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PDB: 4 results

8H5S
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BU of 8h5s by Molmil
Crystal structure of Rv3400 from Mycobacterium tuberculosis
Descriptor: 1,2-ETHANEDIOL, Beta-phosphoglucomutase, CHLORIDE ION, ...
Authors:Singh, L, Karthikeyan, S, Thakur, K.G.
Deposit date:2022-10-13
Release date:2023-10-25
Last modified:2024-05-15
Method:X-RAY DIFFRACTION (1.7 Å)
Cite:Biochemical and structural characterization reveals Rv3400 codes for beta-phosphoglucomutase in Mycobacterium tuberculosis.
Protein Sci., 33, 2024
7YK3
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BU of 7yk3 by Molmil
Crystal structure of DarTG toxin-antitoxin complex from Mycobacterium tuberculosis
Descriptor: DNA ADP-ribosyl glycohydrolase, DNA ADP-ribosyl transferase, PHOSPHATE ION
Authors:Deep, A, Kaur, J, Singh, L, Thakur, K.G.
Deposit date:2022-07-21
Release date:2023-05-31
Last modified:2023-11-15
Method:X-RAY DIFFRACTION (2.2 Å)
Cite:Structural insights into DarT toxin neutralization by cognate DarG antitoxin: ssDNA mimicry by DarG C-terminal domain keeps the DarT toxin inhibited.
Structure, 31, 2023
5EC5
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BU of 5ec5 by Molmil
Crystal structure of lysenin pore
Descriptor: Lysenin, MERCURIBENZOIC ACID, MERCURY (II) ION
Authors:Podobnik, M, Savory, P, Rojko, N, Kisovec, M, Bruce, M, Jayasinghe, L, Anderluh, G.
Deposit date:2015-10-20
Release date:2016-05-18
Last modified:2024-05-08
Method:X-RAY DIFFRACTION (3.1 Å)
Cite:Crystal structure of an invertebrate cytolysin pore reveals unique properties and mechanism of assembly.
Nat Commun, 7, 2016
1NJS
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BU of 1njs by Molmil
human GAR Tfase in complex with hydrolyzed form of 10-trifluoroacetyl-5,10-dideaza-acyclic-5,6,7,8-tetrahydrofolic acid
Descriptor: N-{4-[(1R)-4-[(2R,4R,5S)-2,4-DIAMINO-6-OXOHEXAHYDROPYRIMIDIN-5-YL]-1-(2,2,2-TRIFLUORO-1,1-DIHYDROXYETHYL)BUTYL]BENZOYL}-D-GLUTAMIC ACID, PHOSPHATE ION, Phosphoribosylglycinamide formyltransferase
Authors:Zhang, Y, Desharnais, J, Marsilje, T.H, Li, C, Hedrick, M.P, Gooljarsingh, L.T, Tavassoli, A, Benkovic, S.J, Olson, A.J, Boger, D.L, Wilson, I.A.
Deposit date:2003-01-02
Release date:2003-06-10
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (1.98 Å)
Cite:Rational Design, Synthesis, Evaluation, and Crystal Structure of a Potent Inhibitor of Human GAR Tfase: 10-(Trifluoroacetyl)-5,10-dideazaacyclic-5,6,7,8-tetrahydrofolic Acid
Biochemistry, 42, 2003

224572

数据于2024-09-04公开中

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