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PDBe Entry: 1xmy 
Catalytic Domain Of Human Phosphodiesterase 4B In Complex With (R)-Rolipram
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HYDROLASE
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X-RAY DIFFRACTION
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Resolution: 2.4 Å, R-factor: 24.54%, Free R-factor: 29.805%, Spacegroup: P 21 21 21
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14/12/2004, deposition: 04/10/2004, last revision: 24/02/2009
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Card, G.L. ; England, B.P. ; Suzuki, Y. ; Fong, D. ; Powell, B. ; Lee, B. ; Luu, C. ; Tabrizizad, M. ; Gillette, S. ; Ibrahim, P.N. ; Artis, D.R. ; Bollag, G. ; Milburn, M.V. ; Kim, S.-H. ; Schlessinger, J. ; Zhang, K.Y.J.
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Structural Basis for the Activity of Drugs that Inhibit Phosphodiesterases. STRUCTURE vol:12, pag:2233-2247 (2004) [PubMed ID 15576036 ]
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Phosphodiesterase , PDE , PDE4B , Rolipram , (R)-Rolipram , HYDROLASE
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3.1.4.17 ExPASy BRENDA (A B)
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Homo sapiens(human) 9606 (A B)
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cAMP-specific 3',5'-cyclic phosphodiesterase 4B (EC 3.1.4.17) (DPDE4) (PDE32) Q07343 (A B)
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A, B
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1xlx, 1xlz, 1xm4, 1xm6, 1xmu, 1xn0, 1xom, 1xon, 1xoq, 1xor, 1xos, 1xot, 1xoz, 1xp0
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| A |
cAMP-specific 3',5'-cyclic phosphodiesterase 4B |
Protein |
Q07343 (PDE4B_HUMAN)
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398 |
81% |
| B |
cAMP-specific 3',5'-cyclic phosphodiesterase 4B |
Protein |
Q07343 (PDE4B_HUMAN)
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398 |
81% |
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| A, B |
ZINC ION |
ZN
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| A, B |
MAGNESIUM ION |
MG
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| A, B |
ROLIPRAM |
ROL
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