1C3O
CRYSTAL STRUCTURE OF THE CARBAMOYL PHOSPHATE SYNTHETASE: SMALL SUBUNIT MUTANT C269S WITH BOUND GLUTAMINE
Functional Information from GO Data
| Chain | GOid | namespace | contents |
| A | 0000166 | molecular_function | nucleotide binding |
| A | 0004087 | molecular_function | carbamoyl-phosphate synthase (ammonia) activity |
| A | 0004088 | molecular_function | carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity |
| A | 0005515 | molecular_function | protein binding |
| A | 0005524 | molecular_function | ATP binding |
| A | 0005737 | cellular_component | cytoplasm |
| A | 0005829 | cellular_component | cytosol |
| A | 0005951 | cellular_component | carbamoyl-phosphate synthase complex |
| A | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
| A | 0006526 | biological_process | L-arginine biosynthetic process |
| A | 0006541 | biological_process | glutamine metabolic process |
| A | 0008652 | biological_process | amino acid biosynthetic process |
| A | 0016597 | molecular_function | amino acid binding |
| A | 0016874 | molecular_function | ligase activity |
| A | 0016879 | molecular_function | ligase activity, forming carbon-nitrogen bonds |
| A | 0019856 | biological_process | pyrimidine nucleobase biosynthetic process |
| A | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
| A | 0046872 | molecular_function | metal ion binding |
| B | 0000166 | molecular_function | nucleotide binding |
| B | 0004088 | molecular_function | carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity |
| B | 0004359 | molecular_function | glutaminase activity |
| B | 0005515 | molecular_function | protein binding |
| B | 0005524 | molecular_function | ATP binding |
| B | 0005737 | cellular_component | cytoplasm |
| B | 0005829 | cellular_component | cytosol |
| B | 0005951 | cellular_component | carbamoyl-phosphate synthase complex |
| B | 0006207 | biological_process | 'de novo' pyrimidine nucleobase biosynthetic process |
| B | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
| B | 0006526 | biological_process | L-arginine biosynthetic process |
| B | 0006541 | biological_process | glutamine metabolic process |
| B | 0008652 | biological_process | amino acid biosynthetic process |
| B | 0016874 | molecular_function | ligase activity |
| B | 0019856 | biological_process | pyrimidine nucleobase biosynthetic process |
| B | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
| B | 0046982 | molecular_function | protein heterodimerization activity |
| C | 0000166 | molecular_function | nucleotide binding |
| C | 0004087 | molecular_function | carbamoyl-phosphate synthase (ammonia) activity |
| C | 0004088 | molecular_function | carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity |
| C | 0005515 | molecular_function | protein binding |
| C | 0005524 | molecular_function | ATP binding |
| C | 0005737 | cellular_component | cytoplasm |
| C | 0005829 | cellular_component | cytosol |
| C | 0005951 | cellular_component | carbamoyl-phosphate synthase complex |
| C | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
| C | 0006526 | biological_process | L-arginine biosynthetic process |
| C | 0006541 | biological_process | glutamine metabolic process |
| C | 0008652 | biological_process | amino acid biosynthetic process |
| C | 0016597 | molecular_function | amino acid binding |
| C | 0016874 | molecular_function | ligase activity |
| C | 0016879 | molecular_function | ligase activity, forming carbon-nitrogen bonds |
| C | 0019856 | biological_process | pyrimidine nucleobase biosynthetic process |
| C | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
| C | 0046872 | molecular_function | metal ion binding |
| D | 0000166 | molecular_function | nucleotide binding |
| D | 0004088 | molecular_function | carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity |
| D | 0004359 | molecular_function | glutaminase activity |
| D | 0005515 | molecular_function | protein binding |
| D | 0005524 | molecular_function | ATP binding |
| D | 0005737 | cellular_component | cytoplasm |
| D | 0005829 | cellular_component | cytosol |
| D | 0005951 | cellular_component | carbamoyl-phosphate synthase complex |
| D | 0006207 | biological_process | 'de novo' pyrimidine nucleobase biosynthetic process |
| D | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
| D | 0006526 | biological_process | L-arginine biosynthetic process |
| D | 0006541 | biological_process | glutamine metabolic process |
| D | 0008652 | biological_process | amino acid biosynthetic process |
| D | 0016874 | molecular_function | ligase activity |
