GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaE in Xenophilus azovorans DSM 13620

Align ring 1,2-phenylacetyl-CoA epoxidase PaaE subunit (EC 1.14.13.149) (characterized)
to candidate WP_038218194.1 Q392_RS30125 phenylacetate-CoA oxygenase/reductase subunit PaaK

Query= metacyc::MONOMER-15950
         (357 letters)



>NCBI__GCF_000745855.1:WP_038218194.1
          Length = 364

 Score =  335 bits (859), Expect = 1e-96
 Identities = 168/359 (46%), Positives = 232/359 (64%), Gaps = 6/359 (1%)

Query: 4   FHSLTIKEVRPETRDAVSIAFDVPAELADSFRFTQGQHLVMRTQLDGEEVRRSYSICTGV 63
           FHSL +K + P+T++AV ++F+VP +L ++F FTQGQ+L  R Q++G+++RRSYSIC GV
Sbjct: 5   FHSLKVKAIEPDTQEAVVVSFEVPPDLRETFGFTQGQYLTPRKQIEGQDLRRSYSICAGV 64

Query: 64  NDGELRVAIKRVAGGRFSAYANESLKAGQRLEVMPPSGHFHVELDAARHGNYLAVAAGSG 123
           +DG LRV +++V GG FS + NE L+ G  +  M P G F V L    H ++L +A GSG
Sbjct: 65  DDGVLRVGVRKVRGGVFSNWINEQLQPGDEISAMAPQGRFFVPLAPEEHRHHLGIAGGSG 124

Query: 124 ITPILSIIKTTLETEPHSRVTLLYGNRSSASTLFREQLEDLKNRYLQRLNLIFLFSREQQ 183
           ITPILSI+KT L  EP SR TL+YGNR   ST+F+E+LEDLKNRYL RL L  +FS E  
Sbjct: 125 ITPILSIMKTVLAREPGSRFTLIYGNRHLRSTMFKEELEDLKNRYLTRLVLHHVFSDEHT 184

Query: 184 DVDLYNGRIDADKCGQLFSRWIDVKALDAAFICGPQAMTETVRDQLKANGMAAERIHFEL 243
           D  +  G +D +K G   S  +    +D A+ICGP  M +     L+A G+    IH E 
Sbjct: 185 DAPINMGVLDREKIGDFLSTLVPAWTIDHAYICGPFQMNDEAEAALRAAGVPESAIHIER 244

Query: 244 FAAAGSAQKREA------RESAAQDSSVSQITVISDGRELSFELPRNSQSILDAGNAQGA 297
           F  A +A    A       E+   D+  ++I ++ DG     E  R+  SILD  +A G 
Sbjct: 245 FGIAQAAPGAPAGIGAVMHEARPGDAERARIVIVRDGLRREIEFHRDQPSILDCASAAGL 304

Query: 298 ELPYSCKAGVCSTCKCKVVEGEVEMDSNFALEDYEVAAGYVLSCQTFPISDKVVLDFDQ 356
           E+PYSC +GVC TC+ KV+EG+V M+ NFAL+  EVAAG+VL+CQ  P +++VVL FD+
Sbjct: 305 EVPYSCTSGVCGTCRSKVLEGDVRMERNFALDKAEVAAGFVLTCQAHPTTERVVLSFDE 363


Lambda     K      H
   0.319    0.133    0.377 

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: 325
Number of extensions: 8
Number of successful extensions: 2
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: 357
Length of database: 364
Length adjustment: 29
Effective length of query: 328
Effective length of database: 335
Effective search space:   109880
Effective search space used:   109880
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 24 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