UniProt ID | MED22_HUMAN | |
---|---|---|
UniProt AC | Q15528 | |
Protein Name | Mediator of RNA polymerase II transcription subunit 22 | |
Gene Name | MED22 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 200 | |
Subcellular Localization | Nucleus . | |
Protein Description | Component of the Mediator complex, a coactivator involved in the regulated transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors.. | |
Protein Sequence | MAQQRALPQSKETLLQSYNKRLKDDIKSIMDNFTEIIKTAKIEDETQVSRATQGEQDNYEMHVRAANIVRAGESLMKLVSDLKQFLILNDFPSVNEAIDQRNQQLRTLQEECDRKLITLRDEISIDLYELEEEYYSSSSSLCEANDLPLCEAYGRLDLDTDSADGLSAPLLASPEPSAGPLQVAAPAHSHAGGPGPTEHA | |
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 |
---|---|---|---|---|---|
11 | Ubiquitination | QRALPQSKETLLQSY CCCCCCCHHHHHHHH | 49.85 | 21890473 | |
11 (in isoform 2) | Ubiquitination | - | 49.85 | 21890473 | |
11 (in isoform 1) | Ubiquitination | - | 49.85 | 21890473 | |
20 | Ubiquitination | TLLQSYNKRLKDDIK HHHHHHHHHHHHHHH | 51.37 | - | |
28 | O-linked_Glycosylation | RLKDDIKSIMDNFTE HHHHHHHHHHHHHHH | 24.39 | 30379171 | |
34 | Phosphorylation | KSIMDNFTEIIKTAK HHHHHHHHHHHHHCC | 32.31 | - | |
38 | Ubiquitination | DNFTEIIKTAKIEDE HHHHHHHHHCCCCCC | 48.36 | - | |
39 | O-linked_Glycosylation | NFTEIIKTAKIEDET HHHHHHHHCCCCCCC | 23.83 | 30379171 | |
59 | Phosphorylation | TQGEQDNYEMHVRAA HCCCCCCCHHHHHHH | 23.95 | 28796482 | |
74 | Phosphorylation | NIVRAGESLMKLVSD HHHHHHHHHHHHHHH | 32.61 | - | |
83 | Ubiquitination | MKLVSDLKQFLILND HHHHHHHHHHHHHCC | 43.95 | - | |
107 | Phosphorylation | QRNQQLRTLQEECDR HHHHHHHHHHHHHHH | 41.19 | 19664994 | |
160 | Phosphorylation | YGRLDLDTDSADGLS HCCCCCCCCCCCCCC | 38.87 | 28122231 | |
162 | Phosphorylation | RLDLDTDSADGLSAP CCCCCCCCCCCCCCC | 30.28 | 28122231 | |
167 | Phosphorylation | TDSADGLSAPLLASP CCCCCCCCCCEECCC | 33.11 | 26074081 | |
173 | Phosphorylation | LSAPLLASPEPSAGP CCCCEECCCCCCCCC | 29.75 | 26074081 | |
177 | Phosphorylation | LLASPEPSAGPLQVA EECCCCCCCCCCEEE | 44.17 | 26074081 | |
189 | Phosphorylation | QVAAPAHSHAGGPGP EEECCCCCCCCCCCC | 19.69 | 26074081 | |
197 | Phosphorylation | HAGGPGPTEHA---- CCCCCCCCCCC---- | 46.44 | 26074081 |
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 MED22_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of MED22_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 MED22_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
MED27_HUMAN | MED27 | physical | 12584197 | |
MED7_HUMAN | MED7 | physical | 12584197 | |
MED30_HUMAN | MED30 | physical | 12584197 | |
THOC7_HUMAN | THOC7 | physical | 12584197 | |
MED11_HUMAN | MED11 | physical | 12584197 | |
MED24_HUMAN | MED24 | physical | 22939629 | |
MED4_HUMAN | MED4 | physical | 22939629 |
Kegg Disease | ||||||
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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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