GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ch1CoA in Desulfobacter vibrioformis DSM 8776

Align cyclohex-1-ene-1-carbonyl-CoA dehydrogenase (EC 1.3.8.10) (characterized)
to candidate WP_035238989.1 Q366_RS11450 acyl-CoA dehydrogenase

Query= BRENDA::Q39QF5
         (380 letters)



>NCBI__GCF_000745975.1:WP_035238989.1
          Length = 384

 Score =  278 bits (710), Expect = 2e-79
 Identities = 154/376 (40%), Positives = 228/376 (60%), Gaps = 3/376 (0%)

Query: 4   LTEEQKLTLDMVRDVATREIAPRALELDEKSLFPEYARDLFAKLGLLNPLLPAAYGGTEM 63
           LT+EQ +  +MVR+ + + +AP A E D+ + FP        +LGL+  ++P AYGG   
Sbjct: 5   LTDEQVMIQNMVREFSRKVVAPTAAERDKTTAFPAENFKQMGELGLMGMMVPEAYGGEAA 64

Query: 64  GVLTLALILEELGRVCASTALLLIAQTDGMLPIIHG-GSPELKERYLRRFAGESTLLTAL 122
             ++  L L E+   CAST++++  Q   +   ++  G+ E K+ +L   A    +L A 
Sbjct: 65  DAVSYVLALSEIAYSCASTSVVMSVQNSIVCESLNKFGTEEQKQEFLVPLAS-GEILGAF 123

Query: 123 AATEPAAGSDLLAMKTRAVRQGDKYVINGQKCFITNGSVADVIVVYAYTDPEKGSKGISA 182
           A TEP AGSD ++  T A++ GD+YVING K FIT+G  + V++V A TD   G +GIS 
Sbjct: 124 ALTEPDAGSDPVSQATTAIKDGDEYVINGTKRFITSGENSSVVLVTAKTDETLGHRGISC 183

Query: 183 FVVEKGTPGLVYGRNESKMGMRGSINSELFFENMEVPAENIIGAEGTGFANLMQTLSTNR 242
           F+V K T GL+ G +E KMG+R S  ++L FE+  VPA NI+G EG GF   M  L + R
Sbjct: 184 FIVPKTTAGLIVGHHEDKMGLRASDTTDLIFEDCRVPAANILGKEGDGFKIAMSGLDSGR 243

Query: 243 VFCAAQAVGIAQGALDIAVRHTQDRVQFGKPIAHLAPVQFMVADMATAVEASRLLTRKAA 302
           +  AAQ++G+AQ A D A+++ + R QFG  I     ++F +ADMAT +EA+R LT  AA
Sbjct: 244 IGIAAQSLGVAQAAFDAAIKYARGRKQFGVAITKHQAIRFQIADMATKIEAARQLTLSAA 303

Query: 303 ELLDDGDKKAVLYGSMAKTMASDTAMRVTTDAVQVLGGSGYMKENGVERMMRDAKLTQIY 362
            + D G+ +     SMAK  AS+    +T  A+Q+ GG G+ K+  VER  RDA++  IY
Sbjct: 304 SMKDRGE-RFTREASMAKLFASEMVQDITAQAIQIHGGYGFTKDYAVERFYRDARVFTIY 362

Query: 363 TGTNQITRMVTGRALL 378
            GT++I R+V   A+L
Sbjct: 363 EGTSEIQRIVISNAVL 378


Lambda     K      H
   0.319    0.134    0.371 

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: 308
Number of extensions: 16
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: 380
Length of database: 384
Length adjustment: 30
Effective length of query: 350
Effective length of database: 354
Effective search space:   123900
Effective search space used:   123900
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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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