GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Methylobacterium nodulans ORS 2060

Align Leucine ABC transporter subunit substrate-binding protein LivK (characterized, see rationale)
to candidate WP_043750690.1 MNOD_RS08385 branched-chain amino acid ABC transporter substrate-binding protein

Query= uniprot:A0A160A0J6
         (375 letters)



>NCBI__GCF_000022085.1:WP_043750690.1
          Length = 372

 Score =  295 bits (756), Expect = 1e-84
 Identities = 156/353 (44%), Positives = 220/353 (62%), Gaps = 2/353 (0%)

Query: 15  MVLAGVASHSFAADTIKIGIAGPKTGPVAQYGDMQFSGSKMAIEQINAKGGVNGKQLVAV 74
           ++ AG+A    A   IK+ +AGP TGP A +G    +G+  A+E IN  GG+ GK++  V
Sbjct: 7   VLAAGLAWAGSAQAQIKLAVAGPITGPNAAFGAQLKNGATQAVEDINKAGGILGKKIEIV 66

Query: 75  EYDDACDPKQAVAVANKVVNDGIKFVVGHLCSSSTQPASDIYEDEGVVMITPAATSPDIT 134
            YDDA DPKQ V+VA+K  ++ +  VVGH  S  + PAS++Y + G+V ITPA+T+P  T
Sbjct: 67  IYDDASDPKQGVSVASKAGSEKVVAVVGHFNSGVSIPASEVYAESGIVEITPASTNPKFT 126

Query: 135 ARGYKMIFRTIGLDSAQGPAAGNYIADHVKPKIVAVLHDKQQYGEGIASAVKKTLEDKGV 194
            R     FRT G D  QG  AG Y+A H K K +A++HDK  YG G+A    K L+ KG 
Sbjct: 127 DRKLWNTFRTCGRDDQQGAVAGAYLAQHFKGKNIAIVHDKTPYGRGLADETLKALKAKGG 186

Query: 195 KVAVFEGVNAGDKDFSSMIAKLKQANVDFVYYGGYHPELGLILRQSQEKGLKAKFMGPEG 254
           K  +FEG+N G+KD+S++++KLKQA  D VYYGG H E GLI+RQ  ++GL A  M  +G
Sbjct: 187 KEVLFEGINPGEKDYSALVSKLKQAKADVVYYGGLHTEAGLIVRQMHDQGLNAPLMSGDG 246

Query: 255 VGNDSISQIAKESSEGLLVTLPKSFDQDPANIALADAFKAKKEDPSGPFVFPSYSAVTVI 314
           + +   +QIA   ++G L+T      ++P    +  AFKAK  DP   +   SY+AV ++
Sbjct: 247 ITDKEFAQIAGPGADGTLMTFSPDARKNPNAKDVVAAFKAKNIDPEA-YTLYSYAAVQIL 305

Query: 315 ADAIKAAKSEDAGKVAEAIHAG-TFKTPTGDLSFDKNGDLKDFKFVVYEWHFG 366
             A++ AKS D  KVAE + +G TFKT  GD+S+DK GD+    +V+Y W  G
Sbjct: 306 KTAMEDAKSTDGKKVAEVMRSGKTFKTVIGDISYDKKGDITRPDYVMYMWKKG 358


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: 415
Number of extensions: 21
Number of successful extensions: 4
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: 372
Length adjustment: 30
Effective length of query: 345
Effective length of database: 342
Effective search space:   117990
Effective search space used:   117990
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 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