GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Halomonas desiderata SP1

Align branched-chain-amino-acid aminotransferase; EC 2.6.1.42 (characterized)
to candidate WP_086511983.1 BZY95_RS21775 branched-chain amino acid transaminase

Query= CharProtDB::CH_024500
         (309 letters)



>NCBI__GCF_002151265.1:WP_086511983.1
          Length = 322

 Score =  232 bits (592), Expect = 8e-66
 Identities = 128/303 (42%), Positives = 184/303 (60%), Gaps = 13/303 (4%)

Query: 8   YIWFNGEMVRWEDAKVHVMSHALHYGTSVFEGIRCYDSHKGPVVFRHREHMQRLHDSAKI 67
           +IW +GE + W DAK H+++H LHYG   FEG+R Y    G  +FR  EH +RL DSA  
Sbjct: 10  WIWLDGEWLPWRDAKTHLLTHTLHYGMGCFEGVRAYAGAHGTHLFRVAEHTRRLLDSAHA 69

Query: 68  YRFPVSQSIDELMEACRDVIRKNNLTSAYIRPLIFVGDVGMGVNPPAGYSTDVIIAAFPW 127
              PV+   + L+EA R  + +N L +AY++P +F G  G+G+    G S  V+IAA+  
Sbjct: 70  LDIPVAFDEEVLIEAQRQCLVRNELRNAYLKPTVFFGAEGLGLR-AKGLSVHVMIAAWDL 128

Query: 128 GAYLGAEALEQGIDAMVSSWNRAAPNTIPTAAKAGGNYLSSLLVGSEARRHGYQEGIALD 187
           G Y+ +EA   G+ A+ SSW R   N     AK  G+Y++S+L  + A + G+ E I LD
Sbjct: 129 GDYVSSEAATLGLRALTSSWARHHVNISLCRAKTNGHYVNSILALNTAVKAGFDEAIMLD 188

Query: 188 VNGYISEGAGENLFEVKDGVLFTPPFTSSALPGITRDAIIKLAKE-LGIEVREQVLSRES 246
             GY++E +  N+F ++DG L TP  T S L GITRD++I LA+E LG+EVRE+ ++R+ 
Sbjct: 189 PEGYVAEASAANVFLLRDGALHTPEVT-SCLQGITRDSVIHLAREVLGLEVRERRITRDE 247

Query: 247 LYLADEVFMSGTAAEITPVRSVDGIQVGEGRCGP----------VTKRIQQAFFGLFTGE 296
           LY ADE F++GTAAEI P+R +DG  +G     P          VT ++QQ +  +  GE
Sbjct: 248 LYTADEAFVTGTAAEILPLRELDGRHIGARAGAPLPGQPIDANSVTAQLQQLYRQVTRGE 307

Query: 297 TED 299
            ED
Sbjct: 308 LED 310


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: 268
Number of extensions: 9
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: 322
Length adjustment: 27
Effective length of query: 282
Effective length of database: 295
Effective search space:    83190
Effective search space used:    83190
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