	ENOG4105EI2	Pseudouridine synthase
THA_121	ENOG4105BZY	Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system (By similarity)
THA_1210	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)
THA_1211	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)
THA_1212	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)
THA_1213	ENOG4105CGV	This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis (By similarity)
THA_1214	ENOG4108Z10	Involved in the binding of tRNA to the ribosomes (By similarity)
THA_1215	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)
THA_1216	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)
THA_1217	ENOG4105KZR	One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome (By similarity)
THA_1218	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
THA_1219	ENOG4105K7S	Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA (By similarity)
THA_122	ENOG4105C8U	phosphate abc transporter
THA_1220	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)
THA_1221	ENOG4105CKE	Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation (By similarity)
THA_1222	ENOG4108R70	Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs (By similarity)
THA_1223	ENOG41084ME	50s ribosomal protein l29
THA_1224	ENOG4105K87	One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal
THA_1225	ENOG4108UNN	Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome (By similarity)
THA_1226	ENOG4105KAR	One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit (By similarity)
THA_1227	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
THA_1228	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)
THA_1229	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)
THA_123	ENOG4105E2Z	phosphate ABC transporter (Permease
THA_1230	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)
THA_1231	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)
THA_1232	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)
THA_1233	ENOG4105VPB	50S ribosomal protein L30
THA_1234	ENOG4108UZ0	Binds to the 23S rRNA (By similarity)
THA_1235	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)
THA_1236	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)
THA_1238	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)
THA_1239	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
THA_1240	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)
THA_1241	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)
THA_1242	ENOG4105CTF	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
THA_1243	ENOG4108ZT0	50S ribosomal protein l17
THA_1244	ENOG4107XYV	Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase (By similarity)
THA_1245	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)
THA_1246	ENOG4105CDY	transcriptional regulatory protein
THA_1248	ENOG4105BZU	Histidine kinase
THA_1249	ENOG4105M02	This protein specifically catalyzes the removal of signal peptides from prolipoproteins (By similarity)
THA_125	ENOG4105C26	Dehydrogenase
THA_1250	ENOG4105C34	Pseudouridine synthase
THA_1251	ENOG4105C5F	glutamine synthetase
THA_1252	ENOG4105ZHF	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
THA_1253	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
THA_1262	ENOG4105GSQ	TM1410 hypothetical-related protein
THA_1266	ENOG4107T8Q	Glycosyl transferase (Group 1
THA_1267	ENOG4108MVM	Transposase
THA_127	ENOG41083AI	transcriptional regulator), MarR family
THA_1272	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1275	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
THA_1278	ENOG4108MVM	Transposase
THA_1279	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1280	ENOG4105NBF	ammecr1 domain protein
THA_1285	ENOG4107R56	PP-loop domain protein
THA_1286	ENOG4105CEM	UPF0597 protein
THA_1288	ENOG4105CMG	Carbohydrate kinase
THA_1289	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
THA_129	ENOG4105DE4	1-phosphofructokinase
THA_1291	ENOG4105CMD	Transcriptional regulator, GntR family
THA_1292	ENOG4105CKB	glycosidase
THA_1293	ENOG4105F66	Binding-protein-dependent transport systems inner membrane component
THA_1294	ENOG4105DB9	Binding-protein-dependent transport systems inner membrane component
THA_130	ENOG4105CHR	reductase
THA_1306	ENOG4105CJ4	Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids (By similarity)
THA_1307	ENOG4105VB9	50S ribosomal protein l28
THA_1309	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
THA_1310	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)
THA_1311	ENOG4108UJD	30S ribosomal protein S9
THA_1312	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)
THA_1313	ENOG41081BK	membrane protein-like protein
THA_1314	ENOG4105K46	50S ribosomal protein l27
THA_1316	ENOG4105KK9	This protein binds to 23S rRNA in the presence of protein L20 (By similarity)
THA_1318	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)
THA_1319	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
THA_132	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
THA_1320	ENOG4105MCT	stage V sporulation protein S
THA_1322	ENOG4105CBJ	Metal-dependent enzyme
THA_1323	ENOG4105CJ1	ABC, transporter
THA_1324	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1325	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
THA_1326	ENOG4105CH2	amidohydrolase
THA_1327	ENOG4105CSS	phenylalanyl-tRNA synthetase (alpha subunit)
THA_1328	ENOG4105D0T	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs (By similarity)
THA_1329	ENOG4105C3G	gtp-binding protein
THA_1330	ENOG4105KC4	UPF0296 protein
THA_1331	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)
THA_1332	ENOG4107QPI	nitrilase cyanide hydratase and apolipoprotein n-acyltransferase
THA_1335	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)
THA_1337	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1338	ENOG4105BZU	Histidine kinase
THA_134	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
THA_1340	ENOG4105EAB	amino acid AbC transporter
THA_1341	ENOG4107UU3	sucrose-phosphate synthase (EC 2.4.1.14)
THA_1344	ENOG4107QR0	DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates (By similarity)
THA_1346	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)
THA_1347	ENOG41081WB	50s ribosomal protein L10
THA_135	ENOG4105BZU	Histidine kinase
THA_1351	ENOG4107TVC	Glycosyl transferase, family 2
THA_1352	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
THA_1353	ENOG4105CDU	Replicative dna helicase
THA_1355	ENOG4105KME	endoribonuclease L-psp
THA_1358	ENOG4108Z5K	methylglyoxal synthase
THA_1359	ENOG4108KP7	hydrolase
THA_1362	ENOG4105C5S	asparaginyl-tRNA synthetase
THA_1363	ENOG4105CTD	carboxy-peptidase
THA_1366	ENOG4105DZA	Converts GTP to 7,8-dihydroneopterin triphosphate (By similarity)
THA_1369	ENOG4105X0D	Fimbrial protein
THA_1370	ENOG4105CJ1	ABC, transporter
THA_1374	ENOG41085TI	Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection (By similarity)
THA_1378	ENOG4108QQZ	ErfK YbiS YcfS YnhG family protein
THA_1379	ENOG4108RU0	short-chain dehydrogenase reductase
THA_138	ENOG4109003	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis (By similarity)
THA_1382	ENOG4107QIV	Cytochrome c biogenesis protein
THA_1386	ENOG4108JU3	Alkyl hydroperoxide reductase
THA_139	ENOG4105C89	phosphohexose isomerase
THA_1390	ENOG4105MQ3	flagellar protein FliS
THA_1393	ENOG4108JQ7	(ABC) transporter
THA_1394	ENOG4105C3U	ABC transporter
THA_1396	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
THA_1397	ENOG4107QSI	ABC, transporter
THA_1398	ENOG4106H78	methyltransferase
THA_1399	ENOG4105D38	putrescine abc transporter
THA_14	ENOG4105CMM	transposase
