GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dpkA in Pseudomonas putida KT2440

Align 1-piperideine-2-carboxylate/1-pyrroline-2-carboxylate reductase (NADPH) (EC 1.5.1.21); thiomorpholine-carboxylate dehydrogenase (EC 1.5.1.25) (characterized)
to candidate PP_4431 PP_4431 Ornithine cyclodeaminase 1

Query= BRENDA::Q14894
         (314 letters)



>FitnessBrowser__Putida:PP_4431
          Length = 330

 Score =  115 bits (288), Expect = 1e-30
 Identities = 96/323 (29%), Positives = 154/323 (47%), Gaps = 21/323 (6%)

Query: 8   LSAAEVEEHLRSSSLLIPPLETALANFSSGPEGGVMQPVRTVVPVTKHRGYLGVMPAYSA 67
           L+  E+ E +   +  I  +E A A+ + G    V+ P    + +++H G + V  AY  
Sbjct: 7   LNQREIRECVTLDTDSIDVVENAFASLARGK---VVMPSILRLDISEHNGEVDVKTAYLP 63

Query: 68  AEDALTTKLVT-FYEDRGITSVVPSHQATVLLFEPSNGTLLAVM-DGNVITAKRTAAVSA 125
             +    K+   F+ + G+   +PS    ++L     G L A++ D   +TA RTAA  A
Sbjct: 64  DLENFAIKVSPGFFNNPGLG--LPSLNGMMMLLSGRTGLLQALLLDNGYLTAVRTAAAGA 121

Query: 126 IATKFLKPPSSEVLCILGAGVQAYSHYEIFTEQFSFKEVRIWNRTKENAEKFADTVQG-- 183
           +A ++L    SE + +LGAG QA    +        K VR+W R+   A++ A  +    
Sbjct: 122 VAARWLARQDSEEVALLGAGEQAELQLKALLLVRDIKRVRVWARSSAKAQQLALQLSSLY 181

Query: 184 --EVRVCSSVQEAVAGADVIITVTLATEPILFGEWVKPGAHINAVGASRPDWRELDDELM 241
             E     SV EA++ AD+ +T T + +PIL    ++PG HI A+GA      E+  E++
Sbjct: 182 GLEATAAESVDEAMSSADIAVTCTPSNQPILHRRHLRPGLHITAMGADTEHKNEVAPEVI 241

Query: 242 KEAVLYVD---SQEAALKESGDVLLSGA----EIFAELGEVIKGVKPAHCEKT--TVFKS 292
                YV    SQ A L E    + +G      ++AELG+VI G +      T  T+   
Sbjct: 242 AAVDHYVADRVSQTATLGELHHAINAGVAQDLRVYAELGQVILGDRVGRLTPTDVTLCDL 301

Query: 293 LGMAVEDTVAAKLIYD-SWSSGK 314
            G  V+DT  A L +  + S+GK
Sbjct: 302 TGTGVQDTAIANLAFSRAISTGK 324


Lambda     K      H
   0.315    0.130    0.371 

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: 196
Number of extensions: 8
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: 314
Length of database: 330
Length adjustment: 28
Effective length of query: 286
Effective length of database: 302
Effective search space:    86372
Effective search space used:    86372
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 (21.6 bits)
S2: 48 (23.1 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