GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Malonomonas rubra DSM 5091

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate WP_072908061.1 BUB13_RS08945 glutamate-1-semialdehyde 2,1-aminomutase

Query= BRENDA::P42588
         (459 letters)



>NCBI__GCF_900142125.1:WP_072908061.1
          Length = 427

 Score =  139 bits (349), Expect = 2e-37
 Identities = 104/316 (32%), Positives = 158/316 (50%), Gaps = 19/316 (6%)

Query: 66  VEWQAGSLNTLVDTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPL 125
           +E  AGS   + D  G E+ID +G +G   +GH +P VV A+Q   A             
Sbjct: 38  IEKAAGS--KIYDADGNEYIDYVGSWGPMIMGHCHPKVVEAIQKTAASGASFGAPTAR-- 93

Query: 126 RAMLAKTLAALTPGKLKYSFFCNSGTESVEAALKLAKAYQSPRGKFTFIATSGAFHGK-- 183
              LA+ ++   P   K     +SGTE+  +A++LA+ Y    G+   +   G +HG   
Sbjct: 94  ETQLAEMVSEAYPNIEKVRMV-SSGTEATMSAIRLARGYT---GRDKILKFDGCYHGHAD 149

Query: 184 SLGALSATAKSTFRKPFMPLLPGFRHVPFGNIEAMRTALNECKK----TGDDVAAVILEP 239
           SL   + +  +TF  P  P +P         + A    L+E K+       ++A +ILEP
Sbjct: 150 SLLVKAGSGLATFGVPTSPGVPA--DFAKYTLTATYNDLDEVKQMVAANDKEIACIILEP 207

Query: 240 IQGEGGVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLA 299
           I G  G + P PG+L  +R+LC + G ++I+DEV TG  R     A E  NV+ D++CL 
Sbjct: 208 IAGNMGCVPPVPGFLEGLRELCTQEGIVLIVDEVMTGF-RVAFGGAQERFNVRGDLVCLG 266

Query: 300 KALGGGVMPIGATIATEEVFSVLF-DNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQ 358
           K +GGG +P+GA    +E+   L  +       T  GNPLA +A +AT+N+L E+    Q
Sbjct: 267 KIIGGG-LPVGAFGGKKEIMDSLSPEGGVYQAGTLSGNPLAMSAGIATLNILKEEGFYQQ 325

Query: 359 AEQKGDMLLDGFRQLA 374
            E+K   L  G  Q+A
Sbjct: 326 LEEKSAYLEKGLLQVA 341


Lambda     K      H
   0.320    0.135    0.393 

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: 457
Number of extensions: 27
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: 459
Length of database: 427
Length adjustment: 32
Effective length of query: 427
Effective length of database: 395
Effective search space:   168665
Effective search space used:   168665
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: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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