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IMGVR_UViG_3300025674_007958-3300025674-Ga0208162_100221812
Arc-VirIMGVR_UViG_3300025674_007958-3300025674-Ga0208162_100221812
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 32-142
Domain cluster:
rep: BML_08042016_6_5m_scaffold_2_prodigal-single.1__X__X__00137__D21-104
CATH (32)
| Domain ID | Class ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 1fvuB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.71 | 66.0 | 6.40e-01 | 99.1% | 98.3% |
| 1v7pB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.71 | 66.0 | 6.29e-01 | 100.0% | 98.4% |
| 1h8uB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.71 | 58.0 | 5.73e-01 | 86.5% | 100.0% |
| 3m9zA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.70 | 65.0 | 6.27e-01 | 100.0% | 97.6% |
| 1egiA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.69 | 63.0 | 6.01e-01 | 98.2% | 98.4% |
| 1byfA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.69 | 59.0 | 5.68e-01 | 90.1% | 100.0% |
| 1sb2B00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.68 | 63.0 | 6.06e-01 | 100.0% | 97.6% |
| 5xtsA03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.68 | 61.0 | 5.93e-01 | 96.4% | 100.0% |
| 1jznA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.68 | 62.0 | 5.82e-01 | 99.1% | 97.8% |
| 1c3aA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.68 | 62.0 | 5.85e-01 | 100.0% | 96.3% |
| 6innA04 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.68 | 63.0 | 5.97e-01 | 100.0% | 97.7% |
| 5b1rA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.68 | 62.0 | 6.11e-01 | 100.0% | 94.8% |
| 3vppB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.67 | 62.0 | 6.04e-01 | 100.0% | 97.5% |
| 1ypoA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.67 | 62.0 | 5.92e-01 | 100.0% | 96.9% |
| 2yhfA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.67 | 61.0 | 6.02e-01 | 99.1% | 98.3% |
| 7jptA01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.67 | 60.0 | 5.78e-01 | 96.4% | 100.0% |
| 4yliE00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.67 | 61.0 | 5.53e-01 | 100.0% | 87.2% |
| 3bdwA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.66 | 62.0 | 5.96e-01 | 100.0% | 95.9% |
| 1b7tA02 | 2.30.30.360 | Mainly Beta › Roll › SH3 type barrels. › Myosin S1 fragment, N-terminal | 0.58 | 28.0 | 3.94e-01 | 82.0% | 100.0% |
| 5i4eA01 | 2.30.30.360 | Mainly Beta › Roll › SH3 type barrels. › Myosin S1 fragment, N-terminal | 0.57 | 25.0 | 3.75e-01 | 76.6% | 100.0% |
| 6c6sD02 | 2.30.30.30 | Mainly Beta › Roll › SH3 type barrels. › | 0.56 | 29.0 | 3.76e-01 | 73.0% | 91.7% |
| 6bhdA03 | 2.30.30.140 | Mainly Beta › Roll › SH3 type barrels. › | 0.55 | 27.0 | 3.51e-01 | 71.2% | 82.5% |
| 4m4zA01 | 2.30.30.40 | Mainly Beta › Roll › SH3 type barrels. › SH3 Domains | 0.55 | 25.0 | 3.66e-01 | 73.9% | 100.0% |
| 4ytlA01 | 2.30.30.30 | Mainly Beta › Roll › SH3 type barrels. › | 0.55 | 26.0 | 3.71e-01 | 71.2% | 100.0% |
| 1jw9B00 | 3.40.50.720 | Alpha Beta › 3-Layer(aba) Sandwich › Rossmann fold › NAD(P)-binding Rossmann-like Domain | 0.53 | 40.0 | 3.14e-01 | 79.3% | 70.8% |
| 3oyyA01 | 2.30.30.30 | Mainly Beta › Roll › SH3 type barrels. › | 0.51 | 31.0 | 3.81e-01 | 78.4% | 100.0% |
| 1yn8A00 | 2.30.30.40 | Mainly Beta › Roll › SH3 type barrels. › SH3 Domains | 0.51 | 27.0 | 3.62e-01 | 76.6% | 96.6% |
| 7u32F02 | 2.30.30.10 | Mainly Beta › Roll › SH3 type barrels. › Integrase, C-terminal domain superfamily, retroviral | 0.51 | 24.0 | 3.43e-01 | 75.7% | 98.0% |
| 6bogA01 | 2.30.30.140 | Mainly Beta › Roll › SH3 type barrels. › | 0.51 | 26.0 | 3.46e-01 | 71.2% | 100.0% |
| 2eqkA01 | 2.30.30.140 | Mainly Beta › Roll › SH3 type barrels. › | 0.51 | 29.0 | 3.52e-01 | 74.8% | 86.3% |
