Dboc008056.1
Basic Information
- Insect
- Drosophila bocki
- Gene Symbol
- Tp53
- Assembly
- GCA_008042715.1
- Location
- VNJY01004522.1:19324-20610[-]
Transcription Factor Domain
- TF Family
- P53
- Domain
- P53 domain
- PFAM
- PF00870
- TF Group
- Beta-Scaffold Factors
- Description
- P53 is a tumor suppressor gene product; mutations in p53 or lack of expression are found associated with a large fraction of all human cancers. P53 is activated by DNA damage and acts as a regulator of gene expression that ultimatively blocks progression through the cell cycle. P53 binds to DNA as a tetrameric transcription factor. In its inactive form, p53 is bound to the ring finger protein Mdm2, which promotes its ubiquitinylation and subsequent proteosomal degradation. Phosphorylation of p53 disrupts the Mdm2-p53 complex, while the stable and active p53 binds to regulatory regions of its target genes, such as the cyclin-kinase inhibitor p21, which complexes and inactivates cdk2 and other cyclin complexes [PMID: 20066118, PMID: 12629332, PMID: 1397838, PMID: 6544917, PMID: 19826090, PMID: 19776744, PMID: 6278740, PMID: 221923, PMID: 6318442, PMID: 20030809].This domain is found in p53 transcription factors, where it is responsible for DNA-binding. The DNA-binding domain acts to clamp, or in the case of TonEBP, encircle the DNA target in order to stabilise the protein-DNA complex [PMID: 11780147]. Protein interactions may also serve to stabilise the protein-DNA complex, for example in the STAT-1 dimer the SH2 (Src homology 2) domain in each monomer is coupled to the DNA-binding domain to increase stability [PMID: 9630226]. The DNA-binding domain consists of a beta-sandwich formed of 9 strands in 2 sheets with a Greek-key topology. This structure is found in many transcription factors, often within the DNA-binding domain.
- Hmmscan Out
-
# of c-Evalue i-Evalue score bias hmm coord from hmm coord to ali coord from ali coord to env coord from env coord to acc 1 1 5e-59 8.1e-55 185.5 1.2 2 192 33 224 32 225 0.94
Sequence Information
- Coding Sequence
- ATGAAGCTCTATCAGTTCTACGTGCGCAAACAATCCGTGCTGCGCGAAATGATGCTGCAGGATCTGCAGTCCCAGGTGAATACTTTGCCCAAGCTGGAGAACCACAACCTTGGCGGCTACAATTTCAGCATGGTATTGGATGAACCACCAAAATCTCACTGGATGTTCTCGGTGGCCCTAAACAAGCTCTACATTCGGATGGACAAGATATTTAACGTGGACGTTCAGTTCAAGGCAAAGATGCCCATTCAGCCGCTCAGTCTCCGCGTCTTCCTCTGTTTTGTCAAGGATGTGAGCGGTCCGGTGCTGCGATGCCAGAATCACCTAAGCGTAGAGTCAACGACCATCCCGAACATAAAGGAGCGCGAGAGTTTGCTACGCTGTGAGAATCCCAACACTGTCTACTGTGGATCTGCCCAGGGAAAGGGCATTTCCGAACGCTACTCCGTTCTGATTCCCCTGAATATGTGCCGATCTGGCAGCCGCAGTGCCGGATATGTTCGCCAGACGCTGGCCTTCAAGTTTGTCTGCCAAAATTCGTGTTTTGGCCGAAAGGAAACCTGCTTGGTGTTTTGTCTGGAGAACGCTagTGGCGATATTGTGGGACAGCAGGTTTTGAATGTTAAAATCTGCACGTGCCCGAAACGAGATCGCAACCAGGACGAGCGCCAACTCACTGGCAAGAAGCGCAAATCCGAACCGGCCTGCTCCGATGAGGAGGACGAGCCGGACGTAAAGCCGGCCAAGACGCGTCGCCGCACCGCTTCATACCGGCGGAAAGTAAAGGAGGAGACTGAGAGCAATGACAGCAACGACGAGGAGGTGCCCGCCTCCGAATGGCAGGTGTCGCGTACAGCGGATGGCGAGTACCGTTTGTCGATTACCTGCCCGAAAAAGGATTGGCTCCTTCAGAGCATTGATGGTATGATTAAGGAGGCCGCTGCTGGAGTGCTACAATGTCCAAACCAGGCGAAACTGCGCCGCCATGCCCACAAGTTGGTCAGCCTGAAGAAACGTGCCTGCGACCTTCCGTGA
- Protein Sequence
- MKLYQFYVRKQSVLREMMLQDLQSQVNTLPKLENHNLGGYNFSMVLDEPPKSHWMFSVALNKLYIRMDKIFNVDVQFKAKMPIQPLSLRVFLCFVKDVSGPVLRCQNHLSVESTTIPNIKERESLLRCENPNTVYCGSAQGKGISERYSVLIPLNMCRSGSRSAGYVRQTLAFKFVCQNSCFGRKETCLVFCLENASGDIVGQQVLNVKICTCPKRDRNQDERQLTGKKRKSEPACSDEEDEPDVKPAKTRRRTASYRRKVKEETESNDSNDEEVPASEWQVSRTADGEYRLSITCPKKDWLLQSIDGMIKEAAAGVLQCPNQAKLRRHAHKLVSLKKRACDLP
Similar Transcription Factors
Sequence clustering based on sequence similarity using MMseqs2
- 100% Identity
- iTF_00561518;
- 90% Identity
- iTF_00527079; iTF_00532875; iTF_00612584; iTF_00561518; iTF_00593621; iTF_00484902; iTF_00594317; iTF_00491284; iTF_00613280; iTF_00540862; iTF_00488485; iTF_00491993; iTF_00489853; iTF_00477790; iTF_00524191; iTF_00617407;
- 80% Identity
- -