GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Sinorhizobium fredii NGR234

Align Solute-binding (Aliphatic amino acid) component of ABC transporter (characterized, see rationale)
to candidate YP_002827025.1 NGR_c25150 ABC transporter substrate-binding protein

Query= uniprot:Q1MDE9
         (367 letters)



>NCBI__GCF_000018545.1:YP_002827025.1
          Length = 372

 Score =  334 bits (856), Expect = 3e-96
 Identities = 169/353 (47%), Positives = 227/353 (64%), Gaps = 1/353 (0%)

Query: 10  LVASLAFAPLAHADITIGLIAPLTGPVAAYGDQVKNGAQTAVDEINKKGGILGEKVVLEL 69
           L A +AF+  A AD+ +G+  PLTGP AA+G Q++ GA+ A  +IN  GGI GE++ L L
Sbjct: 11  LTAMVAFSGTAWADLLVGVAGPLTGPNAAFGAQLQKGAEQAAADINAAGGINGEQIKLVL 70

Query: 70  ADDAGEPKQGVSAANKVVGDGIRFVVGPVTSGVAIPVSDVLAENGVLMVTPTATAPDLTK 129
            DD  +PKQG+S ANK V DG++FVVG   SGV+IP S+V AENG+L +TP+AT P  T+
Sbjct: 71  GDDVSDPKQGISVANKFVADGVKFVVGHFNSGVSIPASEVYAENGILEITPSATNPQFTE 130

Query: 130 RGLTNVLRTCGRDDQQAEVAAKYVLKNFKDKRVAIVNDKGAYGKGLADAFKATLNAGGIT 189
           RG+ N  RTCGRDDQQ  VA  Y+  NFKD ++AI++DK  YG+GLAD  K   N  G+T
Sbjct: 131 RGMWNTFRTCGRDDQQGAVAGAYLAANFKDAKIAIIHDKTPYGQGLADETKKATNEAGLT 190

Query: 190 EVVNDAITPGDKDFSALTTRIKSEKVDVVYFGGYHPEGGLLARQLHDLAANATIIGGDGL 249
           E + + I  GDKDFSAL  ++K   V VVY+GG H E GL+ RQ+ D    AT + GDG+
Sbjct: 191 EALYEGINIGDKDFSALIAKMKEAGVSVVYYGGLHTEAGLIMRQMKDQGLKATFMSGDGI 250

Query: 250 SNTEFWAIGTDAAGGTIFTNASDATKSPDSKAAADALAAKNIPAEAFTLNAYAAVEVLKA 309
            + E  +I  DA  GT+ T A D  K+P SK   +   A     EA+TL +YAA++V+ A
Sbjct: 251 VSNELASIAGDAVDGTLMTFAPDPRKNPASKELVEKFRAAGFEPEAYTLYSYAALQVI-A 309

Query: 310 GIEKAGSAEDAEAVATALKDGKEIPTAIGKVTYGETGDLTSQSFSLYKWEAGK 362
              KA    D +AVA A+K      TAIG++ Y E GD+T   + +Y W+ G+
Sbjct: 310 DAAKAAGGNDPQAVAEAIKAKGPFKTAIGELGYDEKGDITRPDYVMYTWKKGE 362


Lambda     K      H
   0.312    0.131    0.362 

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: 436
Number of extensions: 21
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: 367
Length of database: 372
Length adjustment: 30
Effective length of query: 337
Effective length of database: 342
Effective search space:   115254
Effective search space used:   115254
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