GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bztA in Mesorhizobium ciceri biovar biserrulae WSM1271

Align BztA, component of Glutamate/glutamine/aspartate/asparagine porter (characterized)
to candidate WP_013532423.1 MESCI_RS23340 amino acid ABC transporter substrate-binding protein

Query= TCDB::Q52663
         (338 letters)



>NCBI__GCF_000185905.1:WP_013532423.1
          Length = 342

 Score =  373 bits (958), Expect = e-108
 Identities = 187/332 (56%), Positives = 240/332 (72%), Gaps = 5/332 (1%)

Query: 11  ALAALVAGAASASTLDDVKARGQLICGSNPGLTGFAAPDANGVYQGFDVAVCKAVAAAVL 70
           A   L+A AASA+TLD VKA+G + CG + GL GF+APD  G +QG D   C+AVAAAV 
Sbjct: 12  ATLGLMASAASAATLDTVKAKGFIQCGVSTGLAGFSAPDDKGDWQGIDADFCRAVAAAVF 71

Query: 71  GDPMKVKYVPLTGETRFTALASGEVDVLVRNSTWTFSRDTELALDFVAVNYYDGQGFMVN 130
           GD  +VK+ PL+ + RFTAL SGE+D+L RN+TWT +RDT L L+F+ V YYDGQGFM+N
Sbjct: 72  GDGSRVKFTPLSAKERFTALQSGEIDILSRNTTWTINRDTALGLNFIGVTYYDGQGFMIN 131

Query: 131 --KSLGVSSAKELDGATICVQTGTTTEMNLADFFKANNMTYTPVNIADDAEGQQKFAAGA 188
             K  GV+SA +L GA +CVQ+GTTTE+NLAD+FKAN M Y PV      E    + AG 
Sbjct: 132 AKKLPGVNSALQLSGAAVCVQSGTTTELNLADYFKANKMEYNPVVFEKLEEVNAAYDAGR 191

Query: 189 CDSYTTDASGLASSRATLPNAADIVILPEIISKEPLGPVVRHGDNNWGDIVRWSFYALVA 248
           CD YTTD SGL   R TL + AD V+LPEIISKEPLGP VR GD+ W  IV+W+++AL+ 
Sbjct: 192 CDVYTTDQSGLYGIRLTLGSPADHVVLPEIISKEPLGPAVRQGDDQWYHIVKWTYFALLQ 251

Query: 249 AEEYGITKANLEEVAASTQNPEIRRLLGLEGD--MGKKIGLDNDFAKRAILASGNYGEVF 306
           AEE GITKAN++E+  S  +PEI+R+LG E D  +G  +G+ ND+    + A GNYGE+F
Sbjct: 252 AEELGITKANVDEMKNSA-SPEIKRVLGQEADTKIGTDLGVSNDWVVNIVKAVGNYGEMF 310

Query: 307 EANIGASTSIGLARGLNAQWTQGGLMYAPPFR 338
           E N+G+ + + +ARG+NA WT+GGL YAPP R
Sbjct: 311 ERNVGSGSPLKIARGINALWTKGGLQYAPPIR 342


Lambda     K      H
   0.316    0.132    0.384 

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: 368
Number of extensions: 18
Number of successful extensions: 4
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: 338
Length of database: 342
Length adjustment: 28
Effective length of query: 310
Effective length of database: 314
Effective search space:    97340
Effective search space used:    97340
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 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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