Reactive Surfaces Ltd. LLP
`Ex. 1028 (Rozzell Attachment I)
`Reactive Surfaces Ltd. LLP v. Toyota Motor Corp.
`IPR2016-01914
`
`

`

`
`
`II
`I
`
`d")
`
`mail
`
`‘44Iame
`
`In
`
`
`2T© I984, BY ACADEMIC PRESS, INC.
`“HITS RESERVED.
`
`
`WEST OF THIS PUBLICATION MAY BE REPRODUCED OR
`7g e\$\ilTI'ED IN ANY FORM OR BY ANY MEANS. ELECTRONIC
`Cw xIECHANICAL INCLUDING PHOTOCOPY. RECORDING. OR ANV
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`NFORMATION STORAGE AND RETRIEVAL SYSTEM. WITHOUT
`FER\IISSION IN WRITING FROM THE PUBLISHER
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`ACADEMIC PRESS, INC.
`Orlando. Florida 32887
`
`United Kingdom Edition published by
`ACADEMIC PRESS, INC. (LONDON) LTD.
`24/28 Oval Road. London NW1
`7DX
`
`Library of Congress Cataloging in Publication Data
`International Union of Biochemistry. Nomenclature
`Committee.
`Enzyme nomenclature 1984.
`
`"Published for the International Union of
`Biochemistry“
`“Prepared for publication by Edwin C. Webb"
`Includes index.
`2. Enzymes--Classification.
`l. Enzymes--Nomenclature.
`I. Hebb, Edwin C.
`11. International Union of Biochemistry.
`III. Title.
`574.19'25 '014
`I984
`QPGOI . I54
`ISBN 0-12-227162‘9
`ISBN 0-IZ~227163-7 (pbk.)
`
`84-45730
`
`PRINTED I\ THE UNITEDSTATES OF AMERICA
`
`84858687
`
`98765432]
`
`
`
`

`

` Recommended Name
`
`
`
`2.8.3.10
`
`Citrate CoA—transferase
`
`Acetyl-CoA + citrate =
`acetate + (35)-citry|—CoA
`
`2.8.3.11
`
`Citramalate CoA~transferase
`
`Acetyl-CoA + citramalate =
`acetate + (3$)-citramalyl-CoA
`
`2.8.3.12
`
`G lutaconate CoA—transferase
`
`Acetyl-CoA + (E)-glutaconate =
`acetate + 91utaconyl-LC0A
`
`2.8.3.13
`
`Succinate—hydroxymethylglutarate
`CoA-transferase
`
`Succinyl—COA + (S)-3-hydroxy-3-methylglutarate =
`succinate + 3-hydroxy-3-methylglutaryl-COA
`
`3. HYDROLASES
`
`These enzymes catalyse the hydrolysis of various bonds. Some of these enzymes pose problems because
`they have a very wide specificity, and it is not easy to decide if two preparations described by different
`authors are the same, or if they should be listed under different entries.
`
`While the systematic name always includes 'hydrolase', the recommended name is, in most eases, formed
`by the name of the substrate with the suffix use.
`it is understood that the name of the substrate with
`this suffix means a hydrolytic enzyme.
`
`3.1
`
`ACTING ON ESTER BONDS
`
`The esterases are subdivided into those acting on carboxylic esters (3.1.1), thiolesterases (3.1.2),
`phosphoric monoester hydrolases,
`the phosphatases (3.1.3), phosphodiester hydrolases (3.1.4),
`triphosphoric monoester hydrolases (3.1.5), sulfatases (3.1.6), and diphosphoric monoesterases
`(3.1.7), The nucleases, previously included under 3.1.4, are now placed in a number of new sub-
`classes; the exonucleases (3.1.11-16) and the endonucleases (3.1.21-31).
`
`3.1.1 CARBOXYLIC ESTER HYDROLASES
`
`3.1.1.1
`
`Ca rboxylesterase
`
`A carboxylic ester + H20 =
`an alcohol + a carboxylic acid anion
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`

