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ORF30
Euk-VirRanid_herpesvirus_2
ORF30__YP_656538__Ranid_herpesvirus_2__389214
Identity
- Accession:
- YP_656538 ↗
- Protein ID:
- ORF30
- Kingdom:
- euk
Quality
81.1
mean pLDDT
Taxonomy
Heunggongvirae›
Peploviricota›
Herviviricetes›
Herpesvirales›
Alloherpesviridae›
Batravirus›
Ranid_herpesvirus_2
TaxID: 389214
Cluster
Singleton — not in a non-trivial cluster
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 2-64
Domain cluster:
representative
CATH (13)
| Domain ID | Class ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 1sknP00 | 1.10.880.10 | Mainly Alpha › Orthogonal Bundle › Transcription Factor Skn-1; Chain P › Transcription factor, Skn-1-like, DNA-binding domain | 0.78 | 67.0 | 6.32e-01 | 93.7% | 82.4% |
| 1blwC00 | 1.20.1250.10 | Mainly Alpha › Up-down Bundle › Growth Hormone; Chain: A; › | 0.74 | 51.0 | 3.95e-01 | 81.0% | 32.6% |
| 1hqoA02 | 1.20.1050.10 | Mainly Alpha › Up-down Bundle › Glutathione S-transferase Yfyf (Class Pi); Chain A, domain 2 › | 0.71 | 52.0 | 4.09e-01 | 77.8% | 38.9% |
| 2ozbB01 | 1.10.287.4070 | Mainly Alpha › Orthogonal Bundle › Helix Hairpins › | 0.70 | 62.0 | 4.86e-01 | 98.4% | 76.3% |
| 4aflA00 | 6.10.140.1740 | Special › Helix non-globular › Helix Hairpins › | 0.70 | 55.0 | 4.74e-01 | 87.3% | 53.9% |
| 3t5vA00 | 1.25.40.990 | Mainly Alpha › Alpha Horseshoe › Serine Threonine Protein Phosphatase 5, Tetratricopeptide repeat › | 0.70 | 57.0 | 3.64e-01 | 88.9% | 26.1% |
| 1texA00 | 3.40.50.300 | Alpha Beta › 3-Layer(aba) Sandwich › Rossmann fold › P-loop containing nucleotide triphosphate hydrolases | 0.69 | 53.0 | 3.52e-01 | 82.5% | 61.1% |
| 3a1sA02 | 1.10.287.1770 | Mainly Alpha › Orthogonal Bundle › Helix Hairpins › | 0.69 | 55.0 | 4.84e-01 | 84.1% | 87.5% |
| 4h33A00 | 1.10.287.70 | Mainly Alpha › Orthogonal Bundle › Helix Hairpins › | 0.66 | 57.0 | 5.08e-01 | 96.8% | 71.4% |
| 2qksA01 | 1.10.287.70 | Mainly Alpha › Orthogonal Bundle › Helix Hairpins › | 0.63 | 54.0 | 4.57e-01 | 98.4% | 61.3% |
| 3rimB01 | 3.40.50.970 | Alpha Beta › 3-Layer(aba) Sandwich › Rossmann fold › Thiamin diphosphate (ThDP)-binding fold, Pyr/PP domains | 0.61 | 53.0 | 3.35e-01 | 100.0% | 90.8% |
| 3ousA00 | 1.10.287.70 | Mainly Alpha › Orthogonal Bundle › Helix Hairpins › | 0.59 | 43.0 | 4.06e-01 | 82.5% | 80.5% |
| 4dyqA01 | 1.10.10.60 | Mainly Alpha › Orthogonal Bundle › Arc Repressor Mutant, subunit A › Homeodomain-like | 0.56 | 45.0 | 3.96e-01 | 93.7% | 68.0% |
ECOD (10)
| UID | F-ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 3283001 | 605.1.1.4 ↗ | alpha duplicates or obligate multimers › ROP-like › Homodimeric domain of signal transducing histidine kinase › Homodimeric domain of signal transducing histidine kinase › HisKA_3 | 0.83 | 65.0 | 5.64e-01 | 87.3% | 55.8% |
| 3304347 | 109.4.1.1273 ↗ | alpha superhelices › Repetitive alpha hairpins › ARM repeat › ARM repeat › PPR, PPR_3 | 0.77 | 53.0 | 3.65e-01 | 73.0% | 26.0% |
| 3249674 | 604.5.1.32 ↗ | alpha bundles › Spectrin repeat-like › PhoU-like (Pfam 01895) › PhoU-like (Pfam 01895) › TMEM120A-B | 0.73 | 64.0 | 4.28e-01 | 98.4% | 54.6% |
| 4979643 | 606.1.1.1 ↗ | alpha complex topology › Nop N-terminal domain › Nop N-terminal domain › Nop N-terminal domain › Nop | 0.70 | 61.0 | 4.79e-01 | 96.8% | 73.8% |
| 4441096 | 101.1.8.1 ↗ | alpha arrays › HTH › HTH › DNA breaking-rejoining enzymes › Phage_integrase | 0.68 | 51.0 | 5.17e-01 | 82.5% | 86.7% |
| 3591288 | 604.12.1.8 ↗ | alpha bundles › Spectrin repeat-like › MIT domain › MIT domain › KATNA1_MIT | 0.64 | 55.0 | 4.41e-01 | 96.8% | 67.2% |
| 5023625 | 5054.1.1.8 ↗ | alpha complex topology › Voltage-gated ion channels › Voltage-gated ion channels › Voltage-gated ion channels › Ion_trans_2 | 0.62 | 53.0 | 4.63e-01 | 98.4% | 64.0% |
| 3308203 | 601.1.2.80 ↗ | alpha bundles › Four-helical up-and-down bundle › alpha-catenin-related › I/LWEQ domain (Pfam 01608) › Yip1 | 0.61 | 52.0 | 3.72e-01 | 98.4% | 31.0% |
