UniProt ID | RAPSN_HUMAN | |
---|---|---|
UniProt AC | Q13702 | |
Protein Name | 43 kDa receptor-associated protein of the synapse | |
Gene Name | RAPSN | |
Organism | Homo sapiens (Human). | |
Sequence Length | 412 | |
Subcellular Localization |
Cell membrane Peripheral membrane protein Cytoplasmic side. Cell junction, synapse, postsynaptic cell membrane Peripheral membrane protein Cytoplasmic side. Cytoplasm, cytoskeleton. Cytoplasmic surface of postsynaptic membranes. |
|
Protein Description | Postsynaptic protein required for clustering of nicotinic acetylcholine receptors (nAChRs) at the neuromuscular junction. It may link the receptor to the underlying postsynaptic cytoskeleton, possibly by direct association with actin or spectrin.. | |
Protein Sequence | MGQDQTKQQIEKGLQLYQSNQTEKALQVWTKVLEKSSDLMGRFRVLGCLVTAHSEMGRYKEMLKFAVVQIDTARELEDADFLLESYLNLARSNEKLCEFHKTISYCKTCLGLPGTRAGAQLGGQVSLSMGNAFLGLSVFQKALESFEKALRYAHNNDDAMLECRVCCSLGSFYAQVKDYEKALFFPCKAAELVNNYGKGWSLKYRAMSQYHMAVAYRLLGRLGSAMECCEESMKIALQHGDRPLQALCLLCFADIHRSRGDLETAFPRYDSAMSIMTEIGNRLGQVQALLGVAKCWVARKALDKALDAIERAQDLAEEVGNKLSQLKLHCLSESIYRSKGLQRELRAHVVRFHECVEETELYCGLCGESIGEKNSRLQALPCSHIFHLRCLQNNGTRSCPNCRRSSMKPGFV | |
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 | N-myristoyl glycine | ------MGQDQTKQQ ------CCCHHHHHH | 39.51 | - | |
2 | Myristoylation | ------MGQDQTKQQ ------CCCHHHHHH | 39.51 | - | |
59 | Phosphorylation | AHSEMGRYKEMLKFA HCHHCHHHHHHHCHH | 12.93 | 21253578 | |
115 | Phosphorylation | TCLGLPGTRAGAQLG HHHCCCCCHHHHHHC | 18.53 | - | |
126 | Phosphorylation | AQLGGQVSLSMGNAF HHHCCEEEECCCCHH | 13.57 | - | |
145 | Phosphorylation | VFQKALESFEKALRY HHHHHHHHHHHHHHH | 39.29 | 26846344 | |
196 | Phosphorylation | AAELVNNYGKGWSLK HHHHHHHCCCCCCHH | 18.27 | - | |
269 | Phosphorylation | LETAFPRYDSAMSIM HHHHCCCHHHHHHHH | 17.94 | 22210691 | |
271 | Phosphorylation | TAFPRYDSAMSIMTE HHCCCHHHHHHHHHH | 19.55 | 22210691 | |
277 | Phosphorylation | DSAMSIMTEIGNRLG HHHHHHHHHHHHHHH | 23.84 | 22210691 | |
324 | Phosphorylation | EEVGNKLSQLKLHCL HHHHHHHHHHHHHHH | 34.77 | 24719451 | |
405 | Phosphorylation | SCPNCRRSSMKPGFV CCCCCCCCCCCCCCC | 18.55 | - |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of RAPSN_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 RAPSN_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
DAG1_HUMAN | DAG1 | physical | 7619516 | |
HERC1_HUMAN | HERC1 | physical | 26186194 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
H00770 | Congenital myasthenic syndrome | |||||
H00987 | Fetal akinesia deformation sequence (FADS); Pena-Shokeir syndrome, type 1 | |||||
OMIM Disease | ||||||
616326 | Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency (CMS11) | |||||
208150 | Fetal akinesia deformation sequence (FADS) | |||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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