CABP2_HUMAN - dbPTM
CABP2_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID CABP2_HUMAN
UniProt AC Q9NPB3
Protein Name Calcium-binding protein 2
Gene Name CABP2
Organism Homo sapiens (Human).
Sequence Length 220
Subcellular Localization Cytoplasm, perinuclear region . Cell membrane
Lipid-anchor
Cytoplasmic side . Golgi apparatus .
Protein Description Required for sound encoding at inner hair cells (IHCs) synapses, likely via inhibition of the inactivation of voltage-gated calcium channel of type 1.3 (Cav1.3) in the IHCs. [PubMed: 28183797 Required for the normal transfer of light signals through the retina (By similarity]
Protein Sequence MGNCAKRPWRRGPKDPLQWLGSPPRGSCPSPSSSPKEQGDPAPGVQGYSVLNSLVGPACIFLRPSIAATQLDRELRPEEIEELQVAFQEFDRDRDGYIGCRELGACMRTLGYMPTEMELIEISQQISGGKVDFEDFVELMGPKLLAETADMIGVRELRDAFREFDTNGDGRISVGELRAALKALLGERLSQREVDEILQDVDLNGDGLVDFEEFVRMMSR
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
2N-myristoyl glycine------MGNCAKRPW
------CCCCCCCCC
37.61-
2Myristoylation------MGNCAKRPW
------CCCCCCCCC
37.6110625670

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 CABP2_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of CABP2_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 CABP2_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
KCC2G_RATCamk2gphysical
10625670

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
614899Deafness, autosomal recessive, 93 (DFNB93)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of CABP2_HUMAN

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Related Literatures of Post-Translational Modification
Myristoylation
ReferencePubMed
"Five members of a novel Ca(2+)-binding protein (CABP) subfamily withsimilarity to calmodulin.";
Haeseleer F., Sokal I., Verlinde C.L.M.J., Erdjument-Bromage H.,Tempst P., Pronin A.N., Benovic J.L., Fariss R.N., Palczewski K.;
J. Biol. Chem. 275:1247-1260(2000).
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA] (ISOFORMS L-CABP2 ANDS-CABP2), VARIANT GLN-94, AND MYRISTOYLATION AT GLY-2.

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