4FI3: Vitamin B12 import system permease protein BtuC
Structure of vitamin B12 transporter BtuCD-F in a nucleotide-bound state. Determined by X-ray diffraction at 3.47 Å resolution. Released 19 Sept 2012.
- Method
- X-ray diffraction
- Resolution
- 3.47 Å
- Organism
- Escherichia coli
- Chains
- 5
- Atoms
- 10,635
- Mol. weight
- 158.77 kDa
- Ligands
- MG, ANP
- Released
- 19 Sept 2012
Explore 4FI3 in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
4FI3 contains 72 α-helices and 42 β-strands across 5 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: 17 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 3-31 | 29 | |
| α-helix | 42-44 | 3 | |
| α-helix | 49-51 | 3 | |
| α-helix | 56-81 | 26 | |
| α-helix | 88-90 | 3 | |
| α-helix | 93-106 | 14 | |
| α-helix | 114-136 | 23 | |
| α-helix | 142-163 | 22 | |
| α-helix | 169-179 | 11 | |
| α-helix | 188-190 | 3 | |
| α-helix | 191-206 | 16 | |
| α-helix | 209-214 | 6 | |
| α-helix | 218-223 | 6 | |
| α-helix | 228-249 | 22 | |
| α-helix | 256-265 | 10 | |
| α-helix | 272-295 | 24 | |
| α-helix | 305-323 | 19 | |
Chain B: 17 helices, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 3-31 | 29 | |
| α-helix | 42-44 | 3 | |
| α-helix | 49-51 | 3 | |
| α-helix | 56-81 | 26 | |
| α-helix | 88-91 | 4 | |
| α-helix | 93-106 | 14 | |
| α-helix | 114-136 | 23 | |
| α-helix | 142-166 | 25 | |
| α-helix | 169-179 | 11 | |
| α-helix | 188-190 | 3 | |
| α-helix | 191-206 | 16 | |
| α-helix | 209-214 | 6 | |
| α-helix | 218-223 | 6 | |
| α-helix | 228-249 | 22 | |
| α-helix | 256-265 | 10 | |
| α-helix | 272-295 | 24 | |
| α-helix | 305-323 | 19 | |
Chain C: 12 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-12 | 8 | 1 |
| β-strand | 16-23 | 8 | 1 |
| β-strand | 28-32 | 5 | 2 |
| α-helix | 39-47 | 9 | |
| β-strand | 55-58 | 4 | 1 |
| β-strand | 61-62 | 2 | 1 |
| α-helix | 63-65 | 3 | |
| α-helix | 68-74 | 7 | |
| β-strand | 75-78 | 4 | 2 |
| α-helix | 83-85 | 3 | |
| β-strand | 89 | 1 | 3 |
| α-helix | 90-97 | 8 | |
| α-helix | 104-113 | 10 | |
| β-strand | 123 | 1 | 3 |
| α-helix | 124-126 | 3 | |
| α-helix | 129-144 | 16 | |
| β-strand | 154-157 | 4 | 2 |
| α-helix | 166-181 | 16 | |
| β-strand | 185-189 | 5 | 2 |
| α-helix | 193-199 | 7 | |
| β-strand | 202-207 | 6 | 2 |
| β-strand | 210-216 | 7 | 2 |
| α-helix | 217-220 | 4 | |
| α-helix | 223-230 | 8 | |
| β-strand | 233-239 | 7 | 4 |
| β-strand | 242-248 | 7 | 4 |
Chain D: 12 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-12 | 8 | 5 |
| β-strand | 16-23 | 8 | 5 |
| β-strand | 28-32 | 5 | 6 |
| α-helix | 39-46 | 8 | |
| β-strand | 55-58 | 4 | 5 |
| β-strand | 61-62 | 2 | 5 |
| α-helix | 63-65 | 3 | |
| α-helix | 68-74 | 7 | |
| β-strand | 75-78 | 4 | 6 |
| α-helix | 83-85 | 3 | |
| β-strand | 89 | 1 | 7 |
| α-helix | 90-97 | 8 | |
| α-helix | 104-113 | 10 | |
| β-strand | 123 | 1 | 7 |
| α-helix | 124-126 | 3 | |
| α-helix | 129-144 | 16 | |
| β-strand | 154-157 | 4 | 6 |
| α-helix | 166-181 | 16 | |
| β-strand | 185-189 | 5 | 6 |
| α-helix | 193-199 | 7 | |
| β-strand | 202-207 | 6 | 6 |
| β-strand | 210-216 | 7 | 6 |
| α-helix | 217-220 | 4 | |
| α-helix | 223-230 | 8 | |
| β-strand | 233-239 | 7 | 8 |
| β-strand | 242-248 | 7 | 8 |
