GapMind for catabolism of small carbon sources

 

Alignments for a candidate for antC in Pseudomonas simiae WCS417

Align electron transfer component of the anthranilate 1,2-dioxygenase system (EC 1.14.12.1) (characterized)
to candidate GFF1621 PS417_08245 CDP-6-deoxy-L-threo-D-glycero-4-hexulose-3- dehydrase reductase

Query= reanno::WCS417:GFF4631
         (335 letters)



>FitnessBrowser__WCS417:GFF1621
          Length = 329

 Score =  114 bits (284), Expect = 4e-30
 Identities = 106/352 (30%), Positives = 157/352 (44%), Gaps = 49/352 (13%)

Query: 2   NHKVAFSFADGKTLFFPVGANEILLDAALRNGIKIPLDCREGVCGTCQGRCESGDYSQDY 61
           NHK +F+   GK+L          L+ A   G  +   CR G CG C+     GD ++  
Sbjct: 8   NHK-SFTGESGKSL----------LECAKSQGTVLEYSCRTGRCGVCKANVLQGD-TEVM 55

Query: 62  VDEEALSSLDLQQRKMLSCQTRVKSDATFYFDFDSSLCNAPGPVQVKGT---VSAVEQVS 118
             E AL+  +     +L+C     +D     + D         +Q+K     +  +E+++
Sbjct: 56  QPELALTDEERANGAILTCCRAALTDV----ELDIEDLGLLADIQIKTMPCRLDTLERLA 111

Query: 119 ASTA--ILQVQLDQALDFLPGQYARLSVPGTDSWR-SYSFANLPGNH--LQFLVRLLPDG 173
                 +L+     AL +LPGQY  + V G D  R SYS AN       L+  +R +PDG
Sbjct: 112 DDVVRVVLRTPPKSALFYLPGQY--IDVIGKDGVRRSYSIANAVREDAKLELHIRQVPDG 169

Query: 174 VMSNYLRERCQVGDELLMEAPLGAFYLRHV-TQPLVLVAGGTGLSALLGMLDQLAANG-- 230
           VMS Y     QV D L +E PLG F LR+  T  LV +A GTG++ +  ML+ LA+    
Sbjct: 170 VMSQYWFGEAQVNDLLRLEGPLGTFCLRNASTTNLVFMATGTGIAPVKAMLEALASTSEP 229

Query: 231 -CEQPVHLYYGVRGAEDLCEAARIRAYAAKIPNL--RYTEVLSAPSEEWSGKRGY----- 282
              + V++Y+G R   DL        +    P L   Y  VLS   + W G  GY     
Sbjct: 230 LIGKRVYVYWGGRTENDL-------YWLPDFPTLGMTYRPVLSRAGKHWPGATGYVQQAV 282

Query: 283 LTEHFDLAELRDGSADMYLCGPPPMVESIQQWLADQALDGVQLYYEKFTQSN 334
           L E+ DLA+       +Y CG   M+ + ++ L    L     + + F  SN
Sbjct: 283 LAENLDLAD-----TSVYACGSEAMIHTAREMLTQAGLPLKHFHSDAFVSSN 329


Lambda     K      H
   0.320    0.136    0.412 

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: 264
Number of extensions: 13
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: 335
Length of database: 329
Length adjustment: 28
Effective length of query: 307
Effective length of database: 301
Effective search space:    92407
Effective search space used:    92407
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: 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