COX17_HUMAN - dbPTM
COX17_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID COX17_HUMAN
UniProt AC Q14061
Protein Name Cytochrome c oxidase copper chaperone
Gene Name COX17
Organism Homo sapiens (Human).
Sequence Length 63
Subcellular Localization Mitochondrion intermembrane space . Cytoplasm .
Protein Description Copper metallochaperone essential for the assembly of the mitochondrial respiratory chain complex IV (CIV), also known as cytochrome c oxidase. Binds two copper ions and delivers them to the metallochaperone SCO1 which transports the copper ions to the Cu(A) site on the cytochrome c oxidase subunit II (MT-CO2/COX2)..
Protein Sequence MPGLVDSNPAPPESQEKKPLKPCCACPETKKARDACIIEKGEEHCGHLIEAHKECMRALGFKI
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
7Phosphorylation-MPGLVDSNPAPPES
-CCCCCCCCCCCCHH
36.9128450419
14PhosphorylationSNPAPPESQEKKPLK
CCCCCCHHHCCCCCC
49.7925159151
17AcetylationAPPESQEKKPLKPCC
CCCHHHCCCCCCCCC
52.6430585187
17UbiquitinationAPPESQEKKPLKPCC
CCCHHHCCCCCCCCC
52.6433845483
18AcetylationPPESQEKKPLKPCCA
CCHHHCCCCCCCCCC
55.6325953088
21AcetylationSQEKKPLKPCCACPE
HHCCCCCCCCCCCCC
44.5325953088
30AcetylationCCACPETKKARDACI
CCCCCCCCCHHCEEE
42.6525953088
31AcetylationCACPETKKARDACII
CCCCCCCCHHCEEEE
56.957396163
40AcetylationRDACIIEKGEEHCGH
HCEEEEECCHHHHHH
62.3025953088
62UbiquitinationCMRALGFKI------
HHHHHCCCC------
45.79-

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 COX17_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of COX17_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 COX17_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
KATL1_HUMANKATNAL1physical
16189514
RBM48_HUMANRBM48physical
16169070
CXCL7_HUMANPPBPphysical
16169070
CSN6_HUMANCOPS6physical
16169070
ERG28_HUMANC14orf1physical
16169070
EF1A1_HUMANEEF1A1physical
16169070
P53_HUMANTP53physical
16169070
LRIF1_HUMANLRIF1physical
16169070
U119A_HUMANUNC119physical
16169070
ECHB_HUMANHADHBphysical
21988832
KATL1_HUMANKATNAL1physical
25416956
MIF_HUMANMIFphysical
26344197
SCYL2_HUMANSCYL2physical
26344197
TALDO_HUMANTALDO1physical
26344197
TBCA_HUMANTBCAphysical
26344197

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
There are no disease associations of PTM sites.
Regulatory Network of COX17_HUMAN

loading...

Related Literatures of Post-Translational Modification

TOP