| D | 0019856 | biological_process | pyrimidine nucleobase biosynthetic process |
| D | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
| D | 0046982 | molecular_function | protein heterodimerization activity |
| E | 0000166 | molecular_function | nucleotide binding |
| E | 0004087 | molecular_function | carbamoyl-phosphate synthase (ammonia) activity |
| E | 0004088 | molecular_function | carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity |
| E | 0005515 | molecular_function | protein binding |
| E | 0005524 | molecular_function | ATP binding |
| E | 0005737 | cellular_component | cytoplasm |
| E | 0005829 | cellular_component | cytosol |
| E | 0005951 | cellular_component | carbamoyl-phosphate synthase complex |
| E | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
| E | 0006526 | biological_process | L-arginine biosynthetic process |
| E | 0006541 | biological_process | glutamine metabolic process |
| E | 0008652 | biological_process | amino acid biosynthetic process |
| E | 0016597 | molecular_function | amino acid binding |
| E | 0016874 | molecular_function | ligase activity |
| E | 0016879 | molecular_function | ligase activity, forming carbon-nitrogen bonds |
| E | 0019856 | biological_process | pyrimidine nucleobase biosynthetic process |
| E | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
| E | 0046872 | molecular_function | metal ion binding |
| F | 0000166 | molecular_function | nucleotide binding |
| F | 0004088 | molecular_function | carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity |
| F | 0004359 | molecular_function | glutaminase activity |
| F | 0005515 | molecular_function | protein binding |
| F | 0005524 | molecular_function | ATP binding |
| F | 0005737 | cellular_component | cytoplasm |
| F | 0005829 | cellular_component | cytosol |
| F | 0005951 | cellular_component | carbamoyl-phosphate synthase complex |
| F | 0006207 | biological_process | 'de novo' pyrimidine nucleobase biosynthetic process |
| F | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
| F | 0006526 | biological_process | L-arginine biosynthetic process |
| F | 0006541 | biological_process | glutamine metabolic process |
| F | 0008652 | biological_process | amino acid biosynthetic process |
| F | 0016874 | molecular_function | ligase activity |
| F | 0019856 | biological_process | pyrimidine nucleobase biosynthetic process |
| F | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
| F | 0046982 | molecular_function | protein heterodimerization activity |
| G | 0000166 | molecular_function | nucleotide binding |
| G | 0004087 | molecular_function | carbamoyl-phosphate synthase (ammonia) activity |
| G | 0004088 | molecular_function | carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity |
| G | 0005515 | molecular_function | protein binding |
| G | 0005524 | molecular_function | ATP binding |
| G | 0005737 | cellular_component | cytoplasm |
| G | 0005829 | cellular_component | cytosol |
| G | 0005951 | cellular_component | carbamoyl-phosphate synthase complex |
| G | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
| G | 0006526 | biological_process | L-arginine biosynthetic process |
| G | 0006541 | biological_process | glutamine metabolic process |
| G | 0008652 | biological_process | amino acid biosynthetic process |
| G | 0016597 | molecular_function | amino acid binding |
| G | 0016874 | molecular_function | ligase activity |
| G | 0016879 | molecular_function | ligase activity, forming carbon-nitrogen bonds |
| G | 0019856 | biological_process | pyrimidine nucleobase biosynthetic process |
| G | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
| G | 0046872 | molecular_function | metal ion binding |
| H | 0000166 | molecular_function | nucleotide binding |
| H | 0004088 | molecular_function | carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity |
| H | 0004359 | molecular_function | glutaminase activity |
| H | 0005515 | molecular_function | protein binding |
| H | 0005524 | molecular_function | ATP binding |
| H | 0005737 | cellular_component | cytoplasm |
| H | 0005829 | cellular_component | cytosol |
| H | 0005951 | cellular_component | carbamoyl-phosphate synthase complex |
| H | 0006207 | biological_process | 'de novo' pyrimidine nucleobase biosynthetic process |
| H | 0006221 | biological_process | pyrimidine nucleotide biosynthetic process |
| H | 0006526 | biological_process | L-arginine biosynthetic process |
| H | 0006541 | biological_process | glutamine metabolic process |
| H | 0008652 | biological_process | amino acid biosynthetic process |
| H | 0016874 | molecular_function | ligase activity |
