Align Acetolactate synthase small subunit; EC 2.2.1.6; Acetohydroxy-acid synthase small subunit; AHAS; ALS (uncharacterized)
to candidate CA265_RS15810 CA265_RS15810 acetolactate synthase small subunit
Query= curated2:P37252 (172 letters) >FitnessBrowser__Pedo557:CA265_RS15810 Length = 212 Score = 101 bits (251), Expect = 9e-27 Identities = 58/154 (37%), Positives = 89/154 (57%), Gaps = 2/154 (1%) Query: 5 ITLTVVNRSGVLNRITGLFTKRHYNIESITVGHTETAGVSRITFVVHVEGENDVEQLTKQ 64 IT+ NR G+LNRI +F+KR NIES+ +E G+ R V+H EG V +L +Q Sbjct: 24 ITVYAENRIGLLNRIAIIFSKRKINIESLNTSPSEIDGIHRFNIVIH-EGYEVVRKLARQ 82 Query: 65 LNKQIDVLKVTDITNQSIVQRELALIKV-VSAPSTRTEINGIIEPFRASVVDVSRDSIVV 123 + KQI+VLKV TN+ I+ +ELAL KV + + + ++ + AS V + +D V Sbjct: 83 IEKQIEVLKVYFNTNEEIIWQELALYKVSTDEIAEKVTVERLLRQYGASAVVIRKDYTVF 142 Query: 124 QVTGESNKIEALIELLKPYGIKEIARTGTTAFAR 157 VTG + +AL++ L+PY + E R+ A + Sbjct: 143 AVTGHREETDALVKALEPYELIEFVRSARVAIIK 176 Lambda K H 0.315 0.131 0.340 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: 78 Number of extensions: 4 Number of successful extensions: 3 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: 172 Length of database: 212 Length adjustment: 20 Effective length of query: 152 Effective length of database: 192 Effective search space: 29184 Effective search space used: 29184 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 (21.6 bits) S2: 44 (21.6 bits)
Align candidate CA265_RS15810 CA265_RS15810 (acetolactate synthase small subunit)
to HMM TIGR00119 (ilvN: acetolactate synthase, small subunit (EC 2.2.1.6))
# hmmsearch :: search profile(s) against a sequence database # HMMER 3.3.1 (Jul 2020); http://hmmer.org/ # Copyright (C) 2020 Howard Hughes Medical Institute. # Freely distributed under the BSD open source license. # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # query HMM file: ../tmp/path.aa/TIGR00119.hmm # target sequence database: /tmp/gapView.23148.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR00119 [M=158] Accession: TIGR00119 Description: acolac_sm: acetolactate synthase, small subunit Scores for complete sequences (score includes all domains): --- full sequence --- --- best 1 domain --- -#dom- E-value score bias E-value score bias exp N Sequence Description ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 1.3e-31 95.8 3.1 1.6e-31 95.5 3.1 1.1 1 lcl|FitnessBrowser__Pedo557:CA265_RS15810 CA265_RS15810 acetolactate synth Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__Pedo557:CA265_RS15810 CA265_RS15810 acetolactate synthase small subunit # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 95.5 3.1 1.6e-31 1.6e-31 3 156 .. 22 176 .. 20 178 .. 0.96 Alignments for each domain: == domain 1 score: 95.5 bits; conditional E-value: 1.6e-31 TIGR00119 3 hvlsvlvenepGvLsrvsGlfarrgfniesltvgeteekdlsrmtivvegddkvveqiekqleklvdv 70 +++v en+ G L+r++ +f++r+ niesl + +e +++ r iv++ +vv ++ +q+ek+++v lcl|FitnessBrowser__Pedo557:CA265_RS15810 22 YTITVYAENRIGLLNRIAIIFSKRKINIESLNTSPSEIDGIHRFNIVIHEGYEVVRKLARQIEKQIEV 89 5799999************************************************************* PP TIGR00119 71 lkvldlteseivkrelvlvkvsalg.eerneikelteifrgrvvDvsedslivelsgkedkisaflkl 137 lkv t++ei+ +el+l kvs+ e+ +++l +++++ v + +d ++ ++g+ + +a++k+ lcl|FitnessBrowser__Pedo557:CA265_RS15810 90 LKVYFNTNEEIIWQELALYKVSTDEiAEKVTVERLLRQYGASAVVIRKDYTVFAVTGHREETDALVKA 157 *********************9976257889************************************* PP TIGR00119 138 lkefgikevarsGlvalsr 156 l+++ + e +rs va+ + lcl|FitnessBrowser__Pedo557:CA265_RS15810 158 LEPYELIEFVRSARVAIIK 176 ***************9876 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (158 nodes) Target sequences: 1 (212 residues searched) Passed MSV filter: 1 (1); expected 0.0 (0.02) Passed bias filter: 1 (1); expected 0.0 (0.02) Passed Vit filter: 1 (1); expected 0.0 (0.001) Passed Fwd filter: 1 (1); expected 0.0 (1e-05) Initial search space (Z): 1 [actual number of targets] Domain search space (domZ): 1 [number of targets reported over threshold] # CPU time: 0.01u 0.00s 00:00:00.01 Elapsed: 00:00:00.00 # Mc/sec: 5.60 // [ok]
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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