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

2FZG

The Structure of Wild-Type E. Coli Aspartate Transcarbamoylase in Complex with Novel T State Inhibitors at 2.25 Resolution

Functional Information from GO Data
ChainGOidnamespacecontents
A0004070molecular_functionaspartate carbamoyltransferase activity
A0004088molecular_functioncarbamoyl-phosphate synthase (glutamine-hydrolyzing) activity
A0005515molecular_functionprotein binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
A0006221biological_processpyrimidine nucleotide biosynthetic process
A0006520biological_processamino acid metabolic process
A0006541biological_processglutamine metabolic process
A0009347cellular_componentaspartate carbamoyltransferase complex
A0016597molecular_functionamino acid binding
A0016740molecular_functiontransferase activity
A0016743molecular_functioncarboxyl- or carbamoyltransferase activity
A0042802molecular_functionidentical protein binding
A0044205biological_process'de novo' UMP biosynthetic process
A0070207biological_processprotein homotrimerization
B0005515molecular_functionprotein binding
B0005737cellular_componentcytoplasm
B0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
B0006221biological_processpyrimidine nucleotide biosynthetic process
B0008270molecular_functionzinc ion binding
B0009347cellular_componentaspartate carbamoyltransferase complex
B0046872molecular_functionmetal ion binding
C0004070molecular_functionaspartate carbamoyltransferase activity
C0004088molecular_functioncarbamoyl-phosphate synthase (glutamine-hydrolyzing) activity
C0005515molecular_functionprotein binding
C0005737cellular_componentcytoplasm
C0005829cellular_componentcytosol
C0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
C0006221biological_processpyrimidine nucleotide biosynthetic process
C0006520biological_processamino acid metabolic process
C0006541biological_processglutamine metabolic process
C0009347cellular_componentaspartate carbamoyltransferase complex
C0016597molecular_functionamino acid binding
C0016740molecular_functiontransferase activity
C0016743molecular_functioncarboxyl- or carbamoyltransferase activity
C0042802molecular_functionidentical protein binding
C0044205biological_process'de novo' UMP biosynthetic process
C0070207biological_processprotein homotrimerization
D0005515molecular_functionprotein binding
D0005737cellular_componentcytoplasm
D0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
D0006221biological_processpyrimidine nucleotide biosynthetic process
D0008270molecular_functionzinc ion binding
D0009347cellular_componentaspartate carbamoyltransferase complex
D0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 154
ChainResidue
BCYS109
BCYS114
BCYS138
BCYS141

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN D 154
ChainResidue
DCYS109
DCYS114
DCYS138
DCYS141

site_idAC3
Number of Residues14
DetailsBINDING SITE FOR RESIDUE CTP B 901
ChainResidue
BASP4
BALA11
BILE12
BVAL17
BASP19
BHIS20
BLYS60
BILE86
BTYR89
BVAL91
BLYS94
BHOH943
BHOH971
BTHR2

site_idAC4
Number of Residues15
DetailsBINDING SITE FOR RESIDUE CTP D 902
ChainResidue
DTHR2
DALA11
DILE12
DVAL17
DASP19
DHIS20
DLYS60
DILE86
DTYR89
DVAL91
DLYS94
DHOH925
DHOH949
DHOH958
DHOH1000

site_idAC5
Number of Residues16
DetailsBINDING SITE FOR RESIDUE EOB A 611
ChainResidue
ASER52
AARG54
ATHR55
AGLY82
AARG105
AHIS134
AGLN137
AGLY166
AARG167
ATHR168
AARG229
APRO266
ALEU267
AHOH619
AHOH662
AHOH750

site_idAC6
Number of Residues14
DetailsBINDING SITE FOR RESIDUE EOB C 612
ChainResidue
CALA51
CSER52
CTHR53
CARG54
CTHR55
CLYS83
CARG105
CHIS134
CGLN137
CTHR168
CARG229
CGLN231
CHOH644
CHOH738

Functional Information from PROSITE/UniProt
site_idPS00097
Number of Residues8
DetailsCARBAMOYLTRANSFERASE Aspartate and ornithine carbamoyltransferases signature. FfEaSTRT
ChainResidueDetails
APHE48-THR55

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING:
ChainResidueDetails
BCYS109
CHIS106
CPRO135
CTHR138
CPRO268
CARG269
BCYS114
BCYS138
BCYS141
DCYS109
DCYS114
DCYS138
DCYS141
CARG56

site_idSWS_FT_FI2
Number of Residues6
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00001, ECO:0000305|PubMed:3380787
ChainResidueDetails
AGLY85
ATHR168
AVAL230
CGLY85
CTHR168
CVAL230

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1at1
ChainResidueDetails
AARG54
AHIS134
AARG105
ATHR55

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1at1
ChainResidueDetails
CARG54
CHIS134
CARG105
CTHR55

site_idMCSA1
Number of Residues5
DetailsM-CSA 405
ChainResidueDetails
ATHR55electrostatic stabiliser
AARG56electrostatic stabiliser, increase electrophilicity
AGLY85proton shuttle (general acid/base)
AHIS106electrostatic stabiliser, increase electrophilicity
APRO135electrostatic stabiliser, increase electrophilicity

site_idMCSA2
Number of Residues5
DetailsM-CSA 405
ChainResidueDetails
CTHR55electrostatic stabiliser
CARG56electrostatic stabiliser, increase electrophilicity
CGLY85proton shuttle (general acid/base)
CHIS106electrostatic stabiliser, increase electrophilicity
CPRO135electrostatic stabiliser, increase electrophilicity

227111

PDB entries from 2024-11-06

PDB statisticsPDBj update infoContact PDBjnumon