6MBL: SETD3, a Histidine Methyltransferase

SETD3, a Histidine Methyltransferase, in Complex with an Actin Peptide and SAH, Second P212121 Crystal Form. Determined by X-ray diffraction at 2.2 Å resolution. Released 19 Dec 2018.

Method
X-ray diffraction
Resolution
2.2 Å
Organism
Homo sapiens
Chains
2
Atoms
4,252
Mol. weight
70.55 kDa
Ligands
SAH
Released
19 Dec 2018

Explore 6MBL in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6MBL contains 28 α-helices and 16 β-strands across 2 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: 28 helices, 15 β-strands

ElementResiduesLengthSheet
α-helix21-3515
α-helix38-392
α-helix42-443
α-helix45-6117
α-helix74-774
α-helix78-8710
β-strand95-10062
β-strand104-10962
β-strand11313
β-strand118-12361
α-helix124-1263
β-strand128-12924
α-helix130-1345
α-helix139-1446
α-helix146-1505
α-helix152-16413
α-helix172-1754
α-helix185-1873
α-helix190-1945
α-helix201-22525
α-helix233-2353
α-helix240-25314
β-strand255-25844
β-strand265-26954
α-helix273-2753
α-helix2761
β-strand277-27825
β-strand285-28841
β-strand293-29751
β-strand30213
β-strand307-30822
β-strand309-31025
α-helix317-3248
β-strand335-34176
α-helix349-35810
β-strand364-37076
α-helix378-38710
α-helix391-3966
α-helix403-4086
α-helix419-43719
α-helix444-45310
α-helix458-49437
α-helix496-4994
Chain Y: 0 helices, 1 β-strand
ElementResiduesLengthSheet
β-strand7011

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Actin PeptideYprotein15Homo sapiensP60709 (AlphaFold model)
Histone-lysine N-methyltransferase setd3Aprotein599Homo sapiensQ86TU7 (AlphaFold model)
Sequence of entity 1 (Y), FASTA
>6MBL_1 Actin Peptide (chains Y)
TLKYPIEHGIVTNWD
Sequence of entity 2 (A), FASTA
>6MBL_2 Histone-lysine N-methyltransferase setd3 (chains A)
GPLGSMGKKSRVKTQKSGTGATATVSPKEILNLTSELLQKCSSPAPGPGKEWEEYVQIRT
LVEKIRKKQKGLSVTFDGKREDYFPDLMKWASENGASVEGFEMVNFKEEGFGLRATRDIK
AEELFLWVPRKLLMTVESAKNSVLGPLYSQDRILQAMGNIALAFHLLCERASPNSFWQPY
IQTLPSEYDTPLYFEEDEVRYLQSTQAIHDVFSQYKNTARQYAYFYKVIQTHPHANKLPL
KDSFTYEDYRWAVSSVMTRQNQIPTEDGSRVTLALIPLWDMCNHTNGLITTGYNLEDDRC
ECVALQDFRAGEQIYIFYGTRSNAEFVIHSGFFFDNNSHDRVKIKLGVSKSDRLYAMKAE
VLARAGIPTSSVFALHFTEPPISAQLLAFLRVFCMTEEELKEHLLGDSAIDRIFTLGNSE
FPVSWDNEVKLWTFLEDRASLLLKTYKTTIEEDKSVLKNHDLSVRAKMAIKLRLGEKEIL
EKAVKSAAVNREYYRQQMEEKAPLPKYEESNLGLLESSVGDSRLPLVLRNLEEEAGVQDA
LNIREAISKAKATENGLVNGENSIPNGTRSENESLNQESKRAVEDAKGSSSDSTAGVKE

Ligands and cofactors

IDNameFormulaCopies
SAHS-adenosyl-L-homocysteineC14 H20 N6 O5 S1

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

Primary citation

SETD3 is an actin histidine methyltransferase that prevents primary dystocia. Wilkinson, A.W., Diep, J., Dai, S. et al. Nature (2019) 565:372-376. DOI 10.1038/s41586-018-0821-8 · PubMed

Other PDB entries of the same protein (UniProt P60709 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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