GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lysN in Pseudomonas fluorescens GW456-L13

Align L-2-aminoadipate aminotransferase monomer (EC 2.6.1.39) (characterized)
to candidate PfGW456L13_4175 Transcriptional regulator, GntR family domain / Aspartate aminotransferase (EC 2.6.1.1)

Query= metacyc::MONOMER-6727
         (397 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4175
          Length = 388

 Score =  237 bits (604), Expect = 5e-67
 Identities = 147/395 (37%), Positives = 218/395 (55%), Gaps = 20/395 (5%)

Query: 9   AFGKSAGRIQASTIRELLKLTQRPGILSFAGGLPAPELFPKEEAAEAAARILREKGEVAL 68
           AF +   R+++S IRE+L   QRP ++SFAGGLPA  + PK E AE    +         
Sbjct: 2   AFSERVSRLKSSLIREILAAAQRPQVMSFAGGLPAETMLPKVEWAEMPVSMG-------- 53

Query: 69  QYSPTEGYAPLR---AFVAEWIGVRPE--EVLITTGSQQALDLVGKVFLDEGSPVLLEAP 123
           QY  +EG   LR   A  A  +GV  E  +VL+ +GSQQ LDL  K+++D+G+ +LLEAP
Sbjct: 54  QYGMSEGEPALREALAAEARALGVPCEASQVLVVSGSQQTLDLAAKLYIDKGTEILLEAP 113

Query: 124 SYMGAIQAFRLQGPRFLTVPAGEEGPDLDALEEVLKRERPRFLYLIPSFQNPTGGLTPLP 183
           +Y+ A+Q F+L G   LTV    +GP+L AL   L++ RP F+YLIP+FQNP+       
Sbjct: 114 TYLAALQIFQLFGADCLTVSLEADGPNLTALRARLEQHRPAFIYLIPTFQNPSAVRYSEA 173

Query: 184 ARKRLLQMVMERGLVVVEDDAYRELYF-GEARLPSLFELAREAGYPGVIYLGSFSKVLSP 242
            R  +  ++ E G+ ++ED+ YREL F G    P +  L R +     IY G+ SK L P
Sbjct: 174 KRNAVAALLDEFGVTLIEDEPYRELTFDGGCATPIVSRLKRASW----IYTGTVSKTLLP 229

Query: 243 GLRVAFAVAHPEALQKLVQAKQGADLHTPMLNQMLVHELL-KEGFSERLERVRRVYREKA 301
           GLRV + +A P+    L++ KQ ADLHT  + Q    + +  E + +    +R  YR + 
Sbjct: 230 GLRVGYLIASPDLFPHLLKLKQSADLHTNRVGQWQALQWIGTEKYQQHRSELRDFYRGRR 289

Query: 302 QAMLHALDREVPKEVRYTRPKGGMFVWMELPKGLSAEGLFRRALEENVAFVPGGPFFANG 361
            A   AL+        +  P+GG+F W++L +      L   AL  +VAF+PG PFF   
Sbjct: 290 DAFQAALETHFSDLADWNVPQGGLFFWLKLKQPQDTRTLLNAALANDVAFMPGEPFFPEP 349

Query: 362 GGE-NTLRLSYATLDREGIAEGVRRLGRALKGLLA 395
                 LRL+++ +D   + EG++RL   ++   A
Sbjct: 350 DNHPGYLRLNFSHIDPARLDEGLKRLAAVVRAAQA 384


Lambda     K      H
   0.320    0.139    0.401 

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: 395
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: 397
Length of database: 388
Length adjustment: 31
Effective length of query: 366
Effective length of database: 357
Effective search space:   130662
Effective search space used:   130662
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: 50 (23.9 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