GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fdh in Herbaspirillum seropedicae SmR1

Align D-threo-aldose 1-dehydrogenase (EC 1.1.1.122) (characterized)
to candidate HSERO_RS04830 HSERO_RS04830 alcohol dehydrogenase

Query= BRENDA::Q97YM2
         (349 letters)



>FitnessBrowser__HerbieS:HSERO_RS04830
          Length = 341

 Score =  134 bits (336), Expect = 4e-36
 Identities = 104/344 (30%), Positives = 169/344 (49%), Gaps = 17/344 (4%)

Query: 10  KAALLKKFSEPLSIEDVNIPEPQGEEVLIRIGGAGVCRTDLRVWKGVEAKQGFRLPIILG 69
           KAA++++F +PLSIE V +P P   ++L++   +GVC TDL    G    +    P I G
Sbjct: 6   KAAVVREFGKPLSIEQVPVPTPAPGQILVKFEASGVCHTDLHAAHGDWPVKPTP-PFIPG 64

Query: 70  HENAGTIVEVGELAK-VKKGDNVVV---YATWGDLTCRYCREGKFNICKNQIIPGQTTNG 125
           HE  G +  VG   K VK+GD V V   +   G   C  CR G   +C  Q   G + NG
Sbjct: 65  HEGTGYVAAVGAGVKHVKEGDRVGVPWLHTACG--CCSPCRTGWETLCAEQQNTGYSVNG 122

Query: 126 GFSEYMLVKSSRWLVKLNSLSPVEAAPLADAGTTSMGAIRQALPFISKFAEPVVIVNGIG 185
            F+EY L          ++L    AAP+  AG T    +++      ++    V+++GIG
Sbjct: 123 SFAEYGLADPKFVGHLPDNLDFGPAAPVLCAGVTVYKGLKETEVRPGEW----VVISGIG 178

Query: 186 GLAVYTIQILKALMKNITIVGISRSKKHRDFALELGADYVSEMKDAESL--INKLTDGLG 243
           GL    +Q  KA+  ++    I   K     A +LGAD   + ++  ++  + ++  G  
Sbjct: 179 GLGHMAVQYAKAMGMHVVAADIHEDKLA--LAKKLGADLTVDGRNHNAVAEVQRIIGGAH 236

Query: 244 ASIAIDLVGTEETTYNLGKLLAQEGAIILVGMEGKRVSLEAFDTAVWNKKLLGSNYGSLN 303
            ++ +  V  +      G L A+ G + LVG+    +SL  F+T +    + GS  G+  
Sbjct: 237 GAL-VTAVSPKAMEQAFGFLRAR-GTMALVGLPPGDISLPVFNTVLKRITVRGSIVGTRQ 294

Query: 304 DLEDVVRLSESGKIKPYIIKVPLDDINKAFTNLDEGRVDGRQVI 347
           DLE+ +  +  GK+  +     LD+IN  F  ++EG++DGR V+
Sbjct: 295 DLEESLVFAAEGKVAAHFTWDKLDNINAIFARMEEGKIDGRIVL 338


Lambda     K      H
   0.317    0.136    0.389 

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: 290
Number of extensions: 18
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: 349
Length of database: 341
Length adjustment: 29
Effective length of query: 320
Effective length of database: 312
Effective search space:    99840
Effective search space used:    99840
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 (21.6 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