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データを開く
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基本情報
登録情報 | データベース: PDB / ID: 2mta | |||||||||
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タイトル | CRYSTAL STRUCTURE OF A TERNARY ELECTRON TRANSFER COMPLEX BETWEEN METHYLAMINE DEHYDROGENASE, AMICYANIN AND A C-TYPE CYTOCHROME | |||||||||
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![]() | ELECTRON TRANSPORT | |||||||||
機能・相同性 | ![]() methylamine dehydrogenase (amicyanin) / methanol metabolic process / methylamine dehydrogenase (amicyanin) activity / methylamine metabolic process / aliphatic amine dehydrogenase activity / amine metabolic process / outer membrane-bounded periplasmic space / periplasmic space / electron transfer activity / iron ion binding ...methylamine dehydrogenase (amicyanin) / methanol metabolic process / methylamine dehydrogenase (amicyanin) activity / methylamine metabolic process / aliphatic amine dehydrogenase activity / amine metabolic process / outer membrane-bounded periplasmic space / periplasmic space / electron transfer activity / iron ion binding / copper ion binding / heme binding 類似検索 - 分子機能 | |||||||||
生物種 | ![]() | |||||||||
手法 | ![]() | |||||||||
![]() | Chen, L. / Mathews, F.S. | |||||||||
![]() | ![]() タイトル: Structure of an electron transfer complex: methylamine dehydrogenase, amicyanin, and cytochrome c551i. 著者: Chen, L. / Durley, R.C. / Mathews, F.S. / Davidson, V.L. #1: ![]() タイトル: Crystal Structure Analysis of Amicyanin and Apoamicyanin from Paraccus Denitrificans at 2.0 Angstroms and 1.8 Angstroms Resolution 著者: Durley, R. / Chen, L. / Lim, L.W. / Mathews, F.S. / Davidson, V.L. #2: ![]() タイトル: Preliminary Crystal Structure Studies of a Ternary Electron Transfer Complex between a Quinoprotein, a Blue Copper Protein, and a C-Type Cytochrome 著者: Chen, L. / Mathews, F.S. / Davidson, V.L. / Tegoni, M. / Rivetti, C. / Rossi, G.L. #3: ![]() タイトル: Crystal Structure of an Electron-Transfer Complex between Methylamine Dehydrogenase and Amicyanin 著者: Chen, L. / Durley, R. / Poliks, B.J. / Hamada, K. / Chen, Z. / Mathews, F.S. / Davidson, V.L. / Satow, Y. / Huizinga, E. / Vellieux, F.M.D. / Hol, W.G.J. #4: ![]() タイトル: Three-Dimensional Structure of the Quinoprotein Methylamine Dehydrogenase from Paracoccus Denitrificans Determined by Molecular Replacement at 2.8 Angstroms Resolution 著者: Chen, L. / Mathews, F.S. / Davidson, V.L. / Huizinga, E.G. / Vellieux, F.M.D. / Hol, W.G.J. | |||||||||
履歴 |
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構造の表示
構造ビューア | 分子: ![]() ![]() |
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PDBx/mmCIF形式 | ![]() | 163.2 KB | 表示 | ![]() |
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PDB形式 | ![]() | 125.9 KB | 表示 | ![]() |
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その他 | ![]() |
-検証レポート
文書・要旨 | ![]() | 507.2 KB | 表示 | ![]() |
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文書・詳細版 | ![]() | 535.8 KB | 表示 | |
XML形式データ | ![]() | 19.8 KB | 表示 | |
CIF形式データ | ![]() | 29.6 KB | 表示 | |
アーカイブディレクトリ | ![]() ![]() | HTTPS FTP |
-関連構造データ
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リンク
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集合体
登録構造単位 | ![]()
