GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Halomonas desiderata SP1

Align alcohol dehydrogenase (EC 1.1.1.1); long-chain-alcohol dehydrogenase (EC 1.1.1.192) (characterized)
to candidate WP_086510128.1 BZY95_RS11880 alcohol dehydrogenase

Query= BRENDA::A4IP64
         (395 letters)



>NCBI__GCF_002151265.1:WP_086510128.1
          Length = 387

 Score =  197 bits (502), Expect = 3e-55
 Identities = 118/372 (31%), Positives = 200/372 (53%), Gaps = 6/372 (1%)

Query: 15  GWGALDQLVPEVKRLGAKHILVITDPMLVKIGLVDQVTSPLRQEGYSVHVYTDVVPEPPL 74
           G GA   +   V   GA+ +L+++DP +V  G V++V + L ++G     +T V P P  
Sbjct: 19  GDGARRAVANFVGTFGAERVLLVSDPGVVLAGWVEEVEADLAEQGIFSQRFTSVSPNPRA 78

Query: 75  ETGEKAVAFARDGKFDLVIGVGGGSALDLAKLAAVLAVHDGSVADYLNLTGTRTLEKKGL 134
           E         R+     ++ +GGGS +D AK   ++  HDG + D+    G  TL     
Sbjct: 79  EEVMAGAMAYREMGAQAIVAIGGGSPMDCAKGIGIVVAHDGHIIDF---EGVDTLRVPIP 135

Query: 135 PKILIPTTSGTGSEVTNISVLSLETT--KDVVTHDYLLADVAIVDPQLTVSVPPRVTAAT 192
           P I +PTT+GT ++++  +++S +    K  +    ++ DV+++DPQ+T+++ P +TA T
Sbjct: 136 PLIFVPTTAGTSADISQFAIISDQQRRMKFSIVSKSVVPDVSLIDPQVTLTMSPFLTACT 195

Query: 193 GIDALTHAVEAYVSVNASPTSDGLAVAAIRLISRSLRKAVANGSDKQARIDMANGSYLAG 252
           G+DAL HA+EA+VS  + P +D  A+ A+RLI+  L   V    D + R  +  GS  AG
Sbjct: 196 GVDALVHAIEAFVSTGSGPLTDAHALEAMRLINGHLVALVQAPHDLELRSQVMLGSMQAG 255

Query: 253 LAFFNAGVAGVHALAYPLGGQFHIAHGESNAVLLPYVMGYIRQSCTKRMADIFNALGGNS 312
           LAF NA +  VHA+++ LGG   + HG  N++LL +V+ Y  ++  +R   I   LG + 
Sbjct: 256 LAFSNAILGAVHAMSHSLGGFLDLPHGLCNSLLLEHVVAYNFEAAPERFTRIAETLGIDC 315

Query: 313 SFLSEVEASYRCVEELERFVADVGIPKTLGGFGIPESALESLTKDAVQQKRLLARSPLPL 372
             L+  +   R ++ L      VG+  +LG  G+  S +  L + A++   +L  +P   
Sbjct: 316 RGLNSTQVKARLIDHLIELKRAVGLTGSLGRLGVHTSDVPFLARHALEDPCILT-NPRRS 374

Query: 373 LEADIRAIYEAA 384
              D++ +YE A
Sbjct: 375 SPRDVQVVYEEA 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: 405
Number of extensions: 17
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