| H | 0019856 | biological_process | pyrimidine nucleobase biosynthetic process |
| H | 0044205 | biological_process | 'de novo' UMP biosynthetic process |
| H | 0046982 | molecular_function | protein heterodimerization activity |
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE MN A 4001 |
| Chain | Residue |
| A | GLU299 |
| A | ASN301 |
| A | ADP4000 |
| A | MN4002 |
| A | PO44006 |
| A | HOH4092 |
| site_id | AC2 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE MN A 4002 |
| Chain | Residue |
| A | MN4001 |
| A | PO44006 |
| A | K4020 |
| A | HOH4089 |
| A | GLN285 |
| A | GLU299 |
| A | ADP4000 |
| site_id | AC3 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K A 4003 |
| Chain | Residue |
| A | GLU215 |
| A | ASN236 |
| A | ASP238 |
| A | ALA239 |
| A | ILE242 |
| A | SER247 |
| site_id | AC4 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE K A 4004 |
| Chain | Residue |
| A | ALA126 |
| A | GLU127 |
| A | GLU299 |
| A | MET300 |
| A | ASN301 |
| A | HOH4092 |
| A | HOH4093 |
| site_id | AC5 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE MN A 4008 |
| Chain | Residue |
| A | GLN829 |
| A | GLU841 |
| A | ADP4007 |
| A | HOH4557 |
| site_id | AC6 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE K A 4009 |
| Chain | Residue |
| A | GLU841 |
| A | ASN843 |
| A | ADP4007 |
| site_id | AC7 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K A 4010 |
| Chain | Residue |
| A | GLU761 |
| A | HIS781 |
| A | GLU783 |
| A | GLN784 |
| A | VAL787 |
| A | SER792 |
| site_id | AC8 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE CL A 4015 |
| Chain | Residue |
| A | GLN93 |
| A | THR173 |
| A | MET174 |
| A | HOH4028 |
| A | HOH4031 |
| site_id | AC9 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE CL A 4016 |
| Chain | Residue |
| A | ASN289 |
| A | ASN292 |
| A | ARG294 |
| site_id | BC1 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE CL A 4017 |
| Chain | Residue |
| A | ASN371 |
| A | PHE900 |
| A | PRO901 |
| A | GLY902 |
| site_id | BC2 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE CL B 4018 |
| Chain | Residue |
| B | ASP114 |
| B | HOH4081 |
| site_id | BC3 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE K B 4019 |
| Chain | Residue |
| B | HIS16 |
| B | ASP112 |
| B | HOH4082 |
| B | HOH4083 |
| site_id | BC4 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE K A 4020 |
| Chain | Residue |
| A | GLU217 |
| A | THR244 |
| A | ASN283 |
| A | GLN285 |
| A | MN4002 |
| A | PO44006 |
| A | HOH4098 |
| site_id | BC5 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE K A 4021 |
| Chain | Residue |
| A | ASP84 |
| A | GLY112 |
| A | THR114 |
| A | HOH4111 |
| A | HOH4113 |
| site_id | BC6 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE K A 4022 |
| Chain | Residue |
| A | THR143 |
| A | ALA144 |
| A | HOH4203 |
| site_id | BC7 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE MN C 4024 |
| Chain | Residue |
| C | GLU299 |
| C | ASN301 |
| C | ADP4023 |
| C | K4027 |
| C | PO44028 |
| C | HOH4113 |
| site_id | BC8 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE MN C 4025 |
| Chain | Residue |
| C | GLN285 |
| C | GLU299 |
| C | ADP4023 |
| C | PO44028 |
| C | K4042 |
| C | HOH4110 |
| site_id | BC9 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K C 4026 |
| Chain | Residue |
| C | GLU215 |
| C | ASN236 |
| C | ASP238 |
| C | ALA239 |
| C | ILE242 |
| C | SER247 |
| site_id | CC1 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE K C 4027 |
| Chain | Residue |
| C | ALA126 |
| C | GLU127 |
| C | GLU299 |
| C | MET300 |
| C | ASN301 |
| C | MN4024 |
| C | HOH4114 |
| C | HOH4709 |
| site_id | CC2 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE K E 4066 |
| Chain | Residue |
| E | ALA144 |
| E | HOH4263 |
| E | THR143 |
| site_id | CC3 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE MN C 4030 |
| Chain | Residue |
| C | GLN829 |
| C | GLU841 |
| C | ADP4029 |
| C | HOH4570 |
| C | HOH4571 |
| site_id | CC4 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE MN G 4069 |
| Chain | Residue |
| G | GLU299 |
| G | ASN301 |
| G | HOH2947 |
| G | ADP4068 |
| G | MN4070 |
| G | PO44073 |
| site_id | CC5 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE K C 4031 |
| Chain | Residue |
| C | GLU841 |
| C | ASN843 |
| C | ADP4029 |
| C | HOH4123 |
| site_id | CC6 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE MN G 4070 |
| Chain | Residue |
| G | GLN285 |
| G | GLU299 |
| G | HOH2944 |
| G | ADP4068 |
| G | MN4069 |
| G | PO44073 |
| site_id | CC7 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K C 4032 |
