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 | P00429 P00428 P00428 P00415 P00396 P00396 |
2 | P00396 |
3 | P00429 P00415 P00396 |
4 | P00429 P00428 P00415 P00396 |
5 | P00429 P00415 P00396 P00396 |
6 | P00429 P00428 P00415 P00396 P00396 |
7 | P00428 P00415 P00415 P00396 P00396 |
8 | P00429 P00428 P00415 P00396 P00396 P68530 |
9 | P00429 P00428 P00415 P00415 P00396 P00396 |
10 | P00429 P00428 P00428 P00415 P00415 P00396 P00396 |
11 | P00429 P00428 P00428 P00415 P00396 P00396 P68530 |
12 | P00429 P00428 P00415 P00415 P00396 P00396 P68530 |
Only interaction residues |
|
||||||||
|
Residue | AA | Source | dbSNP | Clinical Significance |
Allele Frequency (> 0.0001) |
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 | - |