Homo sapiens Protein: EEF2 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-18153.5 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | EEF2 | ||||||||||||||||||||||
Protein Name | eukaryotic translation elongation factor 2 | ||||||||||||||||||||||
Synonyms | EEF-2; EF-2; EF2; SCA26; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000307940 | ||||||||||||||||||||||
InnateDB Gene | IDBG-18151 (EEF2) | ||||||||||||||||||||||
Protein Structure | |||||||||||||||||||||||
UniProt Annotation | |||||||||||||||||||||||
Function | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome. | ||||||||||||||||||||||
Subcellular Localization | Cytoplasm. | ||||||||||||||||||||||
Disease Associations | Spinocerebellar ataxia 26 (SCA26) [MIM:609306]: A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. {ECO:0000269PubMed:23001565}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | |||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 137 experimentally validated interaction(s) in this database.
They are also associated with 8 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR000640
Translation elongation factor EFG, V domain IPR000795 Elongation factor, GTP-binding domain IPR004161 Translation elongation factor EFTu/EF1A, domain 2 IPR005225 Small GTP-binding protein domain IPR005517 Translation elongation factor EFG/EF2, domain IV IPR009000 Translation protein, beta-barrel domain IPR009022 Elongation factor G, III-V domain IPR020568 Ribosomal protein S5 domain 2-type fold IPR027417 P-loop containing nucleoside triphosphate hydrolase |
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PFAM |
PF00679
PF00009 PF03144 PF03764 PF14492 |
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PRINTS |
PR00315
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PIRSF | |||||||||||||||||||||||
SMART |
SM00838
SM00889 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P13639 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-P13639 | ||||||||||||||||||||||
TrEMBL | Q8TA90 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 1938 | ||||||||||||||||||||||
UniGene | Hs.515070 | ||||||||||||||||||||||
RefSeq | NP_001952 | ||||||||||||||||||||||
HUGO | HGNC:3214 | ||||||||||||||||||||||
OMIM | 130610 | ||||||||||||||||||||||
CCDS | CCDS12117 | ||||||||||||||||||||||
HPRD | 00561 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AK297398 AY942181 BC024689 BC126259 BC136313 CH471139 M19997 X51466 Z11692 | ||||||||||||||||||||||
GenPept | AAA50388 AAH24689 AAI26260 AAI36314 AAX34409 BAG59838 CAA35829 CAA77750 EAW69274 EAW69275 | ||||||||||||||||||||||