GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Acidovorax sp. GW101-3H11

Align C4-dicarboxylate-binding periplasmic protein DctP (characterized)
to candidate Ac3H11_1227 TRAP-type C4-dicarboxylate transport system, periplasmic component

Query= SwissProt::P37735
         (333 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1227
          Length = 334

 Score =  195 bits (495), Expect = 2e-54
 Identities = 122/326 (37%), Positives = 185/326 (56%), Gaps = 10/326 (3%)

Query: 13  ATALSLALSVPAL-AEPIVIKFSHVVAPDTPKGKGAAKFEELAEKYTNGAVDVEVYPNSQ 71
           ATAL  A  +PA  A+   IKF+     D P+ +GA KF +L    T G + V+++P   
Sbjct: 9   ATALVAASLLPAAHAQERTIKFAFQNQKDHPQAQGAQKFADLVAAKTGGRIAVKLFPGGT 68

Query: 72  LYKDKEELEALQLGAVQMLAPSLAKFGPLGVQ--DFEVFDLPYIFKDYEALHKVTQGEAG 129
           L  D + + ALQ G V+M   ++   G L  Q  +F ++D P++F   +    VT G  G
Sbjct: 69  LGGDLQTVSALQGGTVEM---TVLNAGILAAQSKEFGIYDFPFLFATPQEADAVTDGPFG 125

Query: 130 KMLLSKLEAKGITGLAFWDNGFK-IMSANTPLTMPDDFLGLKMRIQSSKVLEAEMNALGA 188
           K LL KL+AK + GL +W+ GF+ + ++  P+T  +D  GLK+R+  S +     NALGA
Sbjct: 126 KKLLDKLQAKNLVGLGYWELGFRNLTNSKKPITKAEDIAGLKIRVIQSPIYIDLFNALGA 185

Query: 189 VPQVMAFSEVYQALQTGVVDGTENPPSNMFTQKMNEVQKHATVSNHGYLGYAVIVNKQFW 248
               M F E+Y A++   VDG ENP S + + K  EVQK+ TV+ H Y   AVIV+K+FW
Sbjct: 186 NAVPMPFPELYTAMEQKAVDGQENPFSTILSSKFAEVQKYLTVTRHMYNPQAVIVSKKFW 245

Query: 249 DGL-PADVRTGLEKAMAESTDYANGIAKEENEKALQAMKDAGTTEFHELTAEERAAWEEV 307
           D L PAD +  L  AMAE+T +  G+++ +   AL+ +K AG  +  E +  E       
Sbjct: 246 DSLNPAD-QKALTDAMAEATTFQRGVSRVQANVALEDLKKAG-MQVSEFSPAELDKLRAK 303

Query: 308 LTPVHDEMAERIGAETIAAVKAATAE 333
           + PV ++ +E++GAET+  V +  A+
Sbjct: 304 VKPVVEKHSEKVGAETVQEVYSTLAK 329


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: 201
Number of extensions: 10
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 333
Length of database: 334
Length adjustment: 28
Effective length of query: 305
Effective length of database: 306
Effective search space:    93330
Effective search space used:    93330
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