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.
Explore 6PGU in 3D Show helices and sheets RCSB PDB PDBe
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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 1294-1295 | 2 | |
| α-helix | 1297-1313 | 17 | |
| β-strand | 1321-1334 | 14 | 1 |
| α-helix | 1335-1336 | 2 | |
| α-helix | 1337-1339 | 3 | |
| α-helix | 1340-1344 | 5 | |
| β-strand | 1352-1366 | 15 | 1 |
| β-strand | 1369-1381 | 13 | 1 |
| α-helix | 1386 | 1 | |
| β-strand | 1392-1400 | 9 | 1 |
| α-helix | 1407-1409 | 3 | |
| α-helix | 1410-1428 | 19 | |
| β-strand | 1432-1436 | 5 | 1 |
| α-helix | 1439-1441 | 3 | |
| α-helix | 1460-1476 | 17 | |
| β-strand | 1482-1485 | 4 | 1 |
| α-helix | 1486-1493 | 8 | |
| α-helix | 1498-1500 | 3 | |
| α-helix | 1508-1516 | 9 | |
| α-helix | 1583-1590 | 8 | |
| α-helix | 1592-1594 | 3 | |
| β-strand | 1595-1599 | 5 | 1 |
| α-helix | 1603-1606 | 4 | |
| α-helix | 1609-1612 | 4 | |
| α-helix | 1617-1618 | 2 | |
| β-strand | 1619 | 1 | 1 |
| α-helix | 1622-1624 | 3 | |
| α-helix | 1628-1637 | 10 | |
| α-helix | 1644-1660 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 1294-1295 | 2 | |
| α-helix | 1297-1313 | 17 | |
| β-strand | 1321-1334 | 14 | 2 |
| α-helix | 1335-1336 | 2 | |
| α-helix | 1337-1339 | 3 | |
| α-helix | 1340-1344 | 5 | |
| β-strand | 1352-1366 | 15 | 2 |
| β-strand | 1369-1381 | 13 | 2 |
| α-helix | 1386 | 1 | |
| β-strand | 1392-1400 | 9 | 2 |
| α-helix | 1407-1409 | 3 | |
| α-helix | 1410-1428 | 19 | |
| β-strand | 1432-1436 | 5 | 2 |
| α-helix | 1439-1441 | 3 | |
| α-helix | 1460-1476 | 17 | |
| β-strand | 1482-1485 | 4 | 2 |
| α-helix | 1486-1492 | 7 | |
| α-helix | 1498-1500 | 3 | |
| α-helix | 1508-1515 | 8 | |
| α-helix | 1583-1590 | 8 | |
| α-helix | 1592-1594 | 3 | |
| β-strand | 1595-1599 | 5 | 2 |
| α-helix | 1603-1607 | 5 | |
| α-helix | 1609-1612 | 4 | |
| α-helix | 1617-1618 | 2 | |
| β-strand | 1619 | 1 | 2 |
| α-helix | 1622-1624 | 3 | |
| α-helix | 1628-1636 | 9 | |
| α-helix | 1644-1660 | 17 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Histone acetyltransferase p300 | A, B | protein | 323 | Homo sapiens | Q09472 (AlphaFold model) |
>6PGU_1 Histone acetyltransferase p300 (chains A, B) GSKFSAKRLPSTRLGTFLENRVNDFLRRQNHPESGEVTVRVVHASDKTVEVKPGMKARFV DSGEMAESFPYRTKALFAFEEIDGVDLCFFGMHVQEYGSDCPPPNQRRVYISYLDSVHFF RPKCLRTAVYHEILIGYLEYVKKLGYTTGHIWACPPSEGDDYIFHCHPPDQKIPKPKRLQ EWFKKMLDKAVSERIVHDYKDIFKQATEDRLTSAKELPYFEGDFWPNVLEESIKESGGSG SQKLYATMEKHKEVFFVIRLIAGPAANSLPPIVDPDPLIPCDLMDGRDAFLTLARDKHLE FSSLRRAQWSTMCMLVELHTQSQ
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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