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3K14

Co-crystal structure of 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase from Burkholderia pseudomallei with FOL fragment 535, ethyl 3-methyl-5,6-dihydroimidazo[2,1-b][1,3]thiazole-2-carboxylate

Functional Information from GO Data
ChainGOidnamespacecontents
A0008299biological_processisoprenoid biosynthetic process
A0008685molecular_function2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase activity
A0016114biological_processterpenoid biosynthetic process
A0016829molecular_functionlyase activity
A0019288biological_processisopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway
A0046872molecular_functionmetal ion binding
B0008299biological_processisoprenoid biosynthetic process
B0008685molecular_function2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase activity
B0016114biological_processterpenoid biosynthetic process
B0016829molecular_functionlyase activity
B0019288biological_processisopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway
B0046872molecular_functionmetal ion binding
C0008299biological_processisoprenoid biosynthetic process
C0008685molecular_function2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase activity
C0016114biological_processterpenoid biosynthetic process
C0016829molecular_functionlyase activity
C0019288biological_processisopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway
C0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 163
ChainResidue
AASP10
AHIS12
AHIS44
A535164

site_idAC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE 535 A 164
ChainResidue
AASP65
AZN163
BGLU137
AASP10
AHIS12
AHIS44
APHE63
ASER64

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE CL A 165
ChainResidue
AGLN103
ATHR135
AASN136
AGLU137
ALYS138
AGLY143
AHOH186

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K A 166
ChainResidue
AHOH235
AHOH294
BHOH207
CHOH239
CHOH275

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 163
ChainResidue
BASP10
BHIS12
BHIS44
B535164

site_idAC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE 535 B 164
ChainResidue
BASP10
BHIS12
BHIS44
BPHE63
BZN163
CLYS134
CGLU137

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN C 163
ChainResidue
CASP10
CHIS12
CHIS44
C535164

site_idAC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE 535 C 164
ChainResidue
AGLU137
CASP10
CHIS12
CHIS44
CPHE63
CZN163

site_idAC9
Number of Residues8
DetailsBINDING SITE FOR RESIDUE ACT C 165
ChainResidue
AGLY140
ATYR141
AARG144
AHOH229
BHOH174
CGLY140
CTYR141
CARG144

Functional Information from PROSITE/UniProt
site_idPS01350
Number of Residues16
DetailsISPF 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase signature. SDADVLlHAitDAlfG
ChainResidueDetails
ASER37-GLY52

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues30
DetailsBinding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_00107","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues55
DetailsBinding site: {}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues5
DetailsSite: {"description":"Transition state stabilizer","evidences":[{"source":"HAMAP-Rule","id":"MF_00107","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

244693

PDB entries from 2025-11-12

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