GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Collimonas pratensis Ter91

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate WP_061942552.1 CPter91_RS17900 sn-glycerol-3-phosphate import ATP-binding protein UgpC

Query= TCDB::G3LHY9
         (356 letters)



>NCBI__GCF_001584185.1:WP_061942552.1
          Length = 359

 Score =  218 bits (555), Expect = 2e-61
 Identities = 118/348 (33%), Positives = 210/348 (60%), Gaps = 8/348 (2%)

Query: 1   MARITLDHIRHAYGANPKSDKDYSLKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQ 60
           MA++ L +++  YG  PK+     +  +  +  DG    ++GPSGCGK+TLL +++GL +
Sbjct: 1   MAQVHLKNVKKTYGKAPKAVD--VIHGISIDIADGEFIVMVGPSGCGKSTLLRMVAGLEE 58

Query: 61  PSHGRILFDGKDVTNLSTQSRNIAQVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRV 120
            S G I+   + V  L  + R+IA VFQ   +Y  M+VY+N+A+ L+ RG+++ D++ RV
Sbjct: 59  VSAGDIVIGERVVNQLEPKDRDIAMVFQNYALYPHMSVYENMAYGLKIRGLSKDDIETRV 118

Query: 121 RDILEMIDLASWARRKAQGLTADQKQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLR 180
           +   ++++L +  +R  + L+  Q+Q++++GR +VR      LFDEPL+ +D  ++  +R
Sbjct: 119 QKAAKILELGALLQRTPRQLSGGQRQRVAMGRAIVREPA-VFLFDEPLSNLDAKLRVQMR 177

Query: 181 SQLKRLHKQFGFTMVYVTHDQTEALTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYF 240
            ++++LH+  G T +YVTHDQ EA+T  ++++VM  G+  QIGTPAE++ RP+ TFV  F
Sbjct: 178 LEIQKLHRTLGTTSLYVTHDQVEAMTLGQRMIVMNGGRAEQIGTPAEVYARPATTFVASF 237

Query: 241 IGSPGMNFMPARI--EGSTVKVGD-ETLTLEYAPKTSGTAKTELGIRPEFIRLGREGMPI 297
           IGSP MN +  R+  +G++  + +   ++L ++          +G+RPE +  G+ G+ +
Sbjct: 238 IGSPPMNLLCGRVAADGNSFAIDNAAAVSLPFSCHPIAGRDCIMGLRPEQLIFGQPGLNL 297

Query: 298 TISKVEDIGRQKIVRARFADQPIAIVVPEDADIPADARVT--FDPSAI 343
               VE +G   +V     DQ + + VP    + A  ++T  FD +A+
Sbjct: 298 RAELVEALGADLLVHVSIGDQLLVMRVPAATAVEAGQQITAGFDAAAL 345


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: 266
Number of extensions: 12
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 356
Length of database: 359
Length adjustment: 29
Effective length of query: 327
Effective length of database: 330
Effective search space:   107910
Effective search space used:   107910
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