GapMind for catabolism of small carbon sources

 

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

Align Broad specificity amino-acid racemase; Broad spectrum racemase; EC 5.1.1.10 (characterized)
to candidate Pf1N1B4_2146 Alanine racemase (EC 5.1.1.1)

Query= SwissProt::Q88GJ9
         (409 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2146
          Length = 357

 Score =  108 bits (269), Expect = 3e-28
 Identities = 102/333 (30%), Positives = 155/333 (46%), Gaps = 22/333 (6%)

Query: 48  VSASALQHNIRTLQAELAGKSKLCAVLKADAYGHGIGLVMPSIIAQGVPCVAVASNEEAR 107
           +   AL+HN + L  E+ G +K  AV+KADAYGHG      ++ A+     AVA  EEA 
Sbjct: 8   IDLQALRHNYQ-LAREVTG-AKALAVIKADAYGHGAVRCAQALEAEA-DGFAVACIEEAL 64

Query: 108 VVRASGFTGQLVRVR-LASLSELEDGLQYDMEELVGSAEFARQADAIA-ARHGKTLRIHM 165
            +RA+G    ++ +       EL   +++D   +V S     Q +AI  A   K + + +
Sbjct: 65  ELRAAGIRAPVLLLEGFFEADELSLIVEHDFWCVVHSLW---QLEAIEKAALSKPITVWL 121

Query: 166 ALNSSGMSRNGVEMATWSGRGEALQITDQKHLKLVALMTHFAVEDKDDVRKGLAAFNEQT 225
            L+S GM R G+  A +    + L +   K  K+V LM+HFA  D+      L       
Sbjct: 122 KLDS-GMHRVGLHPADYQAAYQRL-LASGKVAKIV-LMSHFARADE------LHCQTSAE 172

Query: 226 DWLIKHARLDRSKLTLHAANSFATLEVPEARLDMVRTGGALFGDTV-----PARTEYKRA 280
              +  A        +   NS A L  P+   D VR G  L+G T         +  +  
Sbjct: 173 QVAVFEAARQGLSAEISLRNSPAVLGWPQIPSDWVRPGIMLYGATPFEEANAVASRLQPV 232

Query: 281 MQFKSHVAAVHSYPAGNTVGYDRTFTLARDSRLANITVGYSDGYRRVFTNKGHVLINGHR 340
           M  +S V  V   P G  +GY   F   +  R+  + +GY+DGY R       V++ G R
Sbjct: 233 MTLESKVICVRELPTGEPIGYGAKFITPKPMRVGVVAMGYADGYPRQAPTGTPVMVAGQR 292

Query: 341 VPVVGKVSMNTLMVDVTDFPDVKGGNEVVLFGK 373
             ++G+VSM+ L +D+TD P    G+ V L+GK
Sbjct: 293 SQLIGRVSMDMLCIDLTDVPQAGLGSPVELWGK 325


Lambda     K      H
   0.318    0.132    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: 309
Number of extensions: 12
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: 409
Length of database: 357
Length adjustment: 30
Effective length of query: 379
Effective length of database: 327
Effective search space:   123933
Effective search space used:   123933
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.

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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