GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08260 in Ochrobactrum thiophenivorans DSM 7216

Align Branched-chain amino acid ABC transporter,substrate-binding periplasmic component (characterized, see rationale)
to candidate WP_094505526.1 CEV31_RS03655 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:G8ALJ3
         (366 letters)



>NCBI__GCF_002252445.1:WP_094505526.1
          Length = 372

 Score =  360 bits (925), Expect = e-104
 Identities = 175/360 (48%), Positives = 240/360 (66%), Gaps = 3/360 (0%)

Query: 4   KLSLLVAVAATAMTA--SVAKADIAVATAGPITGQYATFGEQMKKGIEQAVADINAAGGV 61
           K SL   V  +A+ A    + AD+ +    P+TG  A +G+Q+K+G+E AVA+ NA GG+
Sbjct: 2   KKSLFCGVCLSALVAMGGASFADVVLGVGAPLTGGQAAYGDQIKRGVEAAVAEANAKGGM 61

Query: 62  LGQKLKLEVGDDACDPKQAVAVANQLAKAGVKFVAGHFCSGSSIPASQVYAEEGVLQISP 121
            G+++ +  GDDA DP+Q ++VAN+    GV+FV GHF SG SIP S +YAE GVL I+P
Sbjct: 62  NGEQISIVYGDDAADPRQGISVANKFVGDGVQFVIGHFNSGVSIPTSDIYAENGVLMIAP 121

Query: 122 ASTNPKLTEQNLKNVFRVCGRDDQQGQIAGKYLLENYKGKNVAILHDKSAYGKGLADETQ 181
            +TNP  TE++L N FR C RDDQQG +AGKY+ +NYK   VAILHDK+ YG+GLADET+
Sbjct: 122 GTTNPTFTERDLWNTFRTCRRDDQQGIVAGKYIADNYKDGKVAILHDKTPYGQGLADETK 181

Query: 182 KALNAGGQKEKIYEAYTAGEKDYSALVSKLKQEAVDVVYVGGYHTEAGLLARQMKDQGLN 241
           K+LNA G++E +YE    G+KD+SAL+SK+K   +  VY GG H EAGL+ RQM DQGL 
Sbjct: 182 KSLNANGKEETLYEGINQGDKDFSALISKMKAAGITAVYWGGMHPEAGLIIRQMADQGLK 241

Query: 242 APIVSGDALVTNEYWAITGPAGENTMMTFGPDPREMPEAKEAVEKFRKAGYEPEGYTLYT 301
           A  +SGD +V+NE  +I G A    + TFGPDPR+     + ++ FR  G+EPE YT Y 
Sbjct: 242 AQFISGDGIVSNELASIAGDAVGGVLNTFGPDPRDDAANADLIKAFRDKGFEPEAYTFYA 301

Query: 302 YAALQIWAEAAKQANSTDSAKIADVLR-KNSYNTVIGKIGFDAKGDVTSPAYVWYRWNNG 360
           YA +Q   +AA  A + D  ++A  L+ K  + TV+G + +DAKGD +   YV + W  G
Sbjct: 302 YAGVQSLVDAANAAGNNDPQEVAAALKGKGPFKTVLGDLSYDAKGDPSLSPYVMFEWRKG 361


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: 457
Number of extensions: 26
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: 366
Length of database: 372
Length adjustment: 30
Effective length of query: 336
Effective length of database: 342
Effective search space:   114912
Effective search space used:   114912
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