1Q1B: E. coli MalK in the nucleotide-free form

Crystal structure of E. coli MalK in the nucleotide-free form. Determined by X-ray diffraction at 2.8 Å resolution. Released 30 Sept 2003.

Method
X-ray diffraction
Resolution
2.8 Å
Organism
Escherichia coli
Chains
4
Atoms
11,412
Mol. weight
168.97 kDa
Released
30 Sept 2003

Explore 1Q1B in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1Q1B contains 54 α-helices and 108 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.

Chain A: 13 helices, 27 β-strands

ElementResiduesLengthSheet
β-strand5-841
β-strand9-1352
β-strand16-2272
β-strand2511
α-helix26-272
β-strand31-3553
α-helix42-509
β-strand57-6261
β-strand65-6621
α-helix72-743
β-strand77-8153
α-helix106-12015
α-helix124-1263
α-helix136-15015
β-strand154-15853
α-helix169-18214
β-strand186-19053
α-helix194-2007
β-strand203-20863
β-strand211-21663
α-helix218-2236
β-strand22714
α-helix228-2336
β-strand240-24895
β-strand255-25735
α-helix261-2633
β-strand265-26735
β-strand27016
β-strand280-28565
α-helix287-2893
β-strand29117
β-strand299-309117
β-strand313-32087
β-strand323-332107
β-strand342-34657
α-helix349-3513
β-strand353-35535
β-strand36014
β-strand36115
β-strand36416
Chain B: 12 helices, 28 β-strands
ElementResiduesLengthSheet
β-strand518
β-strand6-729
β-strand9-11310
β-strand19-22410
β-strand2518
β-strand31-35511
α-helix38-403
α-helix42-498
β-strand59-6029
β-strand77112
α-helix92-943
α-helix144-1474
β-strand154112
α-helix172-18211
β-strand186112
β-strand187-190411
α-helix194-2007
β-strand203-208611
β-strand211-216611
α-helix218-2236
β-strand227113
α-helix228-2336
α-helix238-2392
β-strand240-248914
β-strand255-257314
α-helix261-2633
β-strand265-267314
β-strand270115
β-strand280-285614
α-helix287-2893
β-strand291116
β-strand299-3091116
β-strand313-320816
β-strand323-3321016
β-strand342-346516
β-strand353-355314
β-strand360113
β-strand361114
β-strand364115
α-helix367-3693
Chain C: 14 helices, 27 β-strands
ElementResiduesLengthSheet
β-strand5-10617
β-strand12118
β-strand17118
β-strand22-25417
β-strand31-35519
α-helix38-403
α-helix42-509
β-strand57-61517
β-strand66117
α-helix72-743
β-strand77-81519
α-helix106-12015
α-helix124-1263
α-helix131-1333
α-helix136-14813
β-strand154-158519
α-helix166-18217
β-strand186-190519
α-helix194-2007
β-strand203-208619
β-strand211-216619
α-helix218-2236
β-strand227120
α-helix228-2336
α-helix238-2392
β-strand240-248921
β-strand255-257321
β-strand265-267321
β-strand270122
β-strand280-285621
α-helix287-2893
β-strand291123
β-strand299-3091123
β-strand313-320823
β-strand323-3321023
β-strand342-346523
α-helix349-3513
β-strand353-355321
β-strand360120
β-strand361121
β-strand364122
Chain D: 15 helices, 26 β-strands
ElementResiduesLengthSheet
β-strand5-13924
β-strand16-251024
β-strand31-35525
α-helix38-403
α-helix42-487
β-strand59-62424
β-strand65-66224
β-strand80126
α-helix92-954
α-helix113-1164
α-helix119-1213
α-helix133-1353
α-helix145-1484
β-strand154-155225
β-strand157126
α-helix169-18214
β-strand186-190525
α-helix194-2007
β-strand203-208625
β-strand211-216625
α-helix218-2236
β-strand227127
α-helix228-2336
α-helix238-2392
β-strand240-2501128
β-strand253-257528
β-strand265-268428
β-strand270129
β-strand280-285628
α-helix287-2893
β-strand291130
β-strand299-3091130
β-strand313-319730
β-strand327-332630
β-strand342-346530
α-helix349-3513
β-strand353-355328
β-strand360127
β-strand361128
β-strand364129
α-helix367-3693

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Maltose/maltodextrin transport ATP-binding protein malKA, B, C, Dprotein381Escherichia coliP68187 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>1Q1B_1 Maltose/maltodextrin transport ATP-binding protein malK (chains A, B, C, D)
MASVQLQNVTKAWGEVVVSKDINLDIHEGEFVVFVGPSGCGKSTLLRMIAGLETITSGDL
FIGEKRMNDTPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVINQRVNQVAEV
LQLAHLLDRKPKALSGGQRQRVAIGRTLVAEPSVFLLDEPLSNLDAALRVQMRIEISRLH
KRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPKMN
FLPVKVTATAIDQVQVELPMPNRQQVWLPVESRDVQVGANMSLGIRPEHLLPSDIADVIL
EGEVQVVEQLGNETQIHIQIPSIRQNLVYRQNDVVLVEEGATFAIGLPPERCHLFREDGT
ACRRLHKEPGVESASHHHHHH

Primary citation

A tweezer-like motion of the ATP-binding cassette dimer in an ABC transport cycle. Chen, J., Lu, G., Lin, J. et al. Mol Cell (2003) 12:651-661. DOI 10.1016/j.molcel.2003.08.004 · PubMed

Other PDB entries of the same protein (UniProt P68187 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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