GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Collinsella tanakaei YIT 12063

Align glycerol dehydrogenase (EC 1.1.1.6) (characterized)
to candidate WP_009140732.1 HMPREF9452_RS03515 iron-containing alcohol dehydrogenase family protein

Query= BRENDA::Q8ZKM9
         (367 letters)



>NCBI__GCF_000225705.1:WP_009140732.1
          Length = 372

 Score =  130 bits (326), Expect = 7e-35
 Identities = 95/327 (29%), Positives = 165/327 (50%), Gaps = 16/327 (4%)

Query: 34  VVGDKFVLGFAEETLRKSLTDAGLSVE-IAPFGGECSQNEIDRLRAVAEKSQCGAVLGIG 92
           V+G +  L  A + L  +L  + +SV     +GG+ + + ++ L +  E ++  A+  +G
Sbjct: 33  VIGGRKALTAASDRLTAALEGSDVSVTGTFWYGGKAAYSCVEELCSSPEVAEADAIFVVG 92

Query: 93  GGKTLDTAKALAHFMNVPVAIAPTIASTDAPCSALSVIYTDAGEFDRYLLLPHNPNMVIV 152
           GGK +DT K +AH +  P+   PTIAS  +P S +S++Y + G F   + L   P    +
Sbjct: 93  GGKAVDTCKIVAHRLAKPLYTFPTIASNCSPVSCISIMYNEDGSFKEIVQLHEPPAHCFI 152

Query: 153 DTQIVAGAPARLLAAGIGDALATWFEARACSRSGATTMAGGKCTQAALALAELCYNTLIE 212
           DTQ++A AP   L AGIGD +A ++E     R  + +           A++ +C   LI+
Sbjct: 153 DTQVIAEAPEMYLWAGIGDTIAKYYEVVFSMRGDSPSYG----PVLGRAISCMCNRPLID 208

Query: 213 EGEKAMLAAEQHVVTPALE----RVIEANTYLSGVGFESGGLAAAHAIHNGLTAIPDAHH 268
              +A    + + V+ AL      ++ +   +SG+       A AHA+  GLT IP    
Sbjct: 209 CALEAYEDCKNNRVSDALTHAALNIVVSTGLVSGLVGVDYNSALAHALFYGLTTIPSIER 268

Query: 269 -YYHGEKVAFGTLTQLVLENAPVEEIETVAALCHSVGLPITLAQLDIK-QDIPAKMRTVA 326
            + HGE V++G L QLV++    E+++ +  L   +GLP  LA L +  +D  A+     
Sbjct: 269 DHCHGEVVSYGVLVQLVMDK-DSEQLDFLMPLYRKLGLPTCLADLGLTVEDDFAEALAAT 327

Query: 327 EASCAEGETIHNMPGGATPDEVYAALL 353
           E +    + + ++P   T D ++ A+L
Sbjct: 328 EVN----QELRHVPYPVTRDLIWQAIL 350


Lambda     K      H
   0.318    0.133    0.391 

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: 345
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: 367
Length of database: 372
Length adjustment: 30
Effective length of query: 337
Effective length of database: 342
Effective search space:   115254
Effective search space used:   115254
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: 49 (23.5 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