1aap
From Proteopedia
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| - | [[Image:1aap.gif|left|200px]] | + | [[Image:1aap.gif|left|200px]] |
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| - | '''X-RAY CRYSTAL STRUCTURE OF THE PROTEASE INHIBITOR DOMAIN OF ALZHEIMER'S AMYLOID BETA-PROTEIN PRECURSOR''' | + | {{Structure |
| + | |PDB= 1aap |SIZE=350|CAPTION= <scene name='initialview01'>1aap</scene>, resolution 1.5Å | ||
| + | |SITE= | ||
| + | |LIGAND= | ||
| + | |ACTIVITY= | ||
| + | |GENE= | ||
| + | }} | ||
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| + | '''X-RAY CRYSTAL STRUCTURE OF THE PROTEASE INHIBITOR DOMAIN OF ALZHEIMER'S AMYLOID BETA-PROTEIN PRECURSOR''' | ||
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==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1AAP is a [ | + | 1AAP is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AAP OCA]. |
==Reference== | ==Reference== | ||
| - | X-ray crystal structure of the protease inhibitor domain of Alzheimer's amyloid beta-protein precursor., Hynes TR, Randal M, Kennedy LA, Eigenbrot C, Kossiakoff AA, Biochemistry. 1990 Oct 30;29(43):10018-22. PMID:[http:// | + | X-ray crystal structure of the protease inhibitor domain of Alzheimer's amyloid beta-protein precursor., Hynes TR, Randal M, Kennedy LA, Eigenbrot C, Kossiakoff AA, Biochemistry. 1990 Oct 30;29(43):10018-22. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/2125487 2125487] |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: proteinase inhibitor (trypsin)]] | [[Category: proteinase inhibitor (trypsin)]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 09:55:09 2008'' |
Revision as of 07:55, 20 March 2008
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X-RAY CRYSTAL STRUCTURE OF THE PROTEASE INHIBITOR DOMAIN OF ALZHEIMER'S AMYLOID BETA-PROTEIN PRECURSOR
Contents |
Overview
Alzheimer's amyloid beta-protein precursor contains a Kunitz protease inhibitor domain (APPI) potentially involved in proteolytic events leading to cerebral amyloid deposition. To facilitate the identification of the physiological target of the inhibitor, the crystal structure of APPI has been determined and refined to 1.5-A resolution. Sequences in the inhibitor-protease interface of the correct protease target will reflect the molecular details of the APPI structure. While the overall tertiary fold of APPI is very similar to that of the Kunitz inhibitor BPTI, a significant rearrangement occurs in the backbone conformation of one of the two protease binding loops. A number of Kunitz inhibitors have similar loop sequences, indicating the structural alteration is conserved and potentially an important determinant of inhibitor specificity. In a separate region of the protease binding loops, APPI side chains Met-17 and Phe-34 create an exposed hydrophobic surface in place of Arg-17 and Val-34 in BPTI. The restriction this change places on protease target sequences is seen when the structure of APPI is superimposed on BPTI complexed to serine proteases, where the hydrophobic surface of APPI faces a complementary group of nonpolar side chains on kallikrein A versus polar side chains on trypsin.
Disease
Known diseases associated with this structure: Alzheimer disease-1, APP-related OMIM:[104760], Amyloidosis, cerebroarterial, Dutch type OMIM:[104760], Amyloidosis, cerebroarterial, Iowa type OMIM:[104760], Blood group, P system OMIM:[607922]
About this Structure
1AAP is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
X-ray crystal structure of the protease inhibitor domain of Alzheimer's amyloid beta-protein precursor., Hynes TR, Randal M, Kennedy LA, Eigenbrot C, Kossiakoff AA, Biochemistry. 1990 Oct 30;29(43):10018-22. PMID:2125487
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