GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ilvE in Dechlorosoma suillum PS

Align Branched-chain-amino-acid transaminase (EC 2.6.1.42) (characterized)
to candidate Dsui_0883 Dsui_0883 transcriptional regulator with HTH domain and aminotransferase domain

Query= reanno::azobra:AZOBR_RS06555
         (404 letters)



>FitnessBrowser__PS:Dsui_0883
          Length = 475

 Score =  158 bits (400), Expect = 3e-43
 Identities = 111/365 (30%), Positives = 177/365 (48%), Gaps = 13/365 (3%)

Query: 21  IRELLKLLERPEIISFAGGIPDPDFFPTAAIARAYEKIFQSNSGAGGALQYTISEGFTPL 80
           I E+L+ ++ P ++ F      P+ +P   + R      +       A    +  G   L
Sbjct: 98  IFEILESVKNPAVVPFGSSFASPELYPLDKLGRCLAAAARHLDPR--ATVTDLPPGNEEL 155

Query: 81  REWICAYLGRRGIQAGLDEVLVTSGSQQALEFVGKLLIGPGEKILVTRPTYLGALQAFSP 140
           R  I      RG      E++VTSG+ + L    + +  PG+ + +  PT+   LQA   
Sbjct: 156 RRQIALRYLSRGANVSPQEIVVTSGAMEGLNLCLQAVTRPGDLVAIESPTFYANLQAIER 215

Query: 141 YEPQYLSVPGDA-EGPDLAAVEAALEQKP-KFFYLVPDFQNPNGTTISLARREALLDLCA 198
              + + +P    EG  LAA+E AL Q P K    + +F NP   ++S AR+  L+ L A
Sbjct: 216 LGLKVIEIPTHPREGISLAALEDALRQHPIKACLCMLNFSNPITGSLSDARKAELVALLA 275

Query: 199 KHGVPIVEDAAYTELRYEGEPIPSMVALDAARNGGKITNVLFCGSFSKTMVPALRVGWIN 258
           ++ VP++ED  Y EL Y G+  P+    +  R+G     VL   SFSK++ P  R+GW+ 
Sbjct: 276 RYQVPLIEDDVYAEL-YFGDQAPAHAKAED-RHG----LVLHVSSFSKSLAPGYRIGWVA 329

Query: 259 GPAEVINRLVLMKQAGDLHTSTINQIVLHDVVSQN-FDSHIRRLRAGYKERRDAMLTALS 317
           G      ++  +K    L T+   QI L + +    +D+H+RRLR  +  +  AM+ A+ 
Sbjct: 330 G-GRFTQKIQRLKLTTSLATTVPVQIALAEYLKHGGYDNHLRRLRRTFSLQEIAMVGAVE 388

Query: 318 EFAPAGVTWTKPEGGMFVWIELPEGTDGVDLLARAIKDANVAFVPGSAFHADRSGKNTLR 377
              PAG    +P GG F+W+ELP G D +  L R   D  ++  PG  F A R   + LR
Sbjct: 389 RHFPAGTRLARPSGGYFLWVELPPGVDTL-ALHRLALDQGISIAPGPIFSAKREYGHCLR 447

Query: 378 LSFSN 382
           L++ +
Sbjct: 448 LNYGH 452


Lambda     K      H
   0.320    0.138    0.410 

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: 473
Number of extensions: 27
Number of successful extensions: 6
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: 404
Length of database: 475
Length adjustment: 32
Effective length of query: 372
Effective length of database: 443
Effective search space:   164796
Effective search space used:   164796
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: 51 (24.3 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