THA_1400	ENOG4105F38	ABC transporter, permease
THA_1401	ENOG4105C53	Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system (By similarity)
THA_1402	ENOG4107RUE	extracellular solute-binding protein family 1
THA_1403	ENOG4105CCX	Catalyzes the production of spermidine from putrescine and decarboxylated S-adenosylmethionine (dcSAM), which serves as an aminopropyl donor (By similarity)
THA_1404	ENOG4105X3E	Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine (By similarity)
THA_1408	ENOG4108UQV	Membrane
THA_141	ENOG41083NY	Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A (By similarity)
THA_1410	ENOG4105KGE	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA (By similarity)
THA_1411	ENOG4105CTJ	Metal Dependent Phosphohydrolase
THA_1412	ENOG4105C9A	Phoh family
THA_1414	ENOG4105DJT	lAO AO transport system ATPase
THA_1416	ENOG4105PV1	biotin lipoyl attachment domaiN-containing protein
THA_1418	ENOG4107QX3	carboxylase
THA_142	ENOG4108KHP	Diguanylate cyclase
THA_1422	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
THA_1423	ENOG4107YDG	Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization (By similarity)
THA_1427	ENOG4105MEW	serine threonine protein phosphatase
THA_1429	ENOG4105Q75	Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body (By similarity)
THA_143	ENOG4105CCW	damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage (By similarity)
THA_1430	ENOG4108ZC9	flagellar basal-body rod protein flgc
THA_1431	ENOG4105VQ0	flagellar hook-basal body complex protein fliE
THA_1433	ENOG4105CFG	Acts as a chaperone (By similarity)
THA_1434	ENOG4105K8R	UPF0145 protein
THA_1435	ENOG4105F6J	Alpha beta hydrolase fold
THA_1436	ENOG4108MVM	Transposase
THA_1439	ENOG410811P	TRANSCRIPTIONAl REGULATOR GntR family
THA_144	ENOG4105F23	Fibronectin-binding protein
THA_1440	ENOG4105CHU	acetyl-coa acetyltransferase
THA_1442	ENOG4107QP7	CoA-transferase subunit A
THA_1443	ENOG4105BZ8	glutamate synthase
THA_1444	ENOG4105CDJ	oxidoreductase FAD NAD(P)-binding domain protein
THA_1445	ENOG4105DD7	kinase (PfkB family
THA_1446	ENOG4105DKQ	ROK family
THA_1450	ENOG4105M3Z	response regulator
THA_1451	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
THA_1452	ENOG4105CBS	Chea signal transduction histidine kinase
THA_1459	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
THA_1460	ENOG4105BZQ	cdp-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase
THA_1461	ENOG41081HM	2'-5' rna ligase
THA_1462	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)
THA_1464	ENOG4105E4Y	Endoribonuclease that initiates mRNA decay (By similarity)
THA_1466	ENOG4108ZK7	protein family UPF0029, Impact, N-terminal protein
THA_1467	ENOG4108RE9	Phosphodiesterase
THA_1468	ENOG4105D53	Catalyzes the hydrolysis of pseudouridine 5'-phosphate (PsiMP) to ribose 5-phosphate and uracil (By similarity)
THA_1470	ENOG4105DJ1	Phosphoenolpyruvate Carboxylase
THA_1471	ENOG4108JIU	phosphoribosylformylglycinamidine synthase ii
THA_1472	ENOG4105D21	Phosphoribosylformylglycinamidine synthase I
THA_1473	ENOG4108A1T	Phosphoribosylformylglycinamidine synthase, purS
THA_1474	ENOG4105C8V	SAICAR synthetase
THA_1475	ENOG4108UM6	Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) (By similarity)
THA_1476	ENOG4105C6T	cysteine synthase
THA_1477	ENOG4105D7W	serine acetyltransferase
THA_1478	ENOG4105C80	Catalyzes the reversible oxidation of malate to oxaloacetate (By similarity)
THA_1487	ENOG4107QF7	multi-drug
THA_1488	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)
THA_1489	ENOG4105K85	Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) in DNA. Repairs alkylated guanine in DNA by stoichiometrically transferring the alkyl group at the O-6 position to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated (By similarity)
THA_149	ENOG4105CDE	UPF0348 protein
THA_1490	ENOG4107XM9	(LipO)protein
THA_1492	ENOG4105BZU	Histidine kinase
THA_1493	ENOG4108QXE	glycerophosphoryl diester phosphodiesterase
THA_1494	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)
THA_1495	ENOG4105CPQ	Dehydrogenase
THA_1499	ENOG4105UQX	Mate efflux family protein
THA_150	ENOG4108JA2	transcriptioN-repair coupling factor
THA_1501	ENOG4105DA5	(ABC) transporter
THA_1505	ENOG4108IJ0	Aspartate ammonia-lyase
THA_1506	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
THA_1510	ENOG4105DBI	uridine monophosphokinase
THA_1511	ENOG4105DCI	Phosphohydrolase
THA_1512	ENOG4105CGM	Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis (By similarity)
THA_1517	ENOG4105F03	Provides the (R)-glutamate required for cell wall biosynthesis (By similarity)
THA_1518	ENOG4105C21	Displays ATPase and GTPase activities (By similarity)
THA_1519	ENOG4105CHW	UPF0052 protein
THA_152	ENOG4105E59	Participates in a DNA-damage check-point. DisA forms globular foci that rapidly scan along the chromosomes searching for lesions (By similarity)
THA_1520	ENOG4105CIE	May be required for sporulation (By similarity)
THA_1521	ENOG4108Z11	Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes (By similarity)
THA_1522	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)
THA_1523	ENOG4105CRK	lysyL-tRNA synthetase
THA_1525	ENOG41082I2	s4 domain protein
THA_1527	ENOG4105BZ1	(ABC) transporter
THA_1529	ENOG4105C3U	ABC transporter
THA_153	ENOG4108UHX	Involved in the hydrolysis of glutamine to glutamate and ammonia. Channels an ammonia molecule to PdxS (By similarity)
THA_1530	ENOG4108JQ7	(ABC) transporter
THA_1533	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
THA_154	ENOG4105CD9	Involved in the production of pyridoxal phosphate, probably by incorporating ammonia into the pyridine ring (By similarity)
THA_1545	ENOG4105PGM	cation diffusion facilitator family transporter
THA_1546	ENOG4107YCR	Transcriptional regulator, ARSR family
THA_1547	ENOG4105C83	adenylosuccinate lyase
THA_155	ENOG4105D5P	Methylmalonyl-coA mutase
THA_1551	ENOG4108R86	Transcriptional regulator
THA_1552	ENOG41084K4	Binds the 23S rRNA (By similarity)
THA_1553	ENOG4105C62	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
THA_1554	ENOG4107QIZ	NADH dehydrogenase
THA_1556	ENOG4107QIZ	NADH dehydrogenase
THA_1559	ENOG410902H	NADH dehydrogenase (Ubiquinone), 24 kDa subunit
THA_156	ENOG4107W7X	Aldolase
THA_1560	ENOG4105CCS	Glutamate formiminotransferase
THA_1561	ENOG4105ECY	inositol monophosphatase
THA_1563	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)
THA_1565	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
THA_1567	ENOG4105KTH	gatB Yqey
THA_1568	ENOG4108YZG	isomerase
THA_1569	ENOG41084GC	stage II sporulation protein
THA_1570	ENOG4105DS7	Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair (By similarity)
THA_1572	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)
THA_1573	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)
THA_1577	ENOG4105ETE	Transcriptional regulator (LacI family
THA_1578	ENOG4105CNT	hydrolase family 2
THA_158	ENOG4105K8U	2-Amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase
THA_1580	ENOG4105F0Z	galactose-1-phosphate uridylyltransferase
THA_1581	ENOG4105CRD	Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) (By similarity)
THA_1582	ENOG4105CXT	aspartate transcarbamylase
THA_1583	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1584	ENOG4105G5W	regulator Fur family
THA_1585	ENOG4105D3R	alkyl hydroperoxide reductase
THA_1586	ENOG4105VCQ	rubredoxin
THA_1587	ENOG4108ESE	uses NADH to detoxify nitric oxide (NO), protecting several 4Fe-4S NO-sensitive enzymes. Has at least 2 reductase partners, only one of which (NorW, flavorubredoxin reductase) has been identified. NO probably binds to the di-iron center
