5LGQ: Mouse CARM1

Crystal structure of mouse CARM1 in complex with ligand P2C3s. Determined by X-ray diffraction at 2.11 Å resolution. Released 22 Mar 2017.

Method
X-ray diffraction
Resolution
2.11 Å
Organisms
Mus musculus, Homo sapiens
Chains
8
Atoms
12,375
Mol. weight
170.52 kDa
Ligands
8ZB, PG6, DXE
Released
22 Mar 2017

Explore 5LGQ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5LGQ contains 72 α-helices and 86 β-strands across 5 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: 18 helices, 21 β-strands

ElementResiduesLengthSheet
α-helix137-1404
α-helix144-15411
α-helix157-1648
α-helix167-17812
α-helix181-1833
β-strand188-19251
α-helix198-2058
β-strand210-21561
α-helix219-22911
β-strand236-24051
β-strand252-25761
β-strand26112
β-strand26412
α-helix266-2683
α-helix269-2757
α-helix276-2794
β-strand280-28781
β-strand290-29893
α-helix301-31111
α-helix312-3143
β-strand31914
β-strand32214
α-helix325-3273
α-helix328-3369
α-helix3391
β-strand340-34233
α-helix346-3483
β-strand34913
α-helix352-3532
β-strand354-35963
α-helix365-3684
β-strand370-37895
β-strand383-397153
β-strand402-40653
β-strand418-429123
β-strand434-444115
β-strand448-457105
β-strand463-46975
β-strand474-47523
Chain B: 18 helices, 21 β-strands
ElementResiduesLengthSheet
α-helix137-1415
α-helix144-15310
α-helix157-1648
α-helix167-17812
α-helix181-1833
β-strand188-19256
α-helix198-2058
β-strand210-21566
α-helix219-22911
β-strand236-24056
β-strand252-25766
β-strand26117
β-strand26417
α-helix266-2683
α-helix269-2757
α-helix276-2794
β-strand280-28786
β-strand290-29898
α-helix301-31111
α-helix312-3154
β-strand31919
β-strand32219
α-helix325-3273
α-helix328-3369
α-helix3391
β-strand340-34238
α-helix346-3483
β-strand34918
α-helix352-3532
β-strand354-35968
α-helix365-3684
β-strand370-378910
β-strand383-397158
β-strand402-40658
β-strand418-429128
β-strand434-4441110
β-strand448-4571010
β-strand462-469810
β-strand474-47528
Chain C: 18 helices, 23 β-strands
ElementResiduesLengthSheet
α-helix137-1404
α-helix144-15411
α-helix157-1648
α-helix167-17812
α-helix181-1833
β-strand188-192511
α-helix198-2058
β-strand210-215611
α-helix219-22911
β-strand236-240511
β-strand252-257611
β-strand261112
β-strand264112
α-helix266-2683
α-helix269-2757
α-helix276-2794
β-strand280-287811
β-strand290-298913
α-helix301-31111
α-helix312-3143
β-strand319114
β-strand322114
α-helix325-3273
α-helix328-3369
α-helix3391
β-strand340-342313
α-helix346-3483
β-strand349113
β-strand351115
α-helix352-3532
β-strand354-359613
α-helix365-3684
β-strand370-378916
β-strand379115
β-strand383-3971513
β-strand402-406513
β-strand418-4291213
β-strand434-4441116
β-strand448-4571016
β-strand463-469716
β-strand474-475213
Chain D: 17 helices, 21 β-strands
ElementResiduesLengthSheet
α-helix137-1404
α-helix144-15411
α-helix157-1659
α-helix167-17913
α-helix181-1833
β-strand188-192517
α-helix198-2058
β-strand210-215617
α-helix219-22911
β-strand236-240517
β-strand252-257617
β-strand261118
β-strand264118
α-helix266-2683
α-helix269-2757
α-helix276-2794
β-strand280-287817
β-strand290-298919
α-helix301-31111
α-helix312-3154
β-strand319120
β-strand322120
α-helix325-3273
α-helix328-33710
β-strand340-342319
α-helix346-3483
β-strand349119
α-helix352-3532
β-strand354-359619
α-helix365-3684
β-strand370-378921
β-strand383-3971519
β-strand402-406519
β-strand418-4291219
β-strand434-4441121
β-strand448-4571021
β-strand462-469821
β-strand474-475219
Chain H: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix2-32

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone-arginine methyltransferase CARM1A, B, C, Dprotein361Mus musculusQ9WVG6 (AlphaFold model)
Polyadenylate-binding protein 1E, F, G, Hprotein11Homo sapiensP11940 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>5LGQ_1 Histone-arginine methyltransferase CARM1 (chains A, B, C, D)
GHMGHTLERSVFSERTEESSAVQYFQFYGYLSQQQNMMQDYVRTGTYQRAILQNHTDFKD
KIVLDVGCGSGILSFFAAQAGARKIYAVEASTMAQHAEVLVKSNNLTDRIVVIPGKVEEV
SLPEQVDIIISEPMGYMLFNERMLESYLHAKKYLKPSGNMFPTIGDVHLAPFTDEQLYME
QFTKANFWYQPSFHGVDLSALRGAAVDEYFRQPVVDTFDIRILMAKSVKYTVNFLEAKEG
DLHRIEIPFKFHMLHSGLVHGLAFWFDVAFIGSIMTVWLSTAPTEPLTHWYQVRCLFQSP
LFAKAGDTLSGTCLLIANKRQSYDISIVAQVDQTGSKSSNLLDLKNPFFRYTGTTPSPPP
G
Sequence of entity 2 (E, F, G, H), FASTA
>5LGQ_2 Polyadenylate-binding protein 1 (chains E, F, G, H)
PAAPRPPFSTM

Ligands and cofactors

IDNameFormulaCopies
8ZB(2~{R},3~{R},4~{S},5~{R})-2-(6-aminopurin-9-yl)-5-propyl-oxolane-3,4-diolC12 H17 N5 O34
PG61-(2-methoxy-ethoxy)-2-{2-[2-(2-methoxy-ethoxy]-ethoxy}-ethaneC12 H26 O61
DXE1,2-dimethoxyethaneC4 H10 O21

Water and common crystallization additives (EDO, PEG, SO4) are not listed.

Primary citation

Transition state mimics are valuable mechanistic probes for structural studies with the arginine methyltransferase CARM1. van Haren, M.J., Marechal, N., Troffer-Charlier, N. et al. Proc Natl Acad Sci U S A (2017) 114:3625-3630. DOI 10.1073/pnas.1618401114 · PubMed

Other PDB entries of the same protein (UniProt Q9WVG6 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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