Metabolic Pathways Med Enzymnumre Og Navne
Metabolic Pathways Med Enzymnumre Og Navne
Metabolic Pathways Med Enzymnumre Og Navne
1.
HO O
UDP -
O
MA NNOS E + C OO
I
4.
(S ialate) OP P U 2.7.7.13 4.2.1.46 OH C H 2 C H(NH 3 )C OO NH C C C H C H 2O P 1.2.1.32
1.
C -C H(OH)C H(OH)C H 2 O P
S
C H2 C C OO
1. 1. 1. 22 G alac tos e-P C H 2 C H 2 NH 2 HOC -C H(OH)C H(OH)C H 2 OP C OO
19
C H 2O P
C OO
NHAC
O G alac turonate 2.7.1.7 2.7.7.27 NH
CH CH OH OH NH 2
1.14.12.1 N
O HO OH HO O P C H 2 OH NH 4.2.1.20 N N O
H H NH 2
UDP -N-A c -
3.1.3.29 5.1.3.7 Mannos e-1-P
T DP -G luc os e
2.7.7.34 2.7.7.9 HO
O
T ryptamine
4.1.1.28
T R Y P TOP HA N Indole-3-glyc erol-P 1-(o-C arboxy phenylamino)
4.1.1.48
N-(5-P -R ibos yl)
2.4.2.18
A nthranilate
OOC
OOC O
AC NH
HO OH G luc os amine
4.1.3.20 HO OH OP P U 5.1.3.6 C H 2O P
O
5.1.3.2
C OO 1-deoxyribulos e-5-P anthranilate 2-A mino
OH 2.7.7.10
pyruvate OH 2.7.7.12 OH OP P U OC
HO
muc onate
N-A c -Mannos amine-6-P UDP -G luc uronate 5.4.2.8
HO OH HO OH
2.7.7.24 C H 2 OH
O OH P OC H 2 C H 2
C OO C OO C OO
C OO C OO C OO
4.1.3.27
OOC C H 2 C OC OO
A
C H 2 OH
C H 2 OH
O
C H 2 OH
O 4.1.3.20 O
C H 2O P
O
HOC H HC OH
C OH OH HO OH
C H2 C H2
C
OH O-C -C OO
H 2.7.1.60 Mannos e-6-P 2.4.1.13 C H 2O P HO OH OP UDP -G alac tos e H OH
4.6.1.3
O OH
4.2.1.10
O
OH
1.1.1.25
OH
2.7.1.71
P O
OH
2.5.1.19
P O
OH OH OC -C OO
5.4.99.5
OH I
S hikimate-5 4.6.1.4
AC NH
HO OH OH HO OH OP P U HO OH OP HO OH O HO 3-Deoxy-D-arabino- Dehydro- Dehydro- S hikimate S hikimate-3-P C horis mate P rephenate D
E OH 2.4.1.9
heptulos onate-7-P quinate s hikimate PEP
enolpyruvate 3-P
X
NHAC NHC OC H 3 5.4.2.3
N-A c -G luc os amine-6-P
NHC OC H 3 G luc os e-1-P O O
OH C H 2 C OC OO
+
C H 2 C H (NH 3 ) C OO C H 2 C H(NH 3 ) C OO
+
S
N-A c -Mannos amine UDP -N-A c -G luc os amine N-A c -G luc os amine-1-P HO OH OH C H 2 OH
O C H 2 C OO
C H 2 C OC OO
4.2.1.51
2. 3. 1.
O 5.1.3.14
C OO
2.7.7.23
OH OH OH H H OH
4 NH 2
-OOC
O
C H 2 C OO
O
C H 2 C OO
1.3.1.13
S OH
5.3.1.8 G luc os amine-6-P HO OH OH
C OO OH OH OH
F umaryl 5.2.1.2 Maleyl 1.13.11.5 Homogentis ate
O C C C CO C H 2 OH 1.13.11.27 2.6.1.5 1.14.16.1 2.6.1.5
OH HOC H 2 Hydroxyphenyl T Y R OS INE P HE NY L A L A NINE P henylpyruvate
E OH H OH OH OP
OH OH H OH
ac etoac etate ac etoac etate pyruvate 4. 3. 1.
