3M8D: Vitamin B12 transporter btuB

Crystal structure of spin-labeled BtuB V10R1 with bound calcium and cyanocobalamin. Determined by X-ray diffraction at 2.44 Å resolution. Released 15 Sept 2010.

Method
X-ray diffraction
Resolution
2.44 Å
Organism
Escherichia coli
Chains
1
Atoms
4,862
Mol. weight
69.97 kDa
Ligands
CA, MTN, C8E, CNC
Released
15 Sept 2010

Explore 3M8D in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3M8D contains 15 α-helices and 38 β-strands across 1 chain. 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: 15 helices, 38 β-strands

ElementResiduesLengthSheet
β-strand8-921
β-strand17-1821
α-helix19-213
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-helix96-983
α-helix101-1033
β-strand106-11162
α-helix115-1184
β-strand125-13062
β-strand137-14594
β-strand149-159114
β-strand164-175124
β-strand18115
β-strand18716
β-strand197-209134
β-strand214-228154
β-strand23316
β-strand242-257164
β-strand261-277174
β-strand289-305174
β-strand309-322144
β-strand334-348154
β-strand351-362124
β-strand366-380154
β-strand383-394124
α-helix395-3973
α-helix398-4025
α-helix410-4123
β-strand413-426144
β-strand429-447194
α-helix448-4503
β-strand452-471204
β-strand475-488144
α-helix4931
β-strand49414
α-helix4951
β-strand501-511114
β-strand514-523104
β-strand526-53057
α-helix5361
β-strand537-54157
β-strand544-554114
β-strand559-56684
β-strand57915
α-helix580-5812
β-strand585-59394

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Vitamin B12 transporter btuBAprotein594Escherichia coliP06129 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>3M8D_1 Vitamin B12 transporter btuB (chains A)
QDTSPDTLVCTANRFEQPRSTVLAPTTVVTRQDIDRWQSTSVNDVLRRLPGVDITQNGGS
GQLSSIFIRGTNASHVLVLIDGVRLNLAGVSGSADLSQFPIALVQRVEYIRGPRSAVYGS
DAIGGVVNIITTRDEPGTEISAGWGSNSYQNYDVSTQQQLGDKTRVTLLGDYAHTHGYDV
VAYGNTGTQAQTDNDGFLSKTLYGALEHNFTDAWSGFVRGYGYDNRTNYDAYYSPGSPLL
DTRKLYSQSWDAGLRYNGELIKSQLITSYSHSKDYNYDPHYGRYDSSATLDEMKQYTVQW
ANNVIVGHGSIGAGVDWQKQTTTPGTGYVEDGYDQRNTGIYLTGLQQVGDFTFEGAARSD
DNSQFGRHGTWQTSAGWEFIEGYRFIASYGTSYKAPNLGQLYGFYGNPNLDPEKSKQWEG
AFEGLTAGVNWRISGYRNDVSDLIDYDDHTLKYYNEGKARIKGVEATANFDTGPLTHTVS
YDYVDARNAITDTPLLRRAKQQVKYQLDWQLYDFDWGITYQYLGTRYDKDYSSYPYQTVK
MGGVSLWDLAVAYPVTSHLTVRGKIANLFDKDYETVYGYQTAGREYTLSGSYTF

Ligands and cofactors

IDNameFormulaCopies
CACalcium ionCa3
MTNS-[(1-oxyl-2,2,5,5-tetramethyl-2,5-dihydro-1H-pyrrol-3-yl)methyl]…C10 H18 N O3 S21
C8E(hydroxyethyloxy)tri(ethyloxy)octaneC16 H34 O56
CNCCyanocobalaminC63 H89 Co N14 O14 P1

Primary citation

Conformational exchange in a membrane transport protein is altered in protein crystals. Freed, D.M., Horanyi, P.S., Wiener, M.C. et al. Biophys J (2010) 99:1604-1610. DOI 10.1016/j.bpj.2010.06.026 · 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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