GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Pseudomonas benzenivorans DSM 8628

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate WP_090448305.1 BLS63_RS23910 1-aminocyclopropane-1-carboxylate deaminase

Query= BRENDA::O57809
         (325 letters)



>NCBI__GCF_900100495.1:WP_090448305.1
          Length = 337

 Score =  171 bits (432), Expect = 3e-47
 Identities = 109/324 (33%), Positives = 168/324 (51%), Gaps = 20/324 (6%)

Query: 8   LLAKFPRVELIPWETPIQYLPNISREIGADV--YIKRDDL-TGLGIGGNKIRKLEYLLGD 64
           +L KF R  L+   TPI+ L  +S  +G ++  Y KR+D  +GL  GGNKIRKLEY++ D
Sbjct: 1   MLEKFERYPLMFGPTPIEKLNRLSECLGGNIQLYAKREDCNSGLAFGGNKIRKLEYIVPD 60

Query: 65  ALSKGADVVITVGAVHSNHAFVTGLAAKKLGLDAILVLRGKEELK-------GNYLLDKI 117
           A++  AD ++++G V SNH       A KLG+   LV       +       GN L+ ++
Sbjct: 61  AIASHADTLVSIGGVQSNHTRQVAAVAAKLGMKCRLVQESWVPFQDAVYDRVGNILMSRV 120

Query: 118 MGIETRVYDAKDSFELMKYAEEIAEELKREGRKPYVIPPGGA----SPIGTLGYVRAVGE 173
           +G E    DA     + +  E   E++K +G KPY IP G +      +G +G+   V E
Sbjct: 121 LGAEIEFADAGFDIGIRESWERALEDVKAKGGKPYAIPAGASVHKYGGLGYVGFAEEVRE 180

Query: 174 IATQSEVKFDSIVVAAGSGGTLAGLSLGLSILNEDIRPVGIAVGRFGEVMTSKLDNLIKE 233
              Q  +KFD I+V   +G T AG+ +G +        +GI      E   +++  + + 
Sbjct: 181 QEAQMGIKFDYIIVCTVTGSTHAGMLVGFAKDGRARHVIGIDASGTPEQTRAQVLAIAQH 240

Query: 234 AAELLGVKVEVRPE----LYDYSFGEYGKITGEVAQIIRKVGTREGIILDPVYTGKAFYG 289
            AEL+G+  E+  +      +Y++  YG  + E    IR     EG++ DPVY GK+  G
Sbjct: 241 TAELVGLGQEITADDVILREEYAYPAYGIPSEETNAAIRLCARMEGMMTDPVYEGKSMQG 300

Query: 290 LVDLARKGEL--GEKILFIHTGGI 311
           L+DL RKG    G K+L+ H GG+
Sbjct: 301 LIDLVRKGFFPDGSKVLYAHLGGV 324


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: 278
Number of extensions: 17
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: 337
Length adjustment: 28
Effective length of query: 297
Effective length of database: 309
Effective search space:    91773
Effective search space used:    91773
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