3M8B: Spin-labeled BtuB V10R1 in the apo state

Crystal structure of spin-labeled BtuB V10R1 in the apo state. 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
4,605
Mol. weight
68.9 kDa
Ligands
MG, MTN, C8E
Released
15 Sept 2010

Explore 3M8B in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3M8B contains 13 α-helices and 34 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: 13 helices, 34 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-helix86-894
α-helix101-1033
β-strand106-11162
α-helix115-1184
β-strand125-13062
β-strand137-14594
α-helix146-1483
β-strand149-159114
β-strand164-175124
β-strand197-209134
β-strand214-227144
β-strand243-257154
β-strand261-276164
β-strand289-305174
β-strand309-322144
β-strand334-348154
β-strand351-362124
β-strand366-380154
β-strand383-394124
α-helix395-3973
α-helix398-4025
β-strand413-426144
β-strand429-447194
β-strand452-472214
β-strand475-488144
α-helix4931
β-strand49414
α-helix4951
β-strand501-510104
β-strand515-52394
β-strand526-52945
β-strand538-54145
α-helix542-5432
β-strand544-554114
β-strand559-56684
β-strand585-59394

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Vitamin B12 transporter btuBAprotein594Escherichia coliP06129 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>3M8B_1 Vitamin B12 transporter btuB (chains A)
QDTSPDTLVCTANRFEQPRSTVLAPTTVVTRQDIDRWQSTSVNDVLRRLPGVDITQNGGS
GQLSSIFIRGTNASHVLVLIDGVRLNLAGVSGSADLSQFPIALVQRVEYIRGPRSAVYGS
DAIGGVVNIITTRDEPGTEISAGWGSNSYQNYDVSTQQQLGDKTRVTLLGDYAHTHGYDV
VAYGNTGTQAQTDNDGFLSKTLYGALEHNFTDAWSGFVRGYGYDNRTNYDAYYSPGSPLL
DTRKLYSQSWDAGLRYNGELIKSQLITSYSHSKDYNYDPHYGRYDSSATLDEMKQYTVQW
ANNVIVGHGSIGAGVDWQKQTTTPGTGYVEDGYDQRNTGIYLTGLQQVGDFTFEGAARSD
DNSQFGRHGTWQTSAGWEFIEGYRFIASYGTSYKAPNLGQLYGFYGNPNLDPEKSKQWEG
AFEGLTAGVNWRISGYRNDVSDLIDYDDHTLKYYNEGKARIKGVEATANFDTGPLTHTVS
YDYVDARNAITDTPLLRRAKQQVKYQLDWQLYDFDWGITYQYLGTRYDKDYSSYPYQTVK
MGGVSLWDLAVAYPVTSHLTVRGKIANLFDKDYETVYGYQTAGREYTLSGSYTF

Ligands and cofactors

IDNameFormulaCopies
MGMagnesium ionMg4
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 O57

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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