GapMind for catabolism of small carbon sources

 

Alignments for a candidate for davT in Sulfuritalea hydrogenivorans DSM 22779

Align 5-aminovalerate transaminase (EC 2.6.1.48) (characterized)
to candidate WP_041100966.1 SUTH_RS17015 glutamate-1-semialdehyde 2,1-aminomutase

Query= BRENDA::Q9I6M4
         (426 letters)



>NCBI__GCF_000828635.1:WP_041100966.1
          Length = 425

 Score =  161 bits (408), Expect = 3e-44
 Identities = 129/373 (34%), Positives = 171/373 (45%), Gaps = 38/373 (10%)

Query: 5   NESLLKRRQAAVPRGVGQIHPVVAERA-----------ENSTVWDVEGREYIDFAGGIAV 53
           NE L  R Q  +P GV    PV A R+             + V D +G+EYID+ G    
Sbjct: 4   NEELFSRAQKTIPGGVNS--PVRAFRSVGGAPCFFASGSGARVRDADGKEYIDYVGSWGP 61

Query: 54  LNTGHLHPKVIAAVQEQLGK-LSHTCFQVLAYEPYIELAEEIAKRVPGDFPKKTLLVTSG 112
           L  GH     + AVQE   K LS         E  IELAE + +RVP    +   LV+SG
Sbjct: 62  LILGHADADTVRAVQEAAMKGLSFGA----PTEAEIELAELLVRRVPS--MEMVRLVSSG 115

Query: 113 SEAVENAVKIARAATGRAGVIAFTGAYHGRTMMTLGLTGKVVPYSAGMGLMP-GGIFRAL 171
           +EA  +A+++AR  TGR  +I F G YHG         G  +   AG GL+  G    A 
Sbjct: 116 TEATMSAIRLARGFTGRDAIIKFEGCYHGH--------GDSLLVKAGSGLLTFGNPSSAG 167

Query: 172 APCELHG---VSEDDSIASIERIFKNDAQPQDIAAIIIEPVQGEGGFYVNSKSFMQRLRA 228
            P +L     V + +    +   F    +   IA +I+EPV G          F+  +R 
Sbjct: 168 VPADLAQHTLVLDYNDAQGLRDAFAKHGKT--IACVIVEPVAGNMNLIAPKPEFLAAMRE 225

Query: 229 LCDQHGILLIADEVQTGAGRTGTFFATEQLGIVPDLTTFAKSVGGGFPISGVAGKAEIMD 288
           LC QHG +LI DEV TG  R G   A    GI PDL+TF K VGGG P+    G+ +IM+
Sbjct: 226 LCTQHGSVLIFDEVMTGF-RVGPGSAQGLYGITPDLSTFGKVVGGGMPLGAFGGRRDIME 284

Query: 289 AIAPGG---LGGTYAGSPIACAAALAVLKVFEEEKLLERSQAVGERLKAGLREIQAKHKV 345
            IAP G     GT +G+P++ AA L  LK        +   A    L  GL     K  V
Sbjct: 285 KIAPLGPVYQAGTLSGNPLSVAAGLVTLKKVGAPGFYDALTAKTRTLVDGLAAAAKKRGV 344

Query: 346 IGDVRGLGSMVAI 358
               + +G M  +
Sbjct: 345 KFSAQSVGGMFGV 357


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: 462
Number of extensions: 36
Number of successful extensions: 7
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: 425
Length adjustment: 32
Effective length of query: 394
Effective length of database: 393
Effective search space:   154842
Effective search space used:   154842
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