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基本情報
登録情報 | ![]() | |||||||||
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タイトル | The Ectodomains of SPRING and S1P with the inhibitor PF-429242 | |||||||||
![]() | map of SPRING/S1P/PF-429242 | |||||||||
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![]() | protease / complex / inhibitor / MEMBRANE PROTEIN / MEMBRANE PROTEIN-INHIBITOR complex | |||||||||
機能・相同性 | ![]() site-1 protease / CREB3 factors activate genes / positive regulation of SREBP signaling pathway / ATF6-mediated unfolded protein response / ATF6 (ATF6-alpha) activates chaperones / ATF6B (ATF6-beta) activates chaperones / regulation of cholesterol biosynthetic process / Assembly of active LPL and LIPC lipase complexes / membrane protein intracellular domain proteolysis / regulation of vesicle-mediated transport ...site-1 protease / CREB3 factors activate genes / positive regulation of SREBP signaling pathway / ATF6-mediated unfolded protein response / ATF6 (ATF6-alpha) activates chaperones / ATF6B (ATF6-beta) activates chaperones / regulation of cholesterol biosynthetic process / Assembly of active LPL and LIPC lipase complexes / membrane protein intracellular domain proteolysis / regulation of vesicle-mediated transport / Regulation of cholesterol biosynthesis by SREBP (SREBF) / Golgi stack / lysosome organization / mitotic G2 DNA damage checkpoint signaling / endoplasmic reticulum unfolded protein response / cholesterol metabolic process / protein maturation / response to endoplasmic reticulum stress / Post-translational protein phosphorylation / protein processing / Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) / protein import into nucleus / endoplasmic reticulum lumen / Golgi membrane / serine-type endopeptidase activity / endoplasmic reticulum membrane / Golgi apparatus / proteolysis 類似検索 - 分子機能 | |||||||||
生物種 | ![]() | |||||||||
手法 | 単粒子再構成法 / クライオ電子顕微鏡法 / 解像度: 2.4 Å | |||||||||
![]() | Kober DL | |||||||||
資金援助 | ![]()
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![]() | ![]() タイトル: Structural basis for substrate selectivity by site-one protease revealed by studies with a small-molecule inhibitor. 著者: Ashley V Bullington / Ilaria Micallo / Bilkish Bajaj / Pankaj Kumar / Netanya Schlamowitz / Aurora Silva / Sebastian Hendrix / Noam Zelcer / Daniel L Kober / ![]() ![]() 要旨: Site-one protease (S1P) carries out the first proteolytic step to activate membrane-bound effector proteins in the Golgi. S1P matures through an autocatalytic process that begins in the endoplasmic ...Site-one protease (S1P) carries out the first proteolytic step to activate membrane-bound effector proteins in the Golgi. S1P matures through an autocatalytic process that begins in the endoplasmic reticulum (ER) and culminates with the displacement of its inhibitory pro-domain by its cofactor, sterol regulatory element binding protein-regulating gene (SPRING). Spatial control of S1P activity and substrate localization underpins signaling pathways governing, among others, lipogenesis, ER stress, and lysosome biogenesis. The factors governing these pathways are activated by S1P-mediated proteolysis upon their regulated transport from the ER to the Golgi. S1P cleaves substrates with the recognition sequence RX(L/I/V)Z, where X is any residue other than Cys or Pro and Z is preferably Leu or Lys. However, the structural basis for substrate recognition by S1P has remained unknown. Here, we used the small molecule PF-429242, a competitive inhibitor of S1P, to investigate substrate recognition by the S1P/SPRING complex. We determined the structure of S1P/SPRING bound to PF-429242 and found that PF-429242 binds S1P in the same pocket that recognizes the substrate's conserved P Arg. Further structural analysis suggests that S1P requires a conformation change to accommodate the substrate's P (L/I/V) residue. We designed an S1P mutation (I308A) to reduce the steric clash at the P position and generated an S1P that was resistant to PF-429242 in biochemical and cell culture assays. Our findings reveal selectivity in the recognition of substrates by S1P and provide a roadmap for the rational design of improved S1P inhibitors. | |||||||||
履歴 |
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構造の表示
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ダウンロードとリンク
-EMDBアーカイブ
マップデータ | ![]() | 51.7 MB | ![]() | |
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ヘッダ (付随情報) | ![]() ![]() | 23.8 KB 23.8 KB | 表示 表示 | ![]() |
FSC (解像度算出) | ![]() | 9.9 KB | 表示 | ![]() |
画像 | ![]() | 103.2 KB | ||
Filedesc metadata | ![]() | 7.8 KB | ||
その他 | ![]() ![]() ![]() | 86.1 MB 95.7 MB 95.7 MB | ||
アーカイブディレクトリ | ![]() ![]() | HTTPS FTP |
-関連構造データ
関連構造データ | ![]() 9csdMC M: このマップから作成された原子モデル C: 同じ文献を引用 ( |
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類似構造データ | 類似検索 - 機能・相同性 ![]() |
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リンク
EMDBのページ | ![]() ![]() |
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「今月の分子」の関連する項目 |
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マップ
ファイル | ![]() | ||||||||||||||||||||||||||||||||||||
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注釈 | map of SPRING/S1P/PF-429242 | ||||||||||||||||||||||||||||||||||||
投影像・断面図 | 画像のコントロール
画像は Spider により作成 | ||||||||||||||||||||||||||||||||||||
ボクセルのサイズ | X=Y=Z: 0.738 Å | ||||||||||||||||||||||||||||||||||||
密度 |
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対称性 | 空間群: 1 | ||||||||||||||||||||||||||||||||||||
詳細 | EMDB XML:
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-添付データ
-追加マップ: deepemhancer map of SPRING/S1P/PF-429242 for model building and...
