Cryo-EM Structure of Human TLR4/MD-2/DLAM3 Complex. Determined by electron microscopy at 2.9 Å resolution. Released 23 Oct 2024.
Explore 8WTA in 3D Show helices and sheets RCSB PDB PDBe
8WTA contains 18 α-helices and 114 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 31-33 | 3 | 1 |
| β-strand | 37-38 | 2 | 1 |
| β-strand | 41 | 1 | 2 |
| β-strand | 57 | 1 | 1 |
| β-strand | 62 | 1 | 2 |
| β-strand | 69 | 1 | 3 |
| β-strand | 79 | 1 | 4 |
| β-strand | 82 | 1 | 5 |
| β-strand | 86 | 1 | 2 |
| β-strand | 92-93 | 2 | 3 |
| β-strand | 102 | 1 | 4 |
| β-strand | 106-108 | 3 | 5 |
| β-strand | 116-117 | 2 | 3 |
| β-strand | 130-132 | 3 | 5 |
| β-strand | 156 | 1 | 5 |
| β-strand | 179-181 | 3 | 5 |
| β-strand | 189-190 | 2 | 6 |
| β-strand | 207-209 | 3 | 5 |
| β-strand | 217-218 | 2 | 6 |
| β-strand | 223 | 1 | 7 |
| β-strand | 231-234 | 4 | 8 |
| α-helix | 240-249 | 10 | |
| β-strand | 250 | 1 | 7 |
| β-strand | 258-261 | 4 | 8 |
| α-helix | 280-282 | 3 | |
| β-strand | 288-291 | 4 | 8 |
| β-strand | 313-316 | 4 | 8 |
| β-strand | 319 | 1 | 9 |
| β-strand | 335-338 | 4 | 8 |
| β-strand | 341 | 1 | 9 |
| α-helix | 345-347 | 3 | |
| β-strand | 349 | 1 | 10 |
| β-strand | 356-359 | 4 | 8 |
| β-strand | 371 | 1 | 10 |
| β-strand | 386 | 1 | 11 |
| β-strand | 411 | 1 | 11 |
| β-strand | 428 | 1 | 12 |
| β-strand | 453 | 1 | 12 |
| β-strand | 460-461 | 2 | 13 |
| β-strand | 475-477 | 3 | 12 |
| β-strand | 482-483 | 2 | 13 |
| α-helix | 484-486 | 3 | |
| β-strand | 488 | 1 | 14 |
| β-strand | 500-502 | 3 | 12 |
| β-strand | 511 | 1 | 14 |
| β-strand | 524-526 | 3 | 12 |
| β-strand | 548-550 | 3 | 12 |
| α-helix | 566-568 | 3 | |
| β-strand | 573-575 | 3 | 12 |
| α-helix | 588-595 | 8 | |
| α-helix | 604-606 | 3 | |
| β-strand | 608-609 | 2 | 15 |
| β-strand | 618-619 | 2 | 15 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 22-23 | 2 | 16 |
| β-strand | 33-36 | 4 | 16 |
| β-strand | 45-49 | 5 | 17 |
| α-helix | 51-52 | 2 | |
| β-strand | 58-65 | 8 | 17 |
| β-strand | 75-82 | 8 | 16 |
| β-strand | 85-93 | 9 | 16 |
| α-helix | 104-106 | 3 | |
| β-strand | 113-120 | 8 | 17 |
| β-strand | 129 | 1 | 18 |
| β-strand | 132-139 | 8 | 16 |
| β-strand | 144-152 | 9 | 16 |
| β-strand | 155 | 1 | 18 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Toll-like receptor 4 | A, B | protein | 605 | Homo sapiens | O00206 (AlphaFold model) |
| Lymphocyte antigen 96 | C, D | protein | 142 | Homo sapiens | Q9Y6Y9 (AlphaFold model) |
>8WTA_1 Toll-like receptor 4 (chains A, B) EPCVEVVPNITYQCMELNFYKIPDNLPFSTKNLDLSFNPLRHLGSYSFFSFPELQVLDLS RCEIQTIEDGAYQSLSHLSTLILTGNPIQSLALGAFSGLSSLQKLVAVETNLASLENFPI GHLKTLKELNVAHNLIQSFKLPEYFSNLTNLEHLDLSSNKIQSIYCTDLRVLHQMPLLNL SLDLSLNPMNFIQPGAFKEIRLHKLTLRNNFDSLNVMKTCIQGLAGLEVHRLVLGEFRNE GNLEKFDKSALEGLCNLTIEEFRLAYLDYYLDDIIDLFNCLTNVSSFSLVSVTIERVKDF SYNFGWQHLELVNCKFGQFPTLKLKSLKRLTFTSNKGGNAFSEVDLPSLEFLDLSRNGLS FKGCCSQSDFGTTSLKYLDLSFNGVITMSSNFLGLEQLEHLDFQHSNLKQMSEFSVFLSL RNLIYLDISHTHTRVAFNGIFNGLSSLEVLKMAGNSFQENFLPDIFTELRNLTFLDLSQC QLEQLSPTAFNSLSSLQVLNMSHNNFFSLDTFPYKCLNSLQVLDYSLNHIMTSKKQELQH FPSSLAFLNLTQNDFACTCEHQSFLQWIKDQRQLLVEVERMECATPSDKQGMPVLSLNIT CQMNK
>8WTA_2 Lymphocyte antigen 96 (chains C, D) QKQYWVCNSSDASISYTYCDKMQYPISINVNPCIELKGSKGLLHIFYIPRRDLKQLYFNL YITVNTMNLPKRKEVICRGSDDDYSFCRALKGETVNTTISFSFKGIKFSKGKYKCVVEAI SGSPEEMLFCLEFVILHQPNSN
| ID | Name | Formula | Copies |
|---|---|---|---|
| GP4 | 2-amino-2-deoxy-4-O-phosphono-alpha-D-glucopyranose | C6 H14 N O8 P | 2 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 6 |
| 2IL | (3R)-3-(dodecanoyloxy)tetradecanoic acid | C26 H50 O4 | 4 |
| 0IL | (3R)-3-(tetradecanoyloxy)tetradecanoic acid | C28 H54 O4 | 2 |
| XIQ | 2-(hydroxymethyl)-5-methoxy-3,6-bis(oxidanyl)pyran-4-one | C7 H8 O6 | 2 |
Structural insight into TLR4/MD-2 activation by synthetic LPS mimetics with distinct binding modes. Fu, Y., Kim, H., Lee, D.S. et al. Nat Commun (2025) 16:4164-4164. DOI 10.1038/s41467-025-59550-3 · PubMed
Other PDB entries of the same protein (UniProt O00206 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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