GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Pseudomonas benzenivorans DSM 8628

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate WP_090447186.1 BLS63_RS18125 ABC transporter ATP-binding protein

Query= TCDB::G3LHY9
         (356 letters)



>NCBI__GCF_900100495.1:WP_090447186.1
          Length = 386

 Score =  210 bits (534), Expect = 6e-59
 Identities = 126/362 (34%), Positives = 197/362 (54%), Gaps = 21/362 (5%)

Query: 1   MARITLDHIRHAYGANPKSDKDYSLKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQ 60
           MA + L ++   YG+        +LK ++   + G    L+GPSGCGK+TL+N I+GL  
Sbjct: 1   MATLELRNVNKTYGSGLPD----TLKNIEIAIDSGEFLILVGPSGCGKSTLMNCIAGLED 56

Query: 61  PSHGRILFDGKDVTNLSTQSRNIAQVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRV 120
            S G IL +G+D++ +S + R+IA VFQ   +Y TMTV DN+AF L+ R +A AD+D  V
Sbjct: 57  ISGGAILVEGQDISGMSPKDRDIAMVFQSYALYPTMTVRDNIAFGLKIRKMAPADIDTEV 116

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

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

Query: 241 IGSPGMNFMPARIE------GSTVKVGDETLTLEYAPKTSGTAKTE--LGIRPEFIRLGR 292
           IGSP MNF+P R++       + +  G     L       G    E  LGIRPE I + +
Sbjct: 236 IGSPPMNFIPLRLQRRDGQLWALLDSGQARCELPLGAMEEGLESREVILGIRPEQIGIAQ 295

Query: 293 EG------MPITISKVEDIGRQKIVRARFADQPIAIVVPEDA--DIPADARVTFDPSAIS 344
            G      +   +   E  G   +V        +   +  DA   + A   + F+PS + 
Sbjct: 296 GGDGSLPSIRAEVQVTEPTGPDTLVFVELNQTKVCCRLAPDAAPQVGASLELQFEPSKVL 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: 314
Number of extensions: 7
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 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