GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hom in Desulfacinum hydrothermale DSM 13146

Align Homoserine dehydrogenase; HDH; EC 1.1.1.3 (uncharacterized)
to candidate WP_084056978.1 B9A12_RS05960 homoserine dehydrogenase

Query= curated2:Q58997
         (336 letters)



>NCBI__GCF_900176285.1:WP_084056978.1
          Length = 362

 Score =  235 bits (599), Expect = 1e-66
 Identities = 134/337 (39%), Positives = 200/337 (59%), Gaps = 8/337 (2%)

Query: 2   DIIIVGFGAIGKGIAKVLYDKKDYLKKNYE-EFKVVAITDSSGAAIDEDGLDLLKAIEVK 60
           +I+++GFG +G+  A+++ +K+D L   Y   F   AI D  GA +D  G   +  I   
Sbjct: 8   NILLLGFGNVGRAFARLVAEKRDELAGRYGVSFGFSAIVDIGGAVVDPAGTLPVLDIHRH 67

Query: 61  EKTGK-IKNYPEKGRE-MSSIDVIKEVDADVVVEVTPSNLETGDPAKTHILESFKNKKHV 118
              GK ++ +PE GR  + +++ I+ V  DV+VE TP+ L  G+PA+TH+LE  +   HV
Sbjct: 68  VAAGKALEEFPELGRPGLGALEAIRTVPCDVMVEATPTCLRDGEPARTHVLEGLRAGCHV 127

Query: 119 VTANKGPLALCYKELIEEAKKHGVIFRHEASVGGAMPIINLAKETLAGNEILSIRGILNG 178
           ++ANKGP    Y  ++E A + G+     A+   A+P +++A+  LAG+ ILS+ GILNG
Sbjct: 128 ISANKGPFIWAYDTIMEAAMERGLAVGLSAATAAALPTLDVAELCLAGSRILSVEGILNG 187

Query: 179 TTNYILTKMEKEGLDFETALKEAKELGIAETDPTQDIEGLDTAAKIVILANSIMGMNKTI 238
           TTNYILT+M + G  +E  L EA+ LGIAETDP  D+EG DTA K++++AN +     T 
Sbjct: 188 TTNYILTRMHQTGCAYEDGLGEAQRLGIAETDPRLDVEGWDTANKLILIANRVFHAGLTP 247

Query: 239 KDVKVKGISRITPEALFLANKRGYTIKLIGQIKDG----YLIVEPMLVPIDSPL-NVKGT 293
           +DV V+GI+ +TPE +  A   G  IKLIG+I        + V P  +P D PL  V G+
Sbjct: 248 RDVAVQGITSVTPERIRRARDEGRVIKLIGRIAPSSHPVRVSVGPEALPGDHPLAAVSGS 307

Query: 294 LNVAMFETDLAKEVVVVGRGAGPIETASAILSDLIHI 330
                FETD    + V G  + P+  A+A+L D + I
Sbjct: 308 EKAVSFETDSMGRITVSGGHSSPLGAAAALLKDALRI 344


Lambda     K      H
   0.314    0.135    0.366 

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: 272
Number of extensions: 9
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: 336
Length of database: 362
Length adjustment: 29
Effective length of query: 307
Effective length of database: 333
Effective search space:   102231
Effective search space used:   102231
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 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