GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Echinicola vietnamensis KMM 6221, DSM 17526

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate Echvi_3285 Echvi_3285 homoserine O-acetyltransferase

Query= SwissProt::A9I0E6
         (424 letters)



>FitnessBrowser__Cola:Echvi_3285
          Length = 351

 Score =  211 bits (537), Expect = 3e-59
 Identities = 132/365 (36%), Positives = 189/365 (51%), Gaps = 30/365 (8%)

Query: 29  VTPQLIRFDTPLPLASGQSLQSYELAVETYGTLNAGRTNAVLVCHALNASHHVAGLAADD 88
           +T +    +  L L SG+SL  +E++  T G L   + N + + HAL            D
Sbjct: 12  MTQETFHCEEELNLESGESLPGFEISYTTQGHLTPKKDNVIWILHALTG----------D 61

Query: 89  PNDVGWWDNMVGPGKPLDTNRFFVIGVNNLGSCFGSTGPASINPATGHPWGAAFPVLTVE 148
            N   WW  +VG  K  D  ++F++  N LGSC+GST P S NP TG P+   FP L+  
Sbjct: 62  ANVHEWWSGLVGEDKFFDPTKYFIVCANLLGSCYGSTQPLSDNPKTGKPYYYDFPNLSTR 121

Query: 149 DWVHAQARLADHFGIERFAAVMGGSLGGMQALSWAITCPERVAHCIVIASTPRLSAQNIG 208
           D   A  RL  H GI++   ++GGSLGG  AL W+    E+V   I++AS  + S   IG
Sbjct: 122 DMAKAFDRLRQHLGIQQIDTIIGGSLGGQVALEWSYNLQEQVKKTIIVASNAKTSPWTIG 181

Query: 209 FNEVARRAIITDPDFHGGDYYAHNTVPRRGLSVARMIGHITYLSDDDMAEKFGRTQREPA 268
           FNE  R AI +D  +      A     ++GL  AR IG ++Y   D     F  +Q E  
Sbjct: 182 FNEAQRMAIESDSTWGQNSPDA----GKKGLEAARAIGMLSYRHQD----IFHASQAETE 233

Query: 269 EGGAYRYGYDVEFEVESYLRYQGEKFSRYFDANTYLLITRALDYFDPARGTGGDLARALK 328
           E   +       F V SYLRYQG+K S  F+A +Y ++T+A+D  D  RG GG  A+AL 
Sbjct: 234 EKTDH-------FRVSSYLRYQGQKLSNRFNALSYWVLTKAMDSHDLGRGRGG-TAKALS 285

Query: 329 PAQADFLLVSFSTDWRFPPERSREIVRALLKNGSPVTYAEIDAPHGHDAFLLDDARYHAV 388
             +A  L +  +TD  F  E S+ I     KN    TY EI + +GHDAFL+++ + + +
Sbjct: 286 AIKAKVLSIGINTDLLFTKEESQFI----SKNVPNGTYREISSIYGHDAFLVENEQLNYI 341

Query: 389 VRGYY 393
           +  +Y
Sbjct: 342 LTSFY 346


Lambda     K      H
   0.320    0.137    0.427 

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: 356
Number of extensions: 20
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: 424
Length of database: 351
Length adjustment: 30
Effective length of query: 394
Effective length of database: 321
Effective search space:   126474
Effective search space used:   126474
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: 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