GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Halomonas desiderata SP1

Align L-asparaginase 1; L-asparaginase I; L-ASNase I; L-asparagine amidohydrolase I; EC 3.5.1.1 (characterized)
to candidate WP_086509657.1 BZY95_RS09260 asparaginase

Query= SwissProt::P0A962
         (338 letters)



>NCBI__GCF_002151265.1:WP_086509657.1
          Length = 350

 Score =  200 bits (508), Expect = 5e-56
 Identities = 125/341 (36%), Positives = 184/341 (53%), Gaps = 11/341 (3%)

Query: 4   KSIYVAYTGGTIGMQRSEQGYIP---VSGHLQRQLALMPEFHRPEMPDFTIHEYTPLMDS 60
           + + V YTGGT+GM  S +G +P   +   L+  L  +P   + ++P+F +H     +DS
Sbjct: 9   RPVLVLYTGGTLGMMPSAEGLVPAGDIETRLRNALDGLPPSRQSQLPEFVVHTVASPIDS 68

Query: 61  SDMTPEDWQHIAEDIKAHYDDYDGFVILHGTDTMAYTASALSFMLENLGKPVIVTGSQIP 120
           S  TP DWQ +A  I      + G V+LHGTDT+A++AS+L+F L+ L +PV+VTG+  P
Sbjct: 69  SAATPHDWQRLAATIADRIGQHAGIVVLHGTDTLAWSASSLAFQLQGLDRPVVVTGAMHP 128

Query: 121 LAELRSDGQINLLNALYVAANYPINEVTLFFNNRLYRGNRTTKAHADGFDAFASPNLPPL 180
           L    SD   N+  AL  AA   + E+ + F  RL RG R++K H++  DAFASPN P L
Sbjct: 129 LEAEGSDALANIELALRFAARPELQEIAVAFAGRLLRGARSSKTHSENDDAFASPNYPLL 188

Query: 181 LE-AGIHI-----RRLNTPPAPHGEGELIVH-PITPQPIGVVTIYPGISADVVRNFLRQP 233
            E  G  +     R L T        EL  + P+    +  + ++PGI A  +  +L   
Sbjct: 189 GEQVGDDVVLYPARCLETQQRGAPRFELPDYSPLAKGGVVRLALWPGIQAWQLEAWLGDD 248

Query: 234 -VKALILRSYGVGNAPQNKAFLQELQEASDRGIVVVNLTQCMSGKVNMGGYATGNALAHA 292
            V+  +L  +G GN P +   +  L +AS  G ++  ++QC  G +  G YA G  L  A
Sbjct: 249 RVQGALLEVWGGGNIPPDPEVIGVLAKASGEGKLIAAISQCRWGGIAPGRYAAGQGLIEA 308

Query: 293 GVIGGADMTVEATLTKLHYLLSQELDTETIRKAMSQNLRGE 333
           GV+ G DMT EA +TKL +LL+  LD    R+     L GE
Sbjct: 309 GVLSGDDMTPEAAITKLVHLLALPLDATERRRLFLTPLVGE 349


Lambda     K      H
   0.318    0.136    0.398 

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: 366
Number of extensions: 21
Number of successful extensions: 3
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: 338
Length of database: 350
Length adjustment: 29
Effective length of query: 309
Effective length of database: 321
Effective search space:    99189
Effective search space used:    99189
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: 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