1aap

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
[[Image:1aap.gif|left|200px]]
[[Image:1aap.gif|left|200px]]
-
{{Structure
+
<!--
-
|PDB= 1aap |SIZE=350|CAPTION= <scene name='initialview01'>1aap</scene>, resolution 1.5&Aring;
+
The line below this paragraph, containing "STRUCTURE_1aap", creates the "Structure Box" on the page.
-
|SITE=
+
You may change the PDB parameter (which sets the PDB file loaded into the applet)
-
|LIGAND=
+
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
-
|ACTIVITY=
+
or leave the SCENE parameter empty for the default display.
-
|GENE=
+
-->
-
|DOMAIN=
+
{{STRUCTURE_1aap| PDB=1aap | SCENE= }}
-
|RELATEDENTRY=
+
-
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1aap FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1aap OCA], [http://www.ebi.ac.uk/pdbsum/1aap PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1aap RCSB]</span>
+
-
}}
+
'''X-RAY CRYSTAL STRUCTURE OF THE PROTEASE INHIBITOR DOMAIN OF ALZHEIMER'S AMYLOID BETA-PROTEIN PRECURSOR'''
'''X-RAY CRYSTAL STRUCTURE OF THE PROTEASE INHIBITOR DOMAIN OF ALZHEIMER'S AMYLOID BETA-PROTEIN PRECURSOR'''
Line 30: Line 27:
[[Category: Kossiakoff, A A.]]
[[Category: Kossiakoff, A A.]]
[[Category: Randal, M.]]
[[Category: Randal, M.]]
-
[[Category: proteinase inhibitor (trypsin)]]
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 10:03:11 2008''
-
 
+
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 18:36:37 2008''
+

Revision as of 07:03, 2 May 2008

Template:STRUCTURE 1aap

X-RAY CRYSTAL STRUCTURE OF THE PROTEASE INHIBITOR DOMAIN OF ALZHEIMER'S AMYLOID BETA-PROTEIN PRECURSOR


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.

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 Page seeded by OCA on Fri May 2 10:03:11 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools