ID   5.3.3.8
DE   Delta(3)-Delta(2)-enoyl-CoA isomerase.
AN   3,2-trans-enoyl-CoA isomerase.
AN   acetylene-allene isomerase.
AN   Delta(3),Delta(2)-enoyl-CoA isomerase.
AN   Delta(3)-cis-Delta(2)-trans-enoyl-CoA isomerase.
AN   dodecenoyl-CoA Delta-isomerase.
AN   dodecenoyl-CoA isomerase.
CA   (1) a (3Z)-enoyl-CoA = a 4-saturated (2E)-enoyl-CoA.
CA   (2) a (3E)-enoyl-CoA = a 4-saturated (2E)-enoyl-CoA.
CC   -!- The enzyme participates in the beta-oxidation of fatty acids with
CC       double bonds at an odd position.
CC   -!- Processing of these substrates via the beta-oxidation system results
CC       in intermediates with a cis- or trans-double bond at position C3,
CC       which cannot be processed further by the regular enzymes of the beta-
CC       oxidation system.
CC   -!- This enzyme isomerizes the bond to a trans bond at position C2, which
CC       can be processed further.
CC   -!- The reaction rate is ten times higher for the (3Z) isomers than for
CC       (3E) isomers.
CC   -!- The enzyme can also catalyze the isomerization of 3-acetylenic fatty
CC       acyl thioesters to 2,3-dienoyl fatty acyl thioesters.
DR   Q9ZPI6, AIM1_ARATH ;  Q58DM8, ECHM_BOVIN ;  P30084, ECHM_HUMAN ;
DR   Q8BH95, ECHM_MOUSE ;  Q5R646, ECHM_PONAB ;  P14604, ECHM_RAT   ;
DR   P55100, ECHP_CAVPO ;  Q6NYL3, ECHP_DANRE ;  Q08426, ECHP_HUMAN ;
DR   Q9DBM2, ECHP_MOUSE ;  Q5R5M8, ECHP_PONAB ;  P07896, ECHP_RAT   ;
DR   O04469, ECI1_ARATH ;  P42126, ECI1_HUMAN ;  P42125, ECI1_MOUSE ;
DR   P23965, ECI1_RAT   ;  Q05871, ECI1_YEAST ;  O23299, ECI2_ARATH ;
DR   O75521, ECI2_HUMAN ;  Q9WUR2, ECI2_MOUSE ;  Q5XIC0, ECI2_RAT   ;
DR   O23300, ECI3_ARATH ;  Q78JN3, ECI3_MOUSE ;  Q4UL32, FAD3_RICFE ;
DR   Q9ZCZ1, FAD3_RICPR ;  Q68WH7, FAD3_RICTY ;  Q6FF68, FADB_ACIAD ;
DR   B7H1I0, FADB_ACIB3 ;  B7I3P1, FADB_ACIB5 ;  B2I2J9, FADB_ACIBC ;
DR   B0VLX4, FADB_ACIBS ;  B0VE45, FADB_ACIBY ;  A0KEL1, FADB_AERHH ;
DR   A4STF2, FADB_AERS4 ;  Q5E8X6, FADB_ALIF1 ;  B5FEW8, FADB_ALIFM ;
DR   B6EGU2, FADB_ALISL ;  A8ACZ4, FADB_CITK8 ;  Q489W3, FADB_COLP3 ;
DR   A7MQP0, FADB_CROS8 ;  A7ZU51, FADB_ECO24 ;  B7UNH4, FADB_ECO27 ;
DR   B7MHD1, FADB_ECO45 ;  B7L9A7, FADB_ECO55 ;  Q8X8I2, FADB_ECO57 ;
DR   B5YY93, FADB_ECO5E ;  B7NV20, FADB_ECO7I ;  B7N2F2, FADB_ECO81 ;
DR   B7M649, FADB_ECO8A ;  C5A020, FADB_ECOBW ;  B1XAK8, FADB_ECODH ;
