GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Beijerinckia mobilis UQM 1969

Align Homoserine O-succinyltransferase; HST; EC 2.3.1.46; Homoserine transsuccinylase; HTS (uncharacterized)
to candidate WP_280949203.1 DL88_RS09745 alpha/beta fold hydrolase

Query= curated2:B1YPU9
         (381 letters)



>NCBI__GCF_000745425.1:WP_280949203.1
          Length = 361

 Score =  108 bits (269), Expect = 3e-28
 Identities = 96/321 (29%), Positives = 141/321 (43%), Gaps = 41/321 (12%)

Query: 9   PQTMHFAEPLRLQSGSVIGNYQLVVETYGELNAARSNAVLVCHALNASHHVAGVYADDPR 68
           P  +H   P  L++G  I N QL   T+GEL+AA  NA+L     + +  +         
Sbjct: 26  PFEIHDLGPFLLENGGTIRNLQLAYATFGELSAAGDNAILFPTWYSGTTKILE------- 78

Query: 69  STGWWDNLVGPGKPLDTNRFFVIGVNNLGSCFGSTGPMSIDPSSGKPYGA-RFPVVTVED 127
                   +GPG+ LD +R+F+I VN +G+     G  S   ++  P+ A RFP+V++ D
Sbjct: 79  -----QAYIGPGRALDPDRYFIILVNQIGN-----GLSSAPSNNPAPFNAARFPLVSIGD 128

Query: 128 WVHAQAR-VADAFGIERFAAVMGGSLGGMQALAWSLMYPERVAHCIDIASTPKLSAQNIA 186
            V AQ R V + FG+ R   V+GGS+G  Q   W++ YPE V     IA T + SA N  
Sbjct: 129 DVRAQHRLVTEHFGLTRLQLVLGGSMGAQQTYEWAVRYPEFVRRAAPIAGTARASAHNQL 188

Query: 187 FNEVARSAILSDPDFHGGDYYAHGVKPKRGLRVARMIGHITYLSDDDMAEKFGRALRRAD 246
             E    AI SD  +  G +Y +     RGLR    +      +    AE+  R L    
Sbjct: 189 LVESFIEAITSDRAYDNG-WYDNAGDIHRGLRRHARLFATAAFTPRLYAEEGWRDL---- 243

Query: 247 GALDAYNFSFDVEFE---VESYLRYQGDKFADYFDANTYLLITRALDYFDPAKAFDGNLT 303
                  FS   +F    VE +   Q        D N  +L+ R     D  +   G++ 
Sbjct: 244 ------GFSSTEDFLTGFVEGHFLPQ--------DPNNLILLARKWQGGDVGRNSGGDIK 289

Query: 304 AALAHTQAKYLIASFSTDWRF 324
            AL+H  A   + +   D  F
Sbjct: 290 KALSHIIATTYVIAIDEDGLF 310


Lambda     K      H
   0.321    0.136    0.415 

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: 348
Number of extensions: 24
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 381
Length of database: 361
Length adjustment: 30
Effective length of query: 351
Effective length of database: 331
Effective search space:   116181
Effective search space used:   116181
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: 49 (23.5 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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