2.7.7.38: 3-deoxy-manno-octulosonate cytidylyltransferase

This is an abbreviated version!
For detailed information about 3-deoxy-manno-octulosonate cytidylyltransferase, go to the full flat file.

Word Map on EC 2.7.7.38

2.7.7.38

lipopolysaccharide

medicine

3-deoxy-d-manno-2-octulosonate

2-deoxy

capsular

cytidylytransferase

agriculture

analysis

Reaction

Synonyms

2-keto-3-deoxy-D-manno-octulosonate cytidylyltransferase, 2-keto-3-deoxyoctonate cytidylyltransferase, 3-deoxy-D-manno-octulosonate cytidylyltransferase, 3-deoxy-manno-octulosonate cytidylyltransferase, arabinose-5-phosphate isomerase, At1g53000, CKS, CMP-3-deoxy-D-manno-octulosonate pyrophosphorylase, CMP-3-deoxy-D-manno-octulosonate synthetase, CMP-KDO synthetase, CMP/KDO synthase, CMP:KDO synthase, CTP:CMP-3-deoxy-D-manno-octulosonate cytidylyltransferase, cytidine monophospho-3-deoxy-D-manno-octulosonate pyrophosphorylase, cytidine monophospho-3-deoxy-D-manno-octulosonate synthetase, K-CKS, K-KDO-CT, Kdo cytidylyltransferase, KDO-CT, KdsB, KpsF, L-CKS, L-KDO-CT

ECTree

2 Transferases

2.7 Transferring phosphorus-containing groups

2.7.7 Nucleotidyltransferases

2.7.7.38 3-deoxy-manno-octulosonate cytidylyltransferase

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Results	in table
1	Activating Compound
20711	AA Sequence
9	Application
1	CAS Registry Number
15	Cloned(Commentary)
7	Crystallization (Commentary)
1	General Information
1	General Stability
3	IC50 Value
19	Inhibitors
2	kcat/KM [mM/s]
2	Ki Value [mM]
29	KM Value [mM]
5	Localization
27	Metals/Ions
13	Molecular Weight [Da]
64	Natural Substrates/ Products (Substrates)
439	Organism
5	Pathway
50	PDB ID
9	pH Optimum
4	pH Range
1	pH Stability
3	pI Value
12	Purification (Commentary)
1	Reaction
2	Reaction Type
72	Reference
5	Specific Activity [micromol/min/mg]
6	Storage Stability
103	Substrates and Products (Substrate)
11	Subunits
57	Synonyms
1	Systematic Name
1	Temperature Optimum [°C]
1	Temperature Range [°C]
1	Temperature Stability [°C]
11	Turnover Number [1/s]

Inhibitors

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Inhibitors on EC 2.7.7.38 - 3-deoxy-manno-octulosonate cytidylyltransferase

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((2-(1-((5-fluoropyridin-2-yl)methyl)-1,6-dihydropyridin-2-yl)-6-methyl-1,4-dihydropyrimidin-4-yl)amino)(2-methyl-2,3-dihydro-1H-pyrazol-4-yl)methanol

Acinetobacter baumannii

A3M4Z0

761537

(1R,4S,5R)-3-[2-[(S)-1-((S)-1-carboxy-ethylcarbamoyl)-ethylamino]-ethyl]-4,5-dihydroxy-cyclohexanecarboxylic acid

Escherichia coli

661340

(Z)-4-((2'-methoxy-[1,1'-biphenyl]-3(2H)-ylidene)methyl)-N-(pyridin-1(4H)-ylmethyl)-4H-pyran-4-carboxamide

Acinetobacter baumannii

A3M4Z0

761537

1-(4-(3-((4,5-dimethylthiazol-2-yl)amino)pyrazin-2-yl)pyridin-1(2H)-yl)-3-(2-methyl-2,5-dihydrothiazol-4-yl)propan-1-ol

Acinetobacter baumannii

A3M4Z0

761537

2,6-Anhydro-3-deoxy-D-glycero-D-talo-octanoate

4 entries

2-(4-chloro-3-methylphenoxy)-1-(3-(5-(2-hydroxypropan-2-yl)-2-methyl-2,3-dihydrofuran-2-yl)-2-oxa-8-azaspiro[4.5]deca-6,9-dien-8-yl)-2-methylpropan-1-ol

Acinetobacter baumannii

A3M4Z0

761537

4,5,6,7-tetrachloro-2',4',5',7'-tetraiodofluorescein

3 entries

4-(3-fluorophenoxy)-1-(4-((5-methylisoxazol-3-yl)methoxy)benzyl)pyrrolidin-3-ol

Acinetobacter baumannii

diphosphate

weak inhibition

Hg2+

strong inhibition

additional information

5 entries