GapMind for catabolism of small carbon sources

 

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

Align branched-chain-2-oxoacid decarboxylase (subunit 2/2) (EC 4.1.1.72) (characterized)
to candidate Pf1N1B4_1019 Branched-chain alpha-keto acid dehydrogenase, E1 component, beta subunit (EC 1.2.4.4)

Query= BRENDA::Q9HIA4
         (319 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1019
          Length = 329

 Score =  297 bits (761), Expect = 2e-85
 Identities = 156/320 (48%), Positives = 220/320 (68%), Gaps = 4/320 (1%)

Query: 1   MNMVQALNSAMDLKMSEDDSVIILGEDVGRDGGVFRVTDGLQAKYGPQRVIDTPLSELGI 60
           + +++A+N A+   MSED++VI+LGEDVG +GGVFR T GL+  +G +RVID+PL+E  +
Sbjct: 6   VTLLEAVNLALHRAMSEDENVIVLGEDVGVNGGVFRATLGLRDTFGFKRVIDSPLAETML 65

Query: 61  VGMAIGMAVNGLKPIPEIQFQDFIYTSMDQIINQMAKIRYRSGGDYTVPLVLRTPVGGGI 120
            G+ +GMA  GLKP+ EIQF  FIY +M+ +++  +++R R+ G  T P+V+R+P+G GI
Sbjct: 66  GGLVVGMAAQGLKPVVEIQFMGFIYATMEHLVSHASRMRNRTRGRITCPMVMRSPMGAGI 125

Query: 121 KGGLYHSQSGEAYFAHTAGLTVVSPSNPYDAKGLLISAIESPDPVIFLEPKRLYRAQKVE 180
           +   +HS+S EA FAH  GL VV PS+P  A GLL++AI+ PDPVIFLEP RLYR     
Sbjct: 126 RAPEHHSESTEALFAHIPGLRVVIPSSPARAYGLLLAAIDDPDPVIFLEPTRLYRMNPQP 185

Query: 181 VPDEKYTIPLRKANVLKQGNDVTIVTYGSMVPTVMSVASK---SKYDVEVIDLRTIAPMD 237
           + D+   +PL     L++G+D+T++++G+ V   +  A+K        EVID+ +I P+D
Sbjct: 186 LLDDGKRLPLDSCFTLREGSDITLISWGASVMETLQAATKLAEQGVSAEVIDVASIKPLD 245

Query: 238 RDTIISSVKKTGRVVIVHEAPRTLGVGAEISAMISERAIEYLYAPIVRVTGPDTPFP-YR 296
            DT+ +SV+KTGR VIVHEAPR+ GVGAEI+A + ER    L API RVT PD P P YR
Sbjct: 246 LDTMEASVRKTGRCVIVHEAPRSCGVGAEIAASLYERVFLELQAPIQRVTAPDIPPPLYR 305

Query: 297 LEEYYLPNEGRINAALDRVM 316
           LE  Y+P    I  A + VM
Sbjct: 306 LESLYMPGIEDILHACNTVM 325


Lambda     K      H
   0.318    0.137    0.388 

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: 305
Number of extensions: 15
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: 319
Length of database: 329
Length adjustment: 28
Effective length of query: 291
Effective length of database: 301
Effective search space:    87591
Effective search space used:    87591
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 48 (23.1 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