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1JFG

TRICHODIENE SYNTHASE FROM FUSARIUM SPOROTRICHIOIDES COMPLEXED WITH DIPHOSPHATE

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
BSER229
BGLU233
BPOP700
BHOH1088

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG B 702
ChainResidue
BHOH1090
BHOH1091
BASP100
BPOP700
BMG703
BHOH1089

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG B 703
ChainResidue
BASP100
BGLU164
BPOP700
BMG702
BHOH1090
BHOH1092

site_idAC4
Number of Residues16
DetailsBINDING SITE FOR RESIDUE POP B 700
ChainResidue
BASP100
BARG182
BASN225
BSER229
BLYS232
BGLU233
BARG304
BTYR305
BMG701
BMG702
BMG703
BGOL751
BHOH1088
BHOH1089
BHOH1091
BHOH1092

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 750
ChainResidue
AMET73
ATYR93
AGLY186
AMET221
ATYR295
AHOH1033
AHOH1064

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL B 751
ChainResidue
BARG182
BGLY186
BMET221
BTYR295
BTYR305
BPOP700

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 752
ChainResidue
ATYR113
ALEU117
AHOH1070
BTYR113
BLEU117
BILE151
BLEU155
BHOH888

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
BASP239
BILE241
AASP239
AILE241

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
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
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
BTYR305electrostatic stabiliser, hydrogen bond donor, increase nucleophilicity, promote heterolysis

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PDB entries from 2024-06-12

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