UniProt ID | HSFX1_HUMAN | |
---|---|---|
UniProt AC | Q9UBD0 | |
Protein Name | Heat shock transcription factor, X-linked | |
Gene Name | HSFX1 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 423 | |
Subcellular Localization | Nucleus . Cytoplasm . | |
Protein Description | ||
Protein Sequence | MEDKRSLSMARCEERNSRGQDHGLERVPFPPQLQSETYLHPADPSPAWDDPGSTGSPNLRLLTEEIAFQPLAEEASFRRPHPDGDVPPQGEDNLLSLPFPQKLWRLVSSNQFSSIWWDDSGACRVINQKLFEKEILKRDVAHKVFATTSIKSFFRQLNLYGFRKRRQCTFRTFTRIFSAKRLVSILNKLEFYCHPYFQRDSPHLLVRMKRRVGVKSAPRHQEEDKPEAAGSCLAPADTEQQDHTSPNENDQVTPQHREPAGPNTQIRSGSAPPATPVMVPDSAVASDNSPVTQPAGEWSEGSQAHVTPVAAVPGPAALPFLYVPGSPTQMNSYGPVVALPTASRSTLAMDTTGLPAPGMLPFCHLWVPVTLVAAGAAQPAASMVMFPHLPALHHHCPHSHRTSQYMPASDGPQAYPDYADQST | |
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 |
---|---|---|---|---|---|
8 | O-linked_Glycosylation | MEDKRSLSMARCEER CCCHHHHHHHHHHHH | 16.19 | 30379171 | |
96 | Phosphorylation | QGEDNLLSLPFPQKL CCCCCCCCCCCCHHH | 36.84 | - | |
137 | Ubiquitination | LFEKEILKRDVAHKV HHHHHHHHHHHHHHH | 52.81 | - | |
152 | Phosphorylation | FATTSIKSFFRQLNL HCHHHHHHHHHHHCH | 28.13 | 24719451 | |
184 | Phosphorylation | FSAKRLVSILNKLEF HCHHHHHHHHHHHHH | 26.42 | 24719451 | |
201 | Phosphorylation | HPYFQRDSPHLLVRM CHHHCCCCCCHHHHH | 19.19 | - | |
215 | Sumoylation | MKRRVGVKSAPRHQE HHHHHCCCCCCCCCC | 34.66 | - | |
215 | Sumoylation | MKRRVGVKSAPRHQE HHHHHCCCCCCCCCC | 34.66 | - |
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 HSFX1_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of HSFX1_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 HSFX1_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
CCD57_HUMAN | CCDC57 | physical | 25036637 | |
SYIM_HUMAN | IARS2 | physical | 25036637 | |
F192A_HUMAN | FAM192A | physical | 25036637 | |
CSPG2_HUMAN | VCAN | physical | 25036637 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
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. | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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