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ORF_ID	e_value	Gene_name	EC_number	COGs	Description
ONINOJAO_00004	1.5e-155			M	Glycosyl hydrolases family 25
ONINOJAO_00005	3.6e-22
ONINOJAO_00006	4.6e-16
ONINOJAO_00007	6e-17
ONINOJAO_00008	4.6e-20			S	Phage uncharacterised protein (Phage_XkdX)
ONINOJAO_00009	1.3e-57
ONINOJAO_00014	3.7e-137
ONINOJAO_00015	3.8e-36
ONINOJAO_00016	2.9e-10
ONINOJAO_00017	1.2e-123	Z012_12235		S	Baseplate J-like protein
ONINOJAO_00018	2.1e-32
ONINOJAO_00019	1.5e-44
ONINOJAO_00020	2.8e-111
ONINOJAO_00021	2.3e-37
ONINOJAO_00022	8.7e-54			M	LysM domain
ONINOJAO_00023	9e-206		3.4.14.13	M	Phage tail tape measure protein TP901
ONINOJAO_00025	5.3e-11
ONINOJAO_00026	1.4e-29
ONINOJAO_00027	6.9e-104	Z012_02110		S	Protein of unknown function (DUF3383)
ONINOJAO_00028	1.7e-35
ONINOJAO_00029	1.5e-28
ONINOJAO_00030	9e-31
ONINOJAO_00031	1.4e-20			S	Protein of unknown function (DUF4054)
ONINOJAO_00032	5e-91	Z012_11565		S	Uncharacterized protein conserved in bacteria (DUF2184)
ONINOJAO_00033	5.7e-34
ONINOJAO_00034	5.7e-52			S	Uncharacterized protein conserved in bacteria (DUF2213)
ONINOJAO_00035	2.1e-10			S	Lysin motif
ONINOJAO_00036	8.8e-49			S	Phage Mu protein F like protein
ONINOJAO_00037	1e-137			S	Protein of unknown function (DUF1073)
ONINOJAO_00038	8.7e-204			S	Terminase-like family
ONINOJAO_00039	2.7e-20	ps333		L	Terminase small subunit
ONINOJAO_00043	2.9e-07
ONINOJAO_00044	2e-41			S	VRR_NUC
ONINOJAO_00061	1.8e-62			L	DnaD domain protein
ONINOJAO_00062	4.7e-47			S	ERF superfamily
ONINOJAO_00063	2.1e-36			S	Protein of unknown function (DUF1351)
ONINOJAO_00066	2.7e-17
ONINOJAO_00071	2.2e-81	ps308		K	AntA/AntB antirepressor
ONINOJAO_00073	2.2e-25			K	Cro/C1-type HTH DNA-binding domain
ONINOJAO_00074	1.2e-10			E	Zn peptidase
ONINOJAO_00080	1.7e-59			L	Belongs to the 'phage' integrase family
ONINOJAO_00081	8.1e-168	era		S	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
ONINOJAO_00082	2.7e-91	ybeY	2.6.99.2, 3.5.4.5	S	Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA
ONINOJAO_00083	1.2e-174	phoH		T	phosphate starvation-inducible protein PhoH
ONINOJAO_00084	2.7e-68	yqeY		S	YqeY-like protein
ONINOJAO_00085	2e-22	rpsU		J	Belongs to the bacterial ribosomal protein bS21 family
ONINOJAO_00086	3.7e-151	yqfL	2.7.11.33, 2.7.4.28	F	Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation
ONINOJAO_00087	8e-106			S	Peptidase family M23
ONINOJAO_00088	9.3e-161	yitT		S	Uncharacterised 5xTM membrane BCR, YitT family COG1284
ONINOJAO_00089	1.4e-105
ONINOJAO_00090	1.1e-37	thrB	2.7.1.39	F	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate
ONINOJAO_00091	9.7e-82	thrB	2.7.1.39	F	Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate
ONINOJAO_00092	1.2e-23	hom	1.1.1.3, 2.7.2.4	E	homoserine dehydrogenase
ONINOJAO_00093	4.7e-122	hom	1.1.1.3, 2.7.2.4	E	homoserine dehydrogenase
ONINOJAO_00094	1.3e-244	thrC	4.2.3.1	E	Threonine synthase
ONINOJAO_00095	4.8e-115	lysC	2.7.2.4	E	Belongs to the aspartokinase family
ONINOJAO_00096	5.1e-84	lysC	2.7.2.4	E	Belongs to the aspartokinase family
ONINOJAO_00097	1.5e-26	lysC	2.7.2.4	E	Belongs to the aspartokinase family
