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5FYC

Crystal structure of human JMJD2A in complex with succinate

Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE NI A 501
ChainResidue
AHIS188
AGLU190
AHIS276
AFUM1354
AHOH2080
AHOH2084

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

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE NI B 501
ChainResidue
BHIS188
BGLU190
BHIS276
BFUM1354
BHOH2093
BHOH2098

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

site_idAC5
Number of Residues11
DetailsBINDING SITE FOR RESIDUE FUM B 1354
ChainResidue
BTYR132
BTYR177
BHIS188
BASN198
BLYS206
BTRP208
BHIS276
BNI501
BHOH2092
BHOH2098
BHOH2151

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE FUM A 1354
ChainResidue
ATYR132
ATYR177
APHE185
AHIS188
AASN198
ALYS206
ATRP208
AHIS276
ANI501
AHOH2084
AHOH2150

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE EDO B 1355
ChainResidue
BTYR121
BTRP122
BPHE185
BTRP187
BLEU244
BILE245
BALA277
BGLY278

site_idAC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO B 1356
ChainResidue
BTHR83
BPHE227
BSER230
BTHR243

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EDO A 1355
ChainResidue
ATHR83
APHE227
ASER230
ATHR243
AHOH2107

site_idBC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EDO A 1356
ChainResidue
ALYS314
ASER316
AMET317
ATRP332
AHOH2151

site_idBC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE EDO B 1357
ChainResidue
BTYR59
BARG98

site_idBC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE EDO A 1357
ChainResidue
ALYS89
ALYS90

site_idBC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EDO A 1358
ChainResidue
AHIS188
ATHR189
ALEU238
AARG239
ATYR275

site_idBC5
Number of Residues8
DetailsBINDING SITE FOR RESIDUE EDO A 1359
ChainResidue
ATYR253
AGLY254
AHOH2112
AHOH2152
AHOH2153
BASP258
BLYS259
BVAL260

site_idBC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 B 1358
ChainResidue
ALYS105
BPHE227
BPRO228
BGLY229
BSER230

site_idBC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 1360
ChainResidue
APHE227
APRO228
AGLY229
ASER230
BLYS105

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:16677698
ChainResidueDetails
ATYR132
AASN198
ALYS206
BTYR132
BASN198
BLYS206

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00538, ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
ChainResidueDetails
AHIS188
AHIS276
BHIS188
BHIS276

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:16677698, ECO:0000305|PubMed:26741168
ChainResidueDetails
AGLU190
BGLU190

site_idSWS_FT_FI4
Number of Residues8
DetailsBINDING: BINDING => ECO:0007744|PDB:5F2W, ECO:0007744|PDB:5F32, ECO:0007744|PDB:5F37, ECO:0007744|PDB:5F39, ECO:0007744|PDB:5F3E, ECO:0007744|PDB:5F3G, ECO:0007744|PDB:5F5I
ChainResidueDetails
ACYS234
AHIS240
ACYS306
ACYS308
BCYS234
BHIS240
BCYS306
BCYS308

site_idSWS_FT_FI5
Number of Residues2
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:B2RXH2
ChainResidueDetails
ALYS241
BLYS241

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 2024-10-30

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