GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Dyadobacter tibetensis Y620-1

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate WP_025763937.1 X939_RS0114125 1-aminocyclopropane-1-carboxylate deaminase/D-cysteine desulfhydrase

Query= BRENDA::O57809
         (325 letters)



>NCBI__GCF_000566685.1:WP_025763937.1
          Length = 301

 Score =  134 bits (337), Expect = 3e-36
 Identities = 95/290 (32%), Positives = 141/290 (48%), Gaps = 21/290 (7%)

Query: 31  SREIGADVYIKRDDLTGLGIGGNKIRKLEYLLGDALSKGADVVITVGAVHSNHAFVTGLA 90
           +++ G  +Y+KRDDL    + GNK RKL+Y L D    G   +++ G  +SNH +    A
Sbjct: 20  TQDAGISLYMKRDDLIHPLVSGNKWRKLKYALADVHRSGNATILSFGGAYSNHLYALAAA 79

Query: 91  AKKLGLDAILVLRGKEELKGNYLLDKIMGIETR----VYDAKDSFELMKYAEEIAEELKR 146
            +  G+  I ++RG EEL G    D +   E +     + +++S+ L +Y  +  E L R
Sbjct: 80  GRLTGISTIGIVRG-EELAGKKRSDTLAFCEAQGMKLHFVSRESYRL-RYNRDYLESLSR 137

Query: 147 EGRKPYVIPPGGASPIGTLGYVRAVGEIATQSEVKFDSIVVAAGSGGTLAG-LSLGLSIL 205
           +  KPY+IP GG S +   G      E+  Q     D   V  GSGGT AG LS G  +L
Sbjct: 138 QFGKPYIIPEGGTSTMALEGVGELAQEVYDQLGRHPDYYTVPVGSGGTTAGLLSAGQQVL 197

Query: 206 NEDIRPVGIAVGRFGEVMTSKLDNLIKEAAELLGVKVEVRPELYDYSFGEYGKITGEVAQ 265
                     V + G  +   + +L  + +  L + +       DY FG YGK   E+ +
Sbjct: 198 -------AFPVLKNGGFLKEVILDLASDHSAHLALSL-----FTDYHFGGYGKWNPELVR 245

Query: 266 IIRKVGTREGIILDPVYTGKAFYGLVDLARKG--ELGEKILFIHTGGISG 313
            I     R  I L+ +YTGK  YGL DL  KG    G  ++ +HTGG+ G
Sbjct: 246 FILDFRDRFQIPLEQIYTGKMMYGLYDLMSKGFFRPGTTVVALHTGGLQG 295


Lambda     K      H
   0.319    0.142    0.402 

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: 277
Number of extensions: 13
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: 325
Length of database: 301
Length adjustment: 27
Effective length of query: 298
Effective length of database: 274
Effective search space:    81652
Effective search space used:    81652
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 (21.7 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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