GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Magnetospirillum magneticum AMB-1

Align Solute-binding (Aliphatic amino acid) component of ABC transporter (characterized, see rationale)
to candidate WP_011385357.1 AMB_RS15010 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:Q1MDE9
         (367 letters)



>NCBI__GCF_000009985.1:WP_011385357.1
          Length = 366

 Score =  313 bits (803), Expect = 4e-90
 Identities = 162/354 (45%), Positives = 222/354 (62%), Gaps = 2/354 (0%)

Query: 9   TLVASLAFAPLAHADITIGLIAPLTGPVAAYGDQVKNGAQTAVDEINKKGGILGEKVVLE 68
           TL A+L  A  A ADITIG+  PL+G  AA+G+Q K GA  AV++IN KGG+LG+K+ L 
Sbjct: 10  TLAAALLMAGAARADITIGVAGPLSGSEAAFGEQFKRGAMKAVEDINAKGGVLGQKLALT 69

Query: 69  LADDAGEPKQGVSAANKVVGDGIRFVVGPVTSGVAIPVSDVLAENGVLMVTPTATAPDLT 128
           L DDA +PKQ V+ AN++    + FV G   SG +IP S+V AE G+L ++P +T P  T
Sbjct: 70  LGDDACDPKQAVAVANEMAAKKVPFVAGHFCSGSSIPASEVYAETGILQISPASTNPKFT 129

Query: 129 KRGLTNVLRTCGRDDQQAEVAAKYVLKNFKDKRVAIVNDKGAYGKGLADAFKATLNAGGI 188
           +RGL N+ RTCGRDDQQ  +AA Y+ K+ KDK VAIV+DK AYGKGLAD  +  L   GI
Sbjct: 130 ERGLPNIFRTCGRDDQQGVIAADYIAKHQKDKVVAIVHDKSAYGKGLADQTRDALGKAGI 189

Query: 189 TEVVNDAITPGDKDFSALTTRIKSEKVDVVYFGGYHPEGGLLARQLHDLAANATIIGGDG 248
              + +AI+ G+KD+SAL T++K+ KVD++YFGGY  E GL+ RQL D      ++GGD 
Sbjct: 190 KAALYEAISAGEKDYSALVTKLKASKVDLLYFGGYKTEAGLIVRQLRDQGMQTRLMGGDA 249

Query: 249 LSNTEFWAIGTDAAGGTIFTNASDATKSPDSKAAADALAAKNIPAEAFTLNAYAAVEVLK 308
           L   E+WAI   A  GT+ T + D  K+P +        A+    EA+TL  Y  ++   
Sbjct: 250 LVTEEYWAITGAAGEGTMMTFSPDPRKNPANADLVKYYRAQKYEPEAYTLYTYGTIQAWA 309

Query: 309 AGIEKAGSAEDAEAVATALKDGKEIPTAIGKVTYGETGDLTSQSFSLYKWEAGK 362
              EKA    D + VA  LK  ++  TAIGK+ +   GD+ +  + +Y W+ GK
Sbjct: 310 QAAEKA-KTTDWKKVAAVLK-AEKFDTAIGKIGFDAKGDVAAPGYVMYVWKGGK 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: 389
Number of extensions: 11
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 Sep 17 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