Mine: New entries

6AL3
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LYS49 PLA2 BPII DERIVED FROM THE VENOM OF PROTOBOTHROPS FLAVOVIRIDIS.
Descriptor:Basic phospholipase A2 BP-II, SULFATE ION
Authors:Matsui, T., Kamata, S., Suzuki, A., Oda-Ueda, N., Ogawa, T., Tanaka, Y.
Deposit date:2018-09-05
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.57 Å)
Cite:SDS-induced oligomerization of Lys49-phospholipase A2 from snake venom.
Sci Rep, 2019
6AN9
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CRYSTAL STRUCTURE OF PPK2 CLASS III IN COMPLEX WITH ADP FROM CYTOPHAGA HUTCHINSONII ATCC 33406
Descriptor:Polyphosphate:AMP phosphotransferase, ADENOSINE-5'-DIPHOSPHATE, GLYCEROL
Authors:Nocek, B., Joachimiak, A., Yakunin, A.
Deposit date:2017-08-12
Release date:2019-01-16
Method:X-RAY DIFFRACTION (1.891 Å)
Cite:Crystal structure of PPK2 class III in complex with ADP from Cytophaga hutchinsonii ATCC 33406
To Be Published
6ANG
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CRYSTAL STRUCTURE OF PPK2 CLASS III IN THE COMPLEX WITH AMP FROM CYTOPHAGA HUTCHINSONII ATCC 33406
Descriptor:Polyphosphate:AMP phosphotransferase, ADENOSINE MONOPHOSPHATE, CHLORIDE ION
Authors:Nocek, B., Joachimiak, A., Yakunin, A.
Deposit date:2017-08-13
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.45 Å)
Cite:Crystal structure of PPK2 class III in complex with ADP from Cytophaga hutchinsonii ATCC 33406
To Be Published
6ANH
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CRYSTAL STRUCTURE OF PPK2 CLASS III IN COMPLEX WITH GUANOSINE 5-TETRAPHOSPHATE
Descriptor:Polyphosphate:AMP phosphotransferase, 5'-O-[(S)-hydroxy{[(S)-hydroxy{[(R)-hydroxy(phosphonooxy)phosphoryl]oxy}phosphoryl]oxy}phosphoryl]guanosine
Authors:Nocek, B., Joachimiak, A., Yakunin, A.
Deposit date:2017-08-13
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.65 Å)
Cite:Crystal structure of PPK2 class III in complex with ADP from Cytophaga hutchinsonii ATCC 33406
To Be Published
6AQE
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CRYSTAL STRUCTURE OF PPK2 IN COMPLEX WITH MG ATP
Descriptor:molecule A, ADENOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, ...
Authors:Nocek, B., Joachimiak, A., Yakunin, A.
Deposit date:2017-08-19
Release date:2019-01-16
Method:X-RAY DIFFRACTION (1.805 Å)
Cite:Crystal structure of PPK2 class III in complex with ADP from Cytophaga hutchinsonii ATCC 33406
To Be Published
6AQN
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CRYSTAL STRUCTURE OF PPK2 IN COMPLEX WITH PHOSPHONIC ACID INHIBITOR
Descriptor:Polyphosphate:AMP phosphotransferase, [(R)-hydroxy(4-methylphenyl)methyl]phosphonic acid, GLYCEROL, ...
Authors:Nocek, B., Berlicki, l., Joachimiak, A., Yakunin, S.
Deposit date:2017-08-20
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.199 Å)
Cite:Crystal structure of PPK2 class III in complex with ADP from Cytophaga hutchinsonii ATCC 33406
To Be Published
6AU0
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CRYSTAL STRUCTURE OF PPK2 (CLASS III) IN COMPLEX WITH BISPHOSPHONATE INHIBITOR (2-((3,5-DICHLOROPHENYL)AMINO)ETHANE-1,1-DIYL)DIPHOSPHONIC ACID
Descriptor:Polyphosphate:AMP phosphotransferase, {[(3,5-dichlorophenyl)amino]methylene}bis(phosphonic acid), GLYCEROL
Authors:Nocek, B., Ruszkowski, M., Joachimiak, A., Berlicki, L., Yakunin, A.
Deposit date:2017-08-29
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:Crystal structure of PPK2 class III in complex with ADP from Cytophaga hutchinsonii ATCC 33406
To Be Published
6B18
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CRYSTAL STRUCTURE OF PPK3 CLASS III IN COMPLEX WITH INHIBITOR
Descriptor:PPK3 Class III, {[(4-benzylphenyl)amino]methylene}bis(phosphonic acid), PHOSPHATE ION, ...
Authors:Nocek, B., Ruszkowski, M., Berlicki, L., Joachimiak, A., Yakunin, A.