| Chain | Residue |
| C | GLU761 |
| C | HIS781 |
| C | GLU783 |
| C | GLN784 |
| C | VAL787 |
| C | SER792 |
| site_id | CC8 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K G 4071 |
| Chain | Residue |
| G | GLU215 |
| G | ASN236 |
| G | ASP238 |
| G | ALA239 |
| G | ILE242 |
| G | SER247 |
| site_id | CC9 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE CL C 4037 |
| Chain | Residue |
| C | THR173 |
| C | MET174 |
| C | HOH4050 |
| site_id | DC1 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE K G 4072 |
| Chain | Residue |
| G | ALA126 |
| G | GLU127 |
| G | GLU299 |
| G | MET300 |
| G | ASN301 |
| G | HOH2947 |
| G | HOH2948 |
| site_id | DC2 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE CL C 4038 |
| Chain | Residue |
| C | ASN289 |
| C | ASN292 |
| C | ARG294 |
| site_id | DC3 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE MN G 4075 |
| Chain | Residue |
| G | GLN829 |
| G | GLU841 |
| G | ADP4074 |
| site_id | DC4 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE CL C 4039 |
| Chain | Residue |
| C | ASN371 |
| C | PHE900 |
| C | PRO901 |
| C | GLY902 |
| site_id | DC5 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE K G 4076 |
| Chain | Residue |
| G | GLU841 |
| G | ASN843 |
| G | ADP4074 |
| site_id | DC6 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE CL D 4040 |
| Chain | Residue |
| C | GLU549 |
| D | ASP114 |
| D | HOH1501 |
| site_id | DC7 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K G 4077 |
| Chain | Residue |
| G | GLU761 |
| G | HIS781 |
| G | GLU783 |
| G | GLN784 |
| G | VAL787 |
| G | SER792 |
| site_id | DC8 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE K D 4041 |
| Chain | Residue |
| C | ARG490 |
| C | HOH4558 |
| D | HIS16 |
| D | ASP112 |
| D | HOH1505 |
| site_id | DC9 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE CL G 4082 |
| Chain | Residue |
| G | GLN93 |
| G | THR173 |
| G | MET174 |
| G | HOH2879 |
| site_id | EC1 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE K C 4042 |
| Chain | Residue |
| C | GLU217 |
| C | THR244 |
| C | ASN283 |
| C | GLN285 |
| C | MN4025 |
| C | PO44028 |
| C | HOH4119 |
| site_id | EC2 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE CL G 4083 |
| Chain | Residue |
| G | ASN289 |
| G | ASN292 |
| G | ARG294 |
| site_id | EC3 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE K C 4043 |
| Chain | Residue |
| C | ASP84 |
| C | GLY112 |
| C | THR114 |
| C | HOH4134 |
| site_id | EC4 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE CL G 4084 |
| Chain | Residue |
| G | ASN371 |
| G | PRO901 |
| G | GLY902 |
| site_id | EC5 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE K C 4044 |
| Chain | Residue |
| C | THR143 |
| C | ALA144 |
| C | HOH4221 |
| C | HOH4226 |
| site_id | EC6 |
| Number of Residues | 2 |
| Details | BINDING SITE FOR RESIDUE CL H 4085 |
| Chain | Residue |
| H | PHE15 |
| H | ASP114 |
| site_id | EC7 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE MN E 4046 |
| Chain | Residue |
| E | GLU299 |
| E | ASN301 |
| E | ADP4045 |
| E | MN4047 |
| E | PO44050 |
| E | HOH4144 |
| site_id | EC8 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE K H 4086 |
| Chain | Residue |
| H | HIS16 |
| H | ASP112 |
| H | HOH3432 |
| H | HOH3435 |
| site_id | EC9 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE MN E 4047 |
| Chain | Residue |
| E | GLN285 |
| E | GLU299 |
| E | ADP4045 |
| E | MN4046 |
| E | PO44050 |
| E | K4064 |
| E | HOH4141 |
| site_id | FC1 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K G 4087 |
| Chain | Residue |
| G | GLU217 |
| G | THR244 |
| G | ASN283 |
| G | GLN285 |
| G | HOH2953 |
| G | PO44073 |
| site_id | FC2 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K E 4048 |
| Chain | Residue |
| E | GLU215 |
| E | ASN236 |
| E | ASP238 |
| E | ALA239 |
| E | ILE242 |
| E | SER247 |
| site_id | FC3 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE K G 4088 |
| Chain | Residue |
| G | ASP84 |
| G | GLY112 |
| G | THR114 |
| G | HOH2968 |
| G | HOH2970 |
| site_id | FC4 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K E 4049 |
| Chain | Residue |
| E | ALA126 |
| E | GLU127 |
| E | GLU299 |
| E | MET300 |
| E | ASN301 |
| E | HOH4145 |
| site_id | FC5 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE K G 4089 |
| Chain | Residue |
| G | THR143 |
| G | ALA144 |
| G | HOH3052 |
| G | HOH3058 |
| site_id | FC6 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE MN E 4052 |
| Chain | Residue |
| E | GLN829 |
| E | GLU841 |
| E | ADP4051 |
| E | HOH4614 |
| E | HOH4615 |
