GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astA in Sphingomonas histidinilytica UM2

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

Query= SwissProt::Q8ZPV1
         (344 letters)



>NCBI__GCF_900167915.1:WP_079649484.1
          Length = 334

 Score =  231 bits (589), Expect = 2e-65
 Identities = 127/334 (38%), Positives = 189/334 (56%), Gaps = 2/334 (0%)

Query: 1   MRVIRPVEHADIAALMQLAGKTGGGLTSLPANEATLAARIERALKTWSGELPKGEQGYVF 60
           M ++RP   +D+A+LM+LA  +G G TSLP +EATL  R+  +  ++ G +   E  Y  
Sbjct: 1   MLIVRPAGPSDLASLMELAVLSGRGFTSLPEDEATLLNRLTLSEASFGGAIAPREAWYTL 60

Query: 61  VLEDSETGEVGGICAIEVAVGLNDPWYNYRVGTLVHASKELNVYNALPTLFLSNDHTGSS 120
           +LEDSETG + G+  +  AVG+  P +++RV TL   S  +N       L L N+  G +
Sbjct: 61  MLEDSETGRIEGLGGVRAAVGVARPHFSFRVMTLAQFSSAINTRFDHKALVLVNECAGWT 120

Query: 121 ELCTLFLDPEWRKEGNGYLLSKSRFMFMAAFRDKFNEKVVAEMRGVIDEHGYSPFWQSLG 180
           E+ +L+L PE R  G G LL++SR+M +   R +F+E V+AE+RG     G  PFW  + 
Sbjct: 121 EVGSLYLRPERRSGGAGSLLARSRYMLIGTERQRFSETVMAELRGYFAPDGTCPFWDGVA 180

Query: 181 KRFFSMDFSRADFLCGTGQKAFIAELMPKHPIYTHFLSEEAQAVIGEVHPQTAPARAVLE 240
            +FF + F  AD +  +    FI +L P+HPIY   +   AQ  IG VH +   ARA+LE
Sbjct: 181 SKFFRLPFDEADHMVMSTDGQFILDLAPRHPIYVELIDTAAQEAIGRVHVEGEAARAMLE 240

Query: 241 KEGFRYRHYIDIFDGGPTLECDIDRVRAIRKSRLVEVAEGQPAPGDYPACLVANENYHHF 300
            EGFR    +DIFDGGPT     D +R I ++ ++   +G PA  D P  LV+  +   F
Sbjct: 241 HEGFRGSGLVDIFDGGPTYSVPRDSIRTIERTEVLAAMKGDPA--DAPERLVSTASIGGF 298

Query: 301 RAALVRADPQTSRLVLTAAQLDALKCRAGDHVRL 334
           RA   +   +    VL    +DAL+ ++G+ VR+
Sbjct: 299 RAIRTKVRIEEGIAVLDGEAIDALRLKSGEMVRV 332


Lambda     K      H
   0.321    0.137    0.416 

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: 296
Number of extensions: 18
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 344
Length of database: 334
Length adjustment: 28
Effective length of query: 316
Effective length of database: 306
Effective search space:    96696
Effective search space used:    96696
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: 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