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3MPU

Crystal structure of the C47A/A241C disulfide-linked E. coli Aspartate Transcarbamoylase holoenzyme

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
E0004070molecular_functionaspartate carbamoyltransferase activity
E0004088molecular_functioncarbamoyl-phosphate synthase (glutamine-hydrolyzing) activity
E0005515molecular_functionprotein binding
E0005737cellular_componentcytoplasm
E0005829cellular_componentcytosol
E0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
E0006221biological_processpyrimidine nucleotide biosynthetic process
E0006520biological_processamino acid metabolic process
E0006541biological_processglutamine metabolic process
E0009347cellular_componentaspartate carbamoyltransferase complex
E0016597molecular_functionamino acid binding
E0016740molecular_functiontransferase activity
E0016743molecular_functioncarboxyl- or carbamoyltransferase activity
E0042802molecular_functionidentical protein binding
E0044205biological_process'de novo' UMP biosynthetic process
E0070207biological_processprotein homotrimerization
F0005515molecular_functionprotein binding
F0005737cellular_componentcytoplasm
F0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
F0006221biological_processpyrimidine nucleotide biosynthetic process
F0008270molecular_functionzinc ion binding
F0009347cellular_componentaspartate carbamoyltransferase complex
F0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PO4 A 311
ChainResidue
ASER52
AHOH514
ATHR53
AARG54
ATHR55
ASER80
ALYS84
AARG105
ALEU267
APO4312

site_idAC2
Number of Residues11
DetailsBINDING SITE FOR RESIDUE PO4 A 312
ChainResidue
ATHR55
ALYS84
AARG105
AHIS134
AARG167
ATHR168
ALEU267
APO4311
AHOH514
AHOH563
AHOH571

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 154
ChainResidue
BCYS109
BCYS114
BCYS138
BCYS141

site_idAC4
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PO4 C 311
ChainResidue
CSER52
CTHR53
CARG54
CTHR55
CSER80
CLYS84
CARG105
CLEU267
CPO4312
CHOH680

site_idAC5
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PO4 C 312
ChainResidue
CTHR55
CLYS84
CARG105
CHIS134
CARG167
CTHR168
CLEU267
CPO4311
CHOH680
CHOH729

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN D 154
ChainResidue
DCYS109
DCYS114
DCYS138
DCYS141

site_idAC7
Number of Residues9
DetailsBINDING SITE FOR RESIDUE PO4 E 311
ChainResidue
ESER52
ETHR53
EARG54
ETHR55
ESER80
EARG105
ELEU267
EPO4312
EHOH709

site_idAC8
Number of Residues10
DetailsBINDING SITE FOR RESIDUE PO4 E 312
ChainResidue
ETHR55
ELYS84
EARG105
EHIS134
EARG167
ETHR168
ELEU267
EPO4311
EHOH319
EHOH709

site_idAC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN F 154
ChainResidue
FCYS109
FCYS114
FCYS138
FCYS141

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 Residues12
DetailsBINDING:
ChainResidueDetails
BCYS109
FCYS114
FCYS138
FCYS141
CLEU267
CPRO268
EARG54
ETHR55
EARG105
EHIS134
EGLN137
BCYS114
ELEU267
EPRO268
BCYS138
BCYS141
DCYS109
DCYS114
DCYS138
DCYS141
FCYS109

site_idSWS_FT_FI2
Number of Residues9
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00001, ECO:0000305|PubMed:3380787
ChainResidueDetails
ALYS84
AARG167
AARG229
CLYS84
CARG167
CARG229
ELYS84
EARG167
EARG229

Catalytic Information from CSA
site_idMCSA1
Number of Residues5
DetailsM-CSA 405
ChainResidueDetails
AARG54electrostatic stabiliser
ATHR55electrostatic stabiliser, increase electrophilicity
ALYS84proton shuttle (general acid/base)
AARG105electrostatic stabiliser, increase electrophilicity
AHIS134electrostatic stabiliser, increase electrophilicity

site_idMCSA2
Number of Residues5
DetailsM-CSA 405
ChainResidueDetails
CARG54electrostatic stabiliser
CTHR55electrostatic stabiliser, increase electrophilicity
CLYS84proton shuttle (general acid/base)
CARG105electrostatic stabiliser, increase electrophilicity
CHIS134electrostatic stabiliser, increase electrophilicity

site_idMCSA3
Number of Residues5
DetailsM-CSA 405
ChainResidueDetails
EARG54electrostatic stabiliser
ETHR55electrostatic stabiliser, increase electrophilicity
ELYS84proton shuttle (general acid/base)
EARG105electrostatic stabiliser, increase electrophilicity
EHIS134electrostatic stabiliser, increase electrophilicity

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PDB entries from 2024-07-10

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