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1YYT

D100E Trichodiene Synthase: Complex With Mg, Pyrophosphate, and (4R)-7-azabisabolene

Functional Information from GO Data
ChainGOidnamespacecontents
A0016106biological_processsesquiterpenoid biosynthetic process
A0016829molecular_functionlyase activity
A0016838molecular_functioncarbon-oxygen lyase activity, acting on phosphates
A0045482molecular_functiontrichodiene synthase activity
A0046872molecular_functionmetal ion binding
B0016106biological_processsesquiterpenoid biosynthetic process
B0016829molecular_functionlyase activity
B0016838molecular_functioncarbon-oxygen lyase activity, acting on phosphates
B0045482molecular_functiontrichodiene synthase activity
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE MG B 701
ChainResidue
BGLU100
BPOP700

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG B 702
ChainResidue
BASN225
BSER229
BGLU233
BPOP700

site_idAC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE POP B 700
ChainResidue
BSER229
BLYS232
BTYR305
BMG701
BMG702
BSAZ704
BGLU100
BARG182
BASN225

site_idAC4
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SAZ B 704
ChainResidue
BMET73
BTYR93
BTHR96
BLEU97
BGLY186
BLEU187
BMET221
BASN225
BTYR295
BTRP298
BPOP700

site_idAC5
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SAZ A 709
ChainResidue
AMET73
ATYR93
ATHR96
AGLY186
ALEU187
AASN225
ATRP298
ATYR305

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:17996718, ECO:0007744|PDB:2PS7
ChainResidueDetails
AGLU100
AGLU164
BGLU100
BGLU164

site_idSWS_FT_FI2
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:15835903, ECO:0000269|PubMed:16171386, ECO:0000269|PubMed:17996718, ECO:0007744|PDB:1YYQ, ECO:0007744|PDB:1YYR, ECO:0007744|PDB:1YYU, ECO:0007744|PDB:2AET, ECO:0007744|PDB:2PS8
ChainResidueDetails
AASN225
ASER229
AGLU233
BASN225
BSER229
BGLU233

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:16171386, ECO:0000269|PubMed:17996718, ECO:0007744|PDB:2AEK, ECO:0007744|PDB:2PS4
ChainResidueDetails
AASP239
AILE241
BASP239
BILE241

Catalytic Information from CSA
site_idMCSA1
Number of Residues8
DetailsM-CSA 262
ChainResidueDetails
ATYR93electrostatic stabiliser, polar/non-polar interaction, van der waals interaction
ATHR96steric role, van der waals interaction
ALEU97steric role, van der waals interaction
AGLU100electrostatic stabiliser, metal ligand
AARG182electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis
ALYS232electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis
AARG304electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis
ATYR305electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis

site_idMCSA2
Number of Residues8
DetailsM-CSA 262
ChainResidueDetails
BTYR93electrostatic stabiliser, polar/non-polar interaction, van der waals interaction
BTHR96steric role, van der waals interaction
BLEU97steric role, van der waals interaction
BGLU100electrostatic stabiliser, metal ligand
BARG182electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis
BLYS232electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis
BARG304electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis
BTYR305electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis

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PDB entries from 2024-11-06

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