| P50 | author | Patricia Babbitt | Q50486645 |
| P2093 | author name string | J A Gerlt | |
| P2860 | cites work | AtzC is a new member of the amidohydrolase protein superfamily and is homologous to other atrazine-metabolizing enzymes. | Q24520516 |
| | On the Evolution of Biochemical Syntheses | Q24522220 |
| | Crystal structure of human glyoxalase I_evidence for gene duplication and 3D domain swapping | Q24532246 |
| | Crystal structure of the biphenyl-cleaving extradiol dioxygenase from a PCB-degrading pseudomonad | Q27729302 |
| | Octahedral coordination at the high-affinity metal site in enolase: crystallographic analysis of the MgII--enzyme complex from yeast at 1.9 A resolution | Q27729931 |
| | The crystal structure of urease from Klebsiella aerogenes | Q27730237 |
| | Three-dimensional structure of the binuclear metal center of phosphotriesterase | Q27730289 |
| | A pre-transition-state mimic of an enzyme: X-ray structure of adenosine deaminase with bound 1-deazaadenosine and zinc-activated water | Q27732093 |
| | Three-dimensional structures of free form and two substrate complexes of an extradiol ring-cleavage type dioxygenase, the BphC enzyme from Pseudomonas sp. strain KKS102 | Q27732711 |
| | Structure of 4-chlorobenzoyl coenzyme A dehalogenase determined to 1.8 A resolution: an enzyme catalyst generated via adaptive mutation | Q27733127 |
| | The crystal structure of enoyl-CoA hydratase complexed with octanoyl-CoA reveals the structural adaptations required for binding of a long chain fatty acid-CoA molecule | Q27748869 |
| | Biochemical characterization and crystallographic structure of an Escherichia coli protein from the phosphotriesterase gene family | Q27749094 |
| | Evolution of enzymatic activities in the enolase superfamily: crystal structure of (D)-glucarate dehydratase from Pseudomonas putida | Q27765687 |
| | Evolution in action | Q28255503 |
| | Metal-catalyzed oxidation and mutagenesis studies on the iron(II) binding site of 1-aminocyclopropane-1-carboxylate oxidase | Q28256458 |
| | One thousand families for the molecular biologist | Q28266140 |
| | Identification of non-heme diiron proteins that catalyze triple bond and epoxy group formation | Q28269789 |
| | Enoyl-coenzyme A hydratase-catalyzed exchange of the alpha-protons of coenzyme A thiol esters: a model for an enolized intermediate in the enzyme-catalyzed elimination? | Q28565389 |
| | Computer analysis of bacterial haloacid dehalogenases defines a large superfamily of hydrolases with diverse specificity. Application of an iterative approach to database search | Q34326151 |
| | Beta1,4-N-acetylgalactosaminyltransferase (GM2 synthase) is released from Golgi membranes as a neuraminidase-sensitive, disulfide-bonded dimer by a cathepsin D-like protease | Q34398985 |
| | An evolutionary treasure: unification of a broad set of amidohydrolases related to urease | Q34425600 |
| | The B12-dependent ribonucleotide reductase from the archaebacterium Thermoplasma acidophila: an evolutionary solution to the ribonucleotide reductase conundrum | Q35899091 |
| | Fosfomycin resistance protein (FosA) is a manganese metalloglutathione transferase related to glyoxalase I and the extradiol dioxygenases | Q36855782 |
| | Evolutionary divergence of substrate specificity within the chymotrypsin-like serine protease fold | Q41646804 |
| | Understanding enzyme superfamilies. Chemistry As the fundamental determinant in the evolution of new catalytic activities | Q41655286 |
| | Molecular characterization of the cai operon necessary for carnitine metabolism in Escherichia coli | Q42487693 |
| | A functionally diverse enzyme superfamily that abstracts the alpha protons of carboxylic acids | Q42689776 |
| | The enolase superfamily: a general strategy for enzyme-catalyzed abstraction of the alpha-protons of carboxylic acids | Q44192562 |
| | How big is the universe of exons? | Q44307823 |
| | Insights into the mechanism of catalysis by the P-C bond-cleaving enzyme phosphonoacetaldehyde hydrolase derived from gene sequence analysis and mutagenesis | Q47901043 |
| | Metabolism of ferulic acid to vanillin. A bacterial gene of the enoyl-SCoA hydratase/isomerase superfamily encodes an enzyme for the hydration and cleavage of a hydroxycinnamic acid SCoA thioester | Q48039366 |
| | Enoyl-CoA Hydratase and Isomerase form a Superfamily with a Common Active-Site Glutamate Residue | Q56442036 |
| | Mandelate racemase and muconate lactonizing enzyme are mechanistically distinct and structurally homologous | Q59012432 |
| | Isomerization of (R)- and (S)- glutathiolactaldehydes by glyoxalase I: the case for dichotomous stereochemical behavior in a single active site | Q68201276 |
| | Identification of active site residues essential to 4-chlorobenzoyl-coenzyme A dehalogenase catalysis by chemical modification and site directed mutagenesis | Q71287905 |
| | Epimerization via carbon-carbon bond cleavage. L-ribulose-5-phosphate 4-epimerase as a masked class II aldolase | Q74457532 |
| | Evolution of enzymatic activities in the enolase superfamily: partitioning of reactive intermediates by (D)-glucarate dehydratase from Pseudomonas putida | Q77409750 |
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 607-612 | |
| P577 | publication date | 1998-10-01 | |
| P1433 | published in | Current Opinion in Chemical Biology | Q15758415 |
| P1476 | title | Mechanistically diverse enzyme superfamilies: the importance of chemistry in the evolution of catalysis | |
| P478 | volume | 2 | |