The ligand-free structure of the mouse TLR4/MD-2 complex. Determined by X-ray diffraction at 2.91 Å resolution. Released 27 Apr 2016.
Explore 5IJB in 3D Show helices and sheets RCSB PDB PDBe
5IJB contains 29 α-helices and 110 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 | 29-32 | 4 | 1 |
| β-strand | 36-38 | 3 | 1 |
| β-strand | 57-59 | 3 | 1 |
| β-strand | 68 | 1 | 2 |
| β-strand | 81-83 | 3 | 1 |
| β-strand | 92 | 1 | 2 |
| β-strand | 105-107 | 3 | 1 |
| β-strand | 129-131 | 3 | 1 |
| β-strand | 153-155 | 3 | 1 |
| α-helix | 168-172 | 5 | |
| β-strand | 178-180 | 3 | 1 |
| β-strand | 188-189 | 2 | 3 |
| α-helix | 195-199 | 5 | |
| β-strand | 206-208 | 3 | 1 |
| β-strand | 216-217 | 2 | 3 |
| β-strand | 225-233 | 9 | 1 |
| α-helix | 239-248 | 10 | |
| β-strand | 252-260 | 9 | 1 |
| α-helix | 273-276 | 4 | |
| β-strand | 283-289 | 7 | 1 |
| α-helix | 297-299 | 3 | |
| α-helix | 303-307 | 5 | |
| β-strand | 312-314 | 3 | 1 |
| β-strand | 332-336 | 5 | 1 |
| α-helix | 343-345 | 3 | |
| β-strand | 353-357 | 5 | 1 |
| β-strand | 364 | 1 | 4 |
| β-strand | 375-377 | 3 | 1 |
| β-strand | 384 | 1 | 4 |
| β-strand | 385-388 | 4 | 5 |
| α-helix | 391-393 | 3 | |
| β-strand | 401-403 | 3 | 1 |
| β-strand | 409-412 | 4 | 5 |
| β-strand | 424-426 | 3 | 1 |
| β-strand | 431-433 | 3 | 5 |
| β-strand | 449-451 | 3 | 1 |
| β-strand | 458-459 | 2 | 6 |
| α-helix | 462-465 | 4 | |
| β-strand | 473-475 | 3 | 1 |
| β-strand | 480-481 | 2 | 6 |
| α-helix | 482-484 | 3 | |
| β-strand | 485-486 | 2 | 7 |
| β-strand | 498-500 | 3 | 1 |
| β-strand | 508-509 | 2 | 7 |
| β-strand | 522-524 | 3 | 1 |
| α-helix | 535-537 | 3 | |
| β-strand | 546-548 | 3 | 1 |
| β-strand | 570-572 | 3 | 1 |
| β-strand | 578 | 1 | 8 |
| α-helix | 586-594 | 9 | |
| α-helix | 596-598 | 3 | |
| β-strand | 599-600 | 2 | 1 |
| β-strand | 604 | 1 | 9 |
| β-strand | 605 | 1 | 8 |
| β-strand | 611 | 1 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 29-32 | 4 | 12 |
| β-strand | 36-38 | 3 | 12 |
| β-strand | 57-59 | 3 | 12 |
| β-strand | 68 | 1 | 13 |
| β-strand | 82-83 | 2 | 12 |
| β-strand | 91 | 1 | 14 |
| β-strand | 92 | 1 | 13 |
| α-helix | 93 | 1 | |
| β-strand | 106-107 | 2 | 12 |
| β-strand | 115 | 1 | 14 |
| β-strand | 122 | 1 | 15 |
| β-strand | 124 | 1 | 15 |
| β-strand | 129-131 | 3 | 16 |
| β-strand | 153-155 | 3 | 16 |
| α-helix | 168-172 | 5 | |
| β-strand | 178-180 | 3 | 16 |
| β-strand | 188-189 | 2 | 17 |
| α-helix | 195-198 | 4 | |
| β-strand | 206-208 | 3 | 16 |
| β-strand | 216-217 | 2 | 17 |
| β-strand | 225-233 | 9 | 16 |
| α-helix | 239-247 | 9 | |
| β-strand | 252-260 | 9 | 16 |
| α-helix | 273-276 | 4 | |
| β-strand | 283-289 | 7 | 16 |
| α-helix | 297-299 | 3 | |
| α-helix | 303-305 | 3 | |
| β-strand | 310-314 | 5 | 16 |
| β-strand | 332-336 | 5 | 16 |
| β-strand | 353-357 | 5 | 16 |
| β-strand | 375-377 | 3 | 16 |
| β-strand | 385-388 | 4 | 18 |
| α-helix | 391-393 | 3 | |
| β-strand | 401-403 | 3 | 16 |
| β-strand | 409-412 | 4 | 18 |
| β-strand | 425-426 | 2 | 16 |
| β-strand | 431-433 | 3 | 18 |
| β-strand | 449-451 | 3 | 16 |
