Summary: Pancreatic ribonuclease
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This is the Wikipedia entry entitled "Pancreatic ribonuclease". More...
Pancreatic ribonuclease Edit Wikipedia article
| Pancreatic ribonuclease | |||||||||
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| Structure of RNase A | |||||||||
| Identifiers | |||||||||
| EC number | 3.1.27.5 | ||||||||
| CAS number | 9001-99-4 | ||||||||
| Databases | |||||||||
| IntEnz | IntEnz view | ||||||||
| BRENDA | BRENDA entry | ||||||||
| ExPASy | NiceZyme view | ||||||||
| KEGG | KEGG entry | ||||||||
| MetaCyc | metabolic pathway | ||||||||
| PRIAM | profile | ||||||||
| PDB structures | RCSB PDB PDBe PDBsum | ||||||||
| Gene Ontology | AmiGO / EGO | ||||||||
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| Pancreatic ribonuclease | |||||||||
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| Identifiers | |||||||||
| Symbol | RNaseA | ||||||||
| Pfam | PF00074 | ||||||||
| InterPro | IPR001427 | ||||||||
| SMART | SM00092 | ||||||||
| PROSITE | PDOC00118 | ||||||||
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Pancreatic ribonucleasea (EC 3.1.27.5, RNase, RNase I, RNase A, pancreatic RNase, ribonuclease I, endoribonuclease I, ribonucleic phosphatase, alkaline ribonuclease, ribonuclease, gene S glycoproteins, Ceratitis capitata alkaline ribonuclease, SLSG glycoproteins, gene S locus-specific glycoproteins, S-genotype-asssocd. glycoproteins, ribonucleate 3'-pyrimidino-oligonucleotidohydrolase) are pyrimidine-specific endonucleases found in high quantity in the pancreas of certain mammals and of some reptiles.[1]
Specifically, the enzymes are involved in endonucleolytic cleavage of 3'-phosphomononucleotides and 3'-phosphooligonucleotides ending in C-P or U-P with 2',3'-cyclic phosphate intermediates. Ribonuclease can unwind the DNA helix by complexing with single-stranded DNA; the complex arises by an extended multi-site cation-anion interaction between lysine and arginine residues of the enzyme and phosphate groups of the nucleotides.
Other proteins belonging to the pancreatic ribonuclease superfamily include: bovine seminal vesicle and brain ribonucleases; kidney non-secretory ribonucleases;[2] liver-type ribonucleases;[3] angiogenin, which induces vascularisation of normal and malignant tissues; eosinophil cationic protein,[4] a cytotoxin and helminthotoxin with ribonuclease activity; and frog liver ribonuclease and frog sialic acid-binding lectin. The sequence of pancreatic ribonucleases contains four conserved disulfide bonds and three amino acid residues involved in the catalytic activity.[5]
[edit] Examples
Human genes encoding proteins containing this domain include:
[edit] References
- ^ van der Laan JM, Beintema JJ (1986). "Comparison of the structure of turtle pancreatic ribonuclease with those of mammalian ribonucleases". FEBS Lett. 194 (2): 338â343. doi:10.1016/0014-5793(86)80113-2. PMID 3940901.
- ^ Rosenberg HF, Ackerman SJ, Tenen DG (1989). "Molecular cloning of the human eosinophil-derived neurotoxin: a member of the ribonuclease gene family". Proc. Natl. Acad. Sci. U.S.A. 86 (12): 4460â4464. doi:10.1073/pnas.86.12.4460. PMC 287289. PMID 2734298.
- ^ Stone SR, Hofsteenge J, Matthies R (1989). "Primary structure of a ribonuclease from porcine liver, a new member of the ribonuclease superfamily". Biochemistry 28 (25): 9806â9813. doi:10.1021/bi00451a040. PMID 2611266.
- ^ Rosenberg HF, Ackerman SJ, Tenen DG (1989). "Human eosinophil cationic protein. Molecular cloning of a cytotoxin and helminthotoxin with ribonuclease activity". J. Exp. Med. 170 (1): 163â176. doi:10.1084/jem.170.1.163. PMC 2189377. PMID 2473157.
- ^ Raines, R. T. (1998). "Ribonuclease A". Chem. Rev. 98: 1045â1066. PMID 11848924.
This article incorporates text from the public domain Pfam and InterPro IPR001427
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This tab holds the annotation information that is stored in the Pfam database. As we move to using Wikipedia as our main source of annotation, the contents of this tab will be gradually replaced by the Wikipedia tab.
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Ribonucleases. Members include pancreatic RNAase A and angiogenins. Structure is an alpha+beta fold -- long curved beta sheet and three helices.
External database links
| HOMSTRAD: | rnasemam |
| PANDIT: | PF00074 |
| PROSITE: | PDOC00118 |
| Pseudofam: | PF00074 |
| SCOP: | 7rsa |
| SYSTERS: | RnaseA |
This tab holds annotation information from the InterPro database.
