nuclear factor 1 C-type isoform 2 [Homo sapiens]
nuclear factor I( domain architecture ID 12106891)
nuclear factor I (NFI) is a CCAAT-box-binding protein active in transcription and DNA replication
List of domain hits
Name | Accession | Description | Interval | E-value | |||||
CTF_NFI | pfam00859 | CTF/NF-I family transcription modulation region; |
208-494 | 2.26e-144 | |||||
CTF/NF-I family transcription modulation region; : Pssm-ID: 459967 [Multi-domain] Cd Length: 288 Bit Score: 415.47 E-value: 2.26e-144
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NfI_DNAbd_pre-N | pfam10524 | Nuclear factor I protein pre-N-terminus; The Nuclear factor I (NFI) family of site-specific ... |
2-38 | 5.36e-20 | |||||
Nuclear factor I protein pre-N-terminus; The Nuclear factor I (NFI) family of site-specific DNA-binding proteins (also known as CTF or CAAT box transcription factor) functions both in viral DNA replication and in the regulation of gene expression in higher organizms. The N-terminal 200 residues contains the DNA-binding and dimerization domain, but also has an 8-47 residue highly conserved region 5' of this, whose function is not known. Deletion of the N-terminal 200 amino acids removes the DNA-binding activity, dimerization-ability and the stimulation of adenovirus DNA replication. : Pssm-ID: 463134 Cd Length: 41 Bit Score: 83.04 E-value: 5.36e-20
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MH1 super family | cl00055 | N-terminal Mad Homology 1 (MH1) domain; The MH1 is a small DNA-binding domain present in SMAD ... |
59-160 | 4.17e-18 | |||||
N-terminal Mad Homology 1 (MH1) domain; The MH1 is a small DNA-binding domain present in SMAD (small mothers against decapentaplegic) family of proteins, which are signal transducers and transcriptional modulators that mediate multiple signaling pathways. MH1 binds to the DNA major groove in an unusual manner via a beta hairpin structure. It negatively regulates the functions of the MH2 domain, the C-terminal domain of SMAD. Receptor-regulated SMAD proteins (R-SMADs, including SMAD1, SMAD2, SMAD3, SMAD5, and SMAD9) are activated by phosphorylation by transforming growth factor (TGF)-beta type I receptors. The active R-SMAD associates with a common mediator SMAD (Co-SMAD or SMAD4) and other cofactors, which together translocate to the nucleus to regulate gene expression. The inhibitory or antagonistic SMADs (I-SMADs, including SMAD6 and SMAD7) negatively regulate TGF-beta signaling by competing with R-SMADs for type I receptor or Co-SMADs. MH1 domains of R-SMAD and SMAD4 contain a nuclear localization signal as well as DNA-binding activity. The activated R-SMAD/SMAD4 complex then binds with very low affinity to a DNA sequence CAGAC called SMAD-binding element (SBE) via the MH1 domain. The actual alignment was detected with superfamily member smart00523: Pssm-ID: 469592 Cd Length: 109 Bit Score: 79.73 E-value: 4.17e-18
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Name | Accession | Description | Interval | E-value | |||||
CTF_NFI | pfam00859 | CTF/NF-I family transcription modulation region; |
208-494 | 2.26e-144 | |||||
CTF/NF-I family transcription modulation region; Pssm-ID: 459967 [Multi-domain] Cd Length: 288 Bit Score: 415.47 E-value: 2.26e-144
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NfI_DNAbd_pre-N | pfam10524 | Nuclear factor I protein pre-N-terminus; The Nuclear factor I (NFI) family of site-specific ... |
2-38 | 5.36e-20 | |||||
Nuclear factor I protein pre-N-terminus; The Nuclear factor I (NFI) family of site-specific DNA-binding proteins (also known as CTF or CAAT box transcription factor) functions both in viral DNA replication and in the regulation of gene expression in higher organizms. The N-terminal 200 residues contains the DNA-binding and dimerization domain, but also has an 8-47 residue highly conserved region 5' of this, whose function is not known. Deletion of the N-terminal 200 amino acids removes the DNA-binding activity, dimerization-ability and the stimulation of adenovirus DNA replication. Pssm-ID: 463134 Cd Length: 41 Bit Score: 83.04 E-value: 5.36e-20
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DWA | smart00523 | Domain A in dwarfin family proteins; |
59-160 | 4.17e-18 | |||||
Domain A in dwarfin family proteins; Pssm-ID: 214708 Cd Length: 109 Bit Score: 79.73 E-value: 4.17e-18
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MH1 | pfam03165 | MH1 domain; The MH1 (MAD homology 1) domain is found at the amino terminus of MAD related ... |
60-164 | 1.76e-17 | |||||
