GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Pseudomonas fluorescens FW300-N2E3

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate AO353_11680 AO353_11680 cysteine desulfhydrase

Query= BRENDA::O57809
         (325 letters)



>FitnessBrowser__pseudo3_N2E3:AO353_11680
          Length = 330

 Score =  218 bits (556), Expect = 1e-61
 Identities = 129/323 (39%), Positives = 196/323 (60%), Gaps = 16/323 (4%)

Query: 9   LAKFPRVELIPWETPIQYLPNISREIGADVYIKRDDLTGLGIGGNKIRKLEYLLGDALSK 68
           LA+F R++L+   T ++ L  +S  +G DVY+KRDDLT L +GGNK+RKLEYL  DAL++
Sbjct: 6   LARFNRLDLLANATALEKLERLSTWLGRDVYVKRDDLTPLAMGGNKLRKLEYLAADALAQ 65

Query: 69  GADVVITVGAVHSNHAFVTGLAAKKLGLDAILVLR---GKEEL----KGNYLLDKIMGIE 121
           GAD +IT GA+ SNH   T   A KLGL  + +L    G ++      GN LL  +   +
Sbjct: 66  GADTLITAGAIQSNHVRQTAALAAKLGLGCVALLENPIGTDDSNYLGNGNRLLLDLFDAK 125

Query: 122 TRVYDAKDSFELMKYAEEIAEELKREGRKPYVIPPGGASPIGTLGYVRAVGEIATQSE-- 179
             + +  D+ +  +  + +AE L+  G+KPY++P GG++ +G LGYVRA  E+A Q E  
Sbjct: 126 VELVENLDNAD--QQLQALAERLRSNGKKPYLVPIGGSNALGALGYVRAGLELAGQIEDS 183

Query: 180 -VKFDSIVVAAGSGGTLAGLSLGLSILNEDIRPVGIAVGRFGEVMTSKLDNLIKEAAELL 238
            ++F ++V+A+GS GT +GL+L LS +  D+  +G+ V R  E    K+  L +  AELL
Sbjct: 184 GLEFAAVVLASGSAGTHSGLALALSEVLPDLPVIGVTVSRSDEDQRPKVQGLAERTAELL 243

Query: 239 GVKV--EVRPELYDYSFG-EYGKITGEVAQIIRKVGTREGIILDPVYTGKAFYGLVD-LA 294
           GV +    + +L+D  F   YG+        ++ + ++EG++LDPVYTGKA  GL+D + 
Sbjct: 244 GVNLPASFKVQLWDEYFAPRYGEPNAGTLAAVKLLASQEGLLLDPVYTGKAMAGLLDGIG 303

Query: 295 RKGELGEKILFIHTGGISGTFHY 317
           R+      I+F+HTGG    F Y
Sbjct: 304 RQRFNDGPIIFLHTGGAPALFAY 326


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: 279
Number of extensions: 14
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: 330
Length adjustment: 28
Effective length of query: 297
Effective length of database: 302
Effective search space:    89694
Effective search space used:    89694
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 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