| site_id | FC7 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE K E 4053 |
| Chain | Residue |
| E | GLU841 |
| E | ASN843 |
| E | ADP4051 |
| E | HOH4154 |
| site_id | FC8 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE K E 4054 |
| Chain | Residue |
| E | GLU761 |
| E | HIS781 |
| E | GLU783 |
| E | GLN784 |
| E | VAL787 |
| E | SER792 |
| site_id | FC9 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE CL E 4059 |
| Chain | Residue |
| E | GLN93 |
| E | THR173 |
| E | MET174 |
| E | HOH4080 |
| E | HOH4083 |
| site_id | GC1 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE CL E 4060 |
| Chain | Residue |
| E | ASN289 |
| E | ASN292 |
| E | ARG294 |
| site_id | GC2 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE CL E 4061 |
| Chain | Residue |
| E | ASN371 |
| E | PHE900 |
| E | PRO901 |
| E | GLY902 |
| site_id | GC3 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE CL F 4062 |
| Chain | Residue |
| E | GLU549 |
| E | HOH4605 |
| F | PHE15 |
| F | ASP114 |
| F | HOH2477 |
| site_id | GC4 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE K F 4063 |
| Chain | Residue |
| E | HOH4605 |
| F | HIS16 |
| F | ASP112 |
| F | HOH2481 |
| F | HOH2482 |
| site_id | GC5 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE K E 4064 |
| Chain | Residue |
| E | GLU217 |
| E | THR244 |
| E | ASN283 |
| E | GLN285 |
| E | MN4047 |
| E | PO44050 |
| E | HOH4150 |
| site_id | GC6 |
| Number of Residues | 5 |
| Details | BINDING SITE FOR RESIDUE K E 4065 |
| Chain | Residue |
| E | ASP84 |
| E | GLY112 |
| E | THR114 |
| E | HOH4166 |
| E | HOH4169 |
| site_id | GC7 |
| Number of Residues | 13 |
| Details | BINDING SITE FOR RESIDUE PO4 E 4050 |
| Chain | Residue |
| E | MET174 |
| E | GLY175 |
| E | HIS243 |
| E | GLN285 |
| E | GLU299 |
| E | ASN301 |
| E | ARG303 |
| E | ARG306 |
| E | ADP4045 |
| E | MN4046 |
| E | MN4047 |
| E | K4064 |
| E | HOH4150 |
| site_id | GC8 |
| Number of Residues | 1 |
| Details | BINDING SITE FOR RESIDUE PO4 E 4067 |
| Chain | Residue |
| E | GLU560 |
| site_id | GC9 |
| Number of Residues | 14 |
| Details | BINDING SITE FOR RESIDUE PO4 G 4073 |
| Chain | Residue |
| G | MET174 |
| G | GLY175 |
| G | HIS243 |
| G | GLN285 |
| G | GLU299 |
| G | ASN301 |
| G | ARG303 |
| G | ARG306 |
| G | HOH2944 |
| G | HOH2953 |
| G | ADP4068 |
| G | MN4069 |
| G | MN4070 |
| G | K4087 |
| site_id | HC1 |
| Number of Residues | 14 |
| Details | BINDING SITE FOR RESIDUE PO4 A 4006 |
| Chain | Residue |
| A | MET174 |
| A | GLY175 |
| A | HIS243 |
| A | GLN285 |
| A | GLU299 |
| A | ASN301 |
| A | ARG303 |
| A | ARG306 |
| A | ADP4000 |
| A | MN4001 |
| A | MN4002 |
| A | K4020 |
| A | HOH4089 |
| A | HOH4098 |
| site_id | HC2 |
| Number of Residues | 15 |
| Details | BINDING SITE FOR RESIDUE PO4 C 4028 |
| Chain | Residue |
| C | MET174 |
| C | GLY175 |
| C | HIS243 |
| C | GLN285 |
| C | GLU299 |
| C | ASN301 |
| C | ARG303 |
| C | ARG306 |
| C | ADP4023 |
| C | MN4024 |
| C | MN4025 |
| C | K4042 |
| C | HOH4110 |
| C | HOH4119 |
| C | HOH4120 |
| site_id | HC3 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE ORN C 4033 |
| Chain | Residue |
| C | GLU783 |
| C | ASP791 |
| C | GLU892 |
| C | LEU907 |
| C | TYR1040 |
| C | ASP1041 |
| C | THR1042 |
| C | HOH4075 |
| C | HOH4077 |
| C | HOH4105 |
| site_id | HC4 |
| Number of Residues | 13 |
| Details | BINDING SITE FOR RESIDUE GLN D 4034 |
| Chain | Residue |
| D | SER47 |
| D | ASN240 |
| D | GLY241 |
| D | GLY243 |
| D | SER269 |
| D | LEU270 |
| D | GLN273 |
| D | ASN311 |
| D | HIS312 |
| D | GLY313 |
| D | PHE314 |
| D | HIS353 |
| D | HOH995 |
| site_id | HC5 |
| Number of Residues | 11 |
| Details | BINDING SITE FOR RESIDUE GLN C 4035 |
| Chain | Residue |
| C | ARG528 |
| C | ALA537 |
| C | THR538 |
| C | GLU552 |
| C | ASN554 |
| C | HOH4450 |
| C | HOH4451 |
| C | HOH4456 |
| C | HOH4566 |
| D | ARG120 |
| D | ARG123 |
| site_id | HC6 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE NET C 4036 |
| Chain | Residue |
| C | GLN22 |
| C | THR94 |
| C | ASN97 |
| C | ASN936 |
| site_id | HC7 |
| Number of Residues | 27 |
| Details | BINDING SITE FOR RESIDUE ADP E 4045 |
| Chain | Residue |
| E | ARG129 |
| E | ILE167 |
| E | ARG169 |
| E | THR173 |
| E | MET174 |
| E | GLY175 |
| E | GLY176 |
| E | GLU208 |
| E | LEU210 |
| E | ILE211 |
| E | GLU215 |
| E | MET240 |
| E | GLY241 |
| E | ILE242 |
| E | HIS243 |
| E | THR244 |
| E | GLN285 |
| E | ILE298 |
| E | GLU299 |
| E | THR376 |
| E | MN4046 |
| E | MN4047 |
| E | PO44050 |
| E | HOH4137 |
| E | HOH4141 |
| E | HOH4144 |
| E | HOH4613 |
| site_id | HC8 |
| Number of Residues | 20 |
