GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Sinorhizobium meliloti 1021

Align L-threonine dehydrogenase (EC 1.1.1.103) (characterized)
to candidate SMa0263 SMa0263 alcohol dehydrogenase

Query= ecocyc::EG12293-MONOMER
         (383 letters)



>FitnessBrowser__Smeli:SMa0263
          Length = 399

 Score =  176 bits (445), Expect = 1e-48
 Identities = 114/334 (34%), Positives = 172/334 (51%), Gaps = 29/334 (8%)

Query: 33  RTLIVTDNMLTKLGMAGDVQ---KALEERNIFSVIYDGTQPNPTTENVAAGLKLLKENNC 89
           R LIVTD   T+L +  D+    + LEE  +  ++   T P+   E+             
Sbjct: 33  RALIVTD---TRLAVDADLLALVRRLEEAGLEVMVDSSTLPDVPVESAIVSAAAASGFAP 89

Query: 90  DSVISLGGGSPHDCAKGIALVAANGGDIRDYEGVDRSAKPQLPMIAINTTAGTASEMTRF 149
           D VI +GGGS  D AK + L+  +GG  +DY G      P +P+IAI TTAGT SE+T  
Sbjct: 90  DLVIGIGGGSCLDMAKCVTLLLTHGGRPQDYYGEYAVPGPVMPLIAIPTTAGTGSEVTPV 149

Query: 150 CIITDEARHIKMAIVDKHVTPLLSVNDSSLMIGMPKSLTAATGMDALTHAIEAYVSIAAT 209
            +++D  R +K+ I   H+ P +S+ D  L +  P  LTA  G DALTHAIEA+ +I   
Sbjct: 150 AVLSDAERSLKVGISSPHLIPAVSICDPELTLSCPPGLTAIAGADALTHAIEAFTAIRRE 209

Query: 210 PI---------------TDACALKAVTMIAENLPLAVEDGSNAKAREAMAYAQFLAGMAF 254
           P+               +D  AL A+T++ + L  A +DG++A ARE +     LAG+AF
Sbjct: 210 PVPGIAQQRVFVGKNELSDHFALSAITLLWQGLERACKDGADAGARETVMLGATLAGLAF 269

Query: 255 NNASLGYVHAMAHQLGGFYNLPHGVCNAVLLPHVQVFNSKVAAARLRDCAAAMGVNVTGK 314
             A     HA+ + +G   +  HG+  A L+P+V  +N+ +    L   A A G+     
Sbjct: 270 GVAGTAAAHAIQYPVGALTHTAHGLGVACLMPYVMTWNAPLIRDELAQIAHAAGLG---- 325

Query: 315 NDAEGAEACINAIRELAKKVDIPAGLRDLNVKEE 348
               G +  I A+  L +++ IPA LRDL ++E+
Sbjct: 326 ----GPDEVIPALVSLFERIGIPATLRDLGLEED 355


Lambda     K      H
   0.318    0.131    0.373 

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: 377
Number of extensions: 16
Number of successful extensions: 3
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: 383
Length of database: 399
Length adjustment: 31
Effective length of query: 352
Effective length of database: 368
Effective search space:   129536
Effective search space used:   129536
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 (21.8 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