GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Cupriavidus basilensis 4G11

Align TM0028, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized)
to candidate RR42_RS35215 RR42_RS35215 peptide ABC transporter ATP-binding protein

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__Cup4G11:RR42_RS35215
          Length = 329

 Score =  206 bits (523), Expect = 8e-58
 Identities = 126/335 (37%), Positives = 186/335 (55%), Gaps = 22/335 (6%)

Query: 1   MKEILLKAENVRAYY--------KLEKVSVKAVDGLSFEILEDEVIGVVGESGCGKTTLS 52
           M + +L+ EN++ ++        K +  SVKAVDG+SF +   E +G+VGESGCGK+T  
Sbjct: 1   MGDEILRVENLKVHFPVTQGVFIKRQVGSVKAVDGVSFTLRRGETLGLVGESGCGKSTTG 60

Query: 53  NVIFMNMVKPLTLVDGKIFLRVNGEFVELSSMTRDEVKRKFWGKEITIIPQAAMNALMPT 112
             I    +K L    G+I      +F   S     + + K + + + ++ Q    +L P 
Sbjct: 61  LAI----IKMLAASGGRIAFD-GDDFATFS-----KAQEKNFRRSVQMVYQDPFGSLNPR 110

Query: 113 IRMEKYVRHLAESHGI--DEEELLDKARRRFEEVGLDPLWIKRYPFELSGGMRQRAVIAI 170
           +++   +    E HG+  D E    +     + VGL P    RYP E SGG RQR  IA 
Sbjct: 111 MKVCDIIGEPLEVHGMANDREHYRARIAELLQMVGLLPYMADRYPHEFSGGQRQRIGIAR 170

Query: 171 ATILNPSLLIADEPTSALDVVNQKVLLKVLMQMKRQGIVKSIIFITHDIATVRQIADRMI 230
           A  + PSL++ DEP SALDV  Q  ++ V M+++R+ +  + IFI HD+A VR I+DR+ 
Sbjct: 171 ALAVEPSLIVCDEPVSALDVSIQAQVVNVFMELQRR-LGLTYIFIAHDLAVVRHISDRIA 229

Query: 231 IMYAGKIVEFAPVESLLEKPLHPYTQGLFNSVLTPEPEVK-KRGITTIPGAPPNLINPPS 289
           +MY G+IVE A  ++L   P HPYT+ L ++V     E + KR    + G  P+ +NPPS
Sbjct: 230 VMYLGRIVEIASRDALYANPRHPYTKALLSAVPVASVEAEAKRQRIVLKGEVPSPLNPPS 289

Query: 290 GCRFHPRCPHAMDVCKEKEPPLTEIEPGRRVACWL 324
           GCRFHPRC  A   C+ ++P L E   G+ VAC L
Sbjct: 290 GCRFHPRCAQATQRCRVEDPVLRERGDGQMVACHL 324


Lambda     K      H
   0.321    0.138    0.405 

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: 297
Number of extensions: 16
Number of successful extensions: 4
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: 330
Length of database: 329
Length adjustment: 28
Effective length of query: 302
Effective length of database: 301
Effective search space:    90902
Effective search space used:    90902
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 Sep 17 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