acyl-CoA-binding domain-containing protein 4 isoform X16 [Homo sapiens]
acyl-CoA-binding protein( domain architecture ID 10087334)
acyl-CoA-binding protein binds acyl-CoA esters and may play a role in housekeeping and/or trafficking
List of domain hits
Name | Accession | Description | Interval | E-value | |||
ACBP | cd00435 | Acyl CoA binding protein (ACBP) binds thiol esters of long fatty acids and coenzyme A in a ... |
13-97 | 3.37e-37 | |||
Acyl CoA binding protein (ACBP) binds thiol esters of long fatty acids and coenzyme A in a one-to-one binding mode with high specificity and affinity. Acyl-CoAs are important intermediates in fatty lipid synthesis and fatty acid degradation and play a role in regulation of intermediary metabolism and gene regulation. The suggested role of ACBP is to act as a intracellular acyl-CoA transporter and pool former. ACBPs are present in a large group of eukaryotic species and several tissue-specific isoforms have been detected. : Pssm-ID: 238248 Cd Length: 85 Bit Score: 126.67 E-value: 3.37e-37
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Atrophin-1 super family | cl38111 | Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian ... |
124-254 | 6.26e-04 | |||
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. The actual alignment was detected with superfamily member pfam03154: Pssm-ID: 460830 [Multi-domain] Cd Length: 991 Bit Score: 41.29 E-value: 6.26e-04
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Name | Accession | Description | Interval | E-value | |||
ACBP | cd00435 | Acyl CoA binding protein (ACBP) binds thiol esters of long fatty acids and coenzyme A in a ... |
13-97 | 3.37e-37 | |||
Acyl CoA binding protein (ACBP) binds thiol esters of long fatty acids and coenzyme A in a one-to-one binding mode with high specificity and affinity. Acyl-CoAs are important intermediates in fatty lipid synthesis and fatty acid degradation and play a role in regulation of intermediary metabolism and gene regulation. The suggested role of ACBP is to act as a intracellular acyl-CoA transporter and pool former. ACBPs are present in a large group of eukaryotic species and several tissue-specific isoforms have been detected. Pssm-ID: 238248 Cd Length: 85 Bit Score: 126.67 E-value: 3.37e-37
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ACBP | pfam00887 | Acyl CoA binding protein; |
13-89 | 1.43e-36 | |||
Acyl CoA binding protein; Pssm-ID: 459982 Cd Length: 76 Bit Score: 124.63 E-value: 1.43e-36
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ACB | COG4281 | Acyl-CoA-binding protein [Lipid transport and metabolism]; |
11-89 | 4.06e-26 | |||
Acyl-CoA-binding protein [Lipid transport and metabolism]; Pssm-ID: 443422 Cd Length: 87 Bit Score: 98.00 E-value: 4.06e-26
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PTZ00458 | PTZ00458 | acyl CoA binding protein; Provisional |
16-89 | 1.01e-12 | |||
acyl CoA binding protein; Provisional Pssm-ID: 185637 Cd Length: 90 Bit Score: 62.53 E-value: 1.01e-12
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Atrophin-1 | pfam03154 | Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian ... |
124-254 | 6.26e-04 | |||
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: 41.29 E-value: 6.26e-04
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Name | Accession | Description | Interval | E-value | |||
ACBP | cd00435 | Acyl CoA binding protein (ACBP) binds thiol esters of long fatty acids and coenzyme A in a ... |
13-97 | 3.37e-37 | |||
Acyl CoA binding protein (ACBP) binds thiol esters of long fatty acids and coenzyme A in a one-to-one binding mode with high specificity and affinity. Acyl-CoAs are important intermediates in fatty lipid synthesis and fatty acid degradation and play a role in regulation of intermediary metabolism and gene regulation. The suggested role of ACBP is to act as a intracellular acyl-CoA transporter and pool former. ACBPs are present in a large group of eukaryotic species and several tissue-specific isoforms have been detected. Pssm-ID: 238248 Cd Length: 85 Bit Score: 126.67 E-value: 3.37e-37
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ACBP | pfam00887 | Acyl CoA binding protein; |
13-89 | 1.43e-36 | |||
Acyl CoA binding protein; Pssm-ID: 459982 Cd Length: 76 Bit Score: 124.63 E-value: 1.43e-36
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ACB | COG4281 | Acyl-CoA-binding protein [Lipid transport and metabolism]; |
11-89 | 4.06e-26 | |||
Acyl-CoA-binding protein [Lipid transport and metabolism]; Pssm-ID: 443422 Cd Length: 87 Bit Score: 98.00 E-value: 4.06e-26
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PTZ00458 | PTZ00458 | acyl CoA binding protein; Provisional |
16-89 | 1.01e-12 | |||
acyl CoA binding protein; Provisional Pssm-ID: 185637 Cd Length: 90 Bit Score: 62.53 E-value: 1.01e-12
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Atrophin-1 | pfam03154 | Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian ... |
124-254 | 6.26e-04 | |||
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: 41.29 E-value: 6.26e-04
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Blast search parameters | ||||
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