4GU1: LSD2

Crystal structure of LSD2. Determined by X-ray diffraction at 2.94 Å resolution. Released 16 Jan 2013.

Method
X-ray diffraction
Resolution
2.94 Å
Organism
Homo sapiens
Chains
2
Atoms
11,971
Mol. weight
178.35 kDa
Ligands
FAD, ZN
Released
16 Jan 2013

Explore 4GU1 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4GU1 contains 97 α-helices and 74 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: 51 helices, 38 β-strands

ElementResiduesLengthSheet
α-helix45-473
α-helix49-502
β-strand82-8651
β-strand89-9241
α-helix93-1008
α-helix107-12014
α-helix124-1252
α-helix127-1304
α-helix131-1355
α-helix137-1382
β-strand139-14132
β-strand150-15232
α-helix157-1593
α-helix161-1666
α-helix184-1863
α-helix188-1903
α-helix191-1966
α-helix199-2046
β-strand21113
α-helix217-2204
α-helix225-2284
β-strand23013
α-helix267-2693
β-strand27214
α-helix273-2742
β-strand28015
β-strand28414
α-helix291-2966
α-helix298-3003
α-helix305-32016
α-helix328-3314
α-helix332-3343
α-helix341-35818
α-helix378-3803
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
α-helix4661
β-strand467-46829
α-helix4691
α-helix4731
β-strand47419
α-helix475-4762
α-helix477-49822
α-helix503-5053
β-strand508110
α-helix509-52113
α-helix527-5293
α-helix530-54718
β-strand554111
β-strand555110
α-helix561-5644
β-strand56715
β-strand572-57438
α-helix579-5868
β-strand592-59326
β-strand598-602512
β-strand608-612512
β-strand617-620412
β-strand622-62546
α-helix629-6335
β-strand638-640312
α-helix642-6432
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-helix716-7194
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-helix805-82016
Chain B: 46 helices, 36 β-strands
ElementResiduesLengthSheet
α-helix45-473
α-helix49-502
β-strand82-84314
β-strand90-92314
α-helix93-1008
α-helix107-11812
α-helix124-1252
α-helix127-1304
α-helix131-1355
α-helix137-1382
β-strand139-141315
β-strand150-152315
α-helix157-1593
α-helix161-1644
α-helix184-1863
α-helix188-1903
α-helix191-1966
α-helix200-2023
β-strand211116
α-helix218-2203
α-helix225-2273
β-strand230116
β-strand272117
α-helix273-2742
β-strand284117
α-helix291-2966
α-helix298-3003
α-helix305-32016
α-helix328-3314
α-helix332-3343
α-helix341-35919
α-helix378-3814
β-strand384-388518
α-helix392-40413
β-strand407-411518
β-strand423-424219
β-strand432-433219
β-strand438-440320
α-helix446-4549
β-strand459-460220
β-strand467-468221
α-helix4691
β-strand474121
α-helix477-49721
α-helix498-5003
α-helix503-5053
β-strand508122
α-helix509-52113
α-helix527-5293
α-helix530-54718
β-strand554123
β-strand555122
α-helix561-5644
β-strand572-574320
α-helix579-5868
β-strand592-593218
β-strand598-602524
β-strand608-612524
β-strand617-620424
β-strand622-625418
α-helix629-6335
β-strand638-640324
α-helix642-6443
α-helix645-6517
β-strand654-657425
β-strand660-665621
β-strand680-683421
α-helix688-6903
β-strand693-699721
β-strand708-713621
α-helix716-7194
α-helix726-74015
α-helix747-7493
β-strand751-754421
α-helix757-7593
β-strand767-770425
β-strand771123
α-helix777-7837
β-strand786118
β-strand790-792318
α-helix795-7973
α-helix805-82016

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Lysine-specific histone demethylase 1BA, Bprotein784Homo sapiensQ8NB78 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>4GU1_1 Lysine-specific histone demethylase 1B (chains A, B)
PLGSEFKGLRRRRKCEKAGCTATCPVCFASASERCAKNGYTSRWYHLSCGEHFCNECFDH
YYRSHKDGYDKYTTWKKIWTSNGKTEPSPKAFMADQQLPYWVQCTKPECRKWRQLTKEIQ
LTPQIAKTYRCGMKPNTAIKPETSDHCSLPEDLRVLEVSNHWWYSMLILPPLLKDSVAAP
LLSAYYPDCVGMSPSCTSTNRAAATGNASPGKLEHSKAALSVHVPGMNRYFQPFYQPNEC
GKALCVRPDVMELDELYEFPEYSRDPTMYLALRNLILALWYTNCKEALTPQKCIPHIIVR
GLVRIRCVQEVERILYFMTRKGLINTGVLSVGADQYLLPKDYHNKSVIIIGAGPAGLAAA
RQLHNFGIKVTVLEAKDRIGGRVWDDKSFKGVTVGRGAQIVNGCINNPVALMCEQLGISM
HKFGERCDLIQEGGRITDPTIDKRMDFHFNALLDVVSEWRKDKTQLQDVPLGEKIEEIYK
AFIKESGIQFSELEGQVLQFHLSNLEYACGSNLHQVSARSWDHNEFFAQFAGDHTLLTPG
YSVIIEKLAEGLDIQLKSPVQCIDYSGDEVQVTTTDGTGYSAQKVLVTVPLALLQKGAIQ
FNPPLSEKKMKAINSLGAGIIEKIALQFPYRFWDSKVQGADFFGHVPPSASKRGLFAVFY
DMDPQKKHSVLMSVIAGEAVASVRTLDDKQVLQQCMATLRELFKEQEVPDPTKYFVTRWS
TDPWIQMAYSFVKTGGSGEAYDIIAEDIQGTVFFAGEATNRHFPQTVTGAYLSGVREASK
IAAF

Ligands and cofactors

IDNameFormulaCopies
FADFlavin-adenine dinucleotideC27 H33 N9 O15 P22
ZNZinc ionZn6

Water and common crystallization additives (CL, NA) are not listed.

Primary citation

LSD2/KDM1B and its cofactor NPAC/GLYR1 endow a structural and molecular model for regulation of H3K4 demethylation. Fang, R., Chen, F., Dong, Z. et al. Mol Cell (2013) 49:558-570. DOI 10.1016/j.molcel.2012.11.019 · PubMed

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

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