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P0_An_pond3_S8_coassembly_k141_133253_prodigal-single.1__X__X__00387
Bact-VirP0_An_pond3_S8_coassembly_k141_133253_prodigal-single.1__X__X__00387
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 11-171
Domain cluster:
rep: IMGVR_UViG_3300038974_000877-3300038974-Ga0416721_000556_5288_6388__D166-273_308-366
Pfam (1)
| Accession | Name | Score | E-value | Q cov | HMM cov |
|---|---|---|---|---|---|
| PF03781.23 best | FGE-sulfatase | 52.0 | 1.10e-13 | 97.5% | 65.1% |
CATH (32)
| Domain ID | Class ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 1y1fX00 | 3.90.1580.10 | Alpha Beta › Alpha-Beta Complex › paralog of FGE (formylglycine-generating enzyme) › paralog of FGE (formylglycine-generating enzyme) | 0.78 | 75.0 | 6.11e-01 | 100.0% | 96.3% |
| 2y3cA00 | 3.90.1580.10 | Alpha Beta › Alpha-Beta Complex › paralog of FGE (formylglycine-generating enzyme) › paralog of FGE (formylglycine-generating enzyme) | 0.77 | 74.0 | 5.99e-01 | 100.0% | 93.5% |
| 1f00I03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.76 | 46.0 | 5.83e-01 | 100.0% | 99.0% |
| 4m1gA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.76 | 38.0 | 5.29e-01 | 100.0% | 95.2% |
| 1yu0A03 | 3.90.1580.10 | Alpha Beta › Alpha-Beta Complex › paralog of FGE (formylglycine-generating enzyme) › paralog of FGE (formylglycine-generating enzyme) | 0.74 | 66.0 | 6.34e-01 | 91.9% | 100.0% |
| 2pf5D00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.73 | 42.0 | 5.42e-01 | 95.7% | 96.9% |
| 2yhfA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.68 | 46.0 | 5.32e-01 | 100.0% | 93.2% |
| 3bdwB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.67 | 43.0 | 5.03e-01 | 100.0% | 89.7% |
| 3hupA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.66 | 44.0 | 5.01e-01 | 100.0% | 88.4% |
| 3vppB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.66 | 45.0 | 5.19e-01 | 100.0% | 91.8% |
| 2h2tB01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.66 | 45.0 | 5.30e-01 | 100.0% | 96.6% |
| 2c6uA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.66 | 45.0 | 5.18e-01 | 100.0% | 91.8% |
| 3bdwA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.66 | 45.0 | 5.08e-01 | 100.0% | 89.4% |
| 6innA04 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.66 | 48.0 | 5.30e-01 | 100.0% | 92.2% |
| 6rygA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.65 | 45.0 | 5.31e-01 | 100.0% | 98.3% |
| 7jptA06 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.65 | 46.0 | 5.34e-01 | 100.0% | 99.1% |
| 1kcgB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.65 | 44.0 | 4.96e-01 | 100.0% | 89.4% |
| 5xtsA03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.64 | 47.0 | 5.36e-01 | 100.0% | 98.4% |
| 1tdqB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.64 | 46.0 | 5.19e-01 | 100.0% | 93.7% |
| 5ew6A01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.64 | 47.0 | 5.32e-01 | 100.0% | 99.2% |
| 5vybA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.63 | 46.0 | 4.93e-01 | 100.0% | 84.6% |
| 3zhgA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.63 | 45.0 | 5.00e-01 | 100.0% | 89.4% |
| 3m9zA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.63 | 44.0 | 4.96e-01 | 100.0% | 91.9% |
| 4ak8A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.62 | 46.0 | 5.10e-01 | 100.0% | 93.8% |
| 2vuvA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.62 | 45.0 | 5.04e-01 | 100.0% | 93.0% |
| 1egiA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.62 | 46.0 | 5.16e-01 | 100.0% | 95.3% |
| 1eslA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.62 | 44.0 | 4.54e-01 | 95.7% | 75.2% |
| 5ktiA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.62 | 46.0 | 4.87e-01 | 100.0% | 85.4% |
| 1wk1A01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.61 | 44.0 | 5.05e-01 | 94.4% | 99.2% |
| 2ox8A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.61 | 46.0 | 5.08e-01 | 100.0% | 96.9% |
| 7jptA03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.60 | 45.0 | 5.04e-01 | 96.3% | 98.4% |
| 1afb100 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.59 | 44.0 | 4.56e-01 | 100.0% | 80.5% |
ECOD (82)
| UID | F-ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 4936908 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.81 | 78.0 | 6.41e-01 | 100.0% | 95.5% |
