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2OL2

High Resolution Structure of Native PCI in Space Group P21

Summary for 2OL2
Entry DOI10.2210/pdb2ol2/pdb
Related1LQ8 2HI9
DescriptorPlasma serine protease inhibitor, GLYCEROL (3 entities in total)
Functional Keywordsserpin, hydrolase inhibitor
Biological sourceHomo sapiens (human)
Cellular locationSecreted: P05154
Total number of polymer chains2
Total formula weight89151.45
Authors
Li, W.,Huntington, J.A. (deposition date: 2007-01-18, release date: 2007-03-13, Last modification date: 2023-08-30)
Primary citationLi, W.,Adams, T.E.,Kjellberg, M.,Stenflo, J.,Huntington, J.A.
Structure of native protein C inhibitor provides insight into its multiple functions.
J.Biol.Chem., 282:13759-13768, 2007
Cited by
PubMed Abstract: Protein C inhibitor (PCI) is a multifunctional serpin with wide ranging protease inhibitory functions, unique cofactor binding activities, and potential non-inhibitory functions akin to the hormone-transporting serpins. To gain insight into the molecular mechanisms utilized by PCI we developed a robust expression system in Escherichia coli and solved the crystal structure of PCI in its native state. The five monomers obtained from our two crystal forms provide an NMR-like ensemble revealing regions of inherent flexibility. The reactive center loop (RCL) of PCI is long and highly flexible with no evidence of hinge region incorporation into beta-sheet A, as seen for other heparin-binding serpins. We adapted an extrinsic fluorescence method for determining dissociation constants for heparin and find that the N-terminal tail of PCI and residues adjacent to helix H are not involved in heparin binding. The minimal heparin length capable of tight binding to PCI was determined to be chains of eight monosaccharide units. A large hydrophobic pocket occupied by hydrophobic crystal contacts was found in an analogous position to the hormone-binding site in thyroxine-binding globulin. In conclusion, the data presented here provide important insights into the mechanisms by which PCI exercises its multiple inhibitory and non-inhibitory functions.
PubMed: 17337440
DOI: 10.1074/jbc.M701074200
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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数据于2025-07-23公开中

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