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CAKLQF020000009.1__CAH1083530.1__SAMEA5780031_02040__00135
Bact-VirCAKLQF020000009.1__CAH1083530.1__SAMEA5780031_02040__00135
3D Structure
Domains
high = three domain segmentations agree, medium = two domain segmentations agree. Numbered high-first then medium, N→C within each tier.
D1
high
residues 3-67
Domain cluster:
rep: ON464759.1__UTV60862.1__JDFnp1_74__00074__D5-72
Pfam (4)
| Accession | Name | Score | E-value | Q cov | HMM cov |
|---|---|---|---|---|---|
| PF13560.13 best | HTH_31 | 53.1 | 4.50e-14 | 92.3% | 89.1% |
| PF12844.14 | HTH_19 | 33.5 | 4.50e-08 | 90.8% | 87.5% |
| PF13443.13 | HTH_26 | 23.0 | 1.00e-04 | 87.7% | 92.1% |
| PF01381.29 | HTH_3 | 57.6 | 1.40e-15 | 84.6% | 98.2% |
CATH (70)
| Domain ID | Class ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 1y9qA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.98 | 94.0 | 8.37e-01 | 100.0% | 76.5% |
| 1y7yA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.97 | 93.0 | 9.12e-01 | 100.0% | 94.2% |
| 6rnzA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.95 | 86.0 | 8.61e-01 | 95.4% | 93.9% |
| 3f51C00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.94 | 88.0 | 7.75e-01 | 100.0% | 73.3% |
| 1b0nA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.93 | 84.0 | 7.02e-01 | 95.4% | 60.2% |
| 3fyaB00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.93 | 88.0 | 8.24e-01 | 100.0% | 88.3% |
| 7zviA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.93 | 81.0 | 6.36e-01 | 92.3% | 68.9% |
| 3g7dA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.92 | 74.0 | 6.66e-01 | 96.9% | 64.0% |
| 6b9sB02 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.92 | 84.0 | 8.09e-01 | 98.5% | 87.7% |
| 2ofyA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.92 | 85.0 | 8.28e-01 | 100.0% | 91.4% |
| 3u3wA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.91 | 81.0 | 7.99e-01 | 96.9% | 89.9% |
| 2xcjA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.91 | 82.0 | 7.43e-01 | 95.4% | 76.2% |
| 7n1nB01 | 1.25.40.10 | Mainly Alpha › Alpha Horseshoe › Serine Threonine Protein Phosphatase 5, Tetratricopeptide repeat › Tetratricopeptide repeat domain | 0.91 | 83.0 | 8.50e-01 | 96.9% | 100.0% |
| 2l49B01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.91 | 70.0 | 7.74e-01 | 81.5% | 100.0% |
| 2ewtA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.90 | 84.0 | 8.19e-01 | 100.0% | 94.4% |
| 3kxaA02 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.90 | 76.0 | 7.61e-01 | 89.2% | 89.4% |
| 2bnmA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.90 | 83.0 | 7.91e-01 | 100.0% | 89.2% |
| 3pxpA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.90 | 83.0 | 7.27e-01 | 100.0% | 82.8% |
| 2awiA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.90 | 79.0 | 7.82e-01 | 98.5% | 91.0% |
| 2r1jL00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.89 | 81.0 | 8.07e-01 | 100.0% | 95.5% |
| 3zhiA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.89 | 80.0 | 7.71e-01 | 96.9% | 100.0% |
| 2kpjA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.89 | 82.0 | 7.99e-01 | 100.0% | 92.9% |
| 4jcyA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.89 | 81.0 | 7.05e-01 | 96.9% | 70.7% |
| 4pu7A00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.89 | 78.0 | 7.57e-01 | 96.9% | 85.9% |
| 1r69A00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.89 | 78.0 | 7.91e-01 | 93.8% | 96.8% |
| 2xi8A00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.88 | 78.0 | 7.85e-01 | 100.0% | 93.9% |
| 2qfcA00 | 1.25.40.10 | Mainly Alpha › Alpha Horseshoe › Serine Threonine Protein Phosphatase 5, Tetratricopeptide repeat › Tetratricopeptide repeat domain | 0.88 | 79.0 | 5.03e-01 | 96.9% | 22.5% |
| 1lliA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.88 | 81.0 | 7.23e-01 | 100.0% | 77.5% |
| 3bs3A00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.88 | 74.0 | 7.73e-01 | 96.9% | 98.3% |
| 4ghjB00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.87 | 80.0 | 7.57e-01 | 100.0% | 84.2% |
| 8dtqA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.87 | 80.0 | 7.32e-01 | 100.0% | 80.5% |
| 4yg1A00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.87 | 76.0 | 7.39e-01 | 96.9% | 86.1% |
| 2wusS00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.86 | 80.0 | 7.31e-01 | 100.0% | 89.0% |
| 4ybaA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.86 | 79.0 | 7.39e-01 | 96.9% | 88.3% |
| 1x57A00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.86 | 78.0 | 6.88e-01 | 96.9% | 70.3% |
| 3fymA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.86 | 76.0 | 6.98e-01 | 95.4% | 85.4% |
| 7zcvA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.86 | 74.0 | 7.59e-01 | 92.3% | 98.4% |
| 2auwB02 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.85 | 68.0 | 6.62e-01 | 89.2% | 78.6% |
| 7xi5A01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.85 | 63.0 | 7.03e-01 | 80.0% | 100.0% |
| 3ivpD01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.84 | 77.0 | 7.31e-01 | 100.0% | 85.3% |
| 3op9A01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.84 | 74.0 | 7.35e-01 | 100.0% | 92.6% |
