1dmk

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="1dmk" size="450" color="white" frame="true" align="right" spinBox="true" caption="1dmk, resolution 1.90&Aring;" /> '''BOVINE ENDOTHELIAL N...)
Line 1: Line 1:
-
[[Image:1dmk.gif|left|200px]]<br /><applet load="1dmk" size="450" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1dmk.gif|left|200px]]<br /><applet load="1dmk" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1dmk, resolution 1.90&Aring;" />
caption="1dmk, resolution 1.90&Aring;" />
'''BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-AMINO-6-PHENYL-TETRAHYDROPTERIDINE'''<br />
'''BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-AMINO-6-PHENYL-TETRAHYDROPTERIDINE'''<br />
==Overview==
==Overview==
-
Pathological nitric oxide (NO) generation in sepsis, inflammation, and, stroke may be therapeutically controlled by inhibiting NO synthases (NOS)., Here we targeted the (6R)-5,6,7,8-tetrahydro-l-biopterin (H(4)Bip)-binding, site of NOS, which, upon cofactor binding, maximally increases enzyme, activity and NO production from substrate l-arginine. The first generation, of H(4)Bip-based NOS inhibitors employed a 4-amino pharmacophore of, H(4)Bip analogous to antifolates such as methotrexate. We developed a, novel series of 4-oxo-pteridine derivatives that were screened for, inhibition against neuronal NOS (NOS-I) and a structure-activity, relationship was determined. To understand the structural basis for pterin, antagonism, selected derivatives were docked into the NOS pterin binding, cavity. Using a reduced 4-oxo-pteridine scaffold, derivatives with certain, modifications such as electron-rich aromatic phenyl or benzoyl groups at, the 5- and 6-positions, were discovered to markedly inhibit NOS-I, possibly due to hydrophobic and electrostatic interactions with Phe(462), and Ser(104), respectively, within the pterin binding pocket. One of the, most effective 4-oxo compounds and, for comparisons an active 4-amino, derivative, were then co-crystallized with the endothelial NOS (NOS-III), oxygenase domain and this structure solved to confirm the hypothetical, binding modes. Collectively, these findings suggest (i) that, unlike the, antifolate principle, the 4-amino substituent is not essential for, developing pterin-based NOS inhibitors and (ii), provide a steric and, electrostatic basis for their rational design.
+
Pathological nitric oxide (NO) generation in sepsis, inflammation, and stroke may be therapeutically controlled by inhibiting NO synthases (NOS). Here we targeted the (6R)-5,6,7,8-tetrahydro-l-biopterin (H(4)Bip)-binding site of NOS, which, upon cofactor binding, maximally increases enzyme activity and NO production from substrate l-arginine. The first generation of H(4)Bip-based NOS inhibitors employed a 4-amino pharmacophore of H(4)Bip analogous to antifolates such as methotrexate. We developed a novel series of 4-oxo-pteridine derivatives that were screened for inhibition against neuronal NOS (NOS-I) and a structure-activity relationship was determined. To understand the structural basis for pterin antagonism, selected derivatives were docked into the NOS pterin binding cavity. Using a reduced 4-oxo-pteridine scaffold, derivatives with certain modifications such as electron-rich aromatic phenyl or benzoyl groups at the 5- and 6-positions, were discovered to markedly inhibit NOS-I, possibly due to hydrophobic and electrostatic interactions with Phe(462) and Ser(104), respectively, within the pterin binding pocket. One of the most effective 4-oxo compounds and, for comparisons an active 4-amino derivative, were then co-crystallized with the endothelial NOS (NOS-III) oxygenase domain and this structure solved to confirm the hypothetical binding modes. Collectively, these findings suggest (i) that, unlike the antifolate principle, the 4-amino substituent is not essential for developing pterin-based NOS inhibitors and (ii), provide a steric and electrostatic basis for their rational design.
==About this Structure==
==About this Structure==
-
1DMK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with ACT, CAC, ZN, HEM, AP6 and ITU as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Nitric-oxide_synthase Nitric-oxide synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.14.13.39 1.14.13.39] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1DMK OCA].
+
1DMK is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] with <scene name='pdbligand=ACT:'>ACT</scene>, <scene name='pdbligand=CAC:'>CAC</scene>, <scene name='pdbligand=ZN:'>ZN</scene>, <scene name='pdbligand=HEM:'>HEM</scene>, <scene name='pdbligand=AP6:'>AP6</scene> and <scene name='pdbligand=ITU:'>ITU</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Nitric-oxide_synthase Nitric-oxide synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.14.13.39 1.14.13.39] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DMK OCA].
==Reference==
==Reference==
Line 16: Line 16:
[[Category: Al-Masoudi, N.]]
[[Category: Al-Masoudi, N.]]
[[Category: Berg, M.]]
[[Category: Berg, M.]]
-
[[Category: Frohlich, L.G.]]
+
[[Category: Frohlich, L G.]]
[[Category: Gerwig, R.]]
[[Category: Gerwig, R.]]
[[Category: Groehn, V.]]
[[Category: Groehn, V.]]
Line 23: Line 23:
[[Category: Li, H.]]
[[Category: Li, H.]]
[[Category: Martasek, P.]]
[[Category: Martasek, P.]]
-
[[Category: Masters, B.S.]]
+
[[Category: Masters, B S.]]
[[Category: Matter, H.]]
[[Category: Matter, H.]]
[[Category: Mohr, D.]]
[[Category: Mohr, D.]]
Line 29: Line 29:
[[Category: Pfleiderer, W.]]
[[Category: Pfleiderer, W.]]
[[Category: Poulos, T.]]
[[Category: Poulos, T.]]
-
[[Category: Raman, C.S.]]
+
[[Category: Raman, C S.]]
-
[[Category: Schmidt, H.H.]]
+
[[Category: Schmidt, H H.]]
[[Category: Schnabel, J.]]
[[Category: Schnabel, J.]]
[[Category: Strobel, H.]]
[[Category: Strobel, H.]]
Line 42: Line 42:
[[Category: alpha-beta fold]]
[[Category: alpha-beta fold]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 13:24:50 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:18:11 2008''

Revision as of 10:18, 21 February 2008


1dmk, resolution 1.90Å

Drag the structure with the mouse to rotate

BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-AMINO-6-PHENYL-TETRAHYDROPTERIDINE

Overview

Pathological nitric oxide (NO) generation in sepsis, inflammation, and stroke may be therapeutically controlled by inhibiting NO synthases (NOS). Here we targeted the (6R)-5,6,7,8-tetrahydro-l-biopterin (H(4)Bip)-binding site of NOS, which, upon cofactor binding, maximally increases enzyme activity and NO production from substrate l-arginine. The first generation of H(4)Bip-based NOS inhibitors employed a 4-amino pharmacophore of H(4)Bip analogous to antifolates such as methotrexate. We developed a novel series of 4-oxo-pteridine derivatives that were screened for inhibition against neuronal NOS (NOS-I) and a structure-activity relationship was determined. To understand the structural basis for pterin antagonism, selected derivatives were docked into the NOS pterin binding cavity. Using a reduced 4-oxo-pteridine scaffold, derivatives with certain modifications such as electron-rich aromatic phenyl or benzoyl groups at the 5- and 6-positions, were discovered to markedly inhibit NOS-I, possibly due to hydrophobic and electrostatic interactions with Phe(462) and Ser(104), respectively, within the pterin binding pocket. One of the most effective 4-oxo compounds and, for comparisons an active 4-amino derivative, were then co-crystallized with the endothelial NOS (NOS-III) oxygenase domain and this structure solved to confirm the hypothetical binding modes. Collectively, these findings suggest (i) that, unlike the antifolate principle, the 4-amino substituent is not essential for developing pterin-based NOS inhibitors and (ii), provide a steric and electrostatic basis for their rational design.

About this Structure

1DMK is a Single protein structure of sequence from Bos taurus with , , , , and as ligands. Active as Nitric-oxide synthase, with EC number 1.14.13.39 Full crystallographic information is available from OCA.

Reference

Structural basis for pterin antagonism in nitric-oxide synthase. Development of novel 4-oxo-pteridine antagonists of (6R)-5,6,7,8-tetrahydrobiopterin., Kotsonis P, Frohlich LG, Raman CS, Li H, Berg M, Gerwig R, Groehn V, Kang Y, Al-Masoudi N, Taghavi-Moghadam S, Mohr D, Munch U, Schnabel J, Martasek P, Masters BS, Strobel H, Poulos T, Matter H, Pfleiderer W, Schmidt HH, J Biol Chem. 2001 Dec 28;276(52):49133-41. Epub 2001 Oct 5. PMID:11590164

Page seeded by OCA on Thu Feb 21 12:18:11 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools