GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dsdA in Cupriavidus basilensis 4G11

Align L-serine ammonia-lyase (EC 4.3.1.17); D-Serine ammonia-lyase (EC 4.3.1.18) (characterized)
to candidate RR42_RS32990 RR42_RS32990 1-aminocyclopropane-1-carboxylate deaminase

Query= BRENDA::O57809
         (325 letters)



>FitnessBrowser__Cup4G11:RR42_RS32990
          Length = 338

 Score =  169 bits (429), Expect = 7e-47
 Identities = 110/322 (34%), Positives = 167/322 (51%), Gaps = 20/322 (6%)

Query: 9   LAKFPRVELIPWETPIQYLPNISREIGA--DVYIKRDDL-TGLGIGGNKIRKLEYLLGDA 65
           L +FPR +L    TPIQ L  +S  +G   D+Y KR+D  +GL  GGNK RKLEY++ DA
Sbjct: 3   LKRFPRHQLTFGPTPIQPLKRLSAHLGGKVDLYAKREDCNSGLAFGGNKTRKLEYIIPDA 62

Query: 66  LSKGADVVITVGAVHSNHAFVTGLAAKKLGLDAILVLR-------GKEELKGNYLLDKIM 118
           L++G D ++++G + SN        A  LGL  +LV            +  GN  + +IM
Sbjct: 63  LAQGCDTLVSIGGIQSNQTRQVAAVAAHLGLKCVLVQEDWVNYSDAVYDRVGNIQMSRIM 122

Query: 119 GIETRVYDAKDSFELMKYAEEIAEELKREGRKPYVIPPG-GASPIGTLGYVRAVGEIATQ 177
           G + R+        + K  EE  E +++ G KPY IP G    P+G LG+V    E+  Q
Sbjct: 123 GADVRLVSDGFDIGIRKSWEEAMESVRQAGGKPYPIPAGCSEHPLGGLGFVGFAEEVRAQ 182

Query: 178 SE---VKFDSIVVAAGSGGTLAGLSLGLSILNEDIRPVGIAVGRFGEVMTSKLDNLIKEA 234
                 KFD +VV + +G T AG+ +G +      R +GI          +++  + +  
Sbjct: 183 EAELGFKFDYVVVCSVTGSTQAGMVVGFAADGRANRVIGIDASAKPAQTRAQILRIARNT 242

Query: 235 AELLGVKVEVRPE--LYDYSFG--EYGKITGEVAQIIRKVGTREGIILDPVYTGKAFYGL 290
           A L+ +  ++  E  + D  +G  EYG  + E  + IR     EG++ DPVY GK+  G+
Sbjct: 243 AHLVDLGRDITDEDVVLDTRYGGPEYGLPSEETLEAIRMSAKLEGMMTDPVYEGKSMQGM 302

Query: 291 VDLARKGEL--GEKILFIHTGG 310
           +DL R+GE   G K+L+ H GG
Sbjct: 303 IDLVRRGEFPEGSKVLYAHLGG 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: 293
Number of extensions: 26
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: 338
Length adjustment: 28
Effective length of query: 297
Effective length of database: 310
Effective search space:    92070
Effective search space used:    92070
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 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