GapMind for catabolism of small carbon sources

 

Alignments for a candidate for davT in Malonomonas rubra DSM 5091

Align 5-aminovalerate transaminase (EC 2.6.1.48) (characterized)
to candidate WP_072908061.1 BUB13_RS08945 glutamate-1-semialdehyde 2,1-aminomutase

Query= BRENDA::Q9I6M4
         (426 letters)



>NCBI__GCF_900142125.1:WP_072908061.1
          Length = 427

 Score =  169 bits (427), Expect = 2e-46
 Identities = 116/376 (30%), Positives = 182/376 (48%), Gaps = 34/376 (9%)

Query: 5   NESLLKRRQAAVPRGVGQ---------IHPVVAERAENSTVWDVEGREYIDFAGGIAVLN 55
           +E+L    +  +P GV           I+P+  E+A  S ++D +G EYID+ G    + 
Sbjct: 6   SEALFSAAKNVIPGGVNSPVRAFKSVGINPIFIEKAAGSKIYDADGNEYIDYVGSWGPMI 65

Query: 56  TGHLHPKVIAAVQEQLGKLSHTCFQVLAYEPYIELAEEIAKRVPGDFPKKTLLVTSGSEA 115
            GH HPKV+ A+Q+     S   F         +LAE +++  P    +K  +V+SG+EA
Sbjct: 66  MGHCHPKVVEAIQKTAA--SGASFGAPTARE-TQLAEMVSEAYPN--IEKVRMVSSGTEA 120

Query: 116 VENAVKIARAATGRAGVIAFTGAYHGRTMMTL-----GLTGKVVPYSAGMGLMPGGIFRA 170
             +A+++AR  TGR  ++ F G YHG     L     GL    VP S G   +P    + 
Sbjct: 121 TMSAIRLARGYTGRDKILKFDGCYHGHADSLLVKAGSGLATFGVPTSPG---VPADFAKY 177

Query: 171 LAPCELHGVSEDDSIASIERIFKNDAQPQDIAAIIIEPVQGEGGFYVNSKSFMQRLRALC 230
                 + + E   + +        A  ++IA II+EP+ G  G       F++ LR LC
Sbjct: 178 TLTATYNDLDEVKQMVA--------ANDKEIACIILEPIAGNMGCVPPVPGFLEGLRELC 229

Query: 231 DQHGILLIADEVQTGAGRTGTFFATEQLGIVPDLTTFAKSVGGGFPISGVAGKAEIMDAI 290
            Q GI+LI DEV TG  R     A E+  +  DL    K +GGG P+    GK EIMD++
Sbjct: 230 TQEGIVLIVDEVMTGF-RVAFGGAQERFNVRGDLVCLGKIIGGGLPVGAFGGKKEIMDSL 288

Query: 291 APGG---LGGTYAGSPIACAAALAVLKVFEEEKLLERSQAVGERLKAGLREIQAKHKVIG 347
           +P G     GT +G+P+A +A +A L + +EE   ++ +     L+ GL ++     V  
Sbjct: 289 SPEGGVYQAGTLSGNPLAMSAGIATLNILKEEGFYQQLEEKSAYLEKGLLQVAGNSSVAT 348

Query: 348 DVRGLGSMVAIELFEG 363
             + +G+M      +G
Sbjct: 349 CWQRVGAMFCTYFQQG 364


Lambda     K      H
   0.319    0.137    0.393 

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: 408
Number of extensions: 26
Number of successful extensions: 5
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: 426
Length of database: 427
Length adjustment: 32
Effective length of query: 394
Effective length of database: 395
Effective search space:   155630
Effective search space used:   155630
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. 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