Detail Information for IndEnz0002001578
IED ID IndEnz0002001578
Enzyme Type ID protease001578
Protein Name Sterol regulatory element-binding protein 2
SREBP-2
Sterol regulatory element-binding transcription factor 2

Cleaved into: Processed sterol regulatory element-binding protein 2
Transcription factor SREBF2
Gene Name Srebf2 Srebp2
Organism Mus musculus (Mouse)
Taxonomic Lineage cellular organisms Eukaryota Opisthokonta Metazoa Eumetazoa Bilateria Deuterostomia Chordata Craniata Vertebrata Gnathostomata (jawed vertebrates) Teleostomi Euteleostomi Sarcopterygii Dipnotetrapodomorpha Tetrapoda Amniota Mammalia Theria Eutheria Boreoeutheria Euarchontoglires Glires (Rodents and rabbits) Rodentia Myomorpha (mice and others) Muroidea Muridae Murinae Mus Mus Mus musculus (Mouse)
Enzyme Sequence MDESSELGVLETMETLTELGDELTLGDIDEMLQFVSNQVGEFPDLFSEQLCSSFPGGGSNGGSGNNSSGRGNNGGATDPAVQRSFSQVPLSTFSPSAASPQAPALQVKVSPTPPRATPVLQPRPQPQPQPPAQLQQQTVMITPTFSTAPQTRIIQQPLIYQNAATSFQVLQPQVQSLVTSPQVQPVTIQQQVQTVQAQRVLTQTANGTLQTLAPATVQTVAAPQVQQVPVLVQPQIIKTDSLVLTTLKTDGSPVMAAVQNPALTALTAPIQTAALQVPTLVGSNGTILTTMPVMMGQEKVPIKQVPGGVKQLDPPKEGERRTTHNIIEKRYRSSINDKIIELKDLVMGTDAKMHKSGVLRKAIDYIKYLQQVNHKLRQENMVLKLANQKNKLLKGIDLGSLVDSDVDLKIDDFNQNVLLMSPPASDSGSQAGFSPYSIDSEPGSPLLDDAKVKDEPDSPPVALGMVDRSRILLCVLTFLGLSFNPLTSLLQWGGAHNTDQHPYSGSGRSVLSLESGAGGWFDWMVPTLLLWLVNGVIVLSVFVKLLVHGEPVIRPHSRPSVTFWRHRKQADLDLAKGDFAAAAANLQTCLSVLGRALPTSRLDLACSLSWNVIRYSLQKLRLVRWLLKKVFQRWRATPATAAGFEDEAKSSARDAALAYHRLHQLHITGKLPAGSACSDVHMALCAVNLAECAEEKILPSTLIEIHLTAAMGLKTRCGGKLGFLASYFLNRAQSLCGPEHSTVPDSLRWLCHPLGQKFFMERSWSIKSAAKESLYCAQRSPADPIAQVHQAFCKNLLERAVESLVKPQAKKKAGDQEEESCEFSSALEYLKLLHSFVDSVGFVTSPFSSSSVLRSALGPDVICRWWTSAVTMAISWLQGDDAAVRSRFTEVERVPKALEVTESPLVKAVFYTCRAMHASLSGKADGQQNSFCHCERASGHLWSSLNVSGTTSDPSLNHVIQLFTCDLLLSLRTALWQKQASASQLLGETYHASGTELAGFQRDLGSLRRLAHSFRPAYRKVFLHEATVRLMAGASPTRTHQLLEHSLRRRPTQNTKHGEVDTWPGQRERATAILLACRHLPLSFLSSPGQRAVLLAEAARTLEKVGDRRSCSDCQQMIVKLGGGTAIAAS
Enzyme Length 1130
Uniprot Accession Number Q3U1N2
Absorption
Active Site
Activity Regulation
Binding Site
Calcium Binding
catalytic Activity
DNA Binding
EC Number
Enzyme Function FUNCTION: [Sterol regulatory element-binding protein 2]: Precursor of the transcription factor form (Processed sterol regulatory element-binding protein 2), which is embedded in the endoplasmic reticulum membrane (By similarity). Low sterol concentrations promote processing of this form, releasing the transcription factor form that translocates into the nucleus and activates transcription of genes involved in cholesterol biosynthesis (PubMed:9616204, PubMed:16100574). {ECO:0000250|UniProtKB:Q12772, ECO:0000269|PubMed:16100574, ECO:0000269|PubMed:9616204}.; FUNCTION: [Processed sterol regulatory element-binding protein 2]: Key transcription factor that regulates expression of genes involved in cholesterol biosynthesis (PubMed:9616204). Binds to the sterol regulatory element 1 (SRE-1) (5'-ATCACCCCAC-3'). Has dual sequence specificity binding to both an E-box motif (5'-ATCACGTGA-3') and to SRE-1 (5'-ATCACCCCAC-3') (By similarity). Regulates transcription of genes related to cholesterol synthesis pathway (PubMed:9616204). {ECO:0000250|UniProtKB:Q12772, ECO:0000269|PubMed:9616204}.
