1u53

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="1u53" size="450" color="white" frame="true" align="right" spinBox="true" caption="1u53, resolution 1.56&Aring;" /> '''Novel X-Ray Structur...)
Line 1: Line 1:
-
[[Image:1u53.gif|left|200px]]<br /><applet load="1u53" size="450" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1u53.gif|left|200px]]<br /><applet load="1u53" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1u53, resolution 1.56&Aring;" />
caption="1u53, resolution 1.56&Aring;" />
'''Novel X-Ray Structure of Na-ASP-2, a PR-1 protein from the nematode parasite Necator americanus and a vaccine antigen for human hookworm infection'''<br />
'''Novel X-Ray Structure of Na-ASP-2, a PR-1 protein from the nematode parasite Necator americanus and a vaccine antigen for human hookworm infection'''<br />
==Overview==
==Overview==
-
Human hookworm infection is a major cause of anemia and malnutrition of, adults and children in the developing world. As part of on-going efforts, to control hookworm infection, The Human Hookworm Vaccine Initiative has, identified candidate vaccine antigens from the infective L3 larval stages, of the parasite, including a family of pathogenesis-related (PR) proteins, known as the Ancylostoma-secreted proteins (ASPs). A novel crystal, structure of Na-ASP-2, a PR-1 protein secreted by infective larvae of the, human hookworm Necator americanus, has been solved to resolution limits of, 1.68 A and to an R-factor of 17% using the recombinant protein expressed, in and secreted by Pichia pastoris. The overall fold of Na-ASP-2 is a, three-layer alphabetaalpha sandwich flanked by an N-terminal loop and a, short, cysteine-rich C terminus. Our structure reveals a large central, cavity that is flanked by His129 and Glu106, two residues that are well, conserved in all parasitic nematode L3 ASPs. Na-ASP-2 has structural and, charge similarities to chemokines, which suggests that Na-ASP-2 may be an, extra-cellular ligand of an unknown receptor. Na-ASP-2 is a useful, homology model for NIF, a natural antagonistic ligand of CR3 receptor., From these modeling studies, possible binding modes were predicted. In, addition, this first structure of a PR-1 protein from parasitic helminths, may shed light on the molecular basis of host-parasite interactions.
+
Human hookworm infection is a major cause of anemia and malnutrition of adults and children in the developing world. As part of on-going efforts to control hookworm infection, The Human Hookworm Vaccine Initiative has identified candidate vaccine antigens from the infective L3 larval stages of the parasite, including a family of pathogenesis-related (PR) proteins known as the Ancylostoma-secreted proteins (ASPs). A novel crystal structure of Na-ASP-2, a PR-1 protein secreted by infective larvae of the human hookworm Necator americanus, has been solved to resolution limits of 1.68 A and to an R-factor of 17% using the recombinant protein expressed in and secreted by Pichia pastoris. The overall fold of Na-ASP-2 is a three-layer alphabetaalpha sandwich flanked by an N-terminal loop and a short, cysteine-rich C terminus. Our structure reveals a large central cavity that is flanked by His129 and Glu106, two residues that are well conserved in all parasitic nematode L3 ASPs. Na-ASP-2 has structural and charge similarities to chemokines, which suggests that Na-ASP-2 may be an extra-cellular ligand of an unknown receptor. Na-ASP-2 is a useful homology model for NIF, a natural antagonistic ligand of CR3 receptor. From these modeling studies, possible binding modes were predicted. In addition, this first structure of a PR-1 protein from parasitic helminths may shed light on the molecular basis of host-parasite interactions.
==About this Structure==
==About this Structure==
-
1U53 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Necator_americanus Necator americanus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1U53 OCA].
+
1U53 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Necator_americanus Necator americanus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1U53 OCA].
==Reference==
==Reference==
Line 13: Line 13:
[[Category: Necator americanus]]
[[Category: Necator americanus]]
[[Category: Single protein]]
[[Category: Single protein]]
-
[[Category: Asojo, O.A.]]
+
[[Category: Asojo, O A.]]
-
[[Category: Borgstahl, G.E.O.]]
+
[[Category: Borgstahl, G E.O.]]
[[Category: Deumic, V.]]
[[Category: Deumic, V.]]
[[Category: Dhar, K.]]
[[Category: Dhar, K.]]
[[Category: Goud, G.]]
[[Category: Goud, G.]]
-
[[Category: Hotez, P.J.]]
+
[[Category: Hotez, P J.]]
[[Category: Liu, S.]]
[[Category: Liu, S.]]
[[Category: Loukas, A.]]
[[Category: Loukas, A.]]
Line 24: Line 24:
[[Category: antibiotic]]
[[Category: antibiotic]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 03:19:23 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:20:37 2008''

Revision as of 13:20, 21 February 2008


1u53, resolution 1.56Å

Drag the structure with the mouse to rotate

Novel X-Ray Structure of Na-ASP-2, a PR-1 protein from the nematode parasite Necator americanus and a vaccine antigen for human hookworm infection

Overview

Human hookworm infection is a major cause of anemia and malnutrition of adults and children in the developing world. As part of on-going efforts to control hookworm infection, The Human Hookworm Vaccine Initiative has identified candidate vaccine antigens from the infective L3 larval stages of the parasite, including a family of pathogenesis-related (PR) proteins known as the Ancylostoma-secreted proteins (ASPs). A novel crystal structure of Na-ASP-2, a PR-1 protein secreted by infective larvae of the human hookworm Necator americanus, has been solved to resolution limits of 1.68 A and to an R-factor of 17% using the recombinant protein expressed in and secreted by Pichia pastoris. The overall fold of Na-ASP-2 is a three-layer alphabetaalpha sandwich flanked by an N-terminal loop and a short, cysteine-rich C terminus. Our structure reveals a large central cavity that is flanked by His129 and Glu106, two residues that are well conserved in all parasitic nematode L3 ASPs. Na-ASP-2 has structural and charge similarities to chemokines, which suggests that Na-ASP-2 may be an extra-cellular ligand of an unknown receptor. Na-ASP-2 is a useful homology model for NIF, a natural antagonistic ligand of CR3 receptor. From these modeling studies, possible binding modes were predicted. In addition, this first structure of a PR-1 protein from parasitic helminths may shed light on the molecular basis of host-parasite interactions.

About this Structure

1U53 is a Single protein structure of sequence from Necator americanus. Full crystallographic information is available from OCA.

Reference

X-ray structure of Na-ASP-2, a pathogenesis-related-1 protein from the nematode parasite, Necator americanus, and a vaccine antigen for human hookworm infection., Asojo OA, Goud G, Dhar K, Loukas A, Zhan B, Deumic V, Liu S, Borgstahl GE, Hotez PJ, J Mol Biol. 2005 Feb 25;346(3):801-14. Epub 2005 Jan 12. PMID:15713464

Page seeded by OCA on Thu Feb 21 15:20:37 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools