GapMind for catabolism of small carbon sources

 

Alignments for a candidate for larD in Clostridium acetobutylicum ATCC 824

Align D/L-lactic acid transporter; Lactate racemization operon protein LarD; Lactic acid channel (characterized)
to candidate NP_347948.1 CA_C1319 glycerol uptake facilitator protein

Query= SwissProt::F9UST3
         (238 letters)



>NCBI__GCF_000008765.1:NP_347948.1
          Length = 233

 Score =  176 bits (447), Expect = 3e-49
 Identities = 94/225 (41%), Positives = 136/225 (60%), Gaps = 7/225 (3%)

Query: 7   AEFMGTALMIIFGVGVHCSSVLKGTKYRGSGHIFAITTWGFGISVALFIFGNVC--INPA 64
           AE +GT L+I+ G GV  + VLK +K   SG I     W F +++   IFG+     NPA
Sbjct: 6   AELVGTLLLILLGDGVVANVVLKNSKGHASGWIVITMGWAFAVAIPALIFGSYSNQFNPA 65

Query: 65  MVLAQCLLGNIAWSLFIPYSVAEVLGGVVGSVIVWIMYADHFKASTDEISPITIRNLFCT 124
           + +A  ++G +AW+    Y   + +G  +G+V+V+++Y D FK S ++   + +   FCT
Sbjct: 66  LTIALAVIGKVAWAKVPIYLAGQFIGAFLGAVLVFVVYYDQFKCSENKTDKLGV---FCT 122

Query: 125 APAVRNLPRNFFVELFDTFIFISGILAI-SEIKTPGIVPIGVGLLVWAIGMGLGGPTGFA 183
            PAVRN   NF  E+  TF+ + GIL + ++    G+  + VG L+  IG+ LGGPTG+A
Sbjct: 123 VPAVRNSLINFLCEVIGTFVLVFGILGVGAQNLKNGMGAVFVGFLILVIGLSLGGPTGYA 182

Query: 184 MNLARDMGPRIAHAILPIANKADSDWQYGIIVPGIAPFVGAAIAA 228
           +N ARD+ PRIAH +LPI NK DS+W Y  I P IAP VG  I A
Sbjct: 183 INPARDLAPRIAHLVLPIPNKGDSNWSYAWI-PIIAPVVGGIIGA 226



 Score = 26.2 bits (56), Expect = 6e-04
 Identities = 28/108 (25%), Positives = 46/108 (42%), Gaps = 21/108 (19%)

Query: 6   IAEFMGTALMIIFGVGVHCSSVLKGTKYRGSGHIFAITTWGFGISVALFIFGN---VCIN 62
           + E +GT +++   +GV   ++  G      G +F     GF I V     G      IN
Sbjct: 134 LCEVIGTFVLVFGILGVGAQNLKNGM-----GAVFV----GFLILVIGLSLGGPTGYAIN 184

Query: 63  PAMVLAQCLL---------GNIAWSLFIPYSVAEVLGGVVGSVIVWIM 101
           PA  LA  +          G+  WS      +A V+GG++G+V   ++
Sbjct: 185 PARDLAPRIAHLVLPIPNKGDSNWSYAWIPIIAPVVGGIIGAVCYMLL 232


Lambda     K      H
   0.330    0.145    0.470 

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: 237
Number of extensions: 15
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 238
Length of database: 233
Length adjustment: 23
Effective length of query: 215
Effective length of database: 210
Effective search space:    45150
Effective search space used:    45150
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 46 (22.3 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