GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bch in Shewanella amazonensis SB2B

Align 3-hydroxy-isobutyryl-CoA hydrolase (EC 3.1.2.4) (characterized)
to candidate 6937209 Sama_1379 enoyl-CoA hydratase/isomerase family protein (RefSeq)

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



>FitnessBrowser__SB2B:6937209
          Length = 368

 Score =  249 bits (635), Expect = 1e-70
 Identities = 142/339 (41%), Positives = 198/339 (58%), Gaps = 6/339 (1%)

Query: 28  IGHLTLNRPAGLNAITLDMVRSLHRQLDAWSKDPHIHAVVLRGAGEKAFCAGGDIRSLYD 87
           IG  TLN  A LNA+ LDMVR+L  QL AW  D +I  V+L GAG+KAFCAGGD+R+LY 
Sbjct: 18  IGVATLNVEAALNALDLDMVRALSAQLKAWQADSNIAMVLLDGAGDKAFCAGGDVRALYQ 77

Query: 88  SFK----SGGTLHEDFFVEEYALDLAIHHYRKPVLALMDGFVLGGGMGLVQGADLRVVTE 143
           + K    S  TL + FF EEY LD  IH + KP +   DG V+GGG+GL+ GA  R+ TE
Sbjct: 78  ASKDAPGSTETLAKTFFEEEYRLDYFIHEFGKPFMVWGDGIVMGGGLGLMAGASHRIATE 137

Query: 144 RSRLAMPEVAIGYFPDVGGSYFLPRIPGELGIYLGVSGVQIRAADALYCGLADWYLESQK 203
           RSR+AMPE+ IG +PDVGG++FL  +P + G++LG++  Q+  ADALY G A++ LES  
Sbjct: 138 RSRIAMPEITIGLYPDVGGTFFLAHMPEKTGVFLGLTAFQMNGADALYAGTANFLLESDD 197

Query: 204 LAELDQHLDSLEWHDTPLKDLQGLLAKLALQQLPD-APLQALRPTIDHFFALPDVPSIVE 262
              L   L  + W D    + Q L   L  + +P+ A        +       D+ +++E
Sbjct: 198 KEPLLDALAEVAWDDHSEANHQRLSDVLGTRAVPEQASFLKDNAELISELCSGDLDTVIE 257

Query: 263 QLRTVTVADSHDWAMTTADLLDSRSPLAMGVTLEMLRRGRQLSLENCFALELHLDRQWFE 322
           + + +   DSH   +   D L + SPL+  +       G +LSL +CF  EL +      
Sbjct: 258 RFKALP-DDSHKSLLRARDTLLAGSPLSAHLVWHQAIIGEELSLNDCFRWELGVSINCCA 316

Query: 323 RGDLIEGVRALLIDKDKSPRWNPPTVQALDAKHVASFFS 361
            GD +EGVRALLIDKD++P W    V ++ A+ + S  S
Sbjct: 317 HGDFVEGVRALLIDKDRNPTWQYADVASVPAEAIGSLLS 355


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: 387
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: 368
Length of database: 368
Length adjustment: 30
Effective length of query: 338
Effective length of database: 338
Effective search space:   114244
Effective search space used:   114244
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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