GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Bradyrhizobium sp. BTAi1

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_012047258.1 BBTA_RS35155 hypothetical protein

Query= SwissProt::A9I0E6
         (424 letters)



>NCBI__GCF_000015165.1:WP_012047258.1
          Length = 341

 Score =  120 bits (302), Expect = 5e-32
 Identities = 110/339 (32%), Positives = 150/339 (44%), Gaps = 40/339 (11%)

Query: 42  LASGQSLQSYELAVETYGTLNAGRTNAVLVCHALNASHHVAGLAADDPNDVGWWDNMVGP 101
           L SG ++ S  LA +TYGTLNA + N +L   + +A H           D  W   +VGP
Sbjct: 17  LQSGATVPSLRLAYKTYGTLNAAKDNVILYPTSFSAQHV----------DTEW---LVGP 63

Query: 102 GKPLDTNRFFVIGVNNLGSCFGSTGPASINPATGHPWGAAFPVLTVEDWVHAQARLADH- 160
              LD++R+F+I  N  G+   S+      P+   P  A FP ++  D V  Q RL +  
Sbjct: 64  ADILDSDRYFIIIPNLFGNGLSSS------PSNTPPADAPFPAISYHDAVAIQRRLVEEQ 117

Query: 161 FGIERFAAVMGGSLGGMQALSWAITCPERVAHCIVIASTPRLSAQNIGFNEVARRAIITD 220
           FGI R A V G S+GGMQA  WA   P+ V    V+  + R S  N  F +  + A+I D
Sbjct: 118 FGITRIALVYGWSMGGMQAYHWAACHPDMVERAAVVCGSARCSPYNHVFLDAVKAALIAD 177

Query: 221 PDFHGGDYYAHNTVPRRGLSVARMIGHITYLSDDDMAEKFGRTQREPAEGGAYRYGYDVE 280
           P +  G + A    P  GL   R +G I   +   M+ +F R +    +G A +      
Sbjct: 178 PAYKNGRFVAK---PVAGL---RAMGRI--YAGWAMSYEFYRDEVWREQGFAAQ------ 223

Query: 281 FEVESYLRYQGEKFSRYFDANTYLLITRALDYFDPAR--GTGGDLARALKPAQADFLLVS 338
              E YL    +    + DAN  L         D +     GGDL RAL    A  LL+ 
Sbjct: 224 ---EDYLAATWDTAFAHRDANNLLAQIAIWQNGDISHCSAFGGDLDRALSAITAHMLLMP 280

Query: 339 FSTDWRFPPERSREIVRALLKNGSPVTYAEIDAPHGHDA 377
             TD R+   R  E     L N S      I + HGH A
Sbjct: 281 GQTD-RYFDWRDNERELPKLVNASSAVLRPIPSIHGHRA 318


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: 347
Number of extensions: 21
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: 341
Length adjustment: 30
Effective length of query: 394
Effective length of database: 311
Effective search space:   122534
Effective search space used:   122534
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 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