| 5078087 | 3646.1.1.1 ↗ | alpha complex topology › T-component of energy-coupling factor (ECF) transporters › T-component of energy-coupling factor (ECF) transporters › T-component of energy-coupling factor (ECF) transporters › CbiQ | 0.59 | 50.0 | 3.43e-01 | 98.4% | 59.2% |
| 5009781 | 131.1.1.0 ↗ | alpha complex topology › PDEase-like › HD-domain/PDEase-like › HD-domain/PDEase-like | 0.57 | 44.0 | 3.57e-01 | 85.7% | 43.3% |
D2
high
residues 74-157
Domain cluster:
rep: putative_C-type_lectin_protein__YP_009552862__Bufonid_herpesvirus_1__2282206__D158-275
CATH (57)
| Domain ID | Class ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 7jptA06 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.83 | 76.0 | 6.79e-01 | 98.8% | 99.1% |
| 3fd4A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.83 | 77.0 | 6.40e-01 | 100.0% | 79.3% |
| 6innA04 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.83 | 77.0 | 6.57e-01 | 100.0% | 93.0% |
| 2ox8A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.83 | 77.0 | 6.54e-01 | 100.0% | 94.6% |
| 3m9zA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.83 | 77.0 | 6.66e-01 | 100.0% | 92.7% |
| 1ypoA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.83 | 77.0 | 6.53e-01 | 100.0% | 91.5% |
| 1jznA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.83 | 76.0 | 6.42e-01 | 100.0% | 94.1% |
| 2c6uA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.83 | 77.0 | 6.67e-01 | 100.0% | 92.6% |
| 2yhfA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 76.0 | 6.73e-01 | 100.0% | 94.1% |
| 1h8uB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 71.0 | 6.33e-01 | 92.9% | 100.0% |
| 3aluA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 76.0 | 6.06e-01 | 100.0% | 90.4% |
| 4uwwA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 75.0 | 6.45e-01 | 100.0% | 93.8% |
| 3vppB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 76.0 | 6.61e-01 | 100.0% | 92.6% |
| 4yliE00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 75.0 | 6.15e-01 | 100.0% | 81.2% |
| 1wmzA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 75.0 | 6.26e-01 | 100.0% | 93.6% |
| 3pbfA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 75.0 | 6.14e-01 | 98.8% | 80.7% |
| 1ja3A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 76.0 | 6.73e-01 | 100.0% | 92.2% |
| 2vuvA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 75.0 | 6.44e-01 | 100.0% | 93.8% |
| 4ak8A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.82 | 75.0 | 6.41e-01 | 100.0% | 94.6% |
| 6rygA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 74.0 | 6.61e-01 | 98.8% | 98.3% |
| 1eslA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 71.0 | 5.69e-01 | 94.0% | 76.4% |
| 5ktiA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 75.0 | 6.16e-01 | 100.0% | 86.1% |
| 2h2tB01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 75.0 | 6.66e-01 | 100.0% | 97.4% |
| 1litA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 74.0 | 6.34e-01 | 100.0% | 95.4% |
| 3rs1A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 75.0 | 6.54e-01 | 100.0% | 89.3% |
| 5xtsA03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 74.0 | 6.47e-01 | 100.0% | 100.0% |
| 5jq1A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 74.0 | 6.36e-01 | 100.0% | 93.8% |
| 5b1rA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 75.0 | 6.65e-01 | 100.0% | 88.8% |
| 5vybA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 74.0 | 6.15e-01 | 100.0% | 85.3% |
| 7jptA01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 74.0 | 6.47e-01 | 100.0% | 100.0% |
| 1tdqB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 74.0 | 6.42e-01 | 100.0% | 94.4% |
| 3zhgA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 74.0 | 6.31e-01 | 100.0% | 90.2% |
| 1gz2A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.81 | 73.0 | 6.15e-01 | 100.0% | 95.0% |
| 1v7pB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.80 | 74.0 | 6.37e-01 | 100.0% | 92.9% |
| 1c3aA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.80 | 73.0 | 6.21e-01 | 100.0% | 91.9% |
| 4iopB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.80 | 74.0 | 6.46e-01 | 100.0% | 94.2% |
