GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Klebsiella michiganensis M5al

Align L-threonine dehydrogenase (EC 1.1.1.103) (characterized)
to candidate BWI76_RS00645 BWI76_RS00645 lactaldehyde reductase

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



>FitnessBrowser__Koxy:BWI76_RS00645
          Length = 382

 Score =  326 bits (835), Expect = 8e-94
 Identities = 169/376 (44%), Positives = 240/376 (63%)

Query: 8   IPSVNVIGADSLTDAMNMMADYGFTRTLIVTDNMLTKLGMAGDVQKALEERNIFSVIYDG 67
           +P +++ GA ++ D + ++A   + + LIVTD  L KLG+   +  A++E+ +   ++D 
Sbjct: 7   LPKISLHGAGAIGDMVKLVAGKRWGKALIVTDGQLVKLGLLDSLFAAMDEQQMAYHLFDE 66

Query: 68  TQPNPTTENVAAGLKLLKENNCDSVISLGGGSPHDCAKGIALVAANGGDIRDYEGVDRSA 127
             PNPT   V  G     E  CD +I+ GGGSP D AK + ++ AN G    Y GV +  
Sbjct: 67  VFPNPTEALVQKGYAAYCEAGCDYLIAFGGGSPIDTAKAVKILTANPGPSTAYSGVGKVT 126

Query: 128 KPQLPMIAINTTAGTASEMTRFCIITDEARHIKMAIVDKHVTPLLSVNDSSLMIGMPKSL 187
            P +P++AINTTAGTA+EMT   +I D  R +K  I+D ++ P ++V+D+S+M+ +P ++
Sbjct: 127 NPGVPLVAINTTAGTAAEMTSNAVIIDAERQVKEVIIDPNIIPDIAVDDASVMLDIPPAI 186

Query: 188 TAATGMDALTHAIEAYVSIAATPITDACALKAVTMIAENLPLAVEDGSNAKAREAMAYAQ 247
           TAATGMDALTHAIEA+VS+ A P+TDA A +A+ +I   LP AV+DG N +ARE MA+ Q
Sbjct: 187 TAATGMDALTHAIEAFVSVGAHPLTDANAQEAIRLINLWLPKAVDDGHNLEAREQMAFGQ 246

Query: 248 FLAGMAFNNASLGYVHAMAHQLGGFYNLPHGVCNAVLLPHVQVFNSKVAAARLRDCAAAM 307
           +LAGMAFN+A LG VHA+AHQ G  +NLPHGVCNA+LLP ++ FN   A +R    A AM
Sbjct: 247 YLAGMAFNSAGLGLVHALAHQPGATHNLPHGVCNAILLPIIENFNRPNAVSRFARVAQAM 306

Query: 308 GVNVTGKNDAEGAEACINAIRELAKKVDIPAGLRDLNVKEEDFAVLATNALKDACGFTNP 367
           GV+  G +D   +   INAIR L+K+V IP G   L V + D       AL D C   NP
Sbjct: 307 GVDTRGMSDEAASMEAINAIRALSKRVGIPQGFSQLGVSKADIEGWLDKALADPCAPCNP 366

Query: 368 IQATHEEIVAIYRAAM 383
             A+ +E+  +Y  A+
Sbjct: 367 RAASRDEVRELYLEAL 382


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: 383
Number of extensions: 13
Number of successful extensions: 1
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.

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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