GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Geobacter metallireducens GS-15

Align Lactaldehyde reductase (characterized, see rationale)
to candidate WP_011365768.1 GMET_RS05275 alcohol dehydrogenase

Query= uniprot:Q8A199
         (384 letters)



>NCBI__GCF_000012925.1:WP_011365768.1
          Length = 382

 Score =  253 bits (647), Expect = 5e-72
 Identities = 145/372 (38%), Positives = 210/372 (56%), Gaps = 3/372 (0%)

Query: 12  FGAGCRSVIAVEAARRGFKKAFFVTDKDLIKFGVAAEIIKVFDDNHIPYELYSDVKANPT 71
           FG G  S I   AAR G  K F V+D+D+I  G   + +       +  E+YS + +NP 
Sbjct: 13  FGQGSLSQIGESAARIGASKVFLVSDEDVISAGWVDKALHYLHAVGLETEIYSSLTSNPK 72

Query: 72  IANVQNGVAAYKASGADFIVALGGGSSIDTAKGIGIVVNNPDFADVKSLEGVADTKHKAV 131
              V  G   Y ASG D IVA+GGGS  D AK + I+ +N    +++  EG+        
Sbjct: 73  DFEVLEGARHYVASGCDAIVAVGGGSPTDVAKAVAILASNG--GELRDYEGINRISRPLP 130

Query: 132 PTFALPTTAGTAAEVTINYVIIDEDARKKMVCVDPNDIPAVAIVDPELMYSMPKGLTAAT 191
           P    P+TAG  +EV+   +I+D + + KM  +  + +P +AIVDPEL+ +    L AAT
Sbjct: 131 PMVIAPSTAGAGSEVSPFAIIVDTERKLKMSIISKSLVPDIAIVDPELLRTKDAKLAAAT 190

Query: 192 GMDALTHAIESYITPGAWAMSDMFELKAIEMIAQNLKAAVDNGKDTVAREAMSQAQYIAG 251
           GMDALTH IESY++  A  ++D+   KAI++IA NL+ AV +  D  A   M+ A   AG
Sbjct: 191 GMDALTHGIESYVSLAATPLTDIHACKAIQLIAANLRRAVADRGDMEANTNMAMASLTAG 250

Query: 252 MGFSNVGLGIVHSMAHPLGAFYDTPHGVANALLLPYVMEYNAESPAAPKYIHIAKAMGVN 311
           + FSN  LG  H+M H +    D  HG ANA +LP+VME+N  S    ++ HIA ++G +
Sbjct: 251 IAFSNAILGATHAMTHQVDGLLDQHHGEANASILPHVMEFNL-SACPERFKHIAWSLGKD 309

Query: 312 TDGMTETEGVKAAIEAVKALSLSIGIPQKLHEINVKEEDIPALAVAAFNDVCTGGNPRPT 371
                + EG + AIE ++ L   IG+ + L  + ++EE IP L+  A ND C   NPR  
Sbjct: 310 VRNTGQEEGARLAIEGIRELIADIGLAKGLGAMGLREEFIPLLSRNALNDACLVTNPRNA 369

Query: 372 SVAEIEVLYRKA 383
           +V +IE ++RKA
Sbjct: 370 TVDDIEAIFRKA 381


Lambda     K      H
   0.317    0.133    0.379 

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: 365
Number of extensions: 11
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: 384
Length of database: 382
Length adjustment: 30
Effective length of query: 354
Effective length of database: 352
Effective search space:   124608
Effective search space used:   124608
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 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