| 3bdwB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.80 | 74.0 | 6.59e-01 | 100.0% | 90.5% |
| 1byfA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.80 | 71.0 | 6.16e-01 | 95.2% | 98.4% |
| 1fvuB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.80 | 73.0 | 6.39e-01 | 100.0% | 94.2% |
| 3ff7C00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.80 | 72.0 | 6.51e-01 | 98.8% | 95.5% |
| 5ew6A01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.79 | 71.0 | 6.26e-01 | 98.8% | 100.0% |
| 3hupA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.79 | 72.0 | 6.35e-01 | 100.0% | 89.3% |
| 1sb2B00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.79 | 72.0 | 6.28e-01 | 100.0% | 92.7% |
| 4m1gA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.79 | 68.0 | 6.89e-01 | 100.0% | 94.0% |
| 7jptA04 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.79 | 71.0 | 6.00e-01 | 98.8% | 86.8% |
| 1wk1A01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.79 | 67.0 | 5.89e-01 | 91.7% | 100.0% |
| 1afb100 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.78 | 72.0 | 5.80e-01 | 100.0% | 79.2% |
| 1egiA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.78 | 71.0 | 6.13e-01 | 100.0% | 96.1% |
| 7jptA03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.78 | 67.0 | 5.86e-01 | 94.0% | 100.0% |
| 3bdwA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.76 | 69.0 | 6.02e-01 | 100.0% | 91.1% |
| 1kcgB00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.75 | 68.0 | 5.99e-01 | 100.0% | 91.1% |
| 1f00I03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.72 | 60.0 | 5.73e-01 | 91.7% | 100.0% |
| 2kv3A00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.72 | 64.0 | 5.52e-01 | 100.0% | 93.9% |
| 2afpA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.65 | 57.0 | 5.02e-01 | 100.0% | 90.7% |
| 2debB02 | 3.30.559.10 | Alpha Beta › 2-Layer Sandwich › Chloramphenicol Acetyltransferase › Chloramphenicol acetyltransferase-like domain | 0.51 | 38.0 | 2.66e-01 | 79.8% | 57.7% |
| 6lcqA00 | 3.30.30.10 | Alpha Beta › 2-Layer Sandwich › Defensin A-like › Knottin, scorpion toxin-like | 0.51 | 32.0 | 3.67e-01 | 97.6% | 100.0% |
| 1mkyA02 | 3.40.50.300 | Alpha Beta › 3-Layer(aba) Sandwich › Rossmann fold › P-loop containing nucleotide triphosphate hydrolases | 0.50 | 34.0 | 2.87e-01 | 71.4% | 49.3% |
ECOD (100)
| UID | F-ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 3878326 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.85 | 79.0 | 6.23e-01 | 100.0% | 78.8% |
| 3562328 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.84 | 79.0 | 6.59e-01 | 100.0% | 87.4% |
| 3243322 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.84 | 78.0 | 6.56e-01 | 100.0% | 88.9% |
| 3768432 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.84 | 78.0 | 5.92e-01 | 100.0% | 68.3% |
| 3506715 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.84 | 78.0 | 6.22e-01 | 100.0% | 91.6% |
| 3848073 | 209.1.1.2 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C,Ly49 | 0.84 | 78.0 | 5.79e-01 | 100.0% | 57.9% |
| 3223044 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.84 | 78.0 | 6.43e-01 | 100.0% | 85.7% |
| 3868403 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.84 | 78.0 | 6.70e-01 | 100.0% | 88.8% |
| 3919376 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 5.95e-01 | 100.0% | 73.7% |
| 3848830 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 5.92e-01 | 100.0% | 65.7% |
| 3521774 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 6.54e-01 | 100.0% | 89.2% |
| 3844896 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 6.16e-01 | 100.0% | 72.9% |
| 2077355 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 6.72e-01 | 100.0% | 94.2% |
| 3774029 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 5.98e-01 | 100.0% | 64.1% |
| 3222327 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 76.0 | 6.42e-01 | 100.0% | 88.1% |
| 4514739 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 6.29e-01 | 100.0% | 86.1% |
| 3213988 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 76.0 | 6.27e-01 | 100.0% | 82.8% |
