5O14: Factor H binding protein variant 1.1
Co-crystal structure of a cross-reactive bactericidal human antibody targeting meningococcal vaccine antigen factor H binding protein. Determined by X-ray diffraction at 2.19 Å resolution. Released 14 Feb 2018.
- Method
- X-ray diffraction
- Resolution
- 2.19 Å
- Organisms
- Neisseria meningitidis serogroup B (strain MC58), Homo sapiens
- Chains
- 6
- Atoms
- 10,853
- Mol. weight
- 153.92 kDa
- Released
- 14 Feb 2018
Explore 5O14 in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
5O14 contains 59 α-helices and 124 β-strands across 6 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.
Chain A: 9 helices, 19 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 16-21 | 6 | |
| α-helix | 23-24 | 2 | |
| α-helix | 29 | 1 | |
| α-helix | 31 | 1 | |
| β-strand | 34-35 | 2 | 1 |
| β-strand | 45-50 | 6 | 2 |
| β-strand | 53-57 | 5 | 2 |
| β-strand | 62-63 | 2 | 1 |
| α-helix | 65-67 | 3 | |
| α-helix | 69 | 1 | |
| β-strand | 73-81 | 9 | 2 |
| β-strand | 90-100 | 11 | 2 |
| β-strand | 104-114 | 11 | 2 |
| β-strand | 124-136 | 13 | 2 |
| β-strand | 138 | 1 | 3 |
| α-helix | 139 | 1 | |
| β-strand | 140 | 1 | 4 |
| α-helix | 141-143 | 3 | |
| β-strand | 149-158 | 10 | 3 |
| β-strand | 161-171 | 11 | 3 |
| β-strand | 176-182 | 7 | 3 |
| α-helix | 187-189 | 3 | |
| β-strand | 192-200 | 9 | 3 |
| β-strand | 205 | 1 | 4 |
| β-strand | 206-214 | 9 | 3 |
| β-strand | 217-227 | 11 | 3 |
| β-strand | 233-242 | 10 | 3 |
| β-strand | 245-254 | 10 | 3 |
Chain B: 8 helices, 19 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 16-21 | 6 | |
| α-helix | 23-24 | 2 | |
| α-helix | 29 | 1 | |
| β-strand | 34-35 | 2 | 5 |
| β-strand | 45-50 | 6 | 6 |
| β-strand | 53-57 | 5 | 6 |
| β-strand | 62-63 | 2 | 5 |
| α-helix | 65-67 | 3 | |
| α-helix | 69 | 1 | |
| β-strand | 73-81 | 9 | 6 |
| β-strand | 90-100 | 11 | 6 |
| β-strand | 104-114 | 11 | 6 |
| β-strand | 124-136 | 13 | 6 |
| β-strand | 138 | 1 | 7 |
| α-helix | 139 | 1 | |
| β-strand | 140 | 1 | 8 |
| α-helix | 141-143 | 3 | |
| β-strand | 149-158 | 10 | 7 |
| β-strand | 161-171 | 11 | 7 |
| β-strand | 176-182 | 7 | 7 |
| α-helix | 187-189 | 3 | |
| β-strand | 192-200 | 9 | 7 |
| β-strand | 205 | 1 | 8 |
| β-strand | 206-214 | 9 | 7 |
| β-strand | 217-227 | 11 | 7 |
| β-strand | 233-242 | 10 | 7 |
| β-strand | 245-254 | 10 | 7 |
Chain C: 13 helices, 22 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-6 | 4 | 9 |
| α-helix | 7-9 | 3 | |
| β-strand | 10-12 | 3 | 10 |
| β-strand | 18-25 | 8 | 9 |
| α-helix | 29-31 | 3 | |
| β-strand | 34-39 | 6 | 10 |
| β-strand | 46-52 | 7 | 10 |
| β-strand | 57-60 | 4 | 10 |
| α-helix | 62-64 | 3 | |
| β-strand | 68-73 | 6 | 9 |
| α-helix | 74-76 | 3 | |
| β-strand | 78-83 | 6 | 9 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-100 | 9 | 10 |
| β-strand | 108-112 | 5 | 10 |
| β-strand | 116-120 | 5 | 10 |
| α-helix | 124-125 | 2 | |
| β-strand | 126 | 1 | 11 |
| α-helix | 127-128 | 2 | |
| β-strand | 129-133 | 5 | 12 |
| α-helix | 134-136 | 3 | |
| α-helix | 139-140 | 2 | |
| β-strand | 144-154 | 11 | 12 |
