GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Caulobacter crescentus NA1000

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate CCNA_02479 CCNA_02479 aryl-alcohol dehydrogenase

Query= curated2:Q72L62
         (343 letters)



>FitnessBrowser__Caulo:CCNA_02479
          Length = 366

 Score =  119 bits (298), Expect = 1e-31
 Identities = 113/373 (30%), Positives = 169/373 (45%), Gaps = 60/373 (16%)

Query: 8   APEEGLTLVDRPVPEPGPGEILVRVEAASICGTDLHIWKWDAWARGRIRP---PLVTGHE 64
           +P    +L    +  P  GEILVRV A  +C TD+ +       R +  P   P+V GHE
Sbjct: 10  SPSGPFSLEALDIEPPRAGEILVRVVATGVCHTDMVM-------RDQHLPTPQPVVLGHE 62

Query: 65  FSGVVEAVGPGVKRPQVGDHVSLESHVVCHACPAC--RTGNY-HVCLNTKILGVDRDGG- 120
            +GVVE VGPGV +  VGDHV +  +  C  CP+C      Y H       +G   DG  
Sbjct: 63  GAGVVEQVGPGVAKVAVGDHVVMTFNS-CGRCPSCSDHAPTYCHEFFPRNFMGAREDGSS 121

Query: 121 ------------------FAEYVVVPAENAWVNPKDLPFEVAAILEPFGNAVHTVYAGSG 162
                             FA Y +    NA    K  P E    L P G  V T   G+G
Sbjct: 122 GLSKGSEVIHANIFGQSSFATYALCHERNAVKVDKTAPLER---LGPLGCGVMT---GAG 175

Query: 163 V--------SGKSVLITGAGPIGLMAAMVARASGAGPILVSDPNPYRLAFARPY-ADRLV 213
                    +G+S+++ GAG +GL A + A+A GAGPI+  D NP RLA A    AD  +
Sbjct: 176 AVMNALKVPAGRSLVVFGAGAVGLSAVLAAKAIGAGPIIAIDINPERLALALELGADHAL 235

Query: 214 NPLEEDLLEVVRRVTGSGVEVLLEFSGNEAAIHQGLMALIPGGEARILG-------IPSD 266
           N  E  ++E ++ +TG+G    ++ + N   + Q +  L   G   ++G       +P D
Sbjct: 236 NGAEGGVVEKIQAITGTGAHFSIDTTANLKVMRQAVDCLGARGVCGLVGASKMGDELPLD 295

Query: 267 PIRFDLAGELVMRGITAFGIAGRRLWQTWMQGTALVYSGRVDLSPLITHRLPLSRYREAF 326
            +   ++G  V+RG+   G A   ++   +   AL  +GR     LI    PL+   +A 
Sbjct: 296 AVSV-MSGGKVVRGVVE-GDADPDVFIPEL--IALHLAGRFPFDRLIQF-YPLAEINQAV 350

Query: 327 GLLASGQAVKVIL 339
               +G+ +K ++
Sbjct: 351 SDGETGRVIKPVV 363


Lambda     K      H
   0.321    0.140    0.432 

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: 385
Number of extensions: 23
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: 343
Length of database: 366
Length adjustment: 29
Effective length of query: 314
Effective length of database: 337
Effective search space:   105818
Effective search space used:   105818
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 (21.8 bits)
S2: 49 (23.5 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