UniProt ID | NGN3_HUMAN | |
---|---|---|
UniProt AC | Q9Y4Z2 | |
Protein Name | Neurogenin-3 | |
Gene Name | NEUROG3 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 214 | |
Subcellular Localization | Nucleus . | |
Protein Description | Acts as a transcriptional regulator. Together with NKX2-2, initiates transcriptional activation of NEUROD1. Involved in neurogenesis. Also required for the specification of a common precursor of the 4 pancreatic endocrine cell types (By similarity).. | |
Protein Sequence | MTPQPSGAPTVQVTRETERSFPRASEDEVTCPTSAPPSPTRTRGNCAEAEEGGCRGAPRKLRARRGGRSRPKSELALSKQRRSRRKKANDRERNRMHNLNSALDALRGVLPTFPDDAKLTKIETLRFAHNYIWALTQTLRIADHSLYALEPPAPHCGELGSPGGSPGDWGSLYSPVSQAGSLSPAASLEERPGLLGATFSACLSPGSLAFSDFL | |
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 |
---|---|---|---|---|---|
73 | Phosphorylation | GGRSRPKSELALSKQ CCCCCCHHHHHHHHH | 40.29 | 28787133 | |
112 | Phosphorylation | ALRGVLPTFPDDAKL HHHCCCCCCCCCCCC | 43.57 | - | |
174 | Phosphorylation | GDWGSLYSPVSQAGS CCHHHCCCCHHHCCC | 24.90 | - | |
183 | Phosphorylation | VSQAGSLSPAASLEE HHHCCCCCCCCCHHC | 17.75 | - |
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 NGN3_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of NGN3_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 NGN3_HUMAN !! |
Kegg Drug | ||||||
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DrugBank | ||||||
There are no disease associations of PTM sites. |
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