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 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
2 |
![]() |
3 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
4 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
6 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
8 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
9 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Only interaction residues |
|
||||||||||
![]() ![]() ![]() |
|
Residue | AA | Source | dbSNP | Clinical Significance |
Allele Frequency (> 0.0001) |
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 | - |