InterPro entry IPR023412
Pancreatic ribonucleases (RNaseA) are pyrimidine-specific endonucleases found in high quantity in the pancreas of certain mammals and of some reptiles [PUBMED:3940901]. Specifically, the enzymes are involved in endonucleolytic cleavage of 3'-phosphomononucleotides and 3'-phosphooligonucleotides ending in C-P or U-P with 2',3'-cyclic phosphate intermediates. Ribonuclease can unwind the DNA helix by complexing with single-stranded DNA; the complex arises by an extended multi-site cation-anion interaction between lysine and arginine residues of the enzyme and phosphate groups of the nucleotides. Other proteins belonging to the pancreatic RNAse family include: bovine seminal vesicle and brain ribonucleases; kidney non-secretory ribonucleases [PUBMED:2734298]; liver-type ribonucleases [PUBMED:2611266]; angiogenin, which induces vascularisation of normal and malignant tissues; eosinophil cationic protein [PUBMED:2473157], a cytotoxin and helminthotoxin with ribonuclease activity; and frog liver ribonuclease and frog sialic acid-binding lectin. The sequence of pancreatic RNases contains four conserved disulphide bonds and three amino acid residues involved in the catalytic activity.Domain organisation
Below is a listing of the unique domain organisations or architectures in which this domain is found. More...
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Alignments
We store a range of different sequence alignments for families. As well as the seed alignment from which the family is built, we provide the full alignment, generated by searching the sequence database using the family HMM. We also generate alignments using four representative proteomes (RP) sets, the NCBI sequence database, and our metagenomics sequence database. More...
View options
We make a range of alignments for each Pfam-A family. You can see a description of each above. You can view these alignments in various ways but please note that some types of alignment are never generated while others may not be available for all families, most commonly because the alignments are too large to handle.
| Seed (108) |
Full (847) |
Representative proteomes | NCBI (891) |
Meta (0) |
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| RP15 (15) |
RP35 (18) |
RP55 (39) |
RP75 (241) |
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| Jalview | ||||||||
| HTML | ||||||||
| PP/heatmap | 1 | |||||||
| Pfam viewer | ||||||||
1Cannot generate PP/Heatmap alignments for seeds; no PP data available
Key:
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not generated,
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Format an alignment
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We make all of our alignments available in Stockholm format. You can download them here as raw, plain text files or as gzip-compressed files.
| Seed (108) |
Full (847) |
Representative proteomes | NCBI (891) |
Meta (0) |
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|---|---|---|---|---|---|---|---|---|
| RP15 (15) |
RP35 (18) |
RP55 (39) |
RP75 (241) |
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| Raw Stockholm | ||||||||
| Gzipped | ||||||||
You can also download a FASTA format file containing the full-length sequences for all sequences in the full alignment.
External links
MyHits provides a collection of tools to handle multiple sequence alignments. For example, one can refine a seed alignment (sequence addition or removal, re-alignment or manual edition) and then search databases for remote homologs using HMMER3.
HMM logo
HMM logos is one way of visualising profile HMMs. Logos provide a quick overview of the properties of an HMM in a graphical form. You can see a more detailed description of HMM logos and find out how you can interpret them here. More...
Trees
This page displays the phylogenetic tree for this family's seed alignment. We use FastTree to calculate neighbour join trees with a local bootstrap based on 100 resamples (shown next to the tree nodes). FastTree calculates approximately-maximum-likelihood phylogenetic trees from our seed alignment.
Note: You can also download the data file for the tree.
Curation and family details
This section shows the detailed information about the Pfam family. You can see the definitions of many of the terms in this section in the glossary and a fuller explanation of the scoring system that we use in the scores section of the help pages.
Curation
| Seed source: | Overington and HMM_iterative_training |
| Previous IDs: | rnaseA; |
| Type: | Domain |
| Author: | Eddy SR |
| Number in seed: | 108 |
| Number in full: | 847 |
| Average length of the domain: | 119.30 aa |
| Average identity of full alignment: | 33 % |
| Average coverage of the sequence by the domain: | 78.61 % |
HMM information
| HMM build commands: |
build method: hmmbuild -o /dev/null HMM SEED
search method: hmmsearch -Z 23193494 -E 1000 --cpu 4 HMM pfamseq
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| Model details: |
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| Model length: | 124 | ||||||||||||
| Family (HMM) version: | 15 | ||||||||||||
| Download: | download the raw HMM for this family |
Species distribution
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Structures
For those sequences which have a structure in the Protein DataBank, we use the mapping between UniProt, PDB and Pfam coordinate systems from the PDBe group, to allow us to map Pfam domains onto UniProt sequences and three-dimensional protein structures. The table below shows the structures on which the RnaseA domain has been found. There are 473 instances of this domain found in the PDB. Note that there may be multiple copies of the domain in a single PDB structure, since many structures contain multiple copies of the same protein seqence.
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Archea
Eukaryota
Bacteria
Other sequences
Viruses
Unclassified
Viroids
Unclassified sequence