PDB ID | 1OCC
|
CHAIN | G |
---|---|---|---|
Protein name | CYTOCHROME C OXIDASE | ||
Uniprot Accession | P07471 | ||
The number of similar proteins | 104 | ||
The number of binding states | 12 | ||
The number of binding partners | 5 |
Unicolor (beige)
The number of binding partners
Group
Binding state |
Binding partners |
---|---|
1OCC (CHAIN: G) | |
1 |
![]() ![]() ![]() ![]() ![]() ![]() |
2 |
![]() |
3 |
![]() ![]() ![]() |
4 |
![]() ![]() ![]() ![]() |
5 |
![]() ![]() ![]() ![]() |
6 |
![]() ![]() ![]() ![]() ![]() |
7 |
![]() ![]() ![]() ![]() ![]() |
8 |
![]() ![]() ![]() ![]() ![]() ![]() |
9 |
![]() ![]() ![]() ![]() ![]() ![]() |
10 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
11 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
12 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Only interaction residues |
|
||||||||
![]() ![]() ![]() |
|
Residue | AA | Source / dbSNP |
Clinical Significance |
Allele Frequency (> 0.0001) |
AlphaMissense pathogenicity |
Disease name | |
---|---|---|---|---|---|---|---|
5_LYS | ILE |
8.3kJPN chr16:31439597 - |
- | 0.0001 | - | - | |
27_SER | ARG |
ClinVar chr16:31439429 rs1597176845 |
Likely pathogenic | - | - | Mitochondrial complex 4 deficiency, nuclear type 18 [MONDO:MONDO:0033653,MedGen:C5436720,OMIM:619062] | |
31_CYS | ARG |
ClinVar chr16:31439419 rs1275864234 |
Likely pathogenic | - | - | Mitochondrial complex 4 deficiency, nuclear type 18 [MONDO:MONDO:0033653,MedGen:C5436720,OMIM:619062] | |
47_PHE | LEU |
8.3kJPN chr16:31439369 - |
- | 0.0001 | - | - | |
57_THR | SER |
8.3kJPN chr16:31439340 - |
- | 0.0002 | - | - | |
61_PRO | ALA |
gnomAD chr16:31439172 rs148307890 |
- | 0.0002607 | - | - | |
75_VAL | MET |
8.3kJPN chr16:31439130 - |
- | 0.0001 | - | - |