GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Paraburkholderia bryophila 376MFSha3.1

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 H281DRAFT_05806 H281DRAFT_05806 dipeptide transport system ATP-binding protein

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__Burk376:H281DRAFT_05806
          Length = 339

 Score =  181 bits (460), Expect = 2e-50
 Identities = 115/327 (35%), Positives = 183/327 (55%), Gaps = 25/327 (7%)

Query: 5   LLKAENVRAYYKLEKV-----SVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNM 59
           +L A+ +  YY +++      +VKA++G+SF +   + + VVGESGCGK+TL+       
Sbjct: 18  VLVADKLARYYTVKRGMFATGTVKALNGVSFALERGKTLAVVGESGCGKSTLA------- 70

Query: 60  VKPLTLVDGKIF--LRVNGEFVELSSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRMEK 117
            + LT+++      L ++GE V  +    D  K     + + ++ Q    +L P   +E+
Sbjct: 71  -RQLTMIEAPSAGRLLIDGEDVAGA----DHAKIAALRRRVQMVFQNPFASLNPRKTVEQ 125

Query: 118 YVRH-LAESHGIDEEELLDKARRRFEEVGLDPLWIKRYPFELSGGMRQRAVIAIATILNP 176
            +   LA +  +   E  ++  +    VGL P   KRYP   SGG RQR  IA A IL+P
Sbjct: 126 TLGEPLAINSQLSVTERAERIAQMMRTVGLRPEHAKRYPHMFSGGQRQRVAIARAMILDP 185

Query: 177 SLLIADEPTSALDVVNQKVLLKVLMQMKRQGIVKSIIFITHDIATVRQIADRMIIMYAGK 236
            +++ADEP SALDV  Q  +L + M + +Q    S +FI+H+++ V  IAD +++MY G 
Sbjct: 186 QIVVADEPVSALDVSIQAQILNLFMDL-QQEFKTSYVFISHNLSVVEHIADDVMVMYFGG 244

Query: 237 IVEFAPVESLLEKPLHPYTQGLFNSVLTPEPEVKKRGI-TTIPGAPPNLINPPSGCRFHP 295
           + E    + +  KP HPYT+ L ++  TP      R I   + G  P+ +NPPSGC FH 
Sbjct: 245 VAELGDKKRIFSKPRHPYTRALMSA--TPSIFEADRTIKIKLQGEMPSPLNPPSGCTFHQ 302

Query: 296 RCPHAMDVCKEKEPPLTEIEPGRRVAC 322
           RCP+ +D C+ +EP L E++ GR+V+C
Sbjct: 303 RCPYVIDRCRSEEPKLREVD-GRQVSC 328


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: 285
Number of extensions: 7
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: 339
Length adjustment: 28
Effective length of query: 302
Effective length of database: 311
Effective search space:    93922
Effective search space used:    93922
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