| 1zuuA00 | 2.30.30.40 | Mainly Beta › Roll › SH3 type barrels. › SH3 Domains | 0.51 | 26.0 | 3.59e-01 | 75.7% | 100.0% |
| 2plqA00 | 3.60.110.10 | Alpha Beta › 4-Layer Sandwich › Nitrilase/N-carbamoyl-D-aminoacid amidohydrolase › Carbon-nitrogen hydrolase | 0.51 | 39.0 | 2.87e-01 | 83.8% | 88.2% |
ECOD (68)
| UID | F-ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 5080286 | 209.1.1.25 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lcl_C | 0.86 | 80.0 | 7.50e-01 | 97.3% | 95.4% |
| 4102050 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 66.0 | 6.65e-01 | 97.3% | 86.4% |
| None | — | 0.77 | 65.0 | 6.61e-01 | 98.2% | 90.9% | |
| 4532283 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.77 | 68.0 | 7.04e-01 | 93.7% | 100.0% |
| 3976043 | 209.1.1.6 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › InvE_AD | 0.74 | 68.0 | 6.31e-01 | 97.3% | 91.1% |
| 3498507 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.73 | 67.0 | 5.83e-01 | 100.0% | 89.1% |
| 3937219 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.72 | 66.0 | 6.08e-01 | 99.1% | 97.9% |
| 3908631 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.72 | 66.0 | 6.19e-01 | 99.1% | 98.5% |
| 3980715 | 209.1.1.6 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › InvE_AD | 0.72 | 66.0 | 6.05e-01 | 98.2% | 87.1% |
| 3219777 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.72 | 66.0 | 5.94e-01 | 100.0% | 94.0% |
| 3230092 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.72 | 66.0 | 5.93e-01 | 100.0% | 86.0% |
| 3581508 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.71 | 66.0 | 6.01e-01 | 100.0% | 84.8% |
| 3243113 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.71 | 66.0 | 6.14e-01 | 100.0% | 95.6% |
| 3218099 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.71 | 65.0 | 5.81e-01 | 100.0% | 82.6% |
| 3234540 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.71 | 65.0 | 5.99e-01 | 100.0% | 92.9% |
| 2884722 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.71 | 65.0 | 5.92e-01 | 99.1% | 92.4% |
| 3976063 | 209.1.1.6 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › InvE_AD | 0.70 | 64.0 | 5.98e-01 | 98.2% | 95.6% |
| 3395123 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 65.0 | 5.75e-01 | 100.0% | 85.9% |
| 3214370 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 64.0 | 5.80e-01 | 100.0% | 88.7% |
| 3245906 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 64.0 | 5.84e-01 | 100.0% | 93.8% |
| 3617774 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 65.0 | 5.84e-01 | 100.0% | 86.5% |
| 2884715 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 65.0 | 5.87e-01 | 100.0% | 87.7% |
| 3794584 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 64.0 | 6.02e-01 | 100.0% | 94.1% |
| 3927884 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 64.0 | 4.91e-01 | 100.0% | 52.2% |
| 3887996 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 64.0 | 5.41e-01 | 100.0% | 76.7% |
| 2066820 | 209.1.1.6 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › InvE_AD | 0.70 | 63.0 | 5.91e-01 | 97.3% | 89.5% |
| 4047155 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.70 | 59.0 | 5.70e-01 | 91.0% | 100.0% |
| 3900658 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 64.0 | 5.76e-01 | 100.0% | 88.0% |
| 3225590 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 6.05e-01 | 99.1% | 99.2% |
| 3919376 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 65.0 | 5.46e-01 | 100.0% | 77.7% |
| 3918361 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.70e-01 | 100.0% | 90.7% |
| 3223044 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 64.0 | 5.88e-01 | 100.0% | 90.0% |
