GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lysN in Shewanella oneidensis MR-1

Align 2-aminoadipate transaminase (EC 2.6.1.39) (characterized)
to candidate 200475 SO1300 glutamate-1-semialdehyde-2,1-aminomutase (NCBI ptt file)

Query= reanno::Putida:PP_4108
         (416 letters)



>FitnessBrowser__MR1:200475
          Length = 430

 Score =  142 bits (358), Expect = 2e-38
 Identities = 102/301 (33%), Positives = 152/301 (50%), Gaps = 17/301 (5%)

Query: 15  PITLSHGRNAEVWDTDGKRYIDFVGGIGVLNLGHCNPAVVEAIQAQATRLTHYAFNAAPH 74
           P+ +     A ++D DGK YID+VG  G + LGH +P + EA+ A       +    AP 
Sbjct: 33  PLFIEKADGAYIYDADGKAYIDYVGSWGPMILGHNHPKIREAVLAAVHNGLSFG---APT 89

Query: 75  GPYLALMEQLSQFVPVSYPLAGMLTNSGAEAAENALKVARGATGKRAIIAFDGGFHGRTL 134
              + + E++   VP    +   + +SG EA  +A+++ARG T +  I+ F+G +HG   
Sbjct: 90  ELEVQMAEKVIAMVPSIEQVR--MVSSGTEATMSAIRLARGFTNRDKILKFEGCYHGHAD 147

Query: 135 ATLNLNGKVAPYKQRVGELPGPVYHLPYPSADTGVTCE-QALKAMDRLFSVELAVEDVAA 193
             L   G  A     +G+   P   +P   A   +T     L ++  LF  E    +++ 
Sbjct: 148 CLLVKAGSGA---LTLGQPSSP--GIPEDFAKHTLTAVYNDLDSVRSLF--EQYPTEISC 200

Query: 194 FIFEPVQGEGGFLALDPAFAQALRRFCDERGILIIIDEIQSGFGRTGQRFAFPRLGIEPD 253
            I EPV G    +   P F + LR  CDE G L+IIDE+ +GF R  +  A    G+ PD
Sbjct: 201 IIIEPVAGNMNCIPPIPGFLEGLRSLCDEFGALLIIDEVMTGF-RVSKSGAQGHYGVTPD 259

Query: 254 LLLLAKSIAGGMPLGAVVGRKELMAALPKGG---LGGTYSGNPISCAAALASLAQMTDEN 310
           L  L K I GGMP+GA  GRK++M  +   G     GT SGNPI+ +A LA +  + +E 
Sbjct: 260 LTTLGKVIGGGMPVGAFGGRKDVMQFIAPTGPVYQAGTLSGNPIAMSAGLAQMEALCEEG 319

Query: 311 L 311
           L
Sbjct: 320 L 320


Lambda     K      H
   0.320    0.137    0.402 

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: 439
Number of extensions: 25
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: 416
Length of database: 430
Length adjustment: 32
Effective length of query: 384
Effective length of database: 398
Effective search space:   152832
Effective search space used:   152832
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