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6MWF

Crystal structure of 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase (IspF) Burkholderia pseudomallei in complex with ligand HGN-0459

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 201
ChainResidue
AASP10
AHIS12
AHIS44
ASFY202

site_idAC2
Number of Residues13
Detailsbinding site for residue SFY A 202
ChainResidue
AHIS44
AILE59
APHE63
AASP65
APHE70
ALEU78
AZN201
BLYS134
AASP10
AHIS12
AGLY35
AHIS36
ASER37

site_idAC3
Number of Residues7
Detailsbinding site for residue DMS A 203
ChainResidue
AALA102
APRO105
ALYS106
ALEU107
ALYS134
ATHR135
AHOH302

site_idAC4
Number of Residues6
Detailsbinding site for residue ACT A 204
ChainResidue
AALA92
AILE93
ALEU122
AASP123
AHOH303
AHOH381

site_idAC5
Number of Residues5
Detailsbinding site for residue ZN B 200
ChainResidue
BASP10
BHIS12
BHIS44
BHOH414
CHOH385

site_idAC6
Number of Residues5
Detailsbinding site for residue ZN C 200
ChainResidue
CASP10
CHIS12
CHIS44
CSFY201
CHOH304

site_idAC7
Number of Residues12
Detailsbinding site for residue SFY C 201
ChainResidue
ALYS134
CASP10
CHIS12
CGLY35
CHIS36
CSER37
CHIS44
CILE59
CPHE63
CLEU78
CZN200
CHOH304

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 Residues21
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00107
ChainResidueDetails
AHIS44
AASP58
APHE63
AARG144
BASP10
BHIS12
BHIS36
BHIS44
BASP58
BPHE63
BARG144
CASP10
CHIS12
CHIS36
CHIS44
CASP58
CPHE63
CARG144
AHIS12
AHIS36
AASP10

site_idSWS_FT_FI2
Number of Residues9
DetailsBINDING:
ChainResidueDetails
BASP40
BALA102
BALA133
CASP40
CALA102
CALA133
AASP40
AALA102
AALA133

site_idSWS_FT_FI3
Number of Residues6
DetailsSITE: Transition state stabilizer => ECO:0000255|HAMAP-Rule:MF_00107
ChainResidueDetails
BTHR135
CHIS36
CTHR135
AHIS36
ATHR135
BHIS36

221051

PDB entries from 2024-06-12

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