| PDB ID | 1BE3
|
CHAIN | A |
|---|---|---|---|
| Protein name | CYTOCHROME BC1 COMPLEX | ||
| Uniprot Accession | P31800 | ||
| The number of similar proteins | 36 | ||
| The number of binding states | 9 | ||
| The number of binding partners | 9 | ||
Unicolor (beige)
The number of binding partners
Group
| Binding state |
Binding partners |
|---|---|
| 1BE3 (CHAIN: A) | |
| 1 |
P07552
P00130
P13272
P13271
P00125
P00157
P23004
P13272
|
| 2 |
P23004
|
| 3 |
P00130
P13272
P13272
P13271
P00125
P00157
P23004
|
| 4 |
P13272
P13271
P00125
P00157
P23004
P13272
P00129
|
| 5 |
P07552
P00130
P13272
P13271
P00125
P00157
P23004
|
| 6 |
P00130
P13272
P13271
P00125
P00157
P23004
P13272
|
| 7 |
P00130
P13272
P13271
P00125
P00157
P23004
P13272
P00129
|
| 8 |
P00130
P13272
P13272
P13271
P00125
P00157
P23004
P00129
|
| 9 |
P07552
P00130
P13272
P13271
P00125
P00157
P23004
P13272
P00129
|
|
Only interaction residues |
|
||||||||||
|
|
| Residue | AA | Source / dbSNP |
Clinical Significance |
Allele Frequency (> 0.0001) |
AlphaMissense pathogenicity |
Disease name | |
|---|---|---|---|---|---|---|---|
| 17_SER | GLY |
gnomAD chr3:48646654 rs117171524 |
- | 0.000754354 | - | - | |
| 17_SER | GLY |
8.3kJPN chr3:48646654 rs117171524 |
- | 0.0001 | - | - | |
| 20_ASP | GLU |
8.3kJPN chr3:48646643 - |
- | 0.0001 | - | - | |
| 55_ALA | SER |
gnomAD chr3:48643235 rs201250580 |
- | 0.000199149 | - | - | |
| 86_LEU | PRO |
ClinVar chr3:48642152 - |
Likely pathogenic | - | - | Parkinsonism with polyneuropathy [MONDO:MONDO:0036193,MedGen:C5543299,OMIM:619279,Orphanet:611237] | |
| 181_ASP | HIS |
gnomAD chr3:48641060 rs17080284 |
- | 0.00222461 | - | - | |
| 181_ASP | HIS |
8.3kJPN chr3:48641060 rs17080284 |
- | 0.0359 | - | - | |
| 212_ALA | THR |
gnomAD chr3:48638871 rs145767014 |
- | 0.000119379 | - | - | |
| 227_ALA | THR |
8.3kJPN chr3:48638826 - |
- | 0.0001 | - | - | |
| 232_THR | SER |
8.3kJPN chr3:48638811 - |
- | 0.0001 | - | - | |
| 233_PRO | ARG |
gnomAD chr3:48638807 rs149245457 |
- | 0.00313314 | - | - | |
| 233_PRO | ARG |
8.3kJPN chr3:48638807 rs149245457 |
- | 0.0027 | - | - | |
| 235_ARG | HIS |
gnomAD chr3:48638801 rs62618742 |
- | 0.0168131 | - | - | |
| 235_ARG | CYS |
gnomAD chr3:48638802 rs533718471 |
- | 0.000131387 | - | - | |
| 242_ARG | CYS |
ClinVar chr3:48638548 rs201911056 |
Likely pathogenic | - | - | Hypertrophic cardiomyopathy [Human Phenotype Ontology:HP:0001639,MONDO:MONDO:0005045,MeSH:D002312,MedGen:C0007194,Orphanet:217569] | |
| 242_ARG | CYS |
8.3kJPN chr3:48638548 rs201911056 |
- | 0.0001 | - | - | |
| 267_ASN | SER |
gnomAD chr3:48638472 rs144710790 |
- | 0.00233837 | - | - | |
| 274_ASN | SER |
gnomAD chr3:48638451 rs187641562 |
- | 0.000319415 | - | - | |
| 274_ASN | SER |
8.3kJPN chr3:48638451 rs187641562 |
- | 0.0003 | - | - | |
| 277_ILE | LEU |
ClinVar chr3:48638443 rs2107843274 |
Pathogenic | - | - | Parkinsonism with polyneuropathy [MONDO:MONDO:0036193,MedGen:C5543299,OMIM:619279,Orphanet:611237] | |
| 278_GLY | SER |
gnomAD chr3:48638440 rs145869559 |
- | 0.00045596 | - | - | |
| 280_TYR | SER |
ClinVar chr3:48638433 rs780978963 |
Pathogenic | - | - | Parkinsonism with polyneuropathy [MONDO:MONDO:0036193,MedGen:C5543299,OMIM:619279,Orphanet:611237] | |
| 281_ASP | GLY |
8.3kJPN chr3:48638430 - |
- | 0.0001 | - | - | |
| 304_CYS | TYR |
8.3kJPN chr3:48638227 - |
- | 0.0001 | - | - | |
| 316_GLU | VAL |
8.3kJPN chr3:48638191 - |
- | 0.0001 | - | - | |
| 340_GLY | ARG |
8.3kJPN chr3:48638120 rs139928470 |
- | 0.0001 | - | - | |
| 356_ARG | GLN |
gnomAD chr3:48637959 rs777309520 |
- | 0.000111346 | - | - | |
| 380_GLY | ARG |
8.3kJPN chr3:48637558 - |
- | 0.0001 | - | - | |
| 381_ARG | CYS |
8.3kJPN chr3:48637555 rs370334893 |
- | 0.0001 | - | - | |
| 388_ARG | CYS |
8.3kJPN chr3:48637534 rs780875481 |
- | 0.0001 | - | - | |
| 408_ARG | CYS |
8.3kJPN chr3:48637122 rs762050976 |
- | 0.0001 | - | - | |
| 425_TYR | ASN |
gnomAD chr3:48637071 rs202030377 |
- | 0.000226902 | - | - | |
| 440_GLY | SER |
8.3kJPN chr3:48636584 rs1393314057 |
- | 0.0001 | - | - |