GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hom in Sinorhizobium fredii NGR234

Align Homoserine dehydrogenase; HDH; EC 1.1.1.3 (uncharacterized)
to candidate YP_002822914.1 NGR_b07030 homoserine dehydrogenase

Query= curated2:Q58997
         (336 letters)



>NCBI__GCF_000018545.1:YP_002822914.1
          Length = 359

 Score =  222 bits (565), Expect = 1e-62
 Identities = 131/340 (38%), Positives = 197/340 (57%), Gaps = 9/340 (2%)

Query: 2   DIIIVGFGAIGKGIAKVLYDKKDYLKKNYE-EFKVVAITDSS-GAAIDEDGLDLLKAIEV 59
           +I ++GFG + + +A+++  K    +++      +VA++D   G+ I  +GLD    +E 
Sbjct: 12  NIALIGFGGVNRALAELIATKNPLWERDLGFRLNIVAVSDLYLGSVISPNGLDAKTLVEA 71

Query: 60  KEKTGKIKNYPEKGREMSSIDVIKEVDADVVVEVTPSNLETGDPAKTHILESFKNKKHVV 119
               G          E  +  +IK   AD++VE T +N + G+PA +H   + ++ KHVV
Sbjct: 72  NFAKGGFGQLSGGSAEADNETIIKTAPADLIVEATFTNPKDGEPAVSHCRWALQSGKHVV 131

Query: 120 TANKGPLALCYKELIEEAKKHGVIFRHEASVGGAMPIINLAKETLAGNEILSIRGILNGT 179
           T NKGP+A+  +EL   A  +GV F +E SV    P+I +A+ TLAG E+    GILNGT
Sbjct: 132 TTNKGPVAIAAQELKAVAHANGVHFEYEGSVMSGTPVIRMAERTLAGAEVKGFEGILNGT 191

Query: 180 TNYILTKMEKEGLDFETALKEAKELGIAETDPTQDIEGLDTAAKIVILANSIMGMNKTIK 239
           +N++L +ME  GLDF TA+KEA+ LG AE DPT D+EG D   K+VILAN ++G +   +
Sbjct: 192 SNFVLGRME-GGLDFATAVKEAQILGYAEADPTADVEGFDVRLKVVILANELLGASLKPE 250

Query: 240 DVKVKGISRITPEALFLANKRGYTIKLIGQI---KDGYLI--VEPMLVPIDSPL-NVKGT 293
           +V  KGIS+++P  +  A       KL+G     +DG +   V P  +P + PL  V G 
Sbjct: 251 EVTCKGISKLSPSDIENAAAANSRWKLVGSAVRNEDGTVTGSVSPKQLPFEHPLAGVNGA 310

Query: 294 LNVAMFETDLAKEVVVVGRGAGPIETASAILSDLIHIYNS 333
            N     T+L   V + G GAG IETA A+LSD+I I+N+
Sbjct: 311 TNAVSLNTELLGSVTITGPGAGRIETAYALLSDIIAIHNA 350


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: 298
Number of extensions: 14
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: 336
Length of database: 359
Length adjustment: 29
Effective length of query: 307
Effective length of database: 330
Effective search space:   101310
Effective search space used:   101310
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.

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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