GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hom in Rhizobium leguminosarum 3841

Align Homoserine dehydrogenase; HDH; EC 1.1.1.3 (uncharacterized)
to candidate WP_011654697.1 RL_RS25505 homoserine dehydrogenase

Query= curated2:Q58997
         (336 letters)



>NCBI__GCF_000009265.1:WP_011654697.1
          Length = 353

 Score =  217 bits (553), Expect = 3e-61
 Identities = 128/340 (37%), Positives = 197/340 (57%), Gaps = 9/340 (2%)

Query: 2   DIIIVGFGAIGKGIAKVLYDKKDYLKKNYE-EFKVVAITDSS-GAAIDEDGLDLLKAIEV 59
           +I ++GFG + + + +++  K    +++      +VA++D   G+ I  +GLD    ++ 
Sbjct: 5   NIALIGFGGVNRALTELIAAKNQLWERDLGFRLNIVAVSDLYLGSVISPNGLDAKTLVDA 64

Query: 60  KEKTGKIKNYPEKGREMSSIDVIKEVDADVVVEVTPSNLETGDPAKTHILESFKNKKHVV 119
           K + G          E  +  +IK   AD+VVE T +N + G+PA +H   + +  KHVV
Sbjct: 65  KFEKGGFGQLSGGSAEADNETIIKTAPADIVVEATYTNPKDGEPAVSHCRWALETGKHVV 124

Query: 120 TANKGPLALCYKELIEEAKKHGVIFRHEASVGGAMPIINLAKETLAGNEILSIRGILNGT 179
           T NKGP+A+    L   AK +GV F +E +V    P+I +A+ TLAG E+    GILNGT
Sbjct: 125 TTNKGPVAIAAPALKAFAKTNGVRFEYEGAVMSGTPVIRMAERTLAGAELKGFEGILNGT 184

Query: 180 TNYILTKMEKEGLDFETALKEAKELGIAETDPTQDIEGLDTAAKIVILANSIMGMNKTIK 239
           +N++L +ME  GLDF +A+KEA++LG AE DPT D+EG D   K+VILAN ++G N   +
Sbjct: 185 SNFVLGRME-SGLDFASAVKEAQKLGYAEADPTADVEGFDVRLKVVILANELLGANLKPE 243

Query: 240 DVKVKGISRITPEALFLANKRGYTIKLIG---QIKDGYLI--VEPMLVPIDSPL-NVKGT 293
           D+  KG+S ++   +  A K     KLIG   +  DG +   V P  + +D PL  V G 
Sbjct: 244 DISCKGVSGLSLSDIEEAAKANSRWKLIGAAVRNDDGSVTGSVSPKRLGLDHPLAGVNGA 303

Query: 294 LNVAMFETDLAKEVVVVGRGAGPIETASAILSDLIHIYNS 333
            N    +T+L   V + G GAG IETA A+LSD++ I+++
Sbjct: 304 TNAVSLDTELLGAVTITGPGAGRIETAYALLSDIVAIHSA 343


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: 311
Number of extensions: 22
Number of successful extensions: 3
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: 353
Length adjustment: 29
Effective length of query: 307
Effective length of database: 324
Effective search space:    99468
Effective search space used:    99468
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