GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Desulfovibrio zosterae DSM 11974

Align branched-chain-amino-acid aminotransferase; EC 2.6.1.42 (characterized)
to candidate WP_027722494.1 H589_RS0113395 branched-chain amino acid transaminase

Query= CharProtDB::CH_024500
         (309 letters)



>NCBI__GCF_000425265.1:WP_027722494.1
          Length = 307

 Score =  288 bits (736), Expect = 1e-82
 Identities = 146/303 (48%), Positives = 201/303 (66%), Gaps = 3/303 (0%)

Query: 4   KKADYIWFNGEMVRWEDAKVHVMSHALHYGTSVFEGIRCYDSHKGP-VVFRHREHMQRLH 62
           +KA+ IWF+GE+V W+ A+VHV++H LHYG  VFEGIR Y +  G   VFR REH+ RL 
Sbjct: 3   QKAEKIWFDGELVDWDAAQVHVLTHTLHYGAGVFEGIRAYATADGKSAVFRLREHVVRLF 62

Query: 63  DSAKIYRFPVSQSIDELMEACRDVIRKNNLTSAYIRPLIFVGDVGMGVNPPAGYSTDVII 122
           DSAKI    +  S++E+  A  + ++ N L   YIRPL+F+GD  MGV+P +     V I
Sbjct: 63  DSAKILGITIPFSVEEIHNAILETLKVNGLKEGYIRPLVFIGDGAMGVHPGSN-PIRVCI 121

Query: 123 AAFPWGAYLGAEALEQGIDAMVSSWNRAAPNTIPTAAKAGGNYLSSLLVGSEARRHGYQE 182
           A +PWGAYLG +ALE+GI    SS+NR   N + T +KA GNY++S+L   EA + GY E
Sbjct: 122 ATWPWGAYLGEDALEKGIRVKTSSFNRHHVNAMMTKSKACGNYVNSILAKVEAVKDGYDE 181

Query: 183 GIALDVNGYISEGAGENLFEVKDGVLFTPPFTSSALPGITRDAIIKLAKELGIEVREQVL 242
            + LD  GY+SE  GEN+F VK+G++ TPP T S LPGITR +++K+A++LG EV EQ+ 
Sbjct: 182 ALMLDTQGYVSEATGENIFIVKNGIIKTPPLT-SVLPGITRASLMKVARDLGYEVEEQLF 240

Query: 243 SRESLYLADEVFMSGTAAEITPVRSVDGIQVGEGRCGPVTKRIQQAFFGLFTGETEDKWG 302
           +R+ LY+ADE F  GTAAE+TP+  VD   +G G+ G V   +Q+ +F    G       
Sbjct: 241 TRDELYIADEAFFCGTAAEVTPICEVDNRTIGAGKRGEVGTLLQKEYFNAVKGGNPKYVD 300

Query: 303 WLD 305
           WL+
Sbjct: 301 WLE 303


Lambda     K      H
   0.319    0.136    0.413 

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: 295
Number of extensions: 12
Number of successful extensions: 4
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: 309
Length of database: 307
Length adjustment: 27
Effective length of query: 282
Effective length of database: 280
Effective search space:    78960
Effective search space used:    78960
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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