| 3b7hA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.84 | 75.0 | 7.17e-01 | 100.0% | 86.8% |
| 2ox6D00 | 1.10.3100.10 | Mainly Alpha › Orthogonal Bundle › Putative cytoplasmic protein › Putative cytoplasmic protein | 0.83 | 67.0 | 4.85e-01 | 90.8% | 34.2% |
| 2ppxA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.83 | 63.0 | 6.49e-01 | 83.1% | 85.2% |
| 2ef8A00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.83 | 74.0 | 6.82e-01 | 100.0% | 86.9% |
| 2ictA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.82 | 76.0 | 6.98e-01 | 100.0% | 84.0% |
| 2ebyA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.82 | 75.0 | 7.02e-01 | 100.0% | 84.8% |
| 3mlfE00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.82 | 68.0 | 6.18e-01 | 89.2% | 67.4% |
| 3cecA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.82 | 75.0 | 6.67e-01 | 100.0% | 72.5% |
| 6f8hC00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.82 | 75.0 | 6.57e-01 | 100.0% | 71.0% |
| 1ic8A01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.81 | 66.0 | 5.84e-01 | 89.2% | 62.8% |
| 2o38A01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.79 | 64.0 | 6.50e-01 | 89.2% | 90.8% |
| 7vjmB01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.76 | 63.0 | 6.35e-01 | 89.2% | 90.6% |
| 3fmyA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.75 | 59.0 | 5.95e-01 | 95.4% | 84.8% |
| 2a6cA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.74 | 64.0 | 6.11e-01 | 96.9% | 82.9% |
| 1dw9A01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.73 | 63.0 | 5.76e-01 | 100.0% | 73.6% |
| 2mqkA00 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.73 | 60.0 | 6.02e-01 | 89.2% | 90.8% |
| 1x2lA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.68 | 56.0 | 5.16e-01 | 92.3% | 76.5% |
| 2fjrA01 | 1.10.260.40 | Mainly Alpha › Orthogonal Bundle › 434 Repressor (Amino-terminal Domain) › lambda repressor-like DNA-binding domains | 0.62 | 49.0 | 4.82e-01 | 100.0% | 82.9% |
| 3lqhA02 | 1.20.920.10 | Mainly Alpha › Up-down Bundle › Histone Acetyltransferase; Chain A › Bromodomain-like | 0.59 | 49.0 | 4.33e-01 | 100.0% | 84.0% |
| 4gkfA00 | 1.10.520.30 | Mainly Alpha › Orthogonal Bundle › Peroxidase; domain 1 › AF1862-like domain | 0.57 | 44.0 | 3.47e-01 | 86.2% | 62.3% |
| 2zcaA00 | 1.10.520.40 | Mainly Alpha › Orthogonal Bundle › Peroxidase; domain 1 › CRISPR-associated protein Cse2 | 0.56 | 38.0 | 2.95e-01 | 70.8% | 86.5% |
| 1ti2A03 | 3.40.228.10 | Alpha Beta › 3-Layer(aba) Sandwich › Dimethylsulfoxide Reductase; domain 2 › Dimethylsulfoxide Reductase, domain 2 | 0.54 | 45.0 | 3.02e-01 | 95.4% | 40.1% |
| 3fd9A01 | 1.10.8.520 | Mainly Alpha › Orthogonal Bundle › Helicase, Ruva Protein; domain 3 › ExsD N-terminal domain-like | 0.54 | 37.0 | 3.68e-01 | 86.2% | 68.1% |
| 2e18A00 | 3.40.50.620 | Alpha Beta › 3-Layer(aba) Sandwich › Rossmann fold › HUPs | 0.53 | 38.0 | 2.61e-01 | 75.4% | 41.0% |
| 2w7nA00 | 1.10.10.2690 | Mainly Alpha › Orthogonal Bundle › Arc Repressor Mutant, subunit A › | 0.53 | 40.0 | 3.65e-01 | 86.2% | 70.2% |
| 3by4A00 | 3.90.70.80 | Alpha Beta › Alpha-Beta Complex › Cathepsin B; Chain A › | 0.53 | 45.0 | 3.39e-01 | 100.0% | 58.7% |
| 3r31A01 | 3.40.605.10 | Alpha Beta › 3-Layer(aba) Sandwich › Aldehyde Dehydrogenase; Chain A, domain 1 › Aldehyde Dehydrogenase; Chain A, domain 1 | 0.52 | 44.0 | 3.04e-01 | 100.0% | 60.9% |
| 4i8qA01 | 3.40.605.10 | Alpha Beta › 3-Layer(aba) Sandwich › Aldehyde Dehydrogenase; Chain A, domain 1 › Aldehyde Dehydrogenase; Chain A, domain 1 | 0.52 | 43.0 | 2.90e-01 | 100.0% | 52.6% |
| 2om6A02 | 1.10.150.400 | Mainly Alpha › Orthogonal Bundle › DNA polymerase; domain 1 › | 0.51 | 41.0 | 3.94e-01 | 90.8% | 79.7% |
ECOD (99)
| UID | F-ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 5003089 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.99 | 90.0 | 8.74e-01 | 93.8% | 87.1% |
| 3277880 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.98 | 94.0 | 8.87e-01 | 100.0% | 86.7% |
| 3941643 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.98 | 94.0 | 9.15e-01 | 100.0% | 92.9% |
| 3957550 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.98 | 87.0 | 8.45e-01 | 92.3% | 85.7% |
| 3978391 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.98 | 91.0 | 8.85e-01 | 96.9% | 90.0% |
| 3944738 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.98 | 94.0 | 8.83e-01 | 100.0% | 86.7% |
| None | — | 0.98 | 78.0 | 8.20e-01 | 83.1% | 90.0% | |
| 4010418 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.98 | 89.0 | 8.19e-01 | 95.4% | 77.5% |
| 3280943 | 101.1.4.18 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_31 | 0.97 | 92.0 | 9.23e-01 | 98.5% | 98.5% |
| 4605318 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.97 | 93.0 | 8.75e-01 | 100.0% | 86.7% |
| 3954613 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.97 | 93.0 | 7.18e-01 | 100.0% | 53.6% |
| 3972208 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.97 | 92.0 | 8.63e-01 | 100.0% | 85.3% |
| 3285035 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.97 | 88.0 | 7.70e-01 | 95.4% | 68.9% |
| 3976255 | 101.1.4.17 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_26 | 0.96 | 89.0 | 8.39e-01 | 100.0% | 84.0% |
