7OKP: Mouse CARM1

Crystal structure of mouse CARM1 in complex with histone H3_13-22 K18 acetylated. Determined by X-ray diffraction at 2.2 Å resolution. Released 27 Oct 2021.

Method
X-ray diffraction
Resolution
2.2 Å
Organisms
Mus musculus, Homo sapiens
Chains
8
Atoms
12,181
Mol. weight
174.12 kDa
Ligands
QVR, MLI
Released
27 Oct 2021

Explore 7OKP in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7OKP contains 72 α-helices and 88 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-helix137-1415
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-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
β-strand354-35963
α-helix365-3684
β-strand370-37895
α-helix3791
β-strand383-397153
β-strand402-40653
β-strand418-429123
β-strand434-443105
β-strand449-45795
β-strand463-46975
β-strand474-47523
α-helix481-4855
Chain B: 18 helices, 23 β-strands
ElementResiduesLengthSheet
α-helix137-1415
α-helix144-15310
α-helix157-1659
α-helix167-17913
α-helix181-1833
β-strand18516
β-strand188-19257
α-helix198-2058
β-strand20816
β-strand210-21567
α-helix219-22911
β-strand236-24057
β-strand252-25767
β-strand26118
β-strand26418
α-helix266-2683
α-helix269-2757
α-helix276-2794
β-strand280-28787
β-strand290-29899
α-helix301-31111
α-helix312-3154
β-strand319110
β-strand322110
α-helix325-3273
α-helix328-3369
α-helix3391
β-strand340-34239
α-helix346-3483
β-strand34919
α-helix352-3532
β-strand354-35969
α-helix365-3684
β-strand370-378911
β-strand383-397159
β-strand402-40659
β-strand418-429129
β-strand434-4431011
β-strand449-457911
β-strand462-469811
β-strand474-47529
Chain C: 19 helices, 23 β-strands
ElementResiduesLengthSheet
α-helix137-1415
α-helix144-15411
α-helix157-1659
α-helix167-17913
α-helix181-1833
β-strand188-192512
α-helix198-2069
β-strand210-215612
α-helix219-22911
β-strand236-240512
β-strand252-257612
β-strand261113
β-strand264113
α-helix266-2683
α-helix269-2757
α-helix276-2794
β-strand280-287812
β-strand290-298914
α-helix301-31111
α-helix312-3143
β-strand319115
β-strand322115
α-helix325-3273
α-helix328-3369
α-helix3391
β-strand340-342314
α-helix346-3483
β-strand349114
β-strand354-359614
α-helix365-3684
β-strand370-378916
β-strand383-3971514
β-strand402-406514
β-strand418-4291214
β-strand431117
β-strand433117
β-strand434-4431016
β-strand449-457916
β-strand463-469716
β-strand474-475214
α-helix481-4855
α-helix493-4953
Chain D: 16 helices, 21 β-strands
ElementResiduesLengthSheet
α-helix137-1404
α-helix144-15310
α-helix157-1659
α-helix167-17812
α-helix181-1833
β-strand188-192518
α-helix198-2058
β-strand210-215618
α-helix219-23012
β-strand236-240518
β-strand252-257618
β-strand261119
β-strand264119
α-helix269-2757
α-helix276-2794
β-strand280-287818
β-strand290-298920
α-helix301-31111
α-helix312-3154
β-strand319121
β-strand322121
α-helix325-3273
α-helix328-33710
β-strand340-342320
α-helix346-3483
β-strand349120
α-helix352-3532
β-strand354-359620
α-helix365-3684
β-strand370-378922
β-strand383-3971520
β-strand402-406520
β-strand418-4291220
β-strand434-4431022
β-strand449-457922
β-strand462-469822
β-strand474-475220
Chain G: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix18-192

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone-arginine methyltransferase CARM1A, B, C, Dprotein371Mus musculusQ9WVG6 (AlphaFold model)
Histone H3.3E, F, G, Hprotein11Homo sapiensP84243 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>7OKP_1 Histone-arginine methyltransferase CARM1 (chains A, B, C, D)
GHMGHTLERSVFSERTEESSAVQYFQFYGYLSQQQNMMQDYVRTGTYQRAILQNHTDFKD
KIVLDVGCGSGILSFFAAQAGARKIYAVEASTMAQHAEVLVKSNNLTDRIVVIPGKVEEV
SLPEQVDIIISEPMGYMLFNERMLESYLHAKKYLKPSGNMFPTIGDVHLAPFTDEQLYME
QFTKANFWYQPSFHGVDLSALRGAAVDEYFRQPVVDTFDIRILMAKSVKYTVNFLEAKEG
DLHRIEIPFKFHMLHSGLVHGLAFWFDVAFIGSIMTVWLSTAPTEPLTHWYQVRCLFQSP
LFAKAGDTLSGTCLLIANKRQSYDISIVAQVDQTGSKSSNLLDLKNPFFRYTGTTPSPPP
GSHYTSPSENM
Sequence of entity 2 (E, F, G, H), FASTA
>7OKP_2 Histone H3.3 (chains E, F, G, H)
XGKAPRKQLAT

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
MLIMalonate ionC3 H2 O45

Primary citation

Structural Studies Provide New Insights into the Role of Lysine Acetylation on Substrate Recognition by CARM1 and Inform the Design of Potent Peptidomimetic Inhibitors. Zhang, Y., Marechal, N., van Haren, M.J. et al. Chembiochem (2021) 22:3469-3476. DOI 10.1002/cbic.202100506 · 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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