Chain F: 14 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 26-28 | 3 | 9 |
| α-helix | 31-40 | 10 | |
| β-strand | 46 | 1 | 9 |
| β-strand | 47 | 1 | 10 |
| α-helix | 55-59 | 5 | |
| α-helix | 61 | 1 | |
| β-strand | 62 | 1 | 10 |
| β-strand | 64 | 1 | 11 |
| β-strand | 69 | 1 | 11 |
| α-helix | 71-76 | 6 | |
| β-strand | 81-84 | 4 | 9 |
| α-helix | 91-99 | 9 | |
| β-strand | 103-106 | 4 | 9 |
| α-helix | 113-122 | 10 | |
| α-helix | 123-125 | 3 | |
| α-helix | 129-151 | 23 | |
| α-helix | 154-155 | 2 | |
| β-strand | 156-160 | 5 | 12 |
| β-strand | 168 | 1 | 13 |
| α-helix | 175-182 | 8 | |
| β-strand | 185-187 | 3 | 12 |
| β-strand | 198 | 1 | 13 |
| α-helix | 201-205 | 5 | |
| β-strand | 211-215 | 5 | 12 |
| α-helix | 222-227 | 6 | |
| β-strand | 236-239 | 4 | 12 |
| α-helix | 241-245 | 5 | |
| α-helix | 251-263 | 13 | |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Vitamin B12 import system permease protein BtuC | A, B | protein | 349 | Escherichia coli | P06609 (AlphaFold model) |
| Vitamin B12 import ATP-binding protein BtuD | C, D | protein | 249 | Escherichia coli | P06611 (AlphaFold model) |
| Vitamin B12-binding protein | F | protein | 255 | Escherichia coli | P37028 (AlphaFold model) |
Sequence of entity 1 (A, B), FASTA
>4FI3_1 Vitamin B12 import system permease protein BtuC (chains A, B)
MGHHHHHHHHHHSSGENLYFQGHMLTLARQQQRQNIRWLLSLSVLMLLALLLSLSAGEQW
ISPGDWFTPRGELFVWQIRLPRTLAVLLVGAALAISGAVMQALFENPLAEPGLLGVSNGA
GVGLIAAVLLGQGQLPNWALGLSAIAGALIITLILLRFARRHLSTSRLLLAGVALGIISS
ALMTWAIYFSTSVDLRQLMYWMMGGFGGVDWRQSWLMLALIPVLLWISSQSRPMNMLALG
EISARQLGLPLWFWRNVLVAATGWMVGVSVALAGAIGFIGLVIPHILRLSGLTDHRVLLP
GCALAGASALLLADIVARLALAAAELPIGVVTATLGAPVFIWLLLKAGR
Sequence of entity 2 (C, D), FASTA
>4FI3_2 Vitamin B12 import ATP-binding protein BtuD (chains C, D)
MSIVMQLQDVAESTRLGPLSGEVRAGEILHLVGPNGAGKSTLLARMAGMTSGKGSIQFAG
QPLEAWSATKLALHRAYLSQQQTPPFATPVWHYLTLHQHDKTRTELLNDVAGALALDDKL
GRSTNQLSGGEWQRVRLAAVVLQITPQANPAGQLLLLDQPMCSLDVAQQSALDKILSALS
QQGLAIVMSSHDLNHTLRHAHRAWLLKGGKMLASGRREEVLTPPNLAQAYGMNFRRLDIE
GHRMLISTI
Sequence of entity 3 (F), FASTA
>4FI3_3 Vitamin B12-binding protein (chains F)
MAAPRVITLSPANTELAFAAGITPVGVSSYSDYPPQAQKIEQVSTWQGMNLERIVALKPD
LVIAWRGGNAERQVDQLASLGIKVMWVDATSIEQIANALRQLAPWSPQPDKAEQAAQSLL
DQYAQLKAQYADKPKKRVFLQFGINPPFTSGKESIQNQVLEVCGGENIFKDSRVPWPQVS
REQVLARSPQAIVITGGPDQIPKIKQYWGEQLKIPVIPLTSDWFERASPRIILAAQQLCN
ALSQVDSGSHHHHHH
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| MG | Magnesium ion | Mg | 2 |
| ANP | Phosphoaminophosphonic acid-adenylate ester | C10 H17 N6 O12 P3 | 2 |
Primary citation
Structure of AMP-PNP-bound vitamin B12 transporter BtuCD-F. Korkhov, V.M., Mireku, S.A., Locher, K.P. Nature (2012) 490:367-372. DOI 10.1038/nature11442 · PubMed
Other PDB entries of the same protein (UniProt P06609 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 2QI9 2.6 Å, ABC-transporter BtuCD in complex with its periplasmic binding protein BtuF
- 4R9U 2.79 Å, Structure of vitamin B12 transporter BtuCD in a nucleotide-bound outward facing state
- 1L7V 3.2 Å, Bacterial ABC Transporter Involved in B12 Uptake
- 4DBL 3.49 Å, Crystal structure of E159Q mutant of BtuCDF
Browse structure collections
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