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2OQ6

Crystal structure of JMJD2A complexed with histone H3 peptide trimethylated at Lys9

Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NI A 501
ChainResidue
AHIS188
AGLU190
AHIS276
AOGA600
AHOH763

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 502
ChainResidue
ACYS234
AHIS240
ACYS306
ACYS308

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NI B 501
ChainResidue
BHIS188
BGLU190
BHIS276
BOGA600
BHOH756

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 502
ChainResidue
BCYS234
BHIS240
BCYS306
BCYS308

site_idAC5
Number of Residues13
DetailsBINDING SITE FOR RESIDUE OGA A 600
ChainResidue
ATYR132
APHE185
AHIS188
AGLU190
ASER196
AASN198
ALYS206
AHIS276
ASER288
ANI501
AHOH763
CM3L9
CHOH41

site_idAC6
Number of Residues14
DetailsBINDING SITE FOR RESIDUE OGA B 600
ChainResidue
BTYR132
BPHE185
BHIS188
BGLU190
BSER196
BASN198
BLYS206
BTRP208
BHIS276
BSER288
BNI501
BHOH756
DM3L9
DHOH75

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsMOD_RES: Symmetric dimethylarginine; by PRMT5; alternate => ECO:0000250|UniProtKB:P68433
ChainResidueDetails
CARG8
DARG8
ALYS206
BTYR132
BASN198
BLYS206

site_idSWS_FT_FI2
Number of Residues2
DetailsMOD_RES: N6-methyllysine; alternate => ECO:0000269|PubMed:11242053, ECO:0000269|PubMed:16185088, ECO:0000269|PubMed:16267050, ECO:0000269|PubMed:16457588, ECO:0000269|PubMed:17194708
ChainResidueDetails
CM3L9
DM3L9
BHIS188
BHIS276

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: Phosphoserine; alternate; by AURKB, AURKC, RPS6KA3, RPS6KA4 and RPS6KA5 => ECO:0000269|PubMed:10464286, ECO:0000269|PubMed:11856369, ECO:0000269|PubMed:12560483, ECO:0000269|PubMed:15681610, ECO:0000269|PubMed:16185088, ECO:0000269|PubMed:16457588
ChainResidueDetails
CSER10
DSER10

site_idSWS_FT_FI4
Number of Residues2
DetailsMOD_RES: Phosphothreonine; by PKC and CHEK1 => ECO:0000269|PubMed:12560483, ECO:0000269|PubMed:18066052, ECO:0000269|PubMed:18243098, ECO:0000269|PubMed:22901803
ChainResidueDetails
CTHR11
DTHR11
ACYS306
ACYS308
BCYS234
BHIS240
BCYS306
BCYS308

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000269|PubMed:22389435
ChainResidueDetails
CALY14
DALY14

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: N-acetylalanine => ECO:0007744|PubMed:19413330
ChainResidueDetails
AALA2
BALA2

Catalytic Information from CSA
site_idMCSA1
Number of Residues6
DetailsM-CSA 370
ChainResidueDetails
AGLY170hydrogen bond acceptor, steric role
ATYR177hydrogen bond donor, steric role
AHIS188metal ligand
AGLU190attractive charge-charge interaction, hydrogen bond acceptor, metal ligand, steric role
AHIS276metal ligand
ASER288hydrogen bond donor, steric role

site_idMCSA2
Number of Residues6
DetailsM-CSA 370
ChainResidueDetails
BGLY170hydrogen bond acceptor, steric role
BTYR177hydrogen bond donor, steric role
BHIS188metal ligand
BGLU190attractive charge-charge interaction, hydrogen bond acceptor, metal ligand, steric role
BHIS276metal ligand
BSER288hydrogen bond donor, steric role

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PDB entries from 2024-07-24

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