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| - | [[Image:1m4j.jpg|left|200px]] | + | {{Seed}} |
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| | {{STRUCTURE_1m4j| PDB=1m4j | SCENE= }} | | {{STRUCTURE_1m4j| PDB=1m4j | SCENE= }} |
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| - | '''CRYSTAL STRUCTURE OF THE N-TERMINAL ADF-H DOMAIN OF MOUSE TWINFILIN ISOFORM-1'''
| + | ===CRYSTAL STRUCTURE OF THE N-TERMINAL ADF-H DOMAIN OF MOUSE TWINFILIN ISOFORM-1=== |
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| - | ==Overview==
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| - | Twinfilin is an evolutionarily conserved actin monomer-binding protein that regulates cytoskeletal dynamics in organisms from yeast to mammals. It is composed of two actin-depolymerization factor homology (ADF-H) domains that show approximately 20% sequence identity to ADF/cofilin proteins. In contrast to ADF/cofilins, which bind both G-actin and F-actin and promote filament depolymerization, twinfilin interacts only with G-actin. To elucidate the molecular mechanisms of twinfilin-actin monomer interaction, we determined the crystal structure of the N-terminal ADF-H domain of twinfilin and mapped its actin-binding site by site-directed mutagenesis. This domain has similar overall structure to ADF/cofilins, and the regions important for actin monomer binding in ADF/cofilins are especially well conserved in twinfilin. Mutagenesis studies show that the N-terminal ADF-H domain of twinfilin and ADF/cofilins also interact with actin monomers through similar interfaces, although the binding surface is slightly extended in twinfilin. In contrast, the regions important for actin-filament interactions in ADF/cofilins are structurally different in twinfilin. This explains the differences in actin-interactions (monomer versus filament binding) between twinfilin and ADF/cofilins. Taken together, our data show that the ADF-H domain is a structurally conserved actin-binding motif and that relatively small structural differences at the actin interfaces of this domain are responsible for the functional variation between the different classes of ADF-H domain proteins.
| + | The line below this paragraph, {{ABSTRACT_PUBMED_12207032}}, adds the Publication Abstract to the page |
| | + | (as it appears on PubMed at http://www.pubmed.gov), where 12207032 is the PubMed ID number. |
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| | + | {{ABSTRACT_PUBMED_12207032}} |
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| | ==About this Structure== | | ==About this Structure== |
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| | [[Category: Mixed beta-sheet]] | | [[Category: Mixed beta-sheet]] |
| | [[Category: Pair of alpha-helice]] | | [[Category: Pair of alpha-helice]] |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 00:37:13 2008'' | + | |
| | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 2 23:11:41 2008'' |
Revision as of 20:11, 2 July 2008
Template:STRUCTURE 1m4j
CRYSTAL STRUCTURE OF THE N-TERMINAL ADF-H DOMAIN OF MOUSE TWINFILIN ISOFORM-1
Template:ABSTRACT PUBMED 12207032
About this Structure
1M4J is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.
Reference
Structural conservation between the actin monomer-binding sites of twinfilin and actin-depolymerizing factor (ADF)/cofilin., Paavilainen VO, Merckel MC, Falck S, Ojala PJ, Pohl E, Wilmanns M, Lappalainen P, J Biol Chem. 2002 Nov 8;277(45):43089-95. Epub 2002 Aug 30. PMID:12207032
Page seeded by OCA on Wed Jul 2 23:11:41 2008
