GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Roseburia faecis M72

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 WP_055067293.1 M72_RS04115 oligopeptide/dipeptide ABC transporter ATP-binding protein

Query= TCDB::Q9WXN5
         (330 letters)



>NCBI__GCF_001406815.1:WP_055067293.1
          Length = 350

 Score =  180 bits (457), Expect = 4e-50
 Identities = 110/342 (32%), Positives = 181/342 (52%), Gaps = 23/342 (6%)

Query: 3   EILLKAENVRAYYKLEK----VSVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMN 58
           + LL+ E+++ Y+ + +    + +KAVD +SF I   E +G+VGESGCGKTT+   + + 
Sbjct: 9   DYLLEVEHLKQYFPVHQGFSTIPLKAVDDISFAIRPGETLGLVGESGCGKTTVGRTL-LR 67

Query: 59  MVKPLT---LVDGKIFLRVNGEFVELSSMTRD-----------EVKRKFWGKEITIIPQA 104
           + +P       DGK+      ++ E   M  D           +V    + KE+ ++ Q 
Sbjct: 68  LYQPTAGKITFDGKVLFDSGEQYDENGKMIVDANGKPVMGKKVDVNMMPYRKEMQMVFQD 127

Query: 105 AMNALMPTIRMEKYVRHLAESHGI--DEEELLDKARRRFEEVGLDPLWIKRYPFELSGGM 162
             ++L P + +E  +    + H +  + +E  +K     E VGL+     RY  E SGG 
Sbjct: 128 PYSSLNPRMTVEDIIGEPLDVHKLYRNRKERREKILDLMELVGLNAEHAMRYAHEFSGGQ 187

Query: 163 RQRAVIAIATILNPSLLIADEPTSALDVVNQKVLLKVLMQMKRQGIVKSIIFITHDIATV 222
           RQR  IA A  +NP  ++ DE  SALDV  Q  ++ +  +++ + +  + +FI HD+  V
Sbjct: 188 RQRIGIARALAVNPKFIVCDEAVSALDVSIQAQVVNMFEELQEK-LGVAYLFIAHDLLVV 246

Query: 223 RQIADRMIIMYAGKIVEFAPVESLLEKPLHPYTQGLFNSVLTPEPE-VKKRGITTIPGAP 281
             I+DR+ +MY GK++E A  + L   P+HPYT  L ++V  P+PE  +K     + G  
Sbjct: 247 HHISDRIAVMYLGKMMEIADADELNANPIHPYTLSLLSAVPIPDPETARKSHRIVLEGDV 306

Query: 282 PNLINPPSGCRFHPRCPHAMDVCKEKEPPLTEIEPGRRVACW 323
           P+ +  P+GC F  RC +A + C ++ P LT+   G  VACW
Sbjct: 307 PSPLKMPTGCPFRTRCKYATEKCGQEMPQLTDRGNGHMVACW 348


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: 289
Number of extensions: 12
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: 350
Length adjustment: 28
Effective length of query: 302
Effective length of database: 322
Effective search space:    97244
Effective search space used:    97244
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