Align Putative acetolactate synthase large subunit IlvX; ALS; EC 2.2.1.6; Acetohydroxy-acid synthase large subunit; AHAS (uncharacterized)
to candidate CCNA_00397 CCNA_00397 acetolactate synthase
Query= curated2:O53554 (515 letters) >FitnessBrowser__Caulo:CCNA_00397 Length = 512 Score = 464 bits (1195), Expect = e-135 Identities = 263/514 (51%), Positives = 316/514 (61%), Gaps = 6/514 (1%) Query: 1 MNGAQALINTLVDGGVDVCFANPGTSEMHFVAALDAVPRMRGMLTLFEGVATGAADGYAR 60 MNGA ALI TL D GV CFANPGTSEM FV+ALD PRMR +L LFEGVATGAADGY R Sbjct: 1 MNGADALITTLADNGVTACFANPGTSEMQFVSALDREPRMRSVLCLFEGVATGAADGYGR 60 Query: 61 IAGRPAAVLLHLGPGLGNGLANLHNARRARVPMVVVVGDHATYHKKYDAPLESDIDAVAG 120 +AG+PA LLHLGPG NG ANLHNARRA P+V V+GDHATYH+ +DAPL SDI A+A Sbjct: 61 MAGKPACTLLHLGPGYANGAANLHNARRAFTPVVNVIGDHATYHRDFDAPLNSDIAALAA 120 Query: 121 TVSGWVRRTEAAADVG-ADAEAAIAASRSGSQIATLILPADVCWSDGAHAAAGVPAQAAA 179 S WV+ E A VG AEA IAA + A L+LPAD W++ V A A Sbjct: 121 PNSVWVKSAETADSVGPLAAEAIIAAYGTPGGNACLVLPADAAWNEATVKGPMVTPPAFA 180 Query: 180 AP--VDVGPVAGVLRSGEPAMMLIGGDATRGPGLTAAARIVQATGARWLCETFPTCLERG 237 AP V VA L ++L+G A L AA R+ A G R L +TF RG Sbjct: 181 APDAASVEAVAKALGGATKPVLLLGSGACGEAALAAAGRLA-AHGVRVLTDTFTARQARG 239 Query: 238 AGIPAVERLAYFAEGAAAQLDGVKHLVLAGARSPVSFFAYPGMPSDLVPAGCEVHVL-AE 296 G ++L YF E A LDGV +VL ++PV+FFAYP PS LVP GC V L Sbjct: 240 EGRFRPDKLPYFGELALKDLDGVDLIVLVATQTPVAFFAYPDRPSVLVPEGCSVETLCGR 299 Query: 297 PGGAADALAALADEVAPGTVAPVAGASRPQLPTGDLTSVSAADVVGALLPERAIVVDESN 356 AA AL ALAD + PV + P P G L + + + +P I+ D++ Sbjct: 300 EVDAAAALNALADALGAPAAGPVETYAAPDAPAGRLDAWAIGAAIARHMPTDTIISDDAV 359 Query: 357 TCGVLLPQATAGAPAHDWLTLTGGAIGYGIPAAVGAAVAAPDRPVLCLESDGSAMYTISG 416 T G+ + T A AHDWL+LTGGAIG GIP A+GAAVA PDR VL L DG+ MYT+ G Sbjct: 360 TAGLPIFTQTKAARAHDWLSLTGGAIGQGIPLAIGAAVACPDRKVLALTGDGAGMYTVQG 419 Query: 417 LWSQARENLDVTTVIYNNGAYDILRIELQRVGAGSDPGPKALDLLDISRPTMDFVKIAEG 476 LW+ RE LDVT V++ N AY IL IEL R GAG +PGP A LLD+ P +D+VK+AEG Sbjct: 420 LWTVVREKLDVTVVVFANHAYRILGIELGRTGAG-NPGPAAAKLLDLGDPRIDWVKLAEG 478 Query: 477 MGVPARRVTTCEEFADALRAAFAEPGPHLIDVVV 510 +G+ A RV T E F +A A A PGP LI+ + Sbjct: 479 LGMAAERVATAEAFEEAFARAMATPGPRLIEAAM 512 Lambda K H 0.318 0.134 0.402 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 613 Number of extensions: 25 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 515 Length of database: 512 Length adjustment: 35 Effective length of query: 480 Effective length of database: 477 Effective search space: 228960 Effective search space used: 228960 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory