GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Desulfobulbus mediterraneus DSM 13871

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate WP_028584555.1 G494_RS0110775 D-cysteine desulfhydrase

Query= BRENDA::O57809
         (325 letters)



>NCBI__GCF_000429965.1:WP_028584555.1
          Length = 332

 Score =  194 bits (494), Expect = 2e-54
 Identities = 128/328 (39%), Positives = 177/328 (53%), Gaps = 18/328 (5%)

Query: 9   LAKFPRVELIPWETPIQYLPNISREIG--ADVYIKRDDLTGLGIGGNKIRKLEYLLGDAL 66
           L +FPR   +   TPI+ LP  S  +G   +++IKRDDL     GGNK RKL++ + DAL
Sbjct: 3   LTQFPRRNYVQDATPIEALPAFSAALGNKVNLFIKRDDLLPGCAGGNKTRKLDFCIADAL 62

Query: 67  SKGADVVITVGAVHSNHAFVTGLAAKKLGLDAILVLRG------KEELKGNYLLDKIMGI 120
            KGAD +IT GAV SNH  +T   A K G+D  LVL        +E+  GN  L K+MG+
Sbjct: 63  EKGADTIITCGAVQSNHCRLTLSWAVKEGMDCHLVLEERVAGSYREDGSGNNFLFKLMGV 122

Query: 121 ETRVYDAKDSFELMKYAEEIAEELKREGRKPYVIPPGGASPIGTLGYVRAVGEIATQ--- 177
           ++ +       ++M   E++A E++  GRKPY+IP G ++ IG  GYV    EI  Q   
Sbjct: 123 KS-ITVVPGGSDMMAAMEQLAAEVEGSGRKPYIIPGGASNAIGATGYVACAQEIQQQLFA 181

Query: 178 SEVKFDSIVVAAGSGGTLAGLSLGLSILNEDIRPVGIAVGRFGEVMTSKLDNLIKEAAEL 237
             +K D +VV +GS GT AG+ +G+   N  I   GI V R   V    +  L  E A  
Sbjct: 182 RNLKIDHMVVPSGSAGTHAGMVVGMYGSNAGIPVSGINVSRTKPVQEEIVHKLALETAAR 241

Query: 238 LGVKVEVRPE---LYDYSFGE-YGKITGEVAQIIRKVGTREGIILDPVYTGKAFYGLVDL 293
           LGV+  V  E    +D   G  Y   T  + + ++ +   E I+LDPVY+GKA  GL+DL
Sbjct: 242 LGVRESVPAEEITCFDGYVGPGYSLPTESMVEAVKLLAQTESILLDPVYSGKAMAGLIDL 301

Query: 294 ARKGEL--GEKILFIHTGGISGTFHYGD 319
            R      G  +LF+HTGG    + Y D
Sbjct: 302 VRNDHFAPGANVLFLHTGGSPALYAYLD 329


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: 254
Number of extensions: 12
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: 325
Length of database: 332
Length adjustment: 28
Effective length of query: 297
Effective length of database: 304
Effective search space:    90288
Effective search space used:    90288
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: 49 (23.5 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