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 GFF2298 PGA1_c23300 putative sarcosine dehydrogenase

Query= curated2:Q2RH46
         (366 letters)



>FitnessBrowser__Phaeo:GFF2298
          Length = 815

 Score =  169 bits (428), Expect = 2e-46
 Identities = 112/352 (31%), Positives = 175/352 (49%), Gaps = 26/352 (7%)

Query: 5   KKTPLYGEHVAAGAKMVEFGGWLMPVQYS---------------------SIIEEHQRVR 43
           +K+PLY      GA   E  GW  P  ++                     ++  EH+  R
Sbjct: 421 RKSPLYDTLKNKGACFGEKLGWERPNWFADATRGETPQDLYSFGRQNWFDAVGREHKAAR 480

Query: 44  NCAGLFDVSHMGEITIKGPDALALVQKLLTNDADRATGDRVIYSPMCYPDGGVVDDLLVY 103
             A LFD +   + T+KGPDALA +  +  ND D+  G  +IY+ M    GG+  DL V 
Sbjct: 481 EAAVLFDQTSFAKFTLKGPDALAAMNWICANDVDKPVGS-LIYTQMLNDKGGIECDLTVG 539

Query: 104 PRGEGEYLLVVNAGNIDKDFAWIQENA-SGFRVEVSNISAATAQLALQGPRALEILRPLT 162
              + E+ +V   G +  DF WI+ N   G   ++ +I+++ A L+L GP+A +IL  +T
Sbjct: 540 RVAQDEFYIVTGTGYVTHDFDWIRRNIPEGMNCQLFDITSSNAVLSLMGPKARDILAAVT 599

Query: 163 RVDLASLGYYRWTEGQVLGVHCLIS--RTGYTGEDGFELYFEAAAAPTMWRNILAAGREA 220
           R D+++ G+   T   +    C +   R  Y GE G+EL+     A T++  ++  G+  
Sbjct: 600 RDDVSNDGFQFGTIRTIGIAGCPVQALRVTYVGELGWELHLPVEYAQTVYAALMGVGQPL 659

Query: 221 GLVPAGLGARDTLRLEAALPLYGHELGPDISPLEAGLHRFVRLEKG-EFNGREALAAQRE 279
           GLV AG  A ++LRLE     +G ++GPD +P EAGL   V+L K   F GR A  A++ 
Sbjct: 660 GLVDAGYRAIESLRLEKGYRAWGSDIGPDHTPFEAGLGWAVKLRKKIAFKGRAAAEARKA 719

Query: 280 AGVRRQLVGLTMIDRGIPRPEYPVLAAGKEIGYVTSGSLAPTLGQNIALALV 331
            GV++ L   T     +      +   GK +G++TSG    T+GQ+I    +
Sbjct: 720 GGVKKMLACFTTDPGVVLMGRETIYRNGKRVGWLTSGGYGYTVGQSIGYGYI 771


Lambda     K      H
   0.320    0.138    0.410 

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: 828
Number of extensions: 49
Number of successful extensions: 6
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: 366
Length of database: 815
Length adjustment: 35
Effective length of query: 331
Effective length of database: 780
Effective search space:   258180
Effective search space used:   258180
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: 52 (24.6 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