| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| MS53_0039 | MS53_0041 | MS53_0039 | MS53_0041 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | Putative ABC transporter ATP-binding protein; Identified by sequence similarity; putative; ORF located using Blastx;COG1136;TC:3.A.1.125.1. | 0.412 |
| MS53_0039 | atpE | MS53_0039 | MS53_0410 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | ATP synthase C chain; 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. | 0.617 |
| MS53_0039 | metG | MS53_0039 | MS53_0303 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | methionyl-tRNA synthetase; Identified by sequence similarity; putative; ORF located using Blastx;COG0143; Belongs to the class-I aminoacyl-tRNA synthetase family. | 0.477 |
| MS53_0039 | pdhD | MS53_0039 | MS53_0275 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | Dihydrolipoamide dehydrogenase; Identified by sequence similarity; putative; ORF located using GeneMark;Blastx;COG1249. | 0.537 |
| MS53_0039 | secD | MS53_0039 | MS53_0167 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | Protein-export membrane protein SecD; 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. | 0.477 |
| MS53_0039 | sipS | MS53_0039 | MS53_0040 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | Signal peptidase I; Identified by sequence similarity; putative; ORF located using Blastx;COG0681; Belongs to the peptidase S26 family. | 0.432 |
| MS53_0039 | topA | MS53_0039 | MS53_0531 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | DNA topoisomerase I; Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA- (5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supe [...] | 0.508 |
| MS53_0041 | MS53_0039 | MS53_0041 | MS53_0039 | Putative ABC transporter ATP-binding protein; Identified by sequence similarity; putative; ORF located using Blastx;COG1136;TC:3.A.1.125.1. | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | 0.412 |
| MS53_0041 | MS53_0689 | MS53_0041 | MS53_0689 | Putative ABC transporter ATP-binding protein; Identified by sequence similarity; putative; ORF located using Blastx;COG1136;TC:3.A.1.125.1. | Hypothetical protein. | 0.516 |
| MS53_0041 | lepA | MS53_0041 | MS53_0489 | Putative ABC transporter ATP-binding protein; Identified by sequence similarity; putative; ORF located using Blastx;COG1136;TC:3.A.1.125.1. | GTP-binding protein LepA; 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. | 0.517 |
| MS53_0041 | secD | MS53_0041 | MS53_0167 | Putative ABC transporter ATP-binding protein; Identified by sequence similarity; putative; ORF located using Blastx;COG1136;TC:3.A.1.125.1. | Protein-export membrane protein SecD; 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. | 0.775 |
| MS53_0041 | sipS | MS53_0041 | MS53_0040 | Putative ABC transporter ATP-binding protein; Identified by sequence similarity; putative; ORF located using Blastx;COG1136;TC:3.A.1.125.1. | Signal peptidase I; Identified by sequence similarity; putative; ORF located using Blastx;COG0681; Belongs to the peptidase S26 family. | 0.779 |
| MS53_0041 | topA | MS53_0041 | MS53_0531 | Putative ABC transporter ATP-binding protein; Identified by sequence similarity; putative; ORF located using Blastx;COG1136;TC:3.A.1.125.1. | DNA topoisomerase I; Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA- (5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supe [...] | 0.833 |
| MS53_0689 | MS53_0041 | MS53_0689 | MS53_0041 | Hypothetical protein. | Putative ABC transporter ATP-binding protein; Identified by sequence similarity; putative; ORF located using Blastx;COG1136;TC:3.A.1.125.1. | 0.516 |
| MS53_0689 | sipS | MS53_0689 | MS53_0040 | Hypothetical protein. | Signal peptidase I; Identified by sequence similarity; putative; ORF located using Blastx;COG0681; Belongs to the peptidase S26 family. | 0.431 |
| atpE | MS53_0039 | MS53_0410 | MS53_0039 | ATP synthase C chain; 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. | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0480. | 0.617 |
| atpE | secD | MS53_0410 | MS53_0167 | ATP synthase C chain; 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. | Protein-export membrane protein SecD; 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. | 0.403 |
| atpE | sipS | MS53_0410 | MS53_0040 | ATP synthase C chain; 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. | Signal peptidase I; Identified by sequence similarity; putative; ORF located using Blastx;COG0681; Belongs to the peptidase S26 family. | 0.871 |
| glyA | metG | MS53_0305 | MS53_0303 | Serine hydroxymethyltransferase; 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. | methionyl-tRNA synthetase; Identified by sequence similarity; putative; ORF located using Blastx;COG0143; Belongs to the class-I aminoacyl-tRNA synthetase family. | 0.660 |
| glyA | pdhD | MS53_0305 | MS53_0275 | Serine hydroxymethyltransferase; 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. | Dihydrolipoamide dehydrogenase; Identified by sequence similarity; putative; ORF located using GeneMark;Blastx;COG1249. | 0.960 |