GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Cronobacter universalis NCTC 9529

Align L-threonine 3-dehydrogenase; TDH; L-threonine dehydrogenase; EC 1.1.1.103 (characterized)
to candidate WP_038857091.1 AFK65_RS10710 alcohol dehydrogenase AdhP

Query= SwissProt::Q8U259
         (348 letters)



>NCBI__GCF_001277175.1:WP_038857091.1
          Length = 343

 Score =  121 bits (304), Expect = 2e-32
 Identities = 109/338 (32%), Positives = 158/338 (46%), Gaps = 29/338 (8%)

Query: 18  ELVEVDVPKPGPGEVLIKILATSICGTDLHIYEWNEWAQTRIRPPQIMGHEVAGEVVEVG 77
           E+ EV VP+  PG+VL+KI AT +C TDLH  E  +W   +  PP I GHE  G VV VG
Sbjct: 19  EIQEVLVPEVTPGKVLVKIAATGVCHTDLHAAE-GDW-PVKPNPPFIPGHEGVGHVVAVG 76

Query: 78  PGVEGIEVGDYVSVE-THIVCGKCYACKRGQYHVCQNTKIFGVDTDGVFAEYAVVPAQNV 136
            GV  I+ GD V V   +  CG C  C  G   +C   +  G   +G FA+Y +  A  V
Sbjct: 77  QGVTHIKEGDRVGVPWLYSACGHCEHCLAGWETLCHGQQNSGYSVNGTFADYCLADANYV 136

Query: 137 WKNPKNIPPEYATLQEPLGNAVDTVLAG-----PIAGKSVLITGAGPLGLLGIAVAKASG 191
              P N+  E+ ++  P+  A  TV  G        G  V+I+G G LG L I  A A G
Sbjct: 137 GILPDNV--EFTSI-APILCAGVTVYKGLKMTDTKPGDWVVISGIGGLGHLAIQYANAMG 193

Query: 192 AYPVIVSEPSEFRRNLAKKVGADYVINPFEEDVVKEVMDITDG-NGVDVFLEFSGAPKAL 250
                V    + + + AK++GA    N  E D      +   G +GV   L  + +PKA 
Sbjct: 194 LNVAAVDIDKD-KLDFAKRLGAQVTANALEVDPGSYFHETFGGAHGV---LVTAVSPKAF 249

Query: 251 EQGLQAVTPAGRVSLLGLFPGKVSIDFNNLIIFKALTVYGI---TGRHLWETWYTVSRLL 307
            Q    +   G + L GL PGK  +   ++++    TV G    T + L E         
Sbjct: 250 AQATTMMRRGGTMVLNGLPPGKFDLSIFDMVL-DGTTVRGSIVGTRKDLQEALDFAGHNK 308

Query: 308 QSGKLNIDPIITHKYKGFDKYEEAFELMRAGK-TGKVV 344
            + ++ ++P+        +   + F+ MR GK TG++V
Sbjct: 309 VAAEIAVEPL--------ENINDIFDRMRNGKITGRIV 338


Lambda     K      H
   0.318    0.138    0.417 

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: 296
Number of extensions: 18
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: 348
Length of database: 343
Length adjustment: 29
Effective length of query: 319
Effective length of database: 314
Effective search space:   100166
Effective search space used:   100166
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 24 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