5
C OO -
1.3.1.13 1.3.1.13
S HOC H 2 C C C C HO OH OH HO OH HO OH
OH
F ruc tos e S UC R OS E 3.2.1.26 3.2.1.48
G L UC OS E C HOHC H 2 NHC H 3 C HOHC H 2 NH 2 C H 2 C H 2 NH 2
+
C H 2 C H (NH 3 ) C OO-
H OH H H OH OH 4 .1
G ulonate
1.1.1.19
G luc uronate
1.13.99.1
Inos itol
3.1.3.25
Inos itol-P 5.5.1.4
.1 .2
5
C H 2 C H 2 NH 2 C H=C HC OO C
OH H OH OH OH H OH 5.4.2.2 OH OH OH OH Ubiquinone C innamate A
OH H OH OH 1. 1. 1.
21
ATP OH OH OH OH
1.14.16.2
Menaquinone
3.1.1.18 HOC H 2 C
H
C C
H
C
H
CO HOC H 2 C
H
C C
H
CO CO
HOC H 2 C C C C CO 1.1.1.14 H H OH H C H 2O P
O
3.1.3.9 2.7.1.2 E pinephrine 2.1.1.28
Norepinephrine 1.14.17.1
Dopamine 4.1.1.28
Dopa
+
C H 2 C H (NH 3 ) C OO
OH
T yramine 1.14.13.11 T
2.7.1.1
O O H O HOC H 2 C C C C C H 2 OH
2.6.1.16 (A drenaline)
C HOHC H 2 NH 2
(Noradrenaline)
HN O E
G ulonolac tone 1.1.3.8 2-Oxogulonolac tone A S C OR B A T E OH OH H OH O A DP .1 .6
1.10.2.1
S orbitol
2. 7 HO OH C H 2 OP 2 .1
1.14.18.1 H2 I I C H=C HC OO
C oumarate
C
1.1.1.45
OH H OH OH H OH H
1.10.3.3 . 1. 1.1.1.49 α-T oc opherol O C
O
HOC H 2 C C CO C C OO - C O C OO -
4 OH
O
C H(OH)C OO OH
OC H 3
C HOHC H 2 OH C H-C OO O
H
H OH H
HOC H 2 C
H
C
OH
CO HOC H 2 C
H
C CO
O
CO CO
2.7.1.3 P -G luc ono G luc os e-6-P Normetepinephrine
(V itamin E )
O
+
NH 3 O
OH
O
1.1.1.130 .1 7
P 3-Dehydrogulonate 2, 3-Dioxogulonate Dehydroas c orbate .1 lac tone HO OH OH OC H 3 (Normetadrenaline) OC H 3 Dopaquinone I I
E
H H OH H
C C OO -
3 .1
NADP + OH OH
1 .4
.3 .4 OH O NH OH L
P OC H 2 C C C 1.14.18.1
N
OH H OH H H OH H H
5.3.1.8 5.3.1.9 4-OH-3-Methoxy- 4-OH-3-Methoxy- P las toquinone ME L A NIN T HY R OXINE L IG NIN T annins P lant P igments A
6-P -G luc onate NA DP H
OH OH H OH
HOC H 2 C C C C HO HOC H 2 C C C C HO HOC H 2 C C C O C H 2 OH
H H OH
D-mandelate phenylglyc ol M
T H OH H OH OH H OH OH
H+ 7 .4 2. 4. 2.