THA_159	ENOG4107QSA	Oxaloacetate decarboxylase
THA_1590	ENOG4105MAX	Superoxide reductase
THA_160	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)
THA_1600	ENOG4107ZIF	6-carboxy-5,6,7,8-tetrahydropterin synthase
THA_1604	ENOG4105XJC	Two component transcriptional regulator (Winged helix family
THA_1605	ENOG4105BZA	Phosphoglycerate kinase
THA_1606	ENOG4105BZA	Phosphoglycerate kinase
THA_1607	ENOG4105C17	glyceraldehyde-3-phosphate dehydrogenase
THA_1612	ENOG4105C6H	Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction (By similarity)
THA_1613	ENOG4105D2N	Aldolase
THA_1615	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
THA_1616	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)
THA_1617	ENOG4107QHF	type ii secretion system protein e
THA_1619	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)
THA_162	ENOG4105C8Q	Methyl-accepting chemotaxis
THA_1620	ENOG4105CR3	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids (By similarity)
THA_1621	ENOG4105KNE	Phosphatidate cytidylyltransferase
THA_1622	ENOG4105CIM	Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain (By similarity)
THA_1623	ENOG4105DFF	Rod shape-determining protein mreb
THA_1626	ENOG4105CDF	Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine (By similarity)
THA_1630	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)
THA_1633	ENOG4105W00	Flagellar hook capping protein
THA_1634	ENOG4105BZE	flagellar hook protein, FlgE
THA_1635	ENOG41068WV	flagellar FlbD family protein
THA_1636	ENOG4105E14	MotA TolQ exbB proton channel
THA_1637	ENOG4107XSU	flagellar motor protein motb
THA_1639	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)
THA_1640	ENOG4105DD5	Flagellar motor switch protein
THA_1642	ENOG4105K8I	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves (By similarity)
THA_1643	ENOG4108KVX	Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves (By similarity)
THA_1644	ENOG4105CJW	magnesium transporter
THA_1646	ENOG4105CJS	Phosphopantothenoylcysteine decarboxylase
THA_1647	ENOG4105CCG	Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is tranferred onto alpha-ketoisovalerate to form ketopantoate (By similarity)
THA_1648	ENOG4108RW0	Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid (By similarity)
THA_1650	ENOG4105E0A	ABC, transporter
THA_1653	ENOG4108ZBE	Binds to sigma F and blocks its ability to form an RNA polymerase holoenzyme (E-sigma F). Phosphorylates SpoIIAA on a serine residue. This phosphorylation may enable SpoIIAA to act as an anti-anti-sigma factor that counteracts SpoIIAB and thus releases sigma F from inhibition (By similarity)
THA_1654	ENOG4105WPN	DNA integration recombination invertion protein
THA_1655	ENOG4108YYA	Hydrolyzes D-tyrosyl-tRNA(Tyr) into D-tyrosine and free tRNA(Tyr). Could be a defense mechanism against a harmful effect of D-tyrosine (By similarity)
THA_1656	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)
THA_1660	ENOG4105C7W	Xanthine dehydrogenase
THA_1661	ENOG4107YV9	domain protein
THA_1665	ENOG4108IYI	Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine (By similarity)
THA_1668	ENOG4105C22	threonyL-tRNA synthetase
THA_1669	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1673	ENOG4105H20	Sporulation integral membrane protein YlbJ
THA_1674	ENOG4105CU5	Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine (By similarity)
THA_1677	ENOG4107YBR	Specifically methylates the N7 position of a guanine in 16S rRNA (By similarity)
THA_1678	ENOG4105C1H	Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 (By similarity)
THA_1681	ENOG4107QQG	Dehydrogenase
THA_1683	ENOG4105BZ8	glutamate synthase
THA_1684	ENOG4105CQV	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient (By similarity)
THA_1685	ENOG4105CYU	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain
THA_1686	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)
THA_1687	ENOG4105CMZ	NDH-1 shuttles electrons from NADH, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. This subunit may bind ubiquinone (By similarity)
THA_1688	ENOG4108JPZ	Monovalent cation H antiporter subunit D
THA_1689	ENOG4108JPZ	Monovalent cation H antiporter subunit D
THA_169	ENOG4105D0C	transport protein
THA_1691	ENOG4105MKQ	Monovalent cation H antiporter subunit C
THA_1692	ENOG4105D65	subunit l
THA_1695	ENOG410684G	monovalent cation H antiporter subunit F
THA_1696	ENOG4105SC1	monovalent cation H antiporter subunit E
THA_1697	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
THA_1699	ENOG4105C87	Aminotransferase class I and II
THA_170	ENOG4105CM3	Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate (By similarity)
THA_1701	ENOG4105CGH	5'-nucleotidase
THA_1702	ENOG4107104	thymidine kinase
THA_1703	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1709	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)
THA_171	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)
THA_1710	ENOG4105CZ5	Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate (By similarity)
THA_1711	ENOG4105C8K	Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA (By similarity)
THA_1712	ENOG4105CZX	twitching motility protein
THA_1713	ENOG4105C6E	dna polymerase iii
THA_1714	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)
THA_1717	ENOG4105D78	K07001 NTE family protein
THA_1718	ENOG4105EFU	Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin (By similarity)
THA_172	ENOG4105CDP	Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) (By similarity)
THA_1720	ENOG4105C4K	Nad synthetase
THA_1724	ENOG4105C3B	Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins (By similarity)
THA_1725	ENOG4105E3H	phosphoglycerate mutase
THA_1726	ENOG4107ZP9	ComEC Rec2-related protein
THA_1727	ENOG4105CHV	Transcription elongation factor NusA
THA_1728	ENOG4108396	Required for maturation of 30S ribosomal subunits (By similarity)
THA_173	ENOG4105DUK	Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate (By similarity)
THA_1733	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)
THA_1736	ENOG4107QJF	Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate (By similarity)
THA_1737	ENOG4105VG1	fes assembly suf system protein
THA_1738	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)
THA_1739	ENOG4105K9Q	Binds to the 23S rRNA (By similarity)
THA_174	ENOG4105DMJ	Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate (By similarity)
THA_1742	ENOG4105D4J	Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate
THA_1748	ENOG4105DN4	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
THA_1749	ENOG4108Z4W	Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis (By similarity)
THA_1750	ENOG4107PHP	CheC --inhibitor of MCP methylation
THA_1754	ENOG4105FZW	flagellar biosynthesis regulator FlhF
THA_1755	ENOG4105D7B	Flagellar biosynthesis protein flha
THA_176	ENOG4105C8Y	Acetylornithine aminotransferase
THA_1764	ENOG4107WSY	Domain of unknown function DUF20
THA_1765	ENOG4105DXN	mazG family
THA_1766	ENOG4105C2N	RNA methyltransferase TrmH family group 3
THA_1770	ENOG4105C40	3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs (By similarity)
THA_1772	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)
THA_1774	ENOG4105C4F	May be involved in recombinational repair of damaged DNA (By similarity)
THA_1775	ENOG4105KG3	cytidine deaminase
THA_1776	ENOG4105C37	(CBS) domain
THA_1777	ENOG4105CCT	upf0313 protein
THA_1778	ENOG4105E06	May play a role in 30S ribosomal subunit biogenesis. Unusual circulary permuted GTPase that catalyzes rapid hydrolysis of GTP with a slow catalytic turnover (By similarity)
