node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
MS53_0016 | MS53_0017 | MS53_0016 | MS53_0017 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Glimmer;Blastx. | 0.813 |
MS53_0016 | MS53_0018 | MS53_0016 | MS53_0018 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | Hypothetical protein. | 0.783 |
MS53_0016 | def | MS53_0016 | MS53_0019 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | Putative polypeptide deformylase; 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. | 0.738 |
MS53_0016 | dnaJ | MS53_0016 | MS53_0593 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | Heat shock protein DnaJ; Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins and by disaggregating proteins, also in an autonomous, DnaK-independent fashion. Unfolded proteins bind initially to DnaJ; upon interaction with the DnaJ-bound protein, DnaK hydrolyzes its bound ATP, resulting in the formation of a stable complex. GrpE releases ADP from DnaK; ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, [...] | 0.767 |
MS53_0016 | dnaK | MS53_0016 | MS53_0351 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | Chaperone protein dnaK - heat shock protein 70; Acts as a chaperone; Belongs to the heat shock protein 70 family. | 0.747 |
MS53_0016 | rplE | MS53_0016 | MS53_0631 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | 50S ribosomal protein L5; 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; this bridge is implicated in subunit movement. Contacts the P site tRNA; the 5S rRNA and some of its associated proteins might help stabilize positioning of ribosome-bound tRNAs. | 0.832 |
MS53_0016 | rplN | MS53_0016 | MS53_0633 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | 50S ribosomal protein L14; Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome; Belongs to the universal ribosomal protein uL14 family. | 0.882 |
MS53_0016 | rpsJ | MS53_0016 | MS53_0644 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | 30S ribosomal protein S10; Involved in the binding of tRNA to the ribosomes. Belongs to the universal ribosomal protein uS10 family. | 0.905 |
MS53_0016 | rpsS | MS53_0016 | MS53_0639 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | 30S ribosomal protein S19; Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA. | 0.832 |
MS53_0016 | tufA | MS53_0016 | MS53_0667 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | Elongation factor Tu; This protein promotes the GTP-dependent binding of aminoacyl- tRNA to the A-site of ribosomes during protein biosynthesis. | 0.752 |
MS53_0017 | MS53_0016 | MS53_0017 | MS53_0016 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Glimmer;Blastx. | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | 0.813 |
MS53_0017 | MS53_0018 | MS53_0017 | MS53_0018 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Glimmer;Blastx. | Hypothetical protein. | 0.783 |
MS53_0017 | def | MS53_0017 | MS53_0019 | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Glimmer;Blastx. | Putative polypeptide deformylase; 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. | 0.735 |
MS53_0018 | MS53_0016 | MS53_0018 | MS53_0016 | Hypothetical protein. | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | 0.783 |
MS53_0018 | MS53_0017 | MS53_0018 | MS53_0017 | Hypothetical protein. | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Glimmer;Blastx. | 0.783 |
MS53_0018 | def | MS53_0018 | MS53_0019 | Hypothetical protein. | Putative polypeptide deformylase; 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. | 0.741 |
def | MS53_0016 | MS53_0019 | MS53_0016 | Putative polypeptide deformylase; 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. | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Blastx;COG0693;TC:3.A.1.112.4. | 0.738 |
def | MS53_0017 | MS53_0019 | MS53_0017 | Putative polypeptide deformylase; 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. | Conserved hypothetical protein; Identified by sequence similarity; putative; ORF located using Glimmer;Blastx. | 0.735 |
def | MS53_0018 | MS53_0019 | MS53_0018 | Putative polypeptide deformylase; 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. | Hypothetical protein. | 0.741 |
def | rplE | MS53_0019 | MS53_0631 | Putative polypeptide deformylase; 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. | 50S ribosomal protein L5; 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; this bridge is implicated in subunit movement. Contacts the P site tRNA; the 5S rRNA and some of its associated proteins might help stabilize positioning of ribosome-bound tRNAs. | 0.970 |