Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

6CZF

The structure of E. coli PurF in complex with ppGpp-Mg

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0004044molecular_functionamidophosphoribosyltransferase activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006164biological_processpurine nucleotide biosynthetic process
A0006189biological_process'de novo' IMP biosynthetic process
A0006541biological_processglutamine metabolic process
A0009113biological_processpurine nucleobase biosynthetic process
A0016757molecular_functionglycosyltransferase activity
A0042802molecular_functionidentical protein binding
A0046872molecular_functionmetal ion binding
A0097216molecular_functionguanosine tetraphosphate binding
B0000287molecular_functionmagnesium ion binding
B0004044molecular_functionamidophosphoribosyltransferase activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006164biological_processpurine nucleotide biosynthetic process
B0006189biological_process'de novo' IMP biosynthetic process
B0006541biological_processglutamine metabolic process
B0009113biological_processpurine nucleobase biosynthetic process
B0016757molecular_functionglycosyltransferase activity
B0042802molecular_functionidentical protein binding
B0046872molecular_functionmetal ion binding
B0097216molecular_functionguanosine tetraphosphate binding
C0000287molecular_functionmagnesium ion binding
C0004044molecular_functionamidophosphoribosyltransferase activity
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0006164biological_processpurine nucleotide biosynthetic process
C0006189biological_process'de novo' IMP biosynthetic process
C0006541biological_processglutamine metabolic process
C0009113biological_processpurine nucleobase biosynthetic process
C0016757molecular_functionglycosyltransferase activity
C0042802molecular_functionidentical protein binding
C0046872molecular_functionmetal ion binding
C0097216molecular_functionguanosine tetraphosphate binding
D0000287molecular_functionmagnesium ion binding
D0004044molecular_functionamidophosphoribosyltransferase activity
D0005737cellular_componentcytoplasm
D0005829cellular_componentcytosol
D0006164biological_processpurine nucleotide biosynthetic process
D0006189biological_process'de novo' IMP biosynthetic process
D0006541biological_processglutamine metabolic process
D0009113biological_processpurine nucleobase biosynthetic process
D0016757molecular_functionglycosyltransferase activity
D0042802molecular_functionidentical protein binding
D0046872molecular_functionmetal ion binding
D0097216molecular_functionguanosine tetraphosphate binding
Functional Information from PDB Data
site_idAC1
Number of Residues1
Detailsbinding site for residue MG A 501
ChainResidue
AG4P502

site_idAC2
Number of Residues21
Detailsbinding site for residue G4P A 502
ChainResidue
ASER83
AGLU84
AMG501
AHOH655
CARG45
CLYS46
CASN48
CARG58
CHIS59
CARG62
AARG45
CSER81
CALA82
CSER83
ALYS46
AASN48
AARG58
AHIS59
AARG62
ASER81
AALA82

site_idAC3
Number of Residues1
Detailsbinding site for residue MG D 501
ChainResidue
DG4P502

site_idAC4
Number of Residues21
Detailsbinding site for residue G4P D 502
ChainResidue
BARG45
BLYS46
BASN48
BARG58
BHIS59
BARG62
BSER81
BALA82
BSER83
BHOH688
DARG45
DLYS46
DASN48
DARG58
DHIS59
DARG62
DSER81
DALA82
DSER83
DMG501
DHOH658

Functional Information from PROSITE/UniProt
site_idPS00103
Number of Residues13
DetailsPUR_PYR_PR_TRANSFER Purine/pyrimidine phosphoribosyl transferases signature. VLLVDDSIVRGtT
ChainResidueDetails
AVAL362-THR374

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Nucleophile => ECO:0000255|HAMAP-Rule:MF_01931, ECO:0000269|PubMed:7037784
ChainResidueDetails
ACYS1
BCYS1
CCYS1
DCYS1

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01931
ChainResidueDetails
ATHR304
DTHR304
DASP366
DASP367
AASP366
AASP367
BTHR304
BASP366
BASP367
CTHR304
CASP366
CASP367

Catalytic Information from CSA
site_idMCSA1
Number of Residues5
DetailsM-CSA 214
ChainResidueDetails
ACYS1covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
AGLY27activator, electrostatic stabiliser, hydrogen bond acceptor
AASN101electrostatic stabiliser, hydrogen bond donor
AGLY102electrostatic stabiliser, hydrogen bond donor
ATYR258electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues5
DetailsM-CSA 214
ChainResidueDetails
BCYS1covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
BGLY27activator, electrostatic stabiliser, hydrogen bond acceptor
BASN101electrostatic stabiliser, hydrogen bond donor
BGLY102electrostatic stabiliser, hydrogen bond donor
BTYR258electrostatic stabiliser, hydrogen bond donor

site_idMCSA3
Number of Residues5
DetailsM-CSA 214
ChainResidueDetails
CCYS1covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
CGLY27activator, electrostatic stabiliser, hydrogen bond acceptor
CASN101electrostatic stabiliser, hydrogen bond donor
CGLY102electrostatic stabiliser, hydrogen bond donor
CTYR258electrostatic stabiliser, hydrogen bond donor

site_idMCSA4
Number of Residues5
DetailsM-CSA 214
ChainResidueDetails
DCYS1covalently attached, nucleofuge, nucleophile, proton acceptor, proton donor
DGLY27activator, electrostatic stabiliser, hydrogen bond acceptor
DASN101electrostatic stabiliser, hydrogen bond donor
DGLY102electrostatic stabiliser, hydrogen bond donor
DTYR258electrostatic stabiliser, hydrogen bond donor

223790

PDB entries from 2024-08-14

PDB statisticsPDBj update infoContact PDBjnumon