GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Marinobacter adhaerens HP15

Align Leucine ABC transporter subunit substrate-binding protein LivK (characterized, see rationale)
to candidate GFF3112 HP15_3055 high-affinity leucine-specific leucine-specific-binding periplasmic protein of high-affinity branched-chain amino acid ABC transporter transport system periplasmic binding protein

Query= uniprot:A0A160A0J6
         (375 letters)



>FitnessBrowser__Marino:GFF3112
          Length = 370

 Score =  487 bits (1253), Expect = e-142
 Identities = 241/369 (65%), Positives = 295/369 (79%), Gaps = 4/369 (1%)

Query: 2   TKATKQISKLFAAMVLAGVASHSFAADTIKIGIAGPKTGPVAQYGDMQFSGSKMAIEQIN 61
           T   K ++ +  ++ L G A H  AA  I+IGIAGP TGPVAQYGDMQFSG++MAIEQIN
Sbjct: 3   TSVKKLVTAVSTSVALMG-AGH--AAAEIQIGIAGPMTGPVAQYGDMQFSGARMAIEQIN 59

Query: 62  AKGGVNGKQLVAVEYDDACDPKQAVAVANKVVNDGIKFVVGHLCSSSTQPASDIYEDEGV 121
           A GGV G++LVAVEYDD CDPKQAV VAN +VNDG++FV+GHLCSSSTQPASDIYEDEG+
Sbjct: 60  ANGGVMGEELVAVEYDDVCDPKQAVTVANSLVNDGVRFVIGHLCSSSTQPASDIYEDEGI 119

Query: 122 VMITPAATSPDITARGYKMIFRTIGLDSAQGPAAGNYIADHVKPKIVAVLHDKQQYGEGI 181
           +M+TPA+TSP+IT RGY+++FRTIGLDS QGP A  YIA    P+ VA++HDKQQYGEGI
Sbjct: 120 LMVTPASTSPEITERGYELVFRTIGLDSMQGPVAARYIASQ-NPERVAIVHDKQQYGEGI 178

Query: 182 ASAVKKTLEDKGVKVAVFEGVNAGDKDFSSMIAKLKQANVDFVYYGGYHPELGLILRQSQ 241
           A+AV+ TL+D GV++A+FEG+ AGDKDFSS++ KLKQA+VD+VYYGGYHPELGLILRQ+ 
Sbjct: 179 ATAVRDTLKDAGVEIAMFEGITAGDKDFSSLVTKLKQADVDYVYYGGYHPELGLILRQAN 238

Query: 242 EKGLKAKFMGPEGVGNDSISQIAKESSEGLLVTLPKSFDQDPANIALADAFKAKKEDPSG 301
              L A+FMGPEGVGN  I+ IA E++EGLLVTLP +FDQ   N AL  AF+ K EDPSG
Sbjct: 239 SADLDARFMGPEGVGNKDINTIAGEAAEGLLVTLPPAFDQKAENQALVKAFEDKGEDPSG 298

Query: 302 PFVFPSYSAVTVIADAIKAAKSEDAGKVAEAIHAGTFKTPTGDLSFDKNGDLKDFKFVVY 361
           PFV  SY+AV ++A+ I+AA S D   VA A+  GTF+TP G + +DK GD+K F+FVVY
Sbjct: 299 PFVLTSYTAVQLVAEGIEAAGSTDPFDVAAALREGTFQTPIGTVEYDKAGDMKSFEFVVY 358

Query: 362 EWHFGKPKT 370
           EWH    KT
Sbjct: 359 EWHSDGSKT 367


Lambda     K      H
   0.314    0.132    0.372 

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: 532
Number of extensions: 28
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: 375
Length of database: 370
Length adjustment: 30
Effective length of query: 345
Effective length of database: 340
Effective search space:   117300
Effective search space used:   117300
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 (22.0 bits)
S2: 50 (23.9 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