Deposit date:2017-09-17
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Crystal structure of PPK2 class III in complex with ADP from Cytophaga hutchinsonii ATCC 33406
To Be Published
6B8C
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CRYSTAL STRUCTURE OF NLPC/P60 DOMAIN OF PEPTIDOGLYCAN HYDROLASE SAGA
Descriptor:NLP/P60
Authors:Kim, B., Oren, D.A., Hang, H.C.
Deposit date:2017-10-06
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.403 Å)
Cite:Crystal structure of NlpC/p60 domain of peptidoglycan hydrolase SagA
To Be Published
6BJG
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CIRV P19 MUTANT T111H IN COMPLEX WITH SIRNA
Descriptor:RNA silencing suppressor p19, RNA (5'-R(P*UP*CP*GP*AP*AP*GP*UP*AP*UP*UP*CP*CP*GP*CP*GP*UP*AP*CP*GP*UP*U)-3'), RNA (5'-R(P*CP*GP*UP*AP*CP*GP*CP*GP*GP*AP*AP*UP*AP*CP*UP*UP*CP*GP*AP*UP*U)-3')
Authors:Foss, D.V., Schirle, N., Pezacki, J.P., Macrae, I.J.
Deposit date:2017-11-06
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.29 Å)
Cite:Structural examination of p19 mutants with high affinity for human miRNA-122
To Be Published
6BJH
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CIRV P19 MUTANT T111S IN COMPLEX WITH SIRNA
Descriptor:RNA silencing suppressor p19, RNA (5'-R(P*UP*CP*GP*AP*AP*GP*UP*AP*UP*UP*CP*CP*GP*CP*GP*UP*AP*CP*GP*UP*U)-3'), RNA (5'-R(P*CP*GP*UP*AP*CP*GP*CP*GP*GP*AP*AP*UP*AP*CP*UP*UP*CP*GP*AP*UP*U)-3')
Authors:Foss, D.V., Schirle, N.T., MacRae, I.J., Pezacki, J.P.
Deposit date:2017-11-06
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.58 Å)
Cite:Structural examination of p19 mutants with high affinity for human miRNA-122.
To Be Published
6BJV
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CIRV P19 PROTEIN IN COMPLEX WITH SIRNA
Descriptor:RNA silencing suppressor p19, RNA (5'-R(P*UP*CP*GP*AP*AP*GP*UP*AP*UP*UP*CP*CP*GP*CP*GP*UP*AP*CP*GP*UP*U)-3'), RNA (5'-R(P*CP*GP*UP*AP*CP*GP*CP*GP*GP*AP*AP*UP*AP*CP*UP*UP*CP*GP*AP*UP*U)-3')
Authors:Foss, D.V., Schirle, N., Pezacki, J.P., Macrae, I.J.
Deposit date:2017-11-07
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.198 Å)
Cite:Structural examination of p19 mutants with high affinity for human miRNA-122
To Be Published
6BWS
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CRYSTAL STRUCTURE OF EFGA FROM METHYLOBACTERIUM EXTORQUENS
Descriptor:Glycolate utilization protein
Authors:Shamoo, Y., Davlieva, M.
Deposit date:2017-12-15
Release date:2019-01-16
Method:X-RAY DIFFRACTION (1.65 Å)
Cite:Crystal structure of Efga from Methylobacterium extorquens
To Be Published
6BZJ
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SOLUTION STRUCTURE OF AGL55
Descriptor:M protein
Authors:Qiu, C., Yuan, Y., Castellino, F.J.
Deposit date:2017-12-24
Release date:2019-01-16
Method:SOLUTION NMR
Cite:The C-Domain Repeats in Plasminogen-binding Group A Streptococcal M-Protein are Essential Determinants for its Dimerization
To Be Published
6BZK
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SOLUTION STRUCTURE OF KTI55
Descriptor:M protein
Authors:Castellino, F.J., Qiu, C., Yuan, Y.
Deposit date:2017-12-24
Release date:2019-01-16
Method:SOLUTION NMR
Cite:Solution structure of truncated PAM
To Be Published
6BZL
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SOLUTION STRUCTURE OF VEK75
Descriptor:M protein
Authors:Qiu, C., Yuan, Y., Castellino, F.J.
Deposit date:2017-12-24
Release date:2019-01-16
Method:SOLUTION NMR
Cite:The C-Domain Repeats in Plasminogen-binding Group A Streptococcal M-Protein are Essential Determinants for its Dimerization
To Be Published
6C00
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SOLUTION STRUCTURE OF TRANSLATION INITIATION FACTOR 1 FROM CLOSTRIDIUM DIFFICILE
Descriptor:Translation initiation factor IF-1
Authors:Zhang, Y., Aguilar, F.
Deposit date:2017-12-26
Release date:2019-01-16
Method:SOLUTION NMR
Cite:Solution structure of translation initiation factor 1 from Clostridium difficile
To be Published
6C07
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CRYSTAL STRUCTURE OF S-ADENOSYLMETHIONINE SYNTHETASE (METK/MAT) FROM CRYPTOSPORIDIUM PARVUM
Descriptor:S-adenosylmethionine synthase, CHLORIDE ION, MAGNESIUM ION, ...
Authors:Ohren, J.F., Viola, R.E.
Deposit date:2017-12-28
Release date:2019-01-16
Method:X-RAY DIFFRACTION (1.85 Å)
Cite:Crystal Structure of S-Adenosylmethionine synthetase (MetK/Mat) from Cryptosporidium parvum
To be Published
6C0A
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ACTININ-1 EF-HAND BOUND TO THE CAV1.2 IQ MOTIF
Descriptor:Alpha-actinin-1, Voltage-dependent L-type calcium channel subunit alpha-1C
Authors:Turner, M.L., Ames, J.B.
Deposit date:2017-12-28
Release date:2019-01-16
Method:SOLUTION NMR
Cite:Structural Basis of the Localization and Activation of Neuronal L-type Ca2+ Channels by a-Actinin1 and Calmodulin
To be Published
6C0Z
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CRYSTAL STRUCTURE OF EFGA FROM METHYLOBACTERIUM EXTORQUENS IN COMPLEX WITH FORMALDEHYDE
Descriptor:Efga, FORMIC ACID, oxydimethanol
Authors:Shamoo, Y., Davlieva, M.
Deposit date:2018-01-03
Release date:2019-01-16
Method:X-RAY DIFFRACTION (1.83 Å)
Cite:Crystal structure of Efga form Methylobacterium extorquens in complex with formaldehyde
To Be Published
6C18
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FGFR1 KINASE COMPLEX WITH INHIBITOR SN37115
Descriptor:Fibroblast growth factor receptor 1, 3-(2,6-dichloro-3,5-dimethoxyphenyl)-1-{(3S)-1-[(2E)-4-(dimethylamino)but-2-enoyl]pyrrolidin-3-yl}-7-[(propan-2-yl)amino]-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one, SULFATE ION
Authors:Yosaatmadja, Y., Smaill, J.B., Squire, C.J.
Deposit date:2018-01-04
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Understanding the structural requirements for covalent inhibition of FGFR1-3
To Be Published
6C19
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FGFR1 KINASE COMPLEX WITH INHIBITOR SN36985
Descriptor:Fibroblast growth factor receptor 1, 3-(2,6-dichloro-3,5-dimethoxyphenyl)-1-{(3S)-1-[(2E)-4-(dimethylamino)but-2-enoyl]pyrrolidin-3-yl}-7-(methylamino)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one, SULFATE ION
Authors:Yosaatmadja, Y., Smaill, J.B., Squire, C.J.
Deposit date:2018-01-04
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.12 Å)
Cite:Understanding the structural requirements for covalent inhibition of FGFR1-3
To Be Published
6C1B
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FGFR1 KINASE COMPLEX WITH INHIBITOR SN37118
Descriptor:Fibroblast growth factor receptor 1, 3-(2,6-dichloro-3,5-dimethoxyphenyl)-1-{(3S)-1-[(2E)-4-(dimethylamino)but-2-enoyl]pyrrolidin-3-yl}-7-(phenylamino)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one
Authors:Yosaatmadja, Y., Smaill, J.B., Squire, C.J.
Deposit date:2018-01-04
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2 Å)
Cite:Understanding the structural requirements for covalent inhibition of FGFR1-3
To Be Published
6C1C
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FGFR1 KINASE COMPLEX WITH INHIBITOR SN37116
Descriptor:Fibroblast growth factor receptor 1, 7-(cyclohexylamino)-3-(2,6-dichloro-3,5-dimethoxyphenyl)-1-{(3S)-1-[(2E)-4-(dimethylamino)but-2-enoyl]pyrrolidin-3-yl}-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one, SULFATE ION
Authors:Yosaatmadja, Y., Smaill, J.B., Squire, C.J.
Deposit date:2018-01-04
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.15 Å)
Cite:Understanding the structural requirements for covalent inhibition of FGFR1-3
To Be Published
6C1O
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FGFR1 KINASE DOMAIN COMPLEXED WITH FIIN-1
Descriptor:Fibroblast growth factor receptor 1, N-(3-{[3-(2,6-dichloro-3,5-dimethoxyphenyl)-7-{[4-(diethylamino)butyl]amino}-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl]methyl}phenyl)prop-2-enamide, SULFATE ION
Authors:Kalyukina, M., Yosaatmadja, Y., Smaill, J.B., Squire, C.J.
Deposit date:2018-01-05
Release date:2019-01-16
Method:X-RAY DIFFRACTION (2.29 Å)
Cite:A new class of FGFR1 inhibitors
To Be Published
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