| UniProt ID | HMGB3_MOUSE | |
|---|---|---|
| UniProt AC | O54879 | |
| Protein Name | High mobility group protein B3 | |
| Gene Name | Hmgb3 | |
| Organism | Mus musculus (Mouse). | |
| Sequence Length | 200 | |
| Subcellular Localization | Nucleus . Chromosome . Cytoplasm . | |
| Protein Description | Multifunctional protein with various roles in different cellular compartments. May act in a redox sensitive manner. Associates with chromatin and binds DNA with a preference to non-canonical DNA structures such as single-stranded DNA. Can bent DNA and enhance DNA flexibility by looping thus providing a mechanism to promote activities on various gene promoters (By similarity). Proposed to be involved in the innate immune response to nucleic acids by acting as a cytoplasmic promiscuous immunogenic DNA/RNA sensor. [PubMed: 19890330 Negatively regulates B-cell and myeloid cell differentiation. In hematopoietic stem cells may regulate the balance between self-renewal and differentiation. Involved in negative regulation of canonical Wnt signaling] | |
| Protein Sequence | MAKGDPKKPKGKMSAYAFFVQTCREEHKKKNPEVPVNFAEFSKKCSERWKTMSSKEKSKFDEMAKADKVRYDREMKDYGPAKGGKKKKDPNAPKRPPSGFFLFCSEFRPKIKSTNPGISIGDVAKKLGEMWNNLSDNEKQPYVTKAAKLKEKYEKDVADYKSKGKFDGAKGPAKVARKKVEEEEEEEEEEEEEEEEEEDE | |
| Overview of Protein Modification Sites with Functional and Structural Information | ||
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* ASA = Accessible Surface Area
| Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
|---|---|---|---|---|---|
| 3 | Acetylation | -----MAKGDPKKPK -----CCCCCCCCCC | 63.65 | - | |
| 12 | Acetylation | DPKKPKGKMSAYAFF CCCCCCCCHHHHHHH | 35.49 | 23806337 | |
| 23 | Cysteine derivative | YAFFVQTCREEHKKK HHHHHHHHHHHHHHH | 2.63 | - | |
| 23 | Oxidation | YAFFVQTCREEHKKK HHHHHHHHHHHHHHH | 2.63 | - | |
| 30 | Acetylation | CREEHKKKNPEVPVN HHHHHHHHCCCCCCC | 80.62 | - | |
| 42 | Phosphorylation | PVNFAEFSKKCSERW CCCHHHHHHHHHHHH | 23.78 | 22817900 | |
| 43 | Acetylation | VNFAEFSKKCSERWK CCHHHHHHHHHHHHH | 64.22 | 22826441 | |
| 45 | Cysteine derivative | FAEFSKKCSERWKTM HHHHHHHHHHHHHHC | 6.16 | - | |
| 45 | Oxidation | FAEFSKKCSERWKTM HHHHHHHHHHHHHHC | 6.16 | - | |
| 95 | Methylation | KDPNAPKRPPSGFFL CCCCCCCCCCCCCEE | 47.50 | 58857841 | |
| 98 | Phosphorylation | NAPKRPPSGFFLFCS CCCCCCCCCCEEEEC | 51.41 | 24719451 | |
| 104 | Oxidation | PSGFFLFCSEFRPKI CCCCEEEECCCCCCC | 4.08 | - | |
| 104 | Cysteine derivative | PSGFFLFCSEFRPKI CCCCEEEECCCCCCC | 4.08 | - | |
| 104 | Glutathionylation | PSGFFLFCSEFRPKI CCCCEEEECCCCCCC | 4.08 | 24333276 | |
| 112 | Acetylation | SEFRPKIKSTNPGIS CCCCCCCCCCCCCCC | 58.30 | - | |
| 113 | Phosphorylation | EFRPKIKSTNPGISI CCCCCCCCCCCCCCH | 36.57 | 22817900 | |
| 114 | Phosphorylation | FRPKIKSTNPGISIG CCCCCCCCCCCCCHH | 40.19 | 20139300 | |
| 125 | Acetylation | ISIGDVAKKLGEMWN CCHHHHHHHHHHHHH | 48.67 | 7627571 | |
| 126 | Acetylation | SIGDVAKKLGEMWNN CHHHHHHHHHHHHHC | 52.57 | 23806337 | |
| 135 | Phosphorylation | GEMWNNLSDNEKQPY HHHHHCCCCCCCCCH | 40.28 | 27087446 | |
| 139 | Acetylation | NNLSDNEKQPYVTKA HCCCCCCCCCHHHHH | 63.93 | - |
| 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 HMGB3_MOUSE !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference |
|---|---|---|---|---|
| 23 | C | Oxidation |
| - |
| 45 | C | Oxidation |
| - |
| 104 | C | Oxidation |
| - |
* 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 HMGB3_MOUSE !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
Oops, there are no PPI records of HMGB3_MOUSE !! | ||||
| Kegg Drug | ||||||
|---|---|---|---|---|---|---|
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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