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1W55

Structure of the Bifunctional IspDF from Campylobacter jejuni

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0008299biological_processisoprenoid biosynthetic process
A0008685molecular_function2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase activity
A0016114biological_processterpenoid biosynthetic process
A0016779molecular_functionnucleotidyltransferase activity
A0016829molecular_functionlyase activity
A0019288biological_processisopentenyl diphosphate biosynthetic process, methylerythritol 4-phosphate pathway
A0046872molecular_functionmetal ion binding
A0050518molecular_function2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase activity
A0070567molecular_functioncytidylyltransferase activity
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A1371
ChainResidue
AASP217
ATHR341
AC1372
AHOH2226
AHOH2244
AHOH2245

site_idAC2
Number of Residues19
DetailsBINDING SITE FOR RESIDUE C A1372
ChainResidue
AALA309
APRO312
ALYS313
ALEU314
ALYS315
ALYS318
AALA340
ATHR341
ATHR342
AMG1371
AHOH2168
AHOH2240
AHOH2241
AHOH2242
AHOH2244
AHOH2245
AHIS243
AASP265
AGLY267

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE C A1373
ChainResidue
ALEU9
AALA10
AALA11
ATHR53
AGLY73
AASP74
ATHR75
AARG76
ASER79
AASP96
AVAL97
AARG139
ALYS191
AHOH2048
AHOH2112
AHOH2246
AHOH2247
AHOH2248

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GPP A1374
ChainResidue
APHE216
AMET308
AGLY347
APHE348
AARG351
AHOH2228

site_idAC5
Number of Residues8
DetailsBINDING SITE FOR RESIDUE EDO A1375
ChainResidue
AASP96
AARG99
AASP128
ATHR129
AILE145
ATHR167
ALYS191
AHOH2112

Functional Information from PROSITE/UniProt
site_idPS01295
Number of Residues8
DetailsISPD 4-diphosphocytidyl-2C-methyl-D-erythritol synthase signature. VMVSDVAR
ChainResidueDetails
AVAL92-ARG99

site_idPS01350
Number of Residues16
DetailsISPF 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase signature. SDGDVLaHSltDAilG
ChainResidueDetails
ASER244-GLY259

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues9
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P62617, ECO:0000255|HAMAP-Rule:MF_01520
ChainResidueDetails
AASP217
AHIS219
AHIS243
AHIS251
AASP265
ATYR270
ATHR341
APHE348
AARG351

site_idSWS_FT_FI2
Number of Residues1
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P62617
ChainResidueDetails
AALA309

site_idSWS_FT_FI3
Number of Residues2
DetailsSITE: Transition state stabilizer => ECO:0000255|HAMAP-Rule:MF_01520
ChainResidueDetails
AARG16
ALYS23

site_idSWS_FT_FI4
Number of Residues2
DetailsSITE: Positions MEP for the nucleophilic attack => ECO:0000255|HAMAP-Rule:MF_01520
ChainResidueDetails
AARG139
ALYS191

site_idSWS_FT_FI5
Number of Residues2
DetailsSITE: Transition state stabilizer => ECO:0000250|UniProtKB:P62617, ECO:0000255|HAMAP-Rule:MF_01520
ChainResidueDetails
AHIS243
ATHR342

Catalytic Information from CSA
site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1hv9
ChainResidueDetails
AARG16

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PDB entries from 2024-07-24

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