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5F5I

Crystal Structure of human JMJD2A complexed with KDOOA011340

Functional Information from PDB Data
site_idAC1
Number of Residues5
Detailsbinding site for residue NI A 501
ChainResidue
AHIS188
AGLU190
AHIS276
A5V1504
AHOH610

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 SO4 A 503
ChainResidue
APHE227
APRO228
AGLY229
ASER230
BLYS105

site_idAC4
Number of Residues15
Detailsbinding site for residue 5V1 A 504
ChainResidue
ATYR132
AGLY170
ATYR175
ATYR177
APHE185
AHIS188
AGLU190
AASN198
ALYS206
ATRP208
AHIS276
ASER288
AASN290
ANI501
AHOH610

site_idAC5
Number of Residues5
Detailsbinding site for residue NI B 501
ChainResidue
BHIS188
BGLU190
BHIS276
B5V1504
BHOH613

site_idAC6
Number of Residues4
Detailsbinding site for residue ZN B 502
ChainResidue
BCYS234
BHIS240
BCYS306
BCYS308

site_idAC7
Number of Residues6
Detailsbinding site for residue SO4 B 503
ChainResidue
ALYS105
BPHE227
BPRO228
BGLY229
BSER230
BHOH649

site_idAC8
Number of Residues14
Detailsbinding site for residue 5V1 B 504
ChainResidue
BTYR132
BTYR175
BTYR177
BPHE185
BHIS188
BGLU190
BASN198
BLYS206
BTRP208
BSER288
BASN290
BNI501
BHOH609
BHOH613

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues84
DetailsDomain: {"description":"JmjN","evidences":[{"source":"PROSITE-ProRule","id":"PRU00537","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues166
DetailsDomain: {"description":"JmjC","evidences":[{"source":"PROSITE-ProRule","id":"PRU00538","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues6
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"16677698","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00538","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"16677698","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"26741168","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"16677698","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"26741168","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues8
DetailsBinding site: {"evidences":[{"source":"PDB","id":"5F2W","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F32","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F37","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F39","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F3E","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F3G","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5F5I","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"UniProtKB","id":"B2RXH2","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

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 Residues5
DetailsM-CSA 370
ChainResidueDetails
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

247536

PDB entries from 2026-01-14

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