GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Pseudomonas benzenivorans DSM 8628

Align L-asparaginase (EC 3.5.1.1) (characterized)
to candidate WP_090446303.1 BLS63_RS15675 asparaginase

Query= reanno::pseudo3_N2E3:AO353_09960
         (334 letters)



>NCBI__GCF_900100495.1:WP_090446303.1
          Length = 329

 Score =  367 bits (942), Expect = e-106
 Identities = 193/325 (59%), Positives = 233/325 (71%)

Query: 8   AAQHVMVLYTGGTIGMQASANGLAPASGFEARMRDYLHSQPDLVVPNWRFREMTPLIDSA 67
           A   ++VLYTGGTIGMQASA+GLAPASGFEAR+R     +    +P W FRE+ P IDSA
Sbjct: 2   ACTKLLVLYTGGTIGMQASADGLAPASGFEARLRAQQALEQGRQLPEWTFRELLPPIDSA 61

Query: 68  NMTPAYWQRLRDAVIEAVDVDGCDSVLILHGTDTLAYSAAAMSFQLLGLHARVLFTGSML 127
           NM  A W  +  A+ +AV+ DGCD+VL+LHGTDTLAYSAAA+SF LLGL   VL TGSM 
Sbjct: 62  NMRQANWLAMVAAIRQAVEQDGCDAVLVLHGTDTLAYSAAALSFLLLGLPLPVLLTGSMQ 121

Query: 128 PAGVPDSDAWENLGGALVALGQGLAPGVQLYFHGELLDPTRCAKIRSFGRHPFARLQRQG 187
           PAGVP SDAW NL GA+ AL QG+APGVQLYF G+LL   R +K+ S     FA L R+ 
Sbjct: 122 PAGVPGSDAWANLFGAMQALQQGVAPGVQLYFDGKLLHGARVSKLASATFGAFAELPRRR 181

Query: 188 GGVKAPALPTALEYRQSKQLAKVGVLPLFPGIGAEQLDGVLNSGIQGLVLECFGSGTGPS 247
            G  A  +P +L+YRQ +Q   + VLP +PGI A  +  +L+SG++GL+LEC+GSGTGPS
Sbjct: 182 QGQHAAGIPASLDYRQPRQPVNLAVLPFYPGIQAAHVRALLDSGVRGLLLECYGSGTGPS 241

Query: 248 DNPEFLASLARARDQGVVVVAITQCHEGGVELDVYEAGSRLRGVGVLSGGGMTREAAFGK 307
           D+ E LA+LA A  +GVV+ AI+QC  G VE  VY AGSRL   G++S GGMTREAA GK
Sbjct: 242 DDAELLATLAAAHARGVVLAAISQCPHGHVEFGVYAAGSRLASAGLVSAGGMTREAALGK 301

Query: 308 LHALLGADLDTAEVRRLVELDLCGE 332
           L ALLGA LD AE  R   LDLCGE
Sbjct: 302 LFALLGAGLDQAETERWFALDLCGE 326


Lambda     K      H
   0.320    0.138    0.415 

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: 362
Number of extensions: 21
Number of successful extensions: 1
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: 334
Length of database: 329
Length adjustment: 28
Effective length of query: 306
Effective length of database: 301
Effective search space:    92106
Effective search space used:    92106
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: 49 (23.5 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