GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Cupriavidus basilensis 4G11

Align L-threonine dehydrogenase (EC 1.1.1.103) (characterized)
to candidate RR42_RS11005 RR42_RS11005 4-hydroxybutyrate dehydrogenase

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



>FitnessBrowser__Cup4G11:RR42_RS11005
          Length = 382

 Score =  177 bits (450), Expect = 3e-49
 Identities = 124/358 (34%), Positives = 184/358 (51%), Gaps = 31/358 (8%)

Query: 30  GFTRTLIVTDNMLTKLGMAGDVQKALEERNIFSVIYDGTQPNPTTENVAAGLKLLKENNC 89
           G  R L+VTD  +   G+A     AL    +   I+D T  NPT   V       +++ C
Sbjct: 28  GIRRPLVVTDKGVVAAGVAQQAIVALG--GLPHEIFDETPSNPTEAMVKKAAAQYRDSGC 85

Query: 90  DSVISLGGGSPHDCAKGIALVAANGGDIRDYEGVD----RSAKPQLPMIAINTTAGTASE 145
           D +I++GGGS  D AKGIA++A + G++  Y  ++    R  +   P+IA+ TT+GT SE
Sbjct: 86  DGLIAVGGGSSIDLAKGIAILATHPGELTTYATIEGGSARLTERAAPLIAVPTTSGTGSE 145

Query: 146 MTRFCIITDEARHIKMAIVDKHVTPLLSVNDSSLMIGMPKSLTAATGMDALTHAIEAYVS 205
           + R  II  E    K+     H+ P  ++ D  L +G+P  LTAATGMDA+ H +E +++
Sbjct: 146 VARGAIIILEDGR-KLGFHSWHLLPKSAICDPGLTLGLPAGLTAATGMDAIAHCVETFLA 204

Query: 206 IAATPITDACALKAVTMIAENLPLAVEDGSNAKAREAMAYAQFLAGMAFNNASLGYVHAM 265
            A  P  D  AL  +    +++  A  DG +  AR  M  A     MAF    LG VH++
Sbjct: 205 PAFNPPADGIALDGLERGWKHIERATRDGQDRDARLNMMSASMQGAMAFQK-GLGCVHSL 263

Query: 266 AHQLGGF-----YNLPHGVCNAVLLPHVQVFNSKVAA-------ARLRDCAAAMGVNVTG 313
           +H LGG        L HG  NAV++P V  FN+   +       ARLR    AMG+    
Sbjct: 264 SHPLGGLKVDGKTGLHHGTLNAVVMPAVLRFNADAPSVVRDNRYARLRH---AMGL---- 316

Query: 314 KNDAEGAEACINAIRELAKKVDIPAGLRDLNVKEEDFAVLATNALKDACGFTNPIQAT 371
             DA+ A+    A+ ++  ++ +P GLR + V E+ F  +   AL D C  TNP +A+
Sbjct: 317 PQDADLAQ----AVHDMTARLGLPTGLRQMGVTEDMFDKVIAGALVDHCHKTNPKEAS 370


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: 368
Number of extensions: 28
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: 382
Length adjustment: 30
Effective length of query: 353
Effective length of database: 352
Effective search space:   124256
Effective search space used:   124256
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