GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Azoarcus sp. BH72

Align Leucine-, isoleucine-, valine-, threonine-, and alanine-binding protein; LIVAT-BP; Leu/Ile/Val/Thr/Ala-binding protein (characterized)
to candidate WP_011767451.1 AZO_RS18710 branched-chain amino acid ABC transporter substrate-binding protein

Query= SwissProt::P21175
         (373 letters)



>NCBI__GCF_000061505.1:WP_011767451.1
          Length = 374

 Score =  207 bits (526), Expect = 5e-58
 Identities = 121/352 (34%), Positives = 192/352 (54%), Gaps = 10/352 (2%)

Query: 11  LFAAMAIAGFASYSMAADTIKIALAGPVTGPVAQYGDMQRAGALMAIEQINKAGGVNGAQ 70
           L A +A+ G  S ++A   +KI  AGP+TGP+A +G     GA +A+E  N  G   G Q
Sbjct: 9   LAATLALVG-NSAALAQTVVKIGHAGPLTGPIAHFGKDGEMGARLAVEDANARGITLGGQ 67

Query: 71  ---LEGVIYDDACDPKQAVAVANKVVNDGVKFVVGHVCSSSTQPATDIYEDEGVLMITPS 127
               E V  DD  DP+ A  VA ++ + GVK VVGHV S ++ PA+ +YE  GV ++TPS
Sbjct: 68  KVKFELVSEDDQGDPRTATTVAQRLTDLGVKGVVGHVTSGASIPASRVYEQAGVPVVTPS 127

Query: 128 ATAPEITSRGYKLIFRTIGLDNMQGPVAGKFIAERYKDKTIAVLHDKQQYGEGIATEVKK 187
           +T+P++T +GYK+ FR I  D  QG    K+ AE  K   +A++ D+  YG+G+A     
Sbjct: 128 STSPKLTRQGYKVTFRVIANDLQQGEATAKYAAETLKAAKVAIIDDRTAYGQGLADAFAD 187

Query: 188 TVEDAGIKVAVFEGLNAGDKDFNALISKLKKAGVQFVYFGGYHPEMGLLLRQAKQAGLDA 247
             +  G++V   E       DF A+++K+K      V++GG   +   +LRQ +Q G  A
Sbjct: 188 AAKQRGLQVVGREFTTDKSTDFLAILTKIKAKAPDAVFYGGMDAQAAPMLRQLRQLGSSA 247

Query: 248 RFMGPEGVGNSEITAIAGDASEGML----ATLPRAFEQDPKNKALIDAFKAKNQDPSGIF 303
            ++G +GV   E+  +AGDA    +    A+LP A  + P     +  FK + +    ++
Sbjct: 248 IYLGGDGVCTGEMIKLAGDAMSDKVYCSQASLPPA--KMPGGTDFLSRFKQRYKADVLLY 305

Query: 304 VLPAYSAVTVIAKGIEKAGEADPEKVAEALRANTFETPTGNLGFDEKGDLKN 355
              +Y A T + + ++ A  ++P K   AL+   F+  TG + FD +GD++N
Sbjct: 306 APYSYDAATALIEAMKAADSSEPAKYLPALQRVAFKGVTGEIAFDPQGDIRN 357


Lambda     K      H
   0.316    0.133    0.377 

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: 352
Number of extensions: 18
Number of successful extensions: 3
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: 373
Length of database: 374
Length adjustment: 30
Effective length of query: 343
Effective length of database: 344
Effective search space:   117992
Effective search space used:   117992
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: 50 (23.9 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