P *- 2.2.1.1 OOC C H 2 N(C H 3 ) 3
+
d-A T P 2 .7
.7 .7 d-C T P .1 1 6.3.5.2
HN
H 2N C
C CH
H 2e- PQ 2e-
2e H+ C
PQ
_
. P OC H 2C HOHC HO
B etaine F OL IC ATP 2.7.7.6
R NA 2.7.7.6
GTP 2.7.4.6
G DP 2.7.4.8
N N RP
O QB
PQH2 1e- 1e-
PQ
H+ 3-P -G lyc eraldehyde 1.2.1.8 2.1.2.1 A C ID 2 .7
T T P 2.7.4 1. 17 .4 G UA NOS INE -P
Fe-S NADP+ HOC H 2 C OC H 2 OP .7 .6
T PQH2 Cyt bf
Dihydroxy-
2.2.1.1
.1 + C1 .6
.1 (G MP )
5 .3 .1
QA 2.4.2.14 OHC C H 2 N(C H 3 ) 3
O 2e- A1
H+
H+
ac etone-P Pi 6.3.4.7 B etaine P OOL NH 2
P
Pi 20 O 2 .7 T DP
O O C
S Pheophytin Cyt bc Chl.A0 (G lyc erone-P ) 5 .3 .1
.1 aldehyde 4.1.2.5 4. 2. 1. C O
.7 .6 C C N CH
Y
Y 2PQ ._ 2e-
2PQ NADPH+H+ NA D+
C H3
C H3
HN C H-C H 3
HN
C
C C H3
2 .7
.4 .9 HN
C -C H 3
CH 2.1.1.45
HN CH
OC CH
P680
Chl.a 2PQH2 P700 Pi ADP
2.7.1.28 1.1.99.1 H 2 NC ONHC H 2 C HC OO
OC CH2
OC CH
OC
N OC CH
N DP
N
DP R
N 2e-
2e-
Fe-S 2e- Cyt.f
PC
H+
Glyceraldehyde
+
HOC H 2 C H 2 N (C H 3) 3
H 2 NC H 2 C HC OO
3-A mino- ß-Ureido
NH
Dihydro
NH
T hymine
2.4.2.4
DP
d-UMP
3.5.4.12
d-C MP
2.7.4.14
d-C DP I
T Mn H+
H+
1.2.1.12 C HOL INE 3.5.1.6 3.5.2.2 1.3.1.2 T HY MIDINE -P
PC PC
Ribulose-1,5-bis-P is obutyrate is obutyrate thymine O
M
α
α α
1.2.1.13 + O 2 .4 .2 NH 2
Pi
1
H 4H + HOC H 2 C H(NH 3 )C OO 2. 1 C C C
a
.4
NA DH 4.2.1.22 . 1. HN C H2 HN CH
8
I
β
H+ H+ H+ A DP N CH 1.17.4.1
S E R INE
8
H 2O Translocated protons
2
13
E
β
H+ C H2
CO2 OC OC CH CH
1
2.6.1.51 H 2 NC ONHC H 2 C H 2 C OO OC
H+ H+ 4.1.1.11
S H+
H+ H+ H+ H+ H+ H+ C H 2O P H 2 NC H 2 C H 2 C OO NH N H NH D
3
3
H+ γ O
P OC H 2C HOHC OO P 1.4.1.7 3.5.1.6 C arbamoyl 3.5.2.2 Dihydro- 1.3.1.2 3.5.4.1 C DP
ATP Fixation ß-A lanine Urac il C ytos ine
I O2 Protons from Water H+ H+ H+
1: 3-bis -P -G lyc erate ß-alanine urac il NH 2
I
H+
εε
2
H+
c
2.7.6.1
2
H+ H+ H+ β2 HOC H 2 C OC OO -OOC O O C
O
H+ C H 2.7.4.6
α
H+ H+ H+ H+ H+ O
α
OP OP 3.1.3.3 O C
S H+ H+
Hydroxy- NH
2 C H2
C C HN
C
CH C HN CH N
N
3
THYLAKOID LUMEN
OH OH C H2 CH HN CH CH
α
HN OC
ATP ATP HN 2.4.2.9
H+
+ N R PPP RPPP
ATP synthase A DP P OC H 2 C H(NH 3 )C OO H NH NH RP RP 6.3.4.2
A DP C arbamoyl Dihydro Orotate Orotidine-P Uridine-P UDP UR IDINE - C Y T IDINE - S
STROMA 3.6.1.34 P hos pho- 3.5.2.3 4.1.1.23 (UMP ) 2.7.4.4
CHLOROPLAST OUTER MEMBRANE 2.7.2.3 s erine as partate orotate 1.3.1.14 2.4.2.10 2.7.4.6 triphos phate triphos phate
1.1.1.29 (UT P ) (C T P )
C OO
