GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glnQ in Mesorhizobium ciceri WSM1271

Align Glutamine ABC transporter ATP-binding protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity (characterized)
to candidate YP_004141734.1 Mesci_2542 ABC transporter

Query= TCDB::Q9CES4
         (247 letters)



>NCBI__GCF_000185905.1:YP_004141734.1
          Length = 268

 Score =  254 bits (649), Expect = 1e-72
 Identities = 132/244 (54%), Positives = 176/244 (72%), Gaps = 10/244 (4%)

Query: 12  LHKSFGKNEVLKGITTKFEKGDVVCIIGPSGSGKSTFLRALNGLETATSGDIIID----G 67
           + KS+G  EVLKG+      G V CIIGPSGSGKSTFLR +N LE  ++G +++D    G
Sbjct: 25  VRKSYGPLEVLKGVDLDVPVGSVACIIGPSGSGKSTFLRCINHLEKLSAGILLVDSQFVG 84

Query: 68  FNLTD------KNTNLNLVRQNVGMVFQHFNLFPNMTVMQNITYAPVELKKMSKDDADKK 121
           ++L D      K+  L   R   GM+FQ FNLF +MTVM+N+  AP +++++  D+A  +
Sbjct: 85  YDLRDDKLYEVKDDLLCRRRAETGMLFQSFNLFSHMTVMENLIEAPTQVRRIPPDEAKAE 144

Query: 122 AIQLLETVGLLDKKDAMPEMLSGGQKQRVAIARALAMNPDVMLFDEPTSALDPEMVGDVL 181
           A  LL  VGLLDK D  P  LSGGQ+QRVAIARA+AM P V+LFDEPTSALDPE+VG+VL
Sbjct: 145 AEILLRRVGLLDKVDRYPRELSGGQQQRVAIARAMAMKPKVLLFDEPTSALDPELVGEVL 204

Query: 182 AVMQKLAEEGMTMLIVTHEMGFARKVANRVIFTDGGVILEDGTPEELFDSPKHPRLQDFL 241
            VM+ LAE GMTM++VTHE+GFAR++ ++++F DGGVI+E G P E+  +P  PR ++FL
Sbjct: 205 QVMRDLAESGMTMVVVTHEVGFAREIGDQLVFMDGGVIIERGAPREMIANPVSPRTREFL 264

Query: 242 SKVL 245
           S+VL
Sbjct: 265 SRVL 268


Lambda     K      H
   0.318    0.136    0.378 

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: 189
Number of extensions: 11
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: 247
Length of database: 268
Length adjustment: 24
Effective length of query: 223
Effective length of database: 244
Effective search space:    54412
Effective search space used:    54412
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 47 (22.7 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