GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Azospirillum brasilense Sp245

Align L-threonine dehydrogenase (EC 1.1.1.103) (characterized)
to candidate AZOBR_RS28580 AZOBR_RS28580 alcohol dehydrogenase

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



>FitnessBrowser__azobra:AZOBR_RS28580
          Length = 387

 Score =  214 bits (544), Expect = 4e-60
 Identities = 124/380 (32%), Positives = 197/380 (51%), Gaps = 1/380 (0%)

Query: 4   STFFIPSVNVIGADSLTDAMNMMADYGFTRTLIVTDNMLTKLGMAGDVQKALEERNIFSV 63
           S+F  P+  V G  +     +++ ++  TR  ++ D  L    +   ++  L    +   
Sbjct: 7   SSFSCPTKIVFGVGAHEQLPDVLREWNATRLFVLLDPALADSAIFRRIEGLLTSNGVALS 66

Query: 64  IYDGTQPNPTTENVAAGLKLLKENNCDSVISLGGGSPHDCAKGIALVAANGGDIRDYEGV 123
           ++ G +P P    V A  +  +E +  +++++GGGS  D AK + ++  NGG I DYEG+
Sbjct: 67  VFTGIEPEPGDRTVQAAYERCREQDAQALLAIGGGSTIDVAKAVGILMTNGGRIADYEGI 126

Query: 124 DRSAKPQLPMIAINTTAGTASEMTRFCIITDEARHIKMAIVDKHVTPL-LSVNDSSLMIG 182
           ++ A   LP+IA+ TTAGT SE++  C+ITD AR  KMAI     +P  +++ D   +  
Sbjct: 127 EKFAIRPLPLIAVPTTAGTGSEVSGACVITDTARKTKMAIRHAAFSPAQVAILDPLAVGS 186

Query: 183 MPKSLTAATGMDALTHAIEAYVSIAATPITDACALKAVTMIAENLPLAVEDGSNAKAREA 242
           MP  + A  G+DA  HA E+Y+S  AT  +DA  L A+T+IA ++   V D +N  A   
Sbjct: 187 MPAHVAAHAGIDAFVHAFESYLSKRATVFSDAVNLHAMTLIAGSIRPFVADRTNVPAALD 246

Query: 243 MAYAQFLAGMAFNNASLGYVHAMAHQLGGFYNLPHGVCNAVLLPHVQVFNSKVAAARLRD 302
           M     LA M+F    LG VH MA  +G  + +PHG+ NAV LP+   FN      R+  
Sbjct: 247 MLCGSALAAMSFGVTGLGNVHCMAMSVGALFPVPHGLANAVCLPYAAAFNVSAKPERMAR 306

Query: 303 CAAAMGVNVTGKNDAEGAEACINAIRELAKKVDIPAGLRDLNVKEEDFAVLATNALKDAC 362
            A  +GV+  G    + AEA ++ +R L   + IP  LRD+ V E+    +A  +     
Sbjct: 307 IAEILGVDTAGLPLDQAAEAAVDGLRTLCADLGIPPRLRDVGVTEDRLDEMARRSYAADY 366

Query: 363 GFTNPIQATHEEIVAIYRAA 382
              NP   +  +   ++RAA
Sbjct: 367 NRWNPRHTSEPDFQDLFRAA 386


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: 316
Number of extensions: 10
Number of successful extensions: 2
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: 387
Length adjustment: 30
Effective length of query: 353
Effective length of database: 357
Effective search space:   126021
Effective search space used:   126021
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