ONINOJAO_00098	1.1e-102	VY92_08690	5.3.1.32	G	Antibiotic biosynthesis monooxygenase
ONINOJAO_00099	2.9e-28
ONINOJAO_00100	5.6e-42
ONINOJAO_00101	3.5e-106			K	LysR substrate binding domain
ONINOJAO_00102	1.2e-18
ONINOJAO_00103	5.3e-212			S	Sterol carrier protein domain
ONINOJAO_00104	6.4e-96	citX	2.4.2.52, 2.7.7.61	HI	Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase
ONINOJAO_00105	6.7e-125	arcC	2.7.2.2	E	Belongs to the carbamate kinase family
ONINOJAO_00106	1.1e-31	arcC	2.7.2.2	E	Belongs to the carbamate kinase family
ONINOJAO_00107	1.4e-187	argF	2.1.3.3, 2.7.2.2	E	Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline
ONINOJAO_00108	8.4e-166	arcA	3.5.3.6	E	Arginine
ONINOJAO_00109	9.2e-26	arcA	3.5.3.6	E	Arginine
ONINOJAO_00110	1.3e-154	lysR5		K	LysR substrate binding domain
ONINOJAO_00111	0.0		3.6.3.2, 3.6.3.6	P	Cation transporter/ATPase, N-terminus
ONINOJAO_00112	7.6e-83		3.4.21.96	S	SLAP domain
ONINOJAO_00113	1.6e-248	cls		I	Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol
ONINOJAO_00114	1.1e-147	metAA	2.3.1.46	E	Transfers an acetyl group from acetyl-CoA to
ONINOJAO_00115	2.6e-30	cysK	2.5.1.47	E	Belongs to the cysteine synthase cystathionine beta- synthase family
ONINOJAO_00116	3e-122	cysK	2.5.1.47	E	Belongs to the cysteine synthase cystathionine beta- synthase family
ONINOJAO_00117	7e-95	apt	2.4.2.22, 2.4.2.7	F	Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis
ONINOJAO_00118	0.0	recJ		L	Single-stranded-DNA-specific exonuclease RecJ
ONINOJAO_00119	1.9e-116	srtA	3.4.22.70	M	sortase family
ONINOJAO_00120	0.0	lepA		M	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
ONINOJAO_00121	2.1e-20
ONINOJAO_00122	6e-200	dnaJ		O	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
ONINOJAO_00123	0.0	dnaK		O	Heat shock 70 kDa protein
ONINOJAO_00124	1.3e-81	grpE		O	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
ONINOJAO_00125	1.2e-186	hrcA		K	Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons
ONINOJAO_00126	1.4e-175	ribF	2.7.1.26, 2.7.7.2	H	Belongs to the ribF family
ONINOJAO_00127	2.8e-165	truB	5.4.99.25	J	Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs
ONINOJAO_00128	1.1e-57	rbfA		J	One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA
ONINOJAO_00129	0.0	infB		J	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
ONINOJAO_00130	1.2e-46	rplGA		J	ribosomal protein
ONINOJAO_00131	1.2e-46	ylxR		K	Protein of unknown function (DUF448)
ONINOJAO_00132	2.9e-194	nusA		K	Participates in both transcription termination and antitermination
ONINOJAO_00133	6.7e-81	rimP		J	Required for maturation of 30S ribosomal subunits
ONINOJAO_00134	0.0	polC	2.7.7.7	L	Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity
ONINOJAO_00135	0.0	proS	6.1.1.15	J	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
ONINOJAO_00136	2.6e-196	rseP	3.4.21.107, 3.4.21.116	M	zinc metalloprotease
ONINOJAO_00137	5.1e-145	cdsA	2.7.7.41	I	Belongs to the CDS family
ONINOJAO_00138	1.6e-137	uppS	2.5.1.31	H	Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids
ONINOJAO_00139	7.6e-92	frr		J	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

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