| UniProt ID | FBX32_HUMAN | |
|---|---|---|
| UniProt AC | Q969P5 | |
| Protein Name | F-box only protein 32 | |
| Gene Name | FBXO32 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 355 | |
| Subcellular Localization | Cytoplasm . Nucleus . Shuttles between cytoplasm and the nucleus. | |
| Protein Description | Substrate recognition component of a SCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Probably recognizes and binds to phosphorylated target proteins during skeletal muscle atrophy. Recognizes TERF1.. | |
| Protein Sequence | MPFLGQDWRSPGQNWVKTADGWKRFLDEKSGSFVSDLSSYCNKEVYNKENLFNSLNYDVAAKKRKKDMLNSKTKTQYFHQEKWIYVHKGSTKERHGYCTLGEAFNRLDFSTAILDSRRFNYVVRLLELIAKSQLTSLSGIAQKNFMNILEKVVLKVLEDQQNIRLIRELLQTLYTSLCTLVQRVGKSVLVGNINMWVYRMETILHWQQQLNNIQITRPAFKGLTFTDLPLCLQLNIMQRLSDGRDLVSLGQAAPDLHVLSEDRLLWKKLCQYHFSERQIRKRLILSDKGQLDWKKMYFKLVRCYPRKEQYGDTLQLCKHCHILSWKGTDHPCTANNPESCSVSLSPQDFINLFKF | |
| 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 |
|---|---|---|---|---|---|
| 17 | Ubiquitination | SPGQNWVKTADGWKR CCCCCCEECCHHHHH | 29.61 | 21890473 | |
| 29 | Ubiquitination | WKRFLDEKSGSFVSD HHHHHHCCCCCHHHH | 60.84 | - | |
| 30 | Phosphorylation | KRFLDEKSGSFVSDL HHHHHCCCCCHHHHH | 37.31 | - | |
| 32 | Phosphorylation | FLDEKSGSFVSDLSS HHHCCCCCHHHHHHH | 29.57 | - | |
| 48 | Ubiquitination | CNKEVYNKENLFNSL CCHHHCCCCHHHHHC | 30.23 | 21906983 | |
| 71 | Phosphorylation | RKKDMLNSKTKTQYF HHHHHHCCCCCCCEE | 37.43 | 29083192 | |
| 73 | Phosphorylation | KDMLNSKTKTQYFHQ HHHHCCCCCCCEEEC | 38.86 | 29083192 | |
| 75 | Phosphorylation | MLNSKTKTQYFHQEK HHCCCCCCCEEECCC | 33.46 | 29083192 | |
| 77 | Phosphorylation | NSKTKTQYFHQEKWI CCCCCCCEEECCCEE | 14.30 | 29083192 | |
| 82 | Ubiquitination | TQYFHQEKWIYVHKG CCEEECCCEEEEECC | 32.11 | - | |
| 143 | Ubiquitination | SLSGIAQKNFMNILE CCHHHHHHHHHHHHH | 43.03 | - | |
| 224 | Phosphorylation | RPAFKGLTFTDLPLC CCCCCCCCCCCHHHH | 32.91 | 27251275 | |
| 226 | Phosphorylation | AFKGLTFTDLPLCLQ CCCCCCCCCHHHHHH | 31.24 | 27251275 | |
| 248 | Phosphorylation | SDGRDLVSLGQAAPD CCCCCHHHHCCCCCC | 33.80 | 28348404 | |
| 260 | Phosphorylation | APDLHVLSEDRLLWK CCCCEECCHHHHHHH | 36.04 | 25850435 | |
| 268 | Ubiquitination | EDRLLWKKLCQYHFS HHHHHHHHHHHHHCC | 42.80 | - | |
| 333 | Phosphorylation | KGTDHPCTANNPESC CCCCCCCCCCCCCCC | 36.55 | - | |
| 345 | Phosphorylation | ESCSVSLSPQDFINL CCCEEECCHHHHHHH | 17.01 | - |
| 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 FBX32_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of FBX32_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 FBX32_HUMAN !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
| SKP1_HUMAN | SKP1 | physical | 11717410 | |
| EIF3F_HUMAN | EIF3F | physical | 19073596 | |
| CDN1A_HUMAN | CDKN1A | physical | 21546904 | |
| MYPC3_HUMAN | MYBPC3 | physical | 19850579 | |
| DUS1_HUMAN | DUSP1 | physical | 19117950 | |
| SPB5_HUMAN | SERPINB5 | physical | 21725612 | |
| UB2R1_HUMAN | CDC34 | physical | 19073596 | |
| MUTYH_MOUSE | Mutyh | physical | 21964591 | |
| UB2D3_HUMAN | UBE2D3 | physical | 21964591 | |
| MYOD1_HUMAN | MYOD1 | physical | 15531760 | |
| EIF3F_HUMAN | EIF3F | physical | 18354498 | |
| KLF4_HUMAN | KLF4 | physical | 28068319 | |
| CUL1_HUMAN | CUL1 | physical | 26753747 | |
| RBX1_HUMAN | RBX1 | physical | 26753747 | |
| SKP1_HUMAN | SKP1 | physical | 26753747 | |
| SH3G2_HUMAN | SH3GL2 | physical | 27720640 | |
| SH3G1_HUMAN | SH3GL1 | physical | 27720640 |
| 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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