GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12055 in Caulobacter crescentus NA1000

Align Putative xylitol transport system substrate-binding protein; SubName: Full=Sugar ABC transporter substrate-binding protein (characterized, see rationale)
to candidate CCNA_00902 CCNA_00902 inositol ABC transporter, periplasmic inositol-binding protein IbpA

Query= uniprot:A0A1N7UEK0
         (335 letters)



>FitnessBrowser__Caulo:CCNA_00902
          Length = 326

 Score =  106 bits (265), Expect = 7e-28
 Identities = 89/278 (32%), Positives = 138/278 (49%), Gaps = 14/278 (5%)

Query: 10  TAALSLLACSIAMAADGKTYKVGAAVYGLKGQFMQNWVRELKEHPAVKDGTVQLTVFDGN 69
           TAAL L+      A  G   +V  +   L   F     REL++  A K G V++ V D  
Sbjct: 22  TAALGLMT---GCARGGAEAEVVVSFNDLSQPFFVAMRRELEDE-AAKLG-VKVQVLDAQ 76

Query: 70  YDALTQNNQIENMVTQRYDAILFVPIDTKAGVGTVKAAMSNDVVVIASNTKVADA--SVP 127
            ++  Q + ++    Q    ++  P D+KA  G     +   V VI+ +  +A    +VP
Sbjct: 77  NNSSKQISDLQAAAVQGAKVVIVAPTDSKALAGAADDLVEQGVAVISVDRNIAGGKTAVP 136

Query: 128 YVGNDDVEGGRLQAQAMVDKLNGKGNVVIIQGPIGQSAQIDREKGELEVLGKH-PDIKII 186
           +VG D+V GGR  A  +V        VV+I    G S+ I+R KG  + L    P  KI+
Sbjct: 137 HVGADNVAGGRAMADWVVKTYPAGARVVVITNDPGSSSSIERVKGVHDGLAAGGPAFKIV 196

Query: 187 EKKTANWDRAQALALTEDWLNAH---PKGINGVIAQNDDMALGAVQALKSHGLTSKDVPV 243
            ++TAN  R QAL +T++ L +    P  +  ++  NDDMA+GA++A+++ GL S  V V
Sbjct: 197 TEQTANSKRDQALTVTQNILTSMRDTPPDV--ILCLNDDMAMGALEAVRAAGLDSAKVKV 254

Query: 244 TSIDGMPDAIQAAKKDE-VTTFLQDAQAQSQGALDVAL 280
              D +P+A+   K  E V T  Q+   Q + AL  A+
Sbjct: 255 IGFDAIPEALARIKAGEMVATVEQNPGLQIRTALRQAV 292


Lambda     K      H
   0.314    0.130    0.373 

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: 229
Number of extensions: 11
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: 335
Length of database: 326
Length adjustment: 28
Effective length of query: 307
Effective length of database: 298
Effective search space:    91486
Effective search space used:    91486
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 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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