GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM0028 in Pseudomonas simiae WCS417

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 GFF796 PS417_04045 peptide ABC transporter ATP-binding protein

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__WCS417:GFF796
          Length = 323

 Score =  194 bits (494), Expect = 2e-54
 Identities = 117/328 (35%), Positives = 191/328 (58%), Gaps = 24/328 (7%)

Query: 4   ILLKAENVRAYYKLEK------VSVKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFM 57
           ++L A ++  +Y++ +       +V+A++G+SFE+   + + VVGESGCGK+TL+     
Sbjct: 3   VVLTARDLTRHYEVSRGLFKGHATVRALNGVSFELEAGKTLAVVGESGCGKSTLA----- 57

Query: 58  NMVKPLTLVD--GKIFLRVNGEFVELSSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRM 115
              + LTL++      L++ G+ V  +    D+ +RK   K++ ++ Q+   +L P  ++
Sbjct: 58  ---RALTLIEEPSSGSLKIAGQEVAGA----DKAQRKQLRKDVQMVFQSPYASLNPRQKV 110

Query: 116 -EKYVRHLAESHGIDEEELLDKARRRFEEVGLDPLWIKRYPFELSGGMRQRAVIAIATIL 174
            ++    L  +  +   E  +K +   ++VGL P   +RYP   SGG RQR  +A A +L
Sbjct: 111 GDQLAEPLLINTNLSAAERREKVQAMMKQVGLRPEHYQRYPHMFSGGQRQRIALARAMML 170

Query: 175 NPSLLIADEPTSALDVVNQKVLLKVLMQMKRQGIVKSIIFITHDIATVRQIADRMIIMYA 234
            P +L+ADEPTSALDV  Q  +L + M + +Q    + +FI+H++A V+ +AD +++MY 
Sbjct: 171 QPKVLVADEPTSALDVSIQAQVLNLFMDL-QQEFNTAYVFISHNLAVVQHVADDVMVMYL 229

Query: 235 GKIVEFAPVESLLEKPLHPYTQGLFNSVLTPEPEVKKRGITTIPGAPPNLINPPSGCRFH 294
           G+ VE  P E +  +PLHPYTQ L ++  T  P+  K  I  I G  PN +NPP GC FH
Sbjct: 230 GRPVEVGPKEDIYARPLHPYTQALLSATPTIHPDPNKPKI-KIVGELPNPLNPPPGCAFH 288

Query: 295 PRCPHAMDVCKEKEPPLTEIEPGRRVAC 322
            RCP+A   C  +EP L  ++  R+VAC
Sbjct: 289 KRCPYATARCSTEEPQLRPLD-NRQVAC 315


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: 303
Number of extensions: 13
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: 323
Length adjustment: 28
Effective length of query: 302
Effective length of database: 295
Effective search space:    89090
Effective search space used:    89090
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: 48 (23.1 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