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PDB: 4 results

1KUF
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BU of 1kuf by Molmil
High-resolution Crystal Structure of a Snake Venom Metalloproteinase from Taiwan Habu
Descriptor: CADMIUM ION, metalloproteinase
Authors:Huang, K.F, Chiou, S.H, Ko, T.P, Yuann, J.M, Wang, A.H.J.
Deposit date:2002-01-21
Release date:2002-07-03
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.35 Å)
Cite:The 1.35 A structure of cadmium-substituted TM-3, a snake-venom metalloproteinase from Taiwan habu: elucidation of a TNFalpha-converting enzyme-like active-site structure with a distorted octahedral geometry of cadmium.
Acta Crystallogr.,Sect.D, 58, 2002
1KUG
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BU of 1kug by Molmil
Crystal Structure of a Taiwan Habu Venom Metalloproteinase complexed with its endogenous inhibitor pENW
Descriptor: CADMIUM ION, ENW, metalloproteinase
Authors:Huang, K.F, Chiou, S.H, Ko, T.P, Wang, A.H.J.
Deposit date:2002-01-22
Release date:2002-07-10
Last modified:2019-12-25
Method:X-RAY DIFFRACTION (1.37 Å)
Cite:Determinants of the inhibition of a Taiwan habu venom metalloproteinase by its endogenous inhibitors revealed by X-ray crystallography and synthetic inhibitor analogues.
Eur.J.Biochem., 269, 2002
1KUK
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BU of 1kuk by Molmil
Crystal Structure of a Taiwan Habu Venom Metalloproteinase complexed with pEKW.
Descriptor: CADMIUM ION, EKW, metalloproteinase
Authors:Huang, K.F, Chiou, S.H, Ko, T.P, Wang, A.H.J.
Deposit date:2002-01-22
Release date:2002-07-10
Last modified:2019-12-25
Method:X-RAY DIFFRACTION (1.45 Å)
Cite:Determinants of the inhibition of a Taiwan habu venom metalloproteinase by its endogenous inhibitors revealed by X-ray crystallography and synthetic inhibitor analogues.
Eur.J.Biochem., 269, 2002
1KUI
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BU of 1kui by Molmil
Crystal Structure of a Taiwan Habu Venom Metalloproteinase complexed with pEQW.
Descriptor: CADMIUM ION, EQW, metalloproteinase
Authors:Huang, K.F, Chiou, S.H, Ko, T.P, Wang, A.H.J.
Deposit date:2002-01-22
Release date:2002-07-10
Last modified:2019-12-25
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:Determinants of the inhibition of a Taiwan habu venom metalloproteinase by its endogenous inhibitors revealed by X-ray crystallography and synthetic inhibitor analogues.
Eur.J.Biochem., 269, 2002

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