| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| ndhL | sync_0330 | sync_1912 | sync_0330 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | Conserved hypothetical protein. | 0.770 |
| ndhL | sync_0445 | sync_1912 | sync_0445 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | Conserved hypothetical protein. | 0.751 |
| ndhL | sync_0697 | sync_1912 | sync_0697 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | Conserved hypothetical protein; Identified by similarity to GB:CAE08191.1. | 0.742 |
| ndhL | sync_0950 | sync_1912 | sync_0950 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | Conserved hypothetical protein. | 0.745 |
| ndhL | sync_1203 | sync_1912 | sync_1203 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | Uncharacterized membrane protein. | 0.766 |
| ndhL | sync_1305 | sync_1912 | sync_1305 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | Uncharacterized protein. | 0.889 |
| ndhL | sync_1780 | sync_1912 | sync_1780 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | AbrB family transciptional regulator. | 0.744 |
| ndhL | sync_1881 | sync_1912 | sync_1881 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | Conserved hypothetical protein. | 0.741 |
| ndhL | sync_2257 | sync_1912 | sync_2257 | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | Uncharacterized conserved membrane protein. | 0.768 |
| sync_0330 | ndhL | sync_0330 | sync_1912 | Conserved hypothetical protein. | Possible inorganic carbon transport protein; NDH-1 shuttles electrons from an unknown electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and/or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon-concentration. | 0.770 |
| sync_0330 | sync_0331 | sync_0330 | sync_0331 | Conserved hypothetical protein. | Conserved hypothetical protein. | 0.773 |
| sync_0330 | sync_0445 | sync_0330 | sync_0445 | Conserved hypothetical protein. | Conserved hypothetical protein. | 0.768 |
| sync_0330 | sync_0697 | sync_0330 | sync_0697 | Conserved hypothetical protein. | Conserved hypothetical protein; Identified by similarity to GB:CAE08191.1. | 0.770 |
| sync_0330 | sync_0950 | sync_0330 | sync_0950 | Conserved hypothetical protein. | Conserved hypothetical protein. | 0.771 |
| sync_0330 | sync_1203 | sync_0330 | sync_1203 | Conserved hypothetical protein. | Uncharacterized membrane protein. | 0.774 |
| sync_0330 | sync_1305 | sync_0330 | sync_1305 | Conserved hypothetical protein. | Uncharacterized protein. | 0.773 |
| sync_0330 | sync_1780 | sync_0330 | sync_1780 | Conserved hypothetical protein. | AbrB family transciptional regulator. | 0.771 |
| sync_0330 | sync_1881 | sync_0330 | sync_1881 | Conserved hypothetical protein. | Conserved hypothetical protein. | 0.770 |
| sync_0330 | sync_2257 | sync_0330 | sync_2257 | Conserved hypothetical protein. | Uncharacterized conserved membrane protein. | 0.774 |
| sync_0331 | sync_0330 | sync_0331 | sync_0330 | Conserved hypothetical protein. | Conserved hypothetical protein. | 0.773 |