GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aldA in Clostridium kluyveri DSM 555

Align NAD+-dependent L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_012102549.1 CKL_RS10825 aldehyde dehydrogenase

Query= metacyc::MONOMER-16246
         (477 letters)



>NCBI__GCF_000016505.1:WP_012102549.1
          Length = 474

 Score =  141 bits (355), Expect = 5e-38
 Identities = 105/332 (31%), Positives = 157/332 (47%), Gaps = 11/332 (3%)

Query: 143 GVVAGILPWNFPFFLIARKMAPALLTGNTIVVKPSEETP--NNCFEFARLVAETDLPRGV 200
           GV   I PWNFPF L    +  A+  GN +++KPSE TP   NC +        +    V
Sbjct: 114 GVSLIISPWNFPFQLAISPLVSAIAAGNCVILKPSEYTPLTGNCIKKMISCIFQEDEVAV 173

Query: 201 FNVVCGAGQVGGALSSHPGVDLISFTGSVETGARIMAAAAPNLTKLNLELGGKAPAIVLA 260
           F    G  ++   L   P  + I FTGS   G  IM AAA NL  + LELGGK+P I+  
Sbjct: 174 FE---GDYRISKMLLEKP-FENIFFTGSPTVGKMIMEAAAKNLATVTLELGGKSPVIIHP 229

Query: 261 DADLELAVKAIRDSRIINSGQVCNCAERVYVQRQVAEPFIERIAAAMAATRYGDPLAEPE 320
            A+L+ A   I   + +N+GQ+C   + + + +   E F E +        YG    + +
Sbjct: 230 SANLDEAAGRIAWGKCLNAGQICVAPDYLLIPQNKEEVFTE-LMVKYIIQYYGTFKKDMD 288

Query: 321 -VEMGPLINRLGLEKIDAKVRTALAQGATLVTGGAIAERPGHHYQPTVLTGCRADTRIMR 379
            ++   +I +    +I   V  A+ +GA +  GG   E     Y PT++T    +++I+ 
Sbjct: 289 NLKYSRIITKEHFFRIKELVEEAVYKGAKIRCGGYFNECDNFIY-PTIITNVDLNSKILE 347

Query: 380 EEIFGPVLPIQIVDDLDEAIALANDCEYGLTSSVFTRDLNKAMHALRELDFGETYINR-- 437
           EEIFGPVLPI   + +DEA+         L   +F+RD     + L   + G+  IN   
Sbjct: 348 EEIFGPVLPIISYESMDEALEYIKSKPKPLVIYIFSRDKKAVNYLLDNTESGDAVINDVV 407

Query: 438 EHFEAMQGFHAGVRKSGIGGADGKHGLYEYTH 469
            H   +     G   SGIG + G +G   +TH
Sbjct: 408 VHAGNINLPFGGFNNSGIGKSHGYYGFMAFTH 439


Lambda     K      H
   0.320    0.136    0.395 

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: 437
Number of extensions: 16
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: 477
Length of database: 474
Length adjustment: 33
Effective length of query: 444
Effective length of database: 441
Effective search space:   195804
Effective search space used:   195804
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 (21.8 bits)
S2: 51 (24.3 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