GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Klebsiella michiganensis M5al

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 BWI76_RS07535 BWI76_RS07535 dipeptide/oligopeptide/nickel ABC transporter ATP-binding protein

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__Koxy:BWI76_RS07535
          Length = 347

 Score =  200 bits (508), Expect = 5e-56
 Identities = 119/326 (36%), Positives = 190/326 (58%), Gaps = 24/326 (7%)

Query: 5   LLKAENVRAYY-----KLEKVSVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNM 59
           LLK  N+  ++     K  +V V+AVD +SF +++ E +GVVGESGCGK+T + ++ M +
Sbjct: 16  LLKVNNLLKHFPAGGGKAREV-VQAVDDVSFAVIKGETLGVVGESGCGKSTTARLL-MQL 73

Query: 60  VKPLTLVDGKIFLRVNGEFV-ELSSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRMEKY 118
           +K           + +GE + +   +    +  K + +++ ++ Q +  +L P + ME+ 
Sbjct: 74  LK-----------QDSGELIFDGLEVGSSRLPMKAYRRQVQMVFQDSYASLNPRMTMEES 122

Query: 119 VRHLAESHGIDEEELLDKARRRFEEVGLDP-LWIKRYPFELSGGMRQRAVIAIATILNPS 177
           +      HG+  +E  + AR     VGL+P  +  RYP  LSGG RQR  IA A  + P 
Sbjct: 123 IAFGQRVHGVSAKEASEYARYLLAHVGLEPERFAHRYPHALSGGQRQRVNIARALAMKPR 182

Query: 178 LLIADEPTSALDVVNQKVLLKVLMQMKRQGIVKSIIFITHDIATVRQIADRMIIMYAGKI 237
           L+I DE  SALD   +  +L++L ++KR  +  + +FI+HD+  VR ++DR+++MY G++
Sbjct: 183 LVILDEAVSALDKSVEAQVLQLLQELKRT-LALTYVFISHDLHVVRWLSDRILVMYLGEV 241

Query: 238 VEFAPVESLLEKPLHPYTQGLFNSVLTPEPEVKKRGITT-IPGAPPNLINPPSGCRFHPR 296
           VE  P E L     HPYT+ L +S+ + +P    R +T+ + G PP+ I+PPSGCRFH R
Sbjct: 242 VEIGPAEQLFTASAHPYTRALLSSMPSMDPH--NRTLTSALNGDPPSPISPPSGCRFHTR 299

Query: 297 CPHAMDVCKEKEPPLTEIEPGRRVAC 322
           CPHA  VC E +P L  +  G + AC
Sbjct: 300 CPHARAVCAEVKPTLQSVGEGHQSAC 325


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: 276
Number of extensions: 18
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: 330
Length of database: 347
Length adjustment: 28
Effective length of query: 302
Effective length of database: 319
Effective search space:    96338
Effective search space used:    96338
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