GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hom in Stenotrophomonas chelatiphaga DSM 21508

Align Homoserine dehydrogenase; HDH; EC 1.1.1.3 (characterized)
to candidate WP_057508710.1 ABB28_RS11205 homoserine dehydrogenase

Query= SwissProt::Q5B998
         (368 letters)



>NCBI__GCF_001431535.1:WP_057508710.1
          Length = 362

 Score =  189 bits (479), Expect = 1e-52
 Identities = 131/370 (35%), Positives = 204/370 (55%), Gaps = 28/370 (7%)

Query: 2   SAPIYLGVIGVGGVGTAFLNQLARLPNA----PKLILLARSSQTLLSPTPSYSPTIPAAE 57
           +AP  L ++G G VGTAF+ +   L +     P+   LA S   L       +P  P   
Sbjct: 11  AAPRRLALLGTGTVGTAFVARYRALQSRGLALPRFDWLANSRAVLACDG---APEQPLHA 67

Query: 58  WKTAVETPSLTKSGALTPDEIATYLASAPGRSILVDNTSDPALASNYPVFLRKGISVVTP 117
            + A   P L  + A  P + A  L +     ++VD T+   +A+ +  +L +G+ VVT 
Sbjct: 68  LRRA---PRLGDAAA--PWKQADSLHAG---DVVVDATASETVAAEHAHWLARGVHVVTA 119

Query: 118 NKKGFSSDLSLWKEIFAAAAEGKALVYHESTVGAGLPVISTLKDLVNTGDEVTRIEGVFS 177
           NK G  +      +I A  A+  A     +TVGAGLP++S+L+ LV  GD + RIEGV S
Sbjct: 120 NKLGQGAHAQRAVQIAAHCADSGARYGDSATVGAGLPLLSSLRALVEGGDRILRIEGVLS 179

Query: 178 GTLSFLFNTFAPASGSSSAKWSEVVSQAKELGYTEPDPRDDLNGMDVARKLTILARIAGL 237
           G+L++LF+ +       S  +S  V +A + G+TEPDPR DL+G DV RKL ILAR +GL
Sbjct: 180 GSLAWLFHRY-----DGSQPFSLAVREALDAGFTEPDPRLDLSGEDVRRKLLILARASGL 234

Query: 238 DVQSPDSFPIESLIPAELTSLPSSADGIAQFMARLPEFDSQMAAIKEGAEKAGKVVRYVG 297
           D+ +     ++SL+PA L +LP      AQ + +L + D+ +      A +AG+V+R++G
Sbjct: 235 DL-ADGQVQVDSLVPAALATLPH-----AQALEQLAQLDAPLHQRWLRAREAGQVLRFIG 288

Query: 298 SVDVAKKEVRVGLQQFDKDSAIAGLKGSDNIISFYTRRYGSNPLIVQGAGAGGDVTAMGV 357
            V+      RVG+Q    D  +A   G+DN ++ ++ RY   PL++QG GAG +VTA  +
Sbjct: 289 CVEAG--AARVGVQSLAADHPLASGAGTDNRVAIHSDRYRDQPLLIQGPGAGAEVTAAAL 346

Query: 358 TADLLKVIER 367
             D+L++  +
Sbjct: 347 LDDVLRIARK 356


Lambda     K      H
   0.314    0.132    0.368 

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: 285
Number of extensions: 14
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: 368
Length of database: 362
Length adjustment: 30
Effective length of query: 338
Effective length of database: 332
Effective search space:   112216
Effective search space used:   112216
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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