GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Pseudomonas putida KT2440

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate PP_1722 PP_1722 ABC transporter, ATP-binding protein

Query= TCDB::G3LHY9
         (356 letters)



>FitnessBrowser__Putida:PP_1722
          Length = 329

 Score =  177 bits (448), Expect = 5e-49
 Identities = 117/349 (33%), Positives = 181/349 (51%), Gaps = 30/349 (8%)

Query: 1   MARITLDHIRHAYGANPKSDKDYSLKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQ 60
           M+ +++  ++ +Y  +P  ++      +D     G    LLGPSGCGK+TLL  I+GL  
Sbjct: 1   MSFVSVQKLQKSYAGSPVFER------IDCHIERGEFVTLLGPSGCGKSTLLRCIAGLTS 54

Query: 61  PSHGRILFDGKDVTNLSTQSRNIAQVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRV 120
              G+IL DG D+  LS Q R I  VFQ   ++  MTV  N+AF LR + V   +   RV
Sbjct: 55  VDSGQILLDGHDIVPLSPQKRGIGMVFQSYALFPNMTVEQNVAFGLRMQKVKADESQLRV 114

Query: 121 RDILEMIDLASWARRKAQGLTADQKQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLR 180
           R++LE+++L  +A R    L+  Q Q+++L R LV      +L DEPL+ +D  ++  LR
Sbjct: 115 REVLELVELGKFAGRYPHQLSGGQCQRVALARSLVTRP-RLLLLDEPLSALDARIRKHLR 173

Query: 181 SQLKRLHKQFGFTMVYVTHDQTEALTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYF 240
            Q++ + ++ G T ++VTHDQ EALT ++++ +M  G+IVQ G    L+  P   F   F
Sbjct: 174 EQIRAIQRELGLTTIFVTHDQEEALTMSDRIFLMNQGRIVQSGDAETLYTAPVDLFAAGF 233

Query: 241 IGSPGMNFMPARIEGSTVKVGDETLTLEYAPKTSGTAKTELGIRPEFIRLGREG-MPITI 299
           IG+   N + A          D    L   P  S      L IRPE I LG  G +   +
Sbjct: 234 IGN--YNLLDA----------DSASRLLQRPVAS-----RLAIRPESITLGEHGELDAEV 276

Query: 300 SKVEDIGR--QKIVRARFADQPIAIVVPEDADIPADAR---VTFDPSAI 343
                +G   +  VR R  +  + ++    AD+ AD +   V+ DP+A+
Sbjct: 277 RSHSLLGNVIRYRVRVREVELVVDVLNRSPADLHADGKRVSVSIDPTAL 325


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: 240
Number of extensions: 8
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: 329
Length adjustment: 29
Effective length of query: 327
Effective length of database: 300
Effective search space:    98100
Effective search space used:    98100
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