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6L2C

Crystal structure of Aspergillus fumigatus mitochondrial acetyl-CoA acetyltransferase in complex with CoA

Functional Information from GO Data
ChainGOidnamespacecontents
A0003985molecular_functionacetyl-CoA C-acetyltransferase activity
A0003988molecular_functionacetyl-CoA C-acyltransferase activity
A0005739cellular_componentmitochondrion
A0006635biological_processfatty acid beta-oxidation
A0016746molecular_functionacyltransferase activity
A0016747molecular_functionacyltransferase activity, transferring groups other than amino-acyl groups
A0046872molecular_functionmetal ion binding
B0003985molecular_functionacetyl-CoA C-acetyltransferase activity
B0003988molecular_functionacetyl-CoA C-acyltransferase activity
B0005739cellular_componentmitochondrion
B0006635biological_processfatty acid beta-oxidation
B0016746molecular_functionacyltransferase activity
B0016747molecular_functionacyltransferase activity, transferring groups other than amino-acyl groups
B0046872molecular_functionmetal ion binding
C0003985molecular_functionacetyl-CoA C-acetyltransferase activity
C0003988molecular_functionacetyl-CoA C-acyltransferase activity
C0005739cellular_componentmitochondrion
C0006635biological_processfatty acid beta-oxidation
C0016746molecular_functionacyltransferase activity
C0016747molecular_functionacyltransferase activity, transferring groups other than amino-acyl groups
C0046872molecular_functionmetal ion binding
D0003985molecular_functionacetyl-CoA C-acetyltransferase activity
D0003988molecular_functionacetyl-CoA C-acyltransferase activity
D0005739cellular_componentmitochondrion
D0006635biological_processfatty acid beta-oxidation
D0016746molecular_functionacyltransferase activity
D0016747molecular_functionacyltransferase activity, transferring groups other than amino-acyl groups
D0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues11
Detailsbinding site for residue COA A 501
ChainResidue
ACSO124
APHE358
AHOH673
ALEU184
ATYR219
AASN257
AARG259
AMET263
AALA280
AGLY281
ASER284

site_idAC2
Number of Residues12
Detailsbinding site for residue COA B 501
ChainResidue
BCSO124
BLEU184
BTYR219
BASN257
BARG259
BLYS262
BLEU266
BALA280
BSER284
BMET286
BHOH628
BHOH635

site_idAC3
Number of Residues14
Detailsbinding site for residue COA C 501
ChainResidue
CCSO124
CLEU184
CMET193
CTYR219
CASN257
CLEU258
CARG259
CMET263
CLEU266
CALA280
CSER284
CTHR285
CPHE358
CHOH612

site_idAC4
Number of Residues11
Detailsbinding site for residue COA D 501
ChainResidue
DCSO124
DTYR219
DASN257
DARG259
DLEU266
DGLY281
DSER284
DMET286
DPHE358
DHOH607
DHOH630

Functional Information from PROSITE/UniProt
site_idPS00098
Number of Residues19
DetailsTHIOLASE_1 Thiolases acyl-enzyme intermediate signature. VNKvCASGLkAValaaqnI
ChainResidueDetails
AVAL120-ILE138

site_idPS00099
Number of Residues14
DetailsTHIOLASE_3 Thiolases active site. GVAAICNGgGaAtA
ChainResidueDetails
AGLY410-ALA423

site_idPS00211
Number of Residues15
DetailsABC_TRANSPORTER_1 ABC transporters family signature. FAQGNRALARIVSTA
ChainResidueDetails
APHE304-ALA318

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Acyl-thioester intermediate => ECO:0000250|UniProtKB:P24752
ChainResidueDetails
ACSO124
BCSO124
CCSO124
DCSO124

site_idSWS_FT_FI2
Number of Residues8
DetailsACT_SITE: Proton acceptor => ECO:0000255|PROSITE-ProRule:PRU10020
ChainResidueDetails
AHIS387
ACYS415
BHIS387
BCYS415
CHIS387
CCYS415
DHIS387
DCYS415

site_idSWS_FT_FI3
Number of Residues20
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:Q4WCL5
ChainResidueDetails
ATYR219
BASN416
CTYR219
CLYS262
CALA280
CSER284
CASN416
DTYR219
DLYS262
DALA280
DSER284
ALYS262
DASN416
AALA280
ASER284
AASN416
BTYR219
BLYS262
BALA280
BSER284

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:32005728, ECO:0007744|PDB:6L2C
ChainResidueDetails
AASN229
BASN229
CASN229
DASN229

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PDB entries from 2024-11-06

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