HO HO
C OO ATP 2.6.1.52
2.6.1.22
NH 2 NH 2
C OO H H H H H H H H H H C ONH 2
+ C N OC N N H H
γ-L inolenate
1.14.99.25 1.13.11.34 P OC H 2 C C C C N C CH P OC H 2 C C C C NH C CH P OC H 2 C C CO C H2 NH C CH
P OC H2C HOH C OO
L inoleate A rac hidonate L eukotriene B 4 OH 1.1.1.95
P OC H 2 C OC OO
HC C HC C HC C P OC H 2 C C C CH
C OO 5. O
3-P -G lyc erate P -Hydroxy- OH OH
N N OH OH
N N OH OH
N N
1 .1 3 . 9 9 C OO O R P (P P ) O RP RP OH OH HN N
1.3.1.35 4 .9 . 3
C OO pyruvate 3.6.1.31 3.5.4.19 C
9 .1 O 2.4.2.17
P -R ibos yl-A T P P -R ibos yl-A MP P -R ibos ylformimino P -R ibulos ylformimino Imidazole H
C OS C oA
L C O-S -AC P
HO OH 5.3.99.5
HO
OH 2.7.1.31 5-aminoimidazole- 5.3.1.16 5-aminoimidazole- glyc erol-P
HC C C H 2 C HC OO
I Oleoyl-C oA P almitoleoyl-A C P P ros taglandin P G E2 T hromboxane B 2 P OC H2 C H(O P ) C OO + c arboxamide-R P +
c arboxamide-R P+
HOC H2C H(OH) C OO N NH NHC OC H 2 C H 2 NH 2 HC C C H 2 C H(NH 3 )C OO + HC C C H 2 C OC H 2 OP
1.14.99.5 2, 3-Diphos pho- 5.4.2.1 HC C C H 2 C H(NH 3 )C HO HC C C H 2 C H(NH 3 )C H 2 OH HC C C H 2 C H(NH 3 )C H 2 OP
P C OS C oA C H 3 (C H 2 ) 14 C H=C HC OS -C oA C H 3 (C H 2 ) 14 C H(OH)C H 2 C OS -C oA C H 3 (C H 2 ) 14 C OC H 2 C OS -C oA
glyc erate G lyc erate C
H C arnos ine N
CH
NH
N NH N NH N NH
N
C
NH
4.2.1.19
O
H R '-C O-OC H O
+ C ardiolipin
O
P hos phatidylglyc erol C H 3 C (OH)C H 2 C HO
1.1.1.37
CH2COO- 2.1.3.1 6.4.1.3 C OOH C OOH +
(C H 3 ) 2 C HC H 2 C H(NH 3 )C OO
F MNH 2 4.1.1.41
O C H 2 O P OC H 2 C H 2 NH 3
-
+ +
1.4.3.8 Mevaldate IS OC IT R A T E 5.1.99.1
(C H 3 ) 2 C HC (OH)C H 2 C OO (C H 3 ) 2 C HC HC H(OH)C OO (C H 3 ) 2 C HC H 2 C OC OO 2.6.1.6
L E UC INE
ADP - OC H 2 C (C H 3 ) 2 C H(OH)C O NHC H 2 C H 2 C O NHC H 2 C H 2 S H
Dephos pho-C oenzyme A
O C P P - OC H 2 C H 2 NH 3 P OC H 2 C H 2 NH 3 + 2-Is opropyl- 3-Is opropyl- 1.1.1.85 Oxoleuc ine
S 2.7.8.1 C DP -E thanolamine 2.7.7.14
E thanolamine-P 2.7 .1. 82
+
HOC H 2 C H 2 NH 3 2H 4.1.3.1 1.1.1.41 C H3 malate 4.2.1.33
malate 1.4.1.9
P hos phatidyl E thanolamine 1.1.1.32
2F e -S 2.7.1.24
P ethanolamine
C H 2 OH
CH3CH(OH)CH2CO.SCoA
OOC -C H-C OS C oA C H3 1.2.1.25
C H 2 O-C O-R (5 C lusters) MA L A T E 4.2 .1. 18 C H3
H C E P HA L IN HOC H O
HOC H O
+ C H 3 C OC H 2 C H 2 N(C H 3 ) 3 -OOCCOCH CH COO-
4.1.1.71