| β-strand | 458-459 | 2 | 19 |
| β-strand | 473-475 | 3 | 16 |
| β-strand | 480-481 | 2 | 19 |
| α-helix | 482-484 | 3 | |
| β-strand | 485-486 | 2 | 20 |
| β-strand | 498-500 | 3 | 16 |
| β-strand | 508-509 | 2 | 20 |
| β-strand | 522-524 | 3 | 16 |
| β-strand | 546-548 | 3 | 16 |
| β-strand | 570-572 | 3 | 16 |
| β-strand | 578-579 | 2 | 21 |
| α-helix | 586-594 | 9 | |
| β-strand | 599 | 1 | 16 |
| β-strand | 604 | 1 | 22 |
| β-strand | 605-606 | 2 | 21 |
| β-strand | 611 | 1 | 22 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 23-27 | 5 | 10 |
| β-strand | 30-36 | 7 | 10 |
| β-strand | 45-49 | 5 | 11 |
| α-helix | 51-53 | 3 | |
| β-strand | 57-65 | 9 | 11 |
| β-strand | 74-82 | 9 | 10 |
| β-strand | 85-93 | 9 | 10 |
| α-helix | 103-106 | 4 | |
| β-strand | 113-121 | 9 | 11 |
| β-strand | 131 | 1 | 10 |
| β-strand | 133-139 | 7 | 10 |
| β-strand | 144-155 | 12 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 25-26 | 2 | 23 |
| β-strand | 31-35 | 5 | 23 |
| β-strand | 37 | 1 | 24 |
| β-strand | 40 | 1 | 24 |
| β-strand | 45-49 | 5 | 25 |
| α-helix | 51-53 | 3 | |
| β-strand | 59-64 | 6 | 25 |
| β-strand | 65 | 1 | 26 |
| β-strand | 74-82 | 9 | 23 |
| β-strand | 85-86 | 2 | 23 |
| α-helix | 87-88 | 2 | |
| β-strand | 90-93 | 4 | 23 |
| α-helix | 103-106 | 4 | |
| α-helix | 107-108 | 2 | |
| β-strand | 113 | 1 | 26 |
| β-strand | 116-119 | 4 | 25 |
| β-strand | 130-139 | 10 | 23 |
| β-strand | 144-154 | 11 | 23 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Toll-like receptor 4, Variable lymphocyte receptor B chimera | A, B | protein | 594 | Mus musculus, Eptatretus burgeri | Q4G1L2 (AlphaFold model), Q9QUK6 (AlphaFold model) |
| Lymphocyte antigen 96 | C, D | protein | 150 | Mus musculus | Q9JHF9 (AlphaFold model) |
>5IJB_1 Toll-like receptor 4, Variable lymphocyte receptor B chimera (chains A, B) NPCIEVVPNITYQCMDQKLSKVPDDIPSSTKNIDLSFNPLKILKSYSFSNFSELQWLDLS RCEIETIEDKAWHGLHHLSNLILTGNPIQSFSPGSFSGLTSLENLVAVETKLASLESFPI GQLITLKKLNVAHNFIHSCKLPAYFSNLTNLVHVDLSYNYIQTITVNDLQFLRENPQVNL SLDMSLNPIDFIQDQAFQGIKLHELTLRGNFNSSNIMKTCLQNLAGLHVHRLILGEFKDE RNLEIFEPSIMEGLCDVTIDEFRLTYTNDFSDDIVKFHCLANVSAMSLAGVSIKYLEDVP KHFKWQSLSIIRCQLKQFPTLDLPFLKSLTLTMNKGSISFKKVALPSLSYLDLSRNALSF SGCCSYSDLGTNSLRHLDLSFNGAIIMSANFMGLEELQHLDFQHSTLKRVTEFSAFLSLE KLLYLDISYTNTKIDFDGIFLGLTSLNTLKMAGNSFKDNTLSNVFANTTNLTFLDLSKCQ LEQISWGVFDTLHRLQLLNMSHNNLLFLDSSHYNQLYSLKELALDTNQLKSVPDGIFDRL TSLQKIWLHTNPWDCSCPRIDYLSRWLNKNSQKEQGSAKCSGSGKPVRSIICPT
>5IJB_2 Lymphocyte antigen 96 (chains C, D) EKQQWFCNSSDAIISYSYCDHLKFPISISSEPCIRLRGTNGFVHVEFIPRGNLKYLYFNL FISVNSIELPKRKEVLCHGHDDDYSFCRALKGETVNTSIPFSFEGILFPKGHYRCVAEAI AGDTEEKLFCLNFTIIHRRDVNKGENLYFQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 6 |
TLR4/MD-2 activation by a synthetic agonist with no similarity to LPS. Wang, Y., Su, L., Morin, M.D. et al. Proc Natl Acad Sci U S A (2016) 113:E884-E893. DOI 10.1073/pnas.1525639113 · PubMed
Other PDB entries of the same protein (UniProt Q4G1L2 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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