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1QJ4

HYDROXYNITRILE-LYASE FROM HEVEA BRASILIENSIS AT ATOMIC RESOLUTION

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0009694biological_processjasmonic acid metabolic process
A0009696biological_processsalicylic acid metabolic process
A0016829molecular_functionlyase activity
A0047606molecular_function(S)-hydroxynitrile lyase activity
A0052891molecular_functionaliphatic (S)-hydroxynitrile lyase activity
A0052892molecular_functionaromatic (S)-hydroxynitrile lyase activity
A0080030molecular_functionmethyl indole-3-acetate esterase activity
A0080031molecular_functionmethyl salicylate esterase activity
A0080032molecular_functionmethyl jasmonate esterase activity
Functional Information from PDB Data
site_idAC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 A 400
ChainResidue
ALYS23
ALYS170
AHOH2112
AHOH2535
AHOH2536
AHOH2537
AHOH2538

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 A 401
ChainResidue
ALYS229
AHOH2473
AHOH2539
AHOH2540
AHOH2541
ATYR116
ATRP217

site_idAC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SO4 A 402
ChainResidue
ATHR137
ALYS138
AASP139
AGLY140
AGLY232
AGLY233
ALYS241
AHOH2357
AHOH2543
AHOH2544
AHOH2547

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 403
ChainResidue
ALYS141
AASN181
ALYS185
AHOH2369
AHOH2548
AHOH2549

site_idAC5
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A 300
ChainResidue
ATHR11
AILE12
ASER80
ACYS81
ATRP128
ALEU148
APHE210
AHIS235
AHOH2501

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton donor/acceptor => ECO:0000305|PubMed:14998991, ECO:0000305|PubMed:18524775
ChainResidueDetails
ASER80
AHIS235

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:10548044, ECO:0000269|PubMed:14998991, ECO:0000269|PubMed:18524775, ECO:0007744|PDB:1SCK, ECO:0007744|PDB:3C6Y, ECO:0007744|PDB:3YAS
ChainResidueDetails
ATHR11
ASER80

site_idSWS_FT_FI3
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:14998991, ECO:0007744|PDB:1SC9
ChainResidueDetails
ALYS236

site_idSWS_FT_FI4
Number of Residues1
DetailsSITE: Increases basicity of active site His => ECO:0000305|PubMed:18524775
ChainResidueDetails
AASP207

Catalytic Information from CSA
site_idCSA1
Number of Residues3
Details
ChainResidueDetails
ASER80
AASP207
AHIS235

site_idMCSA1
Number of Residues6
DetailsM-CSA 217
ChainResidueDetails
ATHR11electrostatic stabiliser, hydrogen bond donor
ASER80electrostatic stabiliser, proton acceptor, proton donor, proton relay
ACYS81electrostatic stabiliser
AASP207electrostatic stabiliser, increase acidity, increase basicity
AHIS235hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
ALYS236activator, electrostatic stabiliser, hydrogen bond donor, steric role

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PDB entries from 2025-06-18

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