P59709 (HEMA_CVBQ) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 67.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Hemagglutinin-esterase Short name=HE protein EC=3.1.1.53 Alternative name(s): E3 glycoprotein | ||||
| Gene names |
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| Organism | Bovine coronavirus (strain Quebec) (BCoV) (BCV) [Complete proteome] | ||||
| Taxonomic identifier | 11133 [NCBI] | ||||
| Taxonomic lineage | Viruses › ssRNA positive-strand viruses, no DNA stage › Nidovirales › Coronaviridae › Coronavirinae › Betacoronavirus › ![]() | ||||
| Virus host | Bos taurus (Bovine) [TaxID: 9913] |
Protein attributes
| Sequence length | 424 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Inferred from homology |
General annotation (Comments)
| Function | Structural protein that makes short spikes at the surface of the virus. Contains receptor binding and receptor-destroying activities. Mediates de-O-acetylation of N-acetyl-9-O-acetylneuraminic acid, which is probably the receptor determinant recognized by the virus on the surface of erythrocytes and susceptible cells. This receptor-destroying activity is important for virus release as it probably helps preventing self-aggregation and ensures the efficient spread of the progeny virus from cell to cell. May serve as a secondary viral attachment protein for initiating infection, the spike protein being the major one. Seems to be a 'luxury' protein that is not absolutely necessary for virus infection in culture. However, its presence in the virus may alter its pathogenicity. May become a target for both the humoral and the cellular branches of the immune system By similarity. |
| Catalytic activity | N-acetyl-O-acetylneuraminate + H2O = N-acetylneuraminate + acetate. |
| Subunit structure | Homodimer; disulfide-linked. Forms a complex with the M protein in the pre-Golgi. Associates then with S-M complex to form a ternary complex S-M-HE. |
| Subcellular location | Virion membrane; Single-pass type I membrane protein Potential. Host cell membrane; Single-pass type I membrane protein Potential. Note: In infected cells becomes incorporated into the envelope of virions during virus assembly at the endoplasmic reticulum and cis Golgi. However, some may escape incorporation into virions and subsequently migrate to the cell surface By similarity. |
| Post-translational modification | N-glycosylated in the RER. |
| Miscellaneous | The sequence shown is that of Quebec reference strain. |
| Sequence similarities | Belongs to the influenza type C/coronaviruses hemagglutinin-esterase family. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Host cell membrane Host membrane Membrane Viral envelope protein Virion |
| Domain | Signal Transmembrane Transmembrane helix |
| Molecular function | Hemagglutinin Hydrolase |
| PTM | Disulfide bond Glycoprotein |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Biological_process | viral entry into host cell via membrane fusion with the plasma membrane Inferred from electronic annotation. Source: InterPro |
| Cellular_component | host cell plasma membrane Inferred from electronic annotation. Source: UniProtKB-SubCell integral to membraneInferred from electronic annotation. Source: UniProtKB-KW viral envelopeInferred from electronic annotation. Source: UniProtKB-KW virion membraneInferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular_function | sialate O-acetylesterase activity Inferred from electronic annotation. Source: EC |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||||
Molecule processing | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 18 | 18 | By similarity | ||||||||
| Chain | 19 – 424 | 406 | Hemagglutinin-esterase | PRO_0000037143 | |||||||
