6PGU: Histone acetyltransferase p300

Crystal structure of the p300 acetyltransferase domain with allosteric inhibitor CPI-076 and CoA. Determined by X-ray diffraction at 1.72 Å resolution. Released 23 Oct 2019.

Method
X-ray diffraction
Resolution
1.72 Å
Organism
Homo sapiens
Chains
2
Atoms
5,754
Mol. weight
76.19 kDa
Ligands
OK7, COA
Released
23 Oct 2019

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

Secondary structure: helices and β-sheets

6PGU contains 42 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: 21 helices, 8 β-strands

ElementResiduesLengthSheet
α-helix1294-12952
α-helix1297-131317
β-strand1321-1334141
α-helix1335-13362
α-helix1337-13393
α-helix1340-13445
β-strand1352-1366151
β-strand1369-1381131
α-helix13861
β-strand1392-140091
α-helix1407-14093
α-helix1410-142819
β-strand1432-143651
α-helix1439-14413
α-helix1460-147617
β-strand1482-148541
α-helix1486-14938
α-helix1498-15003
α-helix1508-15169
α-helix1583-15908
α-helix1592-15943
β-strand1595-159951
α-helix1603-16064
α-helix1609-16124
α-helix1617-16182
β-strand161911
α-helix1622-16243
α-helix1628-163710
α-helix1644-166017
Chain B: 21 helices, 8 β-strands
ElementResiduesLengthSheet
α-helix1294-12952
α-helix1297-131317
β-strand1321-1334142
α-helix1335-13362
α-helix1337-13393
α-helix1340-13445
β-strand1352-1366152
β-strand1369-1381132
α-helix13861
β-strand1392-140092
α-helix1407-14093
α-helix1410-142819
β-strand1432-143652
α-helix1439-14413
α-helix1460-147617
β-strand1482-148542
α-helix1486-14927
α-helix1498-15003
α-helix1508-15158
α-helix1583-15908
α-helix1592-15943
β-strand1595-159952
α-helix1603-16075
α-helix1609-16124
α-helix1617-16182
β-strand161912
α-helix1622-16243
α-helix1628-16369
α-helix1644-166017

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Histone acetyltransferase p300A, Bprotein323Homo sapiensQ09472 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>6PGU_1 Histone acetyltransferase p300 (chains A, B)
GSKFSAKRLPSTRLGTFLENRVNDFLRRQNHPESGEVTVRVVHASDKTVEVKPGMKARFV
DSGEMAESFPYRTKALFAFEEIDGVDLCFFGMHVQEYGSDCPPPNQRRVYISYLDSVHFF
RPKCLRTAVYHEILIGYLEYVKKLGYTTGHIWACPPSEGDDYIFHCHPPDQKIPKPKRLQ
EWFKKMLDKAVSERIVHDYKDIFKQATEDRLTSAKELPYFEGDFWPNVLEESIKESGGSG
SQKLYATMEKHKEVFFVIRLIAGPAANSLPPIVDPDPLIPCDLMDGRDAFLTLARDKHLE
FSSLRRAQWSTMCMLVELHTQSQ

Ligands and cofactors

IDNameFormulaCopies
OK7N-(thiophen-2-yl)acetamideC6 H7 N O S2
COACoenzyme aC21 H36 N7 O16 P3 S2

Primary citation

Make the right measurement: Discovery of an allosteric inhibition site for p300-HAT. Gardberg, A.S., Huhn, A.J., Cummings, R. et al. Struct Dyn (2019) 6:054702-054702. DOI 10.1063/1.5119336 · PubMed

Other PDB entries of the same protein (UniProt Q09472 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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