THA_178	ENOG4105CF4	DegT DnrJ EryC1 StrS aminotransferase
THA_1780	ENOG4105C55	Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs
THA_1781	ENOG4107V1F	Flagellar hook-associated 2 domain-containing protein
THA_1783	ENOG41084NJ	Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Essential for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA (By similarity)
THA_1784	ENOG4108HU6	Metal dependent phosphohydrolase
THA_1785	ENOG4105BZU	Histidine kinase
THA_1787	ENOG4105WHM	Necessary for normal cell division and for the maintenance of normal septation (By similarity)
THA_1788	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)
THA_1789	ENOG4105K8N	protein family UPF0079, ATPase
THA_179	ENOG4105CE8	Transfers the fatty acyl group on membrane lipoproteins (By similarity)
THA_1791	ENOG4105MA4	psp1 domain protein
THA_1792	ENOG4105C0Q	Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP (By similarity)
THA_1793	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)
THA_1795	ENOG4105VKD	bioY protein
THA_1796	ENOG4105CJF	Malonyl coA-acyl carrier protein transacylase
THA_1798	ENOG4105IQJ	Involved in biosynthesis of the thiamine precursor thiazole (By similarity)
THA_1799	ENOG4105CBF	Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction (By similarity)
THA_1801	ENOG4107ZCS	Phosphomethylpyrimidine kinase
THA_1802	ENOG4105CTQ	phosphohexokinase
THA_1803	ENOG4105CPN	adenine deaminase
THA_1804	ENOG4107QW8	radical SAM domain protein
THA_1808	ENOG4107QHI	-hydrogenase
THA_181	ENOG4105D43	The glycine cleavage system catalyzes the degradation of glycine (By similarity)
THA_1811	ENOG4108ZBM	Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Also processes some mRNAs, and tRNAs when they are encoded in the rRNA operon (By similarity)
THA_1812	ENOG4105CM0	Catalyzes the synthesis of GMP from XMP (By similarity)
THA_1813	ENOG4105HJX	Biotin- acetyl-CoA-carboxylase ligase
THA_1814	ENOG4105CJR	Integral membrane protein (MviN
THA_1815	ENOG4108R3D	Electron transport complex
THA_1816	ENOG4105C79	DNA protecting protein DprA
THA_1817	ENOG4108IAA	Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate (By similarity)
THA_1819	ENOG4107QUF	Involved in mRNA degradation. Hydrolyzes single-stranded polyribonucleotides processively in the 3'- to 5'-direction (By similarity)
THA_182	ENOG4107QK8	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
THA_1820	ENOG4105C1V	Peptidase, M16
THA_1821	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1822	ENOG4105C4N	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 (By similarity)
THA_1823	ENOG4105E4X	binding-protein-dependent transport systems inner membrane Component
THA_1824	ENOG4105DRS	transport system, permease
THA_1825	ENOG4105CW3	Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway (By similarity)
THA_1826	ENOG4105C9M	aspartyl-trna synthetase
THA_1827	ENOG41084GC	stage II sporulation protein
THA_1828	ENOG4107RB4	Cytidine monophosphate kinase
THA_1829	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)
THA_183	ENOG4105CBI	The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor
THA_1830	ENOG4105DKZ	GTPase that plays an essential role in the late steps of ribosome biogenesis (By similarity)
THA_1831	ENOG4107TFB	basic membrane
THA_1833	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_1834	ENOG41085QA	50S ribosomal protein l34
THA_1835	ENOG41084AH	RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme (By similarity)
THA_1836	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
THA_184	ENOG4105C0A	alcohol dehydrogenase
THA_1841	ENOG4105C5F	glutamine synthetase
THA_1842	ENOG4105BZU	Histidine kinase
THA_1844	ENOG4105C9U	ATP-dependent DNA helicase RecQ
THA_1847	ENOG4105BZ1	(ABC) transporter
THA_1857	ENOG4105C0B	DNA polymerase III (alpha subunit)
THA_1858	ENOG4105DJV	ribulose-phosphate 3-epimerase
THA_1859	ENOG4105CB1	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (By similarity)
THA_1860	ENOG4105SFS	phosphoesterase RecJ domain protein
THA_1861	ENOG4105BZU	Histidine kinase
THA_1862	ENOG4105D4A	Cell wall formation (By similarity)
THA_1863	ENOG4105DFM	M18 family aminopeptidase
THA_1868	ENOG4105DG6	mannose-6-phosphate isomerase
THA_187	ENOG4105M6F	mutator MutT protein
THA_1870	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
THA_1871	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)
THA_1872	ENOG4105DFA	alanine racemase domain protein
THA_1874	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)
THA_1875	ENOG4105QGT	Phosphate uptake regulator
THA_1877	ENOG4105BZT	Catalyzes the formation of 5-methyl-uridine at position 1939 (m5U1939) in 23S rRNA (By similarity)
THA_1878	ENOG4105DC1	bifunctional purine biosynthesis protein purh
THA_188	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)
THA_1882	ENOG4105CG1	Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA (By similarity)
THA_1883	ENOG4107U53	septum site-determining protein minD
THA_1888	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)
THA_189	ENOG4105CGP	Urocanate hydratase
THA_1890	ENOG41069ER	domain protein
THA_1892	ENOG4105CCJ	Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 (By similarity)
THA_1893	ENOG4105D3U	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
THA_1894	ENOG4108KGH	TRANSCRIPTIONal
THA_1895	ENOG4105Y7X	Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA. Acts in DNA repair (By similarity)
THA_1897	ENOG4105N5T	Radical SAM Protein
THA_1898	ENOG4105D6T	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)
THA_190	ENOG4105DI2	Pyruvate flavodoxin ferredoxin oxidoreductase domain protein
THA_1900	ENOG4105DPM	folylpolyglutamate synthase Dihydrofolate synthase
THA_1901	ENOG4105CA4	amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner (By similarity)
THA_1903	ENOG4107QTR	Required for nitrogen fixation. May be part of a membrane complex functioning as an intermediate in the electron transport to nitrogenase (By similarity)
THA_1904	ENOG4105D6A	Electron transport complex
THA_1906	ENOG4105DZB	Electron transport complex
THA_1907	ENOG4105DGN	Electron transport complex
THA_1912	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)
THA_1914	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
THA_1915	ENOG4108IUK	alpha amylase, catalytic
THA_1916	ENOG410626R	Converts the free carboxyl group of a malonyl-thioester to its methyl ester by transfer of a methyl group from S-adenosyl- L-methionine (SAM). It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway (By similarity)
THA_1918	ENOG4107R3E	Citrate transporter
THA_1919	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
THA_192	ENOG4105D9Q	decarboxylase (Beta subunit)
THA_1921	ENOG4105D0I	Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate (By similarity)
THA_1922	ENOG4105D18	nicotinate-nucleotide pyrophosphorylase
THA_1924	ENOG4105BZU	Histidine kinase
THA_1926	ENOG4105CS2	ec 3.2.1.21
THA_1927	ENOG4105EJ9	Membrane
THA_1929	ENOG4107QSE	Dipeptidase
THA_1932	ENOG4105DB9	Binding-protein-dependent transport systems inner membrane component
THA_1937	ENOG4105C50	Binding-protein-dependent transport systems, inner membrane component
THA_194	ENOG4108JJB	ABC transporter
THA_1940	ENOG4107QM2	Aldo Keto reductase
THA_1942	ENOG4107QK4	glycoside hydrolase, family 3 domain protein
THA_1944	ENOG4105DTQ	mandelate racemase muconate lactonizing
THA_1946	ENOG4105IJJ	transcriptional regulator, crp fnr family
THA_1947	ENOG4108KN7	Removes 5-oxoproline from various penultimate amino acid residues except L-proline (By similarity)