| None | — | 0.96 | 79.0 | 7.64e-01 | 84.6% | 78.6% | |
| 4380509 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.96 | 91.0 | 7.54e-01 | 100.0% | 61.9% |
| 352428 | 101.1.4.18 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_31 | 0.96 | 91.0 | 7.99e-01 | 100.0% | 73.0% |
| 3969553 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.96 | 91.0 | 8.58e-01 | 100.0% | 86.7% |
| 4952242 | 101.1.4.17 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_26 | 0.96 | 85.0 | 8.29e-01 | 93.8% | 87.1% |
| 147355 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.95 | 91.0 | 8.55e-01 | 100.0% | 89.5% |
| None | — | 0.95 | 87.0 | 8.72e-01 | 98.5% | 95.4% | |
| 4656409 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.95 | 90.0 | 8.75e-01 | 100.0% | 92.9% |
| 2773 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.95 | 90.0 | 8.41e-01 | 100.0% | 84.4% |
| 4367316 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.95 | 90.0 | 7.20e-01 | 100.0% | 56.5% |
| 4392992 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.95 | 82.0 | 7.56e-01 | 90.8% | 73.8% |
| 4274007 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.95 | 89.0 | 8.22e-01 | 100.0% | 81.2% |
| 2581392 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.95 | 86.0 | 8.29e-01 | 95.4% | 87.3% |
| 3972189 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.94 | 90.0 | 8.48e-01 | 100.0% | 86.7% |
| 4507416 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.94 | 84.0 | 6.81e-01 | 93.8% | 55.5% |
| 3287571 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.94 | 88.0 | 7.92e-01 | 100.0% | 75.3% |
| 148652 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.94 | 88.0 | 7.81e-01 | 100.0% | 73.0% |
| 4038777 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.94 | 85.0 | 7.29e-01 | 95.4% | 65.3% |
| 3280189 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.93 | 88.0 | 8.30e-01 | 100.0% | 86.7% |
| 3285836 | 101.1.4.18 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_31 | 0.93 | 89.0 | 8.16e-01 | 100.0% | 87.5% |
| 2149183 | 10.12.1.50 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › HTH_26 | 0.93 | 86.0 | 5.74e-01 | 100.0% | 29.3% |
| 5015314 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.93 | 82.0 | 7.55e-01 | 100.0% | 75.0% |
| 4536849 | 10.12.1.146 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › HTH_3 | 0.93 | 87.0 | 5.14e-01 | 100.0% | 15.9% |
| 2577290 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.93 | 86.0 | 7.88e-01 | 98.5% | 79.0% |
| 5003294 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.93 | 87.0 | 8.22e-01 | 100.0% | 86.7% |
| 4860587 | 101.1.1.9 ↗ | alpha arrays › HTH › HTH › Three-helical HTH › HTH_3 | 0.93 | 84.0 | 7.87e-01 | 100.0% | 80.8% |
| 4033847 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.92 | 86.0 | 7.17e-01 | 100.0% | 61.9% |
| 3587838 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.92 | 83.0 | 8.05e-01 | 98.5% | 88.6% |
| 3953562 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.92 | 83.0 | 8.12e-01 | 96.9% | 91.4% |
| 4509221 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.92 | 86.0 | 6.74e-01 | 100.0% | 52.0% |
| 5083215 | 101.1.4.18 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_31 | 0.92 | 82.0 | 8.25e-01 | 95.4% | 95.4% |
| 3277922 | 101.1.4.18 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_31 | 0.92 | 82.0 | 7.80e-01 | 95.4% | 89.3% |
| 5059226 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.91 | 80.0 | 7.35e-01 | 100.0% | 75.0% |
| 3591049 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.91 | 85.0 | 6.28e-01 | 100.0% | 43.3% |
| 3282040 | 101.1.4.18 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_31 | 0.91 | 85.0 | 7.67e-01 | 100.0% | 82.4% |
| 4950501 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.91 | 81.0 | 8.14e-01 | 100.0% | 93.8% |
| 5057975 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.91 | 79.0 | 7.50e-01 | 100.0% | 80.0% |
| 3990067 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.91 | 84.0 | 7.79e-01 | 100.0% | 81.2% |
| 4008186 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.91 | 81.0 | 6.43e-01 | 95.4% | 51.7% |
| 4869547 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.91 | 78.0 | 7.80e-01 | 100.0% | 89.6% |
| 4818340 | 101.1.1.9 ↗ | alpha arrays › HTH › HTH › Three-helical HTH › HTH_3 | 0.90 | 80.0 | 8.13e-01 | 98.5% | 96.8% |
| 3286370 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.90 | 78.0 | 6.14e-01 | 92.3% | 48.0% |
| 4537353 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.90 | 80.0 | 6.31e-01 | 95.4% | 49.6% |
| 3589821 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.90 | 83.0 | 8.15e-01 | 100.0% | 92.9% |
| 4032323 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.90 | 80.0 | 8.04e-01 | 95.4% | 95.4% |
| 4425759 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.90 | 79.0 | 6.48e-01 | 93.8% | 55.5% |
| 3965549 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.90 | 79.0 | 7.55e-01 | 95.4% | 82.7% |
| 1185986 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.89 | 82.0 | 7.39e-01 | 100.0% | 75.6% |
| 3987118 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.89 | 83.0 | 7.48e-01 | 100.0% | 81.2% |
| 4940726 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.89 | 78.0 | 7.83e-01 | 98.5% | 92.3% |
| 3958819 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.89 | 77.0 | 7.99e-01 | 92.3% | 100.0% |
| 3954383 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.89 | 82.0 | 7.56e-01 | 100.0% | 83.7% |
| 3588760 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.89 | 83.0 | 6.90e-01 | 100.0% | 61.9% |
| 3951505 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.88 | 78.0 | 7.45e-01 | 98.5% | 82.7% |
| 5046258 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.88 | 75.0 | 7.12e-01 | 96.9% | 78.7% |
| 137778 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.88 | 81.0 | 8.02e-01 | 98.5% | 95.5% |
| 3062945 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.88 | 78.0 | 7.61e-01 | 96.9% | 87.3% |
| 4956880 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.88 | 77.0 | 7.53e-01 | 98.5% | 87.1% |
| 169605 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.88 | 81.0 | 7.31e-01 | 100.0% | 78.8% |
| 3974079 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.88 | 78.0 | 6.52e-01 | 95.4% | 59.0% |
| 4568698 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.88 | 73.0 | 7.58e-01 | 96.9% | 96.7% |
| 5031045 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.87 | 74.0 | 7.03e-01 | 96.9% | 78.7% |
| 5050903 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.87 | 77.0 | 7.30e-01 | 100.0% | 82.7% |
| 3978875 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.87 | 77.0 | 6.30e-01 | 96.9% | 54.8% |
| 3624238 | 101.1.4.43 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3+MBF1 | 0.87 | 80.0 | 6.37e-01 | 98.5% | 54.2% |
| 3988959 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.87 | 76.0 | 7.64e-01 | 95.4% | 93.8% |
| 3504520 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.87 | 81.0 | 6.86e-01 | 100.0% | 66.0% |
| 3220337 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.86 | 79.0 | 7.00e-01 | 98.5% | 72.2% |
| 5037143 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.86 | 74.0 | 6.85e-01 | 96.9% | 75.0% |
| 3506728 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.86 | 79.0 | 6.26e-01 | 100.0% | 52.0% |
| 4947991 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.85 | 72.0 | 6.85e-01 | 96.9% | 78.7% |
| 4978931 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.85 | 78.0 | 7.58e-01 | 98.5% | 95.7% |
| 4954379 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.85 | 77.0 | 6.40e-01 | 100.0% | 59.1% |
| 4071576 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.84 | 71.0 | 6.44e-01 | 96.9% | 69.4% |
| 4952630 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.84 | 76.0 | 7.29e-01 | 100.0% | 86.7% |
| 3587893 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.84 | 74.0 | 6.38e-01 | 100.0% | 63.0% |
| 5015557 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.84 | 77.0 | 6.61e-01 | 96.9% | 80.0% |
| 4316705 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.83 | 69.0 | 6.43e-01 | 96.9% | 73.8% |
| 5030212 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.83 | 76.0 | 7.39e-01 | 100.0% | 97.1% |
| 4034513 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.82 | 69.0 | 7.19e-01 | 95.4% | 100.0% |
| 4990185 | 101.1.4.18 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_31 | 0.82 | 68.0 | 6.50e-01 | 96.9% | 78.7% |
| 4335698 | 101.1.4.0 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like | 0.82 | 71.0 | 6.40e-01 | 96.9% | 72.2% |
| 4940450 | 101.1.4.18 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_31 | 0.80 | 70.0 | 6.69e-01 | 98.5% | 89.3% |
| 4448496 | 101.1.4.27 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › CYNS_N | 0.79 | 70.0 | 6.82e-01 | 100.0% | 91.4% |
| 5065183 | 101.1.4.3 ↗ | alpha arrays › HTH › HTH › tetra-helical, lambda repressor-like › HTH_3 | 0.75 | 67.0 | 5.83e-01 | 98.5% | 66.3% |
D2
high
residues 82-191
Domain cluster:
rep: rifcsphigho2_12_scaffold_16_prodigal-single.1__X__X__00048__D76-188
CATH (100)
| Domain ID | Class ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 4e2gC00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.88 | 75.0 | 7.16e-01 | 98.2% | 77.8% |
| 7zvmA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.88 | 73.0 | 7.63e-01 | 91.8% | 94.1% |
| 1y9qA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.88 | 71.0 | 7.76e-01 | 89.1% | 100.0% |
| 5zbeA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.87 | 74.0 | 7.56e-01 | 97.3% | 91.6% |
| 1y3tA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.87 | 75.0 | 6.37e-01 | 95.5% | 58.8% |
| 3ibmB00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.87 | 72.0 | 6.43e-01 | 86.4% | 65.1% |
| 3h7jA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.87 | 75.0 | 7.58e-01 | 97.3% | 90.9% |
| 3h7jA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.86 | 73.0 | 7.28e-01 | 98.2% | 86.0% |
| 1y3tA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.86 | 76.0 | 6.60e-01 | 98.2% | 64.4% |
| 2q1zB02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.86 | 70.0 | 7.55e-01 | 95.5% | 100.0% |
| 2pfwA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.85 | 73.0 | 7.33e-01 | 98.2% | 89.2% |
| 1lr5B00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.85 | 79.0 | 6.88e-01 | 98.2% | 73.6% |
| 6m9sD01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.85 | 58.0 | 6.06e-01 | 74.5% | 76.2% |
| 1vj2A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.85 | 79.0 | 7.81e-01 | 98.2% | 94.7% |
| 5fq0A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.84 | 74.0 | 7.42e-01 | 98.2% | 91.8% |
| 2y0oA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.84 | 78.0 | 6.61e-01 | 98.2% | 80.7% |
| 5j7mA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.84 | 77.0 | 7.40e-01 | 100.0% | 86.9% |
| 2oyzA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.84 | 68.0 | 7.31e-01 | 93.6% | 98.9% |
| 2wfpA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 66.0 | 6.95e-01 | 97.3% | 91.8% |
| 3lwcA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 71.0 | 7.35e-01 | 99.1% | 95.1% |
| 5fljA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 78.0 | 6.43e-01 | 99.1% | 61.0% |
| 4e2qA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 77.0 | 5.73e-01 | 100.0% | 42.2% |
| 2vqaA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 74.0 | 6.20e-01 | 94.5% | 60.5% |
| 1qwrA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 64.0 | 7.10e-01 | 93.6% | 100.0% |
| 2bnmA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 75.0 | 7.26e-01 | 95.5% | 93.3% |
| 1j3qB00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 78.0 | 6.39e-01 | 99.1% | 77.0% |
| 2oa2A01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.83 | 69.0 | 6.71e-01 | 87.3% | 79.3% |
| 1o4tA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 77.0 | 7.61e-01 | 99.1% | 97.4% |
| 3es1A02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 72.0 | 6.86e-01 | 91.8% | 92.1% |
| 5cu1A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 76.0 | 6.14e-01 | 98.2% | 59.4% |
| 2q30A01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 63.0 | 7.02e-01 | 84.5% | 100.0% |
| 1sfnA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 77.0 | 5.81e-01 | 100.0% | 44.9% |
| 3ht1A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 76.0 | 6.94e-01 | 99.1% | 78.9% |
| 2f4pA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 76.0 | 7.09e-01 | 99.1% | 85.1% |
| 4lejA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 77.0 | 6.38e-01 | 99.1% | 65.7% |
| 2vqaC01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 76.0 | 6.33e-01 | 98.2% | 63.3% |
| 3i7dA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 76.0 | 6.65e-01 | 99.1% | 76.4% |
| 2opkB01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 67.0 | 7.23e-01 | 89.1% | 100.0% |
| 4b29A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 76.0 | 6.16e-01 | 99.1% | 93.3% |
| 5cadA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 76.0 | 6.17e-01 | 99.1% | 60.6% |
| 1sefA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 74.0 | 6.92e-01 | 96.4% | 80.9% |
| 2vpvA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.82 | 67.0 | 7.21e-01 | 90.9% | 100.0% |
| 6l4cA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 76.0 | 6.26e-01 | 99.1% | 63.6% |
| 3s7iB01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 76.0 | 6.25e-01 | 99.1% | 63.2% |
| 1sq4A02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 75.0 | 7.17e-01 | 99.1% | 85.7% |
| 1cauA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 76.0 | 6.29e-01 | 99.1% | 63.5% |
| 1gqgC01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 75.0 | 6.80e-01 | 98.2% | 76.4% |
| 6l9iA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 75.0 | 6.23e-01 | 98.2% | 61.1% |
| 4lejA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 75.0 | 6.41e-01 | 99.1% | 71.6% |
| 4mv2A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 74.0 | 7.22e-01 | 99.1% | 89.2% |
| 1v70A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 71.0 | 7.32e-01 | 98.2% | 97.1% |
| 3bu7A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 76.0 | 5.13e-01 | 99.1% | 41.1% |
| 3eo6A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 67.0 | 6.84e-01 | 94.5% | 89.6% |
| 1sefA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 71.0 | 6.96e-01 | 95.5% | 86.6% |
| 2pytA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 75.0 | 7.10e-01 | 98.2% | 92.2% |
| 5cadA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 75.0 | 6.17e-01 | 99.1% | 73.7% |
| 2i45D00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.81 | 65.0 | 6.88e-01 | 97.3% | 93.9% |
| 3njzA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.80 | 75.0 | 5.10e-01 | 99.1% | 42.5% |
| 1sq4A01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.80 | 72.0 | 6.49e-01 | 95.5% | 73.6% |
| 5by5A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.80 | 72.0 | 7.16e-01 | 97.3% | 92.2% |
| 4yarA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.80 | 70.0 | 6.74e-01 | 99.1% | 82.9% |
| 1rc6A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.80 | 74.0 | 5.59e-01 | 100.0% | 45.0% |
| 4rd7A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.80 | 72.0 | 7.04e-01 | 99.1% | 89.1% |
| 3myxA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.79 | 71.0 | 7.05e-01 | 100.0% | 90.4% |
| 3hqxA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.79 | 68.0 | 6.95e-01 | 95.5% | 94.3% |
| 3l2hA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.79 | 74.0 | 6.64e-01 | 100.0% | 78.9% |
| 3cewA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.79 | 67.0 | 6.71e-01 | 100.0% | 89.1% |
| 1yllC02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.79 | 74.0 | 7.46e-01 | 100.0% | 100.0% |
| 5jqyA02 | 2.60.120.330 | Mainly Beta › Sandwich › Jelly Rolls › B-lactam Antibiotic, Isopenicillin N Synthase; Chain | 0.79 | 74.0 | 5.97e-01 | 100.0% | 73.5% |
| 3d82A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.79 | 66.0 | 6.85e-01 | 96.4% | 94.1% |
| 6b9tF02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.79 | 70.0 | 7.12e-01 | 95.5% | 95.4% |
| 2o8qA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.79 | 64.0 | 6.17e-01 | 91.8% | 77.0% |
| 3rnsA02 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.78 | 67.0 | 7.03e-01 | 97.3% | 98.0% |
| 3bcwA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.78 | 70.0 | 7.19e-01 | 98.2% | 100.0% |
| 3eqeA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.78 | 73.0 | 6.35e-01 | 98.2% | 70.5% |
| 3es4A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.78 | 73.0 | 7.19e-01 | 99.1% | 94.8% |
| 2fqpA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.78 | 63.0 | 6.72e-01 | 88.2% | 97.9% |
| 1xjaB00 | 2.60.120.280 | Mainly Beta › Sandwich › Jelly Rolls › Regulatory protein AraC | 0.78 | 58.0 | 5.12e-01 | 77.3% | 55.8% |
| 2b8mA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.78 | 69.0 | 6.95e-01 | 99.1% | 94.5% |
| 2d40B00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.78 | 72.0 | 5.21e-01 | 99.1% | 50.0% |
| 3h8uA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.78 | 69.0 | 6.71e-01 | 99.1% | 86.1% |
| 3fjsC00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.77 | 67.0 | 6.82e-01 | 98.2% | 92.5% |
| 2gu9A01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.77 | 68.0 | 7.08e-01 | 94.5% | 99.0% |
| 4mloA01 | 2.60.120.810 | Mainly Beta › Sandwich › Jelly Rolls › | 0.77 | 57.0 | 5.02e-01 | 77.3% | 100.0% |
| 3o14A00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.77 | 66.0 | 5.13e-01 | 100.0% | 45.0% |
| 1e5rB01 | 2.60.120.330 | Mainly Beta › Sandwich › Jelly Rolls › B-lactam Antibiotic, Isopenicillin N Synthase; Chain | 0.77 | 72.0 | 6.03e-01 | 100.0% | 74.9% |
| 3aclA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.76 | 68.0 | 6.70e-01 | 95.5% | 89.8% |
| 3rnsA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.76 | 69.0 | 7.00e-01 | 96.4% | 97.2% |
| 6nwmA01 | 2.60.120.280 | Mainly Beta › Sandwich › Jelly Rolls › Regulatory protein AraC | 0.76 | 62.0 | 5.42e-01 | 85.5% | 60.6% |
| 1ywkC00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.76 | 70.0 | 5.23e-01 | 99.1% | 43.9% |
| 3bb6C00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.75 | 55.0 | 5.55e-01 | 76.4% | 83.9% |
| 5bpxA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.74 | 67.0 | 5.92e-01 | 98.2% | 69.9% |
| 4hslA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.73 | 66.0 | 5.64e-01 | 99.1% | 63.3% |
| 2ozjA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.73 | 66.0 | 6.68e-01 | 97.3% | 96.3% |
| 1yhfA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.73 | 67.0 | 6.77e-01 | 97.3% | 97.3% |
| 1x8mA01 | 2.60.120.520 | Mainly Beta › Sandwich › Jelly Rolls › pectin degrading enzyme 5-keto 4- deoxyuronate isomerase, domain 1 | 0.70 | 63.0 | 6.08e-01 | 96.4% | 90.2% |
| 2qnkA00 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.70 | 65.0 | 4.73e-01 | 100.0% | 95.5% |
| 2vecA01 | 2.60.120.10 | Mainly Beta › Sandwich › Jelly Rolls › Jelly Rolls | 0.70 | 58.0 | 5.96e-01 | 95.5% | 95.1% |
| 5lz6A00 | 2.60.120.680 | Mainly Beta › Sandwich › Jelly Rolls › GOLD domain | 0.67 | 53.0 | 5.09e-01 | 84.5% | 83.3% |
| 6qdiA02 | 3.90.182.10 | Alpha Beta › Alpha-Beta Complex › Toxin - Anthrax Protective Antigen; domain 1 › Toxin - Anthrax Protective Antigen;domain 1 | 0.56 | 46.0 | 4.29e-01 | 90.0% | 79.6% |
ECOD (100)
| UID | F-ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 3967122 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.93 | 86.0 | 8.41e-01 | 99.1% | 89.0% |
| 3941636 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.93 | 87.0 | 8.60e-01 | 99.1% | 93.0% |
| 3973477 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.92 | 84.0 | 8.34e-01 | 98.2% | 91.2% |
| 3969539 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.91 | 80.0 | 8.27e-01 | 95.5% | 97.1% |
| 3971446 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.90 | 77.0 | 7.60e-01 | 96.4% | 85.2% |
| 3973758 | 10.12.1.98 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › MannoseP_isomer | 0.90 | 77.0 | 7.61e-01 | 96.4% | 86.0% |
| 4942033 | 10.12.1.98 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › MannoseP_isomer | 0.89 | 73.0 | 7.22e-01 | 91.8% | 81.6% |
| 3838063 | 10.12.1.98 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › MannoseP_isomer | 0.89 | 77.0 | 7.30e-01 | 96.4% | 78.4% |
| 4827723 | 10.12.1.46 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › CENP-C_C | 0.89 | 61.0 | 7.27e-01 | 73.6% | 100.0% |
| 4954842 | 10.12.1.98 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › MannoseP_isomer | 0.89 | 73.0 | 7.65e-01 | 91.8% | 93.0% |
