2GSK: BtuB:TonB Complex

Structure of the BtuB:TonB Complex. Determined by X-ray diffraction at 2.1 Å resolution. Released 13 Jun 2006.

Method
X-ray diffraction
Resolution
2.1 Å
Organism
Escherichia coli
Chains
2
Atoms
5,658
Mol. weight
78.07 kDa
Ligands
HEX, OCT, LDA, CNC
Released
13 Jun 2006

Explore 2GSK in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2GSK contains 16 α-helices and 45 β-strands across 2 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: 13 helices, 39 β-strands

ElementResiduesLengthSheet
β-strand6-1161
β-strand26-3052
α-helix31-377
α-helix42-465
β-strand52-5653
β-strand64-6853
α-helix73-753
β-strand76-8052
β-strand83-8422
α-helix85-862
α-helix96-983
α-helix101-1033
β-strand106-11162
α-helix115-1184
β-strand125-13062
β-strand137-14594
β-strand149-161134
β-strand164-178154
β-strand18115
β-strand18716
β-strand195-209154
β-strand214-228154
β-strand23316
β-strand242-257164
β-strand261-277174
β-strand289-305174
β-strand309-322144
α-helix326-3283
β-strand333-348164
β-strand351-362124
β-strand366-380154
β-strand383-394124
α-helix395-3973
α-helix398-4025
α-helix410-4123
β-strand413-426144
β-strand429-441134
β-strand444-44747
β-strand452-45547
β-strand459-472144
β-strand475-488144
β-strand493-49424
α-helix4951
β-strand501-511114
β-strand514-523104
β-strand526-53058
β-strand537-54158
α-helix542-5432
β-strand544-554114
β-strand559-56684
β-strand57915
β-strand585-59394
Chain B: 3 helices, 6 β-strands
ElementResiduesLengthSheet
β-strand155-15739
α-helix160-1645
α-helix165-1695
β-strand174-18291
β-strand18719
β-strand188-197101
α-helix203-2108
β-strand214-21529
β-strand221-231111

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Vitamin B12 transporter btuBAprotein590Escherichia coliP06129 (AlphaFold model)
protein TONBBprotein81Escherichia coliP02929 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>2GSK_1 Vitamin B12 transporter btuB (chains A)
PDTLVVTANRFEQPRSTVLAPTTVVTRQDIDRWQSTSVNDVLRRLPGVDITQNGGSGQLS
SIFIRGTNASHVLVLIDGVRLNLAGVSGSADLSQFPIALVQRVEYIRGPRSAVYGSDAIG
GVVNIITTRDEPGTEISAGWGSNSYQNYDVSTQQQLGDKTRVTLLGDYAHTHGYDVVAYG
NTGTQAQTDNDGFLSKTLYGALEHNFTDAWSGFVRGYGYDNRTNYDAYYSPGSPLLDTRK
LYSQSWDAGLRYNGELIKSQLITSYSHSKDYNYDPHYGRYDSSATLDEMKQYTVQWANNV
IVGHGSIGAGVDWQKQTTTPGTGYVEDGYDQRNTGIYLTGLQQVGDFTFEGAARSDDNSQ
FGRHGTWQTSAGWEFIEGYRFIASYGTSYKAPNLGQLYGFYGNPNLDPEKSKQWEGAFEG
LTAGVNWRISGYRNDVSDLIDYDDHTLKYYNEGKARIKGVEATANFDTGPLTHTVSYDYV
DARNAITDTPLLRRAKQQVKYQLDWQLYDFDWGITYQYLGTRYDKDYSSYPYQTVKMGGV
SLWDLAVAYPVTSHLTVRGKIANLFDKDYETVYGYQTAGREYTLSGSYTF
Sequence of entity 2 (B), FASTA
>2GSK_2 protein TONB (chains B)
PRALSRNQPQYPARAQALRIEGQVKVKFDVTPDGRVDNVQILSAKPANMFEREVKNAMRR
WRYEPGKPGSGIVVNILFKIN

Ligands and cofactors

IDNameFormulaCopies
HEXHexaneC6 H142
OCTN-octaneC8 H183
LDALauryl dimethylamine-N-oxideC14 H31 N O4
CNCCyanocobalaminC63 H89 Co N14 O14 P1
CACalcium ionCa2

Primary citation

Outer membrane active transport: structure of the BtuB:TonB complex. Shultis, D.D., Purdy, M.D., Banchs, C.N. et al. Science (2006) 312:1396-1399. DOI 10.1126/science.1127694 · PubMed

Other PDB entries of the same protein (UniProt P06129 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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