THA_1948	ENOG4108JEB	The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine (By similarity)
THA_1954	ENOG4105ZHF	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
THA_1955	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
THA_196	ENOG4105CTQ	phosphohexokinase
THA_1962	ENOG4105KAV	tspo and mbr like protein
THA_1966	ENOG4105ETE	Transcriptional regulator (LacI family
THA_1967	ENOG4105HS6	binding-protein-dependent transport systems inner membrane Component
THA_1968	ENOG4105DRS	transport system, permease
THA_197	ENOG4105EAY	pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for
THA_1970	ENOG4107V4V	glycoside hydrolase family 4
THA_1974	ENOG4105D6J	arsenicaL-resistance protein
THA_1976	ENOG4108UU4	oxidoreductase (Short chain dehydrogenase reductase family)
THA_1978	ENOG4105DQU	oxidoreductase, subunit beta
THA_198	ENOG4107VRQ	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)
THA_1983	ENOG4108MVM	Transposase
THA_1988	ENOG4108IJ9	(ABC) transporter
THA_1989	ENOG4105IRK	Glycosyl transferase (Group 1
THA_199	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)
THA_1990	ENOG4106KNT	transcriptional regulator
THA_1994	ENOG4105KAV	tspo and mbr like protein
THA_20	ENOG4105EJ9	Membrane
THA_200	ENOG4107Z7W	Preprotein translocase YajC subunit
THA_2000	ENOG4107QMH	DNA methylase
THA_2001	ENOG41085W3	Transposase
THA_2006	ENOG4105D7V	transposase
THA_2007	ENOG4105DQ6	Transposase
THA_201	ENOG4105CN0	Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate (By similarity)
THA_2012	ENOG4105DQ6	Transposase
THA_2015	ENOG4105D7V	transposase
THA_2016	ENOG4105DQ6	Transposase
THA_2017	ENOG41085W3	Transposase
THA_2018	ENOG4105DQ6	Transposase
THA_2019	ENOG41085W3	Transposase
THA_2022	ENOG4105DQ6	Transposase
THA_2024	ENOG41085W3	Transposase
THA_203	ENOG41087GE	Catalyzes the formation of dTMP and tetrahydrofolate from dUMP and methylenetetrahydrofolate (By similarity)
THA_2031	ENOG4105DQ6	Transposase
THA_2033	ENOG4105DQ6	Transposase
THA_2038	ENOG41085W3	Transposase
THA_204	ENOG4108UH2	Endonuclease that specifically degrades the RNA of RNA- DNA hybrids (By similarity)
THA_2040	ENOG4105DQ6	Transposase
THA_2041	ENOG41085W3	Transposase
THA_2042	ENOG41085W3	Transposase
THA_207	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)
THA_210	ENOG4105DVS	Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides (By similarity)
THA_211	ENOG4105C2M	dna polymerase I
THA_213	ENOG4105CIT	This protein may be involved in anomalous filament growth. May be a component of the septum (By similarity)
THA_214	ENOG4105C98	muts2 protein
THA_216	ENOG4107QXV	Phosphate transporter
THA_22	ENOG4105CJN	penicillin-binding protein
THA_220	ENOG4105CE5	Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) (By similarity)
THA_221	ENOG4105C1W	two component, sigma54 specific, transcriptional regulator, Fis family
THA_222	ENOG4107RE7	phosphate butyryltransferase
THA_224	ENOG4105CI4	it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids (By similarity)
THA_225	ENOG41084T3	4fe-4S ferredoxin iron-sulfur binding domain-containing protein
THA_227	ENOG4105DIH	basic membrane
THA_228	ENOG4108JQ9	ABC transporter
THA_229	ENOG4105UIB	(ABC) transporter
THA_235	ENOG4105EPR	degv family
THA_236	ENOG4105EPR	degv family
THA_237	ENOG4105DNJ	May play a role in the repair of endogenous alkylation damage (By similarity)
THA_24	ENOG4105CGJ	Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA (By similarity)
THA_243	ENOG4105ENN	converts alpha-aldose to the beta-anomer. It is active on D-glucose, L-arabinose, D-xylose, D-galactose, maltose and lactose (By similarity)
THA_247	ENOG4105C3M	thioredoxin reductase
THA_248	ENOG4108W2Y	isochorismatase
THA_249	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)
THA_25	ENOG4105D6T	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)
THA_251	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)
THA_252	ENOG4105FJ0	thiamine
THA_253	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)
THA_254	ENOG4105JKQ	Part of the ABC transporter complex BtuCDF involved in vitamin B12 import. Binds vitamin B12 and delivers it to the periplasmic surface of BtuC (By similarity)
THA_255	ENOG4105EHG	Permease protein
THA_256	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)
THA_257	ENOG4105DG1	Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released (By similarity)
THA_259	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)
THA_26	ENOG4105C6T	cysteine synthase
THA_260	ENOG4105C66	Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate (By similarity)
THA_261	ENOG4108R6K	riboflavin synthase, subunit alpha
THA_262	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)
THA_263	ENOG4105C8Q	Methyl-accepting chemotaxis
THA_264	ENOG4107YH3	SUF system FeS assembly protein, NifU family
THA_265	ENOG4105C9B	Cysteine desulfurase
THA_266	ENOG4105JRK	feS assembly protein SufD
THA_267	ENOG4105DIW	FeS assembly protein SUFB
THA_269	ENOG4105CJ9	Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions (By similarity)
THA_270	ENOG41083C3	Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter (By similarity)
THA_272	ENOG4105KEB	Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc)
THA_274	ENOG4105D1U	peptidase U62 modulator of DNA gyrase
THA_275	ENOG4105CMS	peptidase U62, modulator of DNA gyrase
THA_276	ENOG4106M28	alanine racemase domain protein
THA_278	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)
THA_279	ENOG4105K77	Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome (By similarity)
THA_28	ENOG4105CPN	adenine deaminase
THA_280	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)
THA_281	ENOG4105C8N	cysteinyl-tRNA synthetase
THA_282	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)
THA_283	ENOG4105C2W	permease
THA_288	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)
THA_289	ENOG4108JYZ	YitT family
THA_294	ENOG4105CXW	Synthesizes alpha-1,4-glucan chains using ADP-glucose (By similarity)
THA_296	ENOG4108JUB	Transcriptional regulator
THA_297	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
THA_298	ENOG4105CPF	Cell wall formation (By similarity)
THA_30	ENOG4108JQ7	(ABC) transporter
THA_301	ENOG4105C5I	Dehydrogenase
THA_302	ENOG4105D1Z	hydroxypyruvate reductase
THA_303	ENOG4107S7H	nh(3)-dependent nad( ) synthetase
THA_304	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)
THA_305	ENOG41085Z1	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
THA_307	ENOG41079KZ	Major Facilitator Superfamily
THA_308	ENOG4108Z3G	3H domain protein
THA_31	ENOG4105C3U	ABC transporter
THA_32	ENOG4105C2T	Binding-protein-dependent transport systems, inner membrane component
THA_321	ENOG4105ZHF	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
THA_322	ENOG4105DYN	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. May be involved in the integration of spacer DNA into the CRISPR cassette (By similarity)
THA_323	ENOG4105ZHF	CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease (By similarity)
THA_325	ENOG41090X3	Peptidyl-prolyl cis-trans isomerase
THA_328	ENOG4105CN9	Peptidase m42 family protein
THA_329	ENOG4105CN9	Peptidase m42 family protein
THA_330	ENOG41065EC	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)
THA_331	ENOG4108UHA	Essential for recycling GMP and indirectly, cGMP (By similarity)
THA_332	ENOG4105KC4	UPF0296 protein
THA_337	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)
THA_339	ENOG4105CKM	Branched-chain carboxylic acid kinase
THA_34	ENOG4105CII	The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision (By similarity)
THA_340	ENOG4107RE7	phosphate butyryltransferase
