GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Paraburkholderia atlantica CCGE1002

Align Solute-binding protein Bamb_6123 (characterized)
to candidate WP_013091519.1 BC1002_RS18505 TRAP transporter substrate-binding protein

Query= SwissProt::Q0B2F6
         (328 letters)



>NCBI__GCF_000092885.1:WP_013091519.1
          Length = 330

 Score =  536 bits (1381), Expect = e-157
 Identities = 260/330 (78%), Positives = 296/330 (89%), Gaps = 2/330 (0%)

Query: 1   MTHRFPRSRTAL--AVALMAGFAMSAQARVFRSADVHGDSFPTNMAVKFMGDELSKLTGG 58
           M  +F  SR ++  A A +A   MSA+ARVFR ADVHGD+FPTNMAVK+MG+++SK T G
Sbjct: 1   MNKKFASSRVSMIVAAAALAFSTMSAEARVFRVADVHGDTFPTNMAVKYMGEQISKATDG 60

Query: 59  KDSIKVFGNSALGSEKDTVDQVRIGAIDMARVNGASFNEIVPESLIPSFPFLFRDVDHFR 118
           KD++KVFGNSALGSE DT+DQVRIGA+DM R NGA+FNEIVPES+IPS PFLFRDV+HFR
Sbjct: 61  KDTVKVFGNSALGSENDTIDQVRIGALDMTRANGAAFNEIVPESMIPSLPFLFRDVEHFR 120

Query: 119 KAMYGPAGQKILDAFAAKGMIALTFYESGARSIYAKRPVRTPADMKGLKVRVQPSDLMVD 178
           K MYGP GQKILDAF AKGMIALTFYESGARS+YAK+ +++PADMKGLKVRVQPSDLMVD
Sbjct: 121 KVMYGPEGQKILDAFTAKGMIALTFYESGARSMYAKKAIKSPADMKGLKVRVQPSDLMVD 180

Query: 179 EIRAMGGTPTPMPFAEVYTGLKTGLVDAAENNLPSYEETKHFEVAPDYSETQHAMTPEVL 238
           EI+AMGGTPTPMPF+EVYTGLKTGLVD AENN+PSYEETKHFEVA  YSETQH+MTPEVL
Sbjct: 181 EIKAMGGTPTPMPFSEVYTGLKTGLVDGAENNIPSYEETKHFEVAQVYSETQHSMTPEVL 240

Query: 239 VFSKKIWDTLSPQEQAAIRKAAADSVPYYQKLWTAREASAQQAVTKGGANILPAAQVDRA 298
           VFSKK+WDTL+PQEQ  I+KAAADSVPYYQKLWTAREA AQ+ VTKGGA ++ A+Q+DRA
Sbjct: 241 VFSKKVWDTLTPQEQQIIKKAAADSVPYYQKLWTAREADAQKTVTKGGATVVAASQIDRA 300

Query: 299 AFVKAMQPLWTKYEKTPQMKQIVDEIEATK 328
           AFVK MQP+WTKYEKTPQMKQIVDEI+A K
Sbjct: 301 AFVKVMQPVWTKYEKTPQMKQIVDEIQAIK 330


Lambda     K      H
   0.318    0.131    0.375 

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: 477
Number of extensions: 14
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: 328
Length of database: 330
Length adjustment: 28
Effective length of query: 300
Effective length of database: 302
Effective search space:    90600
Effective search space used:    90600
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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