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3D53

2.2 A crystal structure of inorganic pyrophosphatase from Rickettsia prowazekii

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0004427molecular_functioninorganic diphosphate phosphatase activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006796biological_processphosphate-containing compound metabolic process
A0016787molecular_functionhydrolase activity
A0046872molecular_functionmetal ion binding
B0000287molecular_functionmagnesium ion binding
B0004427molecular_functioninorganic diphosphate phosphatase activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006796biological_processphosphate-containing compound metabolic process
B0016787molecular_functionhydrolase activity
B0046872molecular_functionmetal ion binding
C0000287molecular_functionmagnesium ion binding
C0004427molecular_functioninorganic diphosphate phosphatase activity
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0006796biological_processphosphate-containing compound metabolic process
C0016787molecular_functionhydrolase activity
C0046872molecular_functionmetal ion binding
D0000287molecular_functionmagnesium ion binding
D0004427molecular_functioninorganic diphosphate phosphatase activity
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0006796biological_processphosphate-containing compound metabolic process
D0016787molecular_functionhydrolase activity
D0046872molecular_functionmetal ion binding
E0000287molecular_functionmagnesium ion binding
E0004427molecular_functioninorganic diphosphate phosphatase activity
E0005737cellular_componentcytoplasm
E0005829cellular_componentcytosol
E0006796biological_processphosphate-containing compound metabolic process
E0016787molecular_functionhydrolase activity
E0046872molecular_functionmetal ion binding
F0000287molecular_functionmagnesium ion binding
F0004427molecular_functioninorganic diphosphate phosphatase activity
F0005737cellular_componentcytoplasm
F0005829cellular_componentcytosol
F0006796biological_processphosphate-containing compound metabolic process
F0016787molecular_functionhydrolase activity
F0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL B 173
ChainResidue
AMET49
AHIS136
BTHR48

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL D 173
ChainResidue
DTHR48
EMET49
EHIS136

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL F 173
ChainResidue
CMET49
CHIS136
FTHR48

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 173
ChainResidue
ATHR48
BMET49
BHIS136

site_idAC5
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL C 173
ChainResidue
CTHR48
FHIS136

site_idAC6
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL E 173
ChainResidue
DHIS136
ETHR48

site_idAC7
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL A 174
ChainResidue
AARG43
AGLN46

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL B 174
ChainResidue
BARG88
BTHR110
BSER111

site_idAC9
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL E 174
ChainResidue
EARG43
EGLN46

site_idBC1
Number of Residues1
DetailsBINDING SITE FOR RESIDUE CL A 175
ChainResidue
ALYS9

site_idBC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL F 174
ChainResidue
FARG43
FGLN46

site_idBC3
Number of Residues1
DetailsBINDING SITE FOR RESIDUE CL B 175
ChainResidue
BLYS9

site_idBC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL E 175
ChainResidue
EARG88
ETHR110
ESER111

site_idBC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 176
ChainResidue
AARG88
ATHR110
ASER111

site_idBC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL C 174
ChainResidue
CARG88
CSER111
CLYS112

site_idBC7
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL C 175
ChainResidue
CARG43
CMET45
CGLN46

site_idBC8
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL D 174
ChainResidue
DARG43
DGLN46

site_idBC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL F 175
ChainResidue
FARG88
FTHR110
FSER111

site_idCC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL D 175
ChainResidue
DARG88
DSER111

site_idCC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL B 176
ChainResidue
BARG43
BGLN46

site_idCC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL E 176
ChainResidue
DLEU144
ELYS132
EHIS136
EGLU139

site_idCC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL B 177
ChainResidue
BLEU123
BASP124
BGLU128
BLYS131
BTRP155

site_idCC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL C 176
ChainResidue
BGLU162
BTHR163
CASP65

Functional Information from PROSITE/UniProt
site_idPS00387
Number of Residues7
DetailsPPASE Inorganic pyrophosphatase signature. DGDPVDV
ChainResidueDetails
AASP65-VAL71

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues42
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00209
ChainResidueDetails
ALYS29
BTYR55
BASP65
BASP70
BASP102
BTYR141
CLYS29
CARG43
CTYR55
CASP65
CASP70
AARG43
CASP102
CTYR141
DLYS29
DARG43
DTYR55
DASP65
DASP70
DASP102
DTYR141
ELYS29
ATYR55
EARG43
ETYR55
EASP65
EASP70
EASP102
ETYR141
FLYS29
FARG43
FTYR55
FASP65
AASP65
FASP70
FASP102
FTYR141
AASP70
AASP102
ATYR141
BLYS29
BARG43

Catalytic Information from CSA
site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1wgi
ChainResidueDetails
AASP67

site_idCSA2
Number of Residues1
DetailsAnnotated By Reference To The Literature 1wgi
ChainResidueDetails
BASP67

site_idCSA3
Number of Residues1
DetailsAnnotated By Reference To The Literature 1wgi
ChainResidueDetails
CASP67

site_idCSA4
Number of Residues1
DetailsAnnotated By Reference To The Literature 1wgi
ChainResidueDetails
DASP67

site_idCSA5
Number of Residues1
DetailsAnnotated By Reference To The Literature 1wgi
ChainResidueDetails
EASP67

site_idCSA6
Number of Residues1
DetailsAnnotated By Reference To The Literature 1wgi
ChainResidueDetails
FASP67

222415

PDB entries from 2024-07-10

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