CX6B1_HUMAN - dbPTM
CX6B1_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID CX6B1_HUMAN
UniProt AC P14854
Protein Name Cytochrome c oxidase subunit 6B1
Gene Name COX6B1
Organism Homo sapiens (Human).
Sequence Length 86
Subcellular Localization Mitochondrion intermembrane space.
Protein Description Connects the two COX monomers into the physiological dimeric form..
Protein Sequence MAEDMETKIKNYKTAPFDSRFPNQNQTRNCWQNYLDFHRCQKAMTAKGGDISVCEWYQRVYQSLCPTSWVTDWDEQRAEGTFPGKI
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
2Acetylation------MAEDMETKI
------CCCHHHHHH
22.8422814378
7Phosphorylation-MAEDMETKIKNYKT
-CCCHHHHHHHHCCC
31.2823532336
8UbiquitinationMAEDMETKIKNYKTA
CCCHHHHHHHHCCCC
38.0723000965
8AcetylationMAEDMETKIKNYKTA
CCCHHHHHHHHCCCC
38.0725953088
8SumoylationMAEDMETKIKNYKTA
CCCHHHHHHHHCCCC
38.07-
10UbiquitinationEDMETKIKNYKTAPF
CHHHHHHHHCCCCCC
56.6423000965
13UbiquitinationETKIKNYKTAPFDSR
HHHHHHCCCCCCCCC
47.8323000965
13AcetylationETKIKNYKTAPFDSR
HHHHHHCCCCCCCCC
47.8325953088
132-HydroxyisobutyrylationETKIKNYKTAPFDSR
HHHHHHCCCCCCCCC
47.83-
30GlutathionylationNQNQTRNCWQNYLDF
CCHHCCCHHHHHHHH
3.4022555962
34PhosphorylationTRNCWQNYLDFHRCQ
CCCHHHHHHHHHHHH
7.7928152594
42UbiquitinationLDFHRCQKAMTAKGG
HHHHHHHHHHHHCCC
43.6922817900
45PhosphorylationHRCQKAMTAKGGDIS
HHHHHHHHHCCCCCC
30.0329759185
47UbiquitinationCQKAMTAKGGDISVC
HHHHHHHCCCCCCHH
55.0221906983
52PhosphorylationTAKGGDISVCEWYQR
HHCCCCCCHHHHHHH
26.0029759185
54S-nitrosocysteineKGGDISVCEWYQRVY
CCCCCCHHHHHHHHH
2.13-
54GlutathionylationKGGDISVCEWYQRVY
CCCCCCHHHHHHHHH
2.1322555962
54S-nitrosylationKGGDISVCEWYQRVY
CCCCCCHHHHHHHHH
2.1322178444
57PhosphorylationDISVCEWYQRVYQSL
CCCHHHHHHHHHHHH
2.4128152594
61PhosphorylationCEWYQRVYQSLCPTS
HHHHHHHHHHHCCCC
8.4527642862
65GlutathionylationQRVYQSLCPTSWVTD
HHHHHHHCCCCCCCC
4.1222555962
67PhosphorylationVYQSLCPTSWVTDWD
HHHHHCCCCCCCCHH
33.9419060867
68PhosphorylationYQSLCPTSWVTDWDE
HHHHCCCCCCCCHHH
12.5119060867
81PhosphorylationDEQRAEGTFPGKI--
HHHHHCCCCCCCC--
20.4021406692
85UbiquitinationAEGTFPGKI------
HCCCCCCCC------
45.5427667366
852-HydroxyisobutyrylationAEGTFPGKI------
HCCCCCCCC------
45.54-

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 CX6B1_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of CX6B1_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 CX6B1_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
COX5A_HUMANCOX5Aphysical
26344197
CX6B1_HUMANCOX6B1physical
27499296
CX6A1_HUMANCOX6A1physical
27499296
COX7R_HUMANCOX7A2Lphysical
27499296
COX6C_HUMANCOX6Cphysical
27499296
NDUS6_HUMANNDUFS6physical
27499296
NDUC2_HUMANNDUFC2physical
27499296
NDUA9_HUMANNDUFA9physical
27499296
NDUA6_HUMANNDUFA6physical
27499296
CX7A2_HUMANCOX7A2physical
27499296
NDUAA_HUMANNDUFA10physical
27499296
NDUV1_HUMANNDUFV1physical
27499296
MIA40_HUMANCHCHD4physical
27499296
SNP29_HUMANSNAP29physical
27499296
UCRI_HUMANUQCRFS1physical
27499296
NDUS1_HUMANNDUFS1physical
27499296
NDUA7_HUMANNDUFA7physical
27499296
NDUS4_HUMANNDUFS4physical
27499296
QCR7_HUMANUQCRBphysical
27499296
C1QBP_HUMANC1QBPphysical
27499296
QCR7_HUMANUQCRBphysical
28514442
SUOX_HUMANSUOXphysical
28514442
SRC_HUMANSRCphysical
28514442

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
220110Mitochondrial complex IV deficiency (MT-C4D)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of CX6B1_HUMAN

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Related Literatures of Post-Translational Modification

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