THA_341	ENOG4105CKM	Branched-chain carboxylic acid kinase
THA_342	ENOG4105C1I	TRANSCRIPTIONAl REGULATOR GntR family
THA_344	ENOG4105C5R	Aminotransferase
THA_345	ENOG4108JQ1	Dehydrogenase
THA_347	ENOG4107S4Y	M20 DapE family protein YgeY
THA_348	ENOG4105IW6	Carbamoyltransferase
THA_351	ENOG4107QYT	Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor (By similarity)
THA_357	ENOG4105MCT	stage V sporulation protein S
THA_358	ENOG4105CGH	5'-nucleotidase
THA_359	ENOG4105BZ1	(ABC) transporter
THA_36	ENOG4105KE9	The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein (By similarity)
THA_365	ENOG4105D8I	Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS (By similarity)
THA_366	ENOG4105EKT	)-iron permease
THA_370	ENOG4105VPX	protein, conserved in bacteria
THA_371	ENOG4105BZ1	(ABC) transporter
THA_375	ENOG4108MVM	Transposase
THA_38	ENOG4105CE1	Ferrous iron transport protein b
THA_380	ENOG4105DPN	Oligoendopeptidase f
THA_381	ENOG4107QJQ	Mate efflux family protein
THA_383	ENOG4105CPC	Aldo Keto reductase
THA_386	ENOG4105CJ1	ABC, transporter
THA_388	ENOG4105D1H	recombination factor protein RarA
THA_389	ENOG4105D1H	recombination factor protein RarA
THA_392	ENOG4108UN4	phage SPO1 DNA polymerase-related protein
THA_393	ENOG4108HRN	Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate (By similarity)
THA_395	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)
THA_396	ENOG4105C5T	Phosphoribosyl pyrophosphate synthase
THA_397	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)
THA_398	ENOG4108ZPD	The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis (By similarity)
THA_4	ENOG4105C1J	atp-dependent rna helicase
THA_402	ENOG4108I67	Catalyzes the synthesis of activated sulfate (By similarity)
THA_403	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)
THA_404	ENOG4108I7H	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)
THA_405	ENOG4105C70	Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis (By similarity)
THA_407	ENOG4105ZU5	s-layer protein
THA_408	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)
THA_41	ENOG4105KQC	Competence protein
THA_410	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
THA_411	ENOG4105C4H	Specifically methylates the guanine in position 2445 (m2G2445) and the guanine in position 2069 (m7G2069) of 23S rRNA (By similarity)
THA_412	ENOG4105KJJ	Uncharacterized ACR, COG1993
THA_413	ENOG4105WMR	Protein CrcB homolog
THA_415	ENOG4108V82	Pyrophosphatase that hydrolyzes non-canonical purine nucleotides such as XTP and ITP dITP to their respective monophosphate derivatives. Might exclude non-canonical purines from DNA precursor pool, thus preventing their incorporation into DNA and avoiding chromosomal lesions (By similarity)
THA_416	ENOG41082VF	Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA (By similarity)
THA_418	ENOG4105F59	Methylates ribosomal protein L11 (By similarity)
THA_419	ENOG4105DR5	peptidase
THA_42	ENOG41074MP	UPF0103 Mediator of ErbB2-driven cell motility-containing protein
THA_421	ENOG4108UYI	beta-alanyl-CoA ammonia lyase
THA_422	ENOG4105DE9	3-keto-5-aminohexanoate cleavage enzyme
THA_423	ENOG4105FRY	Dehydrogenase
THA_424	ENOG4105CK3	Lysine 2,3-aminomutase YodO family protein
THA_425	ENOG4108F01	MaoC domain protein
THA_427	ENOG4105D86	that it carries out the mismatch recognition step. This protein has a weak ATPase activity (By similarity)
THA_428	ENOG4105EQ5	D-Lysine 5,6-aminomutase alpha subunit
THA_429	ENOG4107CHF	5,6-aminomutase beta subunit
THA_43	ENOG4105GVR	general secretion pathway protein D
THA_432	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)
THA_438	ENOG4105CBM	Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 (By similarity)
THA_440	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)
THA_441	ENOG4105D3U	Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine (By similarity)
THA_442	ENOG4105CN9	Peptidase m42 family protein
THA_444	ENOG4105DWR	Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin (By similarity)
THA_445	ENOG4105CI2	imidazolone-5-propionate hydrolase
THA_448	ENOG4108Z03	MAF-like protein
THA_449	ENOG4105W5Q	DNA repair protein (RadC
THA_452	ENOG4105CND	Glycosyl transferase, family 2
THA_453	ENOG4105K64	Glycosyl transferase, family 2
THA_458	ENOG4105CN1	protease
THA_459	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)
THA_462	ENOG4108WF2	Metal Dependent Phosphohydrolase
THA_464	ENOG4108R5P	Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery (By similarity)
THA_465	ENOG4105EK0	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
THA_467	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)
THA_468	ENOG4105DMZ	Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) (By similarity)
THA_469	ENOG4107QXI	Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs (By similarity)
THA_470	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)
THA_473	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)
THA_475	ENOG4105CNB	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
THA_476	ENOG4105CNB	Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans (By similarity)
THA_477	ENOG4105FCI	Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate (By similarity)
THA_478	ENOG4108UH4	Binds specifically to the SsrA RNA (tmRNA) and is required for stable association of SsrA with ribosomes (By similarity)
THA_479	ENOG41084A9	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)
THA_481	ENOG4105W5T	Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum (By similarity)
THA_484	ENOG4105DP4	dak2 domain fusion protein ylov
THA_486	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)
THA_487	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)
THA_488	ENOG4105C35	Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1-P) (By similarity)
THA_489	ENOG4105G6Z	alkaline phosphatase
THA_491	ENOG4105C8T	Leucyl-tRNA synthetase
THA_495	ENOG4108MVM	Transposase
THA_497	ENOG4107R4Q	Functions as an ATPase. May play a role in metal insertion (metal-chelatase) or as a chaperone (By similarity)
THA_499	ENOG4108MVM	Transposase
THA_50	ENOG4108JJB	ABC transporter
THA_501	ENOG4105DZP	Membrane-associated zinc metalloprotease
THA_502	ENOG4105BZU	Histidine kinase
THA_503	ENOG4108MVM	Transposase
THA_504	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_506	ENOG4105C4E	Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (By similarity)
THA_508	ENOG4107VJ5	dihydroorotase
THA_509	ENOG4105I47	Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) (By similarity)
THA_51	ENOG4107Y49	methyltransferase
THA_510	ENOG4107W93	Dihydroorotate dehydrogenase
THA_511	ENOG4107YPM	Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) (By similarity)
THA_512	ENOG4107QV3	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)
THA_515	ENOG4108V3W	Chemotaxis protein, CheW
THA_516	ENOG4105C25	Primosomal protein n'
THA_518	ENOG4105DDK	oxidoreductase, beta subunit
THA_519	ENOG4105D95	Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin (By similarity)
THA_520	ENOG4105WGB	oxidoreductase, delta subunit
THA_521	ENOG4105EJ5	oxidoreductase gamma subunit
THA_522	ENOG4107RFW	hydrolase family 57
THA_524	ENOG4105EJQ	L-serine dehydratase
THA_527	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_53	ENOG4105CV1	Transketolase (EC 2.2.1.1)
THA_530	ENOG4105DW3	Response regulator receiver modulated metal dependent phosphohydrolase
THA_531	ENOG4105F8J	Adenylate Guanylate cyclase
THA_533	ENOG4105I03	Flagellin
THA_534	ENOG4105E1Q	flagellar hook-associated protein
THA_534	ENOG4105E1Q	flagellar hook-associated protein
THA_537	ENOG4105C8Q	Methyl-accepting chemotaxis
