GapMind for Amino acid biosynthesis

 

Aligments for a candidate for aroB in Pseudomonas fluorescens FW300-N2C3

Align 3-dehydroquinate synthase; DHQS; EC 4.2.3.4 (uncharacterized)
to candidate AO356_23655 AO356_23655 3-dehydroquinate synthase

Query= curated2:B2I0J2
         (360 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_23655
          Length = 624

 Score =  170 bits (430), Expect = 1e-46
 Identities = 106/296 (35%), Positives = 161/296 (54%), Gaps = 11/296 (3%)

Query: 68  LPDGEKYKDIQHLNLIFDALLEVGFNRDCTVLALGGGVIGDMAGFASACFQRGVYFVQVP 127
           +P GE  KD Q L  ++  +L+ G +R C VLALGGG + D  G+A A F RG+  +++P
Sbjct: 312 VPAGESSKDSQVLQQLYSDMLQHGLDRHCYVLALGGGAVLDAVGYACATFHRGIRLIRIP 371

Query: 128 TTLLSQVDSSVGGKTGINHPLGKNMLGAFQQPQVVLADMAQLNTLPERELSAGLAEVIKY 187
           +T+L+Q D+ +G K GIN    KN+LGAF     V+ D   L +L  R+  AGLAE +K 
Sbjct: 372 STVLAQNDAGIGVKNGINAFGQKNLLGAFYPATAVINDFQLLTSLSRRDQIAGLAEAVKV 431

Query: 188 ALLGDEDFLVWLEENMDGLVARDADLLAEAVYRSCA--HKARIV-ANDEKEQGERALLNL 244
           AL+ D+ F  W+E+  D L   D      A+ R CA  H A I  A D  E+G    L+ 
Sbjct: 432 ALIKDQAFFQWMEQQADALAHFDHAASRYAI-RRCAELHLAHITGAGDPFERGNGRPLDY 490

Query: 245 GHTFGHAIESYLGYGTWLHGEAVATGMVMAADLSQRLGWISNEDVARTKKIIQRANLPIS 304
           GH   H +E+ L +    HGEAVA GM +    +  LG +S+ D  R   ++ +    ++
Sbjct: 491 GHWAAHKLEN-LSHHRLRHGEAVAVGMALDGLYANALGLLSDADSDRLLHLLLKLGFCLN 549

Query: 305 CPQIPLDDFLGY------MAHDKKVLNGQLRLVLLKQLGQAVITKDFDVELMKQAI 354
            P++ L D  G       +   ++ L GQL + +L ++G++V   + D   M+QA+
Sbjct: 550 PPELTLKDAQGRSQVLLGLEEFRQHLGGQLSIPMLSRIGESVDLHEIDTARMEQAL 605


Lambda     K      H
   0.321    0.138    0.404 

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: 540
Number of extensions: 25
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: 360
Length of database: 624
Length adjustment: 33
Effective length of query: 327
Effective length of database: 591
Effective search space:   193257
Effective search space used:   193257
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 (21.8 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.

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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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.

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