GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Herbaspirillum seropedicae SmR1

Align Leucine ABC transporter subunit substrate-binding protein LivK (characterized, see rationale)
to candidate HSERO_RS08270 HSERO_RS08270 amino acid ABC transporter substrate-binding protein

Query= uniprot:A0A160A0J6
         (375 letters)



>FitnessBrowser__HerbieS:HSERO_RS08270
          Length = 373

 Score =  450 bits (1158), Expect = e-131
 Identities = 228/362 (62%), Positives = 275/362 (75%), Gaps = 7/362 (1%)

Query: 12  FAAMVLAGVASHSFAADTIKIGIAGPKTGPVAQYGDMQFSGSKMAIEQINAKGGVNGKQL 71
           FAA   AGVA     A+T+KI IAGP TG VAQYGDM  +G+  AIEQINA GG NG + 
Sbjct: 17  FAAF--AGVAH----AETVKIAIAGPMTGAVAQYGDMVKAGALTAIEQINAAGGANGNKF 70

Query: 72  VAVEYDDACDPKQAVAVANKVVNDGIKFVVGHLCSSSTQPASDIYEDEGVVMITPAATSP 131
            AV  DDAC+PKQAVAVANK+V+ GIK+V+GH+CS ST PASDIYE+EGVVMITP+AT+P
Sbjct: 71  EAVMMDDACEPKQAVAVANKIVSQGIKYVIGHVCSGSTIPASDIYENEGVVMITPSATAP 130

Query: 132 DIT-ARGYKMIFRTIGLDSAQGPAAGNYIADHVKPKIVAVLHDKQQYGEGIASAVKKTLE 190
            +T A+ +K IFRTIG D  QGPAA  Y+ + +KPK VAVLHDKQ YG+G+AS+VK  L+
Sbjct: 131 QLTEAKPHKFIFRTIGRDDQQGPAAARYVIEKLKPKKVAVLHDKQSYGQGVASSVKAALD 190

Query: 191 DKGVKVAVFEGVNAGDKDFSSMIAKLKQANVDFVYYGGYHPELGLILRQSQEKGLKAKFM 250
              V V VFEG+NAGD D+S+++ KLK   VDFVY+GGYHPE+GLI+RQ++E+G+KA FM
Sbjct: 191 AAKVPVVVFEGINAGDSDYSAIVTKLKSQGVDFVYFGGYHPEMGLIMRQAREQGIKAVFM 250

Query: 251 GPEGVGNDSISQIAKESSEGLLVTLPKSFDQDPANIALADAFKAKKEDPSGPFVFPSYSA 310
           GPEGVGN  I+ IA  +SEG+LVTLP  F  DPAN AL  AF A K DP+GPF  P+YS 
Sbjct: 251 GPEGVGNKDITAIAGPASEGMLVTLPADFAADPANAALVKAFAAAKRDPNGPFQMPAYSG 310

Query: 311 VTVIADAIKAAKSEDAGKVAEAIHAGTFKTPTGDLSFDKNGDLKDFKFVVYEWHFGKPKT 370
           V +IADAI  AKS D  KVA  IHA +FKTP G++ +DK GDLK FKFVV+ WH    KT
Sbjct: 311 VKIIADAIAGAKSTDPEKVAAYIHANSFKTPIGNVEYDKKGDLKSFKFVVFTWHKDASKT 370

Query: 371 EA 372
           EA
Sbjct: 371 EA 372


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: 559
Number of extensions: 28
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 375
Length of database: 373
Length adjustment: 30
Effective length of query: 345
Effective length of database: 343
Effective search space:   118335
Effective search space used:   118335
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