| Details | BINDING SITE FOR RESIDUE ADP E 4051 |
| Chain | Residue |
| E | PRO690 |
| E | ARG715 |
| E | MET725 |
| E | HIS754 |
| E | PHE755 |
| E | LEU756 |
| E | GLU761 |
| E | ALA785 |
| E | GLY786 |
| E | VAL787 |
| E | HIS788 |
| E | SER789 |
| E | GLN829 |
| E | GLU841 |
| E | MN4052 |
| E | K4053 |
| E | HOH4153 |
| E | HOH4154 |
| E | HOH4156 |
| E | HOH4614 |
| site_id | HC9 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE ORN E 4055 |
| Chain | Residue |
| E | GLU783 |
| E | ASP791 |
| E | GLU892 |
| E | LEU907 |
| E | TYR1040 |
| E | ASP1041 |
| E | THR1042 |
| E | HOH4105 |
| E | HOH4136 |
| E | HOH4616 |
| site_id | IC1 |
| Number of Residues | 13 |
| Details | BINDING SITE FOR RESIDUE GLN F 4056 |
| Chain | Residue |
| F | SER47 |
| F | ASN240 |
| F | GLY241 |
| F | PRO242 |
| F | GLY243 |
| F | SER269 |
| F | LEU270 |
| F | GLN273 |
| F | ASN311 |
| F | HIS312 |
| F | GLY313 |
| F | PHE314 |
| F | HOH1956 |
| site_id | IC2 |
| Number of Residues | 11 |
| Details | BINDING SITE FOR RESIDUE GLN E 4057 |
| Chain | Residue |
| E | ARG528 |
| E | ALA537 |
| E | THR538 |
| E | GLU552 |
| E | ASN554 |
| E | HOH4492 |
| E | HOH4493 |
| E | HOH4720 |
| E | HOH4721 |
| F | ARG120 |
| F | ARG123 |
| site_id | IC3 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE NET E 4058 |
| Chain | Residue |
| E | GLN22 |
| E | THR94 |
| E | ASN936 |
| site_id | IC4 |
| Number of Residues | 24 |
| Details | BINDING SITE FOR RESIDUE ADP G 4068 |
| Chain | Residue |
| G | ARG129 |
| G | ILE167 |
| G | ARG169 |
| G | THR173 |
| G | MET174 |
| G | GLY175 |
| G | GLY176 |
| G | GLU208 |
| G | LEU210 |
| G | ILE211 |
| G | GLU215 |
| G | MET240 |
| G | GLY241 |
| G | ILE242 |
| G | HIS243 |
| G | THR244 |
| G | GLN285 |
| G | GLU299 |
| G | HOH2940 |
| G | HOH2944 |
| G | HOH3549 |
| G | MN4069 |
| G | MN4070 |
| G | PO44073 |
| site_id | IC5 |
| Number of Residues | 15 |
| Details | BINDING SITE FOR RESIDUE ADP G 4074 |
| Chain | Residue |
| G | ARG715 |
| G | MET725 |
| G | HIS754 |
| G | PHE755 |
| G | LEU756 |
| G | GLU761 |
| G | ALA785 |
| G | GLY786 |
| G | VAL787 |
| G | HIS788 |
| G | SER789 |
| G | GLN829 |
| G | GLU841 |
| G | MN4075 |
| G | K4076 |
| site_id | IC6 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE ORN G 4078 |
| Chain | Residue |
| G | GLU783 |
| G | ASP791 |
| G | GLU892 |
| G | VAL893 |
| G | LEU907 |
| G | TYR1040 |
| G | ASP1041 |
| G | THR1042 |
| G | HOH2901 |
| G | HOH2932 |
| site_id | IC7 |
| Number of Residues | 26 |
| Details | BINDING SITE FOR RESIDUE ADP A 4000 |
| Chain | Residue |
| A | ARG129 |
| A | ILE167 |
| A | ARG169 |
| A | MET174 |
| A | GLY175 |
| A | GLY176 |
| A | GLU208 |
| A | LEU210 |
| A | ILE211 |
| A | GLU215 |
| A | MET240 |
| A | GLY241 |
| A | ILE242 |
| A | HIS243 |
| A | THR244 |
| A | GLN285 |
| A | ILE298 |
| A | GLU299 |
| A | THR376 |
| A | MN4001 |
| A | MN4002 |
| A | PO44006 |
| A | HOH4085 |
| A | HOH4089 |
| A | HOH4092 |
| A | HOH4556 |
| site_id | IC8 |
| Number of Residues | 15 |
| Details | BINDING SITE FOR RESIDUE GLN H 4079 |
| Chain | Residue |
| H | SER47 |
| H | ASN240 |
| H | GLY241 |
| H | PRO242 |
| H | GLY243 |
| H | SER269 |
| H | LEU270 |
| H | GLN273 |
| H | ASN311 |
| H | HIS312 |
| H | GLY313 |
| H | PHE314 |
| H | HIS353 |
| H | HOH2934 |
| H | HOH2938 |
| site_id | IC9 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE GLN G 4080 |
| Chain | Residue |
| G | ARG528 |
| G | ALA537 |
| G | THR538 |
| G | GLU552 |
| G | ASN554 |
| G | HOH3308 |
| H | ARG120 |
| H | ARG123 |
| site_id | JC1 |
| Number of Residues | 18 |
| Details | BINDING SITE FOR RESIDUE ADP A 4007 |
| Chain | Residue |
| A | PRO690 |
| A | ARG715 |
| A | MET725 |
| A | HIS754 |
| A | PHE755 |
| A | LEU756 |
| A | GLU761 |
| A | ALA785 |
| A | GLY786 |
| A | VAL787 |
| A | HIS788 |
| A | SER789 |
| A | GLN829 |
| A | GLU841 |
| A | MN4008 |
| A | K4009 |
| A | HOH4103 |
| A | HOH4557 |
| site_id | JC2 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE NET G 4081 |
| Chain | Residue |
| G | VAL19 |
| G | THR94 |
| G | ASN97 |
| site_id | JC3 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE ORN A 4011 |
| Chain | Residue |
| A | GLU783 |
| A | ASP791 |
| A | GLU892 |
| A | LEU895 |
| A | LEU907 |
| A | TYR1040 |
| A | ASP1041 |
| A | THR1042 |
| A | HOH4053 |
| A | HOH4084 |
| site_id | JC4 |
| Number of Residues | 15 |
| Details | BINDING SITE FOR RESIDUE GLN B 4012 |
| Chain | Residue |
| B | SER47 |
| B | ASN240 |
| B | GLY241 |
| B | PRO242 |
| B | GLY243 |
| B | SER269 |
| B | LEU270 |
| B | GLN273 |
| B | ASN311 |
| B | HIS312 |
| B | GLY313 |
