GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dadA in Pseudomonas fluorescens FW300-N1B4

Align D-arginine dehydrogenase (EC 1.4.99.6) (characterized)
to candidate Pf1N1B4_2373 D-amino acid dehydrogenase small subunit (EC 1.4.99.1)

Query= BRENDA::Q9HTQ0
         (432 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2373
          Length = 413

 Score =  280 bits (716), Expect = 6e-80
 Identities = 156/412 (37%), Positives = 230/412 (55%), Gaps = 9/412 (2%)

Query: 2   RVLVLGSGVIGTASAYYLARAGFEVVVVDRQDGPALETSFANAGQVSPGYASPWAAPGIP 61
           RV ++G GVIG  +AY L R G +V++++ +D  A ETSFAN GQ+S  Y +P A  G+P
Sbjct: 4   RVCIIGGGVIGLTTAYALVRDGIDVMLIEARDSFASETSFANGGQLSYRYVAPLADAGVP 63

Query: 62  LKAMKWLLEKHAPLAIKLTSDPSQYAWMLQMLRNCTAERYAVNKERMVRLSEYSRDCLDE 121
           L+A+ W+L   +PL ++   DP+Q+ WM   L  C       N   ++RL+  S+  L  
Sbjct: 64  LQALGWMLRGDSPLKLRPRLDPAQWRWMAAFLAACRRSVNQRNGAHLLRLALLSQATLQG 123

Query: 122 LRAETGI-AYEGRTLGTTQLFRTQAQLDAAGKDIAVLERSGVPYEVLDRDGIARVEPALA 180
            R E  +  ++ R  G    FR  A  + A   +A   +     +VL R   A++EPALA
Sbjct: 124 WRDEDRLDGFDWRRNGKLVTFREAASFEHACHSLADPRQQ----QVLSRTECAQLEPALA 179

Query: 181 KVADKLVGALRLPNDQTGDCQLFTTRLAEMAKGLG-VEFRFGQNIERLDFAGDRINGVLV 239
           +     VGA+  P+++  DC  F  +L    K  G  EF  G+ +  +      +  V +
Sbjct: 180 EAP--FVGAIYTPDEEVADCHAFCLQLVARLKASGRCEFLPGRTVTGIRHGDGAVQAVEM 237

Query: 240 NGELLTADHYVLALGSYSPQLLKPLGIKAPVYPLKGYSLTVPITNPEMAPTSTILDETYK 299
             ++L  +  V+A G  SP L  P G+  P+YPLKGYSLT+PI     AP  +I D   K
Sbjct: 238 GAQVLPVEQLVIAAGHRSPALALP-GMNLPLYPLKGYSLTMPIRTEHRAPELSITDYNRK 296

Query: 300 VAITRFDQRIRVGGMAEIAGFDLSLNPRRRETLEMITTDLYPEGGDISQATFWTGLRPAT 359
           +   R   ++RV  M +I GFD +L+P+R   ++    +  P  GD   A  W G+RPAT
Sbjct: 297 IVYARIGAQLRVAAMVDIVGFDPALDPKRLALIKRQAQETLPNAGDYDAAIEWAGMRPAT 356

Query: 360 PDGTPIVGATRYRNLFLNTGHGTLGWTMACGSGRYLADLMAKKRPQISTEGL 411
           P G P++GAT YRNL+LN GHG LG+T+ACGS R L++L+A++ P I  +GL
Sbjct: 357 PSGVPLIGATAYRNLWLNLGHGALGFTLACGSARLLSELIARRTPSIEMQGL 408


Lambda     K      H
   0.318    0.135    0.401 

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: 458
Number of extensions: 19
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: 432
Length of database: 413
Length adjustment: 32
Effective length of query: 400
Effective length of database: 381
Effective search space:   152400
Effective search space used:   152400
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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