GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Collinsella tanakaei YIT 12063

Align alcohol dehydrogenase (EC 1.1.1.1); long-chain-alcohol dehydrogenase (EC 1.1.1.192) (characterized)
to candidate WP_009141551.1 HMPREF9452_RS07580 lactaldehyde reductase

Query= BRENDA::A4IP64
         (395 letters)



>NCBI__GCF_000225705.1:WP_009141551.1
          Length = 386

 Score =  206 bits (523), Expect = 1e-57
 Identities = 128/360 (35%), Positives = 202/360 (56%), Gaps = 8/360 (2%)

Query: 5   RIVFPPLSHVGWGALDQLVPEVKRLGAKHILVITDPMLVKIGLVDQVTSPLRQEGYSVHV 64
           RIV   +S+ G GA+ ++  E+ R G K + V TDP LVK G+  +VT  L + G +  V
Sbjct: 4   RIVLNTISYHGAGAIQEIPGELTRRGYKKVFVCTDPDLVKFGVAAKVTDLLDEAGIAYSV 63

Query: 65  YTDVVPEPPLETGEKAVAFARDGKFDLVIGVGGGSALDLAKLAAVLAVHDGSVADYLNLT 124
           Y+D+ P P ++     V   +  + D ++ +GGGSA+D AK   V+ + +   AD  +L 
Sbjct: 64  YSDIKPNPTIQNVTDGVEAFKAAEADSIVTIGGGSAMDTAKAIGVI-ITNPEFADVRSLE 122

Query: 125 GTRTLEKKGLPKILIPTTSGTGSEVT-NISVLSLETTKDVVTHDYLLA-DVAIVDPQLTV 182
           G    +   +  I +PTT+GT +EVT N  +  +E  +  V  D   A +VA+VDP++  
Sbjct: 123 GVAPTKNHAVFTIAVPTTAGTAAEVTINYVITDVEKVRKFVCVDTNDAPEVAVVDPEMMA 182

Query: 183 SVPPRVTAATGIDALTHAVEAYVSVNASPTSDGLAVAAIRLISRSLRKAVA---NGSDKQ 239
           ++P  +TA+TG+DALTHA+E Y +  A   SD   + AI LIS++LR AVA   +G    
Sbjct: 183 TMPAGLTASTGMDALTHAIEGYTTKGAWEMSDMFHLKAIELISKNLRDAVAEAKSGVPGS 242

Query: 240 ARIDMANGSYLAGLAFFNAGVAGVHALAYPLGGQFHIAHGESNAVLLPYVMGYIRQSCTK 299
            R  MA   Y+AG+ F N G+   H++A+ L   F   HG + A+LLP  M + +    +
Sbjct: 243 GREGMALAQYIAGMGFSNVGLGVDHSMAHTLSAHFDTPHGVACAMLLPIAMEFNKPVVIE 302

Query: 300 RMADIFNALGGNSSFLSEVEASYRCVEELERFVADVGIPKTLGGFGIPESALESLTKDAV 359
           R+A +  A+G +++ +S  EA+   +  +++   DV IP       I E  L++LTKDA+
Sbjct: 303 RLAKVAVAMGVDTTGMSTDEAADAAIAAVKQLSVDVNIPTVCE--AITEDELDTLTKDAM 360


Lambda     K      H
   0.318    0.135    0.381 

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: 349
Number of extensions: 20
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: 395
Length of database: 386
Length adjustment: 31
Effective length of query: 364
Effective length of database: 355
Effective search space:   129220
Effective search space used:   129220
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: 50 (23.9 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