TY  - JOUR
AU  - Sümegi, Balázs
AU  - Sherry, A D
AU  - Malloy, C R
TI  - CHANNELING OF TCA CYCLE INTERMEDIATES IN CULTURED SACCHAROMYCES-CEREVISIAE
JF  - BIOCHEMISTRY
J2  - BIOCHEMISTRY-US
VL  - 29
PY  - 1990
SP  - 9106
EP  - 9110
PG  - 5
SN  - 0006-2960
DO  - 10.1021/bi00491a002
UR  - https://m2.mtmt.hu/api/publication/1060973
ID  - 1060973
N1  - Export Date: 27 January 2024
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Keleti, T.
AU  - Ovádi, Judit
TI  - Control of Metabolism by Dynamic Macromolecular Interactions
JF  - CURRENT TOPICS IN CELLULAR REGULATION
J2  - CURR TOP CELL REGUL
VL  - 29
PY  - 1988
IS  - C
SP  - 1
EP  - 33
PG  - 33
SN  - 0070-2137
DO  - 10.1016/B978-0-12-152829-4.50003-3
UR  - https://m2.mtmt.hu/api/publication/32006019
ID  - 32006019
N1  - Cited By :41            
            Export Date: 10 May 2021            
            Chemicals/CAS: Macromolecular Substances; Multienzyme Complexes
AB  - This chapter discusses the control of metabolism by dynamic macromolecular interactions. Metabolic pathways are controlled and directed by pacemaker, bottleneck, and key enzymes. In general, no single enzyme is responsible for the control of a whole metabolic pathway. In pursuing the pacemaker theory, attempts are made to quantify metabolic regulation, and one studies each enzyme in a sequence separately in situ, determines its kinetic properties in the greatest possible detail and accuracy, and then seeks to determine how it works when it is in the intact cell. In prokaryotes and in eukaryotes the largest macrocompartment is the cytoplasm, containing quantities of soluble enzymes and is full of membranes associated with a great variety of organelles. A theoretical analysis of glycolysis in human erythrocytes has been provided, implicitly assuming that it proceeds in a homogeneous bulk solution without any interaction among the participating enzymes. © 1988 ACADEMIC PRESS, INC.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Robinson, J B
AU  - Inman, L
AU  - Sümegi, Balázs
AU  - Srere, P A
TI  - FURTHER CHARACTERIZATION OF THE KREBS TRICARBOXYLIC-ACID CYCLE METABOLON
JF  - JOURNAL OF BIOLOGICAL CHEMISTRY
J2  - J BIOL CHEM
VL  - 262
PY  - 1987
SP  - 1786
EP  - 1790
PG  - 5
SN  - 0021-9258
UR  - https://m2.mtmt.hu/api/publication/1060979
ID  - 1060979
N1  - Export Date: 27 January 2024
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Ovádi, Judit
AU  - ARAGON, JJ
AU  - SOLS, A
TI  - Phosphofructokinase and fructosebisphosphatase from muscle can interact at physiological concentrations with mutual effects on their kinetic behavior.
JF  - BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
J2  - BIOCHEM BIOPH RES CO
VL  - 135
PY  - 1986
SP  - 852
EP  - 856
PG  - 5
SN  - 0006-291X
UR  - https://m2.mtmt.hu/api/publication/1012878
ID  - 1012878
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Porpáczy, Zoltán
AU  - Sümegi, Balázs
AU  - Alkonyi, István
TI  - Association between the α-ketoglutarate dehydrogenase complex and succinate thiokinase
JF  - BIOCHIMICA ET BIOPHYSICA ACTA
J2  - BIOCHIM BIOPHYS ACTA
VL  - 749
PY  - 1983
IS  - 2
SP  - 172
EP  - 179
PG  - 8
SN  - 0006-3002
DO  - 10.1016/0167-4838(83)90249-2
UR  - https://m2.mtmt.hu/api/publication/1060989
ID  - 1060989
N1  - Export Date: 27 January 2024; CODEN: BBAED
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Sümegi, Balázs
AU  - Alkonyi, István
TI  - A STUDY ON THE PHYSICAL INTERACTION BETWEEN THE PYRUVATE-DEHYDROGENASE COMPLEX AND CITRATE SYNTHASE
JF  - BIOCHIMICA ET BIOPHYSICA ACTA
J2  - BIOCHIM BIOPHYS ACTA
VL  - 749
PY  - 1983
SP  - 163
EP  - 171
PG  - 9
SN  - 0006-3002
DO  - 10.1016/0167-4838(83)90248-0
UR  - https://m2.mtmt.hu/api/publication/1060988
ID  - 1060988
N1  - Export Date: 27 January 2024; CODEN: BBAED
LA  - English
DB  - MTMT
ER  -