5LGS: Mouse CARM1

Crystal structure of mouse CARM1 in complex with ligand P2C3u. Determined by X-ray diffraction at 2.1 Å resolution. Released 22 Mar 2017.

Method
X-ray diffraction
Resolution
2.1 Å
Organisms
Mus musculus, Homo sapiens
Chains
8
Atoms
12,030
Mol. weight
169.12 kDa
Ligands
QVR, DXE
Released
22 Mar 2017

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

Secondary structure: helices and β-sheets

5LGS contains 71 α-helices and 86 β-strands across 7 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: 16 helices, 21 β-strands

ElementResiduesLengthSheet
α-helix137-1415
α-helix144-15310
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-helix270-2756
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
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-strand434-443105
β-strand449-45795
β-strand463-46975
β-strand474-47523
Chain B: 17 helices, 21 β-strands
ElementResiduesLengthSheet
α-helix137-1415
α-helix144-15310
α-helix157-1648
α-helix167-17913
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
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-helix270-2756
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-helix144-15310
α-helix157-1648
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-helix328-3369
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-strand434-4431021
β-strand449-457921
β-strand462-469821
β-strand474-475219
Chains E, F and 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, Hprotein9Homo sapiensP11940 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>5LGS_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
>5LGS_2 Polyadenylate-binding protein 1 (chains E, F, G, H)
PAAPRPPFS

Ligands and cofactors

IDNameFormulaCopies
QVR(2~{R},3~{R},4~{S},5~{R})-2-(6-aminopurin-9-yl)-5-[(~{E})-prop-1-enyl]oxolane-3…C12 H15 N5 O34
DXE1,2-dimethoxyethaneC4 H10 O23

Water and common crystallization additives (EDO, PG4, 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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