Regions | |||||||||||
| Topological domain | 19 – 392 | 374 | Virion surface Potential | ||||||||
| Transmembrane | 393 – 413 | 21 | Helical; Potential | ||||||||
| Topological domain | 414 – 424 | 11 | Intravirion Potential | ||||||||
| Region | 7 – 127 | 121 | Esterase domain first part By similarity | ||||||||
| Region | 128 – 266 | 139 | Receptor binding By similarity | ||||||||
| Region | 267 – 379 | 113 | Esterase domain second part By similarity | ||||||||
Sites | |||||||||||
| Active site | 40 | 1 | Nucleophile By similarity | ||||||||
| Active site | 228 | 1 | Charge relay system By similarity | ||||||||
| Active site | 329 | 1 | Charge relay system By similarity | ||||||||
Amino acid modifications | |||||||||||
| Glycosylation | 54 | 1 | N-linked (GlcNAc...); by host Potential | ||||||||
| Glycosylation | 89 | 1 | N-linked (GlcNAc...); by host Potential | ||||||||
| Glycosylation | 153 | 1 | N-linked (GlcNAc...); by host Potential | ||||||||
| Glycosylation | 236 | 1 | N-linked (GlcNAc...); by host Potential | ||||||||
| Glycosylation | 301 | 1 | N-linked (GlcNAc...); by host Potential | ||||||||
| Glycosylation | 316 | 1 | N-linked (GlcNAc...); by host Potential | ||||||||
| Glycosylation | 358 | 1 | N-linked (GlcNAc...); by host Potential | ||||||||
| Disulfide bond | 44 ↔ 65 | By similarity | |||||||||
| Disulfide bond | 113 ↔ 162 | By similarity | |||||||||
| Disulfide bond | 197 ↔ 276 | By similarity | |||||||||
| Disulfide bond | 205 ↔ 249 | By similarity | |||||||||
| Disulfide bond | 307 ↔ 312 | By similarity | |||||||||
| Disulfide bond | 347 ↔ 371 | By similarity | |||||||||
Natural variations | |||||||||||
| Natural variant | 5 | 1 | L → P in strain: Isolate BCQ.3, Isolate BCQ.1523, Isolate BCQ.2439, Isolate BCQ.2442, Isolate BCQ.2508, Isolate BCQ.2590, Isolate BCQ.3708, Isolate BCQ.3994 and Isolate BCQ.7373. | ||||||||
| Natural variant | 8 | 1 | V → A in strain: Isolate BCQ.2590. | ||||||||
| Natural variant | 11 | 1 | S → C in strain: Isolate BCQ.1523, Isolate BCQ.2442 and Isolate BCQ.2508. | ||||||||
| Natural variant | 49 | 1 | N → T in strain: Isolate BCQ.376, Isolate BCQ.701, Isolate BCQ.1523, Isolate BCQ.2442, Isolate BCQ.2508, Isolate BCQ.3708, Isolate BCQ.3994 and Isolate BCQ.7373. | ||||||||
| Natural variant | 53 | 1 | R → P in strain: Isolate BCQ.2590. | ||||||||
| Natural variant | 66 | 1 | D → G in strain: Isolate BCQ.376, Isolate BCQ.701, Isolate BCQ.3708 and Isolate BCQ.3994. | ||||||||
| Natural variant | 103 | 1 | L → I in strain: Isolate BCQ.2439. | ||||||||
| Natural variant | 103 | 1 | L → V in strain: Isolate BCQ.3, Isolate BCQ.376, Isolate BCQ.701, Isolate BCQ.1523, Isolate BCQ.2442, Isolate BCQ.2508, Isolate BCQ.2590, Isolate BCQ.3708, Isolate BCQ.3994 and Isolate BCQ.7373. | ||||||||
| Natural variant | 114 | 1 | T → I in strain: Isolate BCQ.3708. | ||||||||
| Natural variant | 182 | 1 | G → R in strain: Isolate BCQ.7373. | ||||||||
| Natural variant | 245 | 1 | F → L in strain: Isolate BCQ.7373. | ||||||||
| Natural variant | 282 | 1 | D → G in strain: Isolate BCQ.7373. | ||||||||
| Natural variant | 344 | 1 | D → A in strain: Isolate BCQ.2590. | ||||||||
| Natural variant | 350 | 1 | Q → R in strain: Isolate BCQ.2590. | ||||||||
| Natural variant | 367 | 1 | S → P in strain: Isolate BCQ.376, Isolate BCQ.701, Isolate BCQ.1523, Isolate BCQ.2439, Isolate BCQ.2442, Isolate BCQ.2508, Isolate BCQ.2590, Isolate BCQ.3708, Isolate BCQ.3994 and Isolate BCQ.7373. | ||||||||
| Natural variant | 392 | 1 | L → I in strain: Isolate BCQ.3, Isolate BCQ.376, Isolate BCQ.571, Isolate BCQ.701, Isolate BCQ.1523, Isolate BCQ.2439, Isolate BCQ.2442, Isolate BCQ.2508, Isolate BCQ.3708, Isolate BCQ.3994 and Isolate BCQ.7373. | ||||||||
