GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Herbaspirillum seropedicae SmR1

Align C4-dicarboxylate-binding periplasmic protein DctP (characterized)
to candidate HSERO_RS02540 HSERO_RS02540 ABC transporter substrate-binding protein

Query= SwissProt::P37735
         (333 letters)



>FitnessBrowser__HerbieS:HSERO_RS02540
          Length = 345

 Score =  132 bits (331), Expect = 2e-35
 Identities = 99/310 (31%), Positives = 165/310 (53%), Gaps = 15/310 (4%)

Query: 2   LTRRIL---GALVGATALSLALSVPALAEPIVIKFSHVVAPDTPKGKGAAKFEELAEKYT 58
           +TRR +   GA+  A  L   LS PA A     KF+    P  P  K A +  +     T
Sbjct: 10  VTRRNMLKAGAVGAALPLFSILSRPASAAEFSYKFATGQDPSHPVNKRAQEAIDRIRNAT 69

Query: 59  NGAVDVEVYPNSQLYKDKEELEALQLGAVQMLAPSLAKFGPLGVQDFEVFDLPYIFKDYE 118
           NG ++++++P +QL  D + +  ++ G V+    +      L V    + +  + F DY 
Sbjct: 70  NGRLEIKLFPANQLGSDTDLMSQVRNGGVEFFNQANTVLSTL-VPAAGIVNTGFAFHDYG 128

Query: 119 ALHKVTQGEAGKMLLSKLEAKGITGLAF-WDNGFKIMSANT-PLTMPDDFLGLKMRIQSS 176
           A+ K   G  G  + +++E  G+  ++  WDNGF+ ++ +T P+    D  GLK+R+ ++
Sbjct: 129 AVWKAMDGPLGAHVRAQIEKVGLLTMSKPWDNGFRQITTSTKPVRNAGDVKGLKLRVPAA 188

Query: 177 KVLEAEMNALGAVPQVMAFSEVYQALQTGVVDGTENPPSNMFTQKMNEVQKHATVSNHGY 236
            +L +  +ALGA P  + F+EVY +LQT +V+G ENP + + T ++ EVQK  T+SNH +
Sbjct: 189 PMLTSLFSALGASPTPINFNEVYSSLQTKLVEGQENPLAIISTARLYEVQKFCTISNHVW 248

Query: 237 LGYAVIVNKQFWDGLPAD----VRTGLEKAMA-ESTDYA--NGIAKEE-NEKALQAMKDA 288
             Y ++ N++ ++ LP D    VR  L+KA + E  D A  +G A+ +   K LQ + +A
Sbjct: 249 DAYWILGNRRAFEKLPKDIQEIVRRELDKAASDERADIAAFSGFARNDLASKGLQIV-EA 307

Query: 289 GTTEFHELTA 298
               F E  A
Sbjct: 308 DKDSFKEALA 317


Lambda     K      H
   0.314    0.130    0.364 

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: 264
Number of extensions: 12
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: 333
Length of database: 345
Length adjustment: 28
Effective length of query: 305
Effective length of database: 317
Effective search space:    96685
Effective search space used:    96685
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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