Cryo-EM structure of alpha5beta1 integrin in complex with NeoNectin candidate 2. Determined by electron microscopy at 2.97 Å resolution. Released 18 Jun 2025.
Explore 9DIA in 3D Show helices and sheets RCSB PDB PDBe
9DIA contains 24 α-helices and 69 β-strands across 3 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 | 9-12 | 4 | 1 |
| β-strand | 22-26 | 5 | 2 |
| β-strand | 34-39 | 6 | 2 |
| β-strand | 53 | 1 | 3 |
| β-strand | 54-59 | 6 | 2 |
| β-strand | 68-69 | 2 | 2 |
| β-strand | 79 | 1 | 4 |
| α-helix | 81-85 | 5 | |
| β-strand | 92 | 1 | 4 |
| β-strand | 94-95 | 2 | 5 |
| β-strand | 101 | 1 | 3 |
| β-strand | 104-108 | 5 | 6 |
| β-strand | 111-116 | 6 | 6 |
| β-strand | 120-121 | 2 | 5 |
| β-strand | 130 | 1 | 5 |
| β-strand | 134-139 | 6 | 6 |
| β-strand | 144-148 | 5 | 6 |
| β-strand | 169-172 | 4 | 7 |
| β-strand | 178-182 | 5 | 7 |
| α-helix | 185-188 | 4 | |
| β-strand | 190 | 1 | 8 |
| β-strand | 191-195 | 5 | 7 |
| α-helix | 197-202 | 6 | |
| β-strand | 217-218 | 2 | 7 |
| α-helix | 219-221 | 3 | |
| α-helix | 224-226 | 3 | |
| β-strand | 231 | 1 | 8 |
| β-strand | 235-238 | 4 | 9 |
| α-helix | 246 | 1 | |
| β-strand | 247-252 | 6 | 9 |
| β-strand | 261-265 | 5 | 9 |
| β-strand | 272-277 | 6 | 9 |
| β-strand | 289-292 | 4 | 10 |
| β-strand | 301-306 | 6 | 10 |
| β-strand | 310-312 | 3 | 11 |
| β-strand | 318-320 | 3 | 11 |
| β-strand | 323-327 | 5 | 10 |
| β-strand | 340-343 | 4 | 10 |
| β-strand | 354-359 | 6 | 12 |
| β-strand | 368-373 | 6 | 12 |
| β-strand | 383-387 | 5 | 12 |
| β-strand | 400-402 | 3 | 12 |
| α-helix | 407-408 | 2 | |
| β-strand | 418-421 | 4 | 1 |
| β-strand | 432-437 | 6 | 1 |
| β-strand | 442-447 | 6 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 66-69 | 4 | 13 |
| α-helix | 73-76 | 4 | |
| β-strand | 94 | 1 | 14 |
| β-strand | 98-102 | 5 | 13 |
| β-strand | 104 | 1 | 15 |
| β-strand | 107 | 1 | 15 |
| β-strand | 109-116 | 8 | 14 |
| β-strand | 123-130 | 8 | 16 |
| α-helix | 136-140 | 5 | |
| α-helix | 145-153 | 9 | |
| β-strand | 160-167 | 8 | 16 |
| α-helix | 180-184 | 5 | |
| β-strand | 194 | 1 | 17 |
| β-strand | 199-206 | 8 | 16 |
| α-helix | 209-217 | 9 | |
| β-strand | 222 | 1 | 17 |
| β-strand | 229 | 1 | 18 |
| α-helix | 232-241 | 10 | |
| α-helix | 242-244 | 3 | |
| β-strand | 251-258 | 8 | 16 |
| β-strand | 262 | 1 | 18 |
| α-helix | 267-271 | 5 | |
| β-strand | 275 | 1 | 19 |
| α-helix | 276-277 | 2 | |
| β-strand | 283-284 | 2 | 16 |
| β-strand | 287-288 | 2 | 16 |
| β-strand | 294 | 1 | 19 |
| α-helix | 295-298 | 4 | |
| α-helix | 299-309 | 11 | |
| β-strand | 311-317 | 7 | 16 |
| α-helix | 322-331 | 10 | |
| β-strand | 335-339 | 5 | 16 |
| α-helix | 347-359 | 13 | |
| β-strand | 361-363 | 3 | 20 |
| β-strand | 364-366 | 3 | 13 |
| α-helix | 369-370 | 2 | |
| β-strand | 373-380 | 8 | 14 |
| α-helix | 389-393 | 5 | |
| β-strand | 394-396 | 3 | 20 |
| β-strand | 403-412 | 10 | 14 |
| β-strand | 422-427 | 6 | 13 |
| β-strand | 434-438 | 5 | 13 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-5 | 2 | 21 |
