GapMind for catabolism of small carbon sources

 

Alignments for a candidate for praB in Methylocapsa aurea KYG T

Align 2-hydroxymuconic semialdehyde dehydrogenase; HMSD; EC 1.2.1.85 (characterized)
to candidate WP_036260778.1 DL86_RS09925 aldehyde dehydrogenase family protein

Query= SwissProt::P23105
         (486 letters)



>NCBI__GCF_000746085.1:WP_036260778.1
          Length = 500

 Score =  152 bits (384), Expect = 3e-41
 Identities = 112/341 (32%), Positives = 157/341 (46%), Gaps = 13/341 (3%)

Query: 144 PKGVIGVISPWNLPLLLMTWKVGPALACGNCVVVKPSEETPLTATLLGEVMQAAG----- 198
           P GV+G+I+ +N P+ +  W    AL CG+  V KPSE+TPL A     +   A      
Sbjct: 139 PLGVVGIITAFNFPVAVWAWNAVIALVCGDACVWKPSEKTPLCALAAQALFDKAADALDF 198

Query: 199 VPAGVYNVVHGFGGDSAGAFLTEHPDVDAYTFTGETGTGETIMRAAAKGVRQVSLELGGK 258
           VP  +  +V G  G   G  L   P V   + TG T  G  I    AK   +  LELGG 
Sbjct: 199 VPPNLSQLVTG--GQRTGEALVGDPRVPLVSATGSTRMGREIAPQLAKRFARCILELGGN 256

Query: 259 NAGIVFADCDMDKAIEGTLRSAFANCGQVCLGTERVYVERPIFDAFVARLKAGAEALKIG 318
           NA IV    D+  A    + +A    GQ C    R+ V   +  A + RLK       IG
Sbjct: 257 NAMIVAPSADLSLATRAIVFAAVGTAGQRCTSLRRLIVHDSLRPALIERLKLAYGQATIG 316

Query: 319 EPNDPEANFGPLISHKPREKVPSYYQQAVDDGATVVTGGGVPEMPAHLAGGAWVQPTIWT 378
           +P D     GPLI     + +    ++A   G  V   GG   +        +V+P +  
Sbjct: 317 DPRDRRHLIGPLIDKAAFDSMQRALKEAAAAGGRV--HGGERILIERWPDAYYVRPAL-V 373

Query: 379 GLADDSAVVTEEIFGPCCHIRPFDSEEEAIELANSLPYGLASAIWTENVRRAHRV--AGQ 436
            + D + +V  E F P  ++  +   +EAI L N +P GLAS+I+T ++R A R   A  
Sbjct: 374 EMPDQAPIVHRETFAPILYVLGYRDWDEAIRLHNGVPQGLASSIFTTDLREAERFLSASG 433

Query: 437 IEAGIVWVN-SWFLRDLRTAFGGSKQSGIGREGGVHSLEFY 476
            + GI  VN      ++  AFGG K+SG GRE G  S + Y
Sbjct: 434 SDCGIANVNIGPSGAEIGGAFGGEKESGGGREAGSDSWKAY 474


Lambda     K      H
   0.318    0.136    0.413 

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: 606
Number of extensions: 25
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: 486
Length of database: 500
Length adjustment: 34
Effective length of query: 452
Effective length of database: 466
Effective search space:   210632
Effective search space used:   210632
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: 52 (24.6 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