GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Caminibacter mediatlanticus TB-2

Align C4-dicarboxylate-binding periplasmic protein DctP (characterized)
to candidate WP_007474712.1 CMTB2_RS05780 C4-dicarboxylate ABC transporter

Query= SwissProt::P37735
         (333 letters)



>NCBI__GCF_000170735.1:WP_007474712.1
          Length = 329

 Score =  280 bits (715), Expect = 5e-80
 Identities = 152/317 (47%), Positives = 205/317 (64%), Gaps = 9/317 (2%)

Query: 13  ATALSLALSVPALAEPIVIKFSHVVAPDTPKGKGAAKFEELAEKYTNGAVDVEVYPNSQL 72
           +TAL ++LSV A     VIKFSHVV+P+TPKGK A  F +  E+ + G + VEVYPN+QL
Sbjct: 9   STALIVSLSVAA---DYVIKFSHVVSPNTPKGKAADYFAKRVEELSKGRIKVEVYPNAQL 65

Query: 73  YKDKEELEALQLGAVQMLAPSLAKFGPLGVQDFEVFDLPYIFKDYEALHKVTQGEAGKML 132
            KDK  L  ++  AVQM APS +KF  L V    +FDLP++FKD   LH+V  G+ G+ L
Sbjct: 66  GKDKVILRKMKFNAVQMAAPSFSKFTGL-VPQLGLFDLPFLFKDENHLHRVLDGKVGQKL 124

Query: 133 LSKLEAKGITGLAFWDNGFK-IMSANTPLTMPDDFLGLKMRIQSSKVLEAEMNALGAVPQ 191
           L  +  KG   LA+WDNGFK +  +  PL  PDD  GLK R+ SSKVL  +  ALGA+P 
Sbjct: 125 LDMVTKKGYVALAYWDNGFKQLTDSKRPLIKPDDCKGLKFRVMSSKVLIEQFKALGAIPV 184

Query: 192 VMAFSEVYQALQTGVVDGTENPPSNMFTQKMNEVQKHATVSNHGYLGYAVIVNKQFWDGL 251
           V+ FSEVY ALQ GVVDG EN  SN++T+K  EVQ++ T++NHGYLGY V+++K+FWD L
Sbjct: 185 VLPFSEVYSALQQGVVDGQENTISNIYTKKFYEVQRYMTMTNHGYLGYLVVMSKKFWDKL 244

Query: 252 PADVRTGLEKAMAESTDYANGIAKEENEKALQAMKD----AGTTEFHELTAEERAAWEEV 307
           P D++  +++AM E+T      AKE NE  L  +K+     G  E   LT ++R  WE+ 
Sbjct: 245 PNDLKAVIKQAMKETTAKERVWAKELNEAQLNKIKEYAKKTGKLEIDYLTPQQRLVWEKK 304

Query: 308 LTPVHDEMAERIGAETI 324
           L  ++ +    IG + I
Sbjct: 305 LRTIYPKFYNTIGKDLI 321


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: 277
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: 333
Length of database: 329
Length adjustment: 28
Effective length of query: 305
Effective length of database: 301
Effective search space:    91805
Effective search space used:    91805
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 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