GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Pseudarthrobacter sulfonivorans Ar51

Align L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized)
to candidate WP_058931176.1 AU252_RS13535 NAD(P)-dependent alcohol dehydrogenase

Query= BRENDA::P07913
         (341 letters)



>NCBI__GCF_001484605.1:WP_058931176.1
          Length = 353

 Score =  169 bits (427), Expect = 1e-46
 Identities = 104/340 (30%), Positives = 180/340 (52%), Gaps = 20/340 (5%)

Query: 5   SKLKAEEGIWMTDVPVPELGHNDLLIKIRKTAICGTDVHIYNWDEWSQKTIPVPMVVGHE 64
           S LK +  + M  +P+P+   + +L+++    +CG+DVH Y         +  P+++GHE
Sbjct: 23  SVLKRQGDMVMETLPLPQPDADQVLVQVAAVGVCGSDVHYYEHGRIGDYVVDHPLILGHE 82

Query: 65  YVGEVVGIGQEVKGFKIGDRVSGEGHITCGHCRNCRGGRTHLCRNTIGVGVNRP--GCFA 122
             G +  +G  V   +IG+RV+ E    C  C+ C+ GR +LC + I      P  G FA
Sbjct: 83  LSGRIAAVGSAVDPARIGNRVAVEPQRPCRTCKQCKAGRYNLCPD-IEFYATPPIDGAFA 141

Query: 123 EYLVIPAFNAFKIPDNISDDLAAIFDPFGNAVHTALSFDL-VGEDVLVSGAGPIGIMAAA 181
           EY+ I +  A+ IPD++SD+ AA+ +P    +      ++  G  VL++GAGPIGI+AA 
Sbjct: 142 EYVTIQSDFAYDIPDSVSDEAAALIEPLSVGLWACERAEIKPGSRVLIAGAGPIGIIAAQ 201

Query: 182 VAKHVGARNVVITDVNEYRLELARKMGITRAVNVAKENLNDVMAELGMTEGFDVG--LEM 239
            A+  GA  + ITD+ E RL  A + G T A+N          A+    EG DV   ++ 
Sbjct: 202 AARAFGATEIYITDIAEDRLAFALEHGATHALN----------AKTDSVEGLDVDAFIDA 251

Query: 240 SGAPPAFRTMLDTMNHGGRIAMLGIPPSDMSIDWTKVIFKGLFIKGIYGREMFETWYKMA 299
           SGAP A R+ +  +   GR+ ++G+   D+ +  + +  + +++ G++      TW    
Sbjct: 252 SGAPQAVRSGIKAVGPAGRVILVGLGADDVELPVSYIQNREIWLSGVF--RYTNTWPLAI 309

Query: 300 ALIQSG-LDLSPIITHRFSIDDFQKGFDA-MRSGQSGKVI 337
            LI  G +DL  ++T +F++ + ++   A  ++GQ   V+
Sbjct: 310 QLIADGKVDLDILVTGKFTLAESEEALKAGKQAGQLKAVV 349


Lambda     K      H
   0.322    0.140    0.433 

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: 290
Number of extensions: 13
Number of successful extensions: 4
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: 341
Length of database: 353
Length adjustment: 29
Effective length of query: 312
Effective length of database: 324
Effective search space:   101088
Effective search space used:   101088
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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