`

` Basis for classification
`
`Other N ames
`
`(Systematic Name)
`
`fi 5"(1.71.. O
`
`Acetyl—CoAzcitrate CoA-transferase
`
`2.8.3.11
`
`2.8.3.12
`
`2.8.3.13
`
`Acetyl-CoA :citramalate
`CoA-transferase
`
`(E)-Glutaconate CoA-transferase
`
`Succinate: (Sls-hydroxy-S-methyl—
`gluta'rate CoA-transferase
`
`271
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`.
`
`Comments
`
`References
`
`The enzyme is a component of
`EC 4.1.3.6. Also catalyses the
`transfer of thioacyl carrier
`protein from its acetyl thioester
`to citrate
`
`The enzyme is a component of
`EC 4.1.3.22. Also catalyses the
`transfer of a thioacyl carrier
`protein from its acetyl thioester
`to citramalate
`
`Glutarate, (Rl-2-hydroxyglutar-
`ate, propenoate and propanoate,
`but not (ll-glutaconate. can also
`act as acceptors
`
`Malonyl—CoA can also act as
`donor, more slowly
`
`820
`
`818
`
`474
`
`760
`
`
`
`
`Carboxylic-ester hydroiase
`
`Wide specificity. Als
`vitamin A esters
`
`o hydrolyses
`
`145, 225. 320,
`479, 1594, 3301
`
`3.1.1.1
`
`Ali-esterase,
`Besterase,
`Monobutyrase,
`Cocaine esterase,
`Procaine esterase.
`Methylbutyrase
`
`
`
`
`
`
`
`
`
`
`
`

`

` Recommended Name
`
`Reaction
`
`
`
`
`
`
`3.1.1.2
`
`Arylesterase
`
`3.1.1.3
`
`Triacylglycerol lipase
`
`A phenyl acetate + H20 =
`a phenol + acetate
`
`Triacylglycerol + H20 =
`diacylglycerol + a fatty acid anion
`
`3.1.1.4
`
`Phospholipase A2
`
`Phosphatidylcholine + H20 =
`1acylglycerophosphochollne + a fatty acid anion
`1
`
`3.1.1.5
`
`Lysophospholipase
`
`2-Lysophosphatidylcholine + H20 =
`glycerophosphocholine + a fatty acid anion
`
`3.1.1.6
`
`Acetylesterase
`
`3.1.1.7
`
`Acetylcholinecterase
`
`An acetic ester + H20 =
`an alcohol + acetate
`
`Acetylcholine + H20 =
`choline + acetate
`
`3.1.1.8
`
`Cholinesterase
`
`‘
`
`,
`
`An acylcholine + H20 =
`choline + a carboxylic acid anion
`
`[3.1.1.9 Deleted entry: Benzoy/cho/I‘nestemse; a side reaction of EC 3. l. 7.8]
`
`3.1.1.10
`
`Tropinesterase
`
`3.1.1.11
`
`Pectinesterase
`
`Atropine + H20 =
`tropine + tropate
`
`Pectin + n H20 =
`n methanol + pectate
`
`[3.1. 7.12 Deleted entry: previous/y Vitamin A esterase, now believed to be identical with EC 3.1.7.7]
`
`3.1.1.13
`
`Cholesterol esterase
`
`3.1.1.14
`
`Chlorophyllase
`
`A cholesterol ester+ H20 =
`cholesterol + a fatty acid anion
`
`Chlorophyll + H20 =
`phytol + chlorophyllide
`
`3.1.1.15
`
`L‘Arabinonolactonase
`
`L-Arabinono-1,4—lactone + H20 =
`Larabinonate
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`

