1a4y

Revision as of 16:49, 12 November 2007 by OCA (talk | contribs) (New page: left|200px<br /> <applet load="1a4y" size="450" color="white" frame="true" align="right" spinBox="true" caption="1a4y, resolution 2.0Å" /> '''RIBONUCLEASE INHIBIT...)
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RIBONUCLEASE INHIBITOR-ANGIOGENIN COMPLEX

File:1a4y.gif


1a4y, resolution 2.0Å

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OverviewOverview

Human placental RNase inhibitor (hRI), a leucine-rich repeat protein, binds the blood vessel-inducing protein human angiogenin (Ang) with, extraordinary affinity (Ki <1 fM). Here we report a 2.0 A resolution, crystal structure for the hRI-Ang complex that, together with extensive, mutagenesis data from earlier studies, reveals the molecular features of, this tight interaction. The hRI-Ang binding interface is large and, encompasses 26 residues from hRI and 24 from Ang, recruited from multiple, domains of both proteins. However, a substantial fraction of the, energetically important contacts involve only a single region of each: the, C-terminal segment 434-460 of hRI and the ribonucleolytic active centre of, Ang, most notably the catalytic residue Lys40. Although the overall, docking of Ang resembles that observed for RNase A in the crystal, structure of its complex with the porcine RNase inhibitor, the vast, majority of the interactions in the two complexes are distinctive, indicating that the broad specificity of the inhibitor for pancreatic, RNase superfamily proteins is based largely on its capacity to recognize, features unique to each of them. The implications of these findings for, the development of small, hRI-based inhibitors of Ang for therapeutic use, are discussed.

DiseaseDisease

Known diseases associated with this structure: Amyotrophic lateral sclerosis, susceptibility to OMIM:[105850], Creutzfeldt-Jakob disease OMIM:[176640], Gerstmann-Straussler disease OMIM:[176640], Huntington disease-like 1 OMIM:[176640], Insomnia, fatal familial OMIM:[176640], Prion disease with protracted course OMIM:[176640]

About this StructureAbout this Structure

1A4Y is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Molecular recognition of human angiogenin by placental ribonuclease inhibitor--an X-ray crystallographic study at 2.0 A resolution., Papageorgiou AC, Shapiro R, Acharya KR, EMBO J. 1997 Sep 1;16(17):5162-77. PMID:9311977

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