| 3688349 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.89 | 78.0 | 7.60e-01 | 95.5% | 84.2% |
| 3587816 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.89 | 78.0 | 8.03e-01 | 94.5% | 96.2% |
| 3945556 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.89 | 81.0 | 8.10e-01 | 98.2% | 94.5% |
| 4009299 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.89 | 80.0 | 8.00e-01 | 98.2% | 93.6% |
| 3869575 | 10.12.1.46 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › CENP-C_C | 0.89 | 76.0 | 7.04e-01 | 97.3% | 73.3% |
| 5017338 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.88 | 82.0 | 8.24e-01 | 100.0% | 98.2% |
| 3973849 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.88 | 81.0 | 8.01e-01 | 100.0% | 93.0% |
| 3969412 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.88 | 79.0 | 7.81e-01 | 97.3% | 90.4% |
| 3285287 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.87 | 77.0 | 7.64e-01 | 100.0% | 88.7% |
| 4996252 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.87 | 82.0 | 7.93e-01 | 98.2% | 90.8% |
| 5017493 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.87 | 78.0 | 7.84e-01 | 95.5% | 93.6% |
| 3968593 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.87 | 79.0 | 7.75e-01 | 97.3% | 90.4% |
| 4965910 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.87 | 81.0 | 7.80e-01 | 99.1% | 89.2% |
| 4983916 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.87 | 79.0 | 7.99e-01 | 97.3% | 96.4% |
| 4961572 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 80.0 | 7.52e-01 | 98.2% | 82.3% |
| 1329 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 74.0 | 7.84e-01 | 94.5% | 100.0% |
| 4990612 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.86 | 74.0 | 7.45e-01 | 98.2% | 90.0% |
| 5031628 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 80.0 | 7.73e-01 | 97.3% | 90.0% |
| 4880519 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 74.0 | 7.27e-01 | 98.2% | 84.6% |
| 4659356 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 78.0 | 7.71e-01 | 98.2% | 91.3% |
| 4988640 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 76.0 | 7.63e-01 | 98.2% | 92.7% |
| 4933863 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 80.0 | 7.90e-01 | 98.2% | 94.8% |
| 5062005 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 80.0 | 7.76e-01 | 98.2% | 90.8% |
| 5061863 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.86 | 76.0 | 7.69e-01 | 95.5% | 93.6% |
| 5073275 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.85 | 75.0 | 7.68e-01 | 97.3% | 96.2% |
| 4988382 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.85 | 76.0 | 7.56e-01 | 98.2% | 91.2% |
| 5001494 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.85 | 80.0 | 8.09e-01 | 99.1% | 99.1% |
| 5009241 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.85 | 73.0 | 7.64e-01 | 95.5% | 99.0% |
| 4955761 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.85 | 80.0 | 7.50e-01 | 98.2% | 85.9% |
| 4950350 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.85 | 74.0 | 7.60e-01 | 98.2% | 96.2% |
| 3944739 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.85 | 77.0 | 7.76e-01 | 99.1% | 96.4% |
| 1030916 | 10.12.1.8 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › AraC_binding | 0.85 | 76.0 | 7.82e-01 | 95.5% | 100.0% |
| 1876221 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 74.0 | 7.42e-01 | 98.2% | 91.8% |
| 2900916 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 76.0 | 7.61e-01 | 98.2% | 93.8% |
| 5026683 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 79.0 | 7.67e-01 | 99.1% | 91.7% |
| 3944728 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 77.0 | 7.51e-01 | 100.0% | 89.2% |
| 5067959 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 70.0 | 6.89e-01 | 86.4% | 82.6% |
| 4015504 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 79.0 | 6.91e-01 | 99.1% | 89.0% |
| 5080536 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 72.0 | 7.62e-01 | 99.1% | 99.0% |
| 5018960 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 78.0 | 7.39e-01 | 97.3% | 90.4% |
| 4264620 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 77.0 | 7.46e-01 | 97.3% | 91.7% |
| 3281054 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.84 | 75.0 | 7.54e-01 | 95.5% | 94.5% |
| 3956637 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.84 | 78.0 | 7.20e-01 | 98.2% | 80.0% |
| 4997177 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.83 | 75.0 | 7.45e-01 | 98.2% | 91.3% |
| 4979872 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.83 | 78.0 | 7.54e-01 | 98.2% | 95.0% |
| 4272498 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.83 | 77.0 | 7.19e-01 | 99.1% | 82.3% |
| 5045427 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.83 | 75.0 | 7.72e-01 | 94.5% | 100.0% |
| 4949707 | 10.12.1.98 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › MannoseP_isomer | 0.83 | 79.0 | 6.48e-01 | 99.1% | 81.7% |
| 3166716 | 10.12.1.46 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › CENP-C_C | 0.83 | 79.0 | 6.88e-01 | 100.0% | 71.0% |
| 4357938 | 10.12.1.154 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › MannoseP_isomer, ManC_GMP_beta-helix | 0.83 | 79.0 | 6.55e-01 | 99.1% | 83.4% |