| α-helix | 14-25 | 12 | |
| β-strand | 29-33 | 5 | 21 |
| β-strand | 36-40 | 5 | 21 |
| α-helix | 44-57 | 14 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Integrin alpha-5 | A | protein | 1005 | Homo sapiens | P08648 (AlphaFold model) |
| Integrin beta-1 | B | protein | 738 | Homo sapiens | P05556 (AlphaFold model) |
| NeoNectin candidate 2 | C | protein | 99 | synthetic construct |
>9DIA_1 Integrin alpha-5 (chains A) MGSRTPESPLHAVQLRWGPRRRPPLLPLLLLLLPPPPRVGGFNLDAEAPAVLSGPPGSFF GFSVEFYRPGTDGVSVLVGAPKANTSQPGVLQGGAVYLCPWGASPTQCTPIEFDSKGSRL LESSLSSSEGEEPVEYKSLQWFGATVRAHGSSILACAPLYSWRTEKEPLSDPVGTCYLST DNFTRILEYAPCRSDFSWAAGQGYCQGGFSAEFTKTGRVVLGGPGSYFWQGQILSATQEQ IAESYYPEYLINLVQGQLQTRQASSIYDDSYLGYSVAVGEFSGDDTEDFVAGVPKGNLTY GYVTILNGSDIRSLYNFSGEQMASYFGYAVAATDVNGDGLDDLLVGAPLLMDRTPDGRPQ EVGRVYVYLQHPAGIEPTPTLTLTGHDEFGRFGSSLTPLGDLDQDGYNDVAIGAPFGGET QQGVVFVFPGGPGGLGSKPSQVLQPLWAASHTPDFFGSALRGGRDLDGNGYPDLIVGSFG VDKAVVYRGRPIVSASASLTIFPAMFNPEERSCSLEGNPVACINLSFCLNASGKHVADSI GFTVELQLDWQKQKGGVRRALFLASRQATLTQTLLIQNGAREDCREMKIYLRNESEFRDK LSPIHIALNFSLDPQAPVDSHGLRPALHYQSKSRIEDKAQILLDCGEDNICVPDLQLEVF GEQNHVYLGDKNALNLTFHAQNVGEGGAYEAELRVTAPPEAEYSGLVRHPGNFSSLSCDY FAVNQSRLLVCDLGNPMKAGASLWGGLRFTVPHLRDTKKTIQFDFQILSKNLNNSQSDVV SFRLSVEAQAQVTLNGVSKPEAVLFPVSDWHPRDQPQKEEDLGPAVHHVYELINQGPSSI SQGVLELSCPQALEGQQLLYVTRVTGLNCTTNHPINPKGLELDPEGSLHHQQKREAPSRS SASSGPQILKCPEAECFRLRCELGPLHQQESQSLQLHFRVWAKTFLQREHQPFSLQCEAV YKALKMPYRILPRQLPQKERQVATAVQWTKAEGSYGTGGLEVLFQ
>9DIA_2 Integrin beta-1 (chains B) MNLQPIFWIGLISSVCCVFAQTDENRCLKANAKSCGECIQAGPNCGWCTNSTFLQEGMPT SARCDDLEALKKKGCPPDDIENPRGSKDIKKNKNVTNRSKGTAEKLKPEDITQIQPQQLV LRLRSGEPQTFTLKFKRAEDYPIDLYYLMDLSYSMKDDLENVKSLGTDLMNEMRRITSDF RIGFGSFVEKTVMPYISTTPAKLRNPCTSEQNCTSPFSYKNVLSLTNKGEVFNELVGKQR ISGNLDSPEGGFDAIMQVAVCGSLIGWRNVTRLLVFSTDAGFHFAGDGKLGGIVLPNDGQ CHLENNMYTMSHYYDYPSIAHLVQKLSENNIQTIFAVTEEFQPVYKELKNLIPKSAVGTL SANSSNVIQLIIDAYNSLSSEVILENGKLSEGVTISYKSYCKNGVNGTGENGRKCSNISI GDEVQFEISITSNKCPKKDSDSFKIRPLGFTEEVEVILQYICECECQSEGIPESPKCHEG NGTFECGACRCNEGRVGRHCECSTDEVNSEDMDAYCRKENSSEICSNNGECVCGQCVCRK RDNTNEIYSGKFCECDNFNCDRSNGLICGGNGVCKCRVCECNPNYTGSACDCSLDTSTCE ASNGQICNGRGICECGVCKCTDPKFQGQTCEMCQTCLGVCAEHKECVQCRAFNKGEKKDT CTQECSYFNITKVESRDKLPQPVQPDPVSHCKEKDVDDCWFYFTYSVNGNNEVMVHVVEN PECPTGPDDTSGLEVLFQ
>9DIA_3 NeoNectin candidate 2 (chains C) MGLNDIFEAQKIEWHEGGSGGGEVEVHGRGDIPRSSLELFEKVAKELGLKVERNHRTVTV KGVSEEQIRELEEVAKKLGLWVLVRVTEGGSLEHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| MN | Manganese (II) ion | Mn | 2 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 5 |
| CA | Calcium ion | Ca | 3 |
De Novo Design of Integrin alpha 5 beta 1 Modulating Proteins to Enhance Biomaterial Properties. Wang, X., Guillem-Marti, J., Kumar, S. et al. Adv Mater (2025) 37:e2500872-e2500872. DOI 10.1002/adma.202500872 · PubMed
Other PDB entries of the same protein (UniProt P08648 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 9DIA directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.