Methylmalonyl-C oA OOC C H 2 C = C HC OS C oA C H 3 C = C HC OS C oA (C H 3 ) 2 C HC H 2 C OS C oA P -ADP - OC H 2 C (C H 3 ) 2 C H(OH)C O NHC H 2 C H 2 C O NHC H 2 C H 2 S H
A
C H 2 C OO
4H+
2 2 6.4.1.4 1.3.99.10
O + C H 2 OP O C H 2 C H 2 N(C H 3 ) A c etylc holine 4H+ 2-OXO - 3-Methyl- 3-Methyl- Is ovaleryl-C oA C oenzyme A
2.1.1.17
C H 2 OP O C H 2 C H 2 N(C H 3 ) 3
3.1. 1.5
-
G lyc erophos phoc holine
O
3 .1
C H 3 C (OH)C H 2 C H 2 OH 1.6. 5.3 AS PAR TATE 2 .7 .2 4.2.1.18
glutac onyl-C oA c rotonyl-C oA M
L C H 2 OC H=C HR 2.1.1.71 O - L ys olec ithin .4 .2 Mevalonate 2H+ 4.2.1.2 G L UT A R A T E .4
1.1.1.3
C H 2 O-C O-R 3.1.4.4 2.3.1.6 or 1.2.4.2 I
I R -C O-OC H O
+ R '-C O-OC H O
+
3.1.1.32
3.1.4.3 2.7.1.36
2H+ -
2.3.1.61 +
P OOC C H 2 C H (NH 3 )C OO N
C H 2 OP O C H 2 C H 2 N(C H 3 ) 3 2.7.4.2 OOCCH=CHCOO-
P - O
C H 2 OP O C H 2 C H 2 N(C H 3 ) 3
O -
+
C P P -O C H 2 C H 2 N(C H 3 ) 3
+
OC H 2 C H 2 N(C H 3 ) 3
+
HOC H 2 C H 2 N(C H 3 ) 3 F UMA R A T E
4.3.1.1
A s partyl-P 1 .2
H
C
H2
C
OOC C H 2 C H 2 C ONH
+
NH 3
O
I C holine L E C IT HIN C DP -c holine 2.7.7.15
C holine-P C HOL INE C H 2 C OO UQH 2 6.3.5.4 .1 .1
1 +
HC C H2
C H-C OO
H 2C C H2
C H-C OO
OOC C H 2 C H 2 C ONH OOC C HC H 2 C H 2 C H 2 C H-C OO
+
OOC C H-C H 2 C H 2 C H 2 C HC OO
+
plas malogen 1.3.1.35 2.7.8.2 2.7.1.32 OOC C OOC C
D 2 .7 .8
.3
3.1 .4. 12 C H 3 C (OH)C H 2 C H 2 O P P F ADH 2 +
-OOCCH2CH2CO.SCoA 5.1.99.1 OHC C H 2 C H (NH 3 )C OO N
1.3.1.26
N OOC C OC H 2 C H 2 C H 2 C H-C OO NH 3 NH 3
S erine +NH + + + Diphos pho- S UC C INY L -C oA 5.4.99.2 OOC C H 2 C H 2 C HO A s partyl 4.2.1.52 2, 3-Dihydro- P iperideine- N-S uc c inyl- 2.6.1.17
N-S uc c inyl-2, 63.5.1.18 Diamino- A
S 2.3.1.50 3 NH 3 NH 3 NH 3
mevalonate
F e-S 1.3.5.1
6.2.1.4 S uc c inic S emialdehyde dipic olinate 2, 6-dic arboxylate 2-amino-6-oxo- diaminopimelate pimelate C
C H 3 (C H 2 ) 14 C OC HC H 2 OH C H 3 (C H 2 ) 14 C H(OH)C HC H 2 OH C H 3 (C H 2 ) 12 C H=C HC H(OH)C HC H 2 OH C H 3 (C H 2 ) 12 C H=C HC H(OH)C HC H 2 O- G alac tos e 1.2.1.16
s emialdehyde pimelate
Dehydros phinganin
1.1.1.102
S phinganin 4-S phingenin P s yc hos ine C yt.b F AD
-OOCCH2CH2COO-
S UC C INA T E
OH
+ + + + + + 5 .1 .1
.7 I
H 2 N(C H 2 ) 4 C H(NH 3 )C OO
G anglios ides UDP -S ugars A c yl-C oA
2.4.1.23 UQ II Glycine (C H 3 ) 3 NC H 2 C H(OH)C H 2 C OO (C H 3 ) 3 N(C H 2 ) 3 C H 2 C H(NH 3 )C OO (C H 3 ) 3 N(C H 2 ) 3 C H 2 C H(NH 3 )C OO
4. 1. 1.
