GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Marinobacter adhaerens HP15

Align ABC transporter membrane-spanning permease-branched chain amino acid transport, component of The branched chain hydrophobic amino acid transporter, LivJFGHM (characterized)
to candidate GFF950 HP15_929 branched-chain amino acid ABC transporter, permease protein

Query= TCDB::Q8DQI0
         (292 letters)



>FitnessBrowser__Marino:GFF950
          Length = 315

 Score =  160 bits (404), Expect = 4e-44
 Identities = 94/281 (33%), Positives = 158/281 (56%), Gaps = 3/281 (1%)

Query: 7   QLVNGLILGSVYALLALGYTMVYGIIKLINFAHGDIYMMGAFIGYFLINSFQMNFFVALI 66
           QL+ G+I G+ YALL+LG  +++G++K+INFAHG +YM+GA     + +   +N++VAL+
Sbjct: 35  QLLIGIINGAFYALLSLGLAVIFGLLKIINFAHGAMYMLGAMTTVLMFDYLGVNYWVALL 94

Query: 67  VAMLATAILGVVIEFLAYRPLRHSTRIAVLITAIGVSFLLEYGMVYLVGANTRAFPQA-I 125
           +A L     GV IE+   R +     I  L+   GV+ ++   +V   G +   +    +
Sbjct: 95  LAPLLVGAFGVAIEYFLLRRIAGQDHIYSLLLTFGVALIISGVLVNWFGVSGLRYTMPDM 154

Query: 126 QTVRYDLGPISLTNVQLMILGISLILMILLQVIVQKTKMGKAMRAVSVDSDAAQLMGINV 185
                +LG + +   +  ++  +L++      +++KTK+G  +RA + DS   Q  GINV
Sbjct: 155 FKGGVNLGFMFMPYYRAWVIVAALVVCFATWFVIEKTKLGAYLRAGTEDSQLMQGFGINV 214

Query: 186 NRTISFTFALGSALAGAAGVLIALYYNSLEPLMGVTPGLKSFVAAVLGGIGIIPGAALGG 245
              IS T+  G ALA  AGVL A  Y S+ P+MG    +  F   V+GG+G I GA + G
Sbjct: 215 PLLISLTYGFGVALAAFAGVLAAPIY-SVTPVMGSATLITVFAVVVIGGMGSIGGAIITG 273

Query: 246 FVIGLLETFATAFGMSDFRDAIVYGILLLILIVRPAGILGK 286
            ++G++E     F       AI++ +++L+L+ RP+G+ GK
Sbjct: 274 ILMGVIEGLTKTF-YPPASSAIIFLVMVLVLMFRPSGLFGK 313


Lambda     K      H
   0.330    0.146    0.407 

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: 265
Number of extensions: 17
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: 292
Length of database: 315
Length adjustment: 27
Effective length of query: 265
Effective length of database: 288
Effective search space:    76320
Effective search space used:    76320
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 48 (23.1 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