maturation protein SBDS-like, partial [Colotis evagore]
ribosome maturation protein SBDS( domain architecture ID 1006011)
ribosome maturation protein SBDS is required for the assembly of mature ribosomes and ribosome biogenesis
List of domain hits
Name | Accession | Description | Interval | E-value | |||
PTZ00448 super family | cl29187 | hypothetical protein; Provisional |
2-124 | 1.39e-37 | |||
hypothetical protein; Provisional The actual alignment was detected with superfamily member PTZ00448: Pssm-ID: 185627 [Multi-domain] Cd Length: 373 Bit Score: 130.54 E-value: 1.39e-37
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Name | Accession | Description | Interval | E-value | |||
PTZ00448 | PTZ00448 | hypothetical protein; Provisional |
2-124 | 1.39e-37 | |||
hypothetical protein; Provisional Pssm-ID: 185627 [Multi-domain] Cd Length: 373 Bit Score: 130.54 E-value: 1.39e-37
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RNA_SBDS | TIGR00291 | rRNA metabolism protein, SBDS family; This protein family, possibly universal in both archaea ... |
2-125 | 2.40e-34 | |||
rRNA metabolism protein, SBDS family; This protein family, possibly universal in both archaea and eukaryotes, appears to be involved in (ribosomal) RNA metabolism. Mutations in the human ortholog are associated with Shwachman-Bodian-Diamond syndrome. [Protein synthesis, Other] Pssm-ID: 129392 [Multi-domain] Cd Length: 231 Bit Score: 118.78 E-value: 2.40e-34
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SBDS_domain_II | pfam09377 | SBDS protein, domain II; Members containing this domain are highly conserved in species ... |
67-126 | 4.11e-29 | |||
SBDS protein, domain II; Members containing this domain are highly conserved in species ranging from archaea to vertebrates and plants, including several Shwachman-Bodian-Diamond syndrome (SBDS) proteins from both mouse and humans. Shwachman-Diamond syndrome is an autosomal recessive disorder with clinical features that include pancreatic exocrine insufficiency, haematological dysfunction and skeletal abnormalities. These proteins play a role in RNA metabolism. In yeast Sdo1 is involved in the biogenesis of the 60S ribosomal subunit and translational activation of ribosomes. SBDS protein is composed of three domains. The N-terminal (pfam01172) (FYSH) domain (domain I) is the most frequent target for disease mutations and contains a novel mixed alpha/beta-fold, the central domain (domain II) represented in this entry consists of a three-helical bundle and the C-terminal domain that has a ferredoxin-like fold. Pssm-ID: 462778 Cd Length: 62 Bit Score: 100.20 E-value: 4.11e-29
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Name | Accession | Description | Interval | E-value | |||
PTZ00448 | PTZ00448 | hypothetical protein; Provisional |
2-124 | 1.39e-37 | |||
hypothetical protein; Provisional Pssm-ID: 185627 [Multi-domain] Cd Length: 373 Bit Score: 130.54 E-value: 1.39e-37
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RNA_SBDS | TIGR00291 | rRNA metabolism protein, SBDS family; This protein family, possibly universal in both archaea ... |
2-125 | 2.40e-34 | |||
rRNA metabolism protein, SBDS family; This protein family, possibly universal in both archaea and eukaryotes, appears to be involved in (ribosomal) RNA metabolism. Mutations in the human ortholog are associated with Shwachman-Bodian-Diamond syndrome. [Protein synthesis, Other] Pssm-ID: 129392 [Multi-domain] Cd Length: 231 Bit Score: 118.78 E-value: 2.40e-34
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SBDS_domain_II | pfam09377 | SBDS protein, domain II; Members containing this domain are highly conserved in species ... |
67-126 | 4.11e-29 | |||
SBDS protein, domain II; Members containing this domain are highly conserved in species ranging from archaea to vertebrates and plants, including several Shwachman-Bodian-Diamond syndrome (SBDS) proteins from both mouse and humans. Shwachman-Diamond syndrome is an autosomal recessive disorder with clinical features that include pancreatic exocrine insufficiency, haematological dysfunction and skeletal abnormalities. These proteins play a role in RNA metabolism. In yeast Sdo1 is involved in the biogenesis of the 60S ribosomal subunit and translational activation of ribosomes. SBDS protein is composed of three domains. The N-terminal (pfam01172) (FYSH) domain (domain I) is the most frequent target for disease mutations and contains a novel mixed alpha/beta-fold, the central domain (domain II) represented in this entry consists of a three-helical bundle and the C-terminal domain that has a ferredoxin-like fold. Pssm-ID: 462778 Cd Length: 62 Bit Score: 100.20 E-value: 4.11e-29
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SBDS | pfam01172 | Shwachman-Bodian-Diamond syndrome (SBDS) protein; This family is highly conserved in species ... |
1-56 | 9.55e-21 | |||
Shwachman-Bodian-Diamond syndrome (SBDS) protein; This family is highly conserved in species ranging from archaea to vertebrates and plants. The family contains several Shwachman-Bodian-Diamond syndrome (SBDS) proteins from both mouse and humans. Shwachman-Diamond syndrome is an autosomal recessive disorder with clinical features that include pancreatic exocrine insufficiency, haematological dysfunction and skeletal abnormalities. It is characterized by bone marrow failure and leukemia predisposition. Members of this family play a role in RNA metabolism. In yeast these proteins have been shown to be critical for the release and recycling of the nucleolar shuttling factor Tif6 from pre-60S ribosomes, a key step in 60S maturation and translational activation of ribosomes. This data links defective late 60S subunit maturation to an inherited bone marrow failure syndrome associated with leukemia predisposition. Pssm-ID: 460097 [Multi-domain] Cd Length: 82 Bit Score: 79.39 E-value: 9.55e-21
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Blast search parameters | ||||
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