20
D
2.4 .1. 62 3.5.1.23 A c yl-C oA 4.1.1.33 2.3.1.37 + C arnitine N 6 -T rimethyl- N 6 -T rimethyllys ine LY S INE 1.5.1.7 - 10
UDP -G alac tos e UQH 2 2H+
H 2 NOC C H 2 C H (NH 3 C OO
1.14.11.1
3-OH-lys ine
1.14.11.8 S
NHAcyl O
+ NHC OR
NHC OR A s paragine 2.6.1.19 C OO
C H 3 (C H 2 ) 12 C H=C HC H(OH)C HC H 2 O P O C H 2 C H 2 N(C H 3 ) 3
O - C H 3 (C H 2 ) 12 C H=C HC H(OH)C HC H 2 OH C H 3 (C H 2 ) 12 C H=C HC H(OH)C HC H 2 O- G alac tos e C H2 5-A mino- +
NH C HC H 2 C H 2 C OO
+ +
S P HING OMY E L IN
2.7.8.3
C eramide C erebros ide C H 3 C -C H 2 C H 2 O P P levulinate 1.3.99.7 OOC C H 2 C H 2 C H 2 C OS C oA OOC C H 2 C H 2 C H 2 C OC OO OOC C H 2 C H 2 C H 2 C H (NH 3 ) C OO OHC C H 2 C H 2 C H 2 C H (NH 3 ) C OO C H 2 C H 2 C H 2 C H 2 C H (NH 3 ) C OO
3.1.4.12 3.2.1.46 2.4.1.47 2UQH 2 UQH 2
1.3.99.7 Is opentenyl-P P 1.10.2.2 + 4.1.1.70
G lutaryl-C oA 2-Oxoadipate 2.6.1.39
2-A minoadipate 1.2.1.31 2-A minoadipate 1.5.1.9
S ac c haropine
R -C H(NH 3 ) C OO
C H3
(C 5) 4H+ OOC C H 2 C H 2 C H 2 NH 2 s emialdehyde
I 2H+ 2-A MINO A C ID A denos yl
L yc opene P hytoene
C H 3 C = C HC H 2 O P P
2e- 2UQ _. 4-A minobutyrate
S (C 40) Dimethylallyl-P P III 1e- _ R -C O-C OO (G A B A ) H 2 N(C H 2 ) 3 NH (C H 2 ) 4 NH (C H 2 ) 3 NH 2
C H 3 -S C H 2 C H 2 C HNH 2
+
(C 40) (C 5) 2-OXO A C ID S permine S -A denos ylmethyl
UQ.
TR A
R Metarhodops in R hodops in O
C H 2O P P G eranyl-P P NA
T IO N G L UT A MA T E 2. 7. 2. +
2.5.1.22 C arbohydrates A mino A c ids
11 P OOC C H C H C H (NH ) C OO
E 1.13.11.21 C H 3O C H3
G eranyl-geranyl-P P (C 10) C yt.c 1 2 2 3 H 2 N(C H 2 ) 4 NH (C H 2 ) 3 NH 2
B ios ynthes is B ios ynthes is
C OO - Ops in C H 3O (C 20) G lutamyl-P S permidine Degradation Degradation
N n
2UQ UQ
R etinoate
O Ubiquinone 2.5.1.10 1.10.2.2
O 1.2.1.36
C HO (C oenzyme Q) OPP C yt.c 1.4.1.2 1.4.1.14 3.5.1.2
6.3.1.2 1.2.1.41
L ipids P urines &
C H2 2.5.1.16
I trans -R etinal 5.2.1.3
11-c is -R etinal C HO Menaquinone C H 2 OH B ios ynthes is P yrimidines
D
L ight P hytol (C 20) ting A
s por . 6 . 1 . 3 T P s y NO 3 - NH 4+ +
H 2 NOC C H 2 C H 2 C H (NH 3 ) C OO + H 2 NC H 2 C H 2 C H 2 C H 2 NH 2
Degradation B ios ynthes is
1.1.1.105 1.1.1.105 n
R etinol es ters P las toquinone C uA C uA +-
tra 3 4 nth 1.6.6.1 G lutamine OHC C H 2 C H 2 C H (NH 3 ) C OO
P utres c ine Degradation
S C H3
F arnes yl-P P os cp 1.7.99.4 .7.1
1.7 .6.4 ATP G lutamic
as
O
H
HO CH3
e
1.6 .1 s emialdehyde
NO 2 -
2.3.1.76 (C 15) C O2
3.1.1.21
C H 2 OH
C H 2 OH
CH3 O
C H3 Heme a 2H+ 1.
18
.6
6.3.4.16 C H 3 C OC OO OHC C OO
V itamins C o-enzymes & Hormones
B ios ynthes is Degradation
S 5.2.1.7 6.3.5.5 C H2 C H2
5
δ F1 P yruvate G lyoxylate
3.
