GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcvT in Dinoroseobacter shibae DFL-12

Align Aminomethyltransferase; EC 2.1.2.10; Glycine cleavage system T protein (uncharacterized)
to candidate 3608080 Dshi_1485 FAD dependent oxidoreductase (RefSeq)

Query= curated2:C1F933
         (378 letters)



>FitnessBrowser__Dino:3608080
          Length = 804

 Score =  147 bits (372), Expect = 8e-40
 Identities = 105/333 (31%), Positives = 160/333 (48%), Gaps = 10/333 (3%)

Query: 42  AEHMAVRTGVGLFDVSHMGDIQLRGPGSLDAVQHICMNDASKLAVGQAHYSAMLYPQGTF 101
           AE MAVRTGVG+ ++ + G  ++ GPG+   +  I        A  +   S ML P G  
Sbjct: 470 AEVMAVRTGVGINELQNFGKFRVTGPGARAWLDRIMAGRIP--APRRLSLSPMLAPSGRL 527

Query: 102 VDDVIVHKFSDNDYLIVINAGTREKDYEWIRSHAQPFHCHVSNYSDLYTQLAIQGPRAAE 161
           + D  +   S+ ++ +  + G ++    W ++H       V N SD  T   I GPRA E
Sbjct: 528 IGDFTISCLSETEFQLTASYGAQDYHLRWFQTHLDD-GVTVENISDARTGFQIAGPRARE 586

Query: 162 TLAKLTSVDLAAIKNYRF--TWGTVCNLHNTLIARTGYTGEDGFEIYIPSDEATSERVWN 219
            LA  T  D++A + +RF         + + L+ R  YTG+ G+EIY    E     +++
Sbjct: 587 VLAACTRADVSA-EAFRFFDVAPMTIGMAHCLVQRVSYTGDLGYEIYCSPTE--QRHLFH 643

Query: 220 EVLEAGKEFGIVPCGLGARNTLRLESAMALYGHEISQDIDVFEAGLDRYCKLDKGT-FVG 278
            + EAG+  GI P G+ A  +LRL+     +  E S D    E GLDR+    K T F+G
Sbjct: 644 TLWEAGQPHGIRPFGMRAMMSLRLDKFFGAWSREYSPDYTAAETGLDRFIHFGKNTAFIG 703

Query: 279 SEALKQVVAQGGPKRKLVGLEMIDRGIARDGYRVLNDTQQAVGYVTSGSPAPFLKKNIAL 338
             A +   A   P R+L   E+         Y  ++   + VG+ TSG  A F  K+IAL
Sbjct: 704 RNAAEAERATP-PARQLCAFEVAATDADVVAYEPISLDGEVVGFCTSGGYAHFTGKSIAL 762

Query: 339 AYVPTELATLDREVFVEIRNNPVKARIVPTPFY 371
            +VP E+A    E  +EI  +   A ++ TP +
Sbjct: 763 GFVPREMAQDGLEASIEILGDHCPATLITTPLF 795


Lambda     K      H
   0.320    0.136    0.407 

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: 718
Number of extensions: 41
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 378
Length of database: 804
Length adjustment: 36
Effective length of query: 342
Effective length of database: 768
Effective search space:   262656
Effective search space used:   262656
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: 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