GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Marinobacter adhaerens HP15

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate GFF2209 HP15_2163 sugar ABC transporter, ATP-binding protein

Query= TCDB::G3LHY9
         (356 letters)



>FitnessBrowser__Marino:GFF2209
          Length = 366

 Score =  365 bits (937), Expect = e-105
 Identities = 190/364 (52%), Positives = 251/364 (68%), Gaps = 14/364 (3%)

Query: 1   MARITLDHIRHAYGANPKSDKDYSLKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQ 60
           MA I L  + H+Y   P    DY+++++DH W+ GGAYALLGPSGCGK+T+LNIISGL+Q
Sbjct: 1   MAEIQLKSLAHSYSDMPTGPDDYAIRQLDHVWHKGGAYALLGPSGCGKSTMLNIISGLVQ 60

Query: 61  PSHGRILFDGKDVTNLSTQSRNIAQVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRV 120
           PS G +LFDGK V  LS + RNIAQVFQFPVIYD+MTVYDNLAFPL+N  V  + +  RV
Sbjct: 61  PSEGDVLFDGKRVNELSPRDRNIAQVFQFPVIYDSMTVYDNLAFPLKNNKVPASKIKARV 120

Query: 121 RDILEMIDLASWARRKAQGLTADQKQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLR 180
            +I E++++     +KA+ LTAD+KQK+S+GRGLVR DV+AILFDEPLTVIDP +KW LR
Sbjct: 121 HEIAEVLEIEDKLYKKAKNLTADEKQKVSMGRGLVREDVSAILFDEPLTVIDPQLKWKLR 180

Query: 181 SQLKRLHKQFGFTMVYVTHDQTEALTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYF 240
            +LK++H+QF  TMVYVTHDQ EA TFA+K+ VMY GQIVQ GTP ELFE+P+HTFVG+F
Sbjct: 181 RKLKQIHEQFDITMVYVTHDQLEASTFADKIAVMYGGQIVQFGTPTELFEQPNHTFVGFF 240

Query: 241 IGSPGMNFMPAR------IEGSTVKVGDETLTLEYAPKTSGTAKTELGIRPEFIRLGREG 294
           IGSPGMN +  +        GSTV V  E+  ++   +T  T   ++GIRPEF+ +    
Sbjct: 241 IGSPGMNLIEVQRCPRGVCFGSTV-VSLESWQVDVLQRTRST-NIKIGIRPEFVEVSSVA 298

Query: 295 MPIT----ISKVEDIGRQKIVRARFADQPIAIVVPED--ADIPADARVTFDPSAISIYAD 348
              T    +  VED+G  KIV  +   + + +   E+  A I +   ++F    + +Y D
Sbjct: 299 SDDTFEAEVLDVEDLGTYKIVTVQLDHEKMKVRQSEEFAASIGSKVHLSFPRQWLKLYVD 358

Query: 349 SWRV 352
            + V
Sbjct: 359 EFLV 362


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: 390
Number of extensions: 10
Number of successful extensions: 1
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: 366
Length adjustment: 29
Effective length of query: 327
Effective length of database: 337
Effective search space:   110199
Effective search space used:   110199
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