GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Herbaspirillum seropedicae SmR1

Align L-threonine dehydrogenase (EC 1.1.1.103) (characterized)
to candidate HSERO_RS00730 HSERO_RS00730 4-hydroxybutyrate dehydrogenase

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



>FitnessBrowser__HerbieS:HSERO_RS00730
          Length = 379

 Score =  191 bits (486), Expect = 2e-53
 Identities = 123/360 (34%), Positives = 195/360 (54%), Gaps = 14/360 (3%)

Query: 30  GFTRTLIVTDNMLTKLGMAGDVQKALEERNIFSVIYDGTQPNPTTENVAAGLKLLKENNC 89
           G  + L+VTD  +   G+   V   L+E  + +V+YD T PNP    V A + L +++ C
Sbjct: 28  GIKKPLVVTDMGIRNAGLLDKVLGQLKE-GVGAVVYDQTPPNPNEGAVRAAVALFRQHGC 86

Query: 90  DSVISLGGGSPHDCAKGIALVAANGGDIRDYE----GVDRSAKPQLPMIAINTTAGTASE 145
           D ++++GGGS  D AKG+A+   + G ++ +     G+        P+IAI TTAGT SE
Sbjct: 87  DGIVAVGGGSSIDLAKGVAVCGTHEGPLKSFALIEGGLANITAKTAPVIAIPTTAGTGSE 146

Query: 146 MTRFCI-ITDEARHIKMAIVDKHVTPLLSVNDSSLMIGMPKSLTAATGMDALTHAIEAYV 204
           + R  I I D+ R  K+ I+  ++ P L++ D  L +G+P  +TAATGMDA+ H +E ++
Sbjct: 147 VGRGAILILDDGR--KVGIISPYLVPKLAICDPELTLGLPPLMTAATGMDAIAHCLETFM 204

Query: 205 SIAATPITDACALKAVTMIAENLPLAVEDGSNAKAREAMAYAQFLAGMAFNNASLGYVHA 264
           + +  P  D  AL  +     ++  A  +  + +AR  M  A     MAF    LG VH+
Sbjct: 205 APSFNPPADGIALDGLWRAWAHIERATREPGDREARLNMMSASMQGAMAFQK-GLGCVHS 263

Query: 265 MAHQLGGFY-NLPHGVCNAVLLPHVQVFNSKVAAARLRDCAAAMGVNVTGKNDAEGAEAC 323
           ++H LGG    L HG  NA+ LP +  FN   AA+ ++D   A   +  G     GAE  
Sbjct: 264 LSHSLGGINPRLHHGTLNAIFLPAIIAFNES-AASMVKDNKMARMAHAMGL--GSGAEIG 320

Query: 324 INAIRELAKKVDIPAGLRDLNVKEEDFAVLATNALKDACGFTNPIQATHEEIVAIYRAAM 383
             AIRE+++++ +PAGL +L V E  F  +   AL D    TNP +A+ ++ + + + +M
Sbjct: 321 -PAIREMSRRLGLPAGLGELGVTESMFPQIIQGALADHSHKTNPREASEQDYLHMLQQSM 379


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: 322
Number of extensions: 17
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: 383
Length of database: 379
Length adjustment: 30
Effective length of query: 353
Effective length of database: 349
Effective search space:   123197
Effective search space used:   123197
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.

Links

Downloads

Related tools

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