1w75

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 4: Line 4:
==Overview==
==Overview==
-
Bifunctional derivatives of the alkaloid galanthamine, designed to, interact with both the active site of the enzyme acetylcholinesterase, (AChE) and its peripheral cation binding site, have been assayed with, Torpedo californica AChE (TcAChE), and the three-dimensional structures of, their complexes with the enzyme have been solved by X-ray crystallography., Differences were noted between the IC(50) values obtained for TcAChE and, those for Electrophorus electricus AChE. These differences are ascribed to, sequence differences in one or two residues lining the active-site gorge, of the enzyme. The binding of one of the inhibitors disrupts the native, conformation of one wall of the gorge, formed by the loop Trp279-Phe290., It is proposed that flexibility of this loop may permit the binding of, inhibitors such as galanthamine, which are too bulky to penetrate the, narrow neck of the gorge formed by Tyr121 and Phe330 as seen in the, crystal structure.
+
Bifunctional derivatives of the alkaloid galanthamine, designed to interact with both the active site of the enzyme acetylcholinesterase (AChE) and its peripheral cation binding site, have been assayed with Torpedo californica AChE (TcAChE), and the three-dimensional structures of their complexes with the enzyme have been solved by X-ray crystallography. Differences were noted between the IC(50) values obtained for TcAChE and those for Electrophorus electricus AChE. These differences are ascribed to sequence differences in one or two residues lining the active-site gorge of the enzyme. The binding of one of the inhibitors disrupts the native conformation of one wall of the gorge, formed by the loop Trp279-Phe290. It is proposed that flexibility of this loop may permit the binding of inhibitors such as galanthamine, which are too bulky to penetrate the narrow neck of the gorge formed by Tyr121 and Phe330 as seen in the crystal structure.
==About this Structure==
==About this Structure==
Line 16: Line 16:
[[Category: Argaman, A.]]
[[Category: Argaman, A.]]
[[Category: Botti, S.]]
[[Category: Botti, S.]]
-
[[Category: Greenblatt, H.M.]]
+
[[Category: Greenblatt, H M.]]
[[Category: Silman, I.]]
[[Category: Silman, I.]]
-
[[Category: Sussman, J.L.]]
+
[[Category: Sussman, J L.]]
[[Category: NAG]]
[[Category: NAG]]
[[Category: alzheimer's disease]]
[[Category: alzheimer's disease]]
Line 33: Line 33:
[[Category: synapse]]
[[Category: synapse]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:20:08 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:41:10 2008''

Revision as of 13:41, 21 February 2008


1w75, resolution 2.400Å

Drag the structure with the mouse to rotate

NATIVE ORTHORHOMBIC FORM OF TORPEDO CALIFORNICA ACETYLCHOLINESTERASE (ACHE)

Overview

Bifunctional derivatives of the alkaloid galanthamine, designed to interact with both the active site of the enzyme acetylcholinesterase (AChE) and its peripheral cation binding site, have been assayed with Torpedo californica AChE (TcAChE), and the three-dimensional structures of their complexes with the enzyme have been solved by X-ray crystallography. Differences were noted between the IC(50) values obtained for TcAChE and those for Electrophorus electricus AChE. These differences are ascribed to sequence differences in one or two residues lining the active-site gorge of the enzyme. The binding of one of the inhibitors disrupts the native conformation of one wall of the gorge, formed by the loop Trp279-Phe290. It is proposed that flexibility of this loop may permit the binding of inhibitors such as galanthamine, which are too bulky to penetrate the narrow neck of the gorge formed by Tyr121 and Phe330 as seen in the crystal structure.

About this Structure

1W75 is a Single protein structure of sequence from Torpedo californica with as ligand. Active as Acetylcholinesterase, with EC number 3.1.1.7 Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

The complex of a bivalent derivative of galanthamine with torpedo acetylcholinesterase displays drastic deformation of the active-site gorge: implications for structure-based drug design., Greenblatt HM, Guillou C, Guenard D, Argaman A, Botti S, Badet B, Thal C, Silman I, Sussman JL, J Am Chem Soc. 2004 Dec 1;126(47):15405-11. PMID:15563167

Page seeded by OCA on Thu Feb 21 15:41:10 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools