Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

3C6Z

HNL from Hevea brasiliensis to atomic resolution

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 Residues9
DetailsBINDING SITE FOR RESIDUE SO4 A 2001
ChainResidue
ALYS23
ALYS170
AHOH3029
AHOH3044
AHOH3128
AHOH3152
AHOH3264
AHOH3437
AHOH3686

site_idAC2
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SO4 A 2002
ChainResidue
ATHR137
ALYS138
AASP139
AGLY140
AGLY232
AGLY233
ALYS241
AHOH3225
AHOH3237
AHOH3369
AHOH3370
AHOH3379

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 2003
ChainResidue
ATHR110
AGLY195
ATYR222
AHOH3230
AHOH3529
AHOH3637

site_idAC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 A 2004
ChainResidue
ALYS141
AASN181
ALYS185
AHOH3103
AHOH3124
AHOH3134
AHOH3450

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE BME A 2005
ChainResidue
ACYS94
AGLU95
AGLU192
AHOH3399
AHOH3436

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE IPA A 1001
ChainResidue
ATHR11
ASER80
ALEU148
AHOH3065

site_idAC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE PEG A 1501
ChainResidue
AGLN47
ALYS147
AARG174
ALYS175
AHOH3120
AHOH3272
AHOH3453

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 Residues4
DetailsAnnotated By Reference To The Literature 1c4x
ChainResidueDetails
AASP207
ASER80
ATHR11
AHIS235

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 1c4x
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

222624

PDB entries from 2024-07-17

PDB statisticsPDBj update infoContact PDBjnumon