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 | ||
|
* ASA = Accessible Surface Area
Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
---|---|---|---|---|---|
2 | Acetylation | ------MAEDMETKI ------CCCHHHHHH | 22.84 | 22814378 | |
7 | Phosphorylation | -MAEDMETKIKNYKT -CCCHHHHHHHHCCC | 31.28 | 23532336 | |
8 | Ubiquitination | MAEDMETKIKNYKTA CCCHHHHHHHHCCCC | 38.07 | 23000965 | |
8 | Acetylation | MAEDMETKIKNYKTA CCCHHHHHHHHCCCC | 38.07 | 25953088 | |
8 | Sumoylation | MAEDMETKIKNYKTA CCCHHHHHHHHCCCC | 38.07 | - | |
10 | Ubiquitination | EDMETKIKNYKTAPF CHHHHHHHHCCCCCC | 56.64 | 23000965 | |
13 | Ubiquitination | ETKIKNYKTAPFDSR HHHHHHCCCCCCCCC | 47.83 | 23000965 | |
13 | Acetylation | ETKIKNYKTAPFDSR HHHHHHCCCCCCCCC | 47.83 | 25953088 | |
13 | 2-Hydroxyisobutyrylation | ETKIKNYKTAPFDSR HHHHHHCCCCCCCCC | 47.83 | - | |
30 | Glutathionylation | NQNQTRNCWQNYLDF CCHHCCCHHHHHHHH | 3.40 | 22555962 | |
34 | Phosphorylation | TRNCWQNYLDFHRCQ CCCHHHHHHHHHHHH | 7.79 | 28152594 | |
42 | Ubiquitination | LDFHRCQKAMTAKGG HHHHHHHHHHHHCCC | 43.69 | 22817900 | |
45 | Phosphorylation | HRCQKAMTAKGGDIS HHHHHHHHHCCCCCC | 30.03 | 29759185 | |
47 | Ubiquitination | CQKAMTAKGGDISVC HHHHHHHCCCCCCHH | 55.02 | 21906983 | |
52 | Phosphorylation | TAKGGDISVCEWYQR HHCCCCCCHHHHHHH | 26.00 | 29759185 | |
54 | S-nitrosocysteine | KGGDISVCEWYQRVY CCCCCCHHHHHHHHH | 2.13 | - | |
54 | Glutathionylation | KGGDISVCEWYQRVY CCCCCCHHHHHHHHH | 2.13 | 22555962 | |
54 | S-nitrosylation | KGGDISVCEWYQRVY CCCCCCHHHHHHHHH | 2.13 | 22178444 | |
57 | Phosphorylation | DISVCEWYQRVYQSL CCCHHHHHHHHHHHH | 2.41 | 28152594 | |
61 | Phosphorylation | CEWYQRVYQSLCPTS HHHHHHHHHHHCCCC | 8.45 | 27642862 | |
65 | Glutathionylation | QRVYQSLCPTSWVTD HHHHHHHCCCCCCCC | 4.12 | 22555962 | |
67 | Phosphorylation | VYQSLCPTSWVTDWD HHHHHCCCCCCCCHH | 33.94 | 19060867 | |
68 | Phosphorylation | YQSLCPTSWVTDWDE HHHHCCCCCCCCHHH | 12.51 | 19060867 | |
81 | Phosphorylation | DEQRAEGTFPGKI-- HHHHHCCCCCCCC-- | 20.40 | 21406692 | |
85 | Ubiquitination | AEGTFPGKI------ HCCCCCCCC------ | 45.54 | 27667366 | |
85 | 2-Hydroxyisobutyrylation | AEGTFPGKI------ HCCCCCCCC------ | 45.54 | - |
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 !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of CX6B1_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 CX6B1_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
COX5A_HUMAN | COX5A | physical | 26344197 | |
CX6B1_HUMAN | COX6B1 | physical | 27499296 | |
CX6A1_HUMAN | COX6A1 | physical | 27499296 | |
COX7R_HUMAN | COX7A2L | physical | 27499296 | |
COX6C_HUMAN | COX6C | physical | 27499296 | |
NDUS6_HUMAN | NDUFS6 | physical | 27499296 | |
NDUC2_HUMAN | NDUFC2 | physical | 27499296 | |
NDUA9_HUMAN | NDUFA9 | physical | 27499296 | |
NDUA6_HUMAN | NDUFA6 | physical | 27499296 | |
CX7A2_HUMAN | COX7A2 | physical | 27499296 | |
NDUAA_HUMAN | NDUFA10 | physical | 27499296 | |
NDUV1_HUMAN | NDUFV1 | physical | 27499296 | |
MIA40_HUMAN | CHCHD4 | physical | 27499296 | |
SNP29_HUMAN | SNAP29 | physical | 27499296 | |
UCRI_HUMAN | UQCRFS1 | physical | 27499296 | |
NDUS1_HUMAN | NDUFS1 | physical | 27499296 | |
NDUA7_HUMAN | NDUFA7 | physical | 27499296 | |
NDUS4_HUMAN | NDUFS4 | physical | 27499296 | |
QCR7_HUMAN | UQCRB | physical | 27499296 | |
C1QBP_HUMAN | C1QBP | physical | 27499296 | |
QCR7_HUMAN | UQCRB | physical | 28514442 | |
SUOX_HUMAN | SUOX | physical | 28514442 | |
SRC_HUMAN | SRC | physical | 28514442 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
220110 | Mitochondrial complex IV deficiency (MT-C4D) | |||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
loading...