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1 | ![]()
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単位格子 |
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Atom site foot note | 1: CIS PROLINE - PRO H 145 2: GLN C 146 - PRO C 147 OMEGA =145.73 PEPTIDE BOND DEVIATES SIGNIFICANTLY FROM TRANS CONFORMATION | ||||||||
Components on special symmetry positions |
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要素
-METHYLAMINE DEHYDROGENASE ... , 2種, 2分子 HL
#1: タンパク質 | 分子量: 41063.945 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 参照: UniProt: P29894, EC: 1.4.99.3 |
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#2: タンパク質 | 分子量: 13728.206 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 参照: UniProt: P22619, EC: 1.4.99.3 |
-タンパク質 , 2種, 2分子 AC
#3: タンパク質 | 分子量: 11505.171 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 参照: UniProt: P22364 |
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#4: タンパク質 | 分子量: 16274.852 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) ![]() 参照: UniProt: P29899 |
-非ポリマー , 4種, 130分子 H
A






#5: 化合物 | #6: 化合物 | #7: 化合物 | ChemComp-HEC / | #8: 水 | ChemComp-HOH / | |
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-詳細
構成要素の詳細 | THIS IS THE FIRST TERNARY COMPLEX COMPOSED OF THREE SEQUENTIAL PROTEINS IN AN ELECTRON TRANSFER ...THIS IS THE FIRST TERNARY COMPLEX COMPOSED OF THREE SEQUENTIAL |
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Has protein modification | Y |
非ポリマーの詳細 | THE REDOX COFACTOR TTQ OF MADH IS LOCATED ON EACH L SUBUNIT, WHICH IS COMPRISED OF THE SIDE CHAINS ...THE REDOX COFACTOR TTQ OF MADH IS LOCATED ON EACH L SUBUNIT, WHICH IS COMPRISED OF THE SIDE CHAINS OF TWO TRYPTOPHAN |
配列の詳細 | SEQUENCE ADVISORY NOTICE: AT PRESENT, THE SEQUENCE DATABASES INDICATE THAT RESIDUE 299 OF THE HEAVY ...SEQUENCE ADVISORY NOTICE: AT PRESENT, THE SEQUENCE DATABASES INDICATE THAT RESIDUE 299 OF THE HEAVY CHAIN IS LEU AND RESIDUE 300 IS LEU. THE AUTHORS FOUND THAT THEY MISREAD THE GELS AND THAT RESIDUES 299 AND 300 SHOULD BE PHE AND VAL, RESPECTIVE |
-実験情報
-実験
実験 | 手法: ![]() |
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試料調製
結晶 | マシュー密度: 2.9 Å3/Da / 溶媒含有率: 57.61 % |
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解析
ソフトウェア |
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精密化 | Rfactor Rwork: 0.179 / Rfactor obs: 0.179 / 最高解像度: 2.4 Å 詳細: THE CURRENT MODEL CONTAINS AN AMICYANIN PORTION TRANSFORMED FROM THE MADH-AMICYANIN BINARY COMPLEX (CHEN ET AL., BIOCHEMISTRY, 1992), WHICH WAS NOT INCLUDED IN THE PHASE REFINEMENT. ONLY THE ...詳細: THE CURRENT MODEL CONTAINS AN AMICYANIN PORTION TRANSFORMED FROM THE MADH-AMICYANIN BINARY COMPLEX (CHEN ET AL., BIOCHEMISTRY, 1992), WHICH WAS NOT INCLUDED IN THE PHASE REFINEMENT. ONLY THE CA OF EACH RESIDUE AND THE COPPER ATOM ARE INCLUDED AT THIS STAGE. THE CYTOCHROME PORTION OF THE CURRENT MODEL IS SIMULATED FROM CYTOCHROME C551 DEPOSITED IN PROTEIN DATA BANK (MUTSUURA ET AL., J. MOL. BIOL. 1982). ONLY THE HEME GROUP WAS BUILT TO FIT THE ELECTRON DENSITY AND IS SUBMITTED. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
精密化ステップ | サイクル: LAST / 最高解像度: 2.4 Å
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拘束条件 |
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