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2G4L

Anomalous substructure of hydroxynitrile lyase

Functional Information from GO Data
ChainGOidnamespacecontents
A0009694biological_processjasmonic acid metabolic process
A0009696biological_processsalicylic acid metabolic process
A0016829molecular_functionlyase activity
A0047606molecular_functionhydroxynitrilase 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 Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 301
ChainResidue
ALYS23
ALYS170
AHOH336
AHOH350
AHOH456

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 302
ChainResidue
AGLY233
ALYS241
ATHR137
ALYS138
AASP139
AGLY140

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 303
ChainResidue
ATYR116
ATRP217
ALYS229
AHOH394

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 304
ChainResidue
ALYS141
AASN181
ALYS185
AHOH390
AHOH453

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 305
ChainResidue
ATHR110
AGLY195
ATYR222
AHOH407

site_idAC6
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL A 306
ChainResidue
ATHR190
ALYS191

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_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 2024-04-24

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