| Prior-Knowledge | Description | Expectation | Prediction | Conclusion | Leaf Statistics |
|---|---|---|---|---|---|
| Evidence_70364 | TIGR02779 HMM | None - {{∅}} | True - {{t}} | Unconfirmed presence | |
| Component_51577 | ligase domain | None - {{∅}} | True - {{t}} | Unconfirmed presence | |
| Evidence_70363 | TIGR02778 HMM | None - {{∅}} | True - {{t}} | Unconfirmed presence | |
| Component_51576 | Ku protein, bacterial type | None - {{∅}} | True - {{t}} | Unconfirmed presence | |
| Component_51579 | 3-prime phosphoesterase domain | None - {{∅}} | None - {{∅}} | Unexplained | |
| Evidence_70362 | TIGR02777 HMM | None - {{∅}} | None - {{∅}} | Unexplained | |
| Component_51578 | polymerase domain | None - {{∅}} | True - {{t}} | Unconfirmed presence | |
| Evidence_70361 | TIGR02772 HMM | None - {{∅}} | True - {{t}} | Unconfirmed presence | |
| GenProp0492 | nonhomologous end-joining, bacterial type~This property describes nonhomologous end-joining (NHEJ), a mechanism for DNA repair of double-stranded breaks that appears significantly less common in bacteria than, and uncorrelated with, recombinational repair. The bacterial Ku protein typically is encoded next to the multidomain, multifunctional DNA ligase, LidD. The domains of LigD, which may be permuted, carry separable 3'-phosphoesterase (PE), DNA ligase, and polymerase activities. | None - {{∅}} | True - {{t}} | Unconfirmed presence |