GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Methanobacterium veterum MK4

Align alcohol dehydrogenase (EC 1.1.1.1); long-chain-alcohol dehydrogenase (EC 1.1.1.192) (characterized)
to candidate WP_048082914.1 EJ01_RS11120 alcohol dehydrogenase

Query= BRENDA::A4IP64
         (395 letters)



>NCBI__GCF_000745485.1:WP_048082914.1
          Length = 387

 Score =  198 bits (503), Expect = 3e-55
 Identities = 120/360 (33%), Positives = 201/360 (55%), Gaps = 6/360 (1%)

Query: 27  KRLGAKHILVITDPMLVKIGLVDQVTSPLRQEGYSVHVYTDVVPEPPLETGEKAVAFARD 86
           K  GA+ +L+++DP ++  G +D++   L  EG    +Y DV P        K     ++
Sbjct: 31  KNFGAQKVLIVSDPGIINAGWLDEILPVLESEGLPYEIYKDVKPNSKENDVIKGSELYKN 90

Query: 87  GKFDLVIGVGGGSALDLAKLAAVLAVHDGSVADYLNLTGTRTLEKKGLPKILIPTTSGTG 146
            + + ++ +GGGS LD AK   +++ ++ ++ ++    G   +     P I IPTT+G+ 
Sbjct: 91  EECNAIVALGGGSTLDCAKGIGIVSSNNKNILEF---EGVDKVYNPIPPLICIPTTAGSS 147

Query: 147 SEVTNISVLSLETTKDVVT--HDYLLADVAIVDPQLTVSVPPRVTAATGIDALTHAVEAY 204
           ++V+  +V+  +  K  ++     ++ DVA++DP  T ++   +TA TG+DALTHA+EAY
Sbjct: 148 ADVSQFAVIMDQKRKVKISIISKAVVPDVALIDPITTTTMDNYLTACTGLDALTHAIEAY 207

Query: 205 VSVNASPTSDGLAVAAIRLISRSLRKAVANGSDKQARIDMANGSYLAGLAFFNAGVAGVH 264
           VS  +SP +D  A+ AIRLI  SL K + N +D   R +M  GS  AGLAF NA +  VH
Sbjct: 208 VSNASSPLTDTHALNAIRLIWSSLAKIIHNPNDLGLRGNMMLGSLEAGLAFSNASLGAVH 267

Query: 265 ALAYPLGGQFHIAHGESNAVLLPYVMGYIRQSCTKRMADIFNALGGNSSFLSEVEASYRC 324
           A+A+ LGG   ++HGE NAVLL +V+ +   +   R   I  A+G N S ++++E     
Sbjct: 268 AMAHSLGGFLDLSHGECNAVLLDHVVDFNFDAEPVRYQRIGEAMGINFSRMTKIEKKTAI 327

Query: 325 VEELERFVADVGIPKTLGGFGIPESALESLTKDAVQQKRLLARSPLPLLEADIRAIYEAA 384
           + +L+     +GI  TL   G+ ES +  L+K+A++   ++     P  + DI  I+  A
Sbjct: 328 IHKLKHLKESIGIDHTLRQMGVKESDIAQLSKNAMEDSCIVTNPRRP-EQKDIEEIFRNA 386


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: 354
Number of extensions: 20
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: 395
Length of database: 387
Length adjustment: 31
Effective length of query: 364
Effective length of database: 356
Effective search space:   129584
Effective search space used:   129584
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