| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| def | rplQ | MS53_0019 | MS53_0573 | 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 L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 0.849 |
| def | rplU | MS53_0019 | MS53_0551 | 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 L21; This protein binds to 23S rRNA in the presence of protein L20; Belongs to the bacterial ribosomal protein bL21 family. | 0.831 |
| def | rplV | MS53_0019 | MS53_0638 | 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 L22; This protein binds specifically to 23S rRNA; its binding is stimulated by other ribosomal proteins, e.g. L4, L17, and L20. 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). | 0.856 |
| def | rpmA | MS53_0019 | MS53_0550 | 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 L27; Identified by sequence similarity; putative; ORF located using Glimmer;GeneMark;Blastx;COG0211; Belongs to the bacterial ribosomal protein bL27 family. | 0.828 |
| def | rpmB | MS53_0019 | MS53_0066 | 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 L28; Identified by sequence similarity; putative; ORF located using Blastx;COG0227; Belongs to the bacterial ribosomal protein bL28 family. | 0.831 |
| def | rpsB | MS53_0019 | MS53_0413 | 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. | 30S ribosomal protein S2; Identified by sequence similarity; putative; ORF located using Blastx;COG0052; Belongs to the universal ribosomal protein uS2 family. | 0.828 |
| def | rpsM | MS53_0019 | MS53_0576 | 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. | 30S ribosomal protein S13; 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; these bridges are implicated in subunit movement. Contacts the tRNAs in the A and P-sites. Belongs to the universal ribosomal protein uS13 family. | 0.827 |
| def | rpsP | MS53_0019 | MS53_0010 | 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. | 30S ribosomal protein S16; Identified by sequence similarity; putative; ORF located using Blastx;COG0228; Belongs to the bacterial ribosomal protein bS16 family. | 0.829 |
| def | rpsT | MS53_0019 | MS53_0071 | 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. | 30S ribosomal protein S20; Binds directly to 16S ribosomal RNA. | 0.864 |
| def | tig | MS53_0019 | MS53_0603 | 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. | Putative trigger factor; 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; Belongs to the FKBP-type PPIase family. Tig subfamily. | 0.863 |
| rplQ | def | MS53_0573 | MS53_0019 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 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. | 0.849 |
| rplQ | rplU | MS53_0573 | MS53_0551 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 50S ribosomal protein L21; This protein binds to 23S rRNA in the presence of protein L20; Belongs to the bacterial ribosomal protein bL21 family. | 0.984 |
| rplQ | rplV | MS53_0573 | MS53_0638 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 50S ribosomal protein L22; This protein binds specifically to 23S rRNA; its binding is stimulated by other ribosomal proteins, e.g. L4, L17, and L20. 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). | 0.987 |
| rplQ | rpmA | MS53_0573 | MS53_0550 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 50S ribosomal protein L27; Identified by sequence similarity; putative; ORF located using Glimmer;GeneMark;Blastx;COG0211; Belongs to the bacterial ribosomal protein bL27 family. | 0.977 |
| rplQ | rpmB | MS53_0573 | MS53_0066 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 50S ribosomal protein L28; Identified by sequence similarity; putative; ORF located using Blastx;COG0227; Belongs to the bacterial ribosomal protein bL28 family. | 0.974 |
| rplQ | rpsB | MS53_0573 | MS53_0413 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 30S ribosomal protein S2; Identified by sequence similarity; putative; ORF located using Blastx;COG0052; Belongs to the universal ribosomal protein uS2 family. | 0.982 |
| rplQ | rpsM | MS53_0573 | MS53_0576 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 30S ribosomal protein S13; 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; these bridges are implicated in subunit movement. Contacts the tRNAs in the A and P-sites. Belongs to the universal ribosomal protein uS13 family. | 0.996 |
| rplQ | rpsP | MS53_0573 | MS53_0010 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 30S ribosomal protein S16; Identified by sequence similarity; putative; ORF located using Blastx;COG0228; Belongs to the bacterial ribosomal protein bS16 family. | 0.981 |
| rplQ | rpsT | MS53_0573 | MS53_0071 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | 30S ribosomal protein S20; Binds directly to 16S ribosomal RNA. | 0.939 |
| rplQ | tig | MS53_0573 | MS53_0603 | 50S ribosomal protein L17; Identified by sequence similarity; putative; ORF located using Blastx;COG0203. | Putative trigger factor; 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; Belongs to the FKBP-type PPIase family. Tig subfamily. | 0.957 |