GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt1d in Shewanella amazonensis SB2B

Align mannitol dehydrogenase (EC 1.1.1.255) (characterized)
to candidate 6938606 Sama_2709 D-isomer specific 2-hydroxyacid dehydrogenase family protein (RefSeq)

Query= BRENDA::Q38707
         (365 letters)



>FitnessBrowser__SB2B:6938606
          Length = 348

 Score =  318 bits (815), Expect = 1e-91
 Identities = 158/345 (45%), Positives = 230/345 (66%), Gaps = 4/345 (1%)

Query: 11  VKAFGWAARDTTGLLSPFKFSRRATGEKDVRLKVLFCGVCHSDHHMIHNNWGFTTYPIVP 70
           +K  G+AA+     L+P++++ R   E DV +++L+ GVCHSD H + N+WG+T YP VP
Sbjct: 1   MKTIGYAAQSALSPLAPYEYTCRELREDDVAIEILYSGVCHSDLHTVKNDWGWTVYPTVP 60

Query: 71  GHEIVGVVTEVGSKVEKVKVGDNVGIGCLVGSCRSCESCCDNRESHCENTI-DTYGSI-Y 128
           GHEIVG V ++G+ V + ++GDNV +GC+V SC++C  C    E  CE     TY S   
Sbjct: 61  GHEIVGRVVDIGASVTQFRIGDNVAVGCMVDSCQTCSHCHSGEEQFCEQGFTQTYNSAER 120

Query: 129 FDGTMTHGGYSDTMVADEHFILRWPKNLPLDSGAPLLCAGITTYSPLKYYGLDKPGTKIG 188
             G +T GGY+  +V  + F+L+ P +L L   APLLCAGITTYSPL+ + +  PG+++ 
Sbjct: 121 HSGEITKGGYARHIVVRQEFVLQIPPSLDLARAAPLLCAGITTYSPLRTWQVG-PGSRVA 179

Query: 189 VVGLGGLGHVAVKMAKAFGAQVTVIDISESKRKEALEKLGADSFLLNSDQEQMKGARSSL 248
           V+G+GGLGH+A+K+A A GA VTVI  +  KR +A++ LGA+ FL++S+ E M+ A +  
Sbjct: 180 VIGMGGLGHMAIKLAVAMGAHVTVISRTADKRADAMQ-LGANEFLISSETESMQQAANRF 238

Query: 249 DGIIDTVPVNHPLAPLFDLLKPNGKLVMVGAPEKPFELPVFSLLKGRKLLGGTINGGIKE 308
           + I+DT+PV H + P   LLK +G L +VG      E+    ++ GR+ +  ++ GGI E
Sbjct: 239 ELILDTIPVKHDVTPYMPLLKVDGTLTLVGQVGPMAEVNTVPMIMGRRRIAASLIGGIAE 298

Query: 309 TQEMLDFAAKHNITADVEVIPMDYVNTAMERLVKSDVRYRFVIDI 353
           TQEMLDF A+ NI  +VE+I M+ +N A ERL KSDV YRFVID+
Sbjct: 299 TQEMLDFCARMNILPEVEMITMEQINDAFERLEKSDVHYRFVIDM 343


Lambda     K      H
   0.319    0.137    0.415 

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: 326
Number of extensions: 14
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: 365
Length of database: 348
Length adjustment: 29
Effective length of query: 336
Effective length of database: 319
Effective search space:   107184
Effective search space used:   107184
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 (21.7 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