THA_539	ENOG4105C31	Tryptophanyl-tRNA synthetase
THA_540	ENOG4105DAN	ATP-dependent protease
THA_541	ENOG4107SJN	Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol (By similarity)
THA_544	ENOG4105E8R	UPF0173 metal-dependent hydrolase
THA_546	ENOG4105C91	Plays an important role in the de novo pathway of purine nucleotide biosynthesis
THA_547	ENOG4107YU2	histidine triad (hIT) protein
THA_549	ENOG4105VNB	Carrier of the growing fatty acid chain in fatty acid biosynthesis (By similarity)
THA_550	ENOG4105D82	Glutamate dehydrogenase
THA_553	ENOG4108MVM	Transposase
THA_555	ENOG4105CKU	formyltetrahydrofolate synthetase
THA_556	ENOG4105BZU	Histidine kinase
THA_557	ENOG4107S82	Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress (By similarity)
THA_559	ENOG4105C2R	Single-stranded-DNA-specific exonuclease (RecJ)
THA_56	ENOG4105GRF	N-glycosylase DNA lyase
THA_560	ENOG41084RN	Could be a nuclease that resolves Holliday junction intermediates in genetic recombination (By similarity)
THA_562	ENOG4105DC7	peptidase M24
THA_566	ENOG410855G	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)
THA_567	ENOG4108BYY	F-type ATPase subunit b
THA_568	ENOG41085KK	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)
THA_569	ENOG4105CDG	Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit (By similarity)
THA_570	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)
THA_571	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)
THA_572	ENOG41082J0	Produces ATP from ADP in the presence of a proton gradient across the membrane (By similarity)
THA_573	ENOG4105EPR	degv family
THA_575	ENOG4105MS2	ribosomal subunit Interface protein
THA_576	ENOG4105BZU	Histidine kinase
THA_577	ENOG4108Z2X	Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine (By similarity)
THA_58	ENOG4105C3F	Signal peptidase i
THA_580	ENOG4107S5Z	Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domain of GcvH, an intermediate carrier during protein lipoylation (By similarity)
THA_581	ENOG4105CU0	Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA (By similarity)
THA_582	ENOG4105VEQ	Cold shock protein
THA_584	ENOG4107UKG	Glycosyl transferase, family 4
THA_589	ENOG4105CSM	endonuclease III
THA_59	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)
THA_592	ENOG4105C7N	Xanthine uracil vitamin C permease
THA_595	ENOG4105CB5	ATP-dependent DNA helicase recG
THA_6	ENOG4105C0D	helicase
THA_60	ENOG4108WTY	tRNA (Guanine-N(1)-)-methyltransferase
THA_61	ENOG4105D6X	Specifically methylates guanosine-37 in various tRNAs (By similarity)
THA_610	ENOG4105ETE	Transcriptional regulator (LacI family
THA_611	ENOG4105D22	carbon starvation protein
THA_612	ENOG4105DY9	regulatoR
THA_613	ENOG4108HRK	Histidine kinase
THA_615	ENOG4105EX2	Binding-protein-dependent transport systems, inner membrane component
THA_618	ENOG4107S85	alpha-2-macroglobulin domain protein
THA_62	ENOG410836E	An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes (By similarity)
THA_620	ENOG4108QJJ	Protein of unknown function (DUF1175)
THA_621	ENOG4105DRY	peptidase s9 prolyl oligopeptidase active site domain protein
THA_622	ENOG4105C8J	)-transporter
THA_623	ENOG4105BZU	Histidine kinase
THA_624	ENOG41084X0	Dihydrofolate reductase
THA_626	ENOG4105BZU	Histidine kinase
THA_63	ENOG41084QK	UPF0109 protein
THA_630	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)
THA_631	ENOG4108UIK	This protein binds directly to 23S ribosomal RNA (By similarity)
THA_632	ENOG4105E5V	Participates in transcription elongation, termination and antitermination (By similarity)
THA_633	ENOG410683Z	Preprotein translocase SecE subunit
THA_637	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)
THA_638	ENOG4108UUM	single-stranded DNA-binding protein
THA_639	ENOG41083EQ	Binds together with S18 to 16S ribosomal RNA (By similarity)
THA_64	ENOG4105K5M	30s ribosomal protein S16
THA_642	ENOG4105CNI	cell division protein FtsW
THA_644	ENOG4107QIB	glycyl-tRNA synthetase, alpha subunit
THA_645	ENOG4107RFA	Glycyl-tRNA synthetase beta subunit
THA_646	ENOG4108RAC	Rubrerythrin
THA_647	ENOG4107QJR	hflk protein
THA_648	ENOG4105EPW	hflc protein
THA_649	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)
THA_650	ENOG4105CPM	Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine (By similarity)
THA_651	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)
THA_655	ENOG4108JJB	ABC transporter
THA_658	ENOG4108KHP	Diguanylate cyclase
THA_659	ENOG4107KMQ	bfd domain protein (2fe-2s)-binding domain protein
THA_662	ENOG4108JQ0	Key enzyme in the regulation of glycerol uptake and metabolism (By similarity)
THA_663	ENOG4108ZIA	glycerol-3-phosphate responsive antiterminator
THA_669	ENOG4105MRB	Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose (By similarity)
THA_670	ENOG4105C2J	ABC transporter
THA_671	ENOG4105CNN	ABC, transporter
THA_672	ENOG4105E9V	Periplasmic binding protein LacI transcriptional regulator
THA_674	ENOG4108RVA	ribokinase
THA_676	ENOG4105F1A	Pyruvate formate-lyase
THA_677	ENOG4105CJD	(Anaerobic) ribonucleoside-triphosphate reductase
THA_68	ENOG4106SMU	thiamine transporter membrane protein
THA_682	ENOG4105DIW	FeS assembly protein SUFB
THA_685	ENOG4105DYB	Isoaspartyl dipeptidase
THA_687	ENOG4107FKK	extracellular solute-binding protein family 1
THA_688	ENOG4105D56	permease protein
THA_689	ENOG4105EG2	ABC transporter, permease
THA_697	ENOG4106I92	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
THA_698	ENOG4108J5C	NQR complex catalyzes the reduction of ubiquinone-1 to ubiquinol by two successive reactions, coupled with the transport of Na( ) ions from the cytoplasm to the periplasm. NqrA to NqrE are probably involved in the second step, the conversion of ubisemiquinone to ubiquinol (By similarity)
THA_70	ENOG4107QQN	Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties (By similarity)
THA_701	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)
THA_702	ENOG41076QQ	Glycosyl transferase, family 2
THA_703	ENOG4108X8W	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)
THA_705	ENOG4107EXU	Short-chain dehydrogenase reductase Sdr
THA_706	ENOG4105EWK	phytoene
THA_71	ENOG4105C0H	protease
THA_710	ENOG4105BZU	Histidine kinase
THA_712	ENOG4108YXY	alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen
THA_716	ENOG4105CMR	udp-glucose 4-epimerase
THA_717	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
THA_722	ENOG4105K70	DNA-binding protein
THA_723	ENOG4105KHV	Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate (By similarity)
THA_724	ENOG4108YXI	Secondary thiamine-phosphate synthase enzyme
THA_726	ENOG4107XSR	periplasmic solute binding protein
THA_727	ENOG4105FDK	ABC transporter
THA_728	ENOG41080V6	ABC-3 protein
THA_73	ENOG4105EHH	Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue (By similarity)
THA_730	ENOG4105C1G	acyl-Coa dehydrogenase
THA_731	ENOG4105BZJ	Electron transfer flavoprotein
THA_737	ENOG4108V3E	phosphoribosylglycinamide formyltransferase
THA_738	ENOG4105DC1	bifunctional purine biosynthesis protein purh
THA_739	ENOG4107QNG	Phosphoribosylglycinamide synthetase
THA_742	ENOG4107RA4	Glycosyl transferase (Group 1
THA_746	ENOG4107RA4	Glycosyl transferase (Group 1
THA_75	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)
THA_752	ENOG4105CJ1	ABC, transporter
THA_757	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
THA_758	ENOG4108Z1W	Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) (By similarity)
THA_759	ENOG4105CEH	Catalyzes the synthesis of dihydrouridine a modified base found in the D-loop of most tRNAs (By similarity)
THA_761	ENOG4105CHM	Aminotransferase