| B | PHE314 |
| B | HIS353 |
| B | HOH4021 |
| B | HOH4025 |
| site_id | JC5 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE GLN A 4013 |
| Chain | Residue |
| A | ARG528 |
| A | ALA537 |
| A | THR538 |
| A | GLU552 |
| A | ASN554 |
| A | HOH4436 |
| A | HOH4437 |
| A | HOH4561 |
| B | ARG120 |
| B | ARG123 |
| site_id | JC6 |
| Number of Residues | 3 |
| Details | BINDING SITE FOR RESIDUE NET A 4014 |
| Chain | Residue |
| A | GLN22 |
| A | THR94 |
| A | ASN936 |
| site_id | JC7 |
| Number of Residues | 27 |
| Details | BINDING SITE FOR RESIDUE ADP C 4023 |
| Chain | Residue |
| C | ARG129 |
| C | ILE167 |
| C | ARG169 |
| C | THR173 |
| C | MET174 |
| C | GLY175 |
| C | GLY176 |
| C | GLU208 |
| C | LEU210 |
| C | ILE211 |
| C | GLU215 |
| C | MET240 |
| C | GLY241 |
| C | ILE242 |
| C | HIS243 |
| C | THR244 |
| C | GLN285 |
| C | ILE298 |
| C | GLU299 |
| C | THR376 |
| C | MN4024 |
| C | MN4025 |
| C | PO44028 |
| C | HOH4106 |
| C | HOH4110 |
| C | HOH4113 |
| C | HOH4567 |
| site_id | JC8 |
| Number of Residues | 20 |
| Details | BINDING SITE FOR RESIDUE ADP C 4029 |
| Chain | Residue |
| C | PRO690 |
| C | ARG715 |
| C | MET725 |
| C | HIS754 |
| C | PHE755 |
| C | LEU756 |
| C | GLU761 |
| C | ALA785 |
| C | GLY786 |
| C | VAL787 |
| C | HIS788 |
| C | SER789 |
| C | GLN829 |
| C | GLU841 |
| C | MN4030 |
| C | K4031 |
| C | HOH4122 |
| C | HOH4123 |
| C | HOH4570 |
| C | HOH4571 |
Functional Information from PROSITE/UniProt
| site_id | PS00866 |
| Number of Residues | 15 |
| Details | CPSASE_1 Carbamoyl-phosphate synthase subdomain signature 1. FPCIIRPSftmGGsG |
| Chain | Residue | Details |
| A | PHE164-GLY178 | |
| A | TYR710-ALA724 |
| site_id | PS00867 |
| Number of Residues | 8 |
| Details | CPSASE_2 Carbamoyl-phosphate synthase subdomain signature 2. VIEMNPRV |
| Chain | Residue | Details |
| A | VAL297-VAL304 | |
| A | LEU839-ALA846 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 780 |
| Details | Domain: {"description":"ATP-grasp 1","evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 544 |
| Details | Domain: {"description":"MGS-like","evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI3 |
| Number of Residues | 1604 |
| Details | Region: {"description":"Carboxyphosphate synthetic domain","evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI4 |
| Number of Residues | 596 |
| Details | Region: {"description":"Oligomerization domain","evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI5 |
| Number of Residues | 544 |
| Details | Region: {"description":"Allosteric domain","evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI6 |
| Number of Residues | 72 |
| Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"10029528","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1A9X","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1C30","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1C3O","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1CE8","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1CS0","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1JDB","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1KEE","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1M6V","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"1T36","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI7 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"10428826","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1CE8","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI8 |
| Number of Residues | 8 |
| Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"10029528","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"10089390","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"10428826","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"10587438","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9636022","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1CE8","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI9 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"10428826","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9636022","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1CE8","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI10 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"10029528","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"10089390","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"10428826","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9636022","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1CE8","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI11 |
| Number of Residues | 4 |
| Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01210","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"10029528","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"10089390","evidenceCode":"ECO:0000269"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI12 |
| Number of Residues | 748 |
| Details | Domain: {"description":"Glutamine amidotransferase type-1","evidences":[{"source":"HAMAP-Rule","id":"MF_01209","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI13 |
| Number of Residues | 4 |
| Details | Active site: {"description":"Nucleophile","evidences":[{"source":"HAMAP-Rule","id":"MF_01209","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI14 |
| Number of Residues | 8 |
| Details | Active site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01209","evidenceCode":"ECO:0000255"}]} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI15 |
| Number of Residues | 32 |
| Details | Binding site: {"evidences":[{"source":"HAMAP-Rule","id":"MF_01209","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"10587438","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"1C3O","evidenceCode":"ECO:0007744"}]} |
| Chain | Residue | Details |
Catalytic Information from CSA
| site_id | CSA1 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1bxr |
| Chain | Residue | Details |
| B | HIS353 | |
| B | SER269 |
| site_id | CSA2 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1bxr |
| Chain | Residue | Details |
| D | HIS353 | |
| D | SER269 |
| site_id | CSA3 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1bxr |
| Chain | Residue | Details |
| F | HIS353 | |
| F | SER269 |
| site_id | CSA4 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1bxr |
| Chain | Residue | Details |
| H | HIS353 | |
| H | SER269 |
| site_id | MCSA1 |
| Number of Residues | 3 |
| Details | M-CSA 435 |
| Chain | Residue | Details |
| B | SER269 | covalent catalysis, proton shuttle (general acid/base) |
| A | ARG303 | electrostatic stabiliser |
| A | ARG715 | electrostatic stabiliser |
| A | GLU761 | steric role |
| A | GLN829 | metal ligand |
| A | GLU841 | metal ligand |
| A | ASN843 | metal ligand |
| A | ARG848 | electrostatic stabiliser |
| B | HIS353 | proton shuttle (general acid/base) |
| B | GLU355 | steric role |
| A | GLU215 | steric role |
| A | HIS243 | proton shuttle (general acid/base) |
| A | ASN283 | electrostatic stabiliser |
| A | GLN285 | metal ligand |
| A | GLU299 | metal ligand |
| A | ASN301 | metal ligand |
| site_id | MCSA2 |
| Number of Residues | 3 |
| Details | M-CSA 435 |
| Chain | Residue | Details |
| D | SER269 | covalent catalysis, proton shuttle (general acid/base) |
| C | ARG303 | electrostatic stabiliser |
| C | ARG715 | electrostatic stabiliser |
| C | GLU761 | steric role |
| C | GLN829 | metal ligand |
| C | GLU841 | metal ligand |
| C | ASN843 | metal ligand |
| C | ARG848 | electrostatic stabiliser |
| D | HIS353 | proton shuttle (general acid/base) |
| D | GLU355 | steric role |
| C | GLU215 | steric role |
| C | HIS243 | proton shuttle (general acid/base) |
| C | ASN283 | electrostatic stabiliser |
| C | GLN285 | metal ligand |
| C | GLU299 | metal ligand |
| C | ASN301 | metal ligand |
| site_id | MCSA3 |
| Number of Residues | 3 |
| Details | M-CSA 435 |
| Chain | Residue | Details |
| F | SER269 | covalent catalysis, proton shuttle (general acid/base) |
| E | ARG303 | electrostatic stabiliser |
| E | ARG715 | electrostatic stabiliser |
| E | GLU761 | steric role |
| E | GLN829 | metal ligand |
| E | GLU841 | metal ligand |
| E | ASN843 | metal ligand |
| E | ARG848 | electrostatic stabiliser |
| F | HIS353 | proton shuttle (general acid/base) |
| F | GLU355 | steric role |
| E | GLU215 | steric role |
| E | HIS243 | proton shuttle (general acid/base) |
| E | ASN283 | electrostatic stabiliser |
| E | GLN285 | metal ligand |
| E | GLU299 | metal ligand |
| E | ASN301 | metal ligand |
| site_id | MCSA4 |
| Number of Residues | 3 |
| Details | M-CSA 435 |
| Chain | Residue | Details |
| H | SER269 | covalent catalysis, proton shuttle (general acid/base) |
| G | ARG303 | electrostatic stabiliser |
| G | ARG715 | electrostatic stabiliser |
| G | GLU761 | steric role |
| G | GLN829 | metal ligand |
| G | GLU841 | metal ligand |
| G | ASN843 | metal ligand |
| G | ARG848 | electrostatic stabiliser |
| H | HIS353 | proton shuttle (general acid/base) |
| H | GLU355 | steric role |
| G | GLU215 | steric role |
| G | HIS243 | proton shuttle (general acid/base) |
| G | ASN283 | electrostatic stabiliser |
| G | GLN285 | metal ligand |
| G | GLU299 | metal ligand |
| G | ASN301 | metal ligand |






