6OI9
Crystal Structure of E. coli Biotin Carboxylase Complexed with 7-[3-(aminomethyl)pyrrolidin-1-yl]-6-(2,6-dichlorophenyl)pyrido[2,3-d]pyrimidin-2-amine
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0003824 | molecular_function | catalytic activity |
A | 0003989 | molecular_function | acetyl-CoA carboxylase activity |
A | 0004075 | molecular_function | biotin carboxylase activity |
A | 0005515 | molecular_function | protein binding |
A | 0005524 | molecular_function | ATP binding |
A | 0005737 | cellular_component | cytoplasm |
A | 0005829 | cellular_component | cytosol |
A | 0006633 | biological_process | fatty acid biosynthetic process |
A | 0009317 | cellular_component | acetyl-CoA carboxylase complex |
A | 0016874 | molecular_function | ligase activity |
A | 0042803 | molecular_function | protein homodimerization activity |
A | 0045717 | biological_process | negative regulation of fatty acid biosynthetic process |
A | 0046872 | molecular_function | metal ion binding |
A | 2001295 | biological_process | malonyl-CoA biosynthetic process |
B | 0003824 | molecular_function | catalytic activity |
B | 0003989 | molecular_function | acetyl-CoA carboxylase activity |
B | 0004075 | molecular_function | biotin carboxylase activity |
B | 0005515 | molecular_function | protein binding |
B | 0005524 | molecular_function | ATP binding |
B | 0005737 | cellular_component | cytoplasm |
B | 0005829 | cellular_component | cytosol |
B | 0006633 | biological_process | fatty acid biosynthetic process |
B | 0009317 | cellular_component | acetyl-CoA carboxylase complex |
B | 0016874 | molecular_function | ligase activity |
B | 0042803 | molecular_function | protein homodimerization activity |
B | 0045717 | biological_process | negative regulation of fatty acid biosynthetic process |
B | 0046872 | molecular_function | metal ion binding |
B | 2001295 | biological_process | malonyl-CoA biosynthetic process |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 14 |
Details | binding site for residue MQM A 501 |
Chain | Residue |
A | ILE157 |
A | HIS236 |
A | GLU276 |
A | LEU278 |
A | GLU288 |
A | ILE437 |
A | LYS159 |
A | GLY166 |
A | GLU201 |
A | LYS202 |
A | TYR203 |
A | LEU204 |
A | HIS209 |
A | GLN233 |
site_id | AC2 |
Number of Residues | 4 |
Details | binding site for residue EDO A 502 |
Chain | Residue |
A | HIS236 |
A | GLN237 |
A | LYS238 |
A | ARG338 |
site_id | AC3 |
Number of Residues | 8 |
Details | binding site for residue EDO A 503 |
Chain | Residue |
A | ILE120 |
A | GLY133 |
A | SER134 |
A | ASP135 |
A | GLY136 |
A | TYR199 |
A | HOH660 |
A | HOH708 |
site_id | AC4 |
Number of Residues | 14 |
Details | binding site for residue MQM B 501 |
Chain | Residue |
B | ILE157 |
B | LYS159 |
B | GLY166 |
B | GLU201 |
B | LYS202 |
B | TYR203 |
B | LEU204 |
B | HIS209 |
B | GLN233 |
B | HIS236 |
B | GLU276 |
B | LEU278 |
B | GLU288 |
B | ILE437 |
site_id | AC5 |
Number of Residues | 7 |
Details | binding site for residue EDO B 502 |
Chain | Residue |
A | VAL365 |
A | ARG366 |
A | TRP367 |
B | PRO360 |
B | GLY361 |
B | GLY362 |
B | VAL365 |
Functional Information from PROSITE/UniProt
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | ACT_SITE: ACT_SITE => ECO:0000269|PubMed:19213731 |
Chain | Residue | Details |
A | ARG292 | |
B | ARG292 |
site_id | SWS_FT_FI2 |
Number of Residues | 4 |
Details | BINDING: BINDING => ECO:0000269|PubMed:10821865, ECO:0000269|PubMed:19213731, ECO:0007744|PDB:1DV2, ECO:0007744|PDB:3G8D |
Chain | Residue | Details |
A | LYS116 | |
A | GLY165 | |
B | LYS116 | |
B | GLY165 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:19213731, ECO:0007744|PDB:3G8C, ECO:0007744|PDB:3G8D |
Chain | Residue | Details |
A | LYS159 | |
B | LYS159 |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:10821865, ECO:0000269|PubMed:19213731, ECO:0007744|PDB:1DV2, ECO:0007744|PDB:3G8C, ECO:0007744|PDB:3G8D |
Chain | Residue | Details |
A | GLU201 | |
B | GLU201 |
site_id | SWS_FT_FI5 |
Number of Residues | 10 |
Details | BINDING: BINDING => ECO:0000269|PubMed:19213731, ECO:0007744|PDB:3G8C |
Chain | Residue | Details |
A | HIS209 | |
B | ARG338 | |
A | LYS238 | |
A | ARG292 | |
A | VAL295 | |
A | ARG338 | |
B | HIS209 | |
B | LYS238 | |
B | ARG292 | |
B | VAL295 |
site_id | SWS_FT_FI6 |
Number of Residues | 2 |
Details | BINDING: BINDING => ECO:0000269|PubMed:10821865, ECO:0000269|PubMed:19213731, ECO:0007744|PDB:1DV2, ECO:0007744|PDB:3G8C |
Chain | Residue | Details |
A | HIS236 | |
B | HIS236 |
site_id | SWS_FT_FI7 |
Number of Residues | 6 |
Details | BINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00409 |
Chain | Residue | Details |
A | GLU276 | |
A | GLU288 | |
A | ASN290 | |
B | GLU276 | |
B | GLU288 | |
B | ASN290 |