7XE2: LSD2

Crystal structure of LSD2 in complex with trans-4-Br-PCPA. Determined by X-ray diffraction at 2.05 Å resolution. Released 14 Sept 2022.

Method
X-ray diffraction
Resolution
2.05 Å
Organism
Homo sapiens
Chains
2
Atoms
13,126
Mol. weight
183.22 kDa
Ligands
ZN, FAD, DIJ, FLC
Released
14 Sept 2022

Explore 7XE2 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7XE2 contains 97 α-helices and 78 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: 50 helices, 39 β-strands

ElementResiduesLengthSheet
β-strand5011
β-strand6512
β-strand7911
β-strand83-8642
β-strand89-9132
α-helix93-1008
α-helix107-12014
α-helix124-1252
α-helix127-1304
α-helix131-1355
α-helix137-1382
β-strand139-14133
β-strand150-15233
α-helix153-1542
α-helix157-1593
α-helix161-1666
α-helix1721
α-helix183-1864
α-helix188-1892
α-helix191-1955
α-helix199-2035
β-strand21114
α-helix217-2193
α-helix225-2284
β-strand23014
β-strand27215
α-helix273-2742
β-strand28415
α-helix291-2966
α-helix298-3003
α-helix305-32016
α-helix328-3314
α-helix332-3343
α-helix341-35818
β-strand384-38856
α-helix392-40413
β-strand407-41156
β-strand423-42427
β-strand432-43327
β-strand438-44038
α-helix446-4549
β-strand459-46028
α-helix461-4622
β-strand467-46829
α-helix4691
α-helix4731
β-strand47419
α-helix475-4762
α-helix477-49721
α-helix498-5003
α-helix503-5053
β-strand508110
α-helix509-52416
α-helix530-54718
α-helix551-5533
β-strand554111
β-strand555110
α-helix561-5644
α-helix566-5694
β-strand572-57438
α-helix579-5879
β-strand592-59326
β-strand598-602512
β-strand608-612512
β-strand617-620412
β-strand622-62546
α-helix629-6335
β-strand638-640312
α-helix642-6443
α-helix645-6539
β-strand654-657413
β-strand660-66569
α-helix672-6754
β-strand680-68349
α-helix688-6903
β-strand693-69979
β-strand708-71369
α-helix716-7227
α-helix726-74015
α-helix747-7493
β-strand751-75449
α-helix757-7593
β-strand767-770413
β-strand771111
α-helix777-7837
β-strand78616
β-strand790-79236
α-helix795-7973
α-helix805-82117
Chain B: 47 helices, 39 β-strands
ElementResiduesLengthSheet
β-strand50114
β-strand65115
β-strand79114
β-strand82-84315
β-strand90-92315
α-helix93-1008
α-helix107-12014
α-helix124-1252
α-helix127-1304
α-helix131-1355
α-helix137-1382
β-strand139-141316
β-strand150-152316
α-helix153-1542
α-helix161-1666
α-helix188-1903
α-helix192-1954
α-helix199-2035
β-strand211117
α-helix217-2193
α-helix225-2284
β-strand230117
β-strand272118
α-helix277-2793
β-strand284118
α-helix291-2966
α-helix298-3003
α-helix305-32016
α-helix328-3314
α-helix332-3343
α-helix341-35818
α-helix378-3814
β-strand384-388519
α-helix392-40413
β-strand407-411519
β-strand423-424220
β-strand432-433220
β-strand438-440321
α-helix446-4549
β-strand459-460221
α-helix461-4622
β-strand467-468222
α-helix4691
α-helix4731
β-strand474122
α-helix475-4762
α-helix477-49721
α-helix498-5003
α-helix503-5053
β-strand508123
α-helix509-52416
α-helix530-54718
α-helix551-5533
β-strand554124
β-strand555123
α-helix561-5644
β-strand572-574321
α-helix579-5879
β-strand592-593219
β-strand598-602525
β-strand608-612525
β-strand617-620425
β-strand622-625419
α-helix629-6346
β-strand638-640325
α-helix642-6443
α-helix645-6539
β-strand654-657426
β-strand660-665622
α-helix672-6754
β-strand680-683422
α-helix688-6903
β-strand693-699722
β-strand708-713622
α-helix717-7226
α-helix726-74015
α-helix747-7493
β-strand751-754422
α-helix757-7593
β-strand767-770426
β-strand771124
α-helix777-7837
β-strand786119
β-strand790-792319
α-helix795-7973
α-helix805-82117

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Lysine-specific histone demethylase 1BA, Bprotein793Homo sapiensQ8NB78 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>7XE2_1 Lysine-specific histone demethylase 1B (chains A, B)
AKKKATETTDEDEDGGSEKKYRKCEKAGCTATCPVCFASASERCAKNGYTSRWYHLSCGE
HFCNECFDHYYRSHKDGYDKYTTWKKIWTSNGKTEPSPKAFMADQQLPYWVQCTKPECRK
WRQLTKEIQLTPQIAKTYRCGMKPNTAIKPETSDHCSLPEDLRVLEVSNHWWYSMLILPP
LLKDSVAAPLLSAYYPDCVGMSPSCTSTNRAAATGNASPGKLEHSKAALSVHVPGMNRYF
QPFYQPNECGKALCVRPDVMELDELYEFPEYSRDPTMYLALRNLILALWYTNCKEALTPQ
KCIPHIIVRGLVRIRCVQEVERILYFMTRKGLINTGVLSVGADQYLLPKDYHNKSVIIIG
AGPAGLAAARQLHNFGIKVTVLEAKDRIGGRVWDDKSFKGVTVGRGAQIVNGCINNPVAL
MCEQLGISMHKFGERCDLIQEGGRITDPTIDKRMDFHFNALLDVVSEWRKDKTQLQDVPL
GEKIEEIYKAFIKESGIQFSELEGQVLQFHLSNLEYACGSNLHQVSARSWDHNEFFAQFA
GDHTLLTPGYSVIIEKLAEGLDIQLKSPVQCIDYSGDEVQVTTTDGTGYSAQKVLVTVPL
ALLQKGAIQFNPPLSEKKMKAINSLGAGIIEKIALQFPYRFWDSKVQGADFFGHVPPSAS
KRGLFAVFYDMDPQKKHSVLMSVIAGEAVASVRTLDDKQVLQQCMATLRELFKEQEVPDP
TKYFVTRWSTDPWIQMAYSFVKTGGSGEAYDIIAEDIQGTVFFAGEATNRHFPQTVTGAY
LSGVREASKIAAF

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn6
FADFlavin-adenine dinucleotideC27 H33 N9 O15 P24
DIJ3-(4-bromophenyl)propanalC9 H9 Br O4
FLCCitrate anionC6 H5 O71

Water and common crystallization additives (PGE, GOL) are not listed.

Primary citation

Structure-Activity Relationship and In Silico Evaluation of cis- and trans-PCPA-Derived Inhibitors of LSD1 and LSD2. Niwa, H., Watanabe, C., Sato, S. et al. ACS Med Chem Lett (2022) 13:1485-1492. DOI 10.1021/acsmedchemlett.2c00294

Other PDB entries of the same protein (UniProt Q8NB78 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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