| 5039704 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.78 | 75.0 | 5.99e-01 | 100.0% | 89.8% |
| 2507386 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.77 | 75.0 | 5.85e-01 | 100.0% | 92.4% |
| 4653754 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.77 | 74.0 | 6.23e-01 | 100.0% | 92.8% |
| 7356 | 209.1.2.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like | 0.77 | 74.0 | 6.61e-01 | 100.0% | 91.9% |
| 4871690 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.76 | 73.0 | 5.85e-01 | 100.0% | 96.5% |
| 3899892 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.76 | 45.0 | 5.38e-01 | 100.0% | 85.5% |
| 1948554 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.76 | 73.0 | 5.99e-01 | 100.0% | 96.6% |
| 4481712 | 209.1.1.10 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Intimin_C | 0.76 | 47.0 | 5.82e-01 | 98.8% | 99.0% |
| 3909571 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.75 | 43.0 | 5.58e-01 | 99.4% | 96.8% |
| 4859271 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.75 | 44.0 | 5.12e-01 | 100.0% | 79.7% |
| 4532283 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.75 | 47.0 | 5.78e-01 | 99.4% | 97.1% |
| 1349657 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.73 | 42.0 | 4.33e-01 | 100.0% | 59.7% |
| 3232262 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.72 | 44.0 | 5.30e-01 | 100.0% | 90.0% |
| 3915615 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.72 | 43.0 | 5.14e-01 | 95.7% | 86.4% |
| 314001 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.72 | 42.0 | 4.37e-01 | 100.0% | 62.0% |
| 3893152 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.72 | 44.0 | 5.33e-01 | 98.1% | 90.9% |
| 2464389 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.71 | 68.0 | 5.69e-01 | 100.0% | 90.7% |
| 3917585 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.71 | 44.0 | 5.23e-01 | 97.5% | 89.1% |
| 3908178 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.71 | 44.0 | 5.35e-01 | 97.5% | 94.3% |
| 3634766 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.71 | 67.0 | 5.30e-01 | 100.0% | 90.5% |
| 3744244 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.70 | 67.0 | 5.65e-01 | 100.0% | 88.5% |
| 3535580 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.70 | 43.0 | 5.28e-01 | 100.0% | 95.2% |
| 3899009 | 209.1.1.4 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Xlink | 0.69 | 40.0 | 5.12e-01 | 95.7% | 96.8% |
| 3963924 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.68 | 65.0 | 5.66e-01 | 100.0% | 98.7% |
| 4015023 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.68 | 44.0 | 5.09e-01 | 100.0% | 88.3% |
| 3528373 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.67 | 47.0 | 5.21e-01 | 100.0% | 89.2% |
| 3879573 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.66 | 48.0 | 4.97e-01 | 100.0% | 79.3% |
| 3549112 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.66 | 46.0 | 5.13e-01 | 100.0% | 88.5% |
| 3556397 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.65 | 45.0 | 4.35e-01 | 100.0% | 64.6% |
| 4004045 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.64 | 49.0 | 5.02e-01 | 100.0% | 81.3% |
| 3507882 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.64 | 48.0 | 5.12e-01 | 100.0% | 87.9% |
| 3759902 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.64 | 46.0 | 4.95e-01 | 100.0% | 86.7% |
| 3222327 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.64 | 46.0 | 4.97e-01 | 100.0% | 87.4% |
| 3747037 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.64 | 44.0 | 4.75e-01 | 100.0% | 83.0% |
| 3777546 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.63 | 45.0 | 4.34e-01 | 100.0% | 63.8% |
| 3217654 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.63 | 47.0 | 5.15e-01 | 100.0% | 91.9% |
| 3940222 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.63 | 47.0 | 4.25e-01 | 100.0% | 57.7% |
| 3550006 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.63 | 46.0 | 4.85e-01 | 100.0% | 83.4% |
| 3882780 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.63 | 45.0 | 4.94e-01 | 100.0% | 88.1% |
| 3470338 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.63 | 48.0 | 5.06e-01 | 100.0% | 87.6% |
| 3242909 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.62 | 46.0 | 5.16e-01 | 100.0% | 96.8% |
