Crystal Structure of Bacillus stearothermophilus Phosphofructokinase mutant T156A bound to PEP. Determined by X-ray diffraction at 2.49 Å resolution. Released 31 Jul 2013.
Explore 4I4I in 3D Show helices and sheets RCSB PDB PDBe
4I4I contains 64 α-helices and 52 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 | 3-9 | 7 | 1 |
| α-helix | 16-29 | 14 | |
| β-strand | 33-37 | 5 | 1 |
| α-helix | 40-45 | 6 | |
| β-strand | 49-51 | 3 | 1 |
| α-helix | 74-77 | 4 | |
| α-helix | 79-92 | 14 | |
| β-strand | 96-101 | 6 | 1 |
| α-helix | 103-114 | 12 | |
| β-strand | 119-123 | 5 | 1 |
| β-strand | 124-125 | 2 | 2 |
| β-strand | 137-138 | 2 | 2 |
| α-helix | 139-156 | 18 | |
| β-strand | 163-168 | 6 | 3 |
| α-helix | 175-184 | 10 | |
| β-strand | 188-190 | 3 | 3 |
| α-helix | 198-210 | 13 | |
| β-strand | 216-221 | 6 | 3 |
| α-helix | 227-238 | 12 | |
| β-strand | 242-246 | 5 | 3 |
| α-helix | 248-252 | 5 | |
| α-helix | 255-257 | 3 | |
| α-helix | 258-276 | 19 | |
| β-strand | 282-287 | 6 | 1 |
| β-strand | 290-295 | 6 | 1 |
| α-helix | 296-299 | 4 | |
| α-helix | 303-304 | 2 | |
| α-helix | 308-317 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-9 | 7 | 4 |
| α-helix | 16-29 | 14 | |
| β-strand | 33-37 | 5 | 4 |
| α-helix | 40-45 | 6 | |
| β-strand | 49-52 | 4 | 4 |
| α-helix | 53 | 1 | |
| α-helix | 54-57 | 4 | |
| α-helix | 74-77 | 4 | |
| α-helix | 79-91 | 13 | |
| β-strand | 96-101 | 6 | 4 |
| α-helix | 105-114 | 10 | |
| β-strand | 119-123 | 5 | 4 |
| β-strand | 124-125 | 2 | 5 |
| β-strand | 137-138 | 2 | 5 |
| α-helix | 139-156 | 18 | |
| β-strand | 163-168 | 6 | 6 |
| α-helix | 175-184 | 10 | |
| β-strand | 188-190 | 3 | 6 |
| α-helix | 198-210 | 13 | |
| β-strand | 216-221 | 6 | 6 |
| α-helix | 227-238 | 12 | |
| β-strand | 242-246 | 5 | 6 |
| α-helix | 248-252 | 5 | |
| α-helix | 255-257 | 3 | |
| α-helix | 258-276 | 19 | |
| β-strand | 282-287 | 6 | 4 |
| β-strand | 290-295 | 6 | 4 |
| α-helix | 296-300 | 5 | |
| α-helix | 303-304 | 2 | |
| α-helix | 308-317 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-9 | 7 | 7 |
| α-helix | 16-29 | 14 | |
| β-strand | 33-37 | 5 | 7 |
| α-helix | 40-46 | 7 | |
| β-strand | 49-51 | 3 | 7 |
| α-helix | 54-57 | 4 | |
| α-helix | 75-77 | 3 | |
| α-helix | 79-92 | 14 | |
| β-strand | 96-101 | 6 | 7 |
| α-helix | 103-114 | 12 | |
| β-strand | 119-123 | 5 | 7 |
| β-strand | 124 | 1 | 8 |
| β-strand | 137 | 1 | 8 |
| α-helix | 139-156 | 18 | |
| β-strand | 163-168 | 6 | 6 |
| α-helix | 175-184 | 10 | |
| β-strand | 188-190 | 3 | 6 |
| α-helix | 198-210 | 13 | |
| β-strand | 216-221 | 6 | 6 |
| α-helix | 227-238 | 12 | |
| β-strand | 242-246 | 5 | 6 |
| α-helix | 248-252 | 5 | |
| α-helix | 255-257 | 3 | |
| α-helix | 258-277 | 20 | |
| β-strand | 282-287 | 6 | 7 |
| β-strand | 290-295 | 6 | 7 |
| α-helix | 296-301 | 6 | |
| α-helix | 303-304 | 2 | |
| α-helix | 308-317 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-9 | 7 | 9 |
| α-helix | 16-29 | 14 | |
| β-strand | 33-37 | 5 | 9 |
| α-helix | 40-45 | 6 | |
| β-strand | 49-51 | 3 | 9 |
| α-helix | 54-57 | 4 | |
| α-helix | 75-77 | 3 | |
| α-helix | 79-91 | 13 | |
| β-strand | 96-101 | 6 | 9 |
| α-helix | 103-114 | 12 | |
| β-strand | 119-123 | 5 | 9 |
| β-strand | 124-125 | 2 | 10 |
| β-strand | 137-138 | 2 | 10 |
| α-helix | 139-156 | 18 | |
| β-strand | 163-168 | 6 | 3 |
| α-helix | 175-184 | 10 | |
| β-strand | 188-190 | 3 | 3 |
| α-helix | 198-210 | 13 | |
| β-strand | 216-221 | 6 | 3 |
| α-helix | 227-238 | 12 | |
| β-strand | 242-246 | 5 | 3 |
| α-helix | 248-252 | 5 | |
| α-helix | 255-257 | 3 | |
| α-helix | 258-276 | 19 | |
| β-strand | 282-287 | 6 | 9 |
| β-strand | 290-295 | 6 | 9 |
| α-helix | 296-300 | 5 | |
| α-helix | 303-304 | 2 | |
| α-helix | 308-317 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| 6-phosphofructokinase | A, B, C, D | protein | 319 | Geobacillus stearothermophilus | P00512 (AlphaFold model) |
>4I4I_1 6-phosphofructokinase (chains A, B, C, D) MKRIGVLTSGGDSPGMNAAIRSVVRKAIYHGVEVYGVYHGYAGLIAGNIKKLEVGDVGDI IHRGGTILYTARCPEFKTEEGQKKGIEQLKKHGIEGLVVIGGDGSYQGAKKLTEHGFPCV GVPGTIDNDIPGTDFTIGFDTALNTVIDAIDKIRDAATSHERTYVIEVMGRHAGDIALWS GLAGGAETILIPEADYDMNDVIARLKRGHERGKKHSIIIVAEGVGSGVDFGRQIQEATGF ETRVTVLGHVQRGGSPTAFDRVLASRLGARAVELLLEGKGGRCVGIQNNQLVDHDIAEAL ANKHTIDQRMYALSKELSI
| ID | Name | Formula | Copies |
|---|---|---|---|
| PEP | Phosphoenolpyruvate | C3 H5 O6 P | 4 |
Redefining the Role of the Quaternary Shift in Bacillus stearothermophilus Phosphofructokinase. Mosser, R., Reddy, M.C., Bruning, J.B. et al. Biochemistry (2013) 52:5421-5429. DOI 10.1021/bi4002503 · PubMed
Other PDB entries of the same protein (UniProt P00512 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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