GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gnl in Skermanella stibiiresistens SB22

Align Periplasmic gluconolactonase, PpgL (characterized, see rationale)
to candidate WP_084164774.1 N825_RS15645 lactonase family protein

Query= uniprot:Q9HWH7
         (388 letters)



>NCBI__GCF_000576635.1:WP_084164774.1
          Length = 411

 Score =  159 bits (403), Expect = 1e-43
 Identities = 117/370 (31%), Positives = 167/370 (45%), Gaps = 24/370 (6%)

Query: 17  GVAPQAQAASLYNLLVGTYT----EGSSEGIQVYRFDGADGSVKGPLRVAHTSNPSYLTF 72
           G  P A+    Y   VG  T        EGI VY+ D + G+      +    NPS+L F
Sbjct: 51  GTTPSAKPRFAY---VGCRTTKERNARGEGIGVYQVDASTGAWAPVQLLKDLVNPSFLAF 107

Query: 73  APDQRTLFVVNENGRGGKGDTVGRATSYRFDPISGRLQQISQVQTLADHPTYSSLSHDGR 132
            P QR L+ V+       GD  G  +S+  +  +G L  ++   +   +P + +    GR
Sbjct: 108 DPTQRFLYTVH-------GDQ-GEVSSFAINDRTGELTLLNTASSGGKNPVHLTTDPSGR 159

Query: 133 YLFVANYSVQPEGSVAVLPVRADGSLAPVVQVESHQASKVHPR--QVSGHVHSVVSSPDG 190
           +L VANY+    G VA L + ADG L  +V +     +    +  Q S H H V   P  
Sbjct: 160 FLIVANYAT---GGVATLAIGADGKLGDIVDLVPLAGTPGPHKVEQASSHPHQVAYDPTR 216

Query: 191 QYLFAPDLGADKVFVYRYAPEQAERPLQAADPAFVPTPPGSGPRHLIFSADGRFAYLTLE 250
             L  PD G D VF +R   E+ +  L  A    V     SGPRH+ F   G  AY+  E
Sbjct: 217 DVLAVPDKGLDAVFTFRLDAEKGK--LVPAGAGSVTARSTSGPRHIAFGPSGTHAYVVNE 274

Query: 251 LSGQVMVFAHEGNGR-LRQLQTHDLAPAGFQGKVGAGALHLSADGRFLGVLNRGDDNQLV 309
           L   V  +A++ +   L+ LQ     PA F G+  AG + ++  GRFL   NRG  N + 
Sbjct: 275 LDSTVTTYAYDASAASLKPLQILSTLPATFTGENRAGGIVMAPSGRFLHATNRGH-NHVA 333

Query: 310 TFAVDPASGQLRFVERRSVEGTEPREFAFSPGGRFVLVANQNSDQLRVFARDPQSGQVGK 369
            F VDP +G L+        G  PR     P  RF+  AN+ +D +  F  D  +G +  
Sbjct: 334 IFGVDPRTGLLQSAGWEPTRGKMPRFITLDPSARFLYAANETTDTIVGFQVDAATGALTA 393

Query: 370 TLQSVEVGSP 379
              +V+ GSP
Sbjct: 394 LEPAVQTGSP 403


Lambda     K      H
   0.318    0.135    0.395 

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: 517
Number of extensions: 50
Number of successful extensions: 13
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: 388
Length of database: 411
Length adjustment: 31
Effective length of query: 357
Effective length of database: 380
Effective search space:   135660
Effective search space used:   135660
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: 50 (23.9 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