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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: 9kx6 | ||||||||||||
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| タイトル | Structure of human C5a-desArg bound mouse C5aR1 in complex with Go | ||||||||||||
要素 |
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キーワード | SIGNALING PROTEIN / GPCR / G protein / SIGNALING PROTEIN-IMMUNE SYSTEM complex | ||||||||||||
| 機能・相同性 | 機能・相同性情報complement component C5a binding / cell proliferation in hindbrain / response to peptidoglycan / presynapse organization / complement component C5a signaling pathway / Terminal pathway of complement / Regulation of Complement cascade / Peptide ligand-binding receptors / membrane attack complex / complement component C5a receptor activity ...complement component C5a binding / cell proliferation in hindbrain / response to peptidoglycan / presynapse organization / complement component C5a signaling pathway / Terminal pathway of complement / Regulation of Complement cascade / Peptide ligand-binding receptors / membrane attack complex / complement component C5a receptor activity / Muscarinic acetylcholine receptors / G protein-coupled acetylcholine receptor activity / G alpha (i) signalling events / regulation of locomotion / Activation of C3 and C5 / negative regulation of macrophage chemotaxis / complement activation, GZMK pathway / adenylate cyclase-inhibiting G protein-coupled acetylcholine receptor signaling pathway / mu-type opioid receptor binding / corticotropin-releasing hormone receptor 1 binding / complement receptor mediated signaling pathway / negative regulation of neurotransmitter secretion / G protein-coupled dopamine receptor signaling pathway / positive regulation of neutrophil chemotaxis / chemokine activity / positive regulation of macrophage chemotaxis / endopeptidase inhibitor activity / amyloid-beta clearance / parallel fiber to Purkinje cell synapse / negative regulation of insulin secretion / positive regulation of vascular endothelial growth factor production / G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger / postsynaptic modulation of chemical synaptic transmission / neutrophil chemotaxis / positive regulation of chemokine production / Neutrophil degranulation / positive regulation of epithelial cell proliferation / astrocyte activation / muscle contraction / adenylate cyclase-inhibiting dopamine receptor signaling pathway / Regulation of Complement cascade / adenylate cyclase-inhibiting serotonin receptor signaling pathway / G protein-coupled serotonin receptor binding / Peptide ligand-binding receptors / microglial cell activation / GABA-ergic synapse / mRNA transcription by RNA polymerase II / chemotaxis / cognition / G protein-coupled receptor activity / positive regulation of angiogenesis / apical part of cell / G-protein beta/gamma-subunit complex binding / adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway / adenylate cyclase-modulating G protein-coupled receptor signaling pathway / Olfactory Signaling Pathway / phospholipase C-activating G protein-coupled receptor signaling pathway / Activation of the phototransduction cascade / G protein-coupled acetylcholine receptor signaling pathway / G beta:gamma signalling through PLC beta / Presynaptic function of Kainate receptors / Thromboxane signalling through TP receptor / Activation of G protein gated Potassium channels / Inhibition of voltage gated Ca2+ channels via Gbeta/gamma subunits / G-protein activation / Glucagon signaling in metabolic regulation / G beta:gamma signalling through CDC42 / Prostacyclin signalling through prostacyclin receptor / Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) / photoreceptor disc membrane / G beta:gamma signalling through BTK / ADP signalling through P2Y purinoceptor 12 / Sensory perception of sweet, bitter, and umami (glutamate) taste / Glucagon-type ligand receptors / Adrenaline,noradrenaline inhibits insulin secretion / Vasopressin regulates renal water homeostasis via Aquaporins / G alpha (z) signalling events / Glucagon-like Peptide-1 (GLP1) regulates insulin secretion / ADP signalling through P2Y purinoceptor 1 / cellular response to