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ORF31
Euk-VirRanid_herpesvirus_2
ORF31__YP_656539__Ranid_herpesvirus_2__389214
Identity
- Accession:
- YP_656539 ↗
- Protein ID:
- ORF31
- Kingdom:
- euk
Quality
63.4
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 105-200
Domain cluster:
rep: membrane_protein_UL45__YP_182345__Gallid_alphaherpesvirus_1__10386__D143-254
CATH (12)
| 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 | 0.81 | 68.0 | 6.31e-01 | 87.5% | 99.1% |
| 1byfA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.80 | 67.0 | 6.09e-01 | 88.5% | 100.0% |
| 5xtsA03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.79 | 66.0 | 6.02e-01 | 88.5% | 100.0% |
| 5ew6A01 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.78 | 64.0 | 5.91e-01 | 87.5% | 100.0% |
| 4m1gA00 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.77 | 61.0 | 6.47e-01 | 89.6% | 96.4% |
| 1f00I03 | 3.10.100.10 | Alpha Beta › Roll › Mannose-Binding Protein A; Chain A › Mannose-Binding Protein A, subunit A | 0.72 | 55.0 | 5.52e-01 | 81.2% | 100.0% |
| 3rrkA03 | 3.30.70.2750 | Alpha Beta › 2-Layer Sandwich › Alpha-Beta Plaits › | 0.61 | 35.0 | 3.97e-01 | 90.6% | 74.3% |
| 3gkeA02 | 3.90.380.10 | Alpha Beta › Alpha-Beta Complex › Naphthalene 1,2-dioxygenase Alpha Subunit; Chain A, domain 1 › Naphthalene 1,2-dioxygenase Alpha Subunit; Chain A, domain 1 | 0.55 | 43.0 | 3.38e-01 | 85.4% | 83.3% |
| 2k3iA01 | 3.30.70.860 | Alpha Beta › 2-Layer Sandwich › Alpha-Beta Plaits › | 0.54 | 36.0 | 3.79e-01 | 93.8% | 76.5% |
| 1vigA00 | 3.30.1370.10 | Alpha Beta › 2-Layer Sandwich › Ribosomal Protein S8; Chain: A, domain 1 › K Homology domain, type 1 | 0.51 | 30.0 | 3.43e-01 | 88.5% | 78.9% |
| 7agvB01 | 3.30.70.1450 | Alpha Beta › 2-Layer Sandwich › Alpha-Beta Plaits › Regulator of K+ conductance, C-terminal domain | 0.50 | 36.0 | 3.84e-01 | 89.6% | 87.7% |
| 4gf3A00 | 3.30.1460.10 | Alpha Beta › 2-Layer Sandwich › Yope Regulator; Chain: A, › | 0.50 | 33.0 | 3.05e-01 | 95.8% | 51.2% |
ECOD (36)
| UID | F-ID | Classification | TM-score | Bits | E-value | Q cov | T cov |
|---|---|---|---|---|---|---|---|
| 3623564 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.82 | 70.0 | 6.16e-01 | 90.6% | 91.1% |
| 3217541 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.81 | 68.0 | 5.41e-01 | 89.6% | 90.2% |
| 3228314 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.80 | 72.0 | 5.88e-01 | 94.8% | 96.3% |
| 3241317 | 209.1.1.14 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › PF29411 | 0.80 | 69.0 | 5.46e-01 | 91.7% | 92.9% |
| 3474452 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 71.0 | 5.92e-01 | 94.8% | 94.3% |
| 3215625 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.80 | 68.0 | 6.23e-01 | 89.6% | 93.3% |
| 3233483 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.80 | 68.0 | 5.61e-01 | 91.7% | 93.3% |
| 3933201 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.79 | 70.0 | 6.19e-01 | 94.8% | 93.3% |
| 3392105 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.79 | 66.0 | 5.89e-01 | 88.5% | 100.0% |
| 3855548 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.79 | 68.0 | 5.81e-01 | 92.7% | 84.7% |
| 3900661 | 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 | 6.45e-01 | 99.0% | 97.7% |
