GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Pseudomonas fluorescens FW300-N2C3

Align L-lactate dehydrogenase; EC 1.1.1.27 (uncharacterized)
to candidate AO356_26080 AO356_26080 lactate dehydrogenase

Query= curated2:Q07251
         (349 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_26080
          Length = 343

 Score =  135 bits (341), Expect = 1e-36
 Identities = 102/327 (31%), Positives = 152/327 (46%), Gaps = 21/327 (6%)

Query: 3   ISLTSARQLARDILAAQQVPADIADDVAEHLVESDRCGYISHGLSILPNYRTALDGHSVN 62
           +S  +   L   I        ++A  +AE+   ++R G  SHG+  LP Y + L+   VN
Sbjct: 13  LSFDALVSLLEKIFLRHGTSTEVARCLAENCAGAERDGAHSHGVFRLPGYVSTLNSGWVN 72

Query: 63  PQGRAKCVLDQ--GTLMVFDGDGGFGQHVGKSVMQAAIERVRQHGHCIVTLRRSHHLGRM 120
             G+A  V++      +  D   GF Q    +     +E+ R  G  ++ +R SHH   +
Sbjct: 73  --GKAVPVVEDVASGFVAVDAGNGFAQPALAAARPLLVEKARSAGIAVLAIRNSHHFAAL 130

Query: 121 GHYGEMAAAAGFVLLSFTNVINRAPVVAPFGGRVARLTTNPLCFAGPMPNGRPPLVVDIA 180
               E  A  G V LS   V+N    V P G       TNP+ FA P  +G P +V D+A
Sbjct: 131 WPDVEPFAYEGLVALS---VVNSMTCVVPHGADRPLFGTNPIAFAAPRADGEP-IVFDLA 186

Query: 181 TSAIAINKARVLAEKGEPAPEGSIIGADGNPTTDASTMFGEHPGALLPFGGHKGYALGVV 240
           TSAIA    ++ A KGE  P G  + + G PT D   +     GALLPFGGHKG AL ++
Sbjct: 187 TSAIAHGDVQIAARKGELLPPGMGVDSLGQPTRDPKAIL--EGGALLPFGGHKGSALSMM 244

Query: 241 AELLAGVLSGGGTI----QPDNPRGGVATNNLFAVLLNPALDLGLDWQSAEVEAFVRYLH 296
            ELLA  L+GG         ++P           ++++P+   G D+     E  VR +H
Sbjct: 245 VELLAAALTGGNFSFEFDWSNHPGAKTPWTGQLLIVIDPSKTAGQDFAERSRE-LVRQMH 303

Query: 297 DTPPAPGVDRVQYPGEYEAANRAQASD 323
                 GV   + PG+     R++A++
Sbjct: 304 ------GVGLRRLPGDRRHRERSKANE 324


Lambda     K      H
   0.319    0.136    0.409 

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: 343
Number of extensions: 18
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: 349
Length of database: 343
Length adjustment: 29
Effective length of query: 320
Effective length of database: 314
Effective search space:   100480
Effective search space used:   100480
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 Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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