GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsB in Burkholderia phytofirmans PsJN

Align ABC transporter for D-Galactose and D-Glucose, permease component 1 (characterized)
to candidate BPHYT_RS05030 BPHYT_RS05030 sugar ABC transporter permease

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1895
         (302 letters)



>FitnessBrowser__BFirm:BPHYT_RS05030
          Length = 312

 Score =  375 bits (963), Expect = e-109
 Identities = 177/300 (59%), Positives = 231/300 (77%), Gaps = 1/300 (0%)

Query: 3   SVAVFSKASPFDAL-QRWLPKLVLAPSMLIVLVGFYGYIIWTFILSFTNSSFMPSYKWVG 61
           +  V  +ASP  AL  RW+PKLVLAPS++I L+  YG+I  T  LS +NS  MP Y++VG
Sbjct: 11  TATVTRRASPMAALADRWIPKLVLAPSVVISLIFVYGFIAITGYLSLSNSRLMPRYEFVG 70

Query: 62  LQQYMRLMDNDRWWVASKNLALFGGMFISISLVLGVFLAVLLDQRIRKEGFIRTVYLYPM 121
           L +Y  L DND +W ++ NL  FG  FI + + LG+FLA+LLDQ+IR EG +R V+LYPM
Sbjct: 71  LDRYRELFDNDVFWTSAANLGWFGIPFIGVCIGLGLFLAILLDQQIRNEGALRAVFLYPM 130

Query: 122 ALSMIVTGTAWKWLLNPGLGLDKMLRDWGWEGFRLDWLVDQDRVVYCLVIAAVWQASGFV 181
           ALS IVTGTAW+W++ P +GL+K+  DWGW  F   WL D D+ ++C+VIAAVWQ++GFV
Sbjct: 131 ALSFIVTGTAWQWIMTPSIGLEKVFHDWGWTSFSFSWLGDPDKAIFCVVIAAVWQSTGFV 190

Query: 182 MAMFLAGLRGVDQSIIRAAQVDGASLPTIYLKIVLPSLRPVFFSAFMILAHIAIKSFDLV 241
           MA+FLAGLRGVD  I +AAQ+DGA LPTIY KIV+PS+RPVFFS  +IL HI IK+FDLV
Sbjct: 191 MALFLAGLRGVDGEIFKAAQMDGAGLPTIYRKIVIPSMRPVFFSVLLILCHITIKTFDLV 250

Query: 242 AAMTAGGPGYSSDLPAMFMYSFTFSRGQMGIGSASAMLMLGAVLTILVPYLYSELRGKRH 301
            A+TAGGPG SS LPA+FMY+F+F+RGQ+G+G+AS+M+ML  V+ +LVP +Y E R  R+
Sbjct: 251 VALTAGGPGTSSSLPAIFMYTFSFNRGQLGVGAASSMMMLATVVAVLVPLMYLESRSTRN 310


Lambda     K      H
   0.329    0.141    0.448 

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: 394
Number of extensions: 13
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: 302
Length of database: 312
Length adjustment: 27
Effective length of query: 275
Effective length of database: 285
Effective search space:    78375
Effective search space used:    78375
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 48 (23.1 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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