GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctC in Pseudomonas fluorescens FW300-N1B4

Align lactate dehydrogenase (NAD+, ferredoxin) (subunit 2/3) (EC 1.3.1.110) (characterized)
to candidate Pf1N1B4_391 Electron transfer flavoprotein, alpha subunit

Query= BRENDA::H6LBB1
         (418 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_391
          Length = 309

 Score =  136 bits (343), Expect = 8e-37
 Identities = 100/320 (31%), Positives = 162/320 (50%), Gaps = 14/320 (4%)

Query: 74  ITVYVDHIEGQIHPVTFELIGKARELAAVIGHPVYALLMGTNITEKADELLKY-GVDKVF 132
           I V  +H    + P T   +  A    A IG  ++ L+ G      A+   K  GV KV 
Sbjct: 3   ILVIAEHDNKVLAPATLNTVAAA----AKIGGDIHVLVAGQGAGAVAEAAAKIAGVAKVL 58

Query: 133 VYDKPELKHFVIEPYANVLEDFIEKVKPSSILVGATNVGRSLAPRVAARYRTGLTADCTI 192
           V D     H + E  A ++ +  +    S IL  AT+ G+++ PRVAA       ++   
Sbjct: 59  VADNAAYAHQLPENVAPLVAELGKGY--SHILAAATSNGKNILPRVAANLDVDQISEIIS 116

Query: 193 LEMKENTDLVQIRPAFGGNIMAQIVTENTRPQFCTVRYKVFTAPERVNEPWGDVEMMDIE 252
           +E  +       RP + GN +A  V  N   +  TVR   F  P         VE +   
Sbjct: 117 VESADTFK----RPIYAGNAIAT-VQSNAAVKVITVRATGFD-PVAAEGGSAAVEAVAAA 170

Query: 253 KAKLVSAIEVMEVIKKEKGIDLSEAETIVAVGRGVKCEKDLDMIHEFAEKIGATVACTRP 312
                S+    E+ K ++  +L+ A+ +V+ GRG++   +   ++  A+K+GA V  +R 
Sbjct: 171 HDAGTSSFVGEELAKSDRP-ELTAAKIVVSGGRGMQNGDNFKHLYALADKLGAAVGASRA 229

Query: 313 GIEAGWFDARLQIGLSGRTVKPKLIIALGISGAVQFAAGMQNSEYIIAINSDPKAPIFNI 372
            ++AG+    +Q+G +G+ V P+L IA+GISGA+Q  AGM++S+ I+AIN D +APIF +
Sbjct: 230 AVDAGFVPNDMQVGQTGKIVAPQLYIAVGISGAIQHLAGMKDSKVIVAINKDEEAPIFQV 289

Query: 373 AHCGMVGDLYEILPELLTMI 392
           A  G+V DL+E +PE   ++
Sbjct: 290 ADYGLVADLFEAIPEFEKLV 309


Lambda     K      H
   0.319    0.137    0.395 

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: 299
Number of extensions: 16
Number of successful extensions: 2
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: 418
Length of database: 309
Length adjustment: 29
Effective length of query: 389
Effective length of database: 280
Effective search space:   108920
Effective search space used:   108920
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.

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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