| PDB ID | 1KDX
|
CHAIN | A |
|---|---|---|---|
| Protein name | CBP | ||
| Uniprot Accession | P45481 | ||
| The number of similar proteins | 15 | ||
| The number of binding states | 6 | ||
| The number of binding partners | 6 | ||
Unicolor (beige)
The number of binding partners
Group
| Binding state |
Binding partners |
|---|---|
| 1KDX (CHAIN: A) | |
| 1 | Monomeric state |
| 2 |
Q03164
|
| 3 |
2LQH
|
| 4 |
P16220
|
| 5 |
Q04206
|
| 6 |
Q2Q067
P06876
|
|
Only interaction residues |
|
||||||||||||||
|
|
| Residue | AA | Source / dbSNP |
Clinical Significance |
Allele Frequency (> 0.0001) |
AlphaMissense pathogenicity |
Disease name | |
|---|---|---|---|---|---|---|---|
| 586_GLY | ASP |
8.3kJPN chr16:3830796 - |
- | 0.0002 | - | - | |
| 600_ARG | TER |
ClinVar chr22:41533772 rs137853038 |
Pathogenic/Likely pathogenic | - | - | Carcinoma of colon|Rubinstein-Taybi syndrome due to EP300 haploinsufficiency [MONDO:MONDO:0002032,MedGen:C0699790|MONDO:MONDO:0013364,MedGen:C3150941,OMIM:613684,Orphanet:353284,Orphanet:783] | |
| 600_ARG | TRP |
ClinVar chr16:3830755 rs1354934373 |
Likely pathogenic | - | - | Rubinstein-Taybi syndrome due to CREBBP mutations [MONDO:MONDO:0008393,MedGen:C4551859,OMIM:180849,Orphanet:353277,Orphanet:783] | |
| 601_ASN | SER |
8.3kJPN chr22:41533776 - |
- | 0.0001 | - | - | |
| 607_LEU | PRO |
ClinVar chr16:3830733 rs2053254528 |
Likely pathogenic | - | - | Rubinstein-Taybi syndrome due to CREBBP mutations [MONDO:MONDO:0008393,MedGen:C4551859,OMIM:180849,Orphanet:353277,Orphanet:783] | |
| 626_GLU | ASP |
8.3kJPN chr22:41536201 - |
- | 0.0002 | - | - | |
| 643_ALA | PRO |
ClinVar chr16:3828712 rs2141237064 |
Likely pathogenic | - | - | Rubinstein-Taybi syndrome due to CREBBP mutations [MONDO:MONDO:0008393,MedGen:C4551859,OMIM:180849,Orphanet:353277,Orphanet:783] | |
| 646_ARG | TER |
ClinVar chr22:41536259 - |
Pathogenic | - | - | not provided [MedGen:CN517202] | |
| 658_TYR | TER |
ClinVar chr16:3828148 rs2053190428 |
Pathogenic | - | - | Rubinstein-Taybi syndrome due to CREBBP mutations [MONDO:MONDO:0008393,MedGen:C4551859,OMIM:180849,Orphanet:353277,Orphanet:783] |