GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gabT in Shewanella sp. ANA-3

Align Gamma aminobutyrate transaminase 2; Gamma-aminobutyrate transaminase isozyme 2; LeGABA-TP2; SlGABA-T2; EC 2.6.1.96 (characterized)
to candidate 7025360 Shewana3_2520 aminotransferase (RefSeq)

Query= SwissProt::Q84P53
         (458 letters)



>FitnessBrowser__ANA3:7025360
          Length = 452

 Score =  153 bits (387), Expect = 1e-41
 Identities = 107/359 (29%), Positives = 181/359 (50%), Gaps = 27/359 (7%)

Query: 29  IDKAEGSYVYGVNGKKYLDSLSGLWCTVLGGSEPRLIEAASKQLNKSAFYHSFWNRTTKP 88
           +  A+G  +  V+G+K +D  S  W  V G   P ++ A  +QL++ + +  F   T +P
Sbjct: 30  VHSAQGCELELVDGRKLIDGTSSWWACVHGYGHPAILTAMERQLHQLS-HVMFGGITHEP 88

Query: 89  SLDLAKELINMFTANKMGKVFFTSSGSEANDTQVKLVWYYNNAIGRP-----NKKKIISR 143
           ++ L K+L+ M T   + KVF   SGS A +  +K+   Y      P      K++I++ 
Sbjct: 89  AITLCKKLLAM-TCEPLTKVFLCDSGSIAVEVAIKMALQYWQGQDLPLAQKAQKQRILTV 147

Query: 144 KNAYHGSTYMTAGLSGLPS-LHLKFDLPPPYILHTDCPHYWNYHLPGETEEEYSTRLANN 202
           K  YHG T+    +      +H  F          D P           +  +   L  +
Sbjct: 148 KKGYHGDTFAAMSVCDPEGGMHTMFGEAVTKQCFVDAP-----------QTPFGEPLRQD 196

Query: 203 ----LENLILKEGPETVAAFIAEPVMGGAGVI-IPPATYFEKIQAVLKKYDILFIADEVI 257
               ++ ++ ++ PE +AA I EP+M GAG +    + Y   ++A+  +Y++L I DE+ 
Sbjct: 197 DLAPMQRILREQHPE-IAAVIIEPIMQGAGGMRFYSSEYLRGLRALCDEYNVLLILDEIA 255

Query: 258 CGFGRLGTMFGCDKYNIKPDLVSIAKALSGGYIPIGAVLVSEEISKVIMSQSNQLGVFCH 317
            GFGR G +F  +  +I PD++ + KAL+GGYI + A L ++ +++ I SQS   GVF H
Sbjct: 256 TGFGRTGKLFAYEHADITPDILCLGKALTGGYISLAATLCTDNVAQGI-SQS-PAGVFMH 313

Query: 318 GFTYSGHPVACAVALEALKIYKEKNITEVVNKLSPKLQEGLKAFIDSPIIGEIRGTGLV 376
           G T+ G+P+ACA A  +L +  ++     V  +  ++Q  L   ID P + E+R  G V
Sbjct: 314 GPTFMGNPLACAAACASLDLINQQEWPAQVAAIEQQMQRELADAIDIPSVKEVRVLGAV 372


Lambda     K      H
   0.318    0.136    0.410 

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: 27
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 458
Length of database: 452
Length adjustment: 33
Effective length of query: 425
Effective length of database: 419
Effective search space:   178075
Effective search space used:   178075
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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 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