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 GFF1587 PS417_08075 methionine ABC transporter ATP-binding protein

Query= TCDB::Q9WXN5
         (330 letters)



>FitnessBrowser__WCS417:GFF1587
          Length = 318

 Score =  172 bits (436), Expect = 1e-47
 Identities = 118/305 (38%), Positives = 170/305 (55%), Gaps = 18/305 (5%)

Query: 22  VKAVDGLSFEILEDEVIGVVGESGCGKTTLSNVIFMNMVKPLTLVDGKIFLRVNGEFVEL 81
           V  VD +SF++ E E++G+VGESG GKT     +   +  P   V G   +R+ G+  +L
Sbjct: 20  VTLVDRVSFDLAEGEILGLVGESGSGKTMACRGLMRLLPSPNLRVQGGA-VRLGGQ--DL 76

Query: 82  SSMTRDEVKRKFWGKEITIIPQAAMNALMPTIRMEKYVRHLAESH-GIDEEELLDKARRR 140
            S+  D   R   G ++ +I Q   + L P +R+ + +      H G  +++   +A   
Sbjct: 77  LSLD-DAGMRAVRGGQLGMIFQNPSSHLDPLMRIGEQIAEGIRLHQGASKKDARLQAIEV 135

Query: 141 FEEVGL-DP-LWIKRYPFELSGGMRQRAVIAIATILNPSLLIADEPTSALDVVNQKVLLK 198
             +VG+ DP   +  YP E SGGMRQRA+IA+A   NP +LIADEPT+ALDV  Q  +L+
Sbjct: 136 LRQVGIPDPQARVDNYPQEFSGGMRQRAMIAVALGCNPKVLIADEPTTALDVTVQAQILR 195

Query: 199 VLMQMKRQ-GIVKSIIFITHDIATVRQIADRMIIMYAGKIVEFAPVESLLEKPLHPYTQG 257
           +L++++ Q G+  SII ITHD+  V Q  D + +MYAG + E      +L +P HPYT G
Sbjct: 196 LLLELRDQRGL--SIIMITHDLGVVAQTCDAIAVMYAGCLCEHGSKYDVLAQPQHPYTAG 253

Query: 258 LFNSVLTPEPEVKKRGITTIPGAPPNLINPPSGCRFHPRCPHAMDVCKEKEPPLTEIEPG 317
           L +    P        + TIPG PP L   P+GCRF+PRCP    +C E  P       G
Sbjct: 254 LID--CQPAHSSGHALLRTIPGQPPLLDALPAGCRFNPRCPQVGALCTEVLP------EG 305

Query: 318 RRVAC 322
           +RVAC
Sbjct: 306 QRVAC 310


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: 253
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: 318
Length adjustment: 28
Effective length of query: 302
Effective length of database: 290
Effective search space:    87580
Effective search space used:    87580
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