GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dpkA in Sinorhizobium meliloti 1021

Align Delta(1)-pyrroline-2-carboxylate/Delta(1)-piperideine-2-carboxylate reductase; Pyr2C/Pip2C reductase; N-methyl-L-amino acid dehydrogenase; NMAADH; EC 1.5.1.21; EC 1.4.1.17 (characterized)
to candidate SMa1459 SMa1459 Dehydrogenase, malate/L-lactate family

Query= SwissProt::Q5FB93
         (341 letters)



>FitnessBrowser__Smeli:SMa1459
          Length = 334

 Score =  194 bits (493), Expect = 3e-54
 Identities = 118/305 (38%), Positives = 168/305 (55%), Gaps = 4/305 (1%)

Query: 8   TVVRVPFTELQSLLQAIFQRHGCSEAVARVLAHNCASAQRDGAHSHGVFRMPGYVSTLAS 67
           T V   + E++++       HG +   AR +A     A+ DG    G++ +P +   LA 
Sbjct: 2   TPVETSWEEIEAVCLEALTLHGAAAETARAVAGAITRAEADGNRVCGLYYLPIFCRHLAI 61

Query: 68  GWVDGQATPQVSDVAAGYVRVDAAGGFAQPALAAARELLVAKARSAGIAVLAIHNSHHFA 127
           G VDG+A P+V+      V VDA  GFA PA+AA    L+  AR AG+A +A+ NS++  
Sbjct: 62  GKVDGEAVPEVTTRGVT-VTVDARSGFAHPAIAAGTPALIDLARQAGLAAMAVRNSYNCL 120

Query: 128 ALWPDVEPFAEEGLVALSVVNSMTCVVPHGARKPLFGTNPIAFAAPCAEHDP-IVFDMAT 186
           AL   V P A+ GL+ + V N+   V P GA + LFGTNP+AFA P  E  P IV D + 
Sbjct: 121 ALGHHVRPLADAGLIGICVSNAPASVAPPGATRALFGTNPLAFAVPSKEGAPTIVVDQSM 180

Query: 187 SAMAHGDVQIAARAGQQLPEGMGVDADGQPTTDPKAILEGGALLPFGGHKGSALSMMVEL 246
           SA+   ++ +    G+ +P G   D +GQPTTD    LE G+LLP GG KG+ ++++VE+
Sbjct: 181 SAVTKTEMILRRDRGEAIPIGWAQDGNGQPTTDAATGLE-GSLLPAGGRKGANIALLVEV 239

Query: 247 LAAALTGGHFSWEFDWSGHPGAKTPWTGQLIIVINPGKAEGERFAQRSRELVEHMQAVGL 306
           LAAALTG   S E    G+     P  GQ +I I+P       F++    LV    A G+
Sbjct: 240 LAAALTGSALSTEASAFGNEEGGPPHVGQFLIAIDPDHFAAGHFSEAMDNLVASHDAAGV 299

Query: 307 TRMPG 311
            R+PG
Sbjct: 300 -RLPG 303


Lambda     K      H
   0.318    0.132    0.398 

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: 332
Number of extensions: 17
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: 341
Length of database: 334
Length adjustment: 28
Effective length of query: 313
Effective length of database: 306
Effective search space:    95778
Effective search space used:    95778
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 17 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