| 5012735 | 7516.1.1.1 ↗ | a/b three-layered sandwiches › Nucleotide-diphospho-sugar transferases › Nucleotide-diphospho-sugar transferases › Nucleotide-diphospho-sugar transferases › NTP_transferase | 0.83 | 79.0 | 5.00e-01 | 99.1% | 35.9% |
| 3973004 | 208.4.1.0 ↗ | beta duplicates or obligate multimers › Single-stranded left-handed beta-helix › Guanosine diphospho-D-mannose pyrophosphorylase/mannose-6-phosphate isomerase linker domain › Guanosine diphospho-D-mannose pyrophosphorylase/mannose-6-phosphate isomerase linker domain | 0.83 | 79.0 | 6.32e-01 | 99.1% | 76.2% |
| 4987174 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.83 | 77.0 | 7.49e-01 | 98.2% | 92.5% |
| 2080774 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.83 | 77.0 | 7.52e-01 | 98.2% | 91.5% |
| 4174964 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.83 | 78.0 | 6.39e-01 | 99.1% | 80.0% |
| 5002053 | 7516.1.1.187 ↗ | a/b three-layered sandwiches › Nucleotide-diphospho-sugar transferases › Nucleotide-diphospho-sugar transferases › Nucleotide-diphospho-sugar transferases › MannoseP_isomer | 0.83 | 78.0 | 4.94e-01 | 99.1% | 31.6% |
| 4977034 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.82 | 76.0 | 7.51e-01 | 99.1% | 93.0% |
| 3972190 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.82 | 75.0 | 7.62e-01 | 96.4% | 98.1% |
| 3966359 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.82 | 77.0 | 5.62e-01 | 100.0% | 42.1% |
| 3781431 | 10.12.1.46 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › CENP-C_C | 0.82 | 77.0 | 6.96e-01 | 100.0% | 89.5% |
| 368152 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.82 | 76.0 | 6.63e-01 | 99.1% | 75.9% |
| 168799 | 10.12.1.46 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › CENP-C_C | 0.82 | 67.0 | 7.21e-01 | 90.9% | 100.0% |
| 4164755 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.81 | 76.0 | 6.15e-01 | 99.1% | 67.2% |
| 5010256 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.81 | 76.0 | 6.28e-01 | 99.1% | 68.9% |
| 3975454 | 10.12.1.138 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_3, Cupin_2 | 0.81 | 76.0 | 5.63e-01 | 100.0% | 42.7% |
| 4978598 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.81 | 67.0 | 7.01e-01 | 97.3% | 95.0% |
| 154310 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.81 | 74.0 | 7.17e-01 | 99.1% | 87.7% |
| 1303 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.81 | 71.0 | 7.32e-01 | 98.2% | 97.1% |
| 3740261 | 10.12.1.46 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › CENP-C_C | 0.81 | 76.0 | 6.68e-01 | 100.0% | 86.3% |
| 3651516 | 10.12.1.5 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › PMI_typeI_C | 0.80 | 69.0 | 7.23e-01 | 98.2% | 100.0% |
| 3191666 | 10.12.1.46 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › CENP-C_C | 0.80 | 76.0 | 6.62e-01 | 100.0% | 89.0% |
| 167437 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.80 | 67.0 | 6.57e-01 | 100.0% | 82.9% |
| 4957100 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.80 | 69.0 | 6.16e-01 | 99.1% | 66.7% |
| 5009706 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.80 | 68.0 | 6.52e-01 | 98.2% | 79.2% |
| 3283472 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.80 | 71.0 | 6.05e-01 | 93.6% | 83.6% |
| 1179973 | 10.12.1.27 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_3 | 0.80 | 74.0 | 6.62e-01 | 100.0% | 74.1% |
| 3957537 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.79 | 70.0 | 7.22e-01 | 97.3% | 98.1% |
| 3958311 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.79 | 73.0 | 6.85e-01 | 98.2% | 83.1% |
| 3277879 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.79 | 70.0 | 7.18e-01 | 100.0% | 99.0% |
| 4284515 | 10.12.1.5 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › PMI_typeI_C | 0.79 | 67.0 | 7.07e-01 | 94.5% | 100.0% |
| 2414505 | 10.12.1.26 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Pirin_C | 0.78 | 70.0 | 6.17e-01 | 95.5% | 70.6% |
| 4955697 | 10.12.1.39 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › Cupin_2 | 0.77 | 70.0 | 7.22e-01 | 98.2% | 100.0% |
| 4393329 | 10.12.1.75 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › AraC_binding_2 | 0.77 | 71.0 | 5.65e-01 | 98.2% | 68.8% |
| 3661846 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.76 | 69.0 | 5.99e-01 | 97.3% | 96.2% |
| 3677913 | 10.12.1.144 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › PMI_typeI_C, PMI_typeI_cat | 0.76 | 70.0 | 5.15e-01 | 98.2% | 54.6% |
| 3444636 | 10.12.1.5 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › PMI_typeI_C | 0.75 | 69.0 | 6.05e-01 | 99.1% | 96.9% |
| 3277945 | 10.12.1.75 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › AraC_binding_2 | 0.74 | 70.0 | 5.61e-01 | 100.0% | 65.0% |
| 3195183 | 10.12.1.0 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix | 0.74 | 66.0 | 6.69e-01 | 95.5% | 99.1% |
| 4567075 | 10.12.1.84 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › VKGC_lumenal_dom | 0.73 | 67.0 | 4.87e-01 | 98.2% | 47.7% |
| 3404684 | 10.12.1.84 ↗ | beta sandwiches › jelly-roll › Double-stranded beta-helix › Double-stranded beta-helix › VKGC_lumenal_dom | 0.73 | 67.0 | 5.31e-01 | 99.1% | 67.1% |