GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Azospirillum sp. B510

Align Solute-binding (Aliphatic amino acid) component of ABC transporter (characterized, see rationale)
to candidate WP_042446662.1 AZL_RS31475 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:Q1MDE9
         (367 letters)



>NCBI__GCF_000010725.1:WP_042446662.1
          Length = 366

 Score =  318 bits (814), Expect = 2e-91
 Identities = 160/358 (44%), Positives = 223/358 (62%), Gaps = 2/358 (0%)

Query: 5   TLTATLVASLAFAPLAHADITIGLIAPLTGPVAAYGDQVKNGAQTAVDEINKKGGILGEK 64
           +L A + A+   A  A ADI +    P+TG  A +G+Q+K G + AV +IN  GG+LG+K
Sbjct: 6   SLLAAIAATALSATAAKADIAVATAGPITGQYATFGEQMKKGMEQAVADINAAGGVLGQK 65

Query: 65  VVLELADDAGEPKQGVSAANKVVGDGIRFVVGPVTSGVAIPVSDVLAENGVLMVTPTATA 124
           + LE+ DDA +PKQ V+ AN++   G++FV G   SG +IP S V +E G+L ++P +T 
Sbjct: 66  LKLEVGDDACDPKQAVAVANQLAKAGVKFVAGHFCSGSSIPASQVYSEEGILQISPASTN 125

Query: 125 PDLTKRGLTNVLRTCGRDDQQAEVAAKYVLKNFKDKRVAIVNDKGAYGKGLADAFKATLN 184
           P LT++GL NV R CGRDDQQ  +A KY+L  +K K VAI++DK AYGKGLAD  +  LN
Sbjct: 126 PKLTEQGLKNVFRVCGRDDQQGAIAGKYLLDTYKGKNVAILHDKSAYGKGLADETQKALN 185

Query: 185 AGGITEVVNDAITPGDKDFSALTTRIKSEKVDVVYFGGYHPEGGLLARQLHDLAANATII 244
           AGG  E + +A T G+KD+SAL +++K   VD VY GGYH E GL+ARQ+ D    A I+
Sbjct: 186 AGGQKETIYEAYTAGEKDYSALVSKLKQANVDAVYIGGYHTEAGLIARQMKDQGLKAIIV 245

Query: 245 GGDGLSNTEFWAIGTDAAGGTIFTNASDATKSPDSKAAADALAAKNIPAEAFTLNAYAAV 304
            GD L   E+WAI  DA   T+ T   D  + PD+KA  +         E +TL  YAA+
Sbjct: 246 SGDALVTNEYWAITGDAGEDTMMTFGPDPREKPDAKAVVEKFRKAGYEPEGYTLYTYAAL 305

Query: 305 EVLKAGIEKAGSAEDAEAVATALKDGKEIPTAIGKVTYGETGDLTSQSFSLYKWEAGK 362
           ++    +++A S  DA  VA  L+ G    T IGK+ +   GD+TS ++  YKW AG+
Sbjct: 306 QIWANAVKQANST-DAAKVADVLRKG-SYDTVIGKIGFDAKGDVTSPAYVWYKWHAGQ 361


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: 410
Number of extensions: 23
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: 366
Length adjustment: 30
Effective length of query: 337
Effective length of database: 336
Effective search space:   113232
Effective search space used:   113232
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 Apr 09 2024. 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