7SFC: Human DNMT1(729-1600)

Human DNMT1(729-1600) Bound to Zebularine-Containing 12mer dsDNA and Inhibitor GSK3735967A. Determined by X-ray diffraction at 1.97 Å resolution. Released 30 Mar 2022.

Method
X-ray diffraction
Resolution
1.97 Å
Organism
Homo sapiens
Chains
3
Atoms
7,762
Mol. weight
108.98 kDa
Ligands
ZN, I67
Released
30 Mar 2022

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

Secondary structure: helices and β-sheets

7SFC contains 55 α-helices and 56 β-strands across 1 chain. 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: 55 helices, 56 β-strands

ElementResiduesLengthSheet
β-strand731-73331
β-strand739-74132
β-strand744-74632
β-strand749-75241
β-strand755-75841
β-strand762-76542
β-strand775-785112
β-strand789-799112
α-helix800-8023
α-helix806-8083
β-strand813-824122
α-helix825-8273
β-strand828-83252
β-strand834-83632
α-helix838-8403
α-helix843-8453
α-helix851-8566
β-strand863-87082
β-strand875-87732
α-helix878-8803
α-helix889-8913
α-helix894-90512
β-strand909-91023
β-strand915-91624
β-strand920-92344
β-strand925-92843
β-strand931-93443
β-strand938-94144
α-helix972-9754
α-helix987-9915
β-strand992-1002114
β-strand100315
β-strand100915
β-strand1015-102064
α-helix10211
β-strand102216
α-helix10231
α-helix1024-10263
α-helix1033-10364
β-strand1041-104447
β-strand1048-105254
α-helix1053-10553
β-strand1058-106034
β-strand1061-106447
α-helix1065-10673
α-helix1072-10776
β-strand1082-109097
β-strand1095-109737
α-helix1098-11003
α-helix1101-11033
α-helix1136-11383
β-strand1139-114462
α-helix1150-11589
β-strand1161-116772
α-helix1171-118010
β-strand1185-118732
α-helix1191-11999
β-strand120418
α-helix12091
β-strand121018
α-helix1211-12122
β-strand1219-122242
α-helix1234-12352
α-helix1237-12448
α-helix1247-125812
β-strand1262-126872
α-helix1269-12724
α-helix1278-129013
β-strand1293-130082
α-helix1301-13044
β-strand130819
β-strand1311-131882
α-helix1323-13308
β-strand1332110
α-helix1336-13383
β-strand1343-1345311
β-strand1348-1350311
β-strand1362110
α-helix1363-13653
α-helix1367-13715
α-helix1375-13762
β-strand1385-1386212
α-helix1395-14017
β-strand1409-1410212
α-helix1419-14268
α-helix1436-14383
β-strand1444-1445213
β-strand1451-1452213
β-strand1453114
α-helix1454-14552
β-strand1459115
β-strand1474115
α-helix1477-14793
α-helix1483-14864
α-helix1487-14893
β-strand1494114
α-helix1499-15035
α-helix1504-15063
α-helix1508-15103
α-helix15151
β-strand1516116
α-helix15171
β-strand152319
α-helix1526-15272
β-strand1540116
β-strand1547116
α-helix1548-15492
α-helix1550-15567
α-helix1569-157810
α-helix1580-15812
α-helix1582-159817

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
DNA (cytosine-5)-methyltransferase 1Aprotein874Homo sapiensP26358 (AlphaFold model)
DNA (12-mer)CDNA12Homo sapiens
DNA (12-mer)DDNA12Homo sapiens
Sequence of entity 1 (A), FASTA
>7SFC_1 DNA (cytosine-5)-methyltransferase 1 (chains A)
HMNRISWVGEAVKTDGKKSYYKKVCIDAETLEVGDCVSVIPDDSSKPLYLARVTALWEDS
SNGQMFHAHWFCAGTDTVLGATSDPLELFLVDECEDMQLSYIHSKVKVIYKAPSENWAME
GGMDPESLLEGDDGKTYFYQLWYDQDYARFESPPKTQPTEDNKFKFCVSCARLAEMRQKE
IPRVLEQLEDLDSRVLYYSATKNGILYRVGDGVYLPPEAFTFNIKLSSPVKRPRKEPVDE
DLYPEHYRKYSDYIKGSNLDAPEPYRIGRIKEIFCPKKSNGRPNETDIKIRVNKFYRPEN
THKSTPASYHADINLLYWSDEEAVVDFKAVQGRCTVEYGEDLPECVQVYSMGGPNRFYFL
EAYNAKSKSFEDPPNHARSPGNKGKGKGKGKGKPKSQACEPSEPEIEIKLPKLRTLDVFS
GCGGLSEGFHQAGISDTLWAIEMWDPAAQAFRLNNPGSTVFTEDCNILLKLVMAGETTNS
RGQRLPQKGDVEMLCGGPPCQGFSGMNRFNSRTYSKFKNSLVVSFLSYCDYYRPRFFLLE
NVRNFVSFKRSMVLKLTLRCLVRMGYQCTFGVLQAGQYGVAQTRRRAIILAAAPGEKLPL
FPEPLHVFAPRACQLSVVVDDKKFVSNITRLSSGPFRTITVRDTMSDLPEVRNGASALEI
SYNGEPQSWFQRQLRGAQYQPILRDHICKDMSALVAARMRHIPLAPGSDWRDLPNIEVRL
SDGTMARKLRYTHHDRKNGRSSSGALRGVCSCVEAGKACDPAARQFNTLIPWCLPHTGNR
HNHWAGLYGRLEWDGFFSTTVTNPEPMGKQGRVLHPEQHRVVSVRECARSQGFPDTYRLF
GNILDKHRQVGNAVPPPLAKAIGLEIKLCMLAKA
Sequence of entity 2 (C), FASTA
>7SFC_2 DNA (12-MER) (chains C)
GAGGCCGCCTGC
Sequence of entity 3 (D), FASTA
>7SFC_3 DNA (12-MER) (chains D)
GCAGGUGGCCTC

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn2
I67N-{[4-({[3,5-dicyano-4-ethyl-6-(4-methyl-1,4-diazepan-1-yl)pyridin-2-yl]sulfany…C25 H31 N7 O S3

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

Primary citation

Structural characterization of dicyanopyridine containing DNMT1-selective, non-nucleoside inhibitors. Horton, J.R., Pathuri, S., Wong, K. et al. Structure (2022) 30:793-802.e5. DOI 10.1016/j.str.2022.03.009 · PubMed

Other PDB entries of the same protein (UniProt P26358 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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