GapMind for catabolism of small carbon sources

 

Alignments for a candidate for puuA in Phaeobacter inhibens BS107

Align Glutamate--putrescine ligase (EC 6.3.1.11) (characterized)
to candidate GFF2676 PGA1_c27180 putative glutamine synthetase

Query= reanno::MR1:200446
         (451 letters)



>FitnessBrowser__Phaeo:GFF2676
          Length = 450

 Score =  176 bits (445), Expect = 2e-48
 Identities = 114/374 (30%), Positives = 191/374 (51%), Gaps = 13/374 (3%)

Query: 74  DFVCVPDENAVFMLPWTIEATAQVIHDCYDRMGNP-IELSPRNVLKKVLSLYDEKGWEPV 132
           D+V  PD   +  +PW +E T  V+ D  D   +  +  SPR +LK+ ++   E G++ +
Sbjct: 78  DYVMKPDLATLRPVPW-LEGTVMVLCDVLDHHSHEEVPHSPRAILKRQVNRLKEMGFDAM 136

Query: 133 IAPEMEFYLTSRSDDHDLPLKPPIGRSGRPEAG-RQSFSIDAANEYDPLFEDMYDWCEIQ 191
            A E+EF+L  +S D    ++    R   P +G  + +SI   +  + +   + +     
Sbjct: 137 CATELEFFLFEKSFD---AIRKSGFRDLEPISGYNEDYSILQTSREEHVLRPIRNHLWDA 193

Query: 192 GLDIDTLIHEDGPAQMEINFSHGNPLSLADQVFVFKRTLREAALKHNVCATFMAKPVTDE 251
           GL I+    E    Q E+N  +   +  A    + K  ++E A +     TF+ K   ++
Sbjct: 194 GLPIENSKGEAETGQEELNIKYAAAMDTAAYHTIAKHAVKEIAQQQGHAVTFLPKWSHEK 253

Query: 252 PGSAMHIHQSVINKETGKNIFTNEDGT--QSALFLSYIAGLQKYIPEFLPLMAPNANSFR 309
            GS+ H+HQS+   + GK  F +E      S+L  +Y+AGL KY P++   MAP  NS++
Sbjct: 254 VGSSSHVHQSLW--QDGKPAFFDESDALGMSSLMKAYMAGLLKYAPDYTAFMAPYINSYK 311

Query: 310 RFLPGTSAPVNLEWGIENRTCGLRIPESSPQNRRIENRIPGADANCYLAFAAGLLCGYIG 369
           RF+ GT AP  + W ++NRT G R+     +  R+E RIPG+D N YLA A  L  G  G
Sbjct: 312 RFMKGTFAPTRIIWSVDNRTAGYRLCGVGSKAIRVECRIPGSDMNPYLAIAGMLAAGIAG 371

Query: 370 MVEGLKPSTPVQGKANESRSNNPHCLPLTLEEALVAMEESDACKEYLGESFTTGFVAVKQ 429
           + EGL+   P  G   +  +     +P TL +A  A++ S   +  +G++    +V   +
Sbjct: 372 IEEGLELQAPTTGDVYQGDTG---MIPGTLRDAATALKSSAMLRAAMGDAVVDHYVRAAE 428

Query: 430 AELENFRRVVSSWE 443
            E+E+F R+V+ +E
Sbjct: 429 VEIEDFERIVTDYE 442


Lambda     K      H
   0.319    0.137    0.414 

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: 466
Number of extensions: 17
Number of successful extensions: 4
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: 451
Length of database: 450
Length adjustment: 33
Effective length of query: 418
Effective length of database: 417
Effective search space:   174306
Effective search space used:   174306
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 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