6SQC: PDB entry 6SQC

Crystal structure of complex between nuclear coactivator binding domain of CBP and [1040-1086]ACTR containing alpha-methylated Leu1055 and Leu1076. Determined by X-ray diffraction at 2.28 Å resolution. Released 30 Sept 2020.

Method
X-ray diffraction
Resolution
2.28 Å
Organisms
Escherichia coli (strain K12), Homo sapiens
Chains
2
Atoms
3,759
Mol. weight
51.96 kDa
Ligands
ZN
Released
30 Sept 2020

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

Secondary structure: helices and β-sheets

6SQC contains 32 α-helices and 24 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: 29 helices, 24 β-strands

ElementResiduesLengthSheet
α-helix1690-16923
β-strand1696-169941
α-helix1706-172015
β-strand1724-172741
α-helix1732-17398
α-helix1740-17423
β-strand1748-175251
α-helix1753-17553
α-helix1756-17616
β-strand176512
α-helix1766-17672
β-strand176813
α-helix1772-17754
β-strand177814
α-helix1780-17856
β-strand1787-178823
β-strand1791-179223
β-strand1795-180061
β-strand1803-180755
β-strand181716
α-helix1821-18299
β-strand1834-183635
α-helix1843-18519
β-strand1856-186167
β-strand1864-187187
α-helix1875-188915
α-helix1899-19079
β-strand1911-191665
α-helix1918-19203
α-helix1921-19266
β-strand1931-193445
α-helix1935-19373
β-strand1938-193926
β-strand1942-194326
α-helix19441
β-strand1947-194828
β-strand1949-195571
β-strand195612
α-helix1962-19687
α-helix1969-19735
α-helix1976-198510
β-strand1990-199121
β-strand199314
α-helix1994-19996
α-helix2004-201512
β-strand2017-201828
α-helix2019-20202
α-helix2025-204016
α-helix2046-205510
α-helix2064-20652
α-helix2066-20749
α-helix2080-209213
α-helix2094-211017
Chain B: 3 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix1044-105815
α-helix1062-10709
α-helix1073-10808

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Maltose/maltodextrin-binding periplasmic protein,CREB-binding proteinAprotein424Escherichia coli (strain K12), Homo sapiensP0AEX9 (AlphaFold model), Q92793 (AlphaFold model)
Nuclear receptor coactivator 3Bprotein47Homo sapiensQ9Y6Q9 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6SQC_1 Maltose/maltodextrin-binding periplasmic protein,CREB-binding protein (chains A)
MKIEEGKLVIWINGDKGYNGLAEVGKKFEKDTGIKVTVEHPDKLEEKFPQVAATGDGPDI
IFWAHDRFGGYAQSGLLAEITPAAAFQDKLYPFTWDAVRYNGKLIAYPIAVEALSLIYNK
DLLPNPPKTWEEIPALDKELKAKGKSALMFNLQEPYFTWPLIAADGGYAFKYENGKYDIK
DVGVDNAGAKAGLTFLVDLIKNKHMNADTDYSIAEAAFNKGETAMTINGPWAWSNIDTSA
VNYGVTVLPTFKGQPSKPFVGVLSAGINAASPNKELAKEFLENYLLTDEGLEAVNKDKPL
GAVALKSYEEELAKDPRIAATMENAQKGEIMPNIPQMSAFWYAVRTAVINAASGRQTVDA
ALAAAQTNAAAMSISPSALQDLLRTLKSPSSPQQQQQVLNILKSNPQLMAAFIKQRTAKY
VANQ
Sequence of entity 2 (B), FASTA
>6SQC_2 Nuclear receptor coactivator 3 (chains B)
EGQSDERALLDQLHTLLSNTDATGLEEIDRALGIPELVNQGQALEPK

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn2

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

Primary citation

Conformational editing of intrinsically disordered protein by alpha-methylation. Bauer, V., Schmidtgall, B., Gogl, G. et al. Chem Sci (2020) 12:1080-1089. DOI 10.1039/d0sc04482b · PubMed

Other PDB entries of the same protein (UniProt P0AEX9 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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