Sequences
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References
| [1] | "Cloning and in vitro expression of the gene for the E3 haemagglutinin glycoprotein of bovine coronavirus." Parker M.D., Cox G.J., Deregt D., Fitzpatrick D.R., Babiuk L.A. J. Gen. Virol. 70:155-164(1989) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC RNA]. |
| [2] | "Comparison of bovine coronavirus isolates associated with neonatal calf diarrhoea and winter dysentery in adult dairy cattle in Quebec." Dea S., Michaud L., Milane G. J. Gen. Virol. 76:1263-1270(1995) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC RNA]. Strain: Isolate BCQ.2590, Isolate BCQ.3 and Isolate BCQ.571. |
| [3] | "Identification of specific variations within the HE, S1, and ORF4 genes of bovine coronaviruses associated with enteric and respiratory diseases in dairy cattle." Gelinas A.-M., Sasseville A.M.-J., Dea S. Adv. Exp. Med. Biol. 494:63-67(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC RNA]. Strain: Isolate BCQ.1523, Isolate BCQ.2590, Isolate BCQ.3994, Isolate BCQ.571 and Isolate BCQ.7373. |
| [4] | "Genomic and antigenic variations of the HE glycoprotein of bovine coronaviruses associated with neonatal calf diarrhea and winter dysentery." Kourtesis A.B., Gelinas A.-M., Dea S. Arch. Virol. 146:1219-1230(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC RNA]. Strain: Isolate BCQ.1523, Isolate BCQ.2439, Isolate BCQ.2442, Isolate BCQ.2508, Isolate BCQ.3708, Isolate BCQ.376, Isolate BCQ.701 and Isolate BCQ.7373. |
| [5] | "Bovine coronaviruses associated with enteric and respiratory diseases in Canadian dairy cattle display different reactivities to anti-HE monoclonal antibodies and distinct amino acid changes in their HE, S and ns4.9 protein." Gelinas A.-M., Boutin M., Sasseville A.M.-J., Dea S. Virus Res. 76:43-57(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC RNA]. Strain: Isolate BCQ.3994. |
| [6] | "Full-length genomic sequence of bovine coronavirus (31 kb). Completion of the open reading frame 1a/1b sequences." Yoo D., Pei Y. Adv. Exp. Med. Biol. 494:73-76(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC RNA]. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | L38962 Genomic RNA. Translation: AAA92989.1. L38963 Genomic RNA. Translation: AAA92990.1. U06093 Genomic RNA. Translation: AAA92991.1. AF239306 Genomic RNA. Translation: AAG40594.1. AF239307 Genomic RNA. Translation: AAG40600.1. AF230523 Genomic RNA. Translation: AAG40588.1. AF230524 Genomic RNA. Translation: AAG40589.1. AF230525 Genomic RNA. Translation: AAG40590.1. AF230526 Genomic RNA. Translation: AAG40591.1. AF230527 Genomic RNA. Translation: AAG40592.1. AF230528 Genomic RNA. Translation: AAG40593.1. AF339836 Genomic RNA. Translation: AAK14397.1. AF220295 Genomic RNA. Translation: AAL40399.1. |
| PIR | HMIHBQ. A31684. |
| RefSeq | NP_150076.1. NC_003045.1. |
3D structure databases | |
| ProteinModelPortal | P59709. |
| SMR | P59709. Positions 19-376. |
| ModBase | Search... |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| GeneID | 921684. |
Family and domain databases | |
| InterPro | IPR008980. Capsid_hemagglutn. IPR007142. Hemagglutn-estrase_core. IPR003860. Hemagglutn-estrase_hemagglutn. [Graphical view] |
| Pfam | PF03996. Hema_esterase. 1 hit. PF02710. Hema_HEFG. 1 hit. [Graphical view] |
| SUPFAM | SSF49818. Capsid_hemag. 1 hit. |
| ProtoNet | Search... |
Entry information
| Entry name | HEMA_CVBQ | ||||||||
| Accession | Primary (citable) accession number: P59709 Secondary accession number(s): P24351 Q9DRF5 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Viral Protein Annotation Program | ||||||||
Relevant documents
| SIMILARITY comments Index of protein domains and families |

Clusters with