| β-strand | 155 | 1 | 11 |
| β-strand | 160-163 | 4 | 13 |
| α-helix | 164-166 | 3 | |
| β-strand | 168 | 1 | 13 |
| β-strand | 172-174 | 3 | 12 |
| α-helix | 175-177 | 3 | |
| β-strand | 178-179 | 2 | 12 |
| β-strand | 185-194 | 10 | 12 |
| α-helix | 195-197 | 3 | |
| β-strand | 204-209 | 6 | 13 |
| α-helix | 210-212 | 3 | |
| β-strand | 214-219 | 6 | 13 |
Chain D: 9 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-7 | 4 | 14 |
| β-strand | 10-14 | 5 | 15 |
| β-strand | 19-25 | 7 | 14 |
| β-strand | 33-38 | 6 | 15 |
| β-strand | 45-49 | 5 | 15 |
| β-strand | 53-54 | 2 | 15 |
| α-helix | 55 | 1 | |
| β-strand | 62-67 | 6 | 14 |
| β-strand | 70-75 | 6 | 14 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-90 | 7 | 15 |
| α-helix | 98 | 1 | |
| β-strand | 99 | 1 | 15 |
| α-helix | 100 | 1 | |
| β-strand | 103-108 | 6 | 15 |
| β-strand | 112 | 1 | 16 |
| α-helix | 113-114 | 2 | |
| β-strand | 115-119 | 5 | 17 |
| α-helix | 120-122 | 3 | |
| α-helix | 123-128 | 6 | |
| β-strand | 130-140 | 11 | 17 |
| β-strand | 141 | 1 | 16 |
| β-strand | 146-151 | 6 | 18 |
| β-strand | 154-155 | 2 | 18 |
| β-strand | 160-164 | 5 | 17 |
| α-helix | 165-168 | 4 | |
| β-strand | 174-183 | 10 | 17 |
| α-helix | 184-188 | 5 | |
| β-strand | 192-198 | 7 | 18 |
| β-strand | 206-211 | 6 | 18 |
Chain H: 11 helices, 22 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-6 | 4 | 24 |
| α-helix | 7-9 | 3 | |
| β-strand | 10-12 | 3 | 25 |
| β-strand | 18-25 | 8 | 24 |
| α-helix | 29-31 | 3 | |
| β-strand | 34-39 | 6 | 25 |
| β-strand | 46-52 | 7 | 25 |
| β-strand | 57-60 | 4 | 25 |
| β-strand | 68-73 | 6 | 24 |
| α-helix | 74-76 | 3 | |
| β-strand | 78-83 | 6 | 24 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-100 | 9 | 25 |
| β-strand | 108-112 | 5 | 25 |
| β-strand | 116-120 | 5 | 25 |
| α-helix | 124-125 | 2 | |
| β-strand | 126 | 1 | 26 |
| α-helix | 127-128 | 2 | |
| β-strand | 129-133 | 5 | 27 |
| α-helix | 134-136 | 3 | |
| β-strand | 144-154 | 11 | 27 |
| β-strand | 155 | 1 | 26 |
| β-strand | 160-163 | 4 | 28 |
| α-helix | 164-166 | 3 | |
| β-strand | 168 | 1 | 28 |
| β-strand | 172-174 | 3 | 27 |
| α-helix | 175-177 | 3 | |
| β-strand | 178-179 | 2 | 27 |
| β-strand | 185-194 | 10 | 27 |
| α-helix | 195-197 | 3 | |
| β-strand | 204-209 | 6 | 28 |
| α-helix | 210-212 | 3 | |
| β-strand | 214-219 | 6 | 28 |
Chain L: 9 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-7 | 4 | 19 |
| β-strand | 10-14 | 5 | 20 |
| β-strand | 19-25 | 7 | 19 |
| β-strand | 33-38 | 6 | 20 |
| β-strand | 45-49 | 5 | 20 |
| β-strand | 53-54 | 2 | 20 |
| α-helix | 55 | 1 | |
| β-strand | 62-67 | 6 | 19 |
| β-strand | 70-75 | 6 | 19 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-90 | 7 | 20 |
| α-helix | 98 | 1 | |
| β-strand | 99 | 1 | 20 |
| α-helix | 100 | 1 | |
| β-strand | 103-108 | 6 | 20 |
| β-strand | 112 | 1 | 21 |
| α-helix | 113-114 | 2 | |
| β-strand | 115-119 | 5 | 22 |
| α-helix | 120-122 | 3 | |
| α-helix | 123-127 | 5 | |
| β-strand | 130-140 | 11 | 22 |
| β-strand | 141 | 1 | 21 |
| β-strand | 146-151 | 6 | 23 |
| β-strand | 154-155 | 2 | 23 |
