GapMind for catabolism of small carbon sources

 

Alignments for a candidate for x5p-reductase in Pseudomonas benzenivorans DSM 8628

Align Lmo2664 protein (characterized, see rationale)
to candidate WP_090447360.1 BLS63_RS19025 butanediol dehydrogenase

Query= uniprot:Q8Y413
         (350 letters)



>NCBI__GCF_900100495.1:WP_090447360.1
          Length = 356

 Score =  154 bits (389), Expect = 3e-42
 Identities = 113/362 (31%), Positives = 180/362 (49%), Gaps = 28/362 (7%)

Query: 1   MRAAVLYENNVIKAEQI---DEATCGKDQVRVEVKAVGICGSDIHK-------MQTRWKY 50
           M AAV +    I+ E++   +    G  Q++V     GICGSD+H+       +     +
Sbjct: 1   MTAAVWHGRKDIRLERVAVPEPPQPGWAQIKVHW--CGICGSDLHEYLAGPVFIPMDRPH 58

Query: 51  PLPA-----VMGHEFAGVITEIGSEVTNVAMGDRVAGIPLEPCMECNYCKAGDFALCDNY 105
           PL       ++GHEF G I  +G+ V++ A+G RVA    + C +C +C+ G + LC+N 
Sbjct: 59  PLTGLQGQCILGHEFCGEIVALGAGVSDFAVGQRVAADACQHCGQCLFCRQGQYNLCENL 118

Query: 106 RMVGSHFHGGFAENVVMKADNVISIGD-LDFEEGAMIEPLAVSMHGVLGIQPRLGDTVIV 164
              G   +G FAE V + A+ +  + +    E GA+IEPLAV MH V         TV+V
Sbjct: 119 AFTGLMNNGAFAELVNVPANLLYRLPEGFPSEAGALIEPLAVGMHAVNKAGSLHEQTVVV 178

Query: 165 FGIGTIGILVVQCLLLAGVKDIIAVDISDKKLADAREFGCKYTINPKNEDLKERVFAYTN 224
            G GTIG+  + C   AG   IIA+++S  + A A E G    I+P   D    V   T+
Sbjct: 179 VGAGTIGLCTIMCAKAAGAARIIALEMSAARKAKALEVGASEVIDPSQCDAVAAVRELTD 238

Query: 225 GLGADIALECAGSKITQEQCLLVTKKKGKVGFLGIAYADVLLHEEAFENIFRRELTLKGF 284
           G GA ++ EC G K T +  + V +K G+   +GI        E +  N F    T K  
Sbjct: 239 GYGAAVSFECIGHKSTAKLAIEVIRKAGRCVMVGI------FEEPSEFNFFEIVATEKQV 292

Query: 285 WNSYSAPFPGEEWRTSIEFVKQGRIKLKPLISHRYKLEE-TKEAFDMILSREHDYNKVMI 343
             S +  + G E+   I  +  GR+ + PLI+ R  L++  ++ F+ +++ +    K+++
Sbjct: 293 IGSLA--YAG-EFAEVIALIAAGRLDVAPLITGRIGLQQIIEQGFEELVNNKDHNVKIIV 349

Query: 344 LP 345
            P
Sbjct: 350 SP 351


Lambda     K      H
   0.321    0.139    0.417 

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: 320
Number of extensions: 15
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: 350
Length of database: 356
Length adjustment: 29
Effective length of query: 321
Effective length of database: 327
Effective search space:   104967
Effective search space used:   104967
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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