| 3911761 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 6.21e-01 | 100.0% | 85.3% |
| 3920847 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 77.0 | 5.37e-01 | 100.0% | 53.7% |
| 3541862 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.83 | 76.0 | 6.12e-01 | 100.0% | 91.0% |
| 3389293 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.11e-01 | 100.0% | 85.8% |
| 3843131 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.49e-01 | 100.0% | 88.5% |
| 4645458 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 5.78e-01 | 100.0% | 64.9% |
| 3891050 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.51e-01 | 100.0% | 95.3% |
| 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 | 0.82 | 76.0 | 5.49e-01 | 100.0% | 65.1% |
| 4195315 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.31e-01 | 100.0% | 89.3% |
| 3770046 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 5.67e-01 | 100.0% | 63.6% |
| 3910028 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.29e-01 | 100.0% | 88.6% |
| 3522167 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 5.49e-01 | 100.0% | 54.1% |
| 4003184 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.40e-01 | 100.0% | 90.3% |
| 3233970 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.24e-01 | 100.0% | 91.0% |
| 3540213 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.42e-01 | 100.0% | 91.0% |
| 3902382 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 6.28e-01 | 100.0% | 87.1% |
| None | — | 0.82 | 76.0 | 5.26e-01 | 100.0% | 48.0% | |
| 3844986 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 5.66e-01 | 100.0% | 62.9% |
| 3512203 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.29e-01 | 100.0% | 87.1% |
| 1408194 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 5.98e-01 | 100.0% | 75.9% |
| 3215625 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.65e-01 | 100.0% | 92.5% |
| 3918059 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.53e-01 | 100.0% | 92.8% |
| 168533 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 6.44e-01 | 100.0% | 93.8% |
| 3886474 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 6.14e-01 | 100.0% | 79.2% |
| None | — | 0.82 | 75.0 | 5.89e-01 | 100.0% | 72.2% | |
| 3532419 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 76.0 | 6.06e-01 | 100.0% | 78.7% |
| 3222331 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 6.34e-01 | 100.0% | 89.6% |
| 3897909 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 5.82e-01 | 100.0% | 72.6% |
| 3928853 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 6.10e-01 | 100.0% | 86.0% |
| 3554135 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 71.0 | 6.26e-01 | 94.0% | 100.0% |
| 3890579 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 5.60e-01 | 100.0% | 60.8% |
| 4467446 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 5.83e-01 | 100.0% | 68.4% |
| 3775570 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 75.0 | 6.23e-01 | 100.0% | 87.9% |
| 3521776 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 6.09e-01 | 100.0% | 80.7% |
| 3867607 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 5.14e-01 | 100.0% | 45.6% |
| 3888923 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 6.20e-01 | 100.0% | 86.0% |
| 4049761 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.81 | 72.0 | 5.66e-01 | 95.2% | 73.9% |
| 3852398 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 5.16e-01 | 100.0% | 45.3% |
| 3556397 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 5.79e-01 | 100.0% | 65.1% |
| 3236452 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 6.08e-01 | 100.0% | 86.0% |
| 3245906 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.14e-01 | 100.0% | 89.0% |
| 3227076 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 6.30e-01 | 100.0% | 90.4% |
| 3882577 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 5.26e-01 | 100.0% | 47.3% |
| 3221351 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 6.24e-01 | 100.0% | 88.4% |
| 3900577 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.46e-01 | 100.0% | 94.4% |
