GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Pseudomonas putida KT2440

Align Glyoxylate reductase; EC 1.1.1.26 (uncharacterized)
to candidate PP_1649 PP_1649 D-lactate dehydrogenase

Query= curated2:Q9YAW4
         (335 letters)



>FitnessBrowser__Putida:PP_1649
          Length = 342

 Score =  162 bits (411), Expect = 9e-45
 Identities = 120/349 (34%), Positives = 174/349 (49%), Gaps = 35/349 (10%)

Query: 1   MKRPRVFVTREVFPEALELLSKYYDVEVWDKYQP--------PPYETLLSKAREADALYT 52
           M  PR  + R     AL   S++YD E + K            P    L  A  AD    
Sbjct: 1   MTHPRHALQRSSTMRALLFSSQHYDQESFTKAAGGTALELHFQPARLTLDTAALADGFEV 60

Query: 53  L---LTDRIDCDLLSQ--APRLRIVAQMAVGFDNIDVECATRLGIYVTNTPGVLTEATAE 107
           +   + D +D  +L +  A   R++A  + G++++D+  A RLG+ V   P     A AE
Sbjct: 61  VCAFINDELDAPVLQRLAAAGTRLIALRSAGYNHVDLAAAQRLGLAVVRVPAYSPHAVAE 120

Query: 108 FTWALILAAARRVVEADHFVRWGEWWRLRTGWHPMMMLGVELRGKTLGILGMGRIGSRVA 167
              ALILA  RR+  A +  R G++           + G +L GKT+G++G G+IG   A
Sbjct: 121 HAVALILALNRRLHRAYNRTREGDFTLHG-------LTGFDLHGKTVGVVGTGQIGVAFA 173

Query: 168 EIGKAFGMRIIYHSRSRKREIEKELGAEYRSLEDLLRESDILSIHLPLTDETRHLIGESE 227
            I   FG +++ +      E+   LGA Y  L +LLRE+ I+S+H PLT+ TRHLI    
Sbjct: 174 RIMAGFGCQLLAYDPYPNPEL-LALGARYLPLPELLREARIISLHCPLTEHTRHLINAQS 232

Query: 228 LKLMKKTAILVNTGRGAIVDTGALVKALREGWIAAAALDVFEEE-----------PLNPN 276
           L  ++  A+L+NTGRGA+VDT AL+ AL+ G +    LDV+EEE           PL  +
Sbjct: 233 LAQLQPGAMLINTGRGALVDTPALIDALKSGQLGYLGLDVYEEEAQLFFEDRSDLPLQDD 292

Query: 277 --HPLTAFKNVVLAPHAASATRETRLRMAMMAAENLVAFAQGKVPPNLV 323
               L  F NV++  H A  TRE    +A    +N+  +A G  P NLV
Sbjct: 293 VLARLLTFPNVIITAHQAFLTREALDAIAATTLDNINRWAAGN-PQNLV 340


Lambda     K      H
   0.322    0.136    0.406 

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: 280
Number of extensions: 12
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: 335
Length of database: 342
Length adjustment: 28
Effective length of query: 307
Effective length of database: 314
Effective search space:    96398
Effective search space used:    96398
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 (21.9 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