GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Methanobacterium veterum MK4

Align alcohol dehydrogenase (EC 1.1.1.1) (characterized)
to candidate WP_048082914.1 EJ01_RS11120 alcohol dehydrogenase

Query= BRENDA::Q09669
         (422 letters)



>NCBI__GCF_000745485.1:WP_048082914.1
          Length = 387

 Score =  280 bits (715), Expect = 7e-80
 Identities = 154/383 (40%), Positives = 229/383 (59%), Gaps = 5/383 (1%)

Query: 44  MPVSAFYIPSFNLFGKGCLAEAAKQIKMSGFKNTLIVTDPGIIKVGLYDKVKALLEEQSI 103
           M +  F  P   +FG      A +  K  G +  LIV+DPGII  G  D++  +LE + +
Sbjct: 6   MELRKFVAPEL-VFGLDARLLAGRYAKNFGAQKVLIVSDPGIINAGWLDEILPVLESEGL 64

Query: 104 TVHLYDGVQPNPTVGNVNQGLEIVKKENCDSMVSIGGGSAHDCAKGIALLATNGGKIADY 163
              +Y  V+PN    +V +G E+ K E C+++V++GGGS  DCAKGI ++++N   I ++
Sbjct: 65  PYEIYKDVKPNSKENDVIKGSELYKNEECNAIVALGGGSTLDCAKGIGIVSSNNKNILEF 124

Query: 164 EGVDKSSKPQLPLIAINTTAGTASEMTRFAIITEETRHIKMAIIDKHTMPILSVNDPETM 223
           EGVDK   P  PLI I TTAG+++++++FA+I ++ R +K++II K  +P +++ DP T 
Sbjct: 125 EGVDKVYNPIPPLICIPTTAGSSADVSQFAVIMDQKRKVKISIISKAVVPDVALIDPITT 184

Query: 224 YGLPPSLTAATGMDALTHAVEAYVSTAANPITDACAVKCIELVNKYLKRAVDNGKDEEAR 283
             +   LTA TG+DALTHA+EAYVS A++P+TD  A+  I L+   L + + N  D   R
Sbjct: 185 TTMDNYLTACTGLDALTHAIEAYVSNASSPLTDTHALNAIRLIWSSLAKIIHNPNDLGLR 244

Query: 284 DNMAYAEFLGGMAFNNASLGYVHAMAHQLGGFYGIPHGVCNAVLLAHVQKFN-SRDPRAN 342
            NM       G+AF+NASLG VHAMAH LGGF  + HG CNAVLL HV  FN   +P   
Sbjct: 245 GNMMLGSLEAGLAFSNASLGAVHAMAHSLGGFLDLSHGECNAVLLDHVVDFNFDAEPVRY 304

Query: 343 ARLGD---IAFHLGCEEHTAEAALDRISQLVLEVKIRPHLVDLGVKEKDFDVLVDHAMKD 399
            R+G+   I F    +     A + ++  L   + I   L  +GVKE D   L  +AM+D
Sbjct: 305 QRIGEAMGINFSRMTKIEKKTAIIHKLKHLKESIGIDHTLRQMGVKESDIAQLSKNAMED 364

Query: 400 ACGATNPIQPTHDEVKAIFKSAM 422
           +C  TNP +P   +++ IF++A+
Sbjct: 365 SCIVTNPRRPEQKDIEEIFRNAL 387


Lambda     K      H
   0.319    0.134    0.390 

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: 410
Number of extensions: 17
Number of successful extensions: 2
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: 422
Length of database: 387
Length adjustment: 31
Effective length of query: 391
Effective length of database: 356
Effective search space:   139196
Effective search space used:   139196
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: 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