`

`Other Names
`
`1‘ 1.2
`
`A-esterase,
`Paraoxonase
`
`
`
`
`E ‘ 2.3
`
`3 11.4
`
`Lipase,
`Triglyceride lipase,
`Tributyrase
`
`Lecithinase A,
`Phosphatidase,
`Phosphatidolipase
`
`3.1.1.5
`
`Lecithinase B,
`Lysolecithinase,
`Phospholipase B
`
`Basis for classification
`(Systematic Name)
`
`Aryl—ester hydrolase
`
`Triacylglycerol acylhydrolase
`
`Phosphatidylcholine 2acylhydrolase
`
`2-Lysophosphatidylcholine
`acylhydrolase
`
`"
`
`Comments
`
`References
`
`
`
`
`
`Acts on many phenolic esters; the 51, 148, 397,
`enzyme from sheep serum also
`2353
`hydrolyses paraox on
`
`The pancreatic enzyme acts only
`on an ester-water interface; the
`outer ester links are preferentially
`hydrolysed
`
`2013, 2313,
`3346, 3557
`
`Also acts on phosphatidylethanol- 832, 1057, 1367 ,
`amine, choline plasmalogen and
`2601, 3326,
`phosphatides, removing the fatty
`4076
`acid attached to the 2—position
`
`643, 752, 969,
`3479, 4077
`
`51, 298, 1733
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`3.1.1.6
`
`3.1.1.7
`
`3.1.1.8
`
`3.1.1.10
`
`3.1.1.11
`
`Acetylcholine acetylhydrolase
`
`Acts on a variety of acetic esters;
`also catalyses transacetylations
`
`146, 299, 609,
`2208, 2665,
`4470
`
`Acts on a variety of choline esters
`and a few other compounds
`
`146.148.1981,
`
`2665, 3365,
`3752
`
`Cesterase (in animal Aceticester acetylhydrolase
`tissues)
`
`True cholinesterase,
`Choline esterase l,
`Cholinesterase
`
`Pseudocholinesterase, Acylcholine acylhydrolase
`Butyrylcholine
`esterase,
`Non-specific
`cholinesterase,
`Choline esterase ll
`(unspecific),
`Benzoylcholinesterase
`
`Atropine acylhydrolase
`
`Also acts on cocaine and other
`tropine esters
`
`1220, 2598
`
`800, 2263, 2556
`
`Pectin demethoxylase, Pectin pectylhydrolase
`Pectin methoxylase,
`Pectin methylesterase
`
`3.1.1.13
`
`Sterol-ester acylhydrolase
`
`Also acts on esters of some other
`sterols
`
`500, 1500, 2032,
`3822
`
`3.1.1.14
`
`Chlorophyll chlorophyllido»
`hydrolase
`
`Also catalyses chlorophyllide
`transfer, e.g. converts chloro-
`phyll to methylchlorophyllide
`
`1564, 1961
`
`4219
`
`
`
`
`3.1.1.15
`
`L-Arabinono-1,4-lactone
`lactonohydrolase
`
`
`
`

`

`
`
`274
`
`Number
`
`Recommended Name
`
`Reaction
`
`[3. 7. 7.16 Deleted entry, 4Carboxymethyl-4-hydroxyisocroIona/actonase. This reaction was due to a mixture ofmucono-
`lactone A—Isomerase (EC 533.4) and 30xoadipate-enol-Iactonase (EC 3. 7. 7.24)]
`
`3.1.1.17
`
`G luconolactonase
`
`o~Glucpno—1 ,5-Iactone + H20 =
`D—gluconate
`
`[3. I . I . I 8 Deleted entry: Aldonolactonase. Now included with EC 3.7. 7.7 7]
`
`
`
`
`
`
`
`3.1.1.19
`
`Uronolactonase
`
`3.1.120
`
`Tannase
`
`3.1.121
`
`Hetinyl~palmitate esterase
`
`3.1.122
`
`Hydroxybutyrate-dimer hydrolase
`
`3.1.1.23
`
`Acylglycerol lipase
`
`3.1.124
`
`3-Oxoadipate enol-Iactofiase
`
`3.1.1.25
`
`1 ,ll-Lactonase
`
`D-Glucurono-6,2~lactone + H20 =
`D-glucurofiate
`
`Digallate + H20 =
`2 gallate
`
`Retinyl palmitate + H20=
`retinol + palmitate
`
`(R)-3—((R)~3-Hydroxybutanoyloxy)butanoate + H20 =
`2 (R)-3-hydroxybutanoate
`
`Hydrolyses glycerol monoesters of long-chain fatty acids
`
`3—Oxoadipate enol—Iactone + H20 =
`3-ox oadipate
`
`A 1,4»lac’tone + H20 =
`a 4—hydroxyac1d
`
`3.1.126
`
`Galactot ipase
`
`1,2—Diacyl-3Kio —galactosy1—sn-glycerol + 2 H20 =
`364: —galactosyl-$n.glycerol + 2 fatty acid anions
`
`3.1.127
`
`3.1.128
`
`4-Pyridox olactonase
`
`Acylcarnitine hydrolase
`
`3.1.1.29
`
`Aminoacyl—tRNA hydrolase
`
`3.1.1.30
`
`D -Arabinonolactonase
`
`4—Pyridoxolactone + H20 = 4pyridoxate
`
`O-Acylcarnitine + H20 =
`a fatty acid + L-carnitine
`
`N-Substituted aminoacyl-tRNA + H20 =
`N~substituted amino acid + tRNA
`
`o-Arabinono-1,4-lactone + H20 =
`D-agabinonate
`
`
`
`