ファイル | emd_45892_additional_1.map | ||||||||||||
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注釈 | deepemhancer map of SPRING/S1P/PF-429242 for model building and illustrations | ||||||||||||
投影像・断面図 |
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密度ヒストグラム |
-ハーフマップ: half map A for S1P/SPRING/PF-429242
ファイル | emd_45892_half_map_1.map | ||||||||||||
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注釈 | half map A for S1P/SPRING/PF-429242 | ||||||||||||
投影像・断面図 |
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密度ヒストグラム |
-ハーフマップ: half map B for S1P/SPRING/PF-429242
ファイル | emd_45892_half_map_2.map | ||||||||||||
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注釈 | half map B for S1P/SPRING/PF-429242 | ||||||||||||
投影像・断面図 |
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密度ヒストグラム |
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試料の構成要素
-全体 : Complex of the ectodomains of S1P and SPRING in the presence of t...
全体 | 名称: Complex of the ectodomains of S1P and SPRING in the presence of the small molecule PF-429242 |
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要素 |
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-超分子 #1: Complex of the ectodomains of S1P and SPRING in the presence of t...
超分子 | 名称: Complex of the ectodomains of S1P and SPRING in the presence of the small molecule PF-429242 タイプ: complex / ID: 1 / 親要素: 0 / 含まれる分子: #1-#2 |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 120 KDa |
-分子 #1: Membrane-bound transcription factor site-1 protease
分子 | 名称: Membrane-bound transcription factor site-1 protease / タイプ: protein_or_peptide / ID: 1 詳細: Construct contains 1-998 of human site one protease followed by a 3xFLAG affinity tag コピー数: 1 / 光学異性体: LEVO |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 115.048203 KDa |
組換発現 | 生物種: ![]() |
配列 | 文字列: MKLVNIWLLL LVVLLCGKKH LGDRLEKKSF EKAPCPGCSH LTLKVEFSST VVEYEYIVAF NGYFTAKARN SFISSALKSS EVDNWRIIP RNNPSSDYPS DFEVIQIKEK QKAGLLTLED HPNIKRVTPQ RKVFRSLKYA ESDPTVPCNE TRWSQKWQSS R PLRRASLS ...文字列: MKLVNIWLLL LVVLLCGKKH LGDRLEKKSF EKAPCPGCSH LTLKVEFSST VVEYEYIVAF NGYFTAKARN SFISSALKSS EVDNWRIIP RNNPSSDYPS DFEVIQIKEK QKAGLLTLED HPNIKRVTPQ RKVFRSLKYA ESDPTVPCNE TRWSQKWQSS R PLRRASLS LGSGFWHATG RHSSRRLLRA IPRQVAQTLQ ADVLWQMGYT GANVRVAVFD TGLSEKHPHF KNVKERTNWT NE RTLDDGL GHGTFVAGVI ASMRECQGFA PDAELHIFRV FTNNQVSYTS WFLDAFNYAI LKKIDVLNLS IGGPDFMDHP FVD KVWELT ANNVIMVSAI GNDGPLYGTL NNPADQMDVI GVGGIDFEDN IARFSSRGMT TWELPGGYGR MKPDIVTYGA GVRG SGVKG GCRALSGTSV ASPVVAGAVT LLVSTVQKRE LVNPASMKQA LIASARRLPG VNMFEQGHGK LDLLRAYQIL NSYKP QASL SPSYIDLTEC PYMWPYCSQP IYYGGMPTVV NVTILNGMGV TGRIVDKPDW QPYLPQNGDN IEVAFSYSSV LWPWSG YLA ISISVTKKAA SWEGIAQGHV MITVASPAET ESKNGAEQTS TVKLPIKVKI IPTPPRSKRV LWDQYHNLRY PPGYFPR DN LRMKNDPLDW NGDHIHTNFR DMYQHLRSMG YFVEVLGAPF TCFDASQYGT LLMVDSEEEY FPEEIAKLRR DVDNGLSL V IFSDWYNTSV MRKVKFYDEN TRQWWMPDTG GANIPALNEL LSVWNMGFSD GLYEGEFTLA NHDMYYASGC SIAKFPEDG VVITQTFKDQ GLEVLKQETA VVENVPILGL YQIPAEGGGR IVLYGDSNCL DDSHRQKDCF WLLDALLQYT SYGVTPPSLS HSGNRQRPP SGAGSVTPER MEGNHLHRYS KVLEAHLGDP KPRPLPACPR LSWAKPQPLN ETAPSNLWKH QKLLSIDLDK V VLPNFRSN RPQVRPLSPG ESGAWDIPGG IMPGRYNQEV DYKDDDDKGS DYKDDDDKGS DYKDDDDK UniProtKB: Membrane-bound transcription factor site-1 protease |
