UniProt ID | TGFB2_HUMAN | |
---|---|---|
UniProt AC | P61812 | |
Protein Name | Transforming growth factor beta-2 | |
Gene Name | TGFB2 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 414 | |
Subcellular Localization | Secreted. | |
Protein Description | TGF-beta 2 has suppressive effects on interleukin-2 dependent T-cell growth.. | |
Protein Sequence | MHYCVLSAFLILHLVTVALSLSTCSTLDMDQFMRKRIEAIRGQILSKLKLTSPPEDYPEPEEVPPEVISIYNSTRDLLQEKASRRAAACERERSDEEYYAKEVYKIDMPPFFPSENAIPPTFYRPYFRIVRFDVSAMEKNASNLVKAEFRVFRLQNPKARVPEQRIELYQILKSKDLTSPTQRYIDSKVVKTRAEGEWLSFDVTDAVHEWLHHKDRNLGFKISLHCPCCTFVPSNNYIIPNKSEELEARFAGIDGTSTYTSGDQKTIKSTRKKNSGKTPHLLLMLLPSYRLESQQTNRRKKRALDAAYCFRNVQDNCCLRPLYIDFKRDLGWKWIHEPKGYNANFCAGACPYLWSSDTQHSRVLSLYNTINPEASASPCCVSQDLEPLTILYYIGKTPKIEQLSNMIVKSCKCS | |
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 |
---|---|---|---|---|---|
46 | Phosphorylation | AIRGQILSKLKLTSP HHHHHHHHHHCCCCC | 37.26 | 24719451 | |
72 | N-linked_Glycosylation | PEVISIYNSTRDLLQ HHHHHHHHCHHHHHH | 34.92 | UniProtKB CARBOHYD | |
81 | Ubiquitination | TRDLLQEKASRRAAA HHHHHHHHHHHHHHH | 38.41 | - | |
98 | Phosphorylation | RERSDEEYYAKEVYK HHCCCHHHHHHEEEE | 13.48 | - | |
123 | Phosphorylation | NAIPPTFYRPYFRIV CCCCCCCCCCCEEEE | 17.10 | 18083107 | |
140 | N-linked_Glycosylation | DVSAMEKNASNLVKA EHHHHHHCHHHHHHH | 34.98 | UniProtKB CARBOHYD | |
188 | Ubiquitination | TQRYIDSKVVKTRAE CHHHCCCEEEECCCC | 47.50 | - | |
241 | N-linked_Glycosylation | SNNYIIPNKSEELEA CCCEECCCCCHHHHH | 50.50 | UniProtKB CARBOHYD | |
275 | Phosphorylation | KSTRKKNSGKTPHLL CCCCCCCCCCCCHHH | 51.01 | 29083192 | |
278 | Phosphorylation | RKKNSGKTPHLLLML CCCCCCCCCHHHHHH | 21.33 | 29083192 | |
288 | Phosphorylation | LLLMLLPSYRLESQQ HHHHHHHHHHHHHHH | 23.89 | 24719451 | |
289 | Phosphorylation | LLMLLPSYRLESQQT HHHHHHHHHHHHHHH | 19.78 | 29083192 | |
293 | Phosphorylation | LPSYRLESQQTNRRK HHHHHHHHHHHHHHH | 31.98 | 29083192 | |
296 | Phosphorylation | YRLESQQTNRRKKRA HHHHHHHHHHHHHHH | 24.05 | 29083192 | |
333 | Ubiquitination | FKRDLGWKWIHEPKG EEHHHCCEECCCCCC | 34.18 | - | |
341 | Phosphorylation | WIHEPKGYNANFCAG ECCCCCCCCCCCCCC | 19.75 | - | |
352 | Phosphorylation | FCAGACPYLWSSDTQ CCCCCCCCCCCCCCC | 22.23 | - | |
404 | Phosphorylation | TPKIEQLSNMIVKSC CCCHHHHHHHHHHHC | 24.85 | - |
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 TGFB2_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of TGFB2_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 TGFB2_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
PGS2_HUMAN | DCN | physical | 9675033 | |
A4_HUMAN | APP | physical | 25241761 | |
BMP2_HUMAN | BMP2 | physical | 25241761 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
Note=A chromosomal aberration involving TGFB2 is found in a family with Peters anomaly. Translocation t(1 | ||||||
7)(q41 | ||||||
p21) with HDAC9. | ||||||
614816 | ||||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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