3.4.21.102	additional information	deletion of N-terminal amino acids 206-660, and deletion of C-terminal amino acids 1-334, both peptides are efficiently labelled by a competitive inhibitor of the enzyme marked with photoaffinity lable	137238	
3.4.21.102	V229E	increased Km for 2N-[[(1-sulfono-5-naphthyl)amino]ethyl]aminosuccinyl-Ala-Ala-Arg-Ala-Ala-[Nepsilon-[4-[4-(dimethylamino)phenylazo]benzoyl]lysyl]-(6-aminocaproyl)2-Glu-Asn-Tyr-Ala-Leu-Ala-Ala	137238	
3.4.21.102	V229Q	increased Km for 2N-[[(1-sulfono-5-naphthyl)amino]ethyl]aminosuccinyl-Ala-Ala-Arg-Ala-Ala-[Nepsilon-[4-[4-(dimethylamino)phenylazo]benzoyl]lysyl]-(6-aminocaproyl)2-Glu-Asn-Tyr-Ala-Leu-Ala-Ala	137238	
3.4.21.102	L132M/L210M	crystallization data of selenomethionyl derivative	137239	
3.4.21.102	D369A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	D441A	no hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	D441N	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	D505A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	E433A	no hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	E449A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	G375A	no hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	G376A	no hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	H19A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	H203A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	H34A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	H553A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	H60A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	K455A	no hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	K455R	no hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	R371A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	R444A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	S372A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	S428A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	S430A	no hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	S430C	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	S432A	hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	T452A	no hydrolysis of the 105 variant of N-terminal domain of lambda repressor	137242	
3.4.21.102	D149A	very little protein detectable, processing of D1 protein of photosystem II takes place	137246	
3.4.21.102	D253A	no processing of D1 protein of photosystem II	137246	
3.4.21.102	D376A	very little protein detectable, processing of D1 protein of photosystem II takes place	137246	
3.4.21.102	E316A	no processing of D1 protein of photosystem II	137246	
3.4.21.102	E316Q	no photoautotrophic growth of cells	137246	
3.4.21.102	K338A	no processing of D1 protein of photosystem II	137246	
3.4.21.102	K338H	no photoautotrophic growth of cells	137246	
3.4.21.102	K338R	no photoautotrophic growth of cells	137246	
3.4.21.102	additional information	deletion of enzyme gene, no processing of D1 protein of photosystem II, no photoautotrophic growth of cells	137246	
3.4.21.102	R198A	very little protein detectable, processing of D1 protein of photosystem II takes place	137246	
3.4.21.102	R255A	no processing of D1 protein of photosystem II	137246	
3.4.21.102	R255H	no photoautotrophic growth of cells	137246	
3.4.21.102	S313A	no processing of D1 protein of photosystem II	137246	
3.4.21.102	E97Q	no enzymic activity, but binding of transit peptide is not disturbed	652464	
3.4.21.102	H94L	no enzymic activity, but binding of transit peptide is not disturbed	652464	
3.4.21.102	additional information	the enzyme-deficient strain 1330DELTActpa is generated by allelic exchange, the mutant produces smaller colonies on enriched agar plates and exhibits a 50% decrease in growth rate in enriched liquid medium and no growth in salt-free enriched medium, the mutant cells show a spherical shape, increased cell diameter, and membranes partially dissociated from the cell envelope compared to the wild-type cells, smooth phenotype, overview, the virulence of the wild-type strain 1330 is reduced by the mutant strain 1330DELTAcptA in murine spleen, overview	669103	
3.4.21.102	additional information	downregulation of the enzyme by antisense technique in transgenic plants results in many lines with lethal seedlings	670503	
3.4.21.102	additional information	the [1-874] deletion mutant lacking the C-terminus is inactive	670503	
3.4.21.102	additional information	the Glu945 deletion mutant shows leaf chlorosis at the early seedling stage but inhibition of root growth during the whole growth period	718206	
3.4.21.102	V205M/G282C	mutations mimic Prochlorococcus marinus D1 protein in mutant background accumulating divinyl chlorophyll. Energy transfer in CP47 is interrupted in photosystem II containing divinyl chlorophylls. The V205M/G282C mutation does not recover the energy transfer pathway in CP47, instead, the mutation allows the excitation energy transfer from CP43 to CP47, which neighbors in the photosystem II dimer	731328