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1N21

(+)-Bornyl Diphosphate Synthase: Cocrystal with Mg and 3-aza-2,3-dihydrogeranyl diphosphate

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0009507cellular_componentchloroplast
A0010333molecular_functionterpene synthase activity
A0016102biological_processditerpenoid biosynthetic process
A0016114biological_processterpenoid biosynthetic process
A0016829molecular_functionlyase activity
A0016838molecular_functioncarbon-oxygen lyase activity, acting on phosphates
A0016853molecular_functionisomerase activity
A0042803molecular_functionprotein homodimerization activity
A0046211biological_process(+)-camphor biosynthetic process
A0046872molecular_functionmetal ion binding
A0047926molecular_functiongeranyl-diphosphate cyclase activity
A0050550molecular_functionpinene synthase activity
A0102703molecular_functioncamphene synthase activity
Functional Information from PDB Data
site_idAC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG A 701
ChainResidue
AASP351
AASP355
AGLU429
AMG703
A3AG900
AHOH921
AHOH922

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG A 702
ChainResidue
AGLU504
A3AG900
AHOH919
AASP496
ATHR500

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG A 703
ChainResidue
AASP351
AASP355
AMG701
A3AG900
AHOH920
AHOH921
AHOH923

site_idAC4
Number of Residues23
DetailsBINDING SITE FOR RESIDUE 3AG A 900
ChainResidue
AARG314
AILE344
AASP351
AASP355
AILE457
ALEU492
AARG493
AASP496
ATHR500
AGLU504
ALYS512
ATYR572
APHE578
AMG701
AMG702
AMG703
AHOH919
AHOH920
AHOH921
AHOH922
AHOH923
AHOH925
AHOH926

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsMotif: {"description":"DDXXD motif","evidences":[{"evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues8
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"12432096","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1N1Z","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1n20
ChainResidueDetails
APHE578
ATRP323

site_idMCSA1
Number of Residues9
DetailsM-CSA 259
ChainResidueDetails
ATRP323electrostatic stabiliser, polar/non-polar interaction, steric role, van der waals interaction
AILE344steric role, van der waals interaction
AASP351metal ligand
AASP355metal ligand
AVAL452steric role, van der waals interaction
AASP496metal ligand
ATHR500metal ligand
AGLU504metal ligand
APHE578electrostatic stabiliser, polar/non-polar interaction, steric role, van der waals interaction

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PDB entries from 2025-12-24

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