GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Leeuwenhoekiella blandensis MED217

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_009781175.1 MED217_RS13915 acyl-CoA dehydrogenase

Query= reanno::psRCH2:GFF2392
         (383 letters)



>NCBI__GCF_000152985.1:WP_009781175.1
          Length = 389

 Score =  240 bits (613), Expect = 4e-68
 Identities = 135/377 (35%), Positives = 214/377 (56%), Gaps = 2/377 (0%)

Query: 1   MHDLELSEDQRMIRDMARDFARREIAPHAQAWEKAGWIDDTLVAQMGELGLLGMVVPEEW 60
           M+++  SE+ ++ R+  RDF ++E+ PH + WEK G I+  +  +MG++G  G+  PEE+
Sbjct: 1   MNNVYFSEEHKLFRESLRDFLQKEVVPHIEKWEKTGEIERFIWKKMGDMGYFGLAYPEEY 60

Query: 61  GGSYIDYVAYALAVEEISA-GDGATGALMSIHNSVGCGPVLNYGSQAQKDEWLTELASGR 119
           GG  +D     + +EE+     G   A M  H  +    +   G  A K+++L    SG 
Sbjct: 61  GGLDLDIFYTLIFLEELQRINSGGFAAAMWAHAYLAMTHLKAEGDAAIKEKYLAPSISGD 120

Query: 120 AIGCFALTEPQAGSEAHNLRTRAELVDGHWVLNGSKQFCSNAKRSKLAIVFAVTDPELGK 179
            IGC  +TEP  GS+   +R+ A     H+VLNGSK F +N   S   IV A T PE G 
Sbjct: 121 KIGCLCITEPFGGSDVAGMRSTAVRQGDHYVLNGSKTFITNGVFSDYLIVAAKTSPEKGN 180

Query: 180 KGLSAFLVPTDTPGFAVERSEHKMGIRASDTCGVSLSDCRIPEANLLGERGKGLAIALSN 239
           KGLS F+V  +  G +  + + K+G RASDT  ++ +D ++P ANL+GE  KG +  + +
Sbjct: 181 KGLSIFVVDREAEGVSATKLD-KLGWRASDTGEIAFTDVKVPAANLMGEEDKGFSYIMQH 239

Query: 240 LEGGRIGIGAQALGIARAAFEAALLYARERVQFGKPIAEHQSIANMLADMQTQLNAARLL 299
               R+ +G  A   A  A E AL Y  ER  FGK I + Q++ + +A+M +++   +  
Sbjct: 240 FALERLIMGVNAHARAEYALEYALEYMGEREAFGKTINKFQALRHTVAEMASEIEMVKAF 299

Query: 300 ILHAARLKSAGLPCLSEASQAKLFASEMAEKVCSQAVQIHGGYGYLEDYPVERYYRDARI 359
               A     G   + EAS +KL  +++A++V  + +Q+ GGYGY+EDYP+ R +RD+R+
Sbjct: 300 NYSIAYNLDKGDYVVKEASMSKLMGTKIADEVIYKCLQMLGGYGYMEDYPLARMFRDSRL 359

Query: 360 TQIYEGSSEIQRLLIAR 376
             I  G+SEI + +IA+
Sbjct: 360 GPIGGGTSEILKEIIAK 376


Lambda     K      H
   0.318    0.133    0.390 

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: 323
Number of extensions: 10
Number of successful extensions: 3
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: 383
Length of database: 389
Length adjustment: 30
Effective length of query: 353
Effective length of database: 359
Effective search space:   126727
Effective search space used:   126727
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