`

`
`
`Number
`
`Other Names
`
`3.1.1.17
`
`Lactonase,
`Aldonolactonase
`
`Basis for classification
`(Systematic Name)
`
`),
`
`Comments
`
`References
`
`275
`
`D‘GlUCOflO-i ,5—lactone
`Iactonohydrolase
`
`Acts on a wide range of
`hexono-1,5-Iactones. The hydro-
`lysis of L—guiono-1,5<iactone was
`previously listed as EC 3.1.1.18
`
`442, 467, 3806
`
`o-Glucurono-GZ-lactone
`Iactonohydrolase
`
`4294
`
`Tannin acylhydrolase
`
`Also hydrolyses ester links in
`other tannins
`
`884
`
`Retinyl-palmitate palmitohydrolase
`
`(R)-3—((R)3Hydroxybutanoyloxy)-
`-butanoate hydroxybutanoylhydrolase
`
`Monoacylglycerol
`lipase
`
`Glycerol-ester acylhydrolase
`
`2341
`
`769
`
`3019
`
`'
`
`'
`
`Carboxymethyibuten- 4Carboxymethylbut—3-en4-olide
`olide lactonase
`enolelactonohydroiase
`
`The enzyme acts on the product
`of EC 4.1.1.44
`
`2876, 2878
`
`3.1.1.19
`
`3.1.1.20
`
`3.1.1.21
`
`3.1.1.22
`
`3.1.1.23
`
`3.1.1.24
`
`3.1.1.25
`
`3.1.126
`
`3.1.1.27
`
`3.1.1.28
`
`3.1.1.29
`
`3.1.1.30
`
`lactonohydroiase
`
`'
`
`1,4-Lactone hydroxyacylhydrolase
`
`1,2-Diacyl-3-B-D -galactosyl—
`~sn-glycerol acyihydrolase
`
`4-Pyridoxolactone lactonohydrolase
`
`O-Acylcarnitine acylhydrolase
`
`Aminoacyl-tFiNA aminoacyihydrolase
`
`o -Arabinono-1,4—lactone
`
`1015
`
`The enzyme is specific for
`1,4-Iactones with 4-8 carbon atoms.
`it does not hydrolyse simple
`aliphatic esters, acetylcholine, sugar
`iactones or substituted aliphatic
`lactones, e.g. 3-hydroxy4-butyro—
`lactone; requires Ca2+
`
`Also acts on 2,3-di-O’acyl-
`01-(054-0 -ga|actosyl-
`43-0 galactosyiHi -glycerol, and
`phosphatidylcholine and other
`phospholipids
`
`1478, 1541
`
`Acts on higher fatty acid (C6 to
`C18) esters of Lcarnitine; highest
`activity is with Odecanoyl—
`-L-carnitine
`
`482
`
`2342
`
`1777
`
`2916
`
`

`

` Recommended Name
`
`Reaction
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`
`3.1 .1 .31
`
`6-Phosphogluconolactonase
`
`3.1.1.32
`
`Phospholipase A1
`
`3.1.1.33
`
`B-Acetylglucose deacetylase
`
`3.1.1.34
`
`Lipoprotein lipase
`
`3.1.1.35
`
`Dihydrocoumarin hydrolase
`
`3.1.1.36
`
`Limonin-D-ring-lactonase
`
`3.1.1.37
`
`Steroid—lactonase
`
`3.1.1.38
`
`Triacetate-lactonase
`
`3.1.1.39
`
`Actinomycin lactonase
`
`6—Phosphoo glucono-1 ,5-lactone + H20 =
`6—ph osphoo ~gluconate
`
`Phosphatidylcholine + H20 =
`Zacylglycerophosphocholine + a fatty acid anion
`
`6-Acetyl-D-glucose + H2O =
`glucose + acetate
`
`Triacylglycerol + H20 =
`diacylglycerol + a fatty acid anion
`
`Dihydrocoumarin + H20 =
`meli lotate
`
`Limonoate D—ring—lactone + H20 =
`limonoate
`
`Testololactone + H20 = testolate
`
`Triacetate lactone + H20 = triacetate
`
`Actinomycin + H20 = actinomycinic monolactone
`
`3.1.1.40
`
`Orsellinate-depside hydrolase
`
`Orsellinate depside + H20 =
`2 orsellinate -
`
`3.1.1.41
`
`Cephalosporin-C deacetylase
`
`3.1.1.42
`
`Chlorogenate hydrolase
`
`3.1.1.43
`
`a—Aminoacid esterase
`
`3.1.1.44
`
`4-Methyloxaloacetate esterase
`
`Cephalosporin C + H20 =
`deacetylcephalosporin C + acetate
`
`Chlorogenate + H20 =
`caffeate + quinate
`
`An a—amino acid ester + H20 =
`an a-amino acid + an alcohol
`
`Oxaloacetate 4-methyl ester + H20 =
`oxaloacetate + methanol
`
`3.1.1 .45
`
`Carboxymethylenebutenolidgse
`
`4—Carboxymethylenebut-Z—en-4—olide + H20 =
`4cxohex-2—enedioate
`
`