DR   A8A6V1, FADB_ECOHS ;  Q0TAL0, FADB_ECOL5 ;  Q8FBI2, FADB_ECOL6 ;
DR   B1IW61, FADB_ECOLC ;  P21177, FADB_ECOLI ;  B7NFE7, FADB_ECOLU ;
DR   B6I4I6, FADB_ECOSE ;  B1LM32, FADB_ECOSM ;  Q1R466, FADB_ECOUT ;
DR   A4WFX4, FADB_ENT38 ;  Q9F0Y7, FADB_ENTCL ;  B7LTY9, FADB_ESCF3 ;
DR   Q5QXH7, FADB_IDILO ;  B5XYH0, FADB_KLEP3 ;  A6TGM4, FADB_KLEP7 ;
DR   Q6DAP5, FADB_PECAS ;  Q7MZ92, FADB_PHOLL ;  Q6LW06, FADB_PHOPR ;
DR   Q48GW3, FADB_PSE14 ;  A6V382, FADB_PSEA7 ;  B7UYR6, FADB_PSEA8 ;
DR   Q02PH8, FADB_PSEAB ;  Q9HZJ2, FADB_PSEAE ;  Q1I7D4, FADB_PSEE4 ;
DR   Q4KFC4, FADB_PSEF5 ;  P28793, FADB_PSEFR ;  C3K613, FADB_PSEFS ;
DR   A4XSM8, FADB_PSEMY ;  Q93Q12, FADB_PSEOL ;  A5W6H0, FADB_PSEP1 ;
DR   Q3K9D8, FADB_PSEPF ;  B0KH74, FADB_PSEPG ;  Q88L02, FADB_PSEPK ;
DR   Q9AHY3, FADB_PSEPU ;  B1J5A5, FADB_PSEPW ;  Q87ZB2, FADB_PSESM ;
DR   Q4ZRA0, FADB_PSEU2 ;  Q4FQC6, FADB_PSYA2 ;  Q1Q8J9, FADB_PSYCK ;
DR   A5WH99, FADB_PSYWF ;  B5EZW0, FADB_SALA4 ;  Q57HM6, FADB_SALCH ;
DR   B5QW85, FADB_SALEP ;  B5RFL6, FADB_SALG2 ;  B4SZ85, FADB_SALNS ;
DR   Q5PKQ2, FADB_SALPA ;  A9MYB0, FADB_SALPB ;  B5BIZ0, FADB_SALPK ;
DR   B4TNZ1, FADB_SALSV ;  Q8Z3C6, FADB_SALTI ;  Q9L6L5, FADB_SALTY ;
DR   A8G8D1, FADB_SERP5 ;  A1S1I8, FADB_SHEAM ;  B8E3R3, FADB_SHEB2 ;
DR   A3CYJ4, FADB_SHEB5 ;  A6WHA0, FADB_SHEB8 ;  A9KU91, FADB_SHEB9 ;
DR   Q08A39, FADB_SHEFN ;  B0TLB9, FADB_SHEHH ;  A3Q8U4, FADB_SHELP ;
DR   Q8EKR9, FADB_SHEON ;  A8GYG0, FADB_SHEPA ;  A4Y1B6, FADB_SHEPC ;
DR   B8CH91, FADB_SHEPW ;  A0KR50, FADB_SHESA ;  A8FP63, FADB_SHESH ;
DR   Q0HPB7, FADB_SHESM ;  Q0I0T3, FADB_SHESR ;  A1RDW6, FADB_SHESW ;
DR   B1KCZ3, FADB_SHEWM ;  B2TVJ5, FADB_SHIB3 ;  Q32A21, FADB_SHIDS ;
DR   Q0SZ36, FADB_SHIF8 ;  Q83PG1, FADB_SHIFL ;  Q3YVC1, FADB_SHISS ;
DR   A4VKA3, FADB_STUS1 ;  B7VGL4, FADB_VIBA3 ;  A7N1D2, FADB_VIBC1 ;
DR   A5F465, FADB_VIBC3 ;  Q9KNI1, FADB_VIBCH ;  C3LSI3, FADB_VIBCM ;
DR   Q87TN9, FADB_VIBPA ;  Q8DDK6, FADB_VIBVU ;  Q7MQH9, FADB_VIBVY ;
DR   A1JIG4, FADB_YERE8 ;  A7FDF2, FADB_YERP3 ;  Q1C2C4, FADB_YERPA ;
DR   B2K0Z6, FADB_YERPB ;  Q8ZAN0, FADB_YERPE ;  A9R754, FADB_YERPG ;
DR   Q1CN99, FADB_YERPN ;  A4TR27, FADB_YERPP ;  Q66FR8, FADB_YERPS ;
DR   B1JP63, FADB_YERPY ;  Q9ZPI5, MFP2_ARATH ;  O49809, MFPA_BRANA ;
DR   Q39659, MFPA_CUCSA ;  Q8W1L6, MFP_ORYSJ  ;
//