| 3396278 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.78 | 66.0 | 5.67e-01 | 89.6% | 83.4% |
| 3777546 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.78 | 68.0 | 5.37e-01 | 92.7% | 66.5% |
| 3405168 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.78 | 68.0 | 5.88e-01 | 93.8% | 93.8% |
| 3875222 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.78 | 70.0 | 6.09e-01 | 95.8% | 90.6% |
| 3861713 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.78 | 67.0 | 5.67e-01 | 92.7% | 91.0% |
| 3849974 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.77 | 62.0 | 5.94e-01 | 85.4% | 100.0% |
| 3519333 | 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 | 5.78e-01 | 94.8% | 92.0% |
| 3217654 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.77 | 69.0 | 6.09e-01 | 96.9% | 95.6% |
| 3231013 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.77 | 65.0 | 5.49e-01 | 89.6% | 95.3% |
| 3900659 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.76 | 63.0 | 5.64e-01 | 87.5% | 93.1% |
| 3217054 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.76 | 66.0 | 6.11e-01 | 92.7% | 94.2% |
| 3922342 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.76 | 65.0 | 5.84e-01 | 91.7% | 92.3% |
| 4532283 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.76 | 62.0 | 6.01e-01 | 86.5% | 100.0% |
| 3759902 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.76 | 70.0 | 6.19e-01 | 100.0% | 93.3% |
| 381685 | 209.1.1.7 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Chordopox_A33R | 0.75 | 59.0 | 6.17e-01 | 89.6% | 93.0% |
| 3415917 | 209.1.1.1 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like › Lectin_C | 0.74 | 66.0 | 4.93e-01 | 95.8% | 53.8% |
| 3600247 | 209.1.1.0 ↗ | a+b complex topology › C-type lectin-like › C-type lectin-like › C-type lectin-like | 0.72 | 62.0 | 5.63e-01 | 92.7% | 99.2% |
| 4974179 | 304.4.1.0 ↗ | a+b two layers › Alpha-beta plaits › Dimeric alpha+beta barrel › Dimeric alpha+beta barrel | 0.53 | 28.0 | 2.72e-01 | 71.9% | 43.6% |
| 3817212 | 304.8.1.0 ↗ | a+b two layers › Alpha-beta plaits › ACT-like › ACT-like | 0.51 | 31.0 | 3.48e-01 | 94.8% | 80.0% |
| 3680212 | 109.4.1.1525 ↗ | alpha superhelices › Repetitive alpha hairpins › ARM repeat › ARM repeat › PPR, DYW_deaminase | 0.51 | 35.0 | 2.41e-01 | 72.9% | 18.4% |
| 3370602 | 109.4.1.1520 ↗ | alpha superhelices › Repetitive alpha hairpins › ARM repeat › ARM repeat › PPR, DYW_deaminase, E_motif | 0.51 | 35.0 | 2.52e-01 | 72.9% | 32.1% |
| 3335541 | 109.4.1.2173 ↗ | alpha superhelices › Repetitive alpha hairpins › ARM repeat › ARM repeat › PPR, DYW_deaminase, Eplus_motif | 0.51 | 35.0 | 2.47e-01 | 74.0% | 24.6% |
| 3826564 | 109.4.1.1285 ↗ | alpha superhelices › Repetitive alpha hairpins › ARM repeat › ARM repeat › PPR, PPR_2, DYW_deaminase, Eplus_motif, E_motif | 0.50 | 35.0 | 2.12e-01 | 72.9% | 13.9% |
| 3643646 | 109.4.1.2680 ↗ | alpha superhelices › Repetitive alpha hairpins › ARM repeat › ARM repeat › PPR, DYW_deaminase, TPR_24 | 0.50 | 35.0 | 2.38e-01 | 74.0% | 24.7% |
| 3825377 | 109.4.1.1291 ↗ | alpha superhelices › Repetitive alpha hairpins › ARM repeat › ARM repeat › PPR, PPR_2, PPR_3, DYW_deaminase, E_motif | 0.50 | 35.0 | 2.17e-01 | 74.0% | 15.0% |