GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Stenotrophomonas chelatiphaga DSM 21508

Align serine racemase (EC 5.1.1.18) (characterized)
to candidate WP_057508536.1 ABB28_RS10275 serine dehydratase

Query= BRENDA::Q2PGG3
         (331 letters)



>NCBI__GCF_001431535.1:WP_057508536.1
          Length = 320

 Score =  266 bits (680), Expect = 5e-76
 Identities = 140/310 (45%), Positives = 206/310 (66%), Gaps = 5/310 (1%)

Query: 14  SIKEAHDRIKPYIHRTPVLTSESLNSISGRSLFFKCECLQKGGAFKFRGACNAVLSLDAE 73
           ++ EA  RI P+   TPVL S++L++++G  L FK E LQ+ GAFKFRGACNAV SL A+
Sbjct: 11  AVLEAAARIAPHAAVTPVLRSQTLDALAGAQLAFKAEHLQRSGAFKFRGACNAVWSLSAD 70

Query: 74  QAAKGVVTHSSGNHAAALSLAAKIQGIPAYIVVPKGAPKCKVDNVIRYGGKVIWSEATMS 133
           +A  GVVTHSSGNH AAL+LAA+ +GI  ++VVP GA   K+ N+ R+G  +     T++
Sbjct: 71  RAPAGVVTHSSGNHGAALALAARTRGIACHVVVPDGAVAAKLANIARHGATLWRCAPTIA 130

Query: 134 SREEIASKVLQETGSVLIHPYNDGRIISGQGTIALELLEQIQEIDAIVVPISGGGLISGV 193
           +RE + ++V  +TG+ L+HPY D  +I+GQGT  LELL+     D +VVP+ GGGL +G 
Sbjct: 131 AREAVCAQVQADTGATLVHPYADAAVIAGQGTAVLELLQAEGPFDVVVVPVGGGGLAAGT 190

Query: 194 ALAAKSIKPSIRIIAAEPKGADDAAQSKVAGKIITLPVTNTIADGLRASLGDLTWPVVRD 253
           ALA + + P  R++ AEP GA D A+S  AG+     V +T+ DGLR +LG   + +++ 
Sbjct: 191 ALALQQVSPHTRLVLAEPAGAADTARSLQAGERRIDFVPDTVCDGLRGTLGAPNFQLLQA 250

Query: 254 LVDDVVTLEECEIIEAMKMCYEILKVSVEPSGAIGLAAVLSNSFRNNPSCRDCKNIGIVL 313
              +V+ +++   + AM++ +++LK +VEPS AI LAAVL+      P       +G+VL
Sbjct: 251 AGAEVIVVDDAATVAAMRLLWQVLKQTVEPSSAIALAAVLA-----QPQRFAGLRVGLVL 305

Query: 314 SGGNVDLGSL 323
           SGGNVD+ +L
Sbjct: 306 SGGNVDIDAL 315


Lambda     K      H
   0.316    0.133    0.380 

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: 287
Number of extensions: 11
Number of successful extensions: 2
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: 331
Length of database: 320
Length adjustment: 28
Effective length of query: 303
Effective length of database: 292
Effective search space:    88476
Effective search space used:    88476
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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