2.5.1.21
T Dark N2
6.
β 2.1.3.3 4.1.1.17
4-Hydroxy-
P
H
AαT 1.5.99.8
H H 1.9.3.1
I HO HO HO HO
Pi
P +1 P i α 1.5.1.2
C H2 C H2
2-oxoglutarate
Human Metabolis m is identified as far pos s ible by black arrows
IV AD P +
H B ios ynthes is Degradation
D P regnenolone C HOL E S T E R OL Des mos terol Zymos terol
H
L anos terol 5.4.99.7
S qualene
1/ O
2 2 H+
H+
+
H 2 NC H 2 C H 2 C H 2 C H (NH 3 ) C OO
2.1.3.3
C H2 C HC OO
1.14.99.7
S (C 30) H+
H+
β
F1 OR NIT HINE
NH
2.6.1.23 C OMP A R T ME NT A T ION
γ 6.3.4.5
P R OL INE
HE MOG L OB IN C HL OR OP HY L L H+
C OO -
C OO -
H2O 1.14.11.2
+
OOC C H(OH)C H 2 C H(NH 3 )C OO
T he "B ackbone" of metabolis m involves
ε H 2 NC ONH 2 OOC C HC H 2 C OO G LY C OLY S IS in the C Y T OP LAS M,
P C H2
C H3
C H2 C H2
C OO - C H2 C OO -
C OO -
COO-
CH2
δ F0 2.1.4.1 UR E A N + HOC H C H2
4-Hydroxy- the T C A C Y C LE (mainly) in the Mitochondrial matrix
O CH H CH H2 C H3 C H C H2 H2 C H3 H+ H 2 NC NHC H 2 C H 2 C H 2 C H (NH 3 ) C OO glutamate
TR A NS L O
CH 2 C H2 - OOC C H2 H2 C H2 CH2
and AT P F OR MAT ION s panning the
C C C C H2 a H+ H+ G lyc ine + 3.5.3.1 A rginino- H 2C C HC OO
MIT OC HONDR IAL INNE R ME MB R ANE
R H 3C CH H 3C CH H3C C H2
H 2C
C
C H2
H2NCH2C=O
α
H+ H+
s NH 2
3.5.3.6
NO s uc c inate
N
H 1.5.1.12
HOC H C H2
N N N N N N 5-A mino- n it An electron flow (an electric current) generated from
P HC Fe CH
H H H H N
H H
N
C OO levulinate
-
1 0 c -s ucb- u +
H 2 NC NHC H 2 C H 2 C H 2 C H (NH 3 ) C OO 1.14.13.39 HC C HC OO
NADH and UQH2 drives the translocation of protons
H
H2C
H H
C H2 H 2C
H H
C H2
H 2C C H2
A HY DR OXY 3-Hydroxy-
N
from the matrix to the intermembrane space.
C
N N N N N N
N
H H
N
- OOC
CH 2 TE
D P R OTONS H+ H+ A R G ININE P R OL INE pyrroline-
The retrolocation of these protons through the F0 subunits
Y H3C
C
C H3 H 3C
C
C H3 H 3C
C
C H3
H 2C C H2 CH 2 4.2.1.24 H+ H+ of ATP synthase to the matrix then supplies the energy
H 2C 4.3.2.1 5-c arboxylate
R C H2
H C H2 C H2 H2 C H2 C H2 H2 C H2
-
OOC C H2
C
H2 C H2
C OO - A DP Pi
+ NH + NH 2 + NH 2 HN C
NH CO
needed to form ATP from ADP and phosphate
I C H2
C OO -
C H2
C OO -
C H2
C OO -
C H2
C OO -
C H2
C OO -
C H2
C OO -
C H2 C H2 H 2C N
H X ATP Y
2
H 2 NC NHC H 2 C OO H 2 NC N(C H 3 )C H 2 C OO P - HNC N(C H 3 )C H 2 C OO
N CH2
1.5.1.2
E lectron F low P roton F low
C OO - C OO -
N H2N
G uanidoac etate
2.1.1.2
C reatine 2.7.3.2 P -C reatine
C H3
S mall Numbers ( eg. 2.4.6.7) refer to the IUB MB E nzyme
1.3.3.4 1.3.3.3 4.1.1.37 4.3.1.8 C reatinine
S HE ME P rotoporphyrinogen C oproporphyrinogen Uroporphyrinogen P orphobilinogen
E ND
E R G O N IC R E A C T IO N
