GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PPDCbeta in Pseudomonas fluorescens FW300-N2E3

Align Putative branched-chain alpha keto acid dehydrogenase E1 subunit beta (characterized, see rationale)
to candidate AO353_15580 AO353_15580 2-oxoisovalerate dehydrogenase

Query= uniprot:G1UHX5
         (328 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_15580
          Length = 328

 Score =  280 bits (715), Expect = 5e-80
 Identities = 156/322 (48%), Positives = 205/322 (63%), Gaps = 5/322 (1%)

Query: 3   EITMAKALNTALRDALRDDPRTILFGEDIGALGGVFRITDGLAAEFGDERCFDTPLAESA 62
           ++T+ +A+N AL  A+R+D   I+ GED+G  GGVFR T GL   FG +R  DTPLAE+ 
Sbjct: 5   KVTLLEAINLALHRAMREDENVIVLGEDVGVNGGVFRATLGLRDSFGFKRVIDTPLAETM 64

Query: 63  ILGTAVGMAMYGYRPVVEMQFDAFAYPAFEQLVSHVAKLRNRTRGAIGLPLTIRIPYGGG 122
           + G  +GMA  G +PV+E+QF  F Y A E LVSH +++RNRTRG I  P+ +R P G G
Sbjct: 65  LGGLVIGMAAQGLKPVLEIQFMGFIYAAMEHLVSHASRMRNRTRGRITCPMVLRTPMGAG 124

Query: 123 IGGVEHHSDSSEIYYMATPGLTVVTPATAADAYSLLRRSIASPDPVVFLEPKRLYWRKEA 182
           I   EHHS+S+E  +   PGL VV P++ A AY LL  +I  PDPV+FLEP RLY R   
Sbjct: 125 IRAPEHHSESTEALFAHIPGLRVVIPSSPARAYGLLLAAIDDPDPVIFLEPTRLY-RMNP 183

Query: 183 LGLPVDTG---PLGSAVIRRHGTHATLIAYGPAVTTALEAAEAAAEHGWDLEVIDLRTLM 239
             L +D G   PL +    R G+  TLI++G +V   L+AA+A AE G   EVID+ ++ 
Sbjct: 184 QPL-IDDGKRLPLDTCFTLREGSDITLISWGASVMETLQAADALAEQGISAEVIDVASIK 242

Query: 240 PLDDATVCASVRRTGRAVVVHEAHGFAGPGAEIAARITERCFYHLEAPVRRVTGFDVPYP 299
           PLD  T+ ASVR+TGR V+VHEA    G GAEIAA + ER    L+AP+ RVT  D+P P
Sbjct: 243 PLDLDTLEASVRKTGRCVIVHEAPRTCGVGAEIAASLYERALLDLQAPILRVTAPDIPPP 302

Query: 300 PPLLERHYLPGVDRILDAVASL 321
               E  Y+P V+ IL A  S+
Sbjct: 303 LYRQELLYMPNVEDILHACDSV 324


Lambda     K      H
   0.322    0.138    0.418 

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: 302
Number of extensions: 13
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: 328
Length of database: 328
Length adjustment: 28
Effective length of query: 300
Effective length of database: 300
Effective search space:    90000
Effective search space used:    90000
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 (21.9 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