GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruF in Sphingomonas histidinilytica UM2

Align arginine N-succinyltransferase; EC 2.3.1.109 (characterized)
to candidate WP_079649484.1 B5X82_RS17595 arginine N-succinyltransferase

Query= CharProtDB::CH_107315
         (338 letters)



>NCBI__GCF_900167915.1:WP_079649484.1
          Length = 334

 Score =  176 bits (445), Expect = 1e-48
 Identities = 110/335 (32%), Positives = 172/335 (51%), Gaps = 3/335 (0%)

Query: 1   MLVMRPAQAADLPQVQRLAADSPVGVTSLPDDAERLRDKILASEASFAAEVSYNGEESYF 60
           ML++RPA  +DL  +  LA  S  G TSLP+D   L +++  SEASF   ++   E  Y 
Sbjct: 1   MLIVRPAGPSDLASLMELAVLSGRGFTSLPEDEATLLNRLTLSEASFGGAIAPR-EAWYT 59

Query: 61  FVLEDSASGELVGCSAIVASAGFSEPFYSFRNETFVHASRSLSIHNKIHVLSLCHDLTGN 120
            +LEDS +G + G   + A+ G + P +SFR  T    S +++       L L ++  G 
Sbjct: 60  LMLEDSETGRIEGLGGVRAAVGVARPHFSFRVMTLAQFSSAINTRFDHKALVLVNECAGW 119

Query: 121 SLLTSFYVQRDLVQSVYAELNSRGRLLFMASHPERFADAVVVEIVGYSDEQGESPFWNAV 180
           + + S Y++ +        L +R R + + +  +RF++ V+ E+ GY    G  PFW+ V
Sbjct: 120 TEVGSLYLRPERRSGGAGSLLARSRYMLIGTERQRFSETVMAELRGYFAPDGTCPFWDGV 179

Query: 181 GRNFFDLNYIEAEKLSGLKSRTFLAELMPHYPIYVPLLPDAAQESMGQVHPRAQITFDIL 240
              FF L + EA+ +       F+ +L P +PIYV L+  AAQE++G+VH   +    +L
Sbjct: 180 ASKFFRLPFDEADHMVMSTDGQFILDLAPRHPIYVELIDTAAQEAIGRVHVEGEAARAML 239

Query: 241 MREGFETDNYIDIFDGGPTLHARTSGIRSIAQSRVVPVKIGEAPKSGRPYLVTNGQLQDF 300
             EGF     +DIFDGGPT       IR+I ++ V+    G+ P      LV+   +  F
Sbjct: 240 EHEGFRGSGLVDIFDGGPTYSVPRDSIRTIERTEVLAAMKGD-PADAPERLVSTASIGGF 298

Query: 301 RAVVLDLDWAPGKPVALSVEAAEALGVGEGASVRL 335
           RA+   +    G  V L  EA +AL +  G  VR+
Sbjct: 299 RAIRTKVRIEEGIAV-LDGEAIDALRLKSGEMVRV 332


Lambda     K      H
   0.319    0.135    0.387 

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: 235
Number of extensions: 5
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: 338
Length of database: 334
Length adjustment: 28
Effective length of query: 310
Effective length of database: 306
Effective search space:    94860
Effective search space used:    94860
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