Statements in which the resource exists as a subject.
PredicateObject
rdf:type
biopax3:comment
FUNCTION: May contribute to the transparency and refractive index of the lens. Has chaperone-like activity, preventing aggregation of various proteins under a wide range of stress conditions. SUBCELLULAR LOCATION: Cytoplasm. Nucleus. Note=Translocates to the nucleus during heat shock and resides in sub-nuclear structures known as SC35 speckles or nuclear splicing speckles. PTM: O-glycosylated; contains N-acetylglucosamine side chains. PTM: Deamidation of Asn-101 in lens occurs mostly during the first 30 years of age, followed by a small additional amount of deamidation (approximately 5%) during the next approximately 38 years, resulting in a maximum of approximately 50% deamidation during the lifetime of the individual. PTM: Phosphorylation on Ser-122 seems to be developmentally regulated. Absent in the first months of life, it appears during the first 12 years of human lifetime. The relative amount of phosphorylated form versus unphosphorylated form does not change over the lifetime of the individual. PTM: Acetylation at Lys-70 seems to increase chaperone activity. MASS SPECTROMETRY: Mass=19950; Method=Electrospray; Range=1-173; Source=PubMed:8175657; MASS SPECTROMETRY: Mass=19863; Method=Electrospray; Range=1-172; Source=PubMed:8175657; MASS SPECTROMETRY: Mass=20029; Method=Electrospray; Range=1-173; Note=With 1 phosphate group; Source=PubMed:8175657; MASS SPECTROMETRY: Mass=19951; Method=Electrospray; Range=1-173; Source=PubMed:9655350; MASS SPECTROMETRY: Mass=19864; Method=Electrospray; Range=1-172; Source=PubMed:9655350; MASS SPECTROMETRY: Mass=19947; Method=Electrospray; Range=1-173; Source=PubMed:10930324; MASS SPECTROMETRY: Mass=19851; Method=Electrospray; Range=1-172; Source=PubMed:10930324; DISEASE: Defects in CRYAA are a cause of cataract autosomal dominant (ADC) [MIM:604219]. Cataract is an opacification of the crystalline lens of the eye that frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. Cataract is the most common treatable cause of visual disability in childhood. SIMILARITY: Belongs to the small heat shock protein (HSP20) family. GENE SYNONYMS:CRYAA CRYA1 HSPB4. COPYRIGHT: Protein annotation is derived from the UniProt Consortium (http://www.uniprot.org/). Distributed under the Creative Commons Attribution-NoDerivs License., SEQUENCE 173 AA; 19909 MW; 81804A8439837D50 CRC64;
biopax3:xref
biopax3:displayName
CRYAA_HUMAN
biopax3:name
Alpha-crystallin A chain, short form, CRYAA, Heat shock protein beta-4, HspB4
biopax3:entityFeature
biopax3:organism
biopax3:sequence
MDVTIQHPWFKRTLGPFYPSRLFDQFFGEGLFEYDLLPFLSSTISPYYRQSLFRTVLDSGISEVRSDRDKFVIFLDVKHFSPEDLTVKVQDDFVEIHGKHNERQDDHGYISREFHRRYRLPSNVDQSALSCSLSADGMLTFCGPKIQTGLDATHAERAIPVSREEKPTSAPSS
biopax3:standardName
Alpha-crystallin A chain