GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Dinoroseobacter shibae DFL-12

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate 3607669 Dshi_1078 Alcohol dehydrogenase zinc-binding domain protein (RefSeq)

Query= curated2:Q67N85
         (351 letters)



>FitnessBrowser__Dino:3607669
          Length = 345

 Score =  131 bits (329), Expect = 3e-35
 Identities = 106/343 (30%), Positives = 162/343 (47%), Gaps = 22/343 (6%)

Query: 19  LQEVPIPTIGPRDVLVKVRAASICGTDYHIYTWDPWSAGRVKPPLTIGHELAGEVVAVGR 78
           L++VP P      V++KV A  +C +D+H +  +     RVKP    GHE  GEV+  G 
Sbjct: 15  LEDVPEPVCPEDGVVLKVLACGVCRSDWHGWVGEH---PRVKPGQIGGHEYCGEVIEAGP 71

Query: 79  EVTACKVGDYVSAETHIVCNRCPRCHMGEYHLCENTKILGVDTDGAFAEYVAVPEQNIWV 138
              A K GD V A   + C  CP C  G  + C N ++ G    GAFAEYVAVP  +   
Sbjct: 72  RA-AFKPGDRVVAPFILACGSCPSCQAGAQNTCPNQRLPGFVEPGAFAEYVAVPFDH--- 127

Query: 139 NDKDIPFELQ-SIQEPLGNAVHTALNGDLTARS-------VLITGCGPIGIMSVPVAKMA 190
           N   +P  L  ++   LG  V TA +  LT R+       V + G G IG+ SV +A   
Sbjct: 128 NLSRLPDSLSPTVAAGLGCRVTTAWHA-LTGRAAVQGAEWVAVHGTGGIGLSSVILANAL 186

Query: 191 GAEIVMAMDINEYRLQLAGQLGADVLINPTKQDPVEVVRSYTRGYGADVVLEMSGNPTAI 250
           GA ++ A+D+ + +L  A Q GA+V +N  + D    ++  T G GA V +E  G P  +
Sbjct: 187 GARVI-AVDVVDEKLTHAAQHGAEVTLNAREGDVAARIKQITGG-GAHVAIEALGIPETV 244

Query: 251 RQGLKAARNGARISLLGLP-GRPLELDLAADVIMRG-LVLQGITGRRMWQTWYQVRSLYR 308
              L+  R   R   +GLP G    +++    I +G L + G  G   W+ +  + SL  
Sbjct: 245 NASLECLRPLGRHVQVGLPTGHTARMEINMSAIYQGNLAVYGTRGMPSWR-YPSLLSLIE 303

Query: 309 AGLAERLRPLVTHRMPLEQIDAAMELMGSGQSGKIVLVPDLKA 351
            G  + + PL+   + L    A +          + ++ D ++
Sbjct: 304 TGRVD-MSPLIAREIGLSGTSAELRAFNGPTPPGVAVITDFQS 345


Lambda     K      H
   0.320    0.137    0.415 

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: 339
Number of extensions: 27
Number of successful extensions: 5
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: 351
Length of database: 345
Length adjustment: 29
Effective length of query: 322
Effective length of database: 316
Effective search space:   101752
Effective search space used:   101752
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