2.3.1.12	additional information	-	high molecular mass species in the absence of guanidinium hydrochloride	486225	
2.3.1.12	additional information	-	molecular weight of E2 complexed with E1 or E3	486201	
2.3.1.12	additional information	-	molecular weight of fragments after treatment with trypsin	486175	
2.3.1.12	additional information	-	molecular weight of lipolyl domains	486166, 486167, 486186	
2.3.1.12	additional information	-	molecular weight of proteolytic fragments	486173, 486176, 486184, 486194, 486195, 486196, 486197, 486198, 486224, 486232, 486236	
2.3.1.12	8982	-	x * 45953, recombinant 1-lip E2, mass spectrometry, x * 8982, recombinant unacetylated hybrid lipoyl domain, mass spectrometry, x * 9019, recombinant fully acetylated hybrid lipoyl domain, mass spectrometry	663289	
2.3.1.12	9019	-	x * 45953, recombinant 1-lip E2, mass spectrometry, x * 8982, recombinant unacetylated hybrid lipoyl domain, mass spectrometry, x * 9019, recombinant fully acetylated hybrid lipoyl domain, mass spectrometry	663289	
2.3.1.12	27500	-	24 * 27500, SDS-PAGE, light scattering experiments, quarternary structure	486172	
2.3.1.12	30000	-	gel filtration in the presence of guanidinium hydrochloride	486225	
2.3.1.12	30028	-	x * 30028, catalytic domain, calculated from amino acid sequence	736448	
2.3.1.12	30030	-	x * 30030, catalytic domain, FT mass spectrometry	736448	
2.3.1.12	33100	-	x * 33100, about, E2, sequence calculation	661817	
2.3.1.12	36000	-	2 * 36000, in the presence of dilute acetic acid	486210	
2.3.1.12	36000	-	24 * 36000, linked by noncovalent bonds	486209	
2.3.1.12	40000	-	24 * 40000, linked by noncovalent bonds	486207	
2.3.1.12	42000	-	60 * 42000, SDS-PAGE	486240	
2.3.1.12	45953	-	x * 45953, recombinant 1-lip E2, mass spectrometry, x * 8982, recombinant unacetylated hybrid lipoyl domain, mass spectrometry, x * 9019, recombinant fully acetylated hybrid lipoyl domain, mass spectrometry	663289	
2.3.1.12	46265	-	x * 46265, calculation from nucleotide sequence	393963	
2.3.1.12	46930	-	calculation from nucleotide sequence	486238	
2.3.1.12	48000	-	24 * 48000	348910	
2.3.1.12	48546	-	x * 48546, calculation from nucleotide sequence	486169	
2.3.1.12	50080	-	calculation from nucleotide sequence	486233	
2.3.1.12	51000	-	gel filtration	486197	
2.3.1.12	52000	-	60 * 52000	348910, 348938, 94881	
2.3.1.12	52000	53000	SDS-PAGE	486238	
2.3.1.12	57000	-	SDS-PAGE	348965	
2.3.1.12	58000	59000	SDS-PAGE	348964	
2.3.1.12	58890	-	calculation from nucleotide sequence	486239	
2.3.1.12	59000	-	SDS-PAGE	486239	
2.3.1.12	59000	-	x * 59000, SDS-PAGE, recombinant protein	720722	
2.3.1.12	60000	-	24 * 60000, SDS-PAGE	486168	
2.3.1.12	60000	-	calculation from nucleotide sequence	486227	
2.3.1.12	60000	-	mature protein, SDS-PAGE	486233	
2.3.1.12	60000	-	x * 60000, SDS-PAGE	486168	
2.3.1.12	60100	64500	sedimentation equilibrium, depending on buffer	486198	
2.3.1.12	63000	-	sedimentation equilibrium	486173	
2.3.1.12	64260	-	calculation from nucleotide sequence	393963	
2.3.1.12	64910	-	calculation from nucleotide sequence	486171	
2.3.1.12	65959	-	24 * 65959, calculation from nucleotide sequence	348982	
2.3.1.12	65959	-	x * 65959, calculated from amino acid sequence	725521, 736459	
2.3.1.12	65960	-	calculation from nucleotide sequence	348982	
2.3.1.12	66000	-	30 * 66000, SDS-PAGE, sedimentation equilibrium	486185	
2.3.1.12	67000	-	plastid precursor protein, SDS-PAGE	486233	
2.3.1.12	68000	-	SDS-PAGE	348941	
2.3.1.12	70000	-	SDS-PAGE	486196, 486224	
2.3.1.12	73000	75000	SDS-PAGE	486176	
2.3.1.12	74000	-	SDS-PAGE	348955, 486194, 486197	
2.3.1.12	74000	-	SDS-PAGE and sedimentation equilibrium data	486202	
2.3.1.12	78000	-	SDS-PAGE	486198	
2.3.1.12	80000	-	SDS-PAGE	486186, 486227	
2.3.1.12	80000	-	SDS-PAGE and calculated from amino acid sequence	486206	
2.3.1.12	81000	-	SDS-PAGE, gel filtration	486192	
2.3.1.12	82000	-	3 * 82000, gel filtration, trimeric form occurs in solutions with 4 M guanidine hydrochloride	486231	
2.3.1.12	83000	-	SDS-PAGE	486173	
2.3.1.12	83000	-	wild-type enzyme, SDS-PAGE	486181	
2.3.1.12	87000	-	SDS-PAGE	348948	
2.3.1.12	127000	-	fusion protein of 11000 Da fragment with beta-galactosidase, SDS-PAGE	486180	
2.3.1.12	150000	-	no component of pyruvate dehydrogenase complex, sucrose density gradient centrifugation	486204	
2.3.1.12	200000	-	at 1.8 - 2.8 M guanidine hydrochloride, complex dissociates at higher guanidine hydrochloride levels to a monomeric form with MW 82000	486231	
2.3.1.12	200000	-	sedimentation equilibrium centrifugation, light scattering, sedimentation and diffusion coefficients	486185	
2.3.1.12	500000	-	above, gel filtration	486168	
2.3.1.12	500000	-	gel filtration	486168	
2.3.1.12	530000	-	-	486173	
2.3.1.12	530000	-	gel filtration	486172	
2.3.1.12	670000	-	gel filtration	486236	
2.3.1.12	864000	-	crystallization experiments	486199	
2.3.1.12	1000000	-	sedimentation equilibrium centrifugation	486209	
2.3.1.12	1470000	-	sedimentation equilibrium experiments in 0.83 M acetic and and 0.005 M sodium chloride	486210	
2.3.1.12	1548000	-	native enzyme	486198	
2.3.1.12	1560000	-	fluorescence anisotropy decay experiments	486177	
2.3.1.12	1800000	1970000	calculation from sedimentation and diffusion constants, meniscus depletion method	486202	
2.3.1.12	2700000	-	gel filtration	486238	
2.3.1.12	2800000	-	calculation from subunit composition of pyruvate dehydrogenase complex	486195	
2.3.1.12	3100000	-	-	94881