GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dpkA in Cupriavidus basilensis 4G11

Align Delta(1)-pyrroline-2-carboxylate/Delta(1)-piperideine-2-carboxylate reductase; Pyr2C/Pip2C reductase; N-methyl-L-amino acid dehydrogenase; EC 1.5.1.21; EC 1.4.1.17 (characterized)
to candidate RR42_RS29130 RR42_RS29130 dehydrogenase

Query= SwissProt::Q4U331
         (343 letters)



>FitnessBrowser__Cup4G11:RR42_RS29130
          Length = 364

 Score =  157 bits (396), Expect = 5e-43
 Identities = 108/309 (34%), Positives = 151/309 (48%), Gaps = 20/309 (6%)

Query: 30  GTSPEVADVLAENCASAQRDGSHSHGIFRIPGYLSSLASGWVD-GKAVPVVEDVGAAFVR 88
           G+    A + A++   A   G  SHG+  IP Y+ S     +   + V VV + G   + 
Sbjct: 23  GSDAREARLTADHLVGANLSGHDSHGVGMIPKYVMSWQGEQLQLNQRVSVVHEAGG-ILS 81

Query: 89  VDACNGFAQPALAAARSLLIDKARSAGVAILAIRGSHHFAALWPDVEPFAEQGLVALSMV 148
           +D   G  Q     A  L I++AR  GV +L +R SHH   +    E     G++++  V
Sbjct: 82  LDGNRGMGQAVTEEAMGLAIERAREHGVCVLGLRASHHLGRVGHWAEQATAAGMISIHFV 141

Query: 149 N--SMTCVVPHGARQPLFGTNPIAFGAPRAGGEPIVFDLATSAIAHGDVQIAAREGRLLP 206
           N  S   V PHG  +  +GTNP   G P AGGEP+V D ATSAIA G V++A  +G  +P
Sbjct: 142 NVLSKPIVAPHGGYEARYGTNPFTIGVPVAGGEPLVMDFATSAIALGKVRVANNKGVAVP 201

Query: 207 AGMGVDRDGLPTQEPRAILD-----GGALLPFGGHKGSALSMMVELLAAGLTGGNFSFEF 261
            G  +D +G PT +P  +        GAL PFG HKG  L++M ELL A +TGG+ +   
Sbjct: 202 PGCLLDTEGHPTDDPAVMFPPAGEAQGALRPFGEHKGYVLAVMCELLGAAVTGGH-TIRP 260

Query: 262 DWSKHPGAQTPWTGQLLIVIDPDK-GAGQHFAQRSEELVRQLH------GVGQERLPGD- 313
           +   H  A   W   L IV DP++ G+   F    +  V  L       G     LPG+ 
Sbjct: 261 ETLTHEHA--VWNNMLAIVFDPERLGSSTTFGHEVQAFVDWLRSSHLQPGTDAILLPGEP 318

Query: 314 RRYLERARS 322
            R   RAR+
Sbjct: 319 ERAWRRARA 327


Lambda     K      H
   0.320    0.137    0.412 

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: 390
Number of extensions: 21
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: 343
Length of database: 364
Length adjustment: 29
Effective length of query: 314
Effective length of database: 335
Effective search space:   105190
Effective search space used:   105190
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: 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