JMJD2A complexed with ni(ii), nog and histone H3K27me3 peptide (25-29) ARK(me3)SA. Determined by X-ray diffraction at 2.0 Å resolution. Released 5 Nov 2014.
Explore 4V2V in 3D Show helices and sheets RCSB PDB PDBe
4V2V contains 48 α-helices and 38 β-strands across 4 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 | 4-7 | 4 | |
| α-helix | 13-14 | 2 | |
| β-strand | 15-17 | 3 | 1 |
| α-helix | 21-24 | 4 | |
| α-helix | 27-36 | 10 | |
| α-helix | 39-42 | 4 | |
| β-strand | 44-47 | 4 | 1 |
| α-helix | 48-50 | 3 | |
| α-helix | 60-62 | 3 | |
| β-strand | 66-67 | 2 | 2 |
| β-strand | 71-78 | 8 | 3 |
| β-strand | 81-88 | 8 | 3 |
| β-strand | 92-93 | 2 | 2 |
| α-helix | 94-102 | 9 | |
| α-helix | 108-110 | 3 | |
| α-helix | 114-124 | 11 | |
| β-strand | 131-132 | 2 | 3 |
| β-strand | 133-137 | 5 | 1 |
| α-helix | 158-164 | 7 | |
| β-strand | 169 | 1 | 4 |
| β-strand | 175-179 | 5 | 1 |
| β-strand | 184-188 | 5 | 5 |
| α-helix | 189-190 | 2 | |
| α-helix | 191-193 | 3 | |
| β-strand | 195-203 | 9 | 1 |
| β-strand | 206-211 | 6 | 5 |
| α-helix | 213-215 | 3 | |
| α-helix | 216-226 | 11 | |
| α-helix | 228-233 | 6 | |
| α-helix | 237-240 | 4 | |
| β-strand | 243-245 | 3 | 3 |
| α-helix | 247-252 | 6 | |
| β-strand | 258-262 | 5 | 5 |
| β-strand | 267-270 | 4 | 1 |
| β-strand | 275-280 | 6 | 5 |
| β-strand | 284-291 | 8 | 1 |
| α-helix | 296-302 | 7 | |
| α-helix | 318-324 | 7 | |
| α-helix | 326-328 | 3 | |
| α-helix | 329-334 | 6 | |
| α-helix | 339-341 | 3 | |
| α-helix | 345-347 | 3 | |
| α-helix | 348-350 | 3 | |
| α-helix | 351-354 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 15-17 | 3 | 6 |
| α-helix | 21-24 | 4 | |
| α-helix | 27-36 | 10 | |
| α-helix | 39-42 | 4 | |
| β-strand | 44-47 | 4 | 6 |
| α-helix | 48-50 | 3 | |
| β-strand | 66-67 | 2 | 7 |
| β-strand | 71-78 | 8 | 8 |
| β-strand | 81-88 | 8 | 8 |
| β-strand | 92-93 | 2 | 7 |
| α-helix | 94-102 | 9 | |
| α-helix | 108-110 | 3 | |
| α-helix | 114-124 | 11 | |
| β-strand | 131-132 | 2 | 8 |
| β-strand | 133-137 | 5 | 6 |
| α-helix | 156-158 | 3 | |
| α-helix | 159-162 | 4 | |
| β-strand | 169 | 1 | 9 |
| β-strand | 175-179 | 5 | 6 |
| β-strand | 184-188 | 5 | 10 |
| α-helix | 189-190 | 2 | |
| α-helix | 191-193 | 3 | |
| β-strand | 195-203 | 9 | 6 |
| β-strand | 206-211 | 6 | 10 |
| α-helix | 213-215 | 3 | |
| α-helix | 216-226 | 11 | |
| α-helix | 228-233 | 6 | |
| α-helix | 237-240 | 4 | |
| β-strand | 243-245 | 3 | 8 |
| α-helix | 247-252 | 6 | |
| β-strand | 258-262 | 5 | 10 |
| β-strand | 267-270 | 4 | 6 |
| β-strand | 275-280 | 6 | 10 |
| β-strand | 284-291 | 8 | 6 |
| α-helix | 296-302 | 7 | |
| α-helix | 318-324 | 7 | |
| α-helix | 326-333 | 8 | |
| α-helix | 339-341 | 3 | |
| α-helix | 345-347 | 3 | |
| α-helix | 348-350 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 26 | 1 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Lysine-specific demethylase 4A | A, B | protein | 381 | HOMO SAPIENS | O75164 (AlphaFold model) |
| Histone H3.1T | C, D | protein | 5 | HOMO SAPIENS | Q16695 (AlphaFold model) |
>4V2V_1 LYSINE-SPECIFIC DEMETHYLASE 4A (chains A, B) MHHHHHHSSGVDLGTENLYFQSMASESETLNPSARIMTFYPTMEEFRNFSRYIAYIESQG AHRAGLAKVVPPKEWKPRASYDDIDDLVIPAPIQQLVTGQSGLFTQYNIQKKAMTVREFR KIANSDKYCTPRYSEFEELERKYWKNLTFNPPIYGADVNGTLYEKHVDEWNIGRLRTILD LVEKESGITIEGVNTPYLYFGMWKTSFAWHTEDMDLYSINYLHFGEPKSWYSVPPEHGKR LERLAKGFFPGSAQSCEAFLRHKMTLISPLMLKKYGIPFDKVTQEAGEFMITFPYGYHAG FNHGFNCAESTNFATRRWIEYGKQAVLCSCRKDMVKISMDVFVRKFQPERYKLWKAGKDN TVIDHTLPTPEAAEFLKESEL
>4V2V_2 HISTONE H3.1T (chains C, D) ARKSA
Water and common crystallization additives (CL) are not listed.
Studies on the Catalytic Domains of Multiple Jmjc Oxygenases Using Peptide Substrates. Williams, S.T., Walport, L.J., Hopkinson, R.J. et al. Epigenetics (2014) 9:1596. DOI 10.4161/15592294.2014.983381 · PubMed
Other PDB entries of the same protein (UniProt O75164 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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