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2JV3
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BU of 2jv3 by Molmil
Ets-1 PNT domain (29-138) NMR structure ensemble
Descriptor: ETS1 proto-oncogene
Authors:Lee, G.M, Kang, H, Schaerpf, M, Slupsky, C.M, Lawrence, M.P.
Deposit date:2007-09-11
Release date:2007-10-16
Last modified:2024-05-29
Method:SOLUTION NMR
Cite:Ets-1 PNT domain (29-138) NMR structure ensemble
To be Published
5ILS
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BU of 5ils by Molmil
Autoinhibited ETV1
Descriptor: ETS translocation variant 1
Authors:Whitby, F.G, Currie, S.L.
Deposit date:2016-03-04
Release date:2017-02-22
Last modified:2019-12-25
Method:X-RAY DIFFRACTION (1.399 Å)
Cite:Structured and disordered regions cooperatively mediate DNA-binding autoinhibition of ETS factors ETV1, ETV4 and ETV5.
Nucleic Acids Res., 45, 2017
5ILV
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BU of 5ilv by Molmil
Uninhibited ETV5
Descriptor: ETS translocation variant 5
Authors:Whitby, F.G, Currie, S.L.
Deposit date:2016-03-04
Release date:2017-02-22
Last modified:2019-12-25
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Structured and disordered regions cooperatively mediate DNA-binding autoinhibition of ETS factors ETV1, ETV4 and ETV5.
Nucleic Acids Res., 45, 2017
5ILU
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BU of 5ilu by Molmil
Autoinhibited ETV4
Descriptor: ETS translocation variant 4
Authors:Whitby, F.G, Currie, S.L.
Deposit date:2016-03-04
Release date:2017-02-22
Last modified:2019-12-25
Method:X-RAY DIFFRACTION (1.101 Å)
Cite:Structured and disordered regions cooperatively mediate DNA-binding autoinhibition of ETS factors ETV1, ETV4 and ETV5.
Nucleic Acids Res., 45, 2017
1C6Z
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BU of 1c6z by Molmil
ALTERNATE BINDING SITE FOR THE P1-P3 GROUP OF A CLASS OF POTENT HIV-1 PROTEASE INHIBITORS AS A RESULT OF CONCERTED STRUCTURAL CHANGE IN 80'S LOOP.
Descriptor: (2S)-N-[(2S,3R)-4-[(2S,3S,4aS,8aS)-3-(tert-butylcarbamoyl)-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]-3-hydroxy-1 -phenyl-butan-2-yl]-2-(quinolin-2-ylcarbonylamino)butanediamide, PROTEIN (PROTEASE)
Authors:Munshi, S.
Deposit date:1999-12-28
Release date:2000-12-28
Last modified:2023-12-27
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:An alternate binding site for the P1-P3 group of a class of potent HIV-1 protease inhibitors as a result of concerted structural change in the 80s loop of the protease.
Acta Crystallogr.,Sect.D, 56, 2000
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數據於2024-07-24公開中

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