3.5.2.10 C ommis s ion (E C ) R eference Numbers of E nzymes
4.99.1.1 4.2.1.75
© 2003 International Union of Biochemistry and M olecular Biology 22 nd Edition Designed by Donald E. Nicholson, D.Sc., The University of Leeds, England – and Sigma-A ldrich
Product No. M 3907
www.iubmb.org
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Enzyme Commission Numbers
OXIDOREDUCTASES
1.1.1.205 IMP-dehydrogenase
1.18.6.1 Nitrogenase
TRANSFERASES
2.2.1.1 Transketolase
2.2.1.2 Transaldolase
2.4.1.1 Phosphorylase
2.4.1.9 Inulosucrase
2.4.1.17 Glucuronosyltransferase
2.4.2.14 Amidophosphoribosyltransferase
2.4.99.1-11 Sialyltransferases
2.4.99.7 Sialyltransferase
2.5.1.1 Dimethylallyltranstransferase
2.5.1.10 Geranyltranstransferase
2.5.1.21 Farnesyltransferase
2.5.1.29 Farnesyltranstransferase
2.5.1.32 Geranylgeranyl-diphosphate geranylgeranyl transferase
TRANSAMINASES
PHOSPHOTRANSFERASES
2.7.1.1 Hexokinase
2.7.1.2 Glucokinase
2.7.1.3 Ketohexokinase
2.7.1.4 Fructokinase
2.7.1.6 Galactokinase
2.7.1.7 Mannokinase
2.7.1.11 6-Phosphofructokinase
2.7.1.15 Ribokinase
2.7.1.16 Ribulokinase
2.7.1.17 Xylulokinase
2.7.1.19 Phosphoribulokinase
2.7.1.28 Triokinase
2.7.1.53 l-Xylulokinase
CoA-TRANSFERASES
HYDROLASES
3.1.1.4 Phospholipase A2
3.1.1.5 Lysophospholipase
3.1.1.7 Acetylcholinesterase
3.1.1.17 Gluconolactonase
3.1.1.31 6-Phosphogluconolactonase
3.1.1.32 Phospholipase A1
3.1.3.5 54-Nucleotidase
3.1.3.9 Glucose-6-phosphatase
3.1.3.11 Fructose-bisphosphatase
3.1.3.15 Histidinol-phosphatase
3.1.3.27 Phosphatidylglycerophosphatase
3.1.3.29 N-Acylneuraminate-9-phosphatase
3.1.3.31 Nucleotidase
3.1.4.3 Phospholipase C
3.1.4.4 Phospholipase D
3.2.1.21 _-Glucosidase
3.2.1.23 _-Galactosidase
3.2.1.26 _-Fructofuranosidase
3.2.1.45 Glucosylceramidase
3.2.1.46 Galactosylceramidase
3.3.1.1 Adenosylhomocysteinase
3.5.1.1 Asparaginase
3.5.1.2 Glutaminase
3.5.1.6 _-Ureidopropionase
3.5.1.9 Arylformamidase
3.5.1.22 Pantothenase
3.5.1.23 Ceramidase
3.5.2.2 Dihydropyrimidinase
3.5.2.3 Dihydroorotase
3.5.2.5 Allantoinase
3.5.2.7 Imidazolonepropionase
3.5.2.10 Creatininase
3.5.3.1 Arginase
3.5.3.4 Allantoicase
3.6.1.3 Adenosinetriphosphatase
3.6.1.15 Nucleoside-triphosphatase
3.7.1.2 Fumarylacetoacetase
3.7.1.3 Kynureninase
3.9.1.1 Phosphoamidase
LYASES
4.1.2.12 Ketopantoaldolase
4.99.1.1 Ferrochelatase
ISOMERASES
N-(54-Phospho-d-ribosylformimino)-5-amino-1-(544-
5.3.1.16 phosphoribosyl)-
4-imidazolecarboxamide isomerase
5.4.2.2 Phosphoglucomutase
5.4.2.8 Phosphomannomutase
UDP-N-acetylmuramoylalanyl-D-glutamyl-lysine-D-alanyl-D-alanine
6.3.2.10
ligase
UDP-N-acetylmuramoylalanyl-D-glutamate-2,6-diaminopimelate
6.3.2.13
ligase