GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysY in Dinoroseobacter shibae DFL-12

Align Putative [LysW]-L-2-aminoadipate/[LysW]-L-glutamate phosphate reductase; EC 1.2.1.103; EC 1.2.1.106 (uncharacterized)
to candidate 3608357 Dshi_1759 N-acetyl-gamma-glutamyl-phosphate reductase (RefSeq)

Query= curated2:A8AAF8
         (356 letters)



>FitnessBrowser__Dino:3608357
          Length = 341

 Score =  235 bits (599), Expect = 1e-66
 Identities = 147/356 (41%), Positives = 201/356 (56%), Gaps = 18/356 (5%)

Query: 3   YEVAIVGASGYTGGELLRVLAVHPDVNVKVVTSREYANKPVYYAHPHLRGI-YPASLKFK 61
           Y +AI+GASGYTG EL+R++A HP + +  +++   A + +    PHLR +  PA +K  
Sbjct: 2   YNIAILGASGYTGAELVRLIATHPRMRITALSADRKAGQTMGAVFPHLRHLDLPALVK-- 59

Query: 62  RLDDPDQLSDVVGDVDLVFLALPHKVSLHYVPKALEVGYKVVDLSADYRLKRVEDYKTWY 121
            +DD D      G VDLVF ALPH  S   +  AL    K+VDLSAD+RL+  E Y  WY
Sbjct: 60  -IDDID-----FGGVDLVFCALPHATSQSVIA-ALPKSVKIVDLSADFRLRDPEAYAKWY 112

Query: 122 GYEHPYPDLLEKAVYGLPELYGDKIRGAQLVANPGCNATSSILAVLPPAAERIIDLDRIV 181
           G  H   DL  +AVYGL E Y ++IR A+LVA  GCNA +   A+ P  A  +IDLD I+
Sbjct: 113 GGPHAALDLQAEAVYGLTEFYREQIRDARLVAGTGCNAATGQYALRPLIAAGVIDLDEII 172

Query: 182 VDVKVGSSEAGAKPYRGGHHPEREGTARPYDAEG-HRHVAELEQVIRDYTGRDVKVGFTP 240
           +D+K G S AG        H E    A  Y   G HRH+ E +Q      GR++KV FTP
Sbjct: 173 IDLKTGVSGAGRSLKENLLHAELSEGAHAYAVGGMHRHLGEFDQEFSALAGREIKVQFTP 232

Query: 241 HAVSMIRGSLASAYSWLTKDLAPLDVQRIYAKYYAGKKFVKIVRGAPMPYPDVKNVYGSN 300
           H +   RG LA+ Y    K  A  ++    A  Y  + FV ++      +P  ++V GSN
Sbjct: 233 HLLPANRGILATVY---VKGEA-TEIYDALADAYEDEPFVVMLPEG--EHPSTRHVRGSN 286

Query: 301 YAEVGFALDKRVGRLAMFAAIDNLMKGAAGTAVQNMNLMLGMDEDEGLKNLVPVRP 356
           +  +G   D+  GR  + AA+DNL KG++G A+QN NLML ++E  GL  + PV P
Sbjct: 287 FVHIGVVRDRIPGRAVVIAALDNLTKGSSGQALQNANLMLDIEETTGLM-MTPVFP 341


Lambda     K      H
   0.319    0.138    0.410 

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: 376
Number of extensions: 21
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: 356
Length of database: 341
Length adjustment: 29
Effective length of query: 327
Effective length of database: 312
Effective search space:   102024
Effective search space used:   102024
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 (21.7 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