GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08260 in Azospirillum thiophilum BV-S

Align Branched-chain amino acid ABC transporter,substrate-binding periplasmic component (characterized, see rationale)
to candidate WP_045585665.1 AL072_RS27965 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:G8ALJ3
         (366 letters)



>NCBI__GCF_001305595.1:WP_045585665.1
          Length = 376

 Score =  391 bits (1004), Expect = e-113
 Identities = 187/360 (51%), Positives = 254/360 (70%)

Query: 7   LLVAVAATAMTASVAKADIAVATAGPITGQYATFGEQMKKGIEQAVADINAAGGVLGQKL 66
           L   ++  A+  + A AD+ +  AGP+TGQYA+F EQM++G + AVAD+NAAGG+ G+K+
Sbjct: 17  LRFGISLAALVPTAAAADVKLGLAGPVTGQYASFMEQMRRGADLAVADLNAAGGINGEKV 76

Query: 67  KLEVGDDACDPKQAVAVANQLAKAGVKFVAGHFCSGSSIPASQVYAEEGVLQISPASTNP 126
            L+V DDACDPKQAVAVAN+    GV+ V GHFCS S+IPAS VYAE G++ ++PASTNP
Sbjct: 77  VLQVADDACDPKQAVAVANRFVADGVQAVVGHFCSSSTIPASSVYAESGLVIVTPASTNP 136

Query: 127 KLTEQNLKNVFRVCGRDDQQGQIAGKYLLENYKGKNVAILHDKSAYGKGLADETQKALNA 186
            +TE+ L N+FRVCGRDDQ   +A K ++    G+ +AI+HDKS YG+G+A+  +  L  
Sbjct: 137 TITERGLTNMFRVCGRDDQAAGVAAKQIVGRNLGRTIAIVHDKSTYGQGIAEGVRTELAQ 196

Query: 187 GGQKEKIYEAYTAGEKDYSALVSKLKQEAVDVVYVGGYHTEAGLLARQMKDQGLNAPIVS 246
            G+   ++E  T GE+D+S+LV+++K   VDVV+ GGYHTEAGLL RQ  +QGL    V+
Sbjct: 197 QGRNVVLFEGITQGERDFSSLVARMKALNVDVVFFGGYHTEAGLLVRQASEQGLKTRFVA 256

Query: 247 GDALVTNEYWAITGPAGENTMMTFGPDPREMPEAKEAVEKFRKAGYEPEGYTLYTYAALQ 306
           GD L T E+ +I GPA +  M TF PDPR      + V +FR AG+EPEG+TLYTYAA++
Sbjct: 257 GDGLATTEFASIAGPASDGVMFTFYPDPRANAGTADLVRRFRTAGFEPEGFTLYTYAAVR 316

Query: 307 IWAEAAKQANSTDSAKIADVLRKNSYNTVIGKIGFDAKGDVTSPAYVWYRWNNGQYAQVK 366
           + A+AAK A +    ++AD LR  +Y+TV+G I FD KGD  S  +V Y WNNG YA +K
Sbjct: 317 VLADAAKAAKTMKGDRLADALRAGTYHTVLGDIRFDRKGDPNSEPFVLYAWNNGTYAPLK 376


Lambda     K      H
   0.312    0.129    0.366 

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: 412
Number of extensions: 19
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: 366
Length of database: 376
Length adjustment: 30
Effective length of query: 336
Effective length of database: 346
Effective search space:   116256
Effective search space used:   116256
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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