GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Shewanella loihica PV-4

Align beta-aspartyl-peptidase (EC 3.4.19.5); asparaginase (EC 3.5.1.1) (characterized)
to candidate 5209718 Shew_2171 peptidase T2, asparaginase 2 (RefSeq)

Query= BRENDA::P37595
         (321 letters)



>FitnessBrowser__PV4:5209718
          Length = 348

 Score =  298 bits (763), Expect = 1e-85
 Identities = 162/317 (51%), Positives = 206/317 (64%), Gaps = 9/317 (2%)

Query: 6   IAIHGGAGAISRAQMSLQQELRYIEALSAIVETGQKMLEAGESALDVVTEAVRLLEECPL 65
           IAIHGGAG IS+A ++  Q+  Y + L   V+ G K+LE G  +L  VT A+ +LE+ PL
Sbjct: 31  IAIHGGAGTISKANLTEAQQQAYRDKLKEAVDAGYKVLEKGGDSLTAVTTAINILEDSPL 90

Query: 66  FNAGIGAVFTRDETHELDACVMDGNTLKAGAVAGVSHLRNPVLAARLVMEQSPHVMMIGE 125
           FNAG GAV+T D THE+DA +MDG  L AGAVAGV H++NP+  AR VM++SPHVM+ G+
Sbjct: 91  FNAGKGAVYTYDGTHEMDASIMDGRNLNAGAVAGVKHIKNPINLARAVMDKSPHVMLSGQ 150

Query: 126 GAENFAFARGMERVSPEIFSTSLRYEQLLAAR-KEGATVLDHSGAP--------LDEKQK 176
           GAE FA ++    V    F T  RY+QL+ A+ K  A     +G P        LD   K
Sbjct: 151 GAEEFALSQDFSLVPVTYFDTESRYQQLIDAKAKLKAAESKEAGKPDYQASVNYLDLDYK 210

Query: 177 MGTVGAVALDLDGNLAAATSTGGMTNKLPGRVGDSPLVGAGCYANNASVAVSCTGTGEVF 236
            GTVGAVALD  GNLAA TSTGGMT K  GR+GDSP++GAG YA N   AVS TG GE F
Sbjct: 211 FGTVGAVALDKQGNLAAGTSTGGMTVKRFGRIGDSPVIGAGTYAENQVCAVSATGHGEYF 270

Query: 237 IRALAAYDIAALMDYGGLSLAEACERVVMEKLPALGGSGGLIAIDHEGNVALPFNTEGMY 296
           IR   A DI A + Y   S+ +A + V+ ++L   GG+GG+IAID  GN+A PFNTEGMY
Sbjct: 271 IRYHVAGDICAKVKYQQKSILQAADEVINQRLITAGGTGGVIAIDQRGNIATPFNTEGMY 330

Query: 297 RAWGYAGDTPTTGIYRE 313
           RA    G+     I+++
Sbjct: 331 RATRKGGEPAKVMIWQD 347


Lambda     K      H
   0.316    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: 360
Number of extensions: 16
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: 321
Length of database: 348
Length adjustment: 28
Effective length of query: 293
Effective length of database: 320
Effective search space:    93760
Effective search space used:    93760
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: 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