MyavA.00213.a: Enoyl-CoA hydratase
Target Characteristics
| from organism: | Mycobacterium avium 104 |
| most recent status: | diffraction |
| center reference id: | MyavA.00213.a |
| is community request: | False |
| associated disease: | Johne's disease, paratuberculosis |
| NIH risk group: | 2 |
| is select agent: | False |
| NIH priority pathogens category: |
IIIC |
Ordering Clones & Proteins
If there are materials available for this target, they will be listed below.
Materials can be ordered from SSGCID using the button in the "order material" column.
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You may order multiple materials at a time at no cost to you, as this contract is funded
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Clones*
| CENTER REFERENCE ID |
DOMAIN/REGION DESCRIPTION |
INFO | AA START |
AA STOP |
ORDER MATERIAL |
|---|---|---|---|---|---|
| MyavA.00213.a.A1.GE28486 | Full length( MyavA.00213.a ) | 1 | 274 | GE28486 |
* SSGCID clones represent un-induced expression constructs which have been verified by sequencing from vector primers. Clones may contain a tag, such as N-term 6xHis. Get sequence information
using the button in the "info" column.
Proteins
| CENTER REFERENCE ID |
DOMAIN/REGION DESCRIPTION |
INFO | AA START |
AA STOP |
ORDER MATERIAL |
|---|---|---|---|---|---|
| MyavA.00213.a.A1.PS00573 | Full length( MyavA.00213.a ) | 1 | 274 |
External Resources
| Resource | Reference ID |
|---|---|
| OrthoMCL: | OG5_129459 |
| PATRIC ID: | fig|243243.7.peg.241 |
| RefSeq: | YP_879538.1 |
| UniProt: | A0A0H3A3H3 |
Enzyme & Pathway Information
| Pathway | Pathway ID | EC Number |
|---|---|---|
| fatty acid beta-oxidation I | FAO-PWY | 4.2.1.17 |
| L-isoleucine degradation I | ILEUDEG-PWY | 4.2.1.17 |
| oleate beta-oxidation | PWY0-1337 | 4.2.1.17 |
| phenylacetate degradation I (aerobic) | PWY0-321 | 4.2.1.17 |
| benzoyl-CoA degradation I (aerobic) | PWY-1361 | 4.2.1.17 |
| fermentation to 2-methylbutanoate | PWY-5109 | 4.2.1.17 |
| fatty acid beta-oxidation II (peroxisome) | PWY-5136 | 4.2.1.17 |
| unsaturated, even numbered fatty acid beta-oxidation | PWY-5138 | 4.2.1.17 |
| superpathway of glyoxylate cycle and fatty acid degradation | PWY-561 | 4.2.1.17 |
| superpathway of phenylethylamine degradation | PWY-6071 | 4.2.1.17 |
| 4-hydroxybenzoate biosynthesis III (plants) | PWY-6435 | 4.2.1.17 |
| fatty acid beta-oxidation VI (peroxisome) | PWY66-391 | 4.2.1.17 |
| pyruvate fermentation to hexanol (engineered) | PWY-6863 | 4.2.1.17 |
| superpathway of cholesterol degradation I (cholesterol oxidase) | PWY-6928 | 4.2.1.17 |
| superpathway of testosterone and androsterone degradation | PWY-6937 | 4.2.1.17 |
| androstenedione degradation | PWY-6944 | 4.2.1.17 |
| superpathway of cholesterol degradation II (cholesterol dehydrogenase) | PWY-6947 | 4.2.1.17 |
| methyl ketone biosynthesis (engineered) | PWY-7007 | 4.2.1.17 |
| 4-coumarate degradation (anaerobic) | PWY-7046 | 4.2.1.17 |
| fatty acid salvage | PWY-7094 | 4.2.1.17 |
| jasmonic acid biosynthesis | PWY-735 | 4.2.1.17 |
| docosahexaenoate biosynthesis III (6-desaturase, mammals) | PWY-7606 | 4.2.1.17 |
| (8E,10E)-dodeca-8,10-dienol biosynthesis | PWY-7654 | 4.2.1.17 |
| Spodoptera littoralis pheromone biosynthesis | PWY-7656 | 4.2.1.17 |
| (4Z,7Z,10Z,13Z,16Z)-docosapentaenoate biosynthesis (6-desaturase) | PWY-7726 | 4.2.1.17 |
| toluene degradation to benzoyl-CoA (anaerobic) | PWY-81 | 4.2.1.17 |
| L-valine degradation I | VALDEG-PWY | 4.2.1.17 |
Sequences
These sequences are the native gene sequence; sequences of constructs derived from these sequences may differ due to codon optimization or other protocols.
To find the specific sequence of any material you may have ordered, click on the "more" button next to the name of that material.
AA Sequence
MAQAYESVTV EKKGHVAQVT LIGPGKGNAM GPAFWSELPE LFETLDADPE VRAIVLTGSG KNFSYGLDVP AMGGSFTPLL SGDALAGPRA VFHREVKRMQ GAITAVADCR TPTIASVHGW CIGGGVDLIS AVDIRYASAD AKFSVREVKL AIVADVGSLA RLPYILNDGH LRELALTGKD IDAARAEKIG LVNDVYADAD ACLAAAHATA AEIAANPPLT VHGIKDVLDQ QRASAVAESL RYVAAWNAAF LPSKDLTEGI AATFEKRPAQ FTGE
NT Sequence
ATGGCGCAAG CATACGAATC GGTCACCGTG GAGAAGAAGG GCCACGTCGC TCAGGTGACG CTGATCGGCC CGGGCAAGGG TAACGCGATG GGGCCGGCCT TCTGGTCCGA GCTGCCCGAG CTGTTCGAAA CGCTGGACGC CGACCCCGAG GTGCGGGCCA TCGTGCTGAC CGGTTCCGGC AAGAACTTCA GCTACGGCCT GGACGTGCCG GCGATGGGCG GATCGTTCAC CCCGCTGCTG TCGGGCGACG CGCTGGCCGG GCCGCGCGCC GTCTTCCACC GCGAGGTCAA GCGGATGCAG GGCGCGATCA CCGCCGTCGC CGACTGCCGC ACCCCCACCA TCGCGTCGGT GCACGGCTGG TGCATCGGCG GCGGCGTCGA CCTCATCTCG GCGGTCGACA TCCGCTACGC CAGCGCCGAC GCCAAGTTCT CGGTGCGCGA GGTCAAGCTG GCCATCGTCG CCGACGTCGG CAGCCTGGCC CGGCTGCCGT ACATCCTCAA CGACGGCCAC CTGCGCGAGC TCGCGCTGAC CGGCAAGGAC ATCGACGCCG CCCGCGCCGA GAAGATCGGG CTGGTCAACG ACGTGTACGC CGACGCCGAC GCGTGCCTGG CCGCCGCGCA TGCCACGGCC GCGGAGATCG CCGCCAACCC CCCGCTGACC GTGCACGGCA TCAAGGATGT CCTCGACCAG CAGCGCGCTT CGGCCGTCGC CGAGAGCCTG CGCTACGTGG CCGCCTGGAA CGCGGCCTTC CTGCCGTCCA AGGACCTCAC CGAGGGCATC GCGGCGACGT TCGAGAAGCG GCCGGCGCAG TTCACCGGCG AG