| 3568994 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.70e-01 | 100.0% | 95.3% |
| 3259439 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.69 | 63.0 | 5.73e-01 | 99.1% | 95.9% |
| 3858628 | 3939.1.1.306 ↗ | alpha duplicates or obligate multimers › XRCC4 C-terminal oligomerization domain › XRCC4 C-terminal oligomerization domain › XRCC4 C-terminal oligomerization domain › Lectin_C | 0.69 | 63.0 | 5.00e-01 | 99.1% | 68.3% |
| 3550006 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 64.0 | 5.79e-01 | 100.0% | 89.0% |
| 3213988 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.78e-01 | 100.0% | 86.9% |
| 3859812 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 62.0 | 5.74e-01 | 97.3% | 90.0% |
| 3908630 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.61e-01 | 100.0% | 87.7% |
| 3932192 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.71e-01 | 100.0% | 88.7% |
| 3013484 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 62.0 | 5.78e-01 | 97.3% | 93.4% |
| 3236450 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.91e-01 | 100.0% | 94.8% |
| 3365401 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.69e-01 | 100.0% | 94.0% |
| 3908637 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.78e-01 | 98.2% | 90.0% |
| 3222331 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.92e-01 | 100.0% | 93.3% |
| 3471940 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 62.0 | 5.69e-01 | 99.1% | 99.3% |
| 3528375 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.69e-01 | 100.0% | 86.7% |
| 3521776 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.69 | 63.0 | 5.69e-01 | 100.0% | 84.0% |
| 3216183 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.68 | 63.0 | 5.68e-01 | 100.0% | 88.0% |
| 3222327 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.68 | 63.0 | 5.91e-01 | 100.0% | 92.6% |
| 3479778 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.68 | 63.0 | 5.65e-01 | 100.0% | 96.7% |
| 3879577 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.68 | 63.0 | 5.73e-01 | 100.0% | 95.9% |
| 3908636 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.68 | 63.0 | 5.79e-01 | 100.0% | 92.9% |
| 3825091 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.68 | 62.0 | 5.62e-01 | 100.0% | 95.3% |
| 3775570 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.68 | 62.0 | 5.68e-01 | 98.2% | 90.7% |
| 3578026 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.68 | 62.0 | 5.41e-01 | 100.0% | 92.1% |
| 3795460 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.68 | 62.0 | 5.79e-01 | 99.1% | 94.0% |
| 3554247 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.67 | 62.0 | 5.60e-01 | 100.0% | 86.7% |
| 3528425 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.67 | 56.0 | 5.59e-01 | 90.1% | 100.0% |
| 4467446 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.67 | 62.0 | 5.26e-01 | 100.0% | 72.4% |
| 3756016 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.66 | 56.0 | 5.63e-01 | 89.2% | 100.0% |
| 3757394 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.66 | 60.0 | 5.62e-01 | 98.2% | 100.0% |
| 3506171 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.66 | 59.0 | 4.96e-01 | 99.1% | 96.3% |
| 3908635 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.64 | 59.0 | 5.75e-01 | 100.0% | 93.3% |
| 3577505 | 4.1.1.0 ↗ | beta barrels › SH3 › SH3 › SH3 | 0.57 | 31.0 | 3.56e-01 | 75.7% | 70.6% |
| 3910433 | 4.1.1.0 ↗ | beta barrels › SH3 › SH3 › SH3 | 0.53 | 29.0 | 3.68e-01 | 72.1% | 92.3% |
| 3391556 | 4.1.1.384 ↗ | beta barrels › SH3 › SH3 › SH3 › Tudor_krimper_1st | 0.52 | 31.0 | 3.24e-01 | 78.4% | 61.9% |
| 3233511 | 4.1.1.1 ↗ | beta barrels › SH3 › SH3 › SH3 › SH3_1 | 0.52 | 26.0 | 3.56e-01 | 73.9% | 98.2% |