UniProt ID | SPIDR_MOUSE | |
---|---|---|
UniProt AC | Q8BGX7 | |
Protein Name | DNA repair-scaffolding protein | |
Gene Name | Spidr | |
Organism | Mus musculus (Mouse). | |
Sequence Length | 933 | |
Subcellular Localization | Nucleus. Together with BLM, is redistributed in discrete nuclear DNA damage-induced foci following hydroxyurea (HU) or camptothecin (CPT) treatment.. | |
Protein Description | Plays a role in DNA double-strand break (DBS) repair via homologous recombination (HR). Serves as a scaffolding protein that helps to promote the recruitment of DNA-processing enzymes like the helicase BLM and recombinase RAD51 to site of DNA damage, and hence contributes to maintain genomic integrity (By similarity).. | |
Protein Sequence | MSGARRPGTSKRKRNWHIEHPSFREERSQQLRRGNFKTVEAADSLSKAWLKCGEGFQDTSEILSLASEKTGITEKHLELSPKPKTETTSKNASELPNIIWSSSESDFSDEDKTLPALQRDGRHGPRADRLGDRTISCPEDEDIEDELQVIDWEVNSDKEDPGGPSECEDDKGTLDISDCDSCASLTSDDRLCEPSEPISTEILEYSSDSEKEEDPEHSLFIDSESPHKYQADFKSDARWCLVSQTDSEANSAEPTLTPQKYTVKFPKTPEYSVTKKKLLRGGLAERLQELQNRKRSAISLWRHRCVSYQMTPLGRKSGVLTVKILELHEECSMQVAVCEQLAGPPITSPPGGLAPRPGAYLKVLFTRETADHLMGHPQDIIYIFPPWQKLLIPNGSCSIILNTYFCQKAIAKETVREDLYSPDISLSRRNITLAQTFRIKDITDNSSINQTTYDSLATPGTGWTHGHEKAEQHLIVAAPLRNSLLDIVESQRAGLWSGVRVQVVVQRVYSLLSRDGARSQQGHTVGHADASGAWSCLLVQDACGMFGEVFLNSTLWKSRQLEGKSCSMSGVKVLQKATRGRTPGLFSLIDSLWPPVISLTEPSCGQPSGETKTYLPPPIFCYIFSAHPTLGQIDAIEDHISKLYQPPVVRCLKEILQTNECSTRCSFYARVIYQKPQLKNLLAQKEIWLLVTDITLQTQDERDHSLPKTLPVYIAPSCVLGPEVVEELALLVSYNLLFRDAFKDNGQIVCIERTVILPQKPLLCVPSASCDLPSPVTLDELSALTPVNSICSVQGTVVDVDESTAFSWPVCDRCGNGRLEQKPEDGGTFSCGDCSQLVLSPLQERHLHVFLDCPTRPESTVKVKLLESSISLLLMSAASEDGSYEVESVLGKEMGPLLCFVQSITTQQSSCVVTLEEIELLSTEGATAAQPPP | |
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 |
---|---|---|---|---|---|
80 | Phosphorylation | TEKHLELSPKPKTET CHHHHHCCCCCCCCC | 26824392 | ||
156 | Phosphorylation | VIDWEVNSDKEDPGG EEEEECCCCCCCCCC | 25195567 | ||
218 | Phosphorylation | KEEDPEHSLFIDSES CCCCCCCCCEECCCC | 18846507 | ||
223 | Phosphorylation | EHSLFIDSESPHKYQ CCCCEECCCCCCCEE | 22817900 | ||
225 | Phosphorylation | SLFIDSESPHKYQAD CCEECCCCCCCEECC | 18846507 | ||
255 | Phosphorylation | EANSAEPTLTPQKYT CCCCCCCCCCCCEEE | 25619855 | ||
257 | Phosphorylation | NSAEPTLTPQKYTVK CCCCCCCCCCEEEEE | 25619855 | ||
261 | Phosphorylation | PTLTPQKYTVKFPKT CCCCCCEEEEECCCC | 26643407 | ||
262 | Phosphorylation | TLTPQKYTVKFPKTP CCCCCEEEEECCCCC | 26643407 | ||
268 | Phosphorylation | YTVKFPKTPEYSVTK EEEECCCCCCCCCCH | 25338131 | ||
308 | Phosphorylation | WRHRCVSYQMTPLGR HHHHHCEEECCCCCC | - | ||
311 | Phosphorylation | RCVSYQMTPLGRKSG HHCEEECCCCCCCCC | - | ||
421 | Phosphorylation | TVREDLYSPDISLSR HHHHHHCCCCCCCHH | 25338131 | ||
828 | Phosphorylation | QKPEDGGTFSCGDCS ECCCCCCCEECCCHH | 25293948 | ||
830 | Phosphorylation | PEDGGTFSCGDCSQL CCCCCCEECCCHHHH | 25293948 | ||
835 | Phosphorylation | TFSCGDCSQLVLSPL CEECCCHHHHEECCH | 25293948 | ||
840 | Phosphorylation | DCSQLVLSPLQERHL CHHHHEECCHHHCCE | 28066266 |
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 SPIDR_MOUSE !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of SPIDR_MOUSE !! |
* 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 SPIDR_MOUSE !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
Oops, there are no PPI records of SPIDR_MOUSE !! |
Kegg Drug | ||||||
---|---|---|---|---|---|---|
DrugBank | ||||||
There are no disease associations of PTM sites. |
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