GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtF in Roseburia faecis M72

Align CbtF, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate WP_022046526.1 M72_RS04110 ABC transporter ATP-binding protein

Query= TCDB::Q97VF4
         (324 letters)



>NCBI__GCF_001406815.1:WP_022046526.1
          Length = 338

 Score =  164 bits (414), Expect = 4e-45
 Identities = 97/301 (32%), Positives = 165/301 (54%), Gaps = 16/301 (5%)

Query: 27  ALKDVSLSMNQGDLLIVLGESGAGKT----TLGRVIVGLQKPTSGEVVYDGYNIWKNKRK 82
           A+  VS ++  G  L ++GESG+GK+    ++ +++    K T GEV+Y G +I K   K
Sbjct: 27  AVNGVSFNLEPGKTLGIVGESGSGKSVTSYSIMQILAETGKITGGEVLYRGEDISKWNEK 86

Query: 83  IFKKYRKD-VQLIPQDPYSTLPFNKTVEEILVAPILRWEKINKDELRKRLINLLELVKLT 141
             +K+R +   +I QDP ++L    T+   L+  IL     +K + R+R I +L LV + 
Sbjct: 87  QMQKFRGEKCSIIFQDPMTSLNPVFTIGNQLMEAILLHTDKDKKQARERAIEMLTLVGVN 146

Query: 142 PAEEFLGKYPHQLSGGQKQRLSIARSLSVNPRIIVADEPVTMVDASLRIGILNTLAEIKN 201
             E  L +YPH+LSGG +QR+ IA +L   P I++ADEP T +D +++  IL  + +++ 
Sbjct: 147 EPESRLKQYPHELSGGMRQRVMIAMALVCEPDILIADEPTTALDVTIQAQILELMQDLQK 206

Query: 202 RLNLTMVFITHDIPIARYFYHLFDKGNTIVMFAGRIVERADLEEILKDPLHPYTNDLIKL 261
           +L + ++ +THD+ +             IVM+ GR+ ER   + I   P H YT  L++ 
Sbjct: 207 KLGMAIIMVTHDLGVIASMC-----DEIIVMYGGRVCERGTADAIFYHPAHEYTKGLLRS 261

Query: 262 TPSIDNLYKEI----NVKINYERVEKGCPYRLRCPFAMDICKNEEPKLFKY--SHEVACF 315
            P  DN+ +++       IN  ++ +GC +  RC  AM IC  ++P  F+    H  +C+
Sbjct: 262 IPKADNMNEKLIPIGGTPINLLQMPEGCAFCPRCESAMKICLKQQPAEFRVGEDHLASCW 321

Query: 316 L 316
           +
Sbjct: 322 M 322


Lambda     K      H
   0.321    0.141    0.410 

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: 288
Number of extensions: 15
Number of successful extensions: 5
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: 324
Length of database: 338
Length adjustment: 28
Effective length of query: 296
Effective length of database: 310
Effective search space:    91760
Effective search space used:    91760
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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