GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Phaeacidiphilus oryzae TH49

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate WP_037577072.1 BS73_RS27805 1-aminocyclopropane-1-carboxylate deaminase

Query= BRENDA::O57809
         (325 letters)



>NCBI__GCF_000744815.1:WP_037577072.1
          Length = 335

 Score =  167 bits (423), Expect = 3e-46
 Identities = 112/322 (34%), Positives = 169/322 (52%), Gaps = 21/322 (6%)

Query: 9   LAKFPRVELIPWETPIQYLPNISREIG-ADVYIKRDDL-TGLGIGGNKIRKLEYLLGDAL 66
           LA F R  L+   +P+  L  +S  +G A ++ KR+D  +GL  GGNK RKLEYLL DAL
Sbjct: 3   LADFDRYPLLFGPSPVHPLERLSEHLGGARIWAKREDCNSGLAFGGNKTRKLEYLLPDAL 62

Query: 67  SKGADVVITVGAVHSNHAFVTGLAAKKLGLDAILVLR-------GKEELKGNYLLDKIMG 119
           ++GAD ++++G V SNH       A + GL A+LV            +  GN LL +IMG
Sbjct: 63  AQGADTLVSIGGVQSNHTRQVAAVAARAGLKAVLVQESWVDWPDSVNDKVGNILLSRIMG 122

Query: 120 IETRVYDAKDSFELMKYAEEIAEELKREGRKPYVIPPGGAS-PIGTLGYVRAVGEIATQS 178
            + R+  A          ++   E++  G  PY IP G +  P+G LG+     E+  Q 
Sbjct: 123 ADVRLVRAGFGIGYKDSWQQALAEVRESGGTPYPIPAGASDHPLGGLGFANWAEEVRQQE 182

Query: 179 E---VKFDSIVVAAGSGGTLAGLSLGLSILNEDIRPVGI-AVGRFGEVMTSKLDNLIKEA 234
               V FD++VV + +G T AG+  G +  +   R +GI A  R  E   ++++ + ++ 
Sbjct: 183 RELGVFFDTVVVCSVTGSTQAGMIAGFAGQDRPRRVIGIDASARIAET-RAQVEKIARDT 241

Query: 235 AELLGVKVEVRPE----LYDYSFGEYGKITGEVAQIIRKVGTREGIILDPVYTGKAFYGL 290
           A+ +G+   +R E    L  ++   YG         IR  G  EG+I+DPVY GK+  GL
Sbjct: 242 ADRIGLGRALRDEEITVLEGWAGEAYGVPVRSTLDAIRLTGGLEGMIIDPVYEGKSMAGL 301

Query: 291 VDLARKGELG--EKILFIHTGG 310
           +DL R GE+G    +L+ H GG
Sbjct: 302 IDLVRNGEIGRDSHVLYAHLGG 323


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: 287
Number of extensions: 20
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: 325
Length of database: 335
Length adjustment: 28
Effective length of query: 297
Effective length of database: 307
Effective search space:    91179
Effective search space used:    91179
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 Apr 09 2024. 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