GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Dechlorosoma suillum PS

Align Valine--pyruvate aminotransferase; Alanine--valine transaminase; EC 2.6.1.66 (characterized)
to candidate Dsui_0132 Dsui_0132 aspartate/tyrosine/aromatic aminotransferase

Query= SwissProt::P96847
         (388 letters)



>FitnessBrowser__PS:Dsui_0132
          Length = 385

 Score =  264 bits (674), Expect = 4e-75
 Identities = 154/375 (41%), Positives = 206/375 (54%), Gaps = 5/375 (1%)

Query: 9   AGVPPFYVMDVWLAAAERQRTHGDLVNLSAGQPSAGAPEPVRAAAAAALHLNQLGYSVAL 68
           A + PF+VM++   A E +    D++++  G+P    PEP+ AAA   L   ++ Y+ AL
Sbjct: 9   ADIAPFHVMELLGRARELEAQGRDIIHMEVGEPDFPTPEPILAAAREFLQDGRVFYTPAL 68

Query: 69  GIPELRDAIAADYQRRHGITVEPDAVVITTGSSGGFLLAFLACFDA-GDRVAMASPGYPC 127
           G+PELR+AI+  Y++R+GI V    + IT G+SG   LA LAC  A G    +  PGYPC
Sbjct: 69  GLPELREAISGFYRQRYGIAVPASRIAITAGASGALTLA-LACLAAPGSEWLLTDPGYPC 127

Query: 128 YRNILSALGCEVVEIPCGPQTRFQPTAQMLAEI-DPPLRGVVVASPANPTGTVIPPEELA 186
            R+ + A     V IP G  + FQPT   L +  +    G + ASPANPTGT++   ELA
Sbjct: 128 NRHFVRAFEGVPVSIPVGAASNFQPTRLDLEQHWNERTAGALFASPANPTGTMLDAAELA 187

Query: 187 AIASWCDASDVRLISDEVYHGLVYQGAPQTSCAWQTSRNAVVVNSFSKYYAMTGWRLGWL 246
            IA +      +LI DE+YHGL Y G   T+ A     N  VV SFSKY+ MTGWRLGWL
Sbjct: 188 DIADFVRQRQGQLIIDEIYHGLTYNGDAPTALA--AGDNIFVVQSFSKYFQMTGWRLGWL 245

Query: 247 LVPTVLRRAVDCLTGNFTICPPVLSQIAAVSAFTPEATAEADGNLASYAINRSLLLDGLR 306
           ++P    R V+ L  N  I     +Q AA++AF PE  A  +   A +   R  L   L 
Sbjct: 246 VIPEPFVRDVEKLAQNLFISASTPAQHAALAAFQPETIALLEQRRAEFKARRDYLAPALE 305

Query: 307 RIGIDRLAPTDGAFYVYADVSDFTSDSLAFCSKLLADTGVAIAPGIDFDTARGGSFVRIS 366
            IG    A  +GAFY+YAD S  T DS  F  +LL + GVAI PGIDF      S VR +
Sbjct: 306 AIGFRITAQPEGAFYLYADCSTLTDDSFGFARRLLEEAGVAITPGIDFGNHGASSHVRFA 365

Query: 367 FAGPSGDIEEALRRI 381
           +      + E + RI
Sbjct: 366 YTNAQARLAEGVERI 380


Lambda     K      H
   0.321    0.136    0.416 

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: 430
Number of extensions: 22
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: 388
Length of database: 385
Length adjustment: 30
Effective length of query: 358
Effective length of database: 355
Effective search space:   127090
Effective search space used:   127090
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 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