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_RS24560 RR42_RS24560 alcohol dehydrogenase

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



>FitnessBrowser__Cup4G11:RR42_RS24560
          Length = 389

 Score =  190 bits (482), Expect = 7e-53
 Identities = 118/350 (33%), Positives = 187/350 (53%), Gaps = 3/350 (0%)

Query: 35  LIVTDNMLTKLGMAGDVQKALEERNIFSVIYDGTQPNPTTENVAAGLKLLKENNCDSVIS 94
           L+VTD  L K G+    + +L        ++D    +P    +   ++  +    D VI 
Sbjct: 40  LVVTDGGLHKAGVLEGAKASLAAAGFRVTVFDEVVADPPEAVLLRCVEHARAARVDLVIG 99

Query: 95  LGGGSPHDCAKGIALVAANGGDIRDYEGVDRSAKPQLPMIAINTTAGTASEMTRFCIITD 154
           LGGGS  D AK  A++  +G  + +  G+      ++P++ + TTAGT SE+T   I++ 
Sbjct: 100 LGGGSSMDIAKLAAVLVVSGQPLAEMYGIGNVKGARVPLVQMPTTAGTGSEVTNISIVS- 158

Query: 155 EARHIKMAIVDKHVTPLLSVNDSSLMIGMPKSLTAATGMDALTHAIEAYVSI-AATPITD 213
                KM IV   +     + D+ L +G+P+  TAATG+DA+ HAIEAY S      I+D
Sbjct: 159 VGETTKMGIVAPQLYADRVILDAELTVGLPRQHTAATGIDAMVHAIEAYTSKHKKNAISD 218

Query: 214 ACALKAVTMIAENLPLAVEDGSNAKAREAMAYAQFLAGMAFNNASLGYVHAMAHQLGGFY 273
           A A +A+ +++ NL  A E+G++  AREAM     LAG AF NA +  VHA+A+ LGG +
Sbjct: 219 ALAREALRLLSANLLPACENGNDRGAREAMLLGATLAGQAFANAPVAAVHALAYPLGGHF 278

Query: 274 NLPHGVCNAVLLPHVQVFNSKVAAARLRDCAAAMGVNVTGKNDAEGAEACINAIRELAKK 333
           ++PHG+ NA++L  V  FN+  AAA+  + A A+G+     +D     A I  + +L  +
Sbjct: 279 HIPHGLSNALMLGPVLRFNAAAAAAQYAELAGALGIGQADGDDEARTAAFIGFMEDLMDR 338

Query: 334 VDIPAGLRDLNVKEEDFAVLATNALKDACGF-TNPIQATHEEIVAIYRAA 382
              P  LRD  V  E  A+LA +A++       NP++    + + +Y  A
Sbjct: 339 SGAPRRLRDAGVTRESLAMLAADAMQQQRLLQNNPVEVQQADALRLYEQA 388


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: 327
Number of extensions: 15
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: 389
Length adjustment: 30
Effective length of query: 353
Effective length of database: 359
Effective search space:   126727
Effective search space used:   126727
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