UniProt ID | CREST_HUMAN | |
---|---|---|
UniProt AC | O75177 | |
Protein Name | Calcium-responsive transactivator | |
Gene Name | SS18L1 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 396 | |
Subcellular Localization | Nucleus. Chromosome, centromere, kinetochore. Localizes to nuclear bodies. Colocalizes with SGO1 at kinetochore (By similarity).. | |
Protein Description | Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity).. | |
Protein Sequence | MSVAFASARPRGKGEVTQQTIQKMLDENHHLIQCILEYQSKGKTAECTQYQQILHRNLVYLATIADSNQNMQSLLPAPPTQNMNLGPGALTQSGSSQGLHSQGSLSDAISTGLPPSSLLQGQIGNGPSHVSMQQTAPNTLPTTSMSISGPGYSHAGPASQGVPMQGQGTIGNYVSRTNINMQSNPVSMMQQQAATSHYSSAQGGSQHYQGQSSIAMMGQGSQGSSMMGQRPMAPYRPSQQGSSQQYLGQEEYYGEQYSHSQGAAEPMGQQYYPDGHGDYAYQQSSYTEQSYDRSFEESTQHYYEGGNSQYSQQQAGYQQGAAQQQTYSQQQYPSQQSYPGQQQGYGSAQGAPSQYPGYQQGQGQQYGSYRAPQTAPSAQQQRPYGYEQGQYGNYQQ | |
Overview of Protein Modification Sites with Functional and Structural Information | ||
* ASA = Accessible Surface Area
Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
---|---|---|---|---|---|
2 | Acetylation | ------MSVAFASAR ------CCCCCCCCC | 23.35 | 19413330 | |
3 (in isoform 5) | Phosphorylation | - | 4.98 | 25072903 | |
5 (in isoform 5) | Phosphorylation | - | 5.31 | 25072903 | |
6 (in isoform 5) | Phosphorylation | - | 7.79 | 25072903 | |
10 (in isoform 5) | Phosphorylation | - | 49.44 | 25072903 | |
391 | Phosphorylation | YGYEQGQYGNYQQ-- CCCCCCCCCCCCC-- | 17.73 | - |
Modified Location | Modified Residue | Modification | Type of Upstream Proteins | Gene Name of Upstream Proteins | UniProt AC of Upstream Proteins | Sources |
---|---|---|---|---|---|---|
Oops, there are no upstream regulatory protein records of CREST_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of CREST_HUMAN !! |
* Distance = the distance between SAP position and PTM sites.
Modified Location | Modification | Variant Position (Distance <= 10) |
Residue Change | SAP | Related Disease | Reference |
---|---|---|---|---|---|---|
Oops, there are no SNP-PTM records of CREST_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
RFX6_HUMAN | RFX6 | physical | 16189514 | |
CBP_HUMAN | CREBBP | physical | 14716005 | |
EP300_HUMAN | EP300 | physical | 14716005 | |
SMCA4_HUMAN | SMARCA4 | physical | 19081374 | |
AATF_HUMAN | AATF | physical | 20211142 | |
RNF12_HUMAN | RLIM | physical | 20211142 | |
TAF9B_HUMAN | TAF9B | physical | 20211142 | |
GATD1_HUMAN | GATAD1 | physical | 20211142 | |
PCGF6_HUMAN | PCGF6 | physical | 20211142 | |
MED30_HUMAN | MED30 | physical | 20211142 | |
ANR22_HUMAN | ANKRD22 | physical | 20211142 | |
CREST_HUMAN | SS18L1 | physical | 25416956 | |
MISSL_HUMAN | MAPK1IP1L | physical | 25416956 | |
RSMB_HUMAN | SNRPB | physical | 21516116 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
There are no disease associations of PTM sites. | ||||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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