2h43: Difference between revisions

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New page: left|200px<br /> <applet load="2h43" size="450" color="white" frame="true" align="right" spinBox="true" caption="2h43, resolution 2.7Å" /> '''Crystal Structure of...
 
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[[Image:2h43.gif|left|200px]]<br />
[[Image:2h43.gif|left|200px]]<br /><applet load="2h43" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2h43" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2h43, resolution 2.7&Aring;" />
caption="2h43, resolution 2.7&Aring;" />
'''Crystal Structure of Human Fragment D Complexed with Ala-His-Arg-Pro-amide'''<br />
'''Crystal Structure of Human Fragment D Complexed with Ala-His-Arg-Pro-amide'''<br />


==Overview==
==Overview==
The beta-chain amino-terminal sequences of all known mammalian fibrins, begin with the sequence Gly-His-Arg-Pro- (GHRP-), but the homologous, sequence in chicken fibrin begins with the sequence Ala-His-Arg-Pro-, (AHRP-). Nonetheless, chicken fibrinogen binds the synthetic peptide, GHRPam, and a previously reported crystal structure has revealed that the, binding is in exact conformance with that observed for the human, GHRPam-fragment D complex. We now report that human fibrinogen, which is, known not to bind APRP, binds the synthetic peptide AHRPam. Moreover, a, crystal structure of AHRPam complexed with fragment D from human, fibrinogen shows that AHRPam binds exclusively to the beta-chain hole and, unlike GHRPam, not at all to the homologous gamma-chain hole. The, difference can be attributed to the methyl group of the alanine residue, clashing with a critical carboxyl group in the gammaC hole but being, accommodated in the roomier betaC hole where the equivalent carboxyl is, situated more flexibly.
The beta-chain amino-terminal sequences of all known mammalian fibrins begin with the sequence Gly-His-Arg-Pro- (GHRP-), but the homologous sequence in chicken fibrin begins with the sequence Ala-His-Arg-Pro- (AHRP-). Nonetheless, chicken fibrinogen binds the synthetic peptide GHRPam, and a previously reported crystal structure has revealed that the binding is in exact conformance with that observed for the human GHRPam-fragment D complex. We now report that human fibrinogen, which is known not to bind APRP, binds the synthetic peptide AHRPam. Moreover, a crystal structure of AHRPam complexed with fragment D from human fibrinogen shows that AHRPam binds exclusively to the beta-chain hole and, unlike GHRPam, not at all to the homologous gamma-chain hole. The difference can be attributed to the methyl group of the alanine residue clashing with a critical carboxyl group in the gammaC hole but being accommodated in the roomier betaC hole where the equivalent carboxyl is situated more flexibly.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
2H43 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with CA and NH2 as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2H43 OCA].  
2H43 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=NH2:'>NH2</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2H43 OCA].  


==Reference==
==Reference==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Doolittle, R.F.]]
[[Category: Doolittle, R F.]]
[[Category: Pandi, L.]]
[[Category: Pandi, L.]]
[[Category: CA]]
[[Category: CA]]
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[[Category: knob-hole interaction]]
[[Category: knob-hole interaction]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 22:25:58 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:38:00 2008''