5LV3: Mouse CARM1

Crystal structure of mouse CARM1 in complex with ligand LH1561Br. Determined by X-ray diffraction at 1.8 Å resolution. Released 20 Sept 2017.

Method
X-ray diffraction
Resolution
1.8 Å
Organism
Mus musculus
Chains
4
Atoms
12,241
Mol. weight
165.38 kDa
Ligands
SAH, LHF
Released
20 Sept 2017

Explore 5LV3 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5LV3 contains 64 α-helices and 88 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: 17 helices, 21 β-strands

ElementResiduesLengthSheet
α-helix137-1415
α-helix144-15411
α-helix157-1659
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-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: 16 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-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
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: 16 helices, 23 β-strands
ElementResiduesLengthSheet
α-helix137-1415
α-helix144-15310
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-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
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: 15 helices, 23 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-helix269-2757
α-helix276-2794
β-strand280-287817
β-strand290-298919
α-helix301-31212
α-helix313-3153
β-strand319120
β-strand322120
α-helix325-3273
α-helix328-3369
β-strand340-342319
α-helix346-3483
β-strand349119
β-strand351121
α-helix352-3532
β-strand354-359619
β-strand370-378922
β-strand379121
β-strand383-3971519
β-strand402-406519
β-strand418-4291219
β-strand434-4431022
β-strand449-457922
β-strand462-469822
β-strand474-475219

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone-arginine methyltransferase CARM1A, B, C, Dprotein361Mus musculusQ9WVG6 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>5LV3_1 Histone-arginine methyltransferase CARM1 (chains A, B, C, D)
GHMGHTLERSVFSERTEESSAVQYFQFYGYLSQQQNMMQDYVRTGTYQRAILQNHTDFKD
KIVLDVGCGSGILSFFAAQAGARKIYAVEASTMAQHAEVLVKSNNLTDRIVVIPGKVEEV
SLPEQVDIIISEPMGYMLFNERMLESYLHAKKYLKPSGNMFPTIGDVHLAPFTDEQLYME
QFTKANFWYQPSFHGVDLSALRGAAVDEYFRQPVVDTFDIRILMAKSVKYTVNFLEAKEG
DLHRIEIPFKFHMLHSGLVHGLAFWFDVAFIGSIMTVWLSTAPTEPLTHWYQVRCLFQSP
LFAKAGDTLSGTCLLIANKRQSYDISIVAQVDQTGSKSSNLLDLKNPFFRYTGTTPSPPP
G

Ligands and cofactors

IDNameFormulaCopies
SAHS-adenosyl-L-homocysteineC14 H20 N6 O5 S2
LHF5-[[2-[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-…C24 H28 Br N9 O52

Primary citation

Hijacking DNA methyltransferase transition state analogues to produce chemical scaffolds for PRMT inhibitors. Halby, L., Marechal, N., Pechalrieu, D. et al. Philos Trans R Soc Lond B Biol Sci (2018) 373. DOI 10.1098/rstb.2017.0072 · 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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