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5DTM

Crystal structure of Dot1L in complex with inhibitor CPD1 [4-(2,6-dichlorobenzoyl)-N-methyl-1H-pyrrole-2-carboxamide]

Functional Information from GO Data
ChainGOidnamespacecontents
A0031151molecular_functionhistone H3K79 methyltransferase activity
A0051726biological_processregulation of cell cycle
B0031151molecular_functionhistone H3K79 methyltransferase activity
B0051726biological_processregulation of cell cycle
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue 5F4 A 401
ChainResidue
APHE131
ASER269
ASER311
ATYR312
AHOH550
AHOH552
AHOH562
AHOH635
ASER140
ALEU143
AVAL144
APHE239
AASN241
APHE243
AVAL267
ASER268

site_idAC2
Number of Residues14
Detailsbinding site for residue 5F4 B 401
ChainResidue
BPHE131
BSER140
BLEU143
BVAL144
BPHE239
BASN241
BPHE243
BVAL267
BSER268
BSER269
BSER311
BTYR312
BHOH579
BHOH607

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING:
ChainResidueDetails
ATYR136
APHE159
AGLU186
AASP222
BTYR136
BPHE159
BGLU186
BASP222

site_idSWS_FT_FI2
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163
ChainResidueDetails
ASER297
BSER297

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PDB entries from 2024-09-11

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