GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcvT in Phaeobacter inhibens BS107

Align Aminomethyltransferase; EC 2.1.2.10; Glycine cleavage system T protein (uncharacterized)
to candidate GFF1886 PGA1_c19150 sarcosine oxidase subunit alpha

Query= curated2:C3PHK3
         (370 letters)



>FitnessBrowser__Phaeo:GFF1886
          Length = 1010

 Score =  158 bits (400), Expect = 6e-43
 Identities = 107/355 (30%), Positives = 176/355 (49%), Gaps = 29/355 (8%)

Query: 7   SPLHAEHEKLGATFTPFGPWEMPLKYDNELEE-----HRAVRNAA---GLFDLSHMGEIW 58
           +P+H  H+  GA + P G W  P  Y    E      +R V+N     GL D S +G++ 
Sbjct: 619 TPMHDWHDSNGADWEPVGQWRRPFAYVRSGESLHDAVNREVKNTRENLGLLDASTLGKLV 678

Query: 59  VNGPDAAEFLSYCFISNLTTLKEGKAKYSMICAEDGGIIDDLITYRLEETKFLVVPNAGN 118
           V GPDA +FL   + + ++TLK GK +Y ++C+E+G +IDD +  R++E  +L     G 
Sbjct: 679 VKGPDAGKFLDMMYTNMMSTLKIGKCRYGLMCSENGFLIDDGVVARIDEDTWLCHTTTGG 738

Query: 119 ADTVWDALNE--RAEGFD--VDLKNESRDVAMIAVQGPKALEILVPLVE------DTKQQ 168
           A+ +   + E  + E +D  V + N +  +A +AV GP A ++L  L E      D  ++
Sbjct: 739 AERIHGHMEEWLQTEWWDWKVYVANITEQLAQVAVVGPNARKVLEKLNENAGGGMDLSKE 798

Query: 169 AVMDLPYYAAMTGKVARKYAFICRTGYTGEDGFELIVYNSDAPELWEELLKAGEEYGIKP 228
           A   LP+     G++    A   R  ++GE  +E+ V  SD    W  L++AG+E+G+ P
Sbjct: 799 A---LPFMEWRDGEIGGFKARAYRISFSGELSYEIAVAASDGQAFWTALMEAGKEFGVMP 855

Query: 229 CGLAARDSLRLEAGMPLYGNELTRDITPVEAGMSRAFAKKEQDFVGAEV-LRQRAEEGPQ 287
            G      LR E G  + G+E    + P + G++ A +KK++DF+G     R    +  +
Sbjct: 856 YGTECLHILRAEKGFIMIGDETDGTVIPQDLGLNWALSKKKEDFLGKRAHTRSHMADPDR 915

Query: 288 AVITGLVSSQ-------RRAARAGSEVYVGENKVGTVTSGQPSPTLGHPVALALI 335
             + GL ++          A   G      +N +G VTS   S  LG  +A+ L+
Sbjct: 916 WQLVGLETTDGSVLPDGAYAVGNGVNANGQKNTIGRVTSTYYSSNLGRGIAMGLV 970


Lambda     K      H
   0.316    0.135    0.398 

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: 896
Number of extensions: 34
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: 370
Length of database: 1010
Length adjustment: 37
Effective length of query: 333
Effective length of database: 973
Effective search space:   324009
Effective search space used:   324009
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: 53 (25.0 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