-分子 #2: SREBP regulating gene protein
分子 | 名称: SREBP regulating gene protein / タイプ: protein_or_peptide / ID: 2 詳細: Construct contains an IgK leader peptide followed by human SPRING residues 35-205 followed by a 10-His tag コピー数: 1 / 光学異性体: LEVO |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 23.200291 KDa |
組換発現 | 生物種: ![]() |
配列 | 文字列: METDTLLLWV LLLWVPGSTG DKQEERAVRD RNLLQVHDHN QPIPWKVQFN LGNSSRPSNQ CRNSIQGKHL ITDELGYVCE RKDLLVNGC CNVNVPSTKQ YCCDGCWPNG CCSAYEYCVS CCLQPNKQLL LERFLNRAAV AFQNLFMAVE DHFELCLAKC R TSSQSVQH ...文字列: METDTLLLWV LLLWVPGSTG DKQEERAVRD RNLLQVHDHN QPIPWKVQFN LGNSSRPSNQ CRNSIQGKHL ITDELGYVCE RKDLLVNGC CNVNVPSTKQ YCCDGCWPNG CCSAYEYCVS CCLQPNKQLL LERFLNRAAV AFQNLFMAVE DHFELCLAKC R TSSQSVQH ENTYRDPIAK YCYGESPPEL FPAHHHHHHH HHH UniProtKB: SREBP regulating gene protein |
-分子 #4: 2-acetamido-2-deoxy-beta-D-glucopyranose
分子 | 名称: 2-acetamido-2-deoxy-beta-D-glucopyranose / タイプ: ligand / ID: 4 / コピー数: 1 / 式: NAG |
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分子量 | 理論値: 221.208 Da |
Chemical component information | ![]() ChemComp-NAG: |
-分子 #5: 4-[(diethylamino)methyl]-N-[2-(2-methoxyphenyl)ethyl]-N-[(3R)-pyr...
分子 | 名称: 4-[(diethylamino)methyl]-N-[2-(2-methoxyphenyl)ethyl]-N-[(3R)-pyrrolidin-3-yl]benzamide タイプ: ligand / ID: 5 / コピー数: 1 / 式: A1AZU |
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分子量 | 理論値: 409.564 Da |
-分子 #6: CALCIUM ION
分子 | 名称: CALCIUM ION / タイプ: ligand / ID: 6 / コピー数: 1 / 式: CA |
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分子量 | 理論値: 40.078 Da |
-分子 #7: water
分子 | 名称: water / タイプ: ligand / ID: 7 / コピー数: 42 / 式: HOH |
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分子量 | 理論値: 18.015 Da |
Chemical component information | ![]() ChemComp-HOH: |
-実験情報
-構造解析
手法 | クライオ電子顕微鏡法 |
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![]() | 単粒子再構成法 |
試料の集合状態 | particle |
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試料調製
濃度 | 0.5 mg/mL |
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緩衝液 | pH: 7.5 |
グリッド | モデル: Quantifoil R1.2/1.3 / 材質: GOLD / メッシュ: 400 / 支持フィルム - 材質: CARBON / 前処理 - タイプ: GLOW DISCHARGE / 前処理 - 時間: 80 sec. / 前処理 - 雰囲気: AIR / 前処理 - 気圧: 0.03 kPa |
凍結 | 凍結剤: ETHANE |
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電子顕微鏡法
顕微鏡 | TFS KRIOS |
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撮影 | フィルム・検出器のモデル: FEI FALCON III (4k x 4k) 平均電子線量: 64.0 e/Å2 |
電子線 | 加速電圧: 300 kV / 電子線源: ![]() |
電子光学系 | 照射モード: FLOOD BEAM / 撮影モード: BRIGHT FIELD / 最大 デフォーカス(公称値): 2.0 µm / 最小 デフォーカス(公称値): 1.8 µm |
実験機器 | ![]() モデル: Titan Krios / 画像提供: FEI Company |