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) (characterized)
to candidate WP_028585350.1 G494_RS0116150 serine dehydratase

Query= BRENDA::P20132
         (328 letters)



>NCBI__GCF_000429965.1:WP_028585350.1
          Length = 311

 Score =  290 bits (743), Expect = 2e-83
 Identities = 152/313 (48%), Positives = 206/313 (65%), Gaps = 11/313 (3%)

Query: 7   LHVKTPIRDSMALSKMAGTSVYLKMDSAQPSGSFKIRGIGHFCKRWAKQGCAHFVCSSAG 66
           LH++TP+  S ALS  +  SV+LK+++ QPSGSFK+RG+GH C  +A+QG   F+ SS G
Sbjct: 3   LHIETPLLPSRALSLESRRSVWLKLEALQPSGSFKLRGVGHACTHYARQGARRFISSSGG 62

Query: 67  NAGMAAAYAARQLGVPATIVVPSTTPALTIERLKNEGATVKVVGELLDEAFELAKALAKN 126
           NAG+A AYA R+L +P T+VVP TTP    E L  E A V+V G    EA ELA +L   
Sbjct: 63  NAGLATAYAGRRLEIPVTVVVPETTPERATELLAREQAEVRVHGASWQEANELALSLLGK 122

Query: 127 NPGWVYIPPFDDPLIWEGHASIVKELKETLWEKPGAIALSVGGGGLLCGVVQGLQEVGWG 186
           N  +++  PFDDPL+W+GHA ++ E+      KP AI L+VGGGGLLCGV QGL   GW 
Sbjct: 123 NDAFLH--PFDDPLLWQGHAGLIDEVAAA-GLKPDAIILAVGGGGLLCGVAQGLHRHGWD 179

Query: 187 DVPVIAMETFGAHSFHAATTAGKLVSLPKITSVAKALGVKTVGAQALKLFQEHPIFSEVI 246
           ++P+IA+ET G  SFH A  AG+LV L KI+ VA +LG   V AQAL+    HP+ + ++
Sbjct: 180 ELPIIAVETEGTASFHGAVEAGRLVKLAKISGVATSLGANQVCAQALQWVGRHPVTTTLV 239

Query: 247 SDQEAVAAIEKFVDDEKILVEPACGAALAAVYSHVIQKLQLEGNLRTPLPSLVVIVCGGS 306
           SD+ A++A E+F+DD ++LVEPACGAALA  Y         E  L     +++V+VCGG+
Sbjct: 240 SDRSALSACERFLDDHRLLVEPACGAALAVAYE--------ETALLERYRTVLVVVCGGA 291

Query: 307 NISLAQLRALKEQ 319
             +  QLR  + Q
Sbjct: 292 TATSEQLRQWRRQ 304


Lambda     K      H
   0.318    0.134    0.395 

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: 252
Number of extensions: 8
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: 328
Length of database: 311
Length adjustment: 28
Effective length of query: 300
Effective length of database: 283
Effective search space:    84900
Effective search space used:    84900
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 (21.7 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