GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Pseudomonas simiae WCS417

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate GFF4321 PS417_22130 sugar ABC transporter ATPase

Query= TCDB::G3LHY9
         (356 letters)



>FitnessBrowser__WCS417:GFF4321
          Length = 386

 Score =  200 bits (509), Expect = 5e-56
 Identities = 123/362 (33%), Positives = 195/362 (53%), Gaps = 21/362 (5%)

Query: 1   MARITLDHIRHAYGANPKSDKDYSLKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQ 60
           MA + L ++   YGA        +LK ++    +G    L+GPSGCGK+TL+N I+GL  
Sbjct: 1   MATLELRNVNKTYGAGLPD----TLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLET 56

Query: 61  PSHGRILFDGKDVTNLSTQSRNIAQVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRV 120
            + G I+   +DV+ +S + R+IA VFQ   +Y TM+V +N+ F L+ R + +AD+D  V
Sbjct: 57  ITGGAIMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEV 116

Query: 121 RDILEMIDLASWARRKAQGLTADQKQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLR 180
             + +++ +     RK   L+  Q+Q++++GR L R      LFDEPL+ +D  ++  +R
Sbjct: 117 ARVAKLLQIEHLLNRKPGQLSGGQQQRVAMGRALARRP-KIYLFDEPLSNLDAKLRVEMR 175

Query: 181 SQLKRLHKQFGFTMVYVTHDQTEALTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYF 240
           +++K +H++   T VYVTHDQ EA+T  +KV VM DG I Q GTP E++  P++ FV  F
Sbjct: 176 TEMKLMHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASF 235

Query: 241 IGSPGMNFMPARI---EGSTVKVGDE-TLTLEYAPKTSGTAKTE----LGIRPEFIRL-- 290
           IGSP MNF+P R+   +G  V + D      E A  T+     +    LG+RPE I L  
Sbjct: 236 IGSPPMNFVPLRLQRKDGRLVALLDSGQARCELALNTTEAGLEDRDVILGLRPEQIMLAA 295

Query: 291 ----GREGMPITISKVEDIGRQKIVRARFADQPIAIVVPEDA--DIPADARVTFDPSAIS 344
                   +   +   E  G   +V  +  D  +   +  D    +     + FDPS + 
Sbjct: 296 GEGDSASSIRAEVQVTEPTGPDTLVFVQLNDTKVCCRLAPDVAPQVGETLTLQFDPSKVL 355

Query: 345 IY 346
           ++
Sbjct: 356 LF 357


Lambda     K      H
   0.321    0.137    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: 318
Number of extensions: 9
Number of successful extensions: 2
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: 356
Length of database: 386
Length adjustment: 30
Effective length of query: 326
Effective length of database: 356
Effective search space:   116056
Effective search space used:   116056
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