GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rbsC in Cronobacter condimenti 1330

Align Ribose import permease protein RbsC (characterized)
to candidate WP_007667712.1 BN137_RS14415 ABC transporter permease

Query= SwissProt::P0AGI1
         (321 letters)



>NCBI__GCF_000319285.1:WP_007667712.1
          Length = 333

 Score =  192 bits (487), Expect = 1e-53
 Identities = 114/310 (36%), Positives = 178/310 (57%), Gaps = 6/310 (1%)

Query: 14  KAWLMEQKSLIALLV--LIAIVSTLSPNFFTINNLFNILQQTSVNAIMAVGMTLVILTSG 71
           K  L  +++L+ L++  ++ ++ +  P+F    NL  +   TS+  I+A+G  +V+LT G
Sbjct: 2   KTLLKHREALLGLVIALMLLVIGSRVPSFLAPANLVEMFNDTSILIILALGQMMVLLTKG 61

Query: 72  IDLSVGSLLALTGAVAASIVGIEVNALVAVAAALA--LGAAIGAVTGVIVAKGRVQAFIA 129
           IDLS+ + LALTG + A I     +  VA+  ALA  LG  +G + G++V K  + A + 
Sbjct: 62  IDLSMAANLALTGMIVALINAHHPDIPVALLLALATLLGLLMGVINGLLVWKLGIPAIVV 121

Query: 130 TLVMMLLLRGVTMVYTNGSPVNTGFTENADLFGWFGIGRPLGVPTPVWIMGIVFLAAWYM 189
           TL  M + RG+  + ++G+ VN     +AD  G   +   LG+P   W    V L   Y 
Sbjct: 122 TLGTMSVYRGIIFLLSDGAWVNA-HQMSADFLGLPRLP-VLGLPLLGWCAIAVLLLVSYF 179

Query: 190 LHHTRLGRYIYALGGNEAATRLSGINVNKIKIIVYSLCGLLASLAGIIEVARLSSAQPTA 249
           L ++R GR +Y  GGN  A   +GIN  K++ I + L G LA   G + ++R + A    
Sbjct: 180 LRYSRTGRALYTAGGNATAAYYTGINAGKMQFISFCLSGALAGFCGYLWISRFAMAYVDV 239

Query: 250 GTGYELDAIAAVVLGGTSLAGGKGRIVGTLIGALILGFLNNGLNLLGVSSYYQMIVKAVV 309
             G+EL  +AA V+GG S  GG GR+ G L+GAL LG +NN L ++GVS ++QM V  VV
Sbjct: 240 ANGFELQIVAACVIGGISTMGGIGRVAGCLLGALFLGVINNALPVVGVSPFWQMAVSGVV 299

Query: 310 ILLAVLVDNK 319
           I++AVL++ +
Sbjct: 300 IVVAVLLNER 309


Lambda     K      H
   0.324    0.139    0.393 

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: 235
Number of extensions: 11
Number of successful extensions: 2
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: 321
Length of database: 333
Length adjustment: 28
Effective length of query: 293
Effective length of database: 305
Effective search space:    89365
Effective search space used:    89365
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.6 bits)
S2: 48 (23.1 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