MH1 domain; The MH1 (MAD homology 1) domain is found at the amino terminus of MAD related proteins such as Smads. This domain is separated from the MH2 domain by a non-conserved linker region. The crystal structure of the MH1 domain shows that a highly conserved 11 residue beta hairpin is used to bind the DNA consensus sequence GNCN in the major groove, shown to be vital for the transcriptional activation of target genes. Not all examples of MH1 can bind to DNA however. Smad2 cannot bind DNA and has a large insertion within the hairpin that presumably abolishes DNA binding. A basic helix (H2) in MH1 with the nuclear localization signal KKLKK has been shown to be essential for Smad3 nuclear import. Smads also use the MH1 domain to interact with transcription factors such as Jun, TFE3, Sp1, and Runx. Pssm-ID: 460833 Cd Length: 103 Bit Score: 77.80 E-value: 1.76e-17
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Name | Accession | Description | Interval | E-value | |||||
CTF_NFI | pfam00859 | CTF/NF-I family transcription modulation region; |
208-494 | 2.26e-144 | |||||
CTF/NF-I family transcription modulation region; Pssm-ID: 459967 [Multi-domain] Cd Length: 288 Bit Score: 415.47 E-value: 2.26e-144
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NfI_DNAbd_pre-N | pfam10524 | Nuclear factor I protein pre-N-terminus; The Nuclear factor I (NFI) family of site-specific ... |
2-38 | 5.36e-20 | |||||
Nuclear factor I protein pre-N-terminus; The Nuclear factor I (NFI) family of site-specific DNA-binding proteins (also known as CTF or CAAT box transcription factor) functions both in viral DNA replication and in the regulation of gene expression in higher organizms. The N-terminal 200 residues contains the DNA-binding and dimerization domain, but also has an 8-47 residue highly conserved region 5' of this, whose function is not known. Deletion of the N-terminal 200 amino acids removes the DNA-binding activity, dimerization-ability and the stimulation of adenovirus DNA replication. Pssm-ID: 463134 Cd Length: 41 Bit Score: 83.04 E-value: 5.36e-20
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DWA | smart00523 | Domain A in dwarfin family proteins; |
59-160 | 4.17e-18 | |||||
Domain A in dwarfin family proteins; Pssm-ID: 214708 Cd Length: 109 Bit Score: 79.73 E-value: 4.17e-18
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MH1 | pfam03165 | MH1 domain; The MH1 (MAD homology 1) domain is found at the amino terminus of MAD related ... |
60-164 | 1.76e-17 | |||||
MH1 domain; The MH1 (MAD homology 1) domain is found at the amino terminus of MAD related proteins such as Smads. This domain is separated from the MH2 domain by a non-conserved linker region. The crystal structure of the MH1 domain shows that a highly conserved 11 residue beta hairpin is used to bind the DNA consensus sequence GNCN in the major groove, shown to be vital for the transcriptional activation of target genes. Not all examples of MH1 can bind to DNA however. Smad2 cannot bind DNA and has a large insertion within the hairpin that presumably abolishes DNA binding. A basic helix (H2) in MH1 with the nuclear localization signal KKLKK has been shown to be essential for Smad3 nuclear import. Smads also use the MH1 domain to interact with transcription factors such as Jun, TFE3, Sp1, and Runx. Pssm-ID: 460833 Cd Length: 103 Bit Score: 77.80 E-value: 1.76e-17
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Atrophin-1 | pfam03154 | Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian ... |
315-454 | 4.60e-03 | |||||
Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian atrophy (DRPLA) gene. DRPLA OMIM:125370 is a progressive neurodegenerative disorder. It is caused by the expansion of a CAG repeat in the DRPLA gene on chromosome 12p. This results in an extended polyglutamine region in atrophin-1, that is thought to confer toxicity to the protein, possibly through altering its interactions with other proteins. The expansion of a CAG repeat is also the underlying defect in six other neurodegenerative disorders, including Huntington's disease. One interaction of expanded polyglutamine repeats that is thought to be pathogenic is that with the short glutamine repeat in the transcriptional coactivator CREB binding protein, CBP. This interaction draws CBP away from its usual nuclear location to the expanded polyglutamine repeat protein aggregates that are characteriztic of the polyglutamine neurodegenerative disorders. This interferes with CBP-mediated transcription and causes cytotoxicity. Pssm-ID: 460830 [Multi-domain] Cd Length: 991 Bit Score: 39.75 E-value: 4.60e-03
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Blast search parameters | ||||
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