| β-strand | 160-164 | 5 | 22 |
| α-helix | 165-168 | 4 | |
| β-strand | 174-183 | 10 | 22 |
| α-helix | 184-188 | 5 | |
| β-strand | 192-198 | 7 | 23 |
| β-strand | 206-211 | 6 | 23 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Factor H binding protein variant 1.1 | A, B | protein | 257 | Neisseria meningitidis serogroup B (strain MC58) | Q9JXV4 (AlphaFold model) |
| Fab 1A12 Heavy Chain | C, H | protein | 235 | Homo sapiens | |
| Fab 1A12 Light Chain | D, L | protein | 217 | Homo sapiens | |
Sequence of entity 1 (A, B), FASTA
>5O14_1 Factor H binding protein variant 1.1 (chains A, B)
MVAADIGAGLADALTAPLDHKDKGLQSLTLDQSVRKNEKLKLAAQGAEKTYGNGDSLNTG
KLKNDKVSRFDFIRQIEVDGQLITLESGEFQVYKQSHSALTAFQTEQIQDSEHSGKMVAK
RQFRIGDIAGEHTSFDKLPEGGRATYRGTAFGSDDAGGKLTYTIDFAAKQGNGKIEHLKS
PELNVDLAAADIKPDGKRHAVISGSVLYNQAEKGSYSLGIFGGKAQEVAGSAEVKTVNGI
RHIGLAAKQLEHHHHHH
Sequence of entity 2 (C, H), FASTA
>5O14_2 Fab 1A12 Heavy Chain (chains C, H)
EVQLVQSGAELKKPGESLKISCKASGYTFTNYWVVWVRQMPGEGLEWMGSIHPRDSDARY
SLSFEGRVTFSVDKSTTTAYLQWSSLKVSDSAIYYCARLSQVSGWSPWVGPWGQGTLVTV
SSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQ
SSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKLEHHHHHH
Sequence of entity 3 (D, L), FASTA
>5O14_3 Fab 1A12 Light Chain (chains D, L)
ADIVMTQSPSSLSASVGDRVTITCRASQSISVSLNWYQQKPGKAPKVLIYAASRLQSGIP
SRFSGSGSGSHFTLTISSLQPEDFATYYCQETYSDLMYTFGQGTKVEIKRTVAAPSVFIF
PPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSST
LTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGECS
Primary citation
Crystal structure reveals vaccine elicited bactericidal human antibody targeting a conserved epitope on meningococcal fHbp. Lopez-Sagaseta, J., Beernink, P.T., Bianchi, F. et al. Nat Commun (2018) 9:528-528. DOI 10.1038/s41467-018-02827-7 · PubMed
Other PDB entries of the same protein (UniProt Q9JXV4 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 8UP2 1.6 Å, Murine Fab JAR 4 bound to meningococcal Factor H binding protein
- 5NQZ 1.63 Å, Structure of a fHbp(V1.1):PorA(P1.16) chimera. Fusion at fHbp position 309.
- 7LCV 1.7 Å, Factor H enhancing human antibody fragment (Fab) to meningococcal Factor H binding protein
- 2YPV 1.8 Å, Crystal structure of the Meningococcal vaccine antigen factor H binding protein in…
- 2Y7S 1.9 Å, Structure of a designed meningococcal antigen (factor H binding protein, mutant G1)…
- 7KET 2.0 Å, Factor H enhancing human antibody fragment (Fab) to meningococcal Factor H binding protein
- 2W80 2.35 Å, Structure of a complex between Neisseria meningitidis factor H binding protein and CCPs…
- 2W81 2.35 Å, Structure of a complex between Neisseria meningitidis factor H binding protein and CCPs…
- 4AYD 2.4 Å, Structure of a complex between CCPs 6 and 7 of Human Complement Factor H and Neisseria…
- 6XZW 2.4 Å, Crystal structure of the meningococcal vaccine antigen fHbp in complex with a…
- 4AYE 2.8 Å, Structure of a complex between CCPs 6 and 7 of Human Complement Factor H and Neisseria…
- 7SBZ 2.9 Å, JAR5 Fab bound to fHbp v1.1 crystallized in space group I422
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