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3TKB
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BU of 3tkb by Molmil
crystal structure of human uracil-DNA glycosylase D183G/K302R mutant
Descriptor: IMIDAZOLE, Uracil-DNA glycosylase
Authors:Assefa, N.G, Niiranen, L, Willassen, N.P, Smalas, A.O, Moe, E.
Deposit date:2011-08-26
Release date:2011-10-12
Last modified:2023-09-13
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:Thermal unfolding studies of cold adapted uracil-DNA N-glycosylase (UNG) from Atlantic cod (Gadus morhua). A comparative study with human UNG.
Comp.Biochem.Physiol. B: Biochem.Mol.Biol., 161, 2012
1EJM
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BU of 1ejm by Molmil
CRYSTAL STRUCTURE OF THE BPTI ALA16LEU MUTANT IN COMPLEX WITH BOVINE TRYPSIN
Descriptor: BETA-TRYPSIN, PANCREATIC TRYPSIN INHIBITOR, SULFATE ION
Authors:Otlewski, J, Smalas, A, Helland, R, Grzesiak, A, Krowarsch, D.
Deposit date:2000-03-03
Release date:2001-03-03
Last modified:2021-11-03
Method:X-RAY DIFFRACTION (1.85 Å)
Cite:Substitutions at the P(1) position in BPTI strongly affect the association energy with serine proteinases.
J.Mol.Biol., 301, 2000
5LFZ
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BU of 5lfz by Molmil
T48 deacetylase
Descriptor: ArCE4A, NICKEL (II) ION
Authors:Rothweiler, U.
Deposit date:2016-07-05
Release date:2017-08-02
Last modified:2024-01-10
Method:X-RAY DIFFRACTION (1.561 Å)
Cite:Structure and function of a CE4 deacetylase isolated from a marine environment.
PLoS ONE, 12, 2017
5LGC
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BU of 5lgc by Molmil
T48 deacetylase with substrate
Descriptor: 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ArCE4A
Authors:Rothweiler, U.
Deposit date:2016-07-06
Release date:2017-08-02
Last modified:2024-01-10
Method:X-RAY DIFFRACTION (2.09 Å)
Cite:Structure and function of a CE4 deacetylase isolated from a marine environment.
PLoS ONE, 12, 2017
1BTP
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BU of 1btp by Molmil
UNIQUE BINDING OF A NOVEL SYNTHETIC INHIBITOR, N-[3-[4-[4-(AMIDINOPHENOXY)-CARBONYL]PHENYL]-2-METHYL-2-PROPENOYL]-N-ALLYLGLYCINE METHANESULFONATE TO BOVINE TRYPSIN, REVEALED BY THE CRYSTAL STRUCTURE OF THE COMPLEX
Descriptor: BETA-TRYPSIN, CALCIUM ION
Authors:Odagaki, Y, Nakai, H, Senokuchi, K, Kawamura, M, Hamanaka, N, Nakamura, M, Tomoo, K, Ishida, T.
Deposit date:1995-08-11
Release date:1996-01-29
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Unique binding of a novel synthetic inhibitor, N-[3-[4-[4-(amidinophenoxy)carbonyl]phenyl]-2-methyl-2-propenoyl]- N-allylglycine methanesulfonate, to bovine trypsin, revealed by the crystal structure of the complex.
Biochemistry, 34, 1995

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