GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Verminephrobacter eiseniae EF01-2

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate WP_011811648.1 VEIS_RS19145 DctP family TRAP transporter solute-binding subunit

Query= reanno::SB2B:6938088
         (339 letters)



>NCBI__GCF_000015565.1:WP_011811648.1
          Length = 335

 Score =  140 bits (353), Expect = 5e-38
 Identities = 97/321 (30%), Positives = 149/321 (46%), Gaps = 9/321 (2%)

Query: 21  LATVLGFSFG---AVAEPVEIKFSHVVAENTPKGQMALKFKELVESRLPGEYKVSVFPNS 77
           LA  LG +FG     A    ++ +   A+N+ +G     F + VE R  G YKV  F N+
Sbjct: 18  LALGLGLAFGLGATAAAQTTMRINISTAQNSHQGVAIDTFAKEVEKRTGGRYKVQTFYNA 77

Query: 78  QLFGDNNELAALLLNDVQLVAPSLSKFERYTKKLQVFDLPFLFEDMDAVDRFQQSEAGQQ 137
            L  +   + A+ L   +L   S      +  + ++ D+PFLF D            GQ+
Sbjct: 78  ALGAERESVEAVQLGTHELTFSSSGPIPNFVPETKILDVPFLFRDKAHARAVLDGPIGQE 137

Query: 138 LLNSMSRKGLVGLGYLHNGMKQFS-ANNALSLPGDAAGKKFRIMPSDVIAAQFEAVGAIP 196
           LL     KG   L +  NG +  S +  A+  PGD  G K R M + V  A ++  G + 
Sbjct: 138 LLTRFDGKGFKALAWAENGFRHMSNSKRAVKEPGDLKGLKMRTMENPVHIAAYKGFGIVT 197

Query: 197 VKKPFSEVFTLLQTRAIDGQENTWSNIYSKKFYEVQTHITESNHGVLDYMLVTSETFWKS 256
               FSEVFT LQ   +DGQEN  S I S KF +VQ H+T + H     + + ++  +  
Sbjct: 198 TPMAFSEVFTALQQGTVDGQENPLSVIISAKFDQVQKHLTLTGHVYSPALFLMNKALFDK 257

Query: 257 LPKDKREIIKQSMDEAVALGNKLALEKANE-DRQLILDSKRVELVTLTPEQRQAWVNAMR 315
           LP       +Q+  +A   G KL   + +E D + + D +   +  +    +  +V A+ 
Sbjct: 258 LPAAD----QQAFIDAARQGAKLNRARVDEDDAKGVADLRAKGMTVIDNIDKARFVAALA 313

Query: 316 PVWSQFEDKIGKDLIEAAESA 336
           PV +QFE + GK  +E   SA
Sbjct: 314 PVNAQFEKQFGKAALEQIRSA 334


Lambda     K      H
   0.316    0.132    0.368 

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: 225
Number of extensions: 8
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: 339
Length of database: 335
Length adjustment: 28
Effective length of query: 311
Effective length of database: 307
Effective search space:    95477
Effective search space used:    95477
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 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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