GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Shewanella amazonensis SB2B

Align L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized)
to candidate 6935786 Sama_0004 alcohol dehydrogenase, zinc-binding (RefSeq)

Query= BRENDA::O58389
         (348 letters)



>FitnessBrowser__SB2B:6935786
          Length = 377

 Score =  117 bits (293), Expect = 5e-31
 Identities = 109/360 (30%), Positives = 167/360 (46%), Gaps = 40/360 (11%)

Query: 13  PGYGAELVEVDVPKPGPGEVLIKVLATSICGTDLHIYEWNEWAQSRIKPPQIMGHEVAGE 72
           PG    + EVDV  P  GEVL++++AT +C TD      ++        P I+GHE  G 
Sbjct: 16  PGQPLSVEEVDVMLPKAGEVLVRIVATGVCHTDAFTLSGDD---PEGVFPAILGHEGGGI 72

Query: 73  VVEIGPGVEGIEVGDYVSVETHIVCGKCYACRRGQYHVC---QNTKIFGVDTDG------ 123
           V  +G GV  + VGD+V       CGKC  C  G+ ++C   + T+  G+  DG      
Sbjct: 73  VEMVGEGVTSVAVGDHVIPLYTAECGKCKFCTSGKTNLCSAVRATQGKGLMPDGTTRFYK 132

Query: 124 ------------VFAEYAVVPAQNIWK-NPKSIPPEYATLQEPLGNAVDTVL--AGPISG 168
                        F+EY V+P  ++ K NP++   E   L   +   +  VL  A    G
Sbjct: 133 DGEPIYHYMGCSTFSEYTVLPEISLAKVNPEAPLEEVCLLGCGVTTGMGAVLKTAKVKKG 192

Query: 169 KSVLITGAGPLGLLGIAVAKASGAYPVIVSEPSDFRRELAKKVGADYVINP--FEEDVVK 226
            +V I G G +GL  +  A  +GA  +I  + +D + ELAKK+GA   INP  +++ +  
Sbjct: 193 DTVAIFGLGGIGLSAVIGATMAGASRIIGIDINDSKFELAKKLGATDCINPKDYDKPIQD 252

Query: 227 EVMDITDGNGVDVFLEFSGAPKALEQGLQAVTPA-GRVSLLGLYPGKVTIDFN--NLI-- 281
            ++++TDG GVD   E  G    +   L+      G   ++G+      I      L+  
Sbjct: 253 VIVEMTDG-GVDFSFECIGNVNVMRSALECCHKGWGESVIIGVAGAGQEISTRPFQLVTG 311

Query: 282 -IFKALTIYGITGRHLWETWYTVSRLLQSGKLNLDPIITHKYKGFDKYEEAFELMRAGKT 340
            +++     G+ GR   E    V + L+ G+  L   ITH   G D   EAF+LM  GK+
Sbjct: 312 RVWRGSAFGGVKGRS--ELPGIVEQYLR-GEFALSDFITHT-MGLDAINEAFDLMHEGKS 367


Lambda     K      H
   0.318    0.139    0.418 

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: 335
Number of extensions: 23
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: 348
Length of database: 377
Length adjustment: 29
Effective length of query: 319
Effective length of database: 348
Effective search space:   111012
Effective search space used:   111012
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 (21.7 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