GapMind for Amino acid biosynthesis

 

Alignments for a candidate for thrC in Acidovorax sp. GW101-3H11

Align threonine synthase (EC 4.2.3.1) (characterized)
to candidate Ac3H11_745 Threonine synthase (EC 4.2.3.1)

Query= BRENDA::P83823
         (351 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_745
          Length = 307

 Score =  103 bits (256), Expect = 8e-27
 Identities = 97/317 (30%), Positives = 150/317 (47%), Gaps = 26/317 (8%)

Query: 22  ISLLEGSTPLIPLKGPEEARKKGIR-LYAKYEGLNPTGSFKDRGMTLAVSKAVEGGAQAV 80
           +SL EG+TP + L  P  A++ GIR L AK+EGLNPTGS KDR    AV++A+   A  V
Sbjct: 1   VSLGEGNTPCLGL--PRLAQRLGIRQLSAKHEGLNPTGSHKDRMSAQAVARALAVDAHKV 58

Query: 81  ACASTGNTAASAAAYAARAGILAIVV----LPAGYV-ALGKVAQSLVHGARIVQVEGNFD 135
             AS+GN A SAAAY A AG+   V     +PA +  AL ++      GAR V  +   D
Sbjct: 59  VLASSGNAAVSAAAYCAAAGLPCEVATYRDMPAPFARALDRL------GARRVAFDQGPD 112

Query: 136 DALRLTQKLTEAFPVALVNSVNP------HRLEGQKTLAFEVVDELGDAPHYHALPVGNA 189
               + +++ E    AL N   P        +EG + +A E V E G  P +  +P    
Sbjct: 113 RWAHVRRQVEEEGAFALTNFSVPAVGSPAFGVEGYRAVALECVAE-GCVPDHVIVPTARG 171

Query: 190 GNITAHWMGYKAYHALGKAKRLPRMLGFQA-AGAAPLVLGRPVERPETLATA--IRIGNP 246
             +   +   +   A G   R+PR+   +  A  + ++ G P +     +TA     G+ 
Sbjct: 172 DLLWGMYSALRDLLAAGLIARMPRLWAVEPFARLSQVLAGAPAQADFGGSTAQFSIAGST 231

Query: 247 ASWQGAVRAKEESGGVIEAVTDEEILFAYRYLAREEGIFCEPASAAAMAGVFKLLREGRL 306
            + Q  +  +   GG +  V D +       L   +G++ E  + A +    +L + G +
Sbjct: 232 VTLQQQIAVQRSGGGAV-VVGDADAARGVAELG-AQGLWVELCAGACVGAAAQLCQHGHI 289

Query: 307 EPESTVVLTLTGHGLKD 323
            P+  V+L LT  G +D
Sbjct: 290 APQDHVLLLLTAKGDRD 306


Lambda     K      H
   0.317    0.134    0.385 

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: 213
Number of extensions: 10
Number of successful extensions: 1
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: 351
Length of database: 307
Length adjustment: 28
Effective length of query: 323
Effective length of database: 279
Effective search space:    90117
Effective search space used:    90117
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: 49 (23.5 bits)

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

Links

Downloads

Related tools

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