GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Sinorhizobium fredii NGR234

Align Leucine-, isoleucine-, valine-, threonine-, and alanine-binding protein; LIVAT-BP; Leu/Ile/Val/Thr/Ala-binding protein (characterized)
to candidate YP_002823734.1 NGR_b15300 amino acid ABC transporter substrate-binding protein

Query= SwissProt::P21175
         (373 letters)



>NCBI__GCF_000018545.1:YP_002823734.1
          Length = 364

 Score =  251 bits (642), Expect = 2e-71
 Identities = 135/357 (37%), Positives = 204/357 (57%), Gaps = 10/357 (2%)

Query: 11  LFAAMAIAGFASYSMAADTIKIALAGPVTGPVAQYGDMQRAGALMAIEQINKAGGVNGAQ 70
           L  A  +A    + + A+ I I +AGP+TG +A  G   + GA MA+ +IN AGGV G Q
Sbjct: 5   LVLAAILASTLGFPVQAE-ILIGVAGPMTGKLAWTGTQLKRGAEMAVARINAAGGVLGEQ 63

Query: 71  LEGVIYDDACDPKQAVAVANKVVNDGVKFVVGHVCSSSTQPATDIYEDEGVLMITPSATA 130
           +  ++ DD CD +QAVA A K+V D    V+GH CS ++ PA+ IY   GV+ I+PS+T 
Sbjct: 64  IRLIVADDFCDAQQAVAAAQKLVADKAVLVIGHYCSGASIPASKIYAKAGVVQISPSSTN 123

Query: 131 PEITSRGYKLIFRTIGLDNMQGPVAGKFIAERYKDKTIAVLHDKQQYGEGIATEVKKTVE 190
           P +T +GY  +FR    D+ QG  AG ++A+ + DK IA+LHD   YG+G+A E +K + 
Sbjct: 124 PTLTEQGYANVFRVCSRDDAQGLQAGNYLADHWGDKKIAILHDDTTYGKGLAEETRKQLN 183

Query: 191 DAGIKVAVFEGLNAGDKDFNALISKLKKAGVQFVYFGGYHPEMGLLLRQAKQAGLDARFM 250
             G+   +++    G  D++A I+  + AG+  +Y GGYH E  L++R A++     + +
Sbjct: 184 KRGVNETIYQSYEPGKDDYSAEIAGFQTAGIAVLYLGGYHTEAALMVRAARERAYPVQVI 243

Query: 251 GPEGVGNSEITAIAGDASEGMLATLPRAFEQDPKNKA----LIDAFKAKNQDPSGIFVLP 306
             +         IAG A+EG L T    F  DP+  A    ++  F+A+N +P   + L 
Sbjct: 244 SGDDTATEAFGLIAGPAAEGTLFT----FVADPRRNAEAADVVARFRAENFEPDS-WTLH 298

Query: 307 AYSAVTVIAKGIEKAGEADPEKVAEALRANTFETPTGNLGFDEKGDLKNFDFTVYEW 363
           +Y A  V A+ + KAG  DP+K+ E LR   F+T  G + FDEKGDL   ++  Y W
Sbjct: 299 SYGAAEVWAQAVRKAGSLDPQKITETLRKYQFDTVLGRIDFDEKGDLTVQNWVWYVW 355


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: 330
Number of extensions: 18
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: 373
Length of database: 364
Length adjustment: 30
Effective length of query: 343
Effective length of database: 334
Effective search space:   114562
Effective search space used:   114562
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 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