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2IF7

Crystal Structure of NTB-A

2IF7 の概要
エントリーDOI10.2210/pdb2if7/pdb
分子名称SLAM family member 6, CALCIUM ION, CHLORIDE ION, ... (4 entities in total)
機能のキーワードntb-a, slam6, ly108, homophilic receptor, immune system
由来する生物種Homo sapiens (human)
細胞内の位置Cell membrane ; Single-pass type I membrane protein : Q96DU3
タンパク質・核酸の鎖数4
化学式量合計86857.20
構造登録者
Cao, E.,Ramagopal, U.A.,Fedorov, A.A.,Fedorov, E.V.,Nathenson, S.G.,Almo, S.C. (登録日: 2006-09-20, 公開日: 2006-10-17, 最終更新日: 2017-10-18)
主引用文献Cao, E.,Ramagopal, U.A.,Fedorov, A.,Fedorov, E.,Yan, Q.,Lary, J.W.,Cole, J.L.,Nathenson, S.G.,Almo, S.C.
NTB-A Receptor Crystal Structure: Insights into Homophilic Interactions in the Signaling Lymphocytic Activation Molecule Receptor Family.
Immunity, 25:559-570, 2006
Cited by
PubMed Abstract: The signaling lymphocytic activation molecule (SLAM) family includes homophilic and heterophilic receptors that regulate both innate and adaptive immunity. The ectodomains of most SLAM family members are composed of an N-terminal IgV domain and a C-terminal IgC2 domain. NK-T-B-antigen (NTB-A) is a homophilic receptor that stimulates cytotoxicity in natural killer (NK) cells, regulates bactericidal activities in neutrophils, and potentiates T helper 2 (Th2) responses. The 3.0 A crystal structure of the complete NTB-A ectodomain revealed a rod-like monomer that self-associates to form a highly kinked dimer spanning an end-to-end distance of approximately 100 A. The NTB-A homophilic and CD2-CD58 heterophilic dimers show overall structural similarities but differ in detailed organization and physicochemical properties of their respective interfaces. The NTB-A structure suggests a mechanism responsible for binding specificity within the SLAM family and imposes physical constraints relevant to the colocalization of SLAM-family proteins with other signaling molecules in the immunological synapse.
PubMed: 17045824
DOI: 10.1016/j.immuni.2006.06.020
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3 Å)
構造検証レポート
Validation report summary of 2if7
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-10-30に公開中

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