S10A1_HUMAN - dbPTM
S10A1_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID S10A1_HUMAN
UniProt AC P23297
Protein Name Protein S100-A1
Gene Name S100A1
Organism Homo sapiens (Human).
Sequence Length 94
Subcellular Localization Cytoplasm .
Protein Description Probably acts as a Ca(2+) signal transducer. [PubMed: 22399290 In response to an increase in intracellular Ca(2+) levels, binds calcium which triggers a conformational change]
Protein Sequence MGSELETAMETLINVFHAHSGKEGDKYKLSKKELKELLQTELSGFLDAQKDVDAVDKVMKELDENGDGEVDFQEYVVLVAALTVACNNFFWENS
Overview of Protein Modification Sites with Functional and Structural Information
Experimental Post-Translational Modification Sites

* ASA = Accessible Surface Area

Locations Modification Substrate Peptides
&
Secondary Structure
ASA (%) Reference Orthologous
Protein Cluster
27PhosphorylationSGKEGDKYKLSKKEL
CCCCCCCCCCCHHHH
23.15-
43PhosphorylationELLQTELSGFLDAQK
HHHHHHHHHHHHHHH
22.6728348404
86S-nitrosocysteineVAALTVACNNFFWEN
HHHHHHHHHHHHCCC
3.58-
86S-nitrosylationVAALTVACNNFFWEN
HHHHHHHHHHHHCCC
3.5822989881

Upstream regulatory proteins (kinases for phosphorylation sites, E3 ubiquitin ligases of ubiquitination sites, ...)
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 S10A1_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of S10A1_HUMAN !!

Disease-associated PTM Sites based on SAP

* 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 S10A1_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
S100P_HUMANS100Pphysical
16189514
S10A1_HUMANS100A1physical
16189514
NIF3L_HUMANNIF3L1physical
16189514
S100B_HUMANS100Bphysical
16189514
S10A4_HUMANS100A4physical
16189514
PYGM_HUMANPYGMphysical
12804600
CXA1_HUMANGJA1physical
12804600
AT2A2_HUMANATP2A2physical
12804600
PLB1_HUMANPLB1physical
12804600
PGM1_HUMANPGM1physical
8894274
S10A1_HUMANS100A1physical
9803314
S10A4_HUMANS100A4physical
10753920
RYR1_HUMANRYR1physical
9298970
S10A1_HUMANS100A1physical
25416956
S10A2_HUMANS100A2physical
25416956
S100B_HUMANS100Bphysical
25416956
PKHF2_HUMANPLEKHF2physical
25416956
S100B_HUMANS100Bphysical
21516116

Drug and Disease Associations
Kegg Disease
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
DB00768Olopatadine
Regulatory Network of S10A1_HUMAN

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Related Literatures of Post-Translational Modification

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