| 4857614 | 209.1.2.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like › FGE-sulfatase | 0.62 | 59.0 | 5.29e-01 | 98.8% | 94.8% |
| 3770046 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.62 | 46.0 | 4.30e-01 | 100.0% | 63.1% |
| 3234898 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.61 | 49.0 | 5.22e-01 | 100.0% | 93.1% |
| 3243322 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.61 | 45.0 | 4.93e-01 | 100.0% | 91.1% |
| 3405168 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.61 | 47.0 | 4.95e-01 | 100.0% | 89.0% |
| 3568994 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.61 | 49.0 | 5.13e-01 | 100.0% | 91.3% |
| 4355266 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.60 | 48.0 | 3.96e-01 | 100.0% | 48.9% |
| 3865253 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.60 | 44.0 | 3.44e-01 | 100.0% | 37.5% |
| 3519333 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.60 | 47.0 | 4.88e-01 | 100.0% | 88.0% |
| 3629386 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.59 | 49.0 | 4.98e-01 | 100.0% | 89.0% |
| 3215058 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.59 | 46.0 | 5.01e-01 | 100.0% | 97.0% |
| 5029394 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.59 | 56.0 | 4.99e-01 | 100.0% | 95.8% |
| 5029487 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.58 | 55.0 | 5.05e-01 | 100.0% | 96.6% |
| 3219449 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.58 | 47.0 | 4.81e-01 | 100.0% | 86.2% |
| 3219837 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.58 | 48.0 | 4.84e-01 | 100.0% | 85.5% |
| 3233366 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.58 | 50.0 | 4.91e-01 | 100.0% | 85.8% |
| 3216466 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.57 | 48.0 | 4.88e-01 | 100.0% | 88.7% |
| 5027867 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.57 | 54.0 | 5.06e-01 | 100.0% | 96.9% |
| 3228009 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.57 | 51.0 | 5.10e-01 | 100.0% | 92.7% |
| 3552630 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.56 | 47.0 | 4.82e-01 | 100.0% | 91.0% |
| 3517836 | 209.1.2.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › Sulfatase-modifying factor-like | 0.56 | 52.0 | 4.53e-01 | 100.0% | 73.1% |
| 3242895 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.56 | 52.0 | 4.81e-01 | 100.0% | 82.0% |
| 3801684 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.55 | 48.0 | 4.77e-01 | 100.0% | 89.1% |
| 3217541 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.55 | 52.0 | 4.94e-01 | 100.0% | 89.1% |
| 3216545 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.55 | 51.0 | 5.03e-01 | 100.0% | 96.0% |
| 3223193 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.55 | 51.0 | 4.96e-01 | 100.0% | 92.6% |
| 4854471 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.54 | 48.0 | 4.82e-01 | 100.0% | 92.7% |
| 3215890 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.54 | 51.0 | 4.64e-01 | 100.0% | 89.3% |
| 3226348 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.54 | 51.0 | 5.02e-01 | 100.0% | 95.9% |
| 3239560 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.54 | 51.0 | 4.56e-01 | 100.0% | 80.9% |
| 3246977 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.54 | 46.0 | 4.79e-01 | 95.0% | 97.3% |
| 3224196 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.53 | 49.0 | 4.58e-01 | 100.0% | 79.5% |
| 3405020 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.53 | 48.0 | 4.86e-01 | 100.0% | 95.6% |
| 3227038 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.53 | 50.0 | 4.67e-01 | 100.0% | 92.3% |
| 3238557 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.53 | 49.0 | 4.81e-01 | 100.0% | 92.6% |
| 3242066 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.53 | 48.0 | 4.75e-01 | 100.0% | 93.9% |
| 3241317 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.52 | 49.0 | 4.68e-01 | 100.0% | 90.8% |
| 3918961 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.52 | 47.0 | 4.60e-01 | 100.0% | 90.6% |
| 3594204 | 209.1.1.11 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › DUF5075 | 0.51 | 47.0 | 4.37e-01 | 97.5% | 98.5% |
| 3214893 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.51 | 47.0 | 4.60e-01 | 100.0% | 90.9% |