`

`277
`
`Comments
`
`Reference:
`
`Basis for classification
`(Systematic Name)
`
`6—Phospho-o -glucono—1 ,5-lactone
`lactonohydrolase
`
`3.1.1.31
`
`3.1.1.32
`
`3.1.1.33
`
`3.1.1.34
`
`3.1.1.35
`
`3.1.1.36
`
`3.1.1.37
`
`3.1.1.38
`
`3.1.1.39
`
`Phosphatidylcholine 1-acylhydrolase
`
`This enzyme has a much broader
`specifity than EC 3.1.1.4
`
`6-Acetylo -glucose acetylhydrolase
`
`Triacylglyceroprotein acylhydrolase
`
`Clearing factor lipase,
`Diglyceride lipase,
`Diacylglycerol lipase
`
`Dihydrocoumarin lactonohydrolase
`
`LimonoateD-ring-lactone
`lactonohydrolase
`
`Testololactone lactonohydrolase
`
`Triacetolactone lactonohydrolase
`
`Hydrolyses triacylglycerols in
`chylomicrons and low-density
`lipoproteins. Also hydrolyses
`diacylglycerol
`
`Also hydrolyses some other
`benzenoid 1,4-Iactones
`
`Limonoate is a triterpenoid
`
`Actinomycin lactonohydrolase
`
`Actinomycins are a class of
`antibiotics
`
`
`
`
`
`
`
`
`
`1865
`
`1 155, 3367,
`4076, 4078
`
`867
`
`905, 1003, 1292.
`2627. 2767
`
`2035
`
`2352
`
`1572
`
`1848
`
`1604
`
`3430
`
`
`
`Number
`
`Other Names
`
`3.1.1.40
`
`Lecanorate hydrolase
`
`Orsellinate—depside hydrolase
`
`The enzyme will only hydrolyse
`those substrates based on the
`2,4-dihydroxy-6-methylbenzoate
`structure that also have a free
`hydroxyl ortho to the depside
`linkage
`
`3.1.1.41
`
`Cephalosporin-C acetylhydrolase
`
`r
`
`3.1.1.42
`
`Chlorogenase
`
`Chlorogenate hydrolase
`
`Hydrolyses the acetyl ester bond
`on the 10—position of the anti-
`biotic cephalosporin C
`
`Also acts, more slowly, on iso—
`chlorogenate. No other substrates
`known
`
`1113
`
`3417
`
`a-Amino acid ester
`hydrolase
`
`a—Amino-acid-ester aminoacyl-
`hydrolase _
`
`Also catalyses aeaminoacyl transfer 1845, 3858
`to a number of amine nucleophiles
`
`3.1.1.43
`
`3.1.1.44
`
`Oxal oacetateA-methyl-ester
`oxaloacetohydrolase
`
`3.1.1.45
`
`Maleylacetate
`enol-lactonase
`
`4~Carboxymethylenebut-Z-enA-ol ide
`lactonohydrolase
`
`842
`
`3407
`
`
`
`

