Kristina Djinovic-Carugo

Prof. Kristina Djinovic-Carugo

Department of Structural and Computational Biology, Universitat Wien, Vienna, Austria
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Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 May 2008 in Cellular and Molecular Life Sciences
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Journal Article
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BSB. Sjöblom
B. Sjöblom
ASA. Salmazo
A. Salmazo
Kristina Djinovic-CarugoKristina Djinovic-Carugo
Kristina Djinovic-Carugo

8 June 2004 in Proceedings of the National Academy of Sciences
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Journal Article
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JWJochen Wuerges
Jochen Wuerges
JLJin-Won Lee
Jin-Won Lee
YYYang-In Yim
Yang-In Yim
HYHyung-Soon Yim
Hyung-Soon Yim
SKSa-Ouk Kang
Sa-Ouk Kang
Kristina Djinovic-CarugoKristina Djinovic-Carugo
Kristina Djinovic-Carugo
Superoxide dismutases (SODs, EC 1.15.1.1) are ubiquitous enzymes that efficiently catalyze the dismutation of superoxide radical anions to protect biological molecules from oxidative damage. The crystal structure of nickel-containing SOD (NiSOD) from Streptomyces seoulensis was determined for the resting, x-ray-reduced, and thiosulfate-reduced enzyme state. NiSOD is a homohexamer consisting of four-helix-bundle subunits. The catalytic center resides in the N-terminal active-site loop, where a Ni(III) ion is coordinated by the amino group of His-1, the amide group of Cys-2, two thiolate groups of Cys-2 and Cys-6, and the imidazolate of His-1 as axial ligand that is lost in the chemically reduced state as well as after x-ray-induced reduction. This structure represents a third class of SODs concerning the catalytic metal species, subunit structure, and oligomeric organization. It adds a member to the small number of Ni-metalloenzymes and contributes with its Ni(III) active site to the general understanding of Ni-related biochemistry. NiSOD is shown to occur also in bacteria other than Streptomyces and is predicted to be present in some cyanobacteria.

7 December 2001 in FEBS Letters
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MGMario Gimona
Mario Gimona
Kristina Djinovic-CarugoKristina Djinovic-Carugo
Kristina Djinovic-Carugo
WKWolfgang J. Kranewitter
Wolfgang J. Kranewitter
SWSteven J. Winder
Steven J. Winder

4 January 2002 in FEBS Letters
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Journal Article
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Kristina Djinovic-CarugoKristina Djinovic-Carugo
Kristina Djinovic-Carugo
MGMathias Gautel
Mathias Gautel
JYJari Ylänne
Jari Ylänne
PYPaul Young
Paul Young

1 January 2016 in Journal of Experimental Biology
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MGMathias Gautel
Mathias Gautel
Kristina Djinovic-CarugoKristina Djinovic-Carugo
Kristina Djinovic-Carugo
Highly ordered organisation of striated muscle is the prerequisite for the fast and unidirectional development of force and motion during heart and skeletal muscle contraction. A group of proteins, summarised as the sarcomeric cytoskeleton, is essential for the ordered assembly of actin and myosin filaments into sarcomeres, by combining architectural, mechanical and signalling functions. This review discusses recent cell biological, biophysical and structural insight into the regulated assembly of sarcomeric cytoskeleton proteins and their roles in dissipating mechanical forces in order to maintain sarcomere integrity during passive extension and active contraction. α-Actinin crosslinks in the Z-disk show a pivot-and-rod structure that anchors both titin and actin filaments. In contrast, the myosin crosslinks formed by myomesin in the M-band are of a ball-and-spring type and may be crucial in providing stable yet elastic connections during active contractions, especially eccentric exercise.

1 August 1999 in Cell
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Journal Article
Closed access
Kristina Djinovic-CarugoKristina Djinovic-Carugo
Kristina Djinovic-Carugo
PYPaul Young
Paul Young
MGMathias Gautel
Mathias Gautel
MSMatti Saraste
Matti Saraste