1evs

File:1evs.jpg

spinqualitylabelsall models PDB ID 1evs Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image
1evs, resolution 2.20Å ()
Structural annotation: Resources: CATH : 1Evsa00 InterPro : Ipr012351, Ipr001581, Ipr009079, Ipr003623 Pfam : PF01291 SCOP : d1evsa_ UniProt : P13725
Functional annotation: Cellular component: extracellular space extracellular region Biological process: tyrosine phosphorylation of Stat1 protein response to heat apoptosis multicellular organismal development negative regulation of cell proliferation cell proliferation immune response tyrosine phosphorylation of Stat3 protein peripheral nervous system development negative regulation of hormone secretion tyrosine phosphorylation of Stat5 protein cell-cell signaling behavioral response to pain regulation of cell growth Molecular function: oncostatin-M receptor binding cytokine activity
Resources:	FirstGlance, OCA, RCSB, PDBsum
Coordinates:	save as pdb, mmCIF, xml

CRYSTAL STRUCTURE OF HUMAN ONCOSTATIN M

OverviewOverview

BACKGROUND: The cytokine oncostatin M (OSM) inhibits growth of certain tumour-derived cells, induces proliferation in other cell types (e.g. haemangioblasts) and is a mediator of inflammatory responses. Its mechanism of action is via specific binding to gp130 and either the leukaemia inhibitory factor receptor (LIFR) or oncostatin M receptor (OSMR) systems at the cell surface to form an active signalling complex. RESULTS: We report here the crystal structure of human oncostatin M (hOSM) along with mutagenesis data which map the receptor-binding epitopes of the molecule. The structure was determined to a resolution of 2.2 A and conforms to the haematopoietin cytokine up-up-down-down four-helix bundle topology. The site 2 epitope, responsible for gp130 binding, is centred around Gly120 which forms a 'dimple' on the surface of the molecule located on helices A and C. The site 3 motif, responsible for LIFR and OSMR binding, consists of a protruding Phe160/Lys163 pair located at the start of helix D. CONCLUSIONS: The data presented allow functional dissection of the receptor-binding interfaces to atomic resolution. Modelling suggests that the gp130 residue Phe169 packs into the site 2 dimple in an analogous fashion to structurally equivalent residues at the growth hormone-growth hormone receptor interface, implying that certain key features may underlie recognition across the whole cytokine/receptor superfamily. Conversely, detailed comparison of the available structures suggests that variations on a common theme dictate the specificity of receptor-ligand interactions within the gp130 family of cytokines.

About this StructureAbout this Structure

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

ReferenceReference

Crystal structure and functional dissection of the cytostatic cytokine oncostatin M., Deller MC, Hudson KR, Ikemizu S, Bravo J, Jones EY, Heath JK, Structure. 2000 Aug 15;8(8):863-74. PMID:10997905 Page seeded by OCA on Fri May 2 15:34:37 2008