EMDB/PDB/SASBDBから引用されている文献のデータベース

キーワード
構造解析手法	All X線回折 NMR 電子顕微鏡小角散乱中性子線回折線維回折粉末回折赤外分光 EPR FRET 理論モデルハイブリッド
著者・登録者
ジャーナル
IF	>30 >20 >10 >5 all

タイトル	Exploring the inhibition of the soluble lytic transglycosylase Cj0843c of Campylobacter jejuni via targeting different sites with different scaffolds.
ジャーナル・号・ページ	Protein Sci., Vol. 32, Page e4683-e4683, Year 2023
掲載日	2023年3月7日 (構造データの登録日)
著者	Kumar, V. / Boorman, J. / Greenlee, W.J. / Zeng, X. / Lin, J. / van den Akker, F.
リンク	Protein Sci. / PubMed:37209283
手法	X線回折
解像度	1.83 - 2.48 Å
構造データ	PDB-8gez: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with LV8036 inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.99 Å PDB-8gf0: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with LV8044 inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.89 Å PDB-8gf1: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with LV8060 inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.92 Å PDB-8gfb: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Fv16b inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.17 Å PDB-8gfc: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Fv17b inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.48 Å PDB-8gfd: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z3252 inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.86 Å PDB-8gfe: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z3261 inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.42 Å PDB-8gff: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z7146 inhibitor 手法: X-RAY DIFFRACTION / 解像度: 1.9 Å PDB-8gfg: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z7912 inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.48 Å PDB-8gfh: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z7285 inhibitor soaked at 10 mM concentration 手法: X-RAY DIFFRACTION / 解像度: 1.83 Å PDB-8gfi: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z7285 inhibitor soaked at 3 mM concentration 手法: X-RAY DIFFRACTION / 解像度: 2.15 Å PDB-8gfj: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni dose-response soaking with 1 mM concentration Z7285 inhibitor (no inhibitor binding observed) 手法: X-RAY DIFFRACTION / 解像度: 2.2 Å PDB-8gfl: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with 4-Nitrophenyl N,N' diacetyl-beta-D-chitobioside inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.36 Å PDB-8gfm: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with zanamivir amine inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.38 Å PDB-8gfp: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with N-acetyl-2,3-dehydro-2-deoxyneuraminic acid inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.07 Å PDB-8gfq: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Fv32r inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.3 Å PDB-8gfs: Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with siastatin B inhibitor 手法: X-RAY DIFFRACTION / 解像度: 2.38 Å
化合物	ChemComp-ZMB: methyl (2S)-3-[(2-acetamido-2-deoxy-beta-D-glucopyranosyl)oxy]-2-methylpropanoate ChemComp-CIT: CITRIC ACID ChemComp-DMS: DIMETHYL SULFOXIDE / DMSO, 沈殿剤YM ChemComp-HOH: WATER ChemComp-UM9: 2,2-dimethyl-3-oxobutyl 2-acetamido-2-deoxy-beta-D-glucopyranoside ChemComp-UL6: [(2S)-1,4-dioxan-2-yl]methyl 2-acetamido-2-deoxy-beta-D-glucopyranoside ChemComp-ZG9: [(2S)-1,4-dioxan-2-yl]methyl 2-acetamido-2-deoxy-6-O-methyl-beta-D-glucopyranoside ChemComp-ZI2: [(2S)-1,4-dioxan-2-yl]methyl 2-acetamido-4-amino-2,4-dideoxy-beta-D-glucopyranoside ChemComp-ZHR: 2-(1-benzofuran-5-yl)ethyl 2-acetamido-2-deoxy-beta-D-glucopyranoside ChemComp-ZH8: ~{N}-[(2~{R},3~{R},4~{R},5~{S},6~{R})-6-(hydroxymethyl)-4,5-bis(oxidanyl)-2-[(4-oxidanylidene-3~{H}-pyrido[1,2-a]pyrimidin-2-yl)methoxy]oxan-3-yl]ethanamide ChemComp-ZHE: cyclohexylmethyl 2-acetamido-2-deoxy-beta-D-glucopyranoside ChemComp-ZHL: (3S,3aR,5S,6S,6aS)-2-oxohexahydro-2H-3,5-methanocyclopenta[b]furan-6-yl 2-acetamido-2-deoxy-beta-D-glucopyranoside ChemComp-ZIA: [(2R)-5-oxopyrrolidin-2-yl]methyl 2-acetamido-2-deoxy-beta-D-glucopyranoside ChemComp-ZIE: 4-nitrophenyl 2-acetamido-4-O-(2-acetamido-2-deoxy-beta-D-glucopyranosyl)-2-deoxy-beta-D-glucopyranoside ChemComp-4AM: 4-AMINO-2-DEOXY-2,3-DEHYDRO-N-ACETYL-NEURAMINIC ACID ChemComp-DAN: 2-DEOXY-2,3-DEHYDRO-N-ACETYL-NEURAMINIC ACID ChemComp-1PE: PENTAETHYLENE GLYCOL / 沈殿剤YM ChemComp-9AM: 9-AMINO-2-DEOXY-2,3-DEHYDRO-N-ACETYL-NEURAMINIC ACID ChemComp-PGE: TRIETHYLENE GLYCOL ChemComp-3XR: (2S,3R,4S,5S)-2-(acetylamino)-5-carboxy-3,4-dihydroxypiperidinium
由来	campylobacter jejuni (カンピロバクター)
キーワード	LYASE/INHIBITOR / soluble lytic transglycosylase / inhibitor / LYASE / LYASE-INHIBITOR complex / LYASE/LYASE INHIBITOR / LYASE-LYASE INHIBITOR complex