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New page: left|200px<br /><applet load="1g6h" size="450" color="white" frame="true" align="right" spinBox="true" caption="1g6h, resolution 1.60Å" /> '''CRYSTAL STRUCTURE OF...
 
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[[Image:1g6h.gif|left|200px]]<br /><applet load="1g6h" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1g6h.gif|left|200px]]<br /><applet load="1g6h" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1g6h, resolution 1.60&Aring;" />
caption="1g6h, resolution 1.60&Aring;" />
'''CRYSTAL STRUCTURE OF THE ADP CONFORMATION OF MJ1267, AN ATP-BINDING CASSETTE OF AN ABC TRANSPORTER'''<br />
'''CRYSTAL STRUCTURE OF THE ADP CONFORMATION OF MJ1267, AN ATP-BINDING CASSETTE OF AN ABC TRANSPORTER'''<br />


==Overview==
==Overview==
BACKGROUND: ATP binding cassette (ABC) transporters are ubiquitously, distributed transmembrane solute pumps that play a causative role in, numerous diseases. Previous structures have defined the fold of the ABC, and established the flexibility of its alpha-helical subdomain. But the, nature of the mechanical changes that occur at each step of the chemical, ATPase cycle have not been defined. RESULTS: Crystal structures were, determined of the MJ1267 ABC from Methanococcus jannaschii in Mg-ADP-bound, and nucleotide-free forms. Comparison of these structures reveals an, induced-fit effect at the active site likely to be a consequence of, nucleotide binding. In the Mg-ADP-bound structure, the loop following the, Walker B moves toward the Walker A (P-loop) coupled to backbone, conformational changes in the intervening "H-loop", which contains an, invariant histidine. These changes affect the region believed to mediate, intercassette interaction in the ABC transporter complex. Comparison of, the Mg-ADP-bound structure of MJ1267 to the ATP-bound structure of HisP, suggests that an outward rotation of the alpha-helical subdomain is, coupled to the loss of a molecular contact between the gamma-phosphate of, ATP and an invariant glutamine in a segment connecting this subdomain to, the core of the cassette. CONCLUSIONS: The induced-fit effect and rotation, of the alpha-helical subdomain may play a role in controlling the, nucleotide-dependent change in cassette-cassette interaction affinity, believed to represent the power-stroke of ABC transporters. Outward, rotation of the alpha-helical subdomain also likely facilitates Mg-ADP, release after hydrolysis. The MJ1267 structures therefore define features, of the nucleotide-dependent conformational changes that drive, transmembrane transport in ABC transporters.
BACKGROUND: ATP binding cassette (ABC) transporters are ubiquitously distributed transmembrane solute pumps that play a causative role in numerous diseases. Previous structures have defined the fold of the ABC and established the flexibility of its alpha-helical subdomain. But the nature of the mechanical changes that occur at each step of the chemical ATPase cycle have not been defined. RESULTS: Crystal structures were determined of the MJ1267 ABC from Methanococcus jannaschii in Mg-ADP-bound and nucleotide-free forms. Comparison of these structures reveals an induced-fit effect at the active site likely to be a consequence of nucleotide binding. In the Mg-ADP-bound structure, the loop following the Walker B moves toward the Walker A (P-loop) coupled to backbone conformational changes in the intervening "H-loop", which contains an invariant histidine. These changes affect the region believed to mediate intercassette interaction in the ABC transporter complex. Comparison of the Mg-ADP-bound structure of MJ1267 to the ATP-bound structure of HisP suggests that an outward rotation of the alpha-helical subdomain is coupled to the loss of a molecular contact between the gamma-phosphate of ATP and an invariant glutamine in a segment connecting this subdomain to the core of the cassette. CONCLUSIONS: The induced-fit effect and rotation of the alpha-helical subdomain may play a role in controlling the nucleotide-dependent change in cassette-cassette interaction affinity believed to represent the power-stroke of ABC transporters. Outward rotation of the alpha-helical subdomain also likely facilitates Mg-ADP release after hydrolysis. The MJ1267 structures therefore define features of the nucleotide-dependent conformational changes that drive transmembrane transport in ABC transporters.


==About this Structure==
==About this Structure==
1G6H is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Methanocaldococcus_jannaschii Methanocaldococcus jannaschii] with MG, MMC and ADP as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1G6H OCA].  
1G6H is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Methanocaldococcus_jannaschii Methanocaldococcus jannaschii] with <scene name='pdbligand=MG:'>MG</scene>, <scene name='pdbligand=MMC:'>MMC</scene> and <scene name='pdbligand=ADP:'>ADP</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1G6H OCA].  


==Reference==
==Reference==
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[[Category: Methanocaldococcus jannaschii]]
[[Category: Methanocaldococcus jannaschii]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Hunt, J.F.]]
[[Category: Hunt, J F.]]
[[Category: Karpowich, N.]]
[[Category: Karpowich, N.]]
[[Category: Martsinkevich, O.]]
[[Category: Martsinkevich, O.]]
[[Category: Millen, L.]]
[[Category: Millen, L.]]
[[Category: Thomas, P.J.]]
[[Category: Thomas, P J.]]
[[Category: Yuan, Y.R.]]
[[Category: Yuan, Y R.]]
[[Category: ADP]]
[[Category: ADP]]
[[Category: MG]]
[[Category: MG]]
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[[Category: beta-core domain]]
[[Category: beta-core domain]]


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