GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Pseudomonas benzenivorans DSM 8628

Align C4-dicarboxylate-binding periplasmic protein DctP (characterized)
to candidate WP_090447081.1 BLS63_RS17640 C4-dicarboxylate ABC transporter

Query= SwissProt::Q9HU18
         (331 letters)



>NCBI__GCF_900100495.1:WP_090447081.1
          Length = 335

 Score =  444 bits (1142), Expect = e-129
 Identities = 220/334 (65%), Positives = 276/334 (82%), Gaps = 5/334 (1%)

Query: 1   MLKHTAKALVCALSLTVAGIVQAADP-----IVIKFSHVVAEHTPKGQGALLFKKLVEER 55
           M K T   ++ A S+  A ++QA +P     I IKFSHV A+HTPKGQGALLFKKL EER
Sbjct: 1   MKKLTTHVMLGACSVLFASLLQAGEPESAAPINIKFSHVAADHTPKGQGALLFKKLAEER 60

Query: 56  LPGKVKVEVYPNSSLFGDGKEMEALLLGDVQIIAPSLAKFEQYTKKLQIFDLPFLFDNIQ 115
           LPGKVKV+VY NSSL+GDGKE+EALLL +VQ++AP+ AK +++TK+LQ+FDL FLFD+  
Sbjct: 61  LPGKVKVDVYANSSLYGDGKELEALLLNEVQLLAPAPAKLDKFTKQLQVFDLMFLFDDAA 120

Query: 116 AVDRFQQSPQGKELLTSMQDKGITGLGYWHNGMKQLSANKPLREPKDARGLKFRVQASKV 175
           A +RFQQ+ +   LL+SM+ KG+ GL YW NGM+QL++NKPL EP DARGLKFRVQ S++
Sbjct: 121 AAERFQQTDKALALLSSMESKGLKGLAYWSNGMRQLTSNKPLHEPADARGLKFRVQPSRI 180

Query: 176 LEEQFKAVRANPRKMSFAEVYQGLQTGVVNGTENPWSNIYSQKMHEVQKYITESDHGVLD 235
            +EQ+ A+RA PRKM+FAE+YQGLQTGVVN ++NPWSNIYSQ+ +EVQKY+TE++  + +
Sbjct: 181 WDEQYIALRAVPRKMAFAEIYQGLQTGVVNASDNPWSNIYSQRHYEVQKYLTEANLTMGN 240

Query: 236 YMVITNTKFWNGLPEDVRGVLAKTMDEVTVEVNKQAEALNQGDKQRIVEAKTSEIIELTP 295
           Y+++TNTKFW+GLP+DVR  L K + EVT+EVNKQAEALNQ DKQRIVEA TSEII+LTP
Sbjct: 241 YVLLTNTKFWDGLPQDVRRELDKVVAEVTLEVNKQAEALNQADKQRIVEAGTSEIIQLTP 300

Query: 296 EQRAEWRKAMQPVWKKFEGEIGADLIKAAEAANQ 329
           EQR  WR A++PVW +FE EIGADLIKAAEAANQ
Sbjct: 301 EQRDMWRSAVKPVWAQFEEEIGADLIKAAEAANQ 334


Lambda     K      H
   0.316    0.132    0.376 

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: 376
Number of extensions: 7
Number of successful extensions: 1
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: 331
Length of database: 335
Length adjustment: 28
Effective length of query: 303
Effective length of database: 307
Effective search space:    93021
Effective search space used:    93021
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.

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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