GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gabT in Stenotrophomonas chelatiphaga DSM 21508

Align Probable 4-aminobutyrate aminotransferase; EC 2.6.1.19; (S)-3-amino-2-methylpropionate transaminase; EC 2.6.1.22; GABA aminotransferase; GABA-AT; Gamma-amino-N-butyrate transaminase; GABA transaminase; Glutamate:succinic semialdehyde transaminase; L-AIBAT (uncharacterized)
to candidate WP_057509163.1 ABB28_RS13760 glutamate-1-semialdehyde-2,1-aminomutase

Query= curated2:P94427
         (436 letters)



>NCBI__GCF_001431535.1:WP_057509163.1
          Length = 426

 Score =  144 bits (363), Expect = 5e-39
 Identities = 96/307 (31%), Positives = 157/307 (51%), Gaps = 30/307 (9%)

Query: 35  KGEGAELYDLDGRRFIDFAGAIGTLNVGHSHPKVVEAVKRQAEELIHPGFNVMMYPTYIE 94
           + +GA L+D+DG R+ID+ G+ G + VGH+HP V +AVK+ A+  +  G         + 
Sbjct: 40  RADGAYLHDVDGNRYIDYVGSWGPMIVGHNHPAVRQAVKKAADSGLSFG---APCAAEVT 96

Query: 95  LAEKLCGIAPGSHEKKAIFLNSGAEAVENAVKIARKYTKRQGVVSFTRGFHGRTNMTMSM 154
           +AE L  + P     + +  NSG EA  +A+++AR  T R  +V F   +HG  +  +  
Sbjct: 97  MAETLTRLVPSCEMVRMV--NSGTEATLSAIRLARGATGRSRIVKFEGCYHGHGDSFL-- 152

Query: 155 TSKVKPYKFGFGPFAPEVYQAPFPYYYQKPAGMSDESYDDMVIQAFNDFFIAS----VAP 210
                  K G G     V  +P       PAG+S+ +    +   +NDF  A+       
Sbjct: 153 ------VKAGSGMLTLGVPTSP-----GVPAGLSELT----LTLPYNDFDAATALFEAQG 197

Query: 211 ETVACVVMEPVQGEGGFIIPSKRFVQHVASFCKEHGIVFVADEIQTGFARTGTYFAIEHF 270
           E +A +++EPV G    I P + ++QH+ + C   G V + DE+ TGF R     A  H+
Sbjct: 198 EQIAGLIIEPVVGNANCIPPREGYLQHLRALCTRFGTVLIFDEVMTGF-RVALGGAQAHY 256

Query: 271 DVVPDLITVSKSLAAGLPLSGVIGRAEM---LDAAAPGELGGTYAGSPLGCAAALAVLDI 327
            V PDL T  K +  G+P+    G+ E+   +  A P    GT +G+P+  AA LA+L++
Sbjct: 257 GVTPDLTTFGKIIGGGMPVGAYGGKRELMQQISPAGPIYQAGTLSGNPVAMAAGLAMLEL 316

Query: 328 IEEEGLN 334
           +++ G +
Sbjct: 317 VQQPGFH 323


Lambda     K      H
   0.319    0.136    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: 462
Number of extensions: 22
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: 436
Length of database: 426
Length adjustment: 32
Effective length of query: 404
Effective length of database: 394
Effective search space:   159176
Effective search space used:   159176
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: 51 (24.3 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