1w14

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px <!-- The line below this paragraph, containing "STRUCTURE_1w14", creates the "Structure Box" on the page. You may change the PDB parameter (which sets the PD...)
Line 1: Line 1:
-
[[Image:1w14.jpg|left|200px]]
+
{{Seed}}
 +
[[Image:1w14.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1w14| PDB=1w14 | SCENE= }}
{{STRUCTURE_1w14| PDB=1w14 | SCENE= }}
-
'''UROKINASE TYPE PLASMINOGEN ACTIVATOR'''
+
===UROKINASE TYPE PLASMINOGEN ACTIVATOR===
-
==Overview==
+
<!--
-
Urokinase type plasminogen activator (uPA), a trypsin-like serine proteinase, plays an important role in normal tissue re-modelling, cell adhesion, and cell motility. In addition, studies utilizing normal animals and potent, selective uPA inhibitors or genetically modified mice that lack functional uPA genes have demonstrated that uPA can significantly enhance tumor initiation, growth, progression and metastasis, strongly suggesting that this enzyme may be a promising anti-cancer target. We have investigated the structure-activity relationship (SAR) of peptidomimetic inhibitors of uPA and solved high resolution X-ray structures of key, lead small molecule inhibitors (e.g. phenethylsulfonamidino(P4)-D-seryl(P3)-L-alanyl(P2)-L-argininal(P1) and derivatives thereof) in complex with the uPA proteinase domain. These potent inhibitors are highly selective for uPA. The non-natural D-seryl residue present at the P3 position in these inhibitors contributes substantially to both potency and selectivity because, due to its D-configuration, its side-chain binds in the S4 pocket to interact with the uPA unique residues Leu97b and His99. Additional potency and selectivity can be achieved by optimizing the inhibitor P4 residue to bind a pocket, known as S1sub or S1beta, that is adjacent to the primary specificity pocket of uPA.
+
The line below this paragraph, {{ABSTRACT_PUBMED_12684001}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 12684001 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_12684001}}
==About this Structure==
==About this Structure==
Line 27: Line 31:
[[Category: Plasminogen activator]]
[[Category: Plasminogen activator]]
[[Category: Urokinase]]
[[Category: Urokinase]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu May 22 21:30:31 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 14:23:57 2008''

Revision as of 11:24, 29 July 2008

Template:STRUCTURE 1w14

UROKINASE TYPE PLASMINOGEN ACTIVATOR

Template:ABSTRACT PUBMED 12684001

About this Structure

1W14 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Crystals of urokinase type plasminogen activator complexes reveal the binding mode of peptidomimetic inhibitors., Zeslawska E, Jacob U, Schweinitz A, Coombs G, Bode W, Madison E, J Mol Biol. 2003 Apr 18;328(1):109-18. PMID:12684001

Page seeded by OCA on Tue Jul 29 14:23:57 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools