GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Dechlorosoma suillum PS

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate Dsui_2228 Dsui_2228 Zn-dependent alcohol dehydrogenase

Query= curated2:Q6AAR3
         (345 letters)



>FitnessBrowser__PS:Dsui_2228
          Length = 340

 Score =  118 bits (296), Expect = 2e-31
 Identities = 108/347 (31%), Positives = 162/347 (46%), Gaps = 19/347 (5%)

Query: 1   MKALVKTRPEPGLELVEVPDPVAGPNDVIVKVMRTGICGTDVHIDKWDGWAAKTVHTPLV 60
           MKA V       L + EVP P   P  V+VKV+ +G+C TD+H    D W  K    P +
Sbjct: 5   MKAAVVHEFGKPLVIEEVPVPEVPPGQVLVKVVASGVCHTDLHAADGD-WPVKP-SLPFI 62

Query: 61  LGHEFCGEIVELGSEVNDLEVGQFVSGEG-HYVCGRCRACLAGKRHLCRNTQGIGYAVNG 119
            GHE  G +  +G+ V  ++ G  V     H  CG C  C+ G   LC + Q  GY VNG
Sbjct: 63  PGHEGVGYVAAVGAGVTHVKEGDRVGVPWLHTACGHCEHCITGWETLCDSQQMTGYTVNG 122

Query: 120 AYCQYFVMPAGNVWVHHIPD-LDPDVAAIFDPFGNAVHTALQ-FPCLAED-VLVSGAGPI 176
            Y +Y +   G  +V  +PD L+   AA     G  V+  L+   C   D V +SG G +
Sbjct: 123 GYAEYVLADPG--YVGKLPDTLEFAPAAPVLCAGVTVYKGLKVLECKPGDWVAISGIGGL 180

Query: 177 GIMAALVAQFQGARNVVVTDLSDERLELAQQLGLKNAVNVSREGLETVWDRFDMKEGFDI 236
           G MA   A+  G  +V+  D++DE+L LA+ LG    +N +R  ++ V +     +G   
Sbjct: 181 GHMAVQYAKAMGF-HVIAVDVADEKLALAKTLGADVTLNAAR--VDPVAEIQKQIKGAHG 237

Query: 237 GLEMSGSGTALTSMIDNMTHGGRIALLGTPSTDITLDFSKIIFNMITIQG--VTGRQIFE 294
            L  + S +A    +  +   G ++L+G P  D  L    ++ N  T++G  V  R+  E
Sbjct: 238 ILVTAVSRSAFGQALGMLHKRGTMSLVGLPPGDFGLPIFDVVLNAKTVRGSIVGTRKDLE 297

Query: 295 TWYTMASLIRSGLDISGIITDRYPITEFREAFDVAGSGH-GGKVVMN 340
                A     G   +   TDR  I    + F    +GH  G++V+N
Sbjct: 298 EALAFAG---EGKVKTHYSTDR--IENINDIFGRMKAGHIDGRIVLN 339


Lambda     K      H
   0.322    0.140    0.436 

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: 319
Number of extensions: 17
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: 345
Length of database: 340
Length adjustment: 29
Effective length of query: 316
Effective length of database: 311
Effective search space:    98276
Effective search space used:    98276
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 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