| 3753780 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.45e-01 | 100.0% | 85.6% |
| 3894078 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 5.78e-01 | 100.0% | 70.3% |
| 3901488 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 6.56e-01 | 100.0% | 95.0% |
| 3554247 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.05e-01 | 100.0% | 82.7% |
| 3899094 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 75.0 | 6.02e-01 | 100.0% | 77.1% |
| 3895325 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.27e-01 | 100.0% | 88.1% |
| 3766641 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.27e-01 | 100.0% | 88.9% |
| 3401288 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 72.0 | 6.45e-01 | 96.4% | 98.3% |
| 3244022 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.81 | 74.0 | 5.74e-01 | 100.0% | 89.1% |
| 3544143 | 192.8.1.283 ↗ | alpha bundles › Long alpha-hairpin › Eukaryotic DNA topoisomerase I, dispensable insert domain › Eukaryotic DNA topoisomerase I, dispensable insert domain › Lectin_C | 0.81 | 75.0 | 5.26e-01 | 100.0% | 48.3% |
| 3853381 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.04e-01 | 100.0% | 71.3% |
| 3909263 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.52e-01 | 100.0% | 90.8% |
| 3755280 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.81 | 74.0 | 6.03e-01 | 100.0% | 79.3% |
| 3404181 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 73.0 | 5.77e-01 | 98.8% | 71.5% |
| 3217746 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 73.0 | 6.21e-01 | 100.0% | 88.9% |
| 3550187 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 74.0 | 5.90e-01 | 100.0% | 67.9% |
| 3877111 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 74.0 | 4.59e-01 | 100.0% | 28.4% |
| 3879105 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 74.0 | 4.56e-01 | 100.0% | 26.6% |
| 3244432 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 73.0 | 6.11e-01 | 100.0% | 87.1% |
| 3774700 | 192.8.1.283 ↗ | alpha bundles › Long alpha-hairpin › Eukaryotic DNA topoisomerase I, dispensable insert domain › Eukaryotic DNA topoisomerase I, dispensable insert domain › Lectin_C | 0.80 | 74.0 | 4.70e-01 | 100.0% | 32.8% |
| 3900461 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 73.0 | 5.85e-01 | 100.0% | 78.8% |
| 4047155 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 72.0 | 6.19e-01 | 96.4% | 97.6% |
| 3486433 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.80 | 73.0 | 6.09e-01 | 100.0% | 89.3% |
| 3752197 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 73.0 | 6.25e-01 | 100.0% | 84.6% |
| 3922916 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.79 | 72.0 | 5.90e-01 | 100.0% | 90.7% |
| 3921612 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.79 | 72.0 | 6.69e-01 | 100.0% | 93.3% |
| 3535150 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.79 | 73.0 | 7.19e-01 | 100.0% | 93.3% |
| 368344 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.79 | 72.0 | 6.51e-01 | 100.0% | 93.8% |
| 3939279 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.78 | 72.0 | 5.92e-01 | 100.0% | 84.1% |
| 4884168 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.78 | 72.0 | 6.10e-01 | 100.0% | 88.8% |
| 3748294 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.78 | 72.0 | 6.34e-01 | 100.0% | 90.7% |
| 3576262 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.77 | 67.0 | 5.92e-01 | 95.2% | 99.2% |
| 4054563 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.77 | 70.0 | 5.59e-01 | 100.0% | 68.9% |
| 3538145 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.77 | 71.0 | 5.71e-01 | 100.0% | 71.4% |
| 3530879 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.77 | 68.0 | 6.16e-01 | 96.4% | 100.0% |
| 3757995 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.75 | 68.0 | 5.46e-01 | 100.0% | 70.0% |
| 4872550 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.74 | 67.0 | 6.01e-01 | 100.0% | 93.0% |
| 3247541 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.74 | 67.0 | 6.11e-01 | 100.0% | 93.6% |