catecholamine stimulus / G beta:gamma signalling through PI3Kgamma / ADORA2B mediated anti-inflammatory cytokines production / adenylate cyclase-activating dopamine receptor signaling pathway / negative regulation of neuron apoptotic process / cellular response to prostaglandin E stimulus / Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding / GPER1 signaling / heterotrimeric G-protein complex / G alpha (12/13) signalling events / Inactivation, recovery and regulation of the phototransduction cascade / G-protein beta-subunit binding / extracellular vesicle / positive regulation of cytosolic calcium ion concentration / Thrombin signalling through proteinase activated receptors (PARs) / signaling receptor complex adaptor activity / chemical synaptic transmission / GTPase binding / cell body / G protein activity / cytoplasmic vesicle 類似検索 - 分子機能 | ||||||||||||
| 生物種 | Homo sapiens (ヒト)![]() | ||||||||||||
| 手法 | 電子顕微鏡法 / 単粒子再構成法 / クライオ電子顕微鏡法 / 解像度: 3.11 Å | ||||||||||||
データ登録者 | Banerjee, R. / Yadav, M.K. / Yadav, R. / Ganguly, M. / Mishra, S. / Dalal, A. / Gati, C. / Shukla, A.K. | ||||||||||||
| 資金援助 | インド, 英国, 3件
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引用 | ジャーナル: bioRxiv / 年: 2025タイトル: Molecular fingerprints of a convergent mechanism orchestrating diverse ligand recognition and species-specific pharmacology at the complement anaphylatoxin receptors. 著者: Sudha Mishra / Manish K Yadav / Annu Dalal / Manisankar Ganguly / Ravi Yadav / Kazuhiro Sawada / Divyanshu Tiwari / Nabarun Roy / Nilanjana Banerjee / Jenny N Fung / Jianina Marallag / Cedric ...著者: Sudha Mishra / Manish K Yadav / Annu Dalal / Manisankar Ganguly / Ravi Yadav / Kazuhiro Sawada / Divyanshu Tiwari / Nabarun Roy / Nilanjana Banerjee / Jenny N Fung / Jianina Marallag / Cedric S Cui / Xaria X Li / John D Lee / Calvin Aaron Dsouza / Shirsha Saha / Parishmita Sarma / Ganita Rawat / Houming Zhu / Htet A Khant / Richard J Clark / Fumiya K Sano / Ramanuj Banerjee / Trent M Woodruff / Osamu Nureki / Cornelius Gati / Arun K Shukla / ![]() 要旨: Complement anaphylatoxin receptors (C3aR and C5aR1) are prototypical G protein-coupled receptors (GPCRs) playing crucial physiological roles in innate immunity by combating pathogenic infections and ...Complement anaphylatoxin receptors (C3aR and C5aR1) are prototypical G protein-coupled receptors (GPCRs) playing crucial physiological roles in innate immunity by combating pathogenic infections and orchestrating inflammatory responses. They continue to be important therapeutic targets for multiple disorders including autoimmune diseases, acute and chronic inflammation, and allergy-related conditions. Recent structural coverage has provided important insights into their activation and signaling, however, confounding observations in the literature related to ligand efficacy and functional responses, especially in different model systems, present a major challenge for drug discovery efforts. Here, we systematically and comprehensively profile a broad set of natural and synthetic ligands at C3aR and C5aR1 and discover a previously unanticipated level of functional specialization in terms of species-specific pharmacology and receptor activation. Taking a lead from this, we determine seventeen cryo-EM structures of different ligand-receptor-G-protein complexes and uncover distinct orientation of agonists between the human and mouse receptors despite an overlapping positioning in the orthosteric binding pocket. Combined with extensive mutagenesis and functional assays, these structural snapshots allow us to decode and validate a convergent molecular mechanism involving a "Five-Point-Switch" in these receptors that orchestrates the recognition and efficacy of diverse agonists. We also identify species-specific differences at the level of phosphorylation patterns encoded in the carboxyl-terminus of these receptors and directly visualize their impact on βarr binding and activation using cryo-EM structures. Interestingly, we observe that βarrs engage with the mouse C5aR1 using a variation of previously discovered P-X-P-P phosphorylation motif via a "Sliding-Mechanism" and also exhibit distinct oligomeric state for the human vs. mouse receptors. Taken together, this study elucidates functional specialization at the complement anaphylatoxin receptors and underlying molecular mechanisms, offering a previously lacking framework with direct and immediate implications for the development of novel therapeutics. | ||||||||||||
