UniProt ID | SPIT2_HUMAN | |
---|---|---|
UniProt AC | O43291 | |
Protein Name | Kunitz-type protease inhibitor 2 | |
Gene Name | SPINT2 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 252 | |
Subcellular Localization |
Membrane Single-pass type I membrane protein . |
|
Protein Description | Inhibitor of HGF activator. Also inhibits plasmin, plasma and tissue kallikrein, and factor XIa.. | |
Protein Sequence | MAQLCGLRRSRAFLALLGSLLLSGVLAADRERSIHDFCLVSKVVGRCRASMPRWWYNVTDGSCQLFVYGGCDGNSNNYLTKEECLKKCATVTENATGDLATSRNAADSSVPSAPRRQDSEDHSSDMFNYEEYCTANAVTGPCRASFPRWYFDVERNSCNNFIYGGCRGNKNSYRSEEACMLRCFRQQENPPLPLGSKVVVLAGLFVMVLILFLGASMVYLIRVARRNQERALRTVWSSGDDKEQLVKNTYVL | |
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 |
---|---|---|---|---|---|
19 | Phosphorylation | AFLALLGSLLLSGVL HHHHHHHHHHHHHHH | 18.80 | 24719451 | |
33 | Phosphorylation | LAADRERSIHDFCLV HHHHHCCCHHHHHHH | 21.37 | 28961369 | |
57 | N-linked_Glycosylation | SMPRWWYNVTDGSCQ CCCCEEEEECCCCEE | 19.25 | UniProtKB CARBOHYD | |
81 | Acetylation | NSNNYLTKEECLKKC CCCCCCCHHHHHHHH | 49.25 | 7479639 | |
87 | Ubiquitination | TKEECLKKCATVTEN CHHHHHHHHCCCCCC | 19.02 | - | |
92 | Phosphorylation | LKKCATVTENATGDL HHHHCCCCCCCCCCH | 21.11 | 22210691 | |
94 | N-linked_Glycosylation | KCATVTENATGDLAT HHCCCCCCCCCCHHH | 33.18 | UniProtKB CARBOHYD | |
101 | Phosphorylation | NATGDLATSRNAADS CCCCCHHHCCCCCCC | 35.20 | 22210691 | |
101 | O-linked_Glycosylation | NATGDLATSRNAADS CCCCCHHHCCCCCCC | 35.20 | 55832809 | |
102 | Phosphorylation | ATGDLATSRNAADSS CCCCHHHCCCCCCCC | 20.24 | 22210691 | |
102 | O-linked_Glycosylation | ATGDLATSRNAADSS CCCCHHHCCCCCCCC | 20.24 | 55832813 | |
108 | O-linked_Glycosylation | TSRNAADSSVPSAPR HCCCCCCCCCCCCCC | 28.63 | 55828365 | |
109 | O-linked_Glycosylation | SRNAADSSVPSAPRR CCCCCCCCCCCCCCC | 38.30 | 55828371 | |
112 | O-linked_Glycosylation | AADSSVPSAPRRQDS CCCCCCCCCCCCCCC | 49.07 | 55828377 | |
119 | Phosphorylation | SAPRRQDSEDHSSDM CCCCCCCCCCCCCCC | 36.26 | 28348404 | |
123 | Phosphorylation | RQDSEDHSSDMFNYE CCCCCCCCCCCCCHH | 40.11 | 28348404 | |
124 | Phosphorylation | QDSEDHSSDMFNYEE CCCCCCCCCCCCHHH | 29.67 | 28348404 | |
134 | O-linked_Glycosylation | FNYEEYCTANAVTGP CCHHHHHHHCCCCCC | 23.26 | OGP | |
150 | Phosphorylation | RASFPRWYFDVERNS CCCCCCEEEEECCCC | 7.38 | - | |
163 | Phosphorylation | NSCNNFIYGGCRGNK CCCCCCCCCCCCCCC | 11.88 | - | |
185 | Ubiquitination | ACMLRCFRQQENPPL HHHHHHHHCCCCCCC | 40.68 | 21890473 | |
190 | Ubiquitination | CFRQQENPPLPLGSK HHHCCCCCCCCCCCH | 30.93 | 21890473 | |
234 | Phosphorylation | NQERALRTVWSSGDD HHHHHHHHHHCCCCC | 27.46 | 27251275 | |
237 | Phosphorylation | RALRTVWSSGDDKEQ HHHHHHHCCCCCHHH | 21.80 | 26657352 | |
238 | Phosphorylation | ALRTVWSSGDDKEQL HHHHHHCCCCCHHHH | 30.45 | 29496963 | |
242 | 2-Hydroxyisobutyrylation | VWSSGDDKEQLVKNT HHCCCCCHHHHHHHE | 52.69 | - | |
242 | Ubiquitination | VWSSGDDKEQLVKNT HHCCCCCHHHHHHHE | 52.69 | 21890473 | |
247 | Ubiquitination | DDKEQLVKNTYVL-- CCHHHHHHHEEEC-- | 52.76 | 21890473 | |
250 | Phosphorylation | EQLVKNTYVL----- HHHHHHEEEC----- | 14.78 | 18083107 |
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 SPIT2_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of SPIT2_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 SPIT2_HUMAN !! |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
H01174 | Congenital diarrhea, including: Congenital chloride diarrhea (DIAR1); Microvillus inclusion disease | |||||
OMIM Disease | ||||||
270420 | Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies (DIAR3) | |||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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