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1YYS

Y305F Trichodiene Synthase: Complex With Mg, Pyrophosphate, and (4S)-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 Residues5
DetailsBINDING SITE FOR RESIDUE MG B 701
ChainResidue
BASN225
BASP226
BSER229
BGLU233
BPOP700

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE MG B 702
ChainResidue
BASP100
BPOP700
BMG703

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG B 703
ChainResidue
BGLU164
BASN185
BPOP700
BMG702
BASP100

site_idAC4
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SAZ A 709
ChainResidue
ATYR93
ATHR96
ALEU97
AARG182
AGLY186
ALEU187
AASN225
ATYR295
ATRP298

site_idAC5
Number of Residues10
DetailsBINDING SITE FOR RESIDUE POP B 700
ChainResidue
BASP100
BARG182
BASN185
BASN225
BSER229
BLYS232
BGLU233
BMG701
BMG702
BMG703

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:17996718, ECO:0007744|PDB:2PS7
ChainResidueDetails
AASP100
AGLU164
BASP100
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
AASP100electrostatic 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
APHE305electrostatic 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
BASP100electrostatic 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
BPHE305electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis

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PDB entries from 2024-07-24

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