GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Brevibacterium jeotgali SJ5-8

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_101588281.1 BJEO58_RS04995 ABC transporter ATP-binding protein

Query= TCDB::Q9WXN5
         (330 letters)



>NCBI__GCF_900169175.1:WP_101588281.1
          Length = 348

 Score =  179 bits (454), Expect = 9e-50
 Identities = 117/306 (38%), Positives = 161/306 (52%), Gaps = 11/306 (3%)

Query: 21  SVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNMVKPLTL-VDGKIFLRVNGEFV 79
           ++  V G+   I   EV G+VGESG GK+  + +  M ++ P T  +DG I  R+ G+ +
Sbjct: 22  TIPIVKGIDLTIEPGEVFGLVGESGSGKSVTA-LATMGLLDPRTAHIDGSI--RLQGDEL 78

Query: 80  ELSSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRMEKYVRHLAESHG-IDEEELLDKAR 138
            L   T     R   G  ++++ Q  M AL P   +   +     +H  I  +E   ++ 
Sbjct: 79  -LGGSTGRGANRSLRGSRVSMVFQEPMTALDPVFTIGSQLTETLRAHTRISAKEAKKRSI 137

Query: 139 RRFEEVGL-DPLW-IKRYPFELSGGMRQRAVIAIATILNPSLLIADEPTSALDVVNQKVL 196
              + VG+ DP      YP ELSGGMRQR VIAIA +  P LLIADEPT+A+D   Q  L
Sbjct: 138 DMLDSVGIVDPAARFHSYPHELSGGMRQRVVIAIALLCGPELLIADEPTTAVDATVQLQL 197

Query: 197 LKVLMQMKRQGIVKSIIFITHDIATVRQIADRMIIMYAGKIVEFAPVESLLEKPLHPYTQ 256
           L ++ +   +    S++FITHD+  V  I DRM  MYAG+IVE   V ++L  P HPYT 
Sbjct: 198 LDLIREAC-EATGTSVLFITHDLGVVSHICDRMATMYAGEIVETGDVSAVLSAPQHPYTA 256

Query: 257 GLFNSVLTPEPEVKKRGITTIPGAPPNLINPPSGCRFHPRCPHAMDVCKEKEPPLTEIEP 316
            L  ++  P PE +   +TTIPG  P     P GC F  RC  AMD C++  PPL     
Sbjct: 257 ALLGAL--PRPETRGTTLTTIPGRVPVPGTEPEGCWFADRCAFAMDECRDSHPPLATGPN 314

Query: 317 GRRVAC 322
           G    C
Sbjct: 315 GSLTRC 320


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: 292
Number of extensions: 14
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: 348
Length adjustment: 28
Effective length of query: 302
Effective length of database: 320
Effective search space:    96640
Effective search space used:    96640
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 24 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