4F5I
Substrate Specificity Conversion of E. coli Pyridoxal-5'-Phosphate Dependent Aspartate Aminotransferase to Tyrosine Aminotransferase: Chimera P4.
Entity
Entity ID | Chain ID | Description | Type | Chain length | Formula weight | Number of molecules | DB Name (Accession) | Biological source | Descriptive keywords |
1 | A, B (A, B) | Aspartate aminotransferase | polymer | 406 | 44855.5 | 2 | UniProt (P00509) Pfam (PF00155) | Escherichia coli | AspAT, Transaminase A |
2 | C (B) | (4S)-2-METHYL-2,4-PENTANEDIOL | non-polymer | 118.2 | 1 | Chemie (MPD) | |||
3 | D, E (A, B) | water | water | 18.0 | 743 | Chemie (HOH) |
Sequence modifications
A, B: 12 - 406 (UniProt: P00509)
PDB | External Database | Details |
---|---|---|
Met 1 | - | expression tag |
Ala 2 | - | expression tag |
His 3 | - | expression tag |
His 4 | - | expression tag |
His 5 | - | expression tag |
His 6 | - | expression tag |
His 7 | - | expression tag |
His 8 | - | expression tag |
Val 9 | - | expression tag |
Gly 10 | - | expression tag |
Thr 11 | - | expression tag |
Val 39 | Ile 29 | engineered mutation |
Asp 40 | Asn 30 | engineered mutation |
Val 43 | Ile 33 | engineered mutation |
Met 56 | Leu 46 | engineered mutation |
Thr 74 | Asn 64 | engineered mutation |
Ser 114 | Thr 104 | engineered mutation |
Thr 139 | Ser 129 | engineered mutation |
Ala 145 | Ser 135 | engineered mutation |
Ile 146 | Val 136 | engineered mutation |
Ile 220 | Phe 210 | engineered mutation |
Ile 222 | Phe 212 | engineered mutation |
Gly 228 | Ala 218 | engineered mutation |
Cys 254 | Tyr 244 | engineered mutation |
Ser 259 | Gly 249 | engineered mutation |
Ser 295 | Asn 285 | engineered mutation |
Ile 385 | Val 375 | engineered mutation |
Sequence viewer
Contents of the asymmetric unit
Polymers | Number of chains | 2 |
Total formula weight | 89711.0 | |
Non-Polymers* | Number of molecules | 1 |
Total formula weight | 118.2 | |
All* | Total formula weight | 89829.2 |