Aligments for a candidate for gabT in Paraburkholderia bryophila 376MFSha3.1

GapMind for catabolism of small carbon sources

Aligments for a candidate for gabT in Paraburkholderia bryophila 376MFSha3.1

Align Gamma-aminobutyrate:alpha-ketoglutarate aminotransferase (EC 2.6.1.19) (characterized)
to candidate H281DRAFT_01082 H281DRAFT_01082 putrescine aminotransferase

Query= reanno::BFirm:BPHYT_RS23155
         (482 letters)



>lcl|FitnessBrowser__Burk376:H281DRAFT_01082 H281DRAFT_01082
           putrescine aminotransferase
          Length = 478

 Score =  877 bits (2266), Expect = 0.0
 Identities = 422/482 (87%), Positives = 456/482 (94%), Gaps = 4/482 (0%)

Query: 1   MSYRTEEVAYVQPAQPAASAQASQAAQQQRSTAEYRALDAAHHIHPFSDMGSLNRSGSRV 60
           MSYRTEE+AY+QPA+PAA A+ +Q    QR+TAEYRALDAAHHIHPFSDMG LNRSGSRV
Sbjct: 1   MSYRTEEIAYMQPAEPAAGARTAQ----QRTTAEYRALDAAHHIHPFSDMGELNRSGSRV 56

Query: 61  IVKAQGVYLWDSEGNKVIDGMAGLWCVNVGYGRKELADAAYKQMQELPYYNTFFKTTHPP 120
           IV+A GVYLWDSEGNK+IDGMAGLWCVNVGYGRKELA+AAY+QM+ELPYYNTFFKTTHPP
Sbjct: 57  IVRAHGVYLWDSEGNKIIDGMAGLWCVNVGYGRKELANAAYRQMEELPYYNTFFKTTHPP 116

Query: 121 VIELSALLAELAPEAFNHFFYCNSGSEGNDTVLRIVHQYWATQGKHSKKFVISRKNGYHG 180
           VIELSALLAELAPE FNHFFYCNSGSE NDTVLRIVH+YW TQGKHSKK VISR+NGYHG
Sbjct: 117 VIELSALLAELAPEPFNHFFYCNSGSEANDTVLRIVHRYWTTQGKHSKKVVISRRNGYHG 176

Query: 181 STIAGGTLGGMGYMHEQMPSKVENIVHIDQPYFFGEAQGNLTPEEFALARAQQLEAKILE 240
           STIAGGTLGGMGYMHEQMPSKVENIVHIDQPYFF EA  + TPEEFALARAQQLE KILE
Sbjct: 177 STIAGGTLGGMGYMHEQMPSKVENIVHIDQPYFFAEANSSQTPEEFALARAQQLEMKILE 236

Query: 241 IGADNVAAFIGEPFQGAGGVIFPASTYWPEIQRICRKYDILLVADEVIGGFGRTGEWFAH 300
           IGA NVAAFIGEPFQGAGGVIFPASTYWPEI+RICRKYD+LLVADEVIGGFGRTGEWFAH
Sbjct: 237 IGAHNVAAFIGEPFQGAGGVIFPASTYWPEIERICRKYDVLLVADEVIGGFGRTGEWFAH 296

Query: 301 QHFGFEPDLITLAKGLTSGYVPMGAVGLHDRVAKAIIENGDFNHGLTYSGHPVAAAVAVA 360
           QHFGF+PDLIT+AKGLTSGYVPMGAVGL+DR+AKAIIENG+FNHGLTYSGHPVAAAVAVA
Sbjct: 297 QHFGFQPDLITMAKGLTSGYVPMGAVGLNDRIAKAIIENGEFNHGLTYSGHPVAAAVAVA 356

Query: 361 NLKLLRDEKIVDRVKNDTGPYFQKQLRETFANHPIIGEISGTGLVAGLQLAQDPKARKRF 420
           NLKLLRDEKIV+RVK DTGPYFQK+LR+TFA HPI+GEI+G GLVAGLQLA++P +RKRF
Sbjct: 357 NLKLLRDEKIVERVKTDTGPYFQKKLRDTFARHPIVGEIAGAGLVAGLQLAEEPASRKRF 416

Query: 421 ANGGDVGTICRDFCFNGNLIMRATGDRMLLSPPLVINKLEIDEIVSKAKKAIDATAQQLG 480
           ANGGDVG +CRDFCFNGNLIMRA+GDRMLLSPPLVI+K EID++VSKAK AIDATA QLG
Sbjct: 417 ANGGDVGGVCRDFCFNGNLIMRASGDRMLLSPPLVISKQEIDDLVSKAKNAIDATATQLG 476

Query: 481 IS 482
           IS
Sbjct: 477 IS 478


Lambda     K      H
   0.319    0.136    0.408 

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: 834
Number of extensions: 18
Number of successful extensions: 2
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: 482
Length of database: 478
Length adjustment: 34
Effective length of query: 448
Effective length of database: 444
Effective search space:   198912
Effective search space used:   198912
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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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources