GapMind for catabolism of small carbon sources

 

Alignments for a candidate for patA in Sinorhizobium meliloti 1021

Align putrescine-2-oxoglutarate transaminase (EC 2.6.1.82) (characterized)
to candidate SM_b21186 SM_b21186 4-aminobutyrate aminotransferase

Query= BRENDA::P42588
         (459 letters)



>FitnessBrowser__Smeli:SM_b21186
          Length = 422

 Score =  192 bits (487), Expect = 2e-53
 Identities = 126/349 (36%), Positives = 187/349 (53%), Gaps = 23/349 (6%)

Query: 78  DTQGQEFIDCLGGFGIFNVGHRNPVVVSAVQNQLAKQPLHSQELLDPLR--AMLAKTLAA 135
           D +G  +ID   G  + N GHR+P V++AV+ QL +   H+   + P      LA+ L A
Sbjct: 34  DKEGNRYIDFAAGIAVVNTGHRHPKVIAAVKAQLDRFT-HTCHQVVPYENYVHLAERLNA 92

Query: 136 LTPGKL-KYSFFCNSGTESVEAALKLAKAYQSPRGKFTFIATSGAFHGKSLGALSATAKS 194
           + PG   K + F  +G E+VE A+K+A+A     G+   +A  G FHG++   ++ T K 
Sbjct: 93  IVPGDFAKKTIFVTTGAEAVENAVKIARA---ATGRQAVVAFGGGFHGRTFMGMALTGKV 149

Query: 195 TFRKPFMPLLPG-FRHVPFG------NIEAMRTALNECKKTGDD---VAAVILEPIQGEG 244
              K     +P    H PF        +E   +AL +      D   VAA+I+EP+QGEG
Sbjct: 150 VPYKVGFGAMPADVFHAPFPIELHGVTVEQSLSALKKLFAADVDPARVAAIIIEPVQGEG 209

Query: 245 GVILPPPGYLTAVRKLCDEFGALMILDEVQTGMGRTGKMFACEHENVQPDILCLAKALGG 304
           G    P  ++ A+R++CD+ G L+I DEVQTG  RTGK+FA EH  V PD+  +AK+L G
Sbjct: 210 GFYPVPTAFMKALREVCDQHGILLIADEVQTGFARTGKLFAMEHHGVAPDLTTMAKSLAG 269

Query: 305 GVMPIGATIATEEVFSVLFDNPFLHTTTFGGNPLACAAALATINVLLEQNLPAQAEQKGD 364
           G  P+ A     E+       P     T+GGNPL  AAA A ++V+ E+NL  +A Q G+
Sbjct: 270 G-FPLAAVTGRAEIMDA--PGPGGLGGTYGGNPLGIAAAHAVLDVIAEENLCERANQLGN 326

Query: 365 MLLDGFRQLAREYPDLVQEARGKGMLMAIEFVDNEIGYNFASEMFRQRV 413
            L      +  + P++V + RG G + A+EF  N++  N  S  F  +V
Sbjct: 327 RLKQRLAAIREKAPEIV-DIRGPGFMNAVEF--NDVRTNLPSAEFANKV 372


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: 446
Number of extensions: 17
Number of successful extensions: 6
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: 422
Length adjustment: 32
Effective length of query: 427
Effective length of database: 390
Effective search space:   166530
Effective search space used:   166530
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 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