GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Sulfuricurvum kujiense DSM 16994

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_013459654.1 SULKU_RS04030 homoserine O-acetyltransferase

Query= SwissProt::Q2T284
         (381 letters)



>NCBI__GCF_000183725.1:WP_013459654.1
          Length = 365

 Score =  300 bits (767), Expect = 6e-86
 Identities = 157/363 (43%), Positives = 221/363 (60%), Gaps = 10/363 (2%)

Query: 10  HTMHFAEPLRLQSGSVLGNYQLVVETYGELNAARSNAVLVCHALNASHHVAGVYADDPRS 69
           H+ HF  PL L+SG +L  Y +V ETYGELN AR N +++CHAL  SHH AG Y  D + 
Sbjct: 7   HSEHFTNPLYLESGRILEPYDIVYETYGELNEARDNVIVICHALTGSHHAAGTYEGDNKP 66

Query: 70  TGWWDNMVGPGKPLDTNRFFVIGVNNLGSCFGSTGPMSIDPATGTPYGARFPVVTVEDWV 129
            GWWD ++G GK +DT+RFFVI  N +GSCFGSTGPMS+      PY  +FPV+T+ D V
Sbjct: 67  -GWWDGLIGQGKAVDTDRFFVICTNVIGSCFGSTGPMSLRYPYNDPYRYKFPVITILDMV 125

Query: 130 HAQARVADAFGIERFAAVMGGSLGGMQALAWSLLYPERVAHCIDIASTPKLSAQNIAFNE 189
            AQ  + D  GI +  AV+GGS+GGMQALA+ + +P      I +A+T       IAFN+
Sbjct: 126 KAQRILFDRLGIHQVHAVIGGSMGGMQALAFGVFFPNFAKKIIAMATTAATQPWAIAFNK 185

Query: 190 VARSAILSDPDFHGGDYYAHGVKPR--RGLRVARMIGHITYLSDDDMAEKFGRALRRADG 247
           VA+ AIL DP+F  G Y    ++     G+ + RM GHI++LS   MA+KFGR  +R DG
Sbjct: 186 VAQEAILKDPEFKNGYYDPEVIRENGLSGMAIGRMAGHISFLSHQSMAKKFGREYKRTDG 245

Query: 248 ALDAYNFNFDVEFEVESYLRYQGDKFADYFDANTYLLITRALDYFDPAKAFNGNLSAALA 307
             + +      +F+VESYL Y G  F  +FD  +YL IT+A++ +D ++ F+ ++  AL 
Sbjct: 246 LFELFG-----KFQVESYLEYNGYNFTKWFDPLSYLYITKAINIYDLSRGFD-SIEEALN 299

Query: 308 HTKAKYLVASFTTDWRFAPARSREIVKALLD-NRRSVSYAEIDAPHGHDAFLLDDARYHN 366
              A+  +  F  D  F P+    I  A+L   + +  Y E+ + +GHDAFL++  +  N
Sbjct: 300 KINAELYLVGFEKDILFLPSEMESIHTAMLAMGKTNSDYLEVVSDYGHDAFLVEIDKIEN 359

Query: 367 LVR 369
            VR
Sbjct: 360 YVR 362


Lambda     K      H
   0.322    0.136    0.417 

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: 381
Number of extensions: 20
Number of successful extensions: 5
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: 381
Length of database: 365
Length adjustment: 30
Effective length of query: 351
Effective length of database: 335
Effective search space:   117585
Effective search space used:   117585
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 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