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1dny

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{{STRUCTURE_1dny| PDB=1dny | SCENE= }}
{{STRUCTURE_1dny| PDB=1dny | SCENE= }}
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'''SOLUTION STRUCTURE OF PCP, A PROTOTYPE FOR THE PEPTIDYL CARRIER DOMAINS OF MODULAR PEPTIDE SYNTHETASES'''
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===SOLUTION STRUCTURE OF PCP, A PROTOTYPE FOR THE PEPTIDYL CARRIER DOMAINS OF MODULAR PEPTIDE SYNTHETASES===
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==Overview==
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BACKGROUND: Nonribosomal peptide synthetases (NRPSs) are large modular enzymes responsible for the synthesis of a variety of microbial bioactive peptides. They consist of modules that each recognise and incorporate one specific amino acid into the peptide product. A module comprises several domains, which carry out the individual reaction steps. After activation by the adenylation domain, the amino acid substrate is covalently tethered to a 4'-phosphopantetheinyl cofactor of a peptidyl carrier domain (PCP) that passes the substrate to the reaction centres of the consecutive domains. RESULTS: The solution structure of PCP, a distinct peptidyl carrier protein derived from the equivalent domain of an NRPS, was solved using NMR techniques. PCP is a distorted four-helix bundle with an extended loop between the first two helices. Its overall fold resembles the topology of acyl carrier proteins (ACPs) from Escherichia coli fatty acid synthase and actinorhodin polyketide synthase from Streptomyces coelicolor; however, the surface polarity and the length and relative alignment of the helices are different. The conserved serine, which is the cofactor-binding site, has the same location as in the ACPs and is situated within a stretch of seven flexible residues. CONCLUSIONS: The structure of PCP reflects its character as a protein domain. The fold is well defined between residues 8 and 82 and the structural core of the PCP domain can now be defined as a region spanning 37 amino acids in both directions from the conserved serine. The flexibility of the post-translationally modified site might have implications for interactions with the cooperating proteins or NRPS domains.
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(as it appears on PubMed at http://www.pubmed.gov), where 10801488 is the PubMed ID number.
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{{ABSTRACT_PUBMED_10801488}}
==About this Structure==
==About this Structure==
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1DNY is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Brevibacillus_brevis Brevibacillus brevis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DNY OCA].
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1DNY is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Brevibacillus_brevis Brevibacillus brevis]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DNY OCA].
==Reference==
==Reference==
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[[Category: Modular peptide synthetase]]
[[Category: Modular peptide synthetase]]
[[Category: Nonribosomal peptide synthesis]]
[[Category: Nonribosomal peptide synthesis]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jun 30 23:21:16 2008''

Revision as of 20:21, 30 June 2008

Image:1dny.png

Template:STRUCTURE 1dny

SOLUTION STRUCTURE OF PCP, A PROTOTYPE FOR THE PEPTIDYL CARRIER DOMAINS OF MODULAR PEPTIDE SYNTHETASES

Template:ABSTRACT PUBMED 10801488

About this Structure

1DNY is a Single protein structure of sequence from Brevibacillus brevis. Full experimental information is available from OCA.

Reference

Solution structure of PCP, a prototype for the peptidyl carrier domains of modular peptide synthetases., Weber T, Baumgartner R, Renner C, Marahiel MA, Holak TA, Structure. 2000 Apr 15;8(4):407-18. PMID:10801488

Page seeded by OCA on Mon Jun 30 23:21:16 2008

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