Temperature Dependency
PH Dependency
Pathway
nucleotide Binding
Features Alternative sequence (2); Chain (2); Compositional bias (2); Cross-link (1); Domain (1); Modified residue (1); Mutagenesis (1); Region (4); Sequence conflict (4); Site (3); Topological domain (3); Transmembrane (2)
Keywords Activator;Alternative splicing;Cholesterol metabolism;Cytoplasmic vesicle;DNA-binding;Endoplasmic reticulum;Golgi apparatus;Isopeptide bond;Lipid metabolism;Membrane;Nucleus;Phosphoprotein;Reference proteome;Steroid metabolism;Sterol metabolism;Transcription;Transcription regulation;Transmembrane;Transmembrane helix;Ubl conjugation
Interact With Q9JM73
Induction
Subcellular Location SUBCELLULAR LOCATION: Endoplasmic reticulum membrane {ECO:0000250|UniProtKB:Q12772}; Multi-pass membrane protein {ECO:0000255}. Golgi apparatus membrane {ECO:0000303|PubMed:28849786}; Multi-pass membrane protein {ECO:0000255}. Cytoplasmic vesicle, COPII-coated vesicle membrane {ECO:0000303|PubMed:28849786}; Multi-pass membrane protein {ECO:0000255}. Note=At high sterol concentrations, the SCAP-SREBP is retained in the endoplasmic reticulum (By similarity). Low sterol concentrations promote recruitment into COPII-coated vesicles and transport of the SCAP-SREBP to the Golgi, where it is processed (By similarity). {ECO:0000250|UniProtKB:Q12772}.; SUBCELLULAR LOCATION: [Processed sterol regulatory element-binding protein 2]: Nucleus {ECO:0000269|PubMed:10397761, ECO:0000269|PubMed:11283257, ECO:0000269|PubMed:29068315}. Note=Transported into the nucleus with the help of importin-beta (PubMed:10397761, PubMed:11283257). Dimerization of the bHLH domain is a prerequisite for importin beta-dependent nuclear import (PubMed:10397761, PubMed:11283257). {ECO:0000269|PubMed:10397761, ECO:0000269|PubMed:11283257}.
Modified Residue MOD_RES 1087; /note=Phosphoserine; /evidence=ECO:0000250|UniProtKB:Q12772
Post Translational Modification PTM: [Sterol regulatory element-binding protein 2]: Processed in the Golgi apparatus, releasing the protein from the membrane. At low cholesterol the SCAP-SREBP complex is recruited into COPII vesicles for export from the endoplasmic reticulum. In the Golgi, complex SREBPs are cleaved sequentially by site-1 (MBTPS1, S1P) and site-2 (MBTPS2, S2P) proteases. The first cleavage by site-1 protease occurs within the luminal loop, the second cleavage by site-2 protease occurs within the first transmembrane domain, releasing the transcription factor from the Golgi membrane. Apoptosis triggers cleavage by the cysteine proteases caspase-3 and caspase-7. Cleavage and activation is induced by mediated cholesterol efflux. {ECO:0000250|UniProtKB:Q12772}.; PTM: Phosphorylated by AMPK, leading to suppress protein processing and nuclear translocation, and repress target gene expression. {ECO:0000269|PubMed:21459323}.; PTM: [Processed sterol regulatory element-binding protein 2]: Ubiquitinated; the nuclear form has a rapid turnover and is rapidly ubiquitinated and degraded by the proteasome in the nucleus. {ECO:0000250|UniProtKB:Q12772}.
Signal Peptide
Structure 3D
Cross Reference PDB -
Mapped Pubmed ID 10512203; 10585467; 11090130; 11208732; 11739104; 11829742; 12032166; 12160734; 12242332; 12446768; 12466851; 12520002; 12829694; 12855700; 12904583; 12943732; 14512514; 14522948; 14610273; 14662765; 14673138; 14722362; 15062879; 15102471; 15226823; 15572673; 15589694; 15618518; 15840001; 16046411; 16316337; 16332269; 16455790; 16879892; 16890542; 17300749; 17890326; 17916878; 17921436; 17967808; 18413311; 18557763; 18682608; 18799693; 18846256; 19110480; 19244508; 19500568; 19748890; 19808779; 19915177; 20059953; 20138838; 20466882; 20566875; 20732877; 20926756; 21084441; 21109190; 21459322; 21816276; 21858719; 21944868; 22005015; 22361881; 22441164; 22573382; 22666465; 22675522; 22985732; 22988430; 23000402; 23000407; 23536474; 23542164; 23563690; 23823476; 23838163; 23881913; 24068000; 24360166; 24465397; 24516236; 24675665; 24952961; 25550450; 25593129; 25646300; 25777360; 25794851; 26028026; 26184741; 26199412; 26508642; 26634251; 26685326; 26984409; 27008858; 27137100; 27416896; 27601673; 27752896; 27767079; 28244871; 28549068; 28630260; 28676202; 29472293; 29899135; 30074985; 30195495; 30604742; 30821074; 31303399; 31875875; 32266253; 33591268; 33878353; 33942715; 34021134; 7803821; 8343131; 8827514; 8833906; 9196007; 9329978; 9756919; 9789033; 9974430;
Motif
Gene Encoded By
Mass 122,911
Kinetics
Metal Binding
Rhea ID
Cross Reference Brenda