GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Shewanella sp. ANA-3

Align 3-hydroxy-isobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate 7025616 Shewana3_2767 enoyl-CoA hydratase/isomerase (RefSeq)

Query= reanno::pseudo3_N2E3:AO353_25665
         (368 letters)



>FitnessBrowser__ANA3:7025616
          Length = 383

 Score =  252 bits (644), Expect = 1e-71
 Identities = 148/334 (44%), Positives = 205/334 (61%), Gaps = 13/334 (3%)

Query: 28  IGHLTLNRPAGLNAITLDMVRSLHRQLDAWSKDPHIHAVVLRGAGEKAFCAGGDIRSLYD 87
           +G +TLN    LNA+ LDMVR++  QL+ W KDP I  VVL G+GEKAFCAGGD+R+LY 
Sbjct: 30  VGVVTLNVEKALNALDLDMVRAMTVQLNLWKKDPLIACVVLDGSGEKAFCAGGDVRALYH 89

Query: 88  -SFKSGGTLHED---FFVEEYALDLAIHHYRKPVLALMDGFVLGGGMGLVQGADLRVVTE 143
            S  + G + E    FF EEY LD  +H Y KPVL   DG V+GGG+GL+ GA  RVVTE
Sbjct: 90  ASVAAKGQVTEVAKVFFEEEYRLDYLLHTYGKPVLVWGDGIVMGGGLGLMAGASHRVVTE 149

Query: 144 RSRLAMPEVAIGYFPDVGGSYFLPRIPGELGIYLGVSGVQIRAADALYCGLADWYLESQK 203
            SR+AMPEV IG +PDVGGSYFL R+PG++G++LG++  Q+ AADA Y GLAD YL    
Sbjct: 150 TSRIAMPEVTIGLYPDVGGSYFLNRMPGKMGLFLGLTAYQMNAADACYVGLADHYLNRDD 209

Query: 204 LAELDQHLDSLEWHDTPL---KDLQGLLAKLALQ-QLP--DAPLQALRPTIDHFFALPDV 257
              +   + +L+W DTP    + L  ++ +L+ Q  +P  D+ L   +  ID   A   +
Sbjct: 210 KELMFDAMATLDWSDTPALNHQRLDTMINELSNQVDIPKGDSLLAESQEMIDRLMA-GSL 268

Query: 258 PSIVEQLRTVTVADSHDWAMTTADLLDSRSPLAMGVTLEMLRRGRQLSLENCFALELHLD 317
             IV ++ T++  ++  W       + + SP++  +     + G +LSL  CF  EL + 
Sbjct: 269 TDIVSRMSTLSTEEA--WLNKACATMLAGSPISWHLAYIQTQLGTKLSLAQCFKWELTVS 326

Query: 318 RQWFERGDLIEGVRALLIDKDKSPRWNPPTVQAL 351
                +GD  EGVRALLIDKD+ P+W    VQ++
Sbjct: 327 VNTCAKGDFCEGVRALLIDKDRQPKWQFADVQSV 360


Lambda     K      H
   0.321    0.138    0.418 

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: 342
Number of extensions: 15
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: 368
Length of database: 383
Length adjustment: 30
Effective length of query: 338
Effective length of database: 353
Effective search space:   119314
Effective search space used:   119314
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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