GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Pseudomonas stutzeri RCH2

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate GFF2318 Psest_2366 Homoserine acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>FitnessBrowser__psRCH2:GFF2318
          Length = 340

 Score = 94.0 bits (232), Expect = 6e-24
 Identities = 102/340 (30%), Positives = 144/340 (42%), Gaps = 44/340 (12%)

Query: 31  LALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGFHAETDRKPGWWDSA- 89
           + L+ G  L +  L Y+  G  N    N VLI     G H               W S  
Sbjct: 16  MRLENGERLRNARLCYQVVGTPNRARDNLVLIPSYYGGTH---------------WGSLP 60

Query: 90  -IGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPIVTVKDWVHAQYRL 148
            +G   P+    + VV L NL G   ST P +  P  G     DFP V++ D V AQ  L
Sbjct: 61  LLGADGPLAGGEYCVV-LTNLFGAGWSTSPSNAAPGQG---AADFPRVSLLDNVRAQKAL 116

Query: 149 MQYLGLSGW--AAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSAQNIAFNEVARQ 206
           +  L    W  A V G S+GGMQ L W++ YP+ V   +           N  F E  + 
Sbjct: 117 LDRLYGEDWQLALVTGWSMGGMQTLFWAMAYPERVRAILPFCCTAHCWPHNRVFLEGVKA 176

Query: 207 AIITDPEFYGGRYADHNALPRRGL-MLARMLGHITYLSDDAMRAKFGRELRAGQVQYGFD 265
           A+  D  + GGRY   +  P RGL    R      Y S    R +  REL       GF+
Sbjct: 177 ALCADAAWLGGRY---SVPPERGLRAFGRAYAGWAY-SQAFYRQELWREL-------GFE 225

Query: 266 VEFQVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQA-SNDDLVAALAEVKAHFLVV 324
               +E+ L Y     +++ DAN  L +       DPA++ +   L  AL  V+A  +++
Sbjct: 226 ---SLEALLDYWEQDHLEQ-DANDLLCVLHTWQSADPARSFAAGSLAEALGRVRARSILM 281

Query: 325 SFTSDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDA 364
             +SD  F+ E +R    A L  G ++    +ES+ GH A
Sbjct: 282 PGSSDLYFTVEDARH--EAALIPGAELRV--LESDWGHCA 317


Lambda     K      H
   0.320    0.135    0.412 

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: 341
Number of extensions: 20
Number of successful extensions: 2
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: 403
Length of database: 340
Length adjustment: 30
Effective length of query: 373
Effective length of database: 310
Effective search space:   115630
Effective search space used:   115630
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: 49 (23.5 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