GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Desulfacinum infernum DSM 9756

Align Cyclohex-1-ene-1-carbonyl-CoA dehydrogenase; Ch1CoA; EC 1.3.8.10 (characterized)
to candidate WP_073037063.1 BUB04_RS03730 acyl-CoA dehydrogenase

Query= SwissProt::Q2LQN9
         (414 letters)



>NCBI__GCF_900129305.1:WP_073037063.1
          Length = 382

 Score =  298 bits (762), Expect = 2e-85
 Identities = 163/378 (43%), Positives = 233/378 (61%), Gaps = 4/378 (1%)

Query: 36  ELTEEQKLLMEMVRNLAVREIAPRAIEIDENHSFPVHARDLFADLGLLSPLVPVEYGGTG 95
           ELTEEQ+++ +M R  A REIAP A E+D  H  P        +LGL+   +P EYGG G
Sbjct: 4   ELTEEQRMIQDMARKFAEREIAPVAAELDRTHKHPEEIVKKMGELGLMGITIPPEYGGAG 63

Query: 96  MDITTFAMVLEEIGKVCASTA-LMLLAQADGMLSIILDGSPALKEKYLPRFGEKSTLMTA 154
           MD  ++ + + EI K CAS   +M +  +     +   G+   K+++L        L   
Sbjct: 64  MDYVSYVLAMIEISKACASCGVIMSVCNSLYNFPVYTYGTEEQKQQFLTPVASGEYL-GC 122

Query: 155 FAATEPGAGSDLLAMKTRAVKKGDKYVINGQKCFITNGSVADILTVWAYTDPSKGAKGMS 214
           +  TE GAGSD   M+T AV  G+++VING+K FITNG+VA    + A TD  KG KG+S
Sbjct: 123 YGLTEAGAGSDPAKMRTTAVLDGNEWVINGEKKFITNGNVARYCVLAAVTDKEKGYKGIS 182

Query: 215 TFVVE-RGTPGLIYGHNEKKMGMRGCPNSELFFEDLEVPAENLVGEEGKGFAYLMGALSI 273
           +F+V+   TPG   G  E+K+G+     +EL FED  +P ENL+G+EG+GF  ++  L  
Sbjct: 183 SFLVDLHNTPGFKVGRVEEKLGINASGTAELIFEDARIPKENLLGKEGEGFKQMLTTLDG 242

Query: 274 NRVFCASQAVGIAQGALERAMQHTREREQFGKPIAHLTPIQFMIADMATEVEAARLLVRK 333
            R+  ASQA+GI +  LE A+++ + REQFG+PIA    IQ+ +AD+AT+++AA LL  +
Sbjct: 243 GRIGIASQAIGIGRAVLEEAIEYAKTREQFGRPIASFQAIQWKLADIATQLDAAELLTLR 302

Query: 334 ATTLLDAKDKRGPLIGGMAKTFASDTAMKVTTDAVQVMGGSGYMQEYQVERMMREAKLTQ 393
           A   L+   +       MAK FASDTAM    + VQ++GG GY +EY +ER MR+AK+TQ
Sbjct: 303 A-AWLEQNGRGYEKEAAMAKLFASDTAMWAAVEGVQILGGYGYCKEYPMERHMRDAKITQ 361

Query: 394 IYTGTNQITRMVTGRSLL 411
           IY GTN+I R+V  R++L
Sbjct: 362 IYEGTNEIMRLVISRNIL 379


Lambda     K      H
   0.318    0.133    0.375 

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: 386
Number of extensions: 21
Number of successful extensions: 4
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: 414
Length of database: 382
Length adjustment: 31
Effective length of query: 383
Effective length of database: 351
Effective search space:   134433
Effective search space used:   134433
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 Apr 09 2024. 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