1LVC: Adenylyl cyclase domain of anthrax edema factor

Crystal structure of the adenylyl cyclase domain of anthrax edema factor (EF) in complex with calmodulin and 2' deoxy, 3' anthraniloyl ATP. Determined by X-ray diffraction at 3.6 Å resolution. Released 4 Dec 2002.

Method
X-ray diffraction
Resolution
3.6 Å
Organisms
Bacillus anthracis, Homo sapiens
Chains
6
Atoms
15,302
Mol. weight
228.97 kDa
Ligands
CA, DOT, YB
Released
4 Dec 2002

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

Secondary structure: helices and β-sheets

1LVC contains 102 α-helices and 83 β-strands across 6 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: 25 helices, 24 β-strands

ElementResiduesLengthSheet
β-strand296-29721
α-helix298-3058
α-helix309-32113
β-strand324-32851
α-helix333-3408
α-helix3431
β-strand344-34522
α-helix3461
α-helix352-3554
β-strand36312
β-strand36513
α-helix368-3703
α-helix377-39216
β-strand39513
β-strand398-40253
β-strand40414
α-helix407-41610
β-strand420-42675
β-strand431-43665
β-strand442-44765
β-strand45214
β-strand453-45755
β-strand472-47325
α-helix4741
β-strand475-48173
β-strand484-48743
β-strand488-48922
β-strand494-49961
β-strand50016
α-helix501-5055
α-helix512-5176
α-helix523-53311
α-helix534-5385
β-strand541-54227
β-strand548-54927
α-helix551-56717
α-helix580-5823
β-strand593-59641
β-strand602-60541
α-helix608-61811
β-strand62416
α-helix648-6536
α-helix660-6689
α-helix696-7049
α-helix707-7093
α-helix714-73623
α-helix745-76723
α-helix774-7785
α-helix788-7969
Chain B: 20 helices, 24 β-strands
ElementResiduesLengthSheet
β-strand29718
α-helix299-3057
α-helix309-32113
β-strand324-32858
α-helix333-3408
β-strand344-34529
β-strand365110
α-helix368-3703
α-helix377-39216
β-strand398-402510
β-strand404111
α-helix409-4157
β-strand420-426712
β-strand431-436612
β-strand442-447612
β-strand452111
β-strand453-457512
α-helix4581
β-strand472-473212
β-strand475-481710
β-strand484-487410
β-strand488-48929
β-strand494-49968
β-strand500113
α-helix502-5054
α-helix510-5178
α-helix525-5339
α-helix534-5385
β-strand541-542214
β-strand548-549214
α-helix551-56515
α-helix580-5823
β-strand594-59638
β-strand602-60438
α-helix608-6147
α-helix615-6195
β-strand624113
β-strand635115
β-strand642115
α-helix648-6514
α-helix714-72714
α-helix728-7303
α-helix743-76422
α-helix786-7905
Chain C: 27 helices, 23 β-strands
ElementResiduesLengthSheet
α-helix298-3058
α-helix309-32113
β-strand324-328516
α-helix329-3302
α-helix333-3408
α-helix3431
β-strand344-345217
α-helix3461
α-helix352-3554
β-strand363117
β-strand365118
α-helix368-3703
α-helix377-39216
β-strand395118
β-strand398-402518
β-strand404119
α-helix407-41610
β-strand420-426720
β-strand431-436620
β-strand442-447620
β-strand452119
β-strand453-457520
β-strand472-473220
α-helix4741
β-strand475-481718
β-strand484-487418
β-strand488-489217
β-strand494-499616
β-strand500121
α-helix501-5055
α-helix512-5154
α-helix522-53312
α-helix534-5385
β-strand541-543322
β-strand547-549322
α-helix551-56717
α-helix580-5823
β-strand593-596416
β-strand602-605416
α-helix608-61811
β-strand624121
α-helix648-6514
α-helix653-6553
α-helix661-6699
α-helix696-7049
α-helix707-7093
α-helix714-73623
α-helix745-76521
α-helix774-7785
α-helix787-79610
Chain D: 10 helices, 4 β-strands
ElementResiduesLengthSheet
α-helix8-103
α-helix12-165
β-strand27-28223
α-helix32-365
α-helix45-5511
β-strand62-63223
α-helix65-7511
α-helix78-814
α-helix82-9211
β-strand99-100224
α-helix102-1109
α-helix118-12811
β-strand136-137224
α-helix138-1436
Chains E and F: 10 helices, 4 β-strands
ElementResiduesLengthSheet
α-helix8-103
α-helix12-165
β-strand27-28225
α-helix32-365
α-helix45-5511
β-strand62-63225
α-helix65-7511
α-helix78-814
α-helix82-9211
β-strand99-100226
α-helix102-1109
α-helix118-12811
β-strand136-137226
α-helix138-1469

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
calmodulin-sensitive adenylate cyclaseA, B, Cprotein510Bacillus anthracisP40136 (AlphaFold model)
calmodulinD, E, Fprotein149Homo sapiensP0DP23 (AlphaFold model)
Sequence of entity 1 (A, B, C), FASTA
>1LVC_1 calmodulin-sensitive adenylate cyclase (chains A, B, C)
DRIDVLKGEKALKASGLVPEHADAFKKIARELNTYILFRPVNKLATNLIKSGVATKGLNV
HGKSSDWGPVAGYIPFDQDLSKKHGQQLAVEKGNLENKKSITEHEGEIGKIPLKLDHLRI
EELKENGIILKGKKEIDNGKKYYLLESNNQVYEFRISDENNEVQYKTKEGKITVLGEKFN
WRNIEVMAKNVEGVLKPLTADYDLFALAPSLTEIKKQIPQKEWDKVVNTPNSLEKQKGVT
NLLIKYGIERKPDSTKGTLSNWQKQMLDRLNEAVKYTGYTGGDVVNHGTEQDNEEFPEKD
NEIFIINPEGEFILTKNWEMTGRFIEKNITGKDYLYYFNRSYNKIAPGNKAYIEWTDPIT
KAKINTIPTSAEFIKNLSSIRRSSNVGVYKDSGDKDEFAKKESVKKIAGYLSDYYNSANH
IFSQEKKRKISIFRGIQAYNEIENVLKSKQIAPEYKNYFQYLKERITNQVQLLLTHQKSN
IEFKLLYKQLNFTENETDNFEVFQKIIDEK
Sequence of entity 2 (D, E, F), FASTA
>1LVC_2 calmodulin (chains D, E, F)
MADQLTEEQIAEFKEAFSLFDKDGDGTITTKELGTVMRSLGQNPTEAELQDMINEVDADG
NGTIDFPEFLTMMARKMKDTDSEEEIREAFRVFDKDGNGYISAAELRHVMTNLGEKLTDE
EVDEMIREADIDGDGQVNYEEFVQMMTAK

Ligands and cofactors

IDNameFormulaCopies
CACalcium ionCa6
DOT3'ANTHRANILOYL-2'-deoxy-adenosine-5'-triphosphateC17 H21 N6 O13 P32
YBYtterbium (III) ionYb3

Primary citation

Physiological calcium concentrations regulate calmodulin binding and catalysis of adenylyl cyclase exotoxins. Shen, Y., Lee, Y.-S., Soelaiman, S. et al. EMBO J (2002) 21:6721-6732. DOI 10.1093/emboj/cdf681 · PubMed

Other PDB entries of the same protein (UniProt P40136 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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