GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gabD in Chryseobacterium arthrosphaerae CC-VM-7

Align Succinate-semialdehyde dehydrogenase; SsaDH; EC 1.2.1.16 (characterized)
to candidate WP_065398085.1 BBI00_RS06965 aldehyde dehydrogenase

Query= SwissProt::Q8GAI8
         (450 letters)



>NCBI__GCF_001684965.1:WP_065398085.1
          Length = 453

 Score =  130 bits (327), Expect = 9e-35
 Identities = 105/336 (31%), Positives = 161/336 (47%), Gaps = 25/336 (7%)

Query: 109 PVGPCLLITPWNFPLAMATRKVAPAVAAGCTMVLKPAKLTPLTSQLFAQTMMEAGLPAGV 168
           P+G  L+I  WN+P  ++   V  A+AAG   +LKP+++   T +  AQ + E   PA  
Sbjct: 103 PLGCILVIGAWNYPYQLSLSPVIAAMAAGNCCILKPSEIAENTMKAMAQIINE-NFPAEY 161

Query: 169 LNVVSSSSASGISGPLLKDSRLRKVSFTGSTPVGKRLMSDASRHVLRTSMELGGNAPFVV 228
           L V         +  LLK  +  K+ FTGST VGK +   A+ H+    +ELGG +P +V
Sbjct: 162 LYVYEGGVEE--TTKLLK-LKFDKIFFTGSTRVGKIVYKAAAEHLTPVVLELGGKSPAIV 218

Query: 229 FEDADLDKAVEGAMAAKMRNMGEACTAANRFLVQESVAQEF---TRKFAAAMGALSTGRG 285
            +DA+LD A +  +  K  N G+ C A +  LV+E+V ++F    RK+      +   + 
Sbjct: 219 TKDANLDIAAKRIVWGKFLNAGQTCVAPDYLLVEETVQEQFLEMLRKY------IKEFQY 272

Query: 286 TDPASQVGPLIN--NGARDDIHALVTAAVDAGAVAVTGGAPVDGPGYFYQPTVLADVPNN 343
           T  + Q   +IN  N  R      +T  +D   +   G   V     + +PT+L  +   
Sbjct: 273 TPDSEQYTRIINLKNFER------LTRLIDKEKLYFGGNFNVQ--QLYIEPTILHYIGWQ 324

Query: 344 AAILGQEIFGPVAPVTTFTTEQDAIKLANASEYGLAAYLYSRDFNRLLRVAEQIEFGMVG 403
             I+ +EIFGP+ PV  F     A+      E  LAAYL++ +         ++ FG   
Sbjct: 325 DEIMQEEIFGPLLPVIGFKNYNAALNDILELEKPLAAYLFTHNSEEKEAFTRKLSFGGGC 384

Query: 404 FNAGI--ISNAAAPFGGVKQSGLGREGGSEGIAEYT 437
            N  +  +SN   PFGGV  SG+G   G  G   +T
Sbjct: 385 INDTVMHLSNDHLPFGGVGNSGIGSYHGKFGFEAFT 420


Lambda     K      H
   0.317    0.131    0.376 

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: 382
Number of extensions: 15
Number of successful extensions: 4
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: 450
Length of database: 453
Length adjustment: 33
Effective length of query: 417
Effective length of database: 420
Effective search space:   175140
Effective search space used:   175140
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: 51 (24.3 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