`

`
`
`278
`
`
`Recommended Name
`Number
`
`
`
`
`
`
`3.1.1.46
`
`Deoxylimonate A-ring-lactonase
`
`Deoxylimonate + H20 =
`deoxylimononic acid D-ring—lamone
`
`
`
`3.1.1.47
`
`1-A|ky1-2-acetylglycerophosphocholine esterase
`
`1-AIkyl-2acetyl-sn-glycero-S-phosphocholine + H20 =
`1a1ky1~sn-g|ycero.3-phosphocholine + acetate
`
`3.1.1.48
`
`Fusarinine~C ornithinesterase
`
`AfivAcyl-L-omithine ester + H20 =
`AF-acyl—L-ornithine + an alcohol
`I
`
`3.1.1.49
`
`Sinapine esterase
`
`Sinapoylcholine + H20 = sinapate + choIine
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`3.1.1.50 Wax-ester hydrolase
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`A wax ester + H20 =
`a long—chain alcohol + a long-chain—fatty-acid anion
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`3.1.1.51
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`Phorbol-diester hydrolase
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`Phorbol 12,13-dibutanoate + H20 =
`phorbol 13—butanoate + butanoate
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`3.1.1.52
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`Phosphatidylinositol deacylase
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`1-PhosphatidyI—o-myo~inositol + H20 =
`1acylglycerophosphoinositol + a fatty acid anion
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`3.1.153
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`Sialate Oacetylesterase
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`N~Acety|-0-acetylneu raminate + H20 =
`Nvacetylneuraminate + acetate
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`3.1.2 THIOLESTER HYDROLASES
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`3.1.2.1
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`AcetyI-CoA hydrolase
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`3.1.2.2
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`PalmitoleoA hydrolase
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`AoetyI-COA + H20 =
`CoA + acetate
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`Palmitoyl-CoA + H20 =
`CoA + palmitate
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`3.1.2.3
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`Succinyl-CoA hydrolase
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`Succinyl-CoA + H20 = CoA + succinate
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`

`

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`Number
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`Other Names
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`3.1.1.46
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`3.1.1.47
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`Basis for classification
`(Systematic Name)
`
`Deoxylimonate A-ring—lactono—
`hydrolase
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`1-Alkyl-2.acetyl.5n-glycero-
`-3-phosphocholine acetohydrolase
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`3.1.1.48
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`Ornithine esterase
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`N5 -Acyl—L ornithineester hydrolase
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`Comments
`
`References
`
`The enzyme opens the A—ring—
`-lactone of the triterpenoid deoxy-
`limonic acid, leaving the D-ring-
`-lactone intact
`
`1403
`
`Hydrolyses the 3 ornithine ester
`bonds-in fusarinine C (a cyclic
`trihydroxamic acid formed by
`esterification 013 molecules of
`fusarinine, N5v(cis-5-hydroxy-
`~3-methylpent—2-enoyll-
`Ws-hydroxy-L-ornithine). Also
`acts on Nssdinitrophenyl-
`-L —ornithine methyl ester
`
`Also acts on long«chain
`acylglycerol, but not diacyl—
`or triacylglycerols
`
`Hydrolyses the 12ester bond in
`a variety of 12,13-diacylphorbols
`(phorbol is a diterpenoid);
`this reaction inactivates tumor
`promoter 01 2 ~tetradecanoyl-
`phorbol-13~acetate from croton
`oil
`
`362
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`933
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`2820
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`' 1612, 2609
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`3529
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`1271—2
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`3532
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`1165
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`Sinapoylcholine sinapohydrolase
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`Waxester acylhydrolase
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`D iacylphorbate
`12hydrolase
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`12,13—Diacylphorbate 12-acyl—
`hydrolase
`
`Phosphatidylinositol
`phospholipase A2
`
`1 Phosphatidyl-D myo-inositol
`Zacylhydrolase
`
`N-Acyl-O—acetyl neuraminate
`O-acetylhydrolase
`
`Acts on free and glycosidiully-
`bound N-acety|« or N-glycoloyl-
`neuraminic acid; acts mainly on
`0‘— and 09—acetyl groups
`
`AcetleoA deacylase, Acetyl-CoA hydrolase
`Acetyl—CoA acylase
`
`3.1.1.49
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`3.1.1.50
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`3.1.1.51
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`3.1.1.52
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`3.1.1.53
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`3.1.2.1
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`3.1.2.2
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`1‘,
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`Longchain fatty-acyl- Palmitoyl-COA hydrolase
`-CoA hydrolase
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`Also hydrolyses CoA thioesters
`of other long-chain fatty acids
`
`236, 294, 2578,
`3665, 4342
`
`Succinyl-CoA acylase Succinyl-CoA hydrolase
`
`1165
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