THA_762	ENOG4108N5B	2-phosphosulfolactate phosphatase
THA_765	ENOG4105BZ4	penicillin-binding protein
THA_768	ENOG4108MVM	Transposase
THA_77	ENOG4105CZ1	Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA (By similarity)
THA_770	ENOG4105CJM	Binding-protein-dependent transport systems, inner membrane component
THA_773	ENOG4108JQ7	(ABC) transporter
THA_774	ENOG4105CKB	glycosidase
THA_776	ENOG4105ETE	Transcriptional regulator (LacI family
THA_778	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)
THA_78	ENOG4105CSF	NADPH-dependent glycerol-3-phosphate dehydrogenase
THA_780	ENOG4105EZM	VWA-like domain (DUF2201)
THA_782	ENOG4105Y5S	NADH ubiquinone oxidoreductase, 24 kD
THA_786	ENOG4107QIZ	NADH dehydrogenase
THA_787	ENOG4107QHI	-hydrogenase
THA_788	ENOG4105FF6	Modulates transcription in response to changes in cellular NADH NAD( ) redox state (By similarity)
THA_790	ENOG4108EQQ	Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein (By similarity)
THA_791	ENOG4106HB6	Alpha beta hydrolase
THA_792	ENOG4105CPF	Cell wall formation (By similarity)
THA_793	ENOG41083B7	nucleosidase (EC 3.2.2.9)
THA_794	ENOG4108W5Z	CheC domain protein
THA_795	ENOG4105C9W	Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity (By similarity)
THA_796	ENOG4105C41	Catalyzes the reversible phosphorylation of UMP to UDP (By similarity)
THA_799	ENOG4108IAB	Phoh family
THA_800	ENOG4105DE5	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity (By similarity)
THA_801	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)
THA_802	ENOG4105C1F	The M ring may be actively involved in energy transduction (By similarity)
THA_805	ENOG41085U1	50S ribosomal protein L32
THA_806	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)
THA_807	ENOG4105C46	Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source (By similarity)
THA_808	ENOG4105C1V	Peptidase, M16
THA_810	ENOG4105CGA	flagellar basal-body rod protein FlgG
THA_811	ENOG4105KTQ	flagellar basal-body rod protein
THA_812	ENOG4105DFF	Rod shape-determining protein mreb
THA_818	ENOG4108MVM	Transposase
THA_824	ENOG4105EJ7	Catalyzes the reduction of hydroxylamine to form NH(3) and H(2)O (By similarity)
THA_825	ENOG4105G6Z	alkaline phosphatase
THA_826	ENOG4105CDU	Replicative dna helicase
THA_827	ENOG4108ZEF	Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate (By similarity)
THA_83	ENOG4105DER	m42 family
THA_830	ENOG410631K	Membrane
THA_832	ENOG4105CT4	transporter
THA_833	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)
THA_834	ENOG4105CK6	Two component transcriptional regulator (Winged helix family
THA_835	ENOG4108IUM	Glycogen debranching enzyme
THA_836	ENOG4105EP6	Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB (By similarity)
THA_837	ENOG41062JF	Transcriptional regulator
THA_841	ENOG4107SDU	Methyl-accepting chemotaxis
THA_843	ENOG41088YS	Glycosyl transferase (Group 1
THA_844	ENOG4107T3P	ABC, transporter
THA_847	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)
THA_856	ENOG4108W8W	CRISPR-associated RAMP protein, Csm3 family
THA_867	ENOG4105C1B	dTDP-glucose 4-6-dehydratase
THA_868	ENOG4108UT6	Transferase hexapeptide repeat containing protein
THA_870	ENOG4108I19	Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis (By similarity)
THA_879	ENOG4107R8N	Glycosyl transferase, family 2
THA_881	ENOG4107R5M	Catalyzes the transfer of a N-acetyl-glucosamine moiety to 1D-myo-inositol 3-phosphate to produce 1D-myo-inositol 2- acetamido-2-deoxy-glucopyranoside 3-phosphate in the mycothiol biosynthesis pathway (By similarity)
THA_882	ENOG4108MVM	Transposase
THA_886	ENOG4105CG5	Glycosyl transferase (Group 1
THA_896	ENOG4105CJT	Mannose-1-phosphate guanylyltransferase
THA_899	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)
THA_90	ENOG4108WBT	adenosyltransferase
THA_901	ENOG4105CPY	First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan (By similarity)
THA_902	ENOG4107UKG	Glycosyl transferase, family 4
THA_908	ENOG4105D92	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
THA_909	ENOG4107W7W	Assembles around the rod to form the L-ring and probably protects the motor basal body from shearing forces during rotation (By similarity)
THA_91	ENOG4105C84	Histidine ammonia-lyase
THA_911	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)
THA_913	ENOG4107Z5F	Aminotransferase class IV
THA_914	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)
THA_915	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)
THA_916	ENOG4105DE4	1-phosphofructokinase
THA_917	ENOG4105CJ1	ABC, transporter
THA_92	ENOG4107WTJ	Methyl-accepting chemotaxis sensory transducer
THA_926	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)
THA_927	ENOG4105CTQ	phosphohexokinase
THA_928	ENOG4107QW4	alcohol dehydrogenase
THA_93	ENOG4105ZU5	s-layer protein
THA_930	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)
THA_931	ENOG4105C6A	phenylalanyl-tRNA synthetase (beta subunit)
THA_935	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)
THA_937	ENOG4105EAG	UDP-N-acetylglucosamine 2-epimerase
THA_94	ENOG4105CMP	catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR (By similarity)
THA_940	ENOG4105S9S	Binding-protein-dependent transport systems, inner membrane component
THA_941	ENOG4105DRW	binding-protein-dependent transport systems inner membrane Component
THA_942	ENOG4105EA8	2-Nitropropane dioxygenase
THA_944	ENOG4105BZU	Histidine kinase
THA_945	ENOG4105CWE	NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 (By similarity)
THA_946	ENOG4105C3X	it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP (By similarity)
THA_948	ENOG41080JC	Protein of unknown function DUF47
THA_949	ENOG4105CG3	alpha amylase, catalytic region
THA_950	ENOG4107QXV	Phosphate transporter
THA_951	ENOG4105CJ3	phosphate transporter
THA_955	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
THA_956	ENOG4108VPX	Involved in 1,2-propanediol (1,2-PD) degradation by catalyzing the conversion of propanoyl-CoA to propanoyl-phosphate (By similarity)
THA_957	ENOG4105CB1	The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate (By similarity)
THA_958	ENOG4105C8Q	Methyl-accepting chemotaxis
THA_959	ENOG4105D19	Role in flagellar biosynthesis (By similarity)
THA_960	ENOG4105D00	flagellar biosynthetic protein flhB
THA_962	ENOG4105M7K	Involved in the transcription termination process (By similarity)
THA_964	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)
THA_966	ENOG4105DPZ	Two component transcriptional regulator (Winged helix family
THA_969	ENOG4108IUZ	ABC transporter
THA_97	ENOG4105DQU	oxidoreductase, subunit beta
THA_971	ENOG4105C1J	atp-dependent rna helicase
THA_972	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)
THA_973	ENOG4105CV2	Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates (By similarity)
THA_975	ENOG4105D1F	ATP-binding protein
THA_977	ENOG4105C5H	ABC transporter
THA_978	ENOG4105UQX	Mate efflux family protein
THA_98	ENOG4108UK2	deaminase
THA_982	ENOG4107QMW	pyridine nucleotide-disulfide oxidoreductase
THA_985	ENOG4108MVM	Transposase
THA_989	ENOG4105C8Q	Methyl-accepting chemotaxis
THA_99	ENOG4105C3E	May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine (By similarity)
THA_991	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)
THA_992	ENOG4107RU2	Histidinol phosphate phosphatase, HisJ family
THA_993	ENOG4105C8D	Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen (By similarity)
THA_994	ENOG4105CEV	competence damage-inducible protein
THA_995	ENOG4105ETE	Transcriptional regulator (LacI family
THA_998	ENOG4105C4R	Atp-dependent dna helicase