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構造の表示
| 構造ビューア | 分子: Molmil Jmol/JSmol |
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ダウンロードとリンク
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ダウンロード
| PDBx/mmCIF形式 | 9kx6.cif.gz | 219.4 KB | 表示 | PDBx/mmCIF形式 |
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| PDB形式 | pdb9kx6.ent.gz | 167.5 KB | 表示 | PDB形式 |
| PDBx/mmJSON形式 | 9kx6.json.gz | ツリー表示 | PDBx/mmJSON形式 | |
| その他 | その他のダウンロード |
-検証レポート
| アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/kx/9kx6 ftp://data.pdbj.org/pub/pdb/validation_reports/kx/9kx6 | HTTPS FTP |
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-関連構造データ
| 関連構造データ | ![]() 62624MC ![]() 9kutC ![]() 9kv6C ![]() 9kv8C ![]() 9kvpC ![]() 9kwgC ![]() 9kwxC ![]() 9ky2C ![]() 9kyuC ![]() 9kzkC ![]() 9l0hC ![]() 9umjC ![]() 9umrC ![]() 9umxC M: このデータのモデリングに利用したマップデータ 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 F&H 検索 |
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リンク
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集合体
| 登録構造単位 | ![]()
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要素
-タンパク質 , 2種, 2分子 AD
| #1: タンパク質 | 分子量: 44958.422 Da / 分子数: 1 / 由来タイプ: 組換発現 由来: (組換発現) Homo sapiens (ヒト), (組換発現) ![]() 遺伝子: CHRM4, C5ar1, C5ar, C5r1 発現宿主: ![]() 参照: UniProt: P08173, UniProt: P30993 |
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| #4: タンパク質 | 分子量: 8131.482 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: C5, CPAMD4 / 発現宿主: ![]() |
-Guanine nucleotide-binding protein ... , 3種, 3分子 BCG
| #2: タンパク質 | 分子量: 27024.762 Da / 分子数: 1 / Mutation: G42D,E43N,A227D,G230D,I332A,V335I / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: GNAO1 / 発現宿主: ![]() |
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| #3: タンパク質 | 分子量: 38534.062 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: GNB1発現宿主: ![]() 参照: UniProt: P62873 |
| #5: タンパク質 | 分子量: 7861.143 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: GNG2発現宿主: ![]() 参照: UniProt: P59768 |
-抗体 , 1種, 1分子 H
| #6: 抗体 | 分子量: 27340.482 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) ![]() ![]() |
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-詳細
| Has protein modification | Y |
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-実験情報
-実験
| 実験 | 手法: 電子顕微鏡法 |
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| EM実験 | 試料の集合状態: PARTICLE / 3次元再構成法: 単粒子再構成法 |
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試料調製
| 構成要素 |
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| 由来(天然) |
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| 由来(組換発現) |
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| 緩衝液 | pH: 7.4 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 試料 | 包埋: NO / シャドウイング: NO / 染色: NO / 凍結: YES | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 急速凍結 | 凍結剤: ETHANE |
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電子顕微鏡撮影
| 実験機器 | ![]() モデル: Titan Krios / 画像提供: FEI Company |
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| 顕微鏡 | モデル: TFS KRIOS |
| 電子銃 | 電子線源: FIELD EMISSION GUN / 加速電圧: 300 kV / 照射モード: FLOOD BEAM |
| 電子レンズ | モード: BRIGHT FIELD / 最大 デフォーカス(公称値): 3000 nm / 最小 デフォーカス(公称値): 800 nm |
| 撮影 | 電子線照射量: 57.9 e/Å2 / 検出モード: COUNTING / フィルム・検出器のモデル: GATAN K3 (6k x 4k) |
| 画像スキャン | 動画フレーム数/画像: 40 |
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解析
| EMソフトウェア |
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| CTF補正 | タイプ: NONE | ||||||||||||||||||||||||||||||||||||||||
| 対称性 | 点対称性: C1 (非対称) | ||||||||||||||||||||||||||||||||||||||||
| 3次元再構成 | 解像度: 3.11 Å / 解像度の算出法: FSC 0.143 CUT-OFF / 粒子像の数: 321951 / 対称性のタイプ: POINT | ||||||||||||||||||||||||||||||||||||||||
| 原子モデル構築 | プロトコル: FLEXIBLE FIT / 空間: REAL |
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万見について




Homo sapiens (ヒト)

インド,
英国, 3件
引用




























PDBj









































FIELD EMISSION GUN