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Resource:PRECISE: Predicted and Consensus Interaction Sites in Enzymes

Name: Resource:PRECISE: Predicted and Consensus Interaction Sites in Enzymes
Description:

PRECISE (Predicted and Consensus Interaction Sites in Enzymes) is a database of interactions between the amino acid residues of an enzyme and its ligands. It provides a summary of interactions between the amino acid residues of an enzyme and its various ligands (substrate and transition state analogues, cofactors, inhibitors, and products). In the current version this information is extracted from the enzyme-ligand complexes in the PDB by performing a number of steps as follows.
1. Clustering homologous enzyme chains. Although enzymes with the same EC number have the same function, they may substantially differ in terms of sequence and/or structure. Since consensus binding sites can be defined only for enzymes with appropriate overlap of their sequences and structures, we have clustered the enzymes in the PDB such that in each cluster the proteins have the same EC number, and all chains are sequence-similar, with a BLAST p-value of 10e-40. The clusters are based on chains rather than the entire protein, since enzymes may have chains of different functions and/or non-homologous chains.
2. Selecting a representative for each homologous cluster. The chains within a sequence-similar cluster thus derived are automatically ranked according to the precision and completeness of their structural data. The measures of the structural quality are adopted from the NCBIs Non-Redundant PDB Chain Set (nrpdb).
3. Selecting ligand type. If the PDB file contains a ligand, it is classified as (a) peptide, (b) nucleotide, (c) metal ion, or (d) other.
4. Calculation of hydrogen bonds and non-bonded interactions. The receptor-ligand interactions are determined using the program HBPLUS by Thornton and coworkers. The results are later parsed and extracted into residue-based formats, giving separate files for each residue that is interacting with the ligand.
5. Summing all interactions within a cluster for the aligned residues. The number of hits, or interactions, for a given residue is calculated automatically throughout the entire cluster. Again, the hits are atom based; two interacting residue can have a hit greater than one if several atoms are involved in the interaction.
6. Final output. If there are non-homologues chains present in the query pdb, a subsequent page will let users to specify which chain to show. The output page will show the sequence of the representative of the cluster along with different color codes for each residue representing the number of hits. Optional filtersallow users to restrict the output to (a) selected chains in the cluster (b) non-bonded or hydrogen bonding interactions; and (c) selected ligand types.

Sponsors: This material is based upon work supported by the National Science Foundation under Grant No.DBI-0213832.
Other Name(s): PRECISE
Resource Type(s): web accessible database
Keywords: enzyme, enzyme and enzyme nomenclature databases, function, align, amino acid, analogue, atom, chain, cofactor, complex, hydrogen bond, inhibitor, interaction, ligand, product, residue, sequence, structure, substrate, transition state
Resource: Resource
URL: http://precise.bu.edu/precisedb/
Id: nif-0000-21331
Link to OWL / RDF: Download this content as OWL/RDF

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Akash, Ccdbuser, Nifbot2, Zaidaziz



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Facts about Resource:PRECISE: Predicted and Consensus Interaction Sites in EnzymesRDF feed
CurationStatusuncurated  +
DefiningCitationhttp://precise.bu.edu/precisedb/  +
Definition

PRECISE (Predicted and Consensus I
PRECISE (Predicted and Consensus Interaction Sites in Enzymes) is a database of interactions between the amino acid residues of an enzyme and its ligands. It provides a summary of interactions between the amino acid residues of an enzyme and its various ligands (substrate and transition state analogues, cofactors, inhibitors, and products). In the current version this information is extracted from the enzyme-ligand complexes in the PDB by performing a number of steps as follows.
1. Clustering homologous enzyme chains. Although enzymes with the same EC number have the same function, they may substantially differ in terms of sequence and/or structure. Since consensus binding sites can be defined only for enzymes with appropriate overlap of their sequences and structures, we have clustered the enzymes in the PDB such that in each cluster the proteins have the same EC number, and all chains are sequence-similar, with a BLAST p-value of 10e-40. The clusters are based on chains rather than the entire protein, since enzymes may have chains of different functions and/or non-homologous chains.
2. Selecting a representative for each homologous cluster. The chains within a sequence-similar cluster thus derived are automatically ranked according to the precision and completeness of their structural data. The measures of the structural quality are adopted from the NCBIs Non-Redundant PDB Chain Set (nrpdb).
3. Selecting ligand type. If the PDB file contains a ligand, it is classified as (a) peptide, (b) nucleotide, (c) metal ion, or (d) other.
4. Calculation of hydrogen bonds and non-bonded interactions. The receptor-ligand interactions are determined using the program HBPLUS by Thornton and coworkers. The results are later parsed and extracted into residue-based formats, giving separate files for each residue that is interacting with the ligand.
5. Summing all interactions within a cluster for the aligned residues. The number of hits, or interactions, for a given residue is calculated automatically throughout the entire cluster. Again, the hits are atom based; two interacting residue can have a hit greater than one if several atoms are involved in the interaction.
6. Final output. If there are non-homologues chains present in the query pdb, a subsequent page will let users to specify which chain to show. The output page will show the sequence of the representative of the cluster along with different color codes for each residue representing the number of hits. Optional filtersallow users to restrict the output to (a) selected chains in the cluster (b) non-bonded or hydrogen bonding interactions; and (c) selected ligand types.

Sponsors: This material is based upon work supported by the National Science Foundation under Grant No.DBI-0213832.
undation under Grant No.DBI-0213832.
Has default formThis property is a special property in this wiki.Resource  +
Has roleWeb accessible database  +
Idnif-0000-21331  +
KeywordsEnzyme  +, Enzyme and enzyme nomenclature databases  +, Function  +, Align  +, Amino acid  +, Analogue  +, Atom  +, Chain  +, Cofactor  +, Complex  +, Hydrogen bond  +, Inhibitor  +, Interaction  +, Ligand  +, Product  +, Residue  +, Sequence  +, Structure  +, Substrate  +, and Transition state  +
LabelResource:PRECISE: Predicted and Consensus Interaction Sites in Enzymes  +
ModifiedDate18 May 2011  +
Page has default formThis property is a special property in this wiki.Resource  +
SuperCategoryResource  +
SynonymPRECISE  +