GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cadA in Synechococcus elongatus PCC 7942

Align lysine decarboxylase (EC 4.1.1.18) (characterized)
to candidate Synpcc7942_2310 Synpcc7942_2310 conserved hypothetical protein, L-2,4-diaminobutyrate decarboxylase

Query= BRENDA::Q9L072
         (480 letters)



>FitnessBrowser__SynE:Synpcc7942_2310
          Length = 489

 Score =  197 bits (500), Expect = 9e-55
 Identities = 141/416 (33%), Positives = 211/416 (50%), Gaps = 24/416 (5%)

Query: 56  PLHDTAAVLDELEDVYLRDAVYFHHPRYLAHLNCPVVIPALLGEAVLSAVNSSLDTWDQS 115
           PL D   +L +LE + L  A+   +P YL H++      +++G+A+ + +N++L + + S
Sbjct: 65  PLPD---LLQQLEPL-LAQAMNPANPGYLGHMDPVASTASVIGDAIAALLNNNLLSVEMS 120

Query: 116 AGGTLIERKLIDWTCARIGLGPAADGVFTSGGTQSNLQALLLAREEAKAEDFADLR---- 171
              + +E  ++     R GLG  A G+  SGG+ +NLQA+ LAR  A       L     
Sbjct: 121 PSFSRLETAVLRELAQRFGLGDEAGGLLLSGGSLANLQAIALARNWALQVQETGLAGLTQ 180

Query: 172 ---IFASEASHFSVRKSAKLLGLGPDAVVSIPVDRDKRMQTVALARELERCARDGLVPMA 228
              +FASEA+H S++K+A LLGLG  AV+ I  DR  RMQ  AL   +    R G  P  
Sbjct: 181 RPILFASEAAHTSIQKAAMLLGLGSQAVIPIATDRRGRMQVAALTEAIASARRQGQRPFC 240

Query: 229 VVATGGTTDFGSIDPLPEIAGLCEQYGVWMHVDAAYGCGLLASLKYRDRITGIERADSVT 288
           +VAT GTT  GSIDPLPE++ +    G+W HVDA+YG  ++ S +Y  ++ GIE+A+SVT
Sbjct: 241 LVATAGTTVTGSIDPLPELSAIARTEGLWFHVDASYGGAVIFSPRYAHKLQGIEQANSVT 300

Query: 289 VDYHKSFFQPVSSSAVLVRDAATLRHATYHAEYLNPRRMVQERIPNQVDKSLQTTRRFDA 348
            +  K      +S+++L+RD + L   T H     P     + + N  + S+Q TR  D 
Sbjct: 301 FNPQKWLCVAKTSASLLLRDWSLL---TEHFRIAAPYMGEADDLINLGEVSVQGTRPADI 357

Query: 349 LKLWMTLRVMGADGIGVLFDEVCDLAAEGWKLLAADPRFDVVVQPSLSTLVFRHIPADVT 408
           LKLW+TL+  G  G   L +    L       L   P+  V   P L+ L FR     +T
Sbjct: 358 LKLWLTLQHFGDRGCAALVEHGLRLCRCFVAELRQRPQIQVATPPDLNILCFRLASDRLT 417

Query: 409 DPAEIDRANLYARKALFASGDAVVAGTKVAGRHYLKFTLLNPETTPADIAAVLDLI 464
              +    + Y   +L           +   R +LK  L+NP TTP  I  +   I
Sbjct: 418 AELQQFLLDRYFFLSL----------PRFRDRLWLKAVLVNPFTTPEHIRQLFGAI 463


Lambda     K      H
   0.320    0.135    0.397 

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: 512
Number of extensions: 19
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: 480
Length of database: 489
Length adjustment: 34
Effective length of query: 446
Effective length of database: 455
Effective search space:   202930
Effective search space used:   202930
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: 52 (24.6 bits)

This GapMind analysis is from Sep 17 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