GapMind for catabolism of small carbon sources

 

Alignments for a candidate for citrullinase in Galbibacter marinus ck-I2-15

Align arginine deiminase (EC 3.5.3.6) (characterized)
to candidate WP_008992888.1 I215_RS15245 hypothetical protein

Query= reanno::WCS417:GFF3434
         (308 letters)



>NCBI__GCF_000300875.1:WP_008992888.1
          Length = 310

 Score =  265 bits (677), Expect = 1e-75
 Identities = 140/309 (45%), Positives = 198/309 (64%), Gaps = 7/309 (2%)

Query: 2   QTTNTVLMIRPARFAFNPDTAINNRFQRQPLDPL--GAQQKALEEFDGYVDTLRRHGVEV 59
           Q T+++LM+RPA+F  N  TA+NN FQ Q LD        KA +EFD +V+TLR  G+ V
Sbjct: 3   QITDSILMVRPAQFRMNEQTAVNNFFQ-QDLDMTQDAITIKAQKEFDNFVNTLRGVGINV 61

Query: 60  LVVQDTPAPHTPDSIFPNNWWSSHADGSLVLYPMEGQNRRLERNKGVLQVLEQR-FAINS 118
           +V QD   P TPDSIFPNNW S+H DG++V+YPM  +NRRLER + VL++L+   F I+ 
Sbjct: 62  IVFQDDLVPDTPDSIFPNNWISTHEDGTVVIYPMFAENRRLERREDVLELLDSEGFYIDE 121

Query: 119 TIDLSHLEQQNIFLEGTGSMVLDRQHRISYACHSGRTHQDALRQFAERLDYQ---LCVFH 175
             D +  E    FLEGTGS++LDR H  +Y   S R  +D    F E ++Y       + 
Sbjct: 122 VADFTSFEMDGDFLEGTGSVILDRVHEKAYCALSDRADEDLFIYFCEEMEYTPVWFTAYQ 181

Query: 176 AVDRHHAPIYHSNVMMSVGRDLSVVCLQALPDASERQGLERSLRDTGKDILALDFDQLEG 235
           +V     PIYH+NVMM VG D +V+CL ++ D  ER+ + + L+D GK+I+ +   QL+ 
Sbjct: 182 SVGGVRKPIYHTNVMMCVGVDFAVICLDSIDDKKERKNVVKHLKDNGKEIIEISEGQLDE 241

Query: 236 FAGNMLEIHDRDGQPLLVMSASAWGALQPAQRQHVERHTRPVVVNIDNIERIGGGSARCM 295
           FAGNML++ +  G+  +VMSA+A  +L   QR  +ER+T  +  +++ IE  GGGSARCM
Sbjct: 242 FAGNMLQVQNNKGETFVVMSATAQKSLTNDQRTKLERYTTILSSDLNTIETCGGGSARCM 301

Query: 296 LAEVHLPAR 304
           +AEV LP +
Sbjct: 302 MAEVFLPKK 310


Lambda     K      H
   0.322    0.135    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: 260
Number of extensions: 7
Number of successful extensions: 5
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: 308
Length of database: 310
Length adjustment: 27
Effective length of query: 281
Effective length of database: 283
Effective search space:    79523
Effective search space used:    79523
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 (21.9 bits)
S2: 48 (23.1 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