GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mglC in Cronobacter condimenti 1330

Align MglC aka B2148, component of Galactose/glucose (methyl galactoside) porter (characterized)
to candidate WP_007667712.1 BN137_RS14415 ABC transporter permease

Query= TCDB::P23200
         (336 letters)



>NCBI__GCF_000319285.1:WP_007667712.1
          Length = 333

 Score =  160 bits (404), Expect = 5e-44
 Identities = 101/324 (31%), Positives = 168/324 (51%), Gaps = 19/324 (5%)

Query: 14  KEGGIYVVLLVLLAIIIFQDPTFLSLLNLSNILTQSSVRIIIALGVAGLIVTQGTDLSAG 73
           +E  + +V+ ++L +I  + P+FL+  NL  +   +S+ II+ALG   +++T+G DLS  
Sbjct: 8   REALLGLVIALMLLVIGSRVPSFLAPANLVEMFNDTSILIILALGQMMVLLTKGIDLSMA 67

Query: 74  RQVGLAAVVAATLLQSMDNANKVFPEMATMPIALVILIVCAIGAVIGLINGLIIAYLNVT 133
             + L  ++ A +       N   P++   P+AL++ +   +G ++G+INGL++  L + 
Sbjct: 68  ANLALTGMIVALI-------NAHHPDI---PVALLLALATLLGLLMGVINGLLVWKLGIP 117

Query: 134 PFITTLGTMIIVYGINSLYYD--FVGASPISGFDSGFSTFAQGFVALGSFRLSYITFYAL 191
             + TLGTM +  GI  L  D  +V A  +S    G          LG   L +     L
Sbjct: 118 AIVVTLGTMSVYRGIIFLLSDGAWVNAHQMSADFLGLPRLP----VLGLPLLGWCAIAVL 173

Query: 192 IAVAFVWVLWNKTRFGKNIFAIGGNPEAAKVSGVNVGLNLLMIYALSGVFYAFGGMLEAG 251
           + V++       +R G+ ++  GGN  AA  +G+N G    + + LSG    F G L   
Sbjct: 174 LLVSY---FLRYSRTGRALYTAGGNATAAYYTGINAGKMQFISFCLSGALAGFCGYLWIS 230

Query: 252 RIGSATNNLGFMYELDAIAACVVGGVSFSGGVGTVIGVVTGVIIFTVINYGLTYIGVNPY 311
           R   A  ++   +EL  +AACV+GG+S  GG+G V G + G +   VIN  L  +GV+P+
Sbjct: 231 RFAMAYVDVANGFELQIVAACVIGGISTMGGIGRVAGCLLGALFLGVINNALPVVGVSPF 290

Query: 312 WQYIIKGAIIIFAVALDSLKYARK 335
           WQ  + G +I+ AV L+     RK
Sbjct: 291 WQMAVSGVVIVVAVLLNERGNKRK 314


Lambda     K      H
   0.327    0.143    0.415 

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: 290
Number of extensions: 19
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: 336
Length of database: 333
Length adjustment: